Patent application title: COMPOSITIONS FOR USE IN IDENTIFICATION OF ALPHAVIRUSES
Rangarajan Sampath (San Diego, CA, US)
Thomas A. Hall (Oceanside, CA, US)
Mark W. Eshoo (Solana Beach, CA, US)
IBIS BIOSCIENCES, INC.
IPC8 Class: AG01N2762FI
Class name: Chemistry: molecular biology and microbiology measuring or testing process involving enzymes or micro-organisms; composition or test strip therefore; processes of forming such composition or test strip involving virus or bacteriophage
Publication date: 2012-09-27
Patent application number: 20120244522
The present invention provides oligonucleotide primers and compositions
and kits containing the same for rapid identification of alphaviruses by
amplification of a segment of viral nucleic acid followed by molecular
12. A method for identification of an unknown alphavirus comprising: amplifying nucleic acid from said alphavirus using a composition comprising a purified oligonucleotide primer pair configured to generate amplicons from two or more members of the alphavirus genus by hybridizing a forward primer and a reverse primer to conserved regions of a nsP1 encoding gene in two or more members of said alphavirus genus, said primer pair comprising a forward primer with 100% sequence identity with SEQ ID NO: 93 and a reverse primer with 100% sequence identity with SEQ ID NO: 66 to obtain an amplification product; measuring the molecular mass of said amplification product; optionally, determining the base composition of said amplification product from said molecular mass; and comparing said molecular mass or base composition with a plurality of molecular masses or base compositions of known alphaviral bioagent identifying amplicons, wherein a match between said molecular mass or base composition and a member of said plurality of molecular masses or base compositions identifies said unknown alphavirus.
13. The method of claim 12 wherein said molecular mass is measured by mass spectrometry.
16. A method for determination of the quantity of an unknown alphavirus in a sample comprising: contacting said sample with a composition comprising a purified oligonucleotide primer pair configured to generate amplicons from two or more members of the alphavirus genus by hybridizing a forward primer and a reverse primer to conserved regions of a nsP1 encoding gene in two or more members of said alphavirus genus, said primer pair comprising a forward primer with 100% sequence identity with SEQ ID NO: 93 and a reverse primer with 100% sequence identity with SEQ ID NO: 66 and a known quantity of a calibration polynucleotide comprising a calibration sequence; concurrently amplifying nucleic acid from said alphavirus in said sample with said composition and amplifying nucleic acid from said calibration polynucleotide in said sample with said composition to obtain a first amplification product comprising an alphaviral bioagent identifying amplicon and a second amplification product comprising a calibration amplicon; determining the molecular mass and abundance for said alphaviral bioagent identifying amplicon and said calibration amplicon; and distinguishing said alphaviral bioagent identifying amplicon from said calibration amplicon based on molecular mass, wherein comparison of alphaviral bioagent identifying amplicon abundance and calibration amplicon abundance indicates the quantity of alphavirus in said sample.
17. The method of claim 16 further comprising determining the base composition of said alphaviral bioagent identifying amplicon.
18. The composition of claim 12 wherein either or both of said oligonucleotide primers comprises at least one modified nucleobase.
19. The composition of claim 12 wherein either or both of said oligonucleotide primers comprises a non-templated T residue on the 5' end.
20. The composition of claim 12 wherein either or both of said oligonucleotide primers comprises at least one non-template tag.
21. The composition of claim 1 wherein either or both of said oligonucleotide primers comprises at least one molecular mass modifying tag.
22. A method for identification of an unknown alphavirus comprising: amplifying nucleic acid from said alphavirus using a composition comprising a purified oligonucleotide primer pair configured to generate amplicons from two or more members of the alphavirus genus by hybridizing a forward primer and a reverse primer to conserved regions of a nsP1 encoding gene in two or more members of said alphavirus genus, said primer pair comprising a forward primer with 100% sequence identity with SEQ ID NO: 21 and a reverse primer with 100% sequence identity with SEQ ID NO: 66 to obtain an amplification product; measuring the molecular mass of said amplification product; optionally, determining the base composition of said amplification product from said molecular mass; and comparing said molecular mass or base composition with a plurality of molecular masses or base compositions of known alphaviral bioagent identifying amplicons, wherein a match between said molecular mass or base composition and a member of said plurality of molecular masses or base compositions identifies said unknown alphavirus.
CROSS-REFERENCE TO RELATED APPLICATIONS
 This application is a divisional of U.S. patent application Ser. No. 11/070,632, filed Mar. 2, 2005, which claims the benefit of priority to U.S. Provisional Application Ser. No. 60/550,023, filed Mar. 3, 2004, which is incorporated herein by reference in its entirety.
FIELD OF THE INVENTION
 The present invention relates generally to the field of genetic identification and quantification of alphaviruses and provides methods, compositions and kits useful for this purpose, as well as others, when combined with molecular mass analysis.
BACKGROUND OF THE INVENTION
 Togaviridae is a family of viruses that includes the genus alphavirus. Alphaviruses are enveloped viruses with a linear, positive-sense single-stranded RNA genome. Members of the alphavirus genus include at least 30 species of arthropod-borne viruses, including Aura (AURA), Babanki (BAB), Barmah Forest (BF), Bebaru (BEB), Buggy Creek, Cabassou (CAB), Chikungunya (CHIK), Eastern equine encephalitis (EEE), Everglades (EVE), Fort Morgan (FM), Getah (GET), Highlands J (HJ), Kyzylagach (KYZ), Mayaro (MAY), Middelburg (MID), Mucambo (MUC), Ndumu (NDU), O' nyong-nyong (ONN), Pixuna (PIX), Ross River (RR), Sagiyama (SAG), Salmon pancreas disease (SPDV), Semliki Forest (SF), Una (UNA), Venezuelan equine encephalitis (VEE), Western equine encephalitis (WEE) and Whataroa (WHA) virus ("The Springer Index of Viruses," pgs. 1148-1155, Tidona and Darai eds., 2001, Springer, New York; Strauss and Strauss, Microbiol. Rev., 1994, 58, 491-562). Alphaviruses are evolutionarily differentiated based on nucleotide sequence of the nonstructural proteins, of which there are four (nsP1, nsP2, nsP3 and nsP4). The genus segregates into New World (American) and Old World (Eurasian/African/Australasian) alphaviruses based on geographic distribution. It is estimated that New World and Old World viruses diverged between 2,000 and 3,000 years ago (Harley et al., Clin. Microbiol. Rev., 2001, 14, 909-932).
 Among the alphavirus species, there are seven distinct serocomplexes (SF, EEE, MID, NDU, VEE, WEE and BFV) into which members of the genus are sub-divided (Khan et al., J. Gen. Virol., 2002, 83, 3075-3084; Harley et al., Clin. Microbiol. Rev., 2001, 14, 909-932). Based on genomic sequence data from six of the seven serocomplexes, alphaviruses have been grouped into three large groups VEE/EEE, SFV and SIN. The VEE-EEE group is exclusively made up of New World viruses with a distribution in North America, South America and Central America. Members of this group include EEE, VEE, EVE, MUC and PIX. The SF group is primarily Old World, but contains one member (MAY) that is found in South America. Other members of the SF group include SF, MID, CHIK, ONN, RR, BF, GET, SAG, BEB and UNA. The SIN group is also primarily Old World, with the exception of AURA, which is a New World virus related to SIN and can be found in Brazil and Argentina. Other members of this group include SIN, WHA, BAB and KYZ. WEE, HJ and FM are considered recombinant viruses and are thus not included in any of the three groups. NDU and Buggy Creek are currently unclassified.
 Many members of the alphavirus genus pose a significant health risk to humans, as well as horses, in many different geographic regions. EEE and WEE both cause a fatal encephalitis in humans and horses; however, EEE is more virulent with a mortality rate up to 50%, compared with 3-4% for WEE. VEE can also cause disease in humans and horses, but symptoms are typically flu-like and rarely lead to encephalitis. The geographic distribution for the encephalitis viruses is primarily in the Americas ("The Springer Index of Viruses," pgs. 1148-1155, Tidona and Darai eds., 2001, Springer, New York; Strauss and Strauss, Microbiol. Rev., 1994, 58, 491-562).
 The SIN group of Old World viruses, including RR, ONN and CHIK, have been associated with outbreaks of acute and persistent arthritis and arthralgia (joint pain) in humans. Epidemics of acute, debilitating arthralgia have been caused by ONN and CHIK in Africa and Asia. RR, which is the etiological agent of epidemic polyarthritis, is endemic to Australia and caused a major epidemic throughout the Pacific islands in 1979. The outbreak affected over 50,000 people on the island of Fiji. Other alphaviruses have been linked to acute and persistent arthralgia in northern Europe and South Africa. Although each virus induces a somewhat different disease, infection with RR, ONN or CHIK typically causes symptoms such as generalized to severe joint pain, fever, rash, headache, nausea, myalgia and lymphadenitis. It has been reported that arthralgia associated with alphavirus infection can persist for months or years. CHIK has also been associated with a fatal hemorrhagic condition ("The Springer Index of Viruses," pgs. 1148-1155, Tidona and Darai eds., 2001, Springer, New York; Strauss and Strauss, Microbiol. Rev., 1994, 58, 491-562; Hossain et al., J. Gen. Virol., 2002, 83, 3075-3084).
 Another alphavirus causing human disease and mortality is MAY, which is found in the Caribbean and South America. Mayaro virus infection causes fever, rash and arthropathy (diseases of the joint), and exhibits a mortality rate of up to 7% ("The Springer Index of Viruses," pgs. 1148-1155, Tidona and Darai eds., 2001, Springer, New York).
B. Bioagent Detection
 A problem in determining the cause of a natural infectious outbreak or a bioterrorist attack is the sheer variety of organisms that can cause human disease. There are over 1400 organisms infectious to humans; many of these have the potential to emerge suddenly in a natural epidemic or to be used in a malicious attack by bioterrorists (Taylor et al., Philos. Trans. R. Soc. London B. Biol. Sci., 2001, 356, 983-989). This number does not include numerous strain variants, bioengineered versions, or pathogens that infect plants or animals.
 Much of the new technology being developed for detection of biological weapons incorporates a polymerase chain reaction (PCR) step based upon the use of highly specific primers and probes designed to selectively detect individual pathogenic organisms. Although this approach is appropriate for the most obvious bioterrorist organisms, like smallpox and anthrax, experience has shown that it is very difficult to predict which of hundreds of possible pathogenic organisms might be employed in a terrorist attack. Likewise, naturally emerging human disease that has caused devastating consequence in public health has come from unexpected families of bacteria, viruses, fungi, or protozoa. Plants and animals also have their natural burden of infectious disease agents and there are equally important biosafety and security concerns for agriculture.
 An alternative to single-agent tests is to do broad-range consensus priming of a gene target conserved across groups of bioagents. Broad-range priming has the potential to generate amplification products across entire genera, families, or, as with bacteria, an entire domain of life. This strategy has been successfully employed using consensus 16S ribosomal RNA primers for determining bacterial diversity, both in environmental samples (Schmidt et al., J. Bact., 1991, 173, 4371-4378) and in natural human flora (Kroes et al., Proc Nat Acad Sci (USA), 1999, 96, 14547-14552). The drawback of this approach for unknown bioagent detection and epidemiology is that analysis of the PCR products requires the cloning and sequencing of hundreds to thousands of colonies per sample, which is impractical to perform rapidly or on a large number of samples.
 Conservation of sequence is not as universal for viruses, however, large groups of viral species share conserved protein-coding regions, such as regions encoding viral polymerases or helicases. Like bacteria, consensus priming has also been described for detection of several viral families, including coronaviruses (Stephensen et al., Vir. Res., 1999, 60, 181-189), enteroviruses (Oberste et al., J. Virol., 2002, 76, 1244-51); Oberste et al., J. Clin. Virol., 2003, 26, 375-7); Oberste et al., Virus Res., 2003, 91, 241-8), retroid viruses (Mack et al., Proc. Natl. Acad. Sci. U.S.A., 1988, 85, 6977-81); Seifarth et al., AIDS Res. Hum. Retroviruses, 2000, 16, 721-729); Donehower et al., J. Vir. Methods, 1990, 28, 33-46), and adenoviruses (Echavarria et al., J. Clin. Micro., 1998, 36, 3323-3326). However, as with bacteria, there is no adequate analytical method other than sequencing to identify the viral bioagent present.
 In contrast to PCR-based methods, mass spectrometry provides detailed information about the molecules being analyzed, including high mass accuracy. It is also a process that can be easily automated. DNA chips with specific probes can only determine the presence or absence of specifically anticipated organisms. Because there are hundreds of thousands of species of benign pathogens, some very similar in sequence to threat organisms, even arrays with 10,000 probes lack the breadth needed to identify a particular organism.
 There is a need for a method for identification of bioagents which is both specific and rapid, and in which no culture or nucleic acid sequencing is required. Disclosed in U.S. Pre-Grant Publication Nos. 2003-0027135, 2003-0082539, 2003-0228571, 2004-0209260, 2004-0219517 and 2004-0180328, and in U.S. application Ser. Nos. 10/660,997, 10/728,486, 10/754,415 and 10/829,826, all of which are commonly owned and incorporated herein by reference in their entirety, are methods for identification of bioagents (any organism, cell, or virus, living or dead, or a nucleic acid derived from such an organism, cell or virus) in an unbiased manner by molecular mass and base composition analysis of "bioagent identifying amplicons" which are obtained by amplification of segments of essential and conserved genes which are involved in, for example, translation, replication, recombination and repair, transcription, nucleotide metabolism, amino acid metabolism, lipid metabolism, energy generation, uptake, secretion and the like. Examples of these proteins include, but are not limited to, ribosomal RNAs, ribosomal proteins, DNA and RNA polymerases, RNA-dependent RNA polymerases, RNA capping and methylation enzymes, elongation factors, tRNA synthetases, protein chain initiation factors, heat shock protein groEL, phosphoglycerate kinase, NADH dehydrogenase, DNA ligases, DNA gyrases and DNA topoisomerases, helicases, metabolic enzymes, and the like.
 To obtain bioagent identifying amplicons, primers are selected to hybridize to conserved sequence regions which bracket variable sequence regions to yield a segment of nucleic acid which can be amplified and which is amenable to methods of molecular mass analysis. The variable sequence regions provide the variability of molecular mass which is used for bioagent identification. Upon amplification by PCR or other amplification methods with the specifically chosen primers, an amplification product that represents a bioagent identifying amplicon is obtained. The molecular mass of the amplification product, obtained by mass spectrometry for example, provides the means to uniquely identify the bioagent without a requirement for prior knowledge of the possible identity of the bioagent. The molecular mass of the amplification product or the corresponding base composition (which can be calculated from the molecular mass of the amplification product) is compared with a database of molecular masses or base compositions and a match indicates the identity of the bioagent. Furthermore, the method can be applied to rapid parallel analyses (for example, in a multi-well plate format) the results of which can be employed in a triangulation identification strategy which is amenable to rapid throughput and does not require nucleic acid sequencing of the amplified target sequence for bioagent identification.
 The result of determination of a previously unknown base composition of a previously unknown bioagent (for example, a newly evolved and heretofore unobserved virus) has downstream utility by providing new bioagent indexing information with which to populate base composition databases. The process of subsequent bioagent identification analyses is thus greatly improved as more base composition data for bioagent identifying amplicons becomes available.
 The present invention provides methods of identifying unknown viruses, including viruses of the Togaviridae family and alphavirus genus. Also provided are oligonucleotide primers, compositions and kits containing the oligonucleotide primers, which define alphaviral identifying amplicons and, upon amplification, produce corresponding amplification products whose molecular masses provide the means to identify alphaviruses at the sub-species level.
SUMMARY OF THE INVENTION
 The present invention provides primers and compositions comprising pairs of primers, and kits containing the same for use in identification of alphaviruses. The primers are designed to produce alphaviral bioagent identifying amplicons of DNA encoding genes essential to alphavirus replication. The invention further provides compositions comprising pairs of primers and kits containing the same, which are designed to provide species and sub-species characterization of alphaviruses.
BRIEF DESCRIPTION OF THE DRAWINGS
 FIG. 1 is a process diagram illustrating a representative primer selection process.
 FIG. 2 is a representative process diagram for identification and determination of the quantity of a bioagent in a sample.
 FIG. 3 is a pseudo four-dimensional plot of expected base compositions of alphavirus identifying amplicons obtained from amplification with primer pair no: 316 the epidemic, epizootic VEEV viruses of classes IAB-IC, ID and IIIA (which have the potential to cause severe disease in humans and animals) can be distinguished from the enzootic VEE types IE, IF, I, IIIB, IIIC, IV, V, and VI, which, in turn, are generally distinguishable from each other.
 In the context of the present invention, a "bioagent" is any organism, cell, or virus, living or dead, or a nucleic acid derived from such an organism, cell or virus. Examples of bioagents include, but are not limited, to cells, including but not limited to human clinical samples, cell cultures, bacterial cells and other pathogens), viruses, viroids, fungi, protists, parasites, and pathogenicity markers (including but not limited to: pathogenicity islands, antibiotic resistance genes, virulence factors, toxin genes and other bioregulating compounds). Samples may be alive or dead or in a vegetative state (for example, vegetative bacteria or spores) and may be encapsulated or bioengineered. In the context of this invention, a "pathogen" is a bioagent which causes a disease or disorder.
 As used herein, "intelligent primers" are primers that are designed to bind to highly conserved sequence regions of a bioagent identifying amplicon that flank an intervening variable region and yield amplification products which ideally provide enough variability to distinguish each individual bioagent, and which are amenable to molecular mass analysis. By the term "highly conserved," it is meant that the sequence regions exhibit between about 80-100%, or between about 90-100%, or between about 95-100% identity among all or at least 70%, at least 80%, at least 90%, at least 95%, or at least 99% of species or strains.
 As used herein, "broad range survey primers" are intelligent primers designed to identify an unknown bioagent at the genus level. In some cases, broad range survey primers are able to identify unknown bioagents at the species or sub-species level. As used herein, "division-wide primers" are intelligent primers designed to identify a bioagent at the species level and "drill-down" primers are intelligent primers designed to identify a bioagent at the sub-species level. As used herein, the "sub-species" level of identification includes, but is not limited to, strains, subtypes, variants, and isolates.
 As used herein, a "bioagent division" is defined as group of bioagents above the species level and includes but is not limited to, orders, families, classes, clades, genera or other such groupings of bioagents above the species level.
 As used herein, a "sub-species characteristic" is a genetic characteristic that provides the means to distinguish two members of the same bioagent species. For example, one viral strain could be distinguished from another viral strain of the same species by possessing a genetic change (e.g., for example, a nucleotide deletion, addition or substitution) in one of the viral genes, such as the RNA-dependent RNA polymerase. In this case, the sub-species characteristic that can be identified using the methods of the present invention, is the genetic change in the viral polymerase.
 As used herein, the term "bioagent identifying amplicon" refers to a polynucleotide that is amplified from a bioagent in an amplification reaction and which 1) provides enough variability to distinguish each individual bioagent and 2) whose molecular mass is amenable to molecular mass determination.
 As used herein, a "base composition" is the exact number of each nucleobase (A, T, C and G) in a given sequence.
 As used herein, a "base composition signature" (BCS) is the exact base composition (i.e., the number of A, T, G and C nucleobases) determined from the molecular mass of a bioagent identifying amplicon.
 As used herein, a "base composition probability cloud" is a representation of the diversity in base composition resulting from a variation in sequence that occurs among different isolates of a given species. The "base composition probability cloud" represents the base composition constraints for each species and is typically visualized using a pseudo four-dimensional plot.
 As used herein, a "wobble base" is a variation in a codon found at the third nucleotide position of a DNA triplet. Variations in conserved regions of sequence are often found at the third nucleotide position due to redundancy in the amino acid code.
 In the context of the present invention, the term "unknown bioagent" may mean either: (i) a bioagent whose existence is known (such as the well known bacterial species Staphylococcus aureus for example) but which is not known to be in a sample to be analyzed, or (ii) a bioagent whose existence is not known (for example, the SARS coronavirus was unknown prior to April 2003). For example, if the method for identification of coronaviruses disclosed in commonly owned U.S. patent Ser. No. 10/829,826 (incorporated herein by reference in its entirety) was to be employed prior to April 2003 to identify the SARS coronavirus in a clinical sample, both meanings of "unknown" bioagent are applicable since the SARS coronavirus was unknown to science prior to April, 2003 and since it was not known what bioagent (in this case a coronavirus) was present in the sample. On the other hand, if the method of U.S. patent Ser. No. 10/829,826 was to be employed subsequent to April 2003 to identify the SARS coronavirus in a clinical sample, only the first meaning (i) of "unknown" bioagent would apply since the SARS coronavirus became known to science subsequent to April 2003 and since it was not known what bioagent was present in the sample.
 As used herein, "triangulation identification" means the employment of more than one bioagent identifying amplicons for identification of a bioagent.
 In the context of the present invention, "viral nucleic acid" includes, but is not limited to, DNA, RNA, or DNA that has been obtained from viral RNA, such as, for example, by performing a reverse transcription reaction. Viral RNA can either be single-stranded (of positive or negative polarity) or double-stranded.
 As used herein, the term "etiology" refers to the causes or origins, of diseases or abnormal physiological conditions.
 As used herein, the term "nucleobase" is synonymous with other terms in use in the art including "nucleotide," "deoxynucleotide," "nucleotide residue," "deoxynucleotide residue," "nucleotide triphosphate (NTP)," or deoxynucleotide triphosphate (dNTP).
 The present invention provides methods for detection and identification of bioagents in an unbiased manner using bioagent identifying amplicons. Intelligent primers are selected to hybridize to conserved sequence regions of nucleic acids derived from a bioagent and which bracket variable sequence regions to yield a bioagent identifying amplicon which can be amplified and which is amenable to molecular mass determination. The molecular mass then provides a means to uniquely identify the bioagent without a requirement for prior knowledge of the possible identity of the bioagent. The molecular mass or corresponding base composition signature (BCS) of the amplification product is then matched against a database of molecular masses or base composition signatures. Furthermore, the method can be applied to rapid parallel multiplex analyses, the results of which can be employed in a triangulation identification strategy. The present method provides rapid throughput and does not require nucleic acid sequencing of the amplified target sequence for bioagent detection and identification.
 Despite enormous biological diversity, all forms of life on earth share sets of essential, common features in their genomes. Since genetic data provide the underlying basis for identification of bioagents by the methods of the present invention, it is necessary to select segments of nucleic acids which ideally provide enough variability to distinguish each individual bioagent and whose molecular mass is amenable to molecular mass determination.
 Unlike bacterial genomes, which exhibit conversation of numerous genes (i.e. housekeeping genes) across all organisms, viruses do not share a gene that is essential and conserved among all virus families. Therefore, viral identification is achieved within smaller groups of related viruses, such as members of a particular virus family or genus. For example, RNA-dependent RNA polymerase is present in all single-stranded RNA viruses and can be used for broad priming as well as resolution within the virus family.
 In some embodiments of the present invention, at least one viral nucleic acid segment is amplified in the process of identifying the bioagent. Thus, the nucleic acid segments that can be amplified by the primers disclosed herein and that provide enough variability to distinguish each individual bioagent and whose molecular masses are amenable to molecular mass determination are herein described as bioagent identifying amplicons.
 In some embodiments of the present invention, bioagent identifying amplicons comprise from about 45 to about 200 nucleobases (i.e. from about 45 to about 200 linked nucleosides). One of ordinary skill in the art will appreciate that the invention embodies compounds of 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, and 200 nucleobases in length, or any range therewithin.
 It is the combination of the portions of the bioagent nucleic acid segment to which the primers hybridize (hybridization sites) and the variable region between the primer hybridization sites that comprises the bioagent identifying amplicon.
 In some embodiments, bioagent identifying amplicons amenable to molecular mass determination which are produced by the primers described herein are either of a length, size or mass compatible with the particular mode of molecular mass determination or compatible with a means of providing a predictable fragmentation pattern in order to obtain predictable fragments of a length compatible with the particular mode of molecular mass determination. Such means of providing a predictable fragmentation pattern of an amplification product include, but are not limited to, cleavage with restriction enzymes or cleavage primers, for example. Thus, in some embodiments, bioagent identifying amplicons are larger than 200 nucleobases and are amenable to molecular mass determination following restriction digestion. Methods of using restriction enzymes and cleavage primers are well known to those with ordinary skill in the art.
 In some embodiments, amplification products corresponding to bioagent identifying amplicons are obtained using the polymerase chain reaction (PCR) which is a routine method to those with ordinary skill in the molecular biology arts. Other amplification methods may be used such as ligase chain reaction (LCR), low-stringency single primer PCR, and multiple strand displacement amplification (MDA) which are also well known to those with ordinary skill.
 Intelligent primers are designed to bind to highly conserved sequence regions of a bioagent identifying amplicon that flank an intervening variable region and yield amplification products which ideally provide enough variability to distinguish each individual bioagent, and which are amenable to molecular mass analysis. In some embodiments, the highly conserved sequence regions exhibit between about 80-100%, or between about 90-100%, or between about 95-100% identity, or between about 99-100% identity. The molecular mass of a given amplification product provides a means of identifying the bioagent from which it was obtained, due to the variability of the variable region. Thus design of intelligent primers requires selection of a variable region with appropriate variability to resolve the identity of a given bioagent. Bioagent identifying amplicons are ideally specific to the identity of the bioagent.
 Identification of bioagents can be accomplished at different levels using intelligent primers suited to resolution of each individual level of identification. Broad range survey intelligent primers are designed with the objective of identifying a bioagent as a member of a particular division (e.g., an order, family, class, clade, genus or other such grouping of bioagents above the species level of bioagents). As a non-limiting example, members of the alphavirus genus may be identified as such by employing broad range survey intelligent primers such as primers which target nsP1 or nsP4. In some embodiments, broad range survey intelligent primers are capable of identification of bioagents at the species or sub-species level.
 Division-wide intelligent primers are designed with an objective of identifying a bioagent at the species level. As a non-limiting example, eastern equine encephalitis (EEE) virus, western equine encephalitis (WEE) virus and Venezuelan equine encephalitis (VEE) virus can be distinguished from each other using division-wide intelligent primers. Division-wide intelligent primers are not always required for identification at the species level because broad range survey intelligent primers may provide sufficient identification resolution to accomplishing this identification objective.
 Drill-down intelligent primers are designed with the objective of identifying a bioagent at the sub-species level (including strains, subtypes, variants and isolates) based on sub-species characteristics. As one non-limiting example, subtypes IC, ID and IE of Venezuelan equine encephalitis virus can be distinguished from each other using drill-down primers. Drill-down intelligent primers are not always required for identification at the sub-species level because broad range survey intelligent primers may provide sufficient identification resolution to accomplishing this identification objective.
 A representative process flow diagram used for primer selection and validation process is outlined in FIG. 1. For each group of organisms, candidate target sequences are identified (200) from which nucleotide alignments are created (210) and analyzed (220). Primers are then designed by selecting appropriate priming regions (230) which then makes possible the selection of candidate primer pairs (240). The primer pairs are then subjected to in silico analysis by electronic PCR (ePCR) (300) wherein bioagent identifying amplicons are obtained from sequence databases such as GenBank or other sequence collections (310) and checked for specificity in silico (320). Bioagent identifying amplicons obtained from GenBank sequences (310) can also be analyzed by a probability model which predicts the capability of a given amplicon to identify unknown bioagents such that the base compositions of amplicons with favorable probability scores are then stored in a base composition database (325). Alternatively, base compositions of the bioagent identifying amplicons obtained from the primers and GenBank sequences can be directly entered into the base composition database (330). Candidate primer pairs (240) are validated by in vitro amplification by a method such as PCR analysis (400) of nucleic acid from a collection of organisms (410). Amplification products thus obtained are analyzed to confirm the sensitivity, specificity and reproducibility of the primers used to obtain the amplification products (420).
 Many of the important pathogens, including the organisms of greatest concern as biological weapons agents, have been completely sequenced. This effort has greatly facilitated the design of primers and probes for the detection of unknown bioagents. The combination of broad-range priming with division-wide and drill-down priming has been used very successfully in several applications of the technology, including environmental surveillance for biowarfare threat agents and clinical sample analysis for medically important pathogens.
 Synthesis of primers is well known and routine in the art. The primers may be conveniently and routinely made through the well-known technique of solid phase synthesis. Equipment for such synthesis is sold by several vendors including, for example, Applied Biosystems (Foster City, Calif.). Any other means for such synthesis known in the art may additionally or alternatively be employed.
 The primers are employed as compositions for use in methods for identification of viral bioagents as follows: a primer pair composition is contacted with nucleic acid (such as, for example, DNA from a DNA virus, or DNA reverse transcribed from the RNA of an RNA virus) of an unknown viral bioagent. The nucleic acid is then amplified by a nucleic acid amplification technique, such as PCR for example, to obtain an amplification product that represents a bioagent identifying amplicon. The molecular mass of each strand of the double-stranded amplification product is determined by a molecular mass measurement technique such as mass spectrometry for example, wherein the two strands of the double-stranded amplification product are separated during the ionization process. In some embodiments, the mass spectrometry is electrospray Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS) or electrospray time of flight mass spectrometry (ESI-TOF-MS). A list of possible base compositions can be generated for the molecular mass value obtained for each strand and the choice of the correct base composition from the list is facilitated by matching the base composition of one strand with a complementary base composition of the other strand. The molecular mass or base composition thus determined is then compared with a database of molecular masses or base compositions of analogous bioagent identifying amplicons for known viral bioagents. A match between the molecular mass or base composition of the amplification product and the molecular mass or base composition of an analogous bioagent identifying amplicon for a known viral bioagent indicates the identity of the unknown bioagent. In some embodiments, the primer pair used is one of the primer pairs of Table 1. In some embodiments, the method is repeated using a different primer pair to resolve possible ambiguities in the identification process or to improve the confidence level for the identification assignment.
 In some embodiments, a bioagent identifying amplicon may be produced using only a single primer (either the forward or reverse primer of any given primer pair), provided an appropriate amplification method is chosen, such as, for example, low stringency single primer PCR (LSSP-PCR). Adaptation of this amplification method in order to produce bioagent identifying amplicons can be accomplished by one with ordinary skill in the art without undue experimentation.
 In some embodiments, the oligonucleotide primers are broad range survey primers which hybridize to conserved regions of nucleic acid encoding nsP1 of all (or between 80% and 100%, between 85% and 100%, between 90% and 100% or between 95% and 100%) known alphaviruses and produce bioagent identifying amplicons. In some embodiments, the oligonucleotide primers are broad range survey primers which hybridize to conserved regions of nucleic acid encoding nsP4 of all (or between 80% and 100%, between 85% and 100%, between 90% and 100% or between 95% and 100%) known alphaviruses and produce bioagent identifying amplicons. As used herein, the term broad range survey primers refers to primers that bind to nucleic acid encoding genes essential to alphavirus replication (e.g., for example, nsP1 and nsP4) of all (or between 80% and 100%, between 85% and 100%, between 90% and 100% or between 95% and 100%) known species of alphaviruses. In some embodiments, the broad range survey primer pairs comprise oligonucleotides ranging in length from 13-35 nucleobases, each of which have from 70% to 100% sequence identity with primer pair number 966, which corresponds to SEQ ID NOs: 21:66. In some embodiments, the broad range survey primer pairs comprise oligonucleotides ranging in length from 13-35 nucleobases, each of which have from 70% to 100% sequence identity with primer pair number 1131, which corresponds to SEQ ID NOs: 33:78.
 In some cases, the molecular mass or base composition of a viral bioagent identifying amplicon defined by a broad range survey primer pair does not provide enough resolution to unambiguously identify a viral bioagent at the species level. These cases benefit from further analysis of one or more viral bioagent identifying amplicons generated from at least one additional broad range survey primer pair or from at least one additional division-wide primer pair. The employment of more than one bioagent identifying amplicon for identification of a bioagent is herein referred to as triangulation identification.
 In other embodiments, the oligonucleotide primers are division-wide primers which hybridize to nucleic acid encoding genes of species within a genus of viruses. In other embodiments, the oligonucleotide primers are drill-down primers which enable the identification of sub-species characteristics. Drill down primers provide the functionality of producing bioagent identifying amplicons for drill-down analyses such as strain typing when contacted with nucleic acid under amplification conditions. Identification of such sub-species characteristics is often critical for determining proper clinical treatment of viral infections. In some embodiments, sub-species characteristics are identified using only broad range survey primers and division-wide and drill-down primers are not used.
 In some embodiments, the primers used for amplification hybridize to and amplify genomic DNA, DNA of bacterial plasmids, DNA of DNA viruses or DNA reverse transcribed from RNA of an RNA virus.
 In some embodiments, the primers used for amplification hybridize directly to viral RNA and act as reverse transcription primers for obtaining DNA from direct amplification of viral RNA. Methods of amplifying RNA using reverse transcriptase are well known to those with ordinary skill in the art and can be routinely established without undue experimentation.
 One with ordinary skill in the art of design of amplification primers will recognize that a given primer need not hybridize with 100% complementarity in order to effectively prime the synthesis of a complementary nucleic acid strand in an amplification reaction. Moreover, a primer may hybridize over one or more segments such that intervening or adjacent segments are not involved in the hybridization event. (e.g., for example, a loop structure or a hairpin structure). The primers of the present invention may comprise at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 99% sequence identity with any of the primers listed in Table 1. Thus, in some embodiments of the present invention, an extent of variation of 70% to 100%, or any range therewithin, of the sequence identity is possible relative to the specific primer sequences disclosed herein. Determination of sequence identity is described in the following example: a primer 20 nucleobases in length which is identical to another 20 nucleobase primer having two non-identical residues has 18 of 20 identical residues (18/20=0.9 or 90% sequence identity). In another example, a primer 15 nucleobases in length having all residues identical to a 15 nucleobase segment of primer 20 nucleobases in length would have 15/20=0.75 or 75% sequence identity with the 20 nucleobase primer.
 Percent homology, sequence identity or complementarity, can be determined by, for example, the Gap program (Wisconsin Sequence Analysis Package, Version 8 for Unix, Genetics Computer Group, University Research Park, Madison Wis.), using default settings, which uses the algorithm of Smith and Waterman (Adv. Appl. Math., 1981, 2, 482-489). In some embodiments, complementarity of primers with respect to the conserved priming regions of viral nucleic acid, is between about 70% and about 80%. In other embodiments, homology, sequence identity or complementarity, is between about 80% and about 90%. In yet other embodiments, homology, sequence identity or complementarity, is at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or is 100%.
 In some embodiments, the primers described herein comprise at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 92%, at least 94%, at least 95%, at least 96%, at least 98%, or at least 99%, or 100% (or any range therewithin) sequence identity with the primer sequences specifically disclosed herein. Thus, for example, a primer may have between 70% and 100%, between 75% and 100%, between 80% and 100%, and between 95% and 100% sequence identity with SEQ ID NO: 21. Likewise, a primer may have similar sequence identity with any other primer whose nucleotide sequence is disclosed herein.
 One with ordinary skill is able to calculate percent sequence identity or percent sequence homology and able to determine, without undue experimentation, the effects of variation of primer sequence identity on the function of the primer in its role in priming synthesis of a complementary strand of nucleic acid for production of an amplification product of a corresponding bioagent identifying amplicon.
 In some embodiments of the present invention, the oligonucleotide primers are 13 to 35 nucleobases in length (13 to 35 linked nucleotide residues). These embodiments comprise oligonucleotide primers 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34 or 35 nucleobases in length, or any range therewithin.
 In some embodiments, any given primer comprises a modification comprising the addition of a non-templated T residue to the 5' end of the primer (i.e., the added T residue does not necessarily hybridize to the nucleic acid being amplified). The addition of a non-templated T residue has an effect of minimizing the addition of non-templated A residues as a result of the non-specific enzyme activity of Taq polymerase (Magnuson et al., Biotechniques, 1996, 21, 700-709), an occurrence which may lead to ambiguous results arising from molecular mass analysis.
 In some embodiments of the present invention, primers may contain one or more universal bases. Because any variation (due to codon wobble in the 3rd position) in the conserved regions among species is likely to occur in the third position of a DNA (or RNA) triplet, oligonucleotide primers can be designed such that the nucleotide corresponding to this position is a base which can bind to more than one nucleotide, referred to herein as a "universal nucleobase." For example, under this "wobble" pairing, inosine (I) binds to U, C or A; guanine (G) binds to U or C, and uridine (U) binds to U or C. Other examples of universal nucleobases include nitroindoles such as 5-nitroindole or 3-nitropyrrole (Loakes et al., Nucleosides and Nucleotides, 1995, 14, 1001-1003), the degenerate nucleotides dP or dK (Hill et al.), an acyclic nucleoside analog containing 5-nitroindazole (Van Aerschot et al., Nucleosides and Nucleotides, 1995, 14, 1053-1056) or the purine analog 1-(2-deoxy-β-D-ribofuranosyl)-imidazole-4-carboxamide (Sala et al., Nucl. Acids Res., 1996, 24, 3302-3306).
 In some embodiments, to compensate for the somewhat weaker binding by the wobble base, the oligonucleotide primers are designed such that the first and second positions of each triplet are occupied by nucleotide analogs which bind with greater affinity than the unmodified nucleotide. Examples of these analogs include, but are not limited to, 2,6-diaminopurine which binds to thymine, 5-propynyluracil which binds to adenine and 5-propynylcytosine and phenoxazines, including G-clamp, which binds to G. Propynylated pyrimidines are described in U.S. Pat. Nos. 5,645,985, 5,830,653 and 5,484,908, each of which is commonly owned and incorporated herein by reference in its entirety. Propynylated primers are described in U.S Pre-Grant Publication No. 2003-0170682, which is also commonly owned and incorporated herein by reference in its entirety. Phenoxazines are described in U.S. Pat. Nos. 5,502,177, 5,763,588, and 6,005,096, each of which is incorporated herein by reference in its entirety. G-clamps are described in U.S. Pat. Nos. 6,007,992 and 6,028,183, each of which is incorporated herein by reference in its entirety.
 In some embodiments, to enable broad priming of rapidly evolving RNA viruses, primer hybridization is enhanced using primers and probes containing 5-propynyl deoxy-cytidine and deoxy-thymidine nucleotides. These modified primers and probes offer increased affinity and base pairing selectivity.
 In some embodiments, non-template primer tags are used to increase the melting temperature (Tm) of a primer-template duplex in order to improve amplification efficiency. A non-template tag is at least three consecutive A or T nucleotide residues on a primer which are not complementary to the template. In any given non-template tag, A can be replaced by C or G and T can also be replaced by C or G. Although Watson-Crick hybridization is not expected to occur for a non-template tag relative to the template, the extra hydrogen bond in a G-C pair relative to an A-T pair confers increased stability of the primer-template duplex and improves amplification efficiency for subsequent cycles of amplification when the primers hybridize to strands synthesized in previous cycles.
 In other embodiments, propynylated tags may be used in a manner similar to that of the non-template tag, wherein two or more 5-propynylcytidine or 5-propynyluridine residues replace template matching residues on a primer. In other embodiments, a primer contains a modified internucleoside linkage such as a phosphorothioate linkage, for example.
 In some embodiments, the primers contain mass-modifying tags. Reducing the total number of possible base compositions of a nucleic acid of specific molecular weight provides a means of avoiding a persistent source of ambiguity in determination of base composition of amplification products. Addition of mass-modifying tags to certain nucleobases of a given primer will result in simplification of de novo determination of base composition of a given bioagent identifying amplicon from its molecular mass.
 In some embodiments of the present invention, the mass modified nucleobase comprises one or more of the following: for example, 7-deaza-2'-deoxyadenosine-5-triphosphate, 5-iodo-2'-deoxyuridine-5'-triphosphate, 5-bromo-2'-deoxyuridine-5'-triphosphate, 5-bromo-2'-deoxycytidine-5'-triphosphate, 5-iodo-2'-deoxycytidine-5'-triphosphate, 5-hydroxy-2'-deoxyuridine-5'-triphosphate, 4-thiothymidine-5'-triphosphate, 5-aza-2'-deoxyuridine-5'-triphosphate, 5-fluoro-2'-deoxyuridine-5'-triphosphate, O6-methyl-2'-deoxyguanosine-5'-triphosphate, N2-methyl-2'-deoxyguanosine-5'-triphosphate, 8-oxo-2'-deoxyguanosine-5'-triphosphate or thiothymidine-5'-triphosphate. In some embodiments, the mass-modified nucleobase comprises 15N or 13C or both 15N and 13C.
 In some cases, a molecular mass of a given bioagent identifying amplicon alone does not provide enough resolution to unambiguously identify a given bioagent. The employment of more than one bioagent identifying amplicon for identification of a bioagent is herein referred to as triangulation identification. Triangulation identification is pursued by analyzing a plurality of bioagent identifying amplicons selected within multiple core genes. This process is used to reduce false negative and false positive signals, and enable reconstruction of the origin of hybrid or otherwise engineered bioagents. For example, identification of the three part toxin genes typical of B. anthracis (Bowen et al., J. Appl. Microbiol., 1999, 87, 270-278) in the absence of the expected signatures from the B. anthracis genome would suggest a genetic engineering event.
 In some embodiments, the triangulation identification process can be pursued by characterization of bioagent identifying amplicons in a massively parallel fashion using the polymerase chain reaction (PCR), such as multiplex PCR where multiple primers are employed in the same amplification reaction mixture, or PCR in multi-well plate format wherein a different and unique pair of primers is used in multiple wells containing otherwise identical reaction mixtures. Such multiplex and multi-well PCR methods are well known to those with ordinary skill in the arts of rapid throughput amplification of nucleic acids.
 In some embodiments, the molecular mass of a given bioagent identifying amplicon is determined by mass spectrometry. Mass spectrometry has several advantages, not the least of which is high bandwidth characterized by the ability to separate (and isolate) many molecular peaks across a broad range of mass to charge ratio (m/z). Thus mass spectrometry is intrinsically a parallel detection scheme without the need for radioactive or fluorescent labels, since every amplification product is identified by its molecular mass. The current state of the art in mass spectrometry is such that less than femtomole quantities of material can be readily analyzed to afford information about the molecular contents of the sample. An accurate assessment of the molecular mass of the material can be quickly obtained, irrespective of whether the molecular weight of the sample is several hundred, or in excess of one hundred thousand atomic mass units (amu) or Daltons.
 In some embodiments, intact molecular ions are generated from amplification products using one of a variety of ionization techniques to convert the sample to gas phase. These ionization methods include, but are not limited to, electrospray ionization (ES), matrix-assisted laser desorption ionization (MALDI) and fast atom bombardment (FAB). Upon ionization, several peaks are observed from one sample due to the formation of ions with different charges. Averaging the multiple readings of molecular mass obtained from a single mass spectrum affords an estimate of molecular mass of the bioagent identifying amplicon. Electrospray ionization mass spectrometry (ESI-MS) is particularly useful for very high molecular weight polymers such as proteins and nucleic acids having molecular weights greater than 10 kDa, since it yields a distribution of multiply-charged molecules of the sample without causing a significant amount of fragmentation.
 The mass detectors used in the methods of the present invention include, but are not limited to, Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS), time of flight (TOF), ion trap, quadrupole, magnetic sector, Q-TOF, and triple quadrupole.
 Although the molecular mass of amplification products obtained using intelligent primers provides a means for identification of bioagents, conversion of molecular mass data to a base composition signature is useful for certain analyses. As used herein, a base composition signature (BCS) is the exact base composition determined from the molecular mass of a bioagent identifying amplicon. In one embodiment, a BCS provides an index of a specific gene in a specific organism.
 In some embodiments, conversion of molecular mass data to a base composition is useful for certain analyses. As used herein, a base composition is the exact number of each nucleobase (A, T, C and G).
 RNA viruses depend on error-prone polymerases for replication and therefore their nucleotide sequences (and resultant base compositions) drift over time within the functional constraints allowed by selection pressure. Base composition probability distribution of a viral species or group represents a probabilistic distribution of the above variation in the A, C, G and T base composition space and can be derived by analyzing base compositions of all known isolates of that particular species.
 In some embodiments, assignment of base compositions to experimentally determined molecular masses is accomplished using base composition probability clouds. Base compositions, like sequences, vary slightly from isolate to isolate within species. It is possible to manage this diversity by building base composition probability clouds around the composition constraints for each species. This permits identification of organisms in a fashion similar to sequence analysis. A pseudo four-dimensional plot can be used to visualize the concept of base composition probability clouds. Optimal primer design requires optimal choice of bioagent identifying amplicons and maximizes the separation between the base composition signatures of individual bioagents. Areas where clouds overlap indicate regions that may result in a misclassification, a problem which is overcome by a triangulation identification process using bioagent identifying amplicons not affected by overlap of base composition probability clouds.
 In some embodiments, base composition probability clouds provide the means for screening potential primer pairs in order to avoid potential misclassifications of base compositions. In other embodiments, base composition probability clouds provide the means for predicting the identity of a bioagent whose assigned base composition was not previously observed and/or indexed in a bioagent identifying amplicon base composition database due to evolutionary transitions in its nucleic acid sequence. Thus, in contrast to probe-based techniques, mass spectrometry determination of base composition does not require prior knowledge of the composition or sequence in order to make the measurement.
 The present invention provides bioagent classifying information similar to DNA sequencing and phylogenetic analysis at a level sufficient to identify a given bioagent. Furthermore, the process of determination of a previously unknown base composition for a given bioagent (for example, in a case where sequence information is unavailable) has downstream utility by providing additional bioagent indexing information with which to populate base composition databases. The process of future bioagent identification is thus greatly improved as more BCS indexes become available in base composition databases.
 In some embodiments, the identity and quantity of an unknown bioagent can be determined using the process illustrated in FIG. 2. Primers (500) and a known quantity of a calibration polynucleotide (505) are added to a sample containing nucleic acid of an unknown bioagent. The total nucleic acid in the sample is then subjected to an amplification reaction (510) to obtain amplification products. The molecular masses of amplification products are determined (515) from which are obtained molecular mass and abundance data. The molecular mass of the bioagent identifying amplicon (520) provides the means for its identification (525) and the molecular mass of the calibration amplicon obtained from the calibration polynucleotide (530) provides the means for its identification (535). The abundance data of the bioagent identifying amplicon is recorded (540) and the abundance data for the calibration data is recorded (545), both of which are used in a calculation (550) which determines the quantity of unknown bioagent in the sample.
 A sample comprising an unknown bioagent is contacted with a pair of primers which provide the means for amplification of nucleic acid from the bioagent, and a known quantity of a polynucleotide that comprises a calibration sequence. The nucleic acids of the bioagent and of the calibration sequence are amplified and the rate of amplification is reasonably assumed to be similar for the nucleic acid of the bioagent and of the calibration sequence. The amplification reaction then produces two amplification products: a bioagent identifying amplicon and a calibration amplicon. The bioagent identifying amplicon and the calibration amplicon should be distinguishable by molecular mass while being amplified at essentially the same rate. Effecting differential molecular masses can be accomplished by choosing as a calibration sequence, a representative bioagent identifying amplicon (from a specific species of bioagent) and performing, for example, a 2-8 nucleobase deletion or insertion within the variable region between the two priming sites. The amplified sample containing the bioagent identifying amplicon and the calibration amplicon is then subjected to molecular mass analysis by mass spectrometry, for example. The resulting molecular mass analysis of the nucleic acid of the bioagent and of the calibration sequence provides molecular mass data and abundance data for the nucleic acid of the bioagent and of the calibration sequence. The molecular mass data obtained for the nucleic acid of the bioagent enables identification of the unknown bioagent and the abundance data enables calculation of the quantity of the bioagent, based on the knowledge of the quantity of calibration polynucleotide contacted with the sample.
 In some embodiments, construction of a standard curve where the amount of calibration polynucleotide spiked into the sample is varied, provides additional resolution and improved confidence for the determination of the quantity of bioagent in the sample. The use of standard curves for analytical determination of molecular quantities is well known to one with ordinary skill and can be performed without undue experimentation.
 In some embodiments, multiplex amplification is performed where multiple bioagent identifying amplicons are amplified with multiple primer pairs which also amplify the corresponding standard calibration sequences. In this or other embodiments, the standard calibration sequences are optionally included within a single vector which functions as the calibration polynucleotide. Multiplex amplification methods are well known to those with ordinary skill and can be performed without undue experimentation.
 In some embodiments, the calibrant polynucleotide is used as an internal positive control to confirm that amplification conditions and subsequent analysis steps are successful in producing a measurable amplicon. Even in the absence of copies of the genome of a bioagent, the calibration polynucleotide should give rise to a calibration amplicon. Failure to produce a measurable calibration amplicon indicates a failure of amplification or subsequent analysis step such as amplicon purification or molecular mass determination. Reaching a conclusion that such failures have occurred is in itself, a useful event.
 In some embodiments, the calibration sequence is comprised of DNA. In some embodiments, the calibration sequence is comprised of RNA.
 In some embodiments, the calibration sequence is inserted into a vector which then itself functions as the calibration polynucleotide. In some embodiments, more than one calibration sequence is inserted into the vector that functions as the calibration polynucleotide. Such a calibration polynucleotide is herein termed a "combination calibration polynucleotide." The process of inserting polynucleotides into vectors is routine to those skilled in the art and can be accomplished without undue experimentation. Thus, it should be recognized that the calibration method should not be limited to the embodiments described herein. The calibration method can be applied for determination of the quantity of any bioagent identifying amplicon when an appropriate standard calibrant polynucleotide sequence is designed and used. The process of choosing an appropriate vector for insertion of a calibrant is also a routine operation that can be accomplished by one with ordinary skill without undue experimentation.
 Bioagents that can be identified by the methods of the present invention include RNA viruses. The genomes of RNA viruses can be positive-sense single-stranded RNA, negative-sense single-stranded RNA or double-stranded RNA. Examples of RNA viruses with positive-sense single-stranded genomes include, but are not limited to members of the Caliciviridae, Picornaviridae, Flaviviridae, Togaviridae, Retroviridae and Coronaviridae families. Examples of RNA viruses with negative-sense single-stranded RNA genomes include, but are not limited to, members of the Filoviridae, Rhabdoviridae, Bunyaviridae, Orthomyxoviridae, Paramyxoviridae and Arenaviridae families. Examples of RNA viruses with double-stranded RNA genomes include, but are not limited to, members of the Reoviridae and Birnaviridae families.
 In some embodiments of the present invention, RNA viruses are identified by first obtaining RNA from an RNA virus, or a sample containing or suspected of containing an RNA virus, obtaining corresponding DNA from the RNA by reverse transcription, amplifying the DNA to obtain one or more amplification products using one or more pairs of oligonucleotide primers that bind to conserved regions of the RNA viral genome, which flank a variable region of the genome, determining the molecular mass or base composition of the one or more amplification products and comparing the molecular masses or base compositions with calculated or experimentally determined molecular masses or base compositions of known RNA viruses, wherein at least one match identifies the RNA virus. Methods of isolating RNA from RNA viruses and/or samples containing RNA viruses, and reverse transcribing RNA to DNA are well known to those of skill in the art.
 Alphaviruses represent RNA virus examples of bioagents which can be identified by the methods of the present invention. Alphaviruses are extremely diverse at the nucleotide and protein sequence levels and are thus difficult to detect and identify using currently available diagnostic techniques.
 In one embodiment of the present invention, the alphavirus target gene is nsP4, which is the viral RNA-dependent RNA polymerase. In another embodiment, the target gene is nsP1, which functions to cap and methylate the 5' end of genomic and subgenomic alphaviral RNAs.
 In other embodiments of the present invention, the intelligent primers produce bioagent identifying amplicons within stable and highly conserved regions of alphaviral genomes. The advantage to characterization of an amplicon in a highly conserved region is that there is a low probability that the region will evolve past the point of primer recognition, in which case, the amplification step would fail. Such a primer set is thus useful as a broad range survey-type primer. In another embodiment of the present invention, the intelligent primers produce bioagent identifying amplicons in a region which evolves more quickly than the stable region described above. The advantage of characterization bioagent identifying amplicon corresponding to an evolving genomic region is that it is useful for distinguishing emerging strain variants.
 The present invention also has significant advantages as a platform for identification of diseases caused by emerging viruses. The present invention eliminates the need for prior knowledge of bioagent sequence to generate hybridization probes. Thus, in another embodiment, the present invention provides a means of determining the etiology of a virus infection when the process of identification of viruses is carried out in a clinical setting and, even when the virus is a new species never observed before. This is possible because the methods are not confounded by naturally occurring evolutionary variations (a major concern for characterization of viruses which evolve rapidly) occurring in the sequence acting as the template for production of the bioagent identifying amplicon. Measurement of molecular mass and determination of base composition is accomplished in an unbiased manner without sequence prejudice.
 Another embodiment of the present invention also provides a means of tracking the spread of any species or strain of virus when a plurality of samples obtained from different locations are analyzed by the methods described above in an epidemiological setting. In one embodiment, a plurality of samples from a plurality of different locations are analyzed with primers which produce bioagent identifying amplicons, a subset of which contain a specific virus. The corresponding locations of the members of the virus-containing subset indicate the spread of the specific virus to the corresponding locations.
 The present invention also provides kits for carrying out the methods described herein. In some embodiments, the kit may comprise a sufficient quantity of one or more primer pairs to perform an amplification reaction on a target polynucleotide from a bioagent to form a bioagent identifying amplicon. In some embodiments, the kit may comprise from one to fifty primer pairs, from one to twenty primer pairs, from one to ten primer pairs, or from two to five primer pairs. In some embodiments, the kit may comprise one or more primer pairs recited in Table 1.
 In some embodiments, the kit may comprise one or more broad range survey primer(s), division wide primer(s), or drill-down primer(s), or any combination thereof. A kit may be designed so as to comprise particular primer pairs for identification of a particular bioagent. For example, a broad range survey primer kit may be used initially to identify an unknown bioagent as a member of the alphavirus genus. Another example of a division-wide kit may be used to distinguish eastern equine encephalitis virus, western equine encephalitis virus and Venezuelan equine encephalitis virus from each other. A drill-down kit may be used, for example, to distinguish different subtypes of Venezuelan equine encephalitis virus, or to identify genetically engineered alphaviruses. In some embodiments, any of these kits may be combined to comprise a combination of broad range survey primers and division-wide primers so as to be able to identify the species of an unknown bioagent.
 In some embodiments, the kit may contain standardized calibration polynucleotides for use as internal amplification calibrants. Internal calibrants are described in commonly owned U.S. Patent Application Ser. No. 60/545,425 which is incorporated herein by reference in its entirety.
 In some embodiments, the kit may also comprise a sufficient quantity of reverse transcriptase (if an RNA virus is to be identified for example), a DNA polymerase, suitable nucleoside triphosphates (including any of those described above), a DNA ligase, and/or reaction buffer, or any combination thereof, for the amplification processes described above. A kit may further include instructions pertinent for the particular embodiment of the kit, such instructions describing the primer pairs and amplification conditions for operation of the method. A kit may also comprise amplification reaction containers such as microcentrifuge tubes and the like. A kit may also comprise reagents or other materials for isolating bioagent nucleic acid or bioagent identifying amplicons from amplification, including, for example, detergents, solvents, or ion exchange resins which may be linked to magnetic beads. A kit may also comprise a table of measured or calculated molecular masses and/or base compositions of bioagents using the primer pairs of the kit.
 While the present invention has been described with specificity in accordance with certain of its embodiments, the following examples serve only to illustrate the invention and are not intended to limit the same. In order that the invention disclosed herein may be more efficiently understood, examples are provided below. It should be understood that these examples are for illustrative purposes only and are not to be construed as limiting the invention in any manner.
Selection of Primers That Define Alphavirus Identifying Amplicons
 For design of primers that define alphaviral bioagent identifying amplicons, relevant sequences from, for example, GenBank were obtained, aligned and scanned for regions where pairs of PCR primers would amplify products of about 45 to about 200 nucleotides in length and distinguish species and/or sub-species from each other by their molecular masses or base compositions. A typical process shown in FIG. 1 is employed.
 A database of expected base compositions for each primer region is generated using an in silico PCR search algorithm, such as (ePCR). An existing RNA structure search algorithm (Macke et al., Nucl. Acids Res., 2001, 29, 4724-4735, which is incorporated herein by reference in its entirety) has been modified to include PCR parameters such as hybridization conditions, mismatches, and thermodynamic calculations (SantaLucia, Proc. Natl. Acad. Sci. U.S.A., 1998, 95, 1460-1465, which is incorporated herein by reference in its entirety). This also provides information on primer specificity of the selected primer pairs.
 Table 1 represents a collection of primers (sorted by forward primer name) designed to identify alphaviruses using the methods described herein. Primer sites were identified on two essential alphaviral genes, nsP1 (the RNA capping and methylation enzyme) and nsP4, the RNA-dependent RNA polymerase). The forward or reverse primer name shown in Table 1 indicates the gene region of the viral genome to which the primer hybridizes relative to a reference sequence. For example, the forward primer name AV_NC001449--888--901P_F indicates a forward primer that hybridizes to residues 888-901 of an alphavirus reference sequence represented by GenBank Accession No. NC001449 (SEQ ID NO: 1). In Table 1, Ua=5-propynyluracil; Ca=5-propynylcytosine; *=phosphorothioate linkage. The primer pair number is an in-house database index number. In some embodiments, primer pairs for identification of alphavirus bioagents comprise forward primer sequence GCTAGAGCGTTTTCGCA (SEQ. ID NO: 93).
TABLE-US-00001 TABLE 1 Primer Pairs for Identification of Alphavirus Bioagents For. Primer For. SEQ Reverse pair primer ID Reverse SEQ ID number name Forward sequence NO: primer name Reverse sequence NO: 302 AV_NC0014 AATGCTAGAGCaGUaUaTUa 2 AV_NC001449_ GCACTTCaCaAAUaGUaCa 47 49_159_17 CaGCA 225_244P_R CAGGAT 8P_F 303 AV_NC0014 AATGCTAGAGCaGUaUaTUa 3 AV_NC001449_ GCACTTCaCaAAUaGUaCa 48 49_159_17 CaGCA 225_244P_2_R TAGGAT 8P_F 304 AV_NC0014 GCTAGAGCaGUaUaTUaCaGC 4 AV_NC001449_ GGCGCaACaUaTCaCaAAU 49 49_162_17 A 231_247P_R aGUaC 8P_F 306 AV_NC0014 TGCaGAAGGGUaACGTCGT 5 AV_NC001449_ TTGCaAGCACAAGAATCa 50 49_888_90 972_991P_R CaCTC 4P_F 307 AV_NC0014 TGUaGTGACaCaAGAUaGAC 6 AV_NC001449_ TGGUaUaGAGCaCaCaAAC 51 49_1057_1 1122_1135P_ 072P_F R 314 AV_NC0014 AATGCTAGAGCGTTTTCGC 7 AV_NC001449_ GCACTTCCAATGTCCAG 52 49_159_17 A 225_244_R GAT 8_F 315 AV_NC0014 AATGCTAGAGCGTTTTCGC 8 AV_NC001449_ GCACTTCCAATGTCTAG 53 49_159_17 A 225_244_2_R GAT 8_F 316 AV_NC0014 GCTAGAGCGTTTTCGCA 9 AV_NC001449_ GGCGCACTTCCAATGTC 54 49_162_17 231_247_R 8_F 317 AV_NC0014 TGCGAAGGGTACGT 10 AV_NC001449_ TTGCAGCACAAGAATCC 55 49_888_90 972_991_R CTC 1_F 318 AV_NC0014 TGCGAAGGGTACGTCGT 11 AV_NC001449_ TTGCAGCACAAGAATCC 56 49_888_90 972_991_R CTC 4_F 319 AV_NC0014 TGTGTGACCAGATGAC 12 AV_NC001449_ TGGTTGAGCCCAAC 57 49_1057_1 1122_1135_ 072_F R 494 AV_NC0014 TAATGCTAGAGCaGUaUaTU 13 AV_NC001449_ TGCACTTCaCaAAUaGUa 58 49_158_17 CaGCA 225_245P_R CaCAGGAT 8P_F 494 AV_NC0014 TAATGCTAGAGCaGUaUaTU 14 AV_NC001449_ TGCACTTCaCaAAUaGUa 59 49_158_17 aCaGCA 225_245P_R CaCAGGAT 8P_F 495 AV_NC0014 TAATGCTAGAGCaGUaUaTU 15 AV_NC001449_ TGCACTTCaCaAAUaGUa 60 49_158_17 CaGCA 225_245P_2_ CaTAGGAT 8P_F R 496 AV_NC0014 TGCTAGAGCaGUaUaTUaCaG 16 AV_NC001449_ TGGCGCaACaUaTCaCaAA 61 49_161_17 CA 231_248P_R UaGUaC 8P_F 497 AV_NC0014 TTGCaGAAGGGUaACGT 17 AV_NC001449_ TTTGCaAGCACAAGAAT 62 49_887_90 972_992P_R CaCaCTC 1P_F 498 AV_NC0014 TTGCaGAAGGGUaACGTCGT 18 AV_NC001449_ TTTGCaAGCACAAGAAT 63 49_887_90 972_992P_R CaCaCTC 4P_F 498 AV_NC0014 TTGCaGAAGGGUaACGTCGT 19 AV_NC001449_ TTTGCaAGCACAAGAAT 64 49_887_90 972_992P_R CaCaCTC 4P_F 499 AV_NC0014 TTGUaGTGACaCaAGAUaGA 20 AV_NC001449_ TTGGUaUaGAGCaCaCaAA 65 49_1056_1 C 1122_1136P_ C 072P_F R 966 AV_NC_001 TCCATGCTAATGCTAGAGC 21 AV_NC_00144 TGGCGCACTTCCAATGT 66 449_151_1 GTTTTCGCA 9_225_248_R CCAGGAT 78_F 967 AV_NC_001 TGTCAGTTGCGAAGGGTAC 22 AV_NC_00144 TCTGTCACTTTGCAGCA 67 449_881_9 GTCGT 9_972_1000_ CAAGAATCCCTC 04_F R 968 AV_NC_001 TAATGCTAGAGCGTTTTCG 23 AV_NC_00144 TGCACTTCCAATGTCCA 68 449_158_1 CA 9_225_245_R GGAT 78_F 969 AV_NC_001 TTGCGAAGGGTACGTCGT 24 AV_NC_00144 TTTGCAGCACAAGAATC 69 449_887_9 9_972_992_R CCTC 04_F 970 AV_NC_001 UaCaCaAATGCTAGAGCGTT 25 AV_NC_00144 UaCaCaGCACTTCCAATG 70 449_156_1 TTCGCA 9_225_247P_ TCCAGGAT 78P_F R 971 AV_NC_001 UaCaCaTGCGAAGGGTACGT 26 AV_NC_00144 UaCaCaTTGCAGCACAAG 71 449_885_9 CGT 9_972_994P_ AATCCCTC 04P_F R 972 AV_NC_001 UaCaCaUaAATGCTAGAGCG 27 AV_NC_00144 UaCaCaUaGCACTTCCAA 72 449_155_1 TTTTCGCA 9_225_248P_ TGTCCAGGAT 78P_F R 973 AV_NC_001 UaCaCaUaTGCGAAGGGTAC 28 AV_NC_00144 UaCaCaUaTTGCAGCACA 73 449_884_9 GTCGT 9_972_995P_ AGAATCCCTC 04P_F R 974 AV_NC_001 UaCaCaUaUaAATGCTAGAGC 29 AV_NC_00144 UaCaCaUaUaGCACTTCCA 74 449_154_1 GTTTTCGCA 9_225_249P_ ATGTCCAGGAT 78P_F R 975 AV_NC_001 UaCaCaUaUaTGCGAAGGGTA 30 AV_NC_00144 UaCaCaUaUaTTGCAGCAC 75 449_883_9 CGTCGT 9_972_996P_ AAGAATCCCTC 04P_F R 976 AV_NC_001 TCCTTCAATGCTAGAGCGT 31 AV_NC_00144 TCCTTCGCACTTCCAAT 76 449_153_1 TTTCGCA 9_225_250_R GTCCAGGAT 78_F 977 AV_NC_001 TCCTTCTGCGAAGGGTACG 32 AV_NC_00144 TCCTTCTTGCAGCACAA 77 449_882_9 TCGT 9_972_997_R GAATCCCTC 04_F 1131 AV_NC_001 TGCCAGCTACACTGTGCGA 33 AV_NC_00144 TGACGACTATCCGCTGG 78 449_1045_ CCAGATGAC 9_1122_1149_ TTGAGCCCAAC 107_F R 1146 AV_NC_001 TATTGTCAGTTGCGAAGGG 34 AV_NC_00144 TGTCACTTTGCAACACA 79 449_878_9 TACGT 9_972_998_R AGAATCCCTC 01_F 1147 AV_NC_001 TATTGTCAGTTGCGACGGG 35 AV_NC_00144 TGTCACTTTGCAACACA 80 449_878_9 TACGT 9_972_998_R AGAATCCCTC 01_2_F 1148 AV_NC_001 TCTATAGTCAGTTGCGACG 36 AV_NC_00144 TGTCACTTTGCAGCACA 81 449_876_9 GGTACGT 9_972_998_2_ AGAATCCCTC 01_F R 1149 AV_NC_001 TGTCAGCTACATTGTGTGA 37 AV_NC_00144 TGACGACTATCCGCTGG 82 449_1045_ CCAAATGACTGG 9_1122_1149_ TTGAGCCCAAC 1075_F 2_R 1150 AV_NC_001 TACCAGCCACACTTTGCGA 38 AV_NC_00144 TGACGACTATCCGCTGG 83 449_1045_ TCAGATGACAGG 9_1122_1149_ TTGAGCCCAAC 1075_2_F 2_R 2048 AV_NC_001 TCCATGCTAACGCCAGAGC 39 AV_NC_00144 TGCTGGTGCACTTCCAA 84 449_151_1 GTTTTCGCA 9_225_251_R TATCCAGGAT 78_2_F 2049 AV_NC_001 TCCATGCTAACGCCAGAGC 40 AV_NC_00144 TGCCGGTGCGCTGCCTA 85 449_151_1 GTTTTCGCA 9_228_251_R TGTCCAA 78_2_F 2050 AV NC 001 TGACGTAGACCCCCAGAGT 41 AV_NC_00144 TCGCTCTGGCATTAGCA 86 449_62_86_ CCGTTT 9_147_171_R TGGTCATT F 2051 AV_NC_001 TGGCGCTATGATGAAATCT 42 AV_NC_00144 TATGTTGTCGTCGCCGA 87 449_6791_ GGAATGTT 9_7083_7106_ TGAACGC 6997_F R 2052 AV_NC_001 TGGCGCTATGATGAAATCT 43 AV_NC_00144 TACGATGTTGTCGTCGC 88 449_6971_ GGAATGTT 9_7086_7109_ CGATGAA 6997_F R 2053 AV_NC_001 TGCCTTCATCGGCGATGAC 44 AV_NC_00144 TCCAAGTGGCGCACCTG 89 449_7082_ AACAT 9_7134_7158_ TCTGCCAT 7105_F R 2054 AV_NC_001 TGTCGGCCGAGGATTTTGA 45 AV_NC_00144 TCATCTTGGCTTTTGTC 90 449_6742_ TGCTATCATAGC 9_6816_6841_ AAAGGAGGC 6772_F R 2055 AV_NC_001 TGCGGTACCGTCACCATTT 46 AV_NC_00144 TGGTAGTTCTCTCATTT 91 449_6254_ CAGAACAC 9_6318_6347_ GTGTGACGTTGCA 6280_F R
One-step RT-PCR of RNA Virus Samples
 RNA was isolated from virus-containing samples according to methods well known in the art. To generate bioagent identifying amplicons for RNA viruses, a one-step RT-PCR protocol was developed. All RT-PCR reactions were assembled in 50 μl reactions in the 96 well microtiter plate format using a Packard MPII liquid handling robotic platform and MJ Dyad® thermocyclers (MJ research, Waltham, Mass.). The RT-PCR reaction consisted of 4 units of Amplitaq Gold®, 1.5× buffer II (Applied Biosystems, Foster City, Calif.), 1.5 mM MgCl2, 0.4 M betaine, 10 mM DTT, 20 mM sorbitol, 50 ng random primers (Invitrogen, Carlsbad, Calif.), 1.2 units Superasin (Ambion, Austin, Tex.), 100 ng polyA DNA, 2 units Superscript III (Invitrogen, Carlsbad, Calif.), 400 ng T4 Gene 32 Protein (Roche Applied Science, Indianapolis, Ind.), 800 μM dNTP mix, and 250 nM of each primer.
 The following RT-PCR conditions were used to amplify the sequences used for mass spectrometry analysis: 60° C. for 5 minutes, 4° C. for 10 minutes, 55° C. for 45 minutes, 95° C. for 10 minutes followed by 8 cycles of 95° C. for 30 seconds, 48° C. for 30 seconds, and 72° C. for 30 seconds, with the 48° C. annealing temperature increased 0.9° C. after each cycle. The PCR reaction was then continued for 37 additional cycles of 95° C. for 15 seconds, 56° C. for 20 seconds, and 72° C. for 20 seconds. The reaction concluded with 2 minutes at 72° C.
Solution Capture Purification of PCR Products for Mass Spectrometry with Ion Exchange Resin-Magnetic Beads
 For solution capture of nucleic acids with ion exchange resin linked to magnetic beads, 25 μl of a 2.5 mg/mL suspension of BioClon amine terminated supraparamagnetic beads were added to 25 to 50 μl of a PCR (or RT-PCR) reaction containing approximately 10 pM of a typical PCR amplification product. The above suspension was mixed for approximately 5 minutes by vortexing or pipetting, after which the liquid was removed after using a magnetic separator. The beads containing bound PCR amplification product were then washed 3× with 50 mM ammonium bicarbonate/50% MeOH or 100 mM ammonium bicarbonate/50% MeOH, followed by three more washes with 50% MeOH. The bound PCR amplicon was eluted with 25 mM piperidine, 25 mM imidazole, 35% MeOH, plus peptide calibration standards.
Mass Spectrometry and Base Composition Analysis
 The ESI-FTICR mass spectrometer is based on a Bruker Daltonics (Billerica, Mass.) Apex II 70e electrospray ionization Fourier transform ion cyclotron resonance mass spectrometer that employs an actively shielded 7 Tesla superconducting magnet. The active shielding constrains the majority of the fringing magnetic field from the superconducting magnet to a relatively small volume. Thus, components that might be adversely affected by stray magnetic fields, such as CRT monitors, robotic components, and other electronics, can operate in close proximity to the FTICR spectrometer. All aspects of pulse sequence control and data acquisition were performed on a 600 MHz Pentium II data station running Bruker's Xmass software under Windows NT 4.0 operating system. Sample aliquots, typically 15 μl were extracted directly from 96-well microtiter plates using a CTC HTS PAL autosampler (LEAP Technologies, Carrboro, N.C.) triggered by the FTICR data station. Samples were injected directly into a 10 μl sample loop integrated with a fluidics handling system that supplies the 100 μl/hr flow rate to the ESI source. Ions were formed via electrospray ionization in a modified Analytica (Branford, Conn.) source employing an off axis, grounded electrospray probe positioned approximately 1.5 cm from the metalized terminus of a glass desolvation capillary. The atmospheric pressure end of the glass capillary was biased at 6000 V relative to the ESI needle during data acquisition. A counter-current flow of dry N2 was employed to assist in the desolvation process. Ions were accumulated in an external ion reservoir comprised of an rf-only hexapole, a skimmer cone, and an auxiliary gate electrode, prior to injection into the trapped ion cell where they were mass analyzed. Ionization duty cycles>99% were achieved by simultaneously accumulating ions in the external ion reservoir during ion detection. Each detection event consisted of 1M data points digitized over 2.3 s. To improve the signal-to-noise ratio (S/N), 32 scans were co-added for a total data acquisition time of 74 s.
 The ESI-TOF mass spectrometer is based on a Bruker Daltonics MicroTOFT®. Ions from the ESI source undergo orthogonal ion extraction and are focused in a reflectron prior to detection. The TOF and FTICR are equipped with the same automated sample handling and fluidics described above. Ions are formed in the standard MicroTOFT® ESI source that is equipped with the same off-axis sprayer and glass capillary as the FTICR ESI source. Consequently, source conditions were the same as those described above. External ion accumulation was also employed to improve ionization duty cycle during data acquisition. Each detection event on the TOF was comprised of 75,000 data points digitized over 75 μs.
 The sample delivery scheme allows sample aliquots to be rapidly injected into the electrospray source at high flow rate and subsequently be electrosprayed at a much lower flow rate for improved ESI sensitivity. Prior to injecting a sample, a bolus of buffer was injected at a high flow rate to rinse the transfer line and spray needle to avoid sample contamination/carryover. Following the rinse step, the autosampler injected the next sample and the flow rate was switched to low flow. Following a brief equilibration delay, data acquisition commenced. As spectra were co-added, the autosampler continued rinsing the syringe and picking up buffer to rinse the injector and sample transfer line. In general, two syringe rinses and one injector rinse were required to minimize sample carryover. During a routine screening protocol a new sample mixture was injected every 106 seconds. More recently a fast wash station for the syringe needle has been implemented which, when combined with shorter acquisition times, facilitates the acquisition of mass spectra at a rate of just under one spectrum/minute.
 Raw mass spectra were post-calibrated with an internal mass standard and deconvoluted to monoisotopic molecular masses. Unambiguous base compositions were derived from the exact mass measurements of the complementary single-stranded oligonucleotides. Quantitative results are obtained by comparing the peak heights with an internal PCR calibration standard present in every PCR well at 500 molecules per well. Calibration methods are commonly owned and disclosed in U.S. Provisional Patent Application Ser. No. 60/545,425.
De Novo Determination of Base Composition of Amplification Products using Molecular Mass Modified Deoxynucleotide Triphosphates
 Because the molecular masses of the four natural nucleobases have a relatively narrow molecular mass range (A=313.058, G=329.052, C=289.046, T=304.046--See Table 2), a persistent source of ambiguity in assignment of base composition can occur as follows: two nucleic acid strands having different base composition may have a difference of about 1 Da when the base composition difference between the two strands is G⇄A (-15.994) combined with C⇄T (+15.000). For example, one 99-mer nucleic acid strand having a base composition of A27G30C21T21 has a theoretical molecular mass of 30779.058 while another 99-mer nucleic acid strand having a base composition of A26G31C22T20 has a theoretical molecular mass of 30780.052. A 1 Da difference in molecular mass may be within the experimental error of a molecular mass measurement and thus, the relatively narrow molecular mass range of the four natural nucleobases imposes an uncertainty factor.
 The present invention provides for a means for removing this theoretical 1 Da uncertainty factor through amplification of a nucleic acid with one mass-tagged nucleobase and three natural nucleobases. The term "nucleobase" as used herein is synonymous with other terms in use in the art including "nucleotide," "deoxynucleotide," "nucleotide residue," "deoxynucleotide residue," "nucleotide triphosphate (NTP)," or deoxynucleotide triphosphate (dNTP).
 Addition of significant mass to one of the 4 nucleobases (dNTPs) in an amplification reaction, or in the primers themselves, will result in a significant difference in mass of the resulting amplification product (significantly greater than 1 Da) arising from ambiguities arising from the G⇄A combined with C⇄T event (Table 2). Thus, the same the G⇄A (-15.994) event combined with 5-Iodo-C⇄T (-110.900) event would result in a molecular mass difference of 126.894. If the molecular mass of the base composition A27G30 5-Iodo-C21T21 (33422.958) is compared with A26G31 5-Iodo-C22T20, (33549.852) the theoretical molecular mass difference is +126.894. The experimental error of a molecular mass measurement is not significant with regard to this molecular mass difference. Furthermore, the only base composition consistent with a measured molecular mass of the 99-mer nucleic acid is A27G30 5-Iodo-C21T21. In contrast, the analogous amplification without the mass tag has 18 possible base compositions.
TABLE-US-00002 TABLE 2 Molecular Masses of Natural Nucleobases and the Mass-Modified Nucleobase 5-Iodo-C and Molecular Mass Differences Resulting from Transitions Nucleobase Molecular Mass Transition Δ Molecular Mass A 313.058 A-->T -9.012 A 313.058 A-->C -24.012 A 313.058 A-->5-Iodo-C 101.888 A 313.058 A-->G 15.994 T 304.046 T-->A 9.012 T 304.046 T-->C -15.000 T 304.046 T-->5-Iodo-C 110.900 T 304.046 T-->G 25.006 C 289.046 C-->A 24.012 C 289.046 C-->T 15.000 C 289.046 C-->G 40.006 5-Iodo-C 414.946 5-Iodo-C-->A -101.888 5-Iodo-C 414.946 5-Iodo-C-->T -110.900 5-Iodo-C 414.946 5-Iodo-C-->G -85.894 G 329.052 G-->A -15.994 G 329.052 G-->T -25.006 G 329.052 G-->C -40.006 G 329.052 G-->5-Iodo-C 85.894
 Mass spectra of bioagent identifying amplicons are analyzed independently using a maximum-likelihood processor, such as is widely used in radar signal processing. This processor, referred to as GenX, first makes maximum likelihood estimates of the input to the mass spectrometer for each primer by running matched filters for each base composition aggregate on the input data. This includes the GenX response to a calibrant for each primer.
 The algorithm emphasizes performance predictions culminating in probability-of-detection versus probability-of-false-alarm plots for conditions involving complex backgrounds of naturally occurring organisms and environmental contaminants. Matched filters consist of a priori expectations of signal values given the set of primers used for each of the bioagents. A genomic sequence database is used to define the mass base count matched filters. The database contains the sequences of known bacterial bioagents and includes threat organisms as well as benign background organisms. The latter is used to estimate and subtract the spectral signature produced by the background organisms. A maximum likelihood detection of known background organisms is implemented using matched filters and a running-sum estimate of the noise covariance. Background signal strengths are estimated and used along with the matched filters to form signatures which are then subtracted. The maximum likelihood process is applied to this "cleaned up" data in a similar manner employing matched filters for the organisms and a running-sum estimate of the noise-covariance for the cleaned up data.
 The amplitudes of all base compositions of bioagent identifying amplicons for each primer are calibrated and a final maximum likelihood amplitude estimate per organism is made based upon the multiple single primer estimates. Models of all system noise are factored into this two-stage maximum likelihood calculation. The processor reports the number of molecules of each base composition contained in the spectra. The quantity of amplification product corresponding to the appropriate primer set is reported as well as the quantities of primers remaining upon completion of the amplification reaction.
Alignment of Alphavirus Sequences using an nsP1 Primer Pair
 A total of 42 alphavirus sequences, including two strains of EEEV, 20 strains of VEEV, one strain of Chikungnya virus, one strain of Igbo Ora virus, two strains of O'nyong-nyong virus, one strain of Ross River virus, one strain of Sagiyama virus, one strain of Mayaro virus, one strain of Barmah forest virus, two strains of Semliki forest virus, one strain of aura virus, one strain of Ockelbo virus, and seven strains of Sindbois virus were aligned and evaluated for identification of useful priming regions. In a representative example, with reference to the reference sequence NC--001449 (SEQ ID NO: 1) representing the genome of Venezualan equine encephalitis virus (VEEV), a pair of primers (no. 316--SEQ ID NOs: 9:54) was designed to produce an alphavirus identifying amplicon 86 nucleobases long corresponding to positions 162-247 of the nsP1 gene of VEEV. This pair of primers is expected to produce an alphavirus identifying amplicon that can provide the means to identify the virus strains described above.
 As shown in FIG. 3, in a pseudo four-dimensional plot of expected base compositions of alphavirus identifying amplicons arising from amplification with primer pair no: 316 the epidemic, epizootic VEEV viruses of classes IAB-IC, ID and IIIA (which have the potential to cause severe disease in humans and animals) can be distinguished from the enzootic VEE types IE, IF, I, IIIB, IIIC, IV, V, and VI, which, in turn, are generally distinguishable from each other.
 Table 3 lists the results of base composition analysis of nine laboratory test isolates of alphaviruses obtained according to the methods described herein by amplification with primer pair 316 to obtain alphavirus identifying amplicons.
TABLE-US-00003 TABLE 3 Expected and Observed Base Compositions of Alphavirus Identifying Amplicons Produced with Primer Pair No: 316 (SEQ ID NOs: 9:54) Expected Base Observed Base Sequence Composition Composition Virus Strain Available [A G C T] [A G C T] VEE 3908 Yes [21 23 23 19] [21 23 23 19] (subtype IC, 1995) VEE 66637 Yes [21 23 23 19] [21 23 23 19] (subtype ID, 1981) VEE 68U201 Yes [22 25 19 20] [22 25 19 20] (Subtype 1E, 1968) VEE 243937 Yes [21 23 23 19] [21 23 23 19] (subtype 1C, 1992) WEE OR71 (71V1658) Yes [22 26 19 19] [22 26 19 19] WEE SD83 (R43738) No -- [22 26 19 19] WEE ON41 (McMillan) No -- [22 27 18 19] WEE Fleming (Fleming) No -- [22 25 19 20] EEE (Parker Strain) Yes [23 25 19 19] [23 25 19 19]
Identification of Six Alphavirus Strains
 Two primers pairs (numbers 966 and 1131) which each amplify a sequence of the alphavirus gene nsP1 were tested for their ability to detect and differentiate among eight different known alphavirus strains using the methods described herein. The strains included in the study were the North American strain of Eastern equine encephalitis virus and the Tonate CaAn 410d, 78V3531, AG80-663, Cabassou CaAr 508 and Everglades Fe3-7c strains of Venezuelan equine encephalitis virus. RT-PCR reactions were spiked with either 10-fold or 100-fold dilutions of virus stock and performed according to the method described in Example 2. Each reaction also contained 500 RNA copies of a calibration sequence to quantitate the amount of virus present in each reaction. The calibration sequence is contained within a combination calibration polynucleotide designated RT-PCR calibrant pVIR001 (SEQ ID NO: 92). This calibration sequence was designed with reference to Venezuelan equine encephalitis virus (VEE) strain 3908, subtype IC (GenBank gi number 20800454) such that all primers disclosed herein with the exception of primer pair numbers 2050-2055, hybridize to the calibration sequence and produce alphavirus calibration amplicons that are distinguishable from alphavirus identifying amplicons. Mass spectral analysis of the alphavirus bioagent identifying amplicons resulted in the correct identification of all six alphavirus strains.
Identification of Related Alphavirus Species
 A series of eight strains of alphaviruses whose alphavirus identifying amplicon sequences (from primer pairs 966 and 1131) are unknown were analyzed using primer pairs 966 and 1131 by the methods described herein. These experiments were carried out without the presence of a calibrant. A representative set of results is shown in Table 4 where it is indicated that the "unknown" alphavirus strains can be assigned to related "known" strains.
TABLE-US-00004 TABLE 4 Representative Result Set of Identification of Alphaviruses with Primer Pair Nos: 966 (SEQ ID NOs: 21:66) and 1131 (SEQ ID NOs: 33:78) Primer Base Spiked Pair Composition Match Alphavirus Strain Sample Virus No: [A G C T] Type Matched 1 Sindbis 966 [24 25 26 23] exact Sindbis virus Virus (NoStrain_14_1, genome strain) 1 Sindbis 1131 [29 26 27 23] exact Sindbis virus (DI-2, Virus NoStrain_14_1, genome strain) 2 Nduma 966 [26 27 22 23] exact Eastern equine Virus encephalitis virus (North American) 2 Nduma 1131 ND Virus 3 Middleburg 966 [26 27 22 23] exact Eastern equine Virus encephalitis virus (North American) 3 Middleburg 1131 [28 29 27 20] Deconvolved BC (none) Virus 4 Mayaro 966 [31 24 22 21] Mayaro virus Virus (NoStrain_5_1, NoStrain_6_2) 4 Mayaro 1131 [26 30 26 23] mass Venezuelan equine Virus adjust encephalitis virus +-1 (78V3531) 5 Highlands 966 [28 28 22 20] no Deconvolved BC (none) J Virus match 5 Highlands 1131 [28 31 28 18] cloud Venezuelan equine J Virus offset encephalitis virus [-1 (243937, 3908, 6119, 0 0 66457, 66637, 71-180; 1] 600035-71-180/4, 83U434, P676, PMCHo5, SH3, TC-83, Trinidad donkey, V198, ZPC738) 6 Getah 966 [25 24 26 23] cloud Sindbis virus Virus offset (NoStrain_14_1, genome [-1 strain) 0 0 1] 6 Getah 1131 ND Virus 1 Barmah 966 [30 23 23 22] exact Barmah Forest virus Virus (BH2193) 1 Barmah 1131 [25 27 30 22] no Deconvolved BC (none) Virus match 2 Semliki 966 [28 23 26 21] exact Semliki forest virus Virus (A7-74, DI-19, DI-6, Defective RNA particle, L10, genome strain) 2 Semliki 1131 ND Virus
 Various modifications of the invention, in addition to those described herein, will be apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. Each reference (including, but not limited to, journal articles, U.S, and non-U.S. patents, patent application publications, international patent application publications, gene bank accession numbers, internet web sites, and the like) cited in the present application is incorporated herein by reference in its entirety. Those skilled in the art will appreciate that numerous changes and modifications may be made to the embodiments of the invention and that such changes and modifications may be made without departing from the spirit of the invention. It is therefore intended that the appended claims cover all such equivalent variations as fall within the true spirit and scope of the invention.
93111444DNAVenezuelan equine encephalitis virus 1atgggcggcg caagagagaa gcccaaacca attacctacc caaaatggag aaagttcacg 60ttgacatcga ggaagacagc ccattcctca gagctttaca acggagcttc ccgcagtttg 120aggtagaagc caagcaggtc actgataatg accatgctaa tgccagagcg ttttcgcatc 180tggcttcaaa actgatcgaa acggaggtgg acccatccga cacgatcctt gacattggaa 240gtgcgcccgc ccgcagaatg tattctaagc ataagtatca ttgcatctgt ccgatgagat 300gtgcggaaga tccggacaga ttgtacaagt atgcaactaa gctgaagaaa aattgcaagg 360aaataactga caaggaattg gacaagaaaa tgaaggagct cgccgccgtc atgagcgacc 420ctgacctgga aactgagact atgtgcctcc acgacgatga gtcatgtcgc tacgaggggc 480aagtcgctgt ttaccaggat gtatacgcag ttgacggacc gacaagtctc tatcaccaag 540ccaacaaggg agttagagtc gcctactgga taggctttga caccacccct tttatgttta 600agaacttggc tggagcatat ccatcatact ctaccaactg ggccgacgaa accgtgttaa 660cggctcgtaa cataggccta tgcagctccg acgtcatgga gcggtcacgt agagggatgt 720ccattcttag gaagaagtat ttgaaaccat ccaataatgt cctattctct gttggctcga 780ccatctacca cgagaagagg gacttactga ggagctggca cctgccgtct gtatttcact 840tacgtggcaa gcaaaattac acatgtcggt gtgagactat agttagttgc gacgggtacg 900tcgttaaaag aatagctatc agtccaggcc tgtatgggaa gccttcaggc tatgctgcta 960cgatgcaccg cgagggattc ttgtgctgca aagtgacaga cacattgaac ggggagaggg 1020tctcttttcc cgtgtgcacg tatgtgccag ctacattgtg tgaccaaatg actggcatac 1080tggcaacaga tgtcagtgcg gacgacgcgc aaaaactgct ggttgggctc aaccagcgca 1140tagtcgtcaa cggtcgcacc caaagaaaca ccaataccat gaagaattat cttttgcccg 1200tagtggccca ggcatttgct aggtgggcaa aggaatataa ggaagatcaa gaagatgaga 1260ggccactagg actacgagat agacagttag tcatggggtg ctgctgggct tttagaaggc 1320acaagataac atctatttat aagcgcccag atacccaaac catcatcaaa gtgaacagcg 1380atttccactc attcgtgctg cccaggatag gcagtaacac actggagatc gggctgagaa 1440cgagaatcag gaaaatgcta gaagagcaca aggagccgtc acctctcatt actgccgagg 1500acatacaaga ggctaagtgc gcagccgatg aggctaagga agtgcgtgaa gccgaggagc 1560tgcgcgctgc tctaccacct ttggcagctg attttgagga gcccactctg gaagccgatg 1620tcgacttgat gttacaagag gctggggccg gctcagtgga gacacctcgt ggcttgataa 1680aggttaccag ctatgccggc gaggacaaga tcggctctta cgcagtgctt tctccacagg 1740ctgtactcaa gagtgagaaa ctatcttgca ttcaccctct cgctgaacaa gtcatagtga 1800taacacactc tggccgaaaa gggcgttatg ccgtggaacc ctaccatgga aaagtagtgg 1860tgccagaggg acatgcaata cccgtccagg actttcaagc tctgagtgaa agtgccacca 1920tcgtgtacaa cgaacgagag ttcgtaaaca ggtacctgca ccatattgcc acacatggag 1980gagcgctgaa cacagatgaa gaatattaca aaactgtcaa gcccagcgag cacgacggcg 2040aatacctgta cgacatcgac aggaaacaat gcgtcaagaa agaattagtc actgggctag 2100ggcttacagg cgagctggtg gatcctccct tccatgaatt tgcctacgag agtctgagaa 2160cacgtccggc cgctccttac caagtaccaa ccataggggt gtatggcgtg ccggggtcag 2220gcaagtctgg catcattaaa agcgcagtca ccaaaaaaga tctggtggtg agcgccaaga 2280aagaaaactg cgcagaaata ataagggacg tcaagaaaat gaaagggctg gacgtcaatg 2340ccagaactgt ggactcagtg ctcttgaatg gatgcaaaca ccccgtagag accctgtata 2400ttgacgaagc ttttgcttgt catgcaggca ctctcagagc gctcatagcc atcataagac 2460ctaaaaaggc agtgctctgc ggggatccaa aacagtgtgg ctttttcaat atgatgtgcc 2520tgaaagtgca ttttaaccac gagatttgca cgcaggtctt ccacaaaagc atctctcgcc 2580gttgcactaa atccgtgact tcggtcgtct caaccttgtt ttacgacaaa aggatgagaa 2640cgacgaaccc gaaagagact aagattgtga ttgacactac tggcagtacc aaaccgaagc 2700aggacgatct cattctcact tgtttcagag ggtgggtgaa gcagttgcaa atagattaca 2760aaggcaacga aataatgacg gcagctgcct ctcaagggct gacccgtaaa ggcgtgtatg 2820ccgttcggta caaggtgaat gaaaatcccc tgtacgcacc cacctcagaa catgtgaacg 2880tcctactgac ccgcacggag gaccgtatcg tgtggaaaac actagccggt gatccatgga 2940taaaaatact gacggccaag tatcctggga acttcactgc cacgatagag gaatggcaag 3000cagagcatga tgccatcatg aggcacatct tggagagacc ggaccctacc gacgttttcc 3060aaaataaggc gaacgtgtgt tgggccaagg ctttggtgcc ggtactgaag actgcaggca 3120tagacatgac cactgaacaa tggaacactg tggattactt cgaaacggac aaagctcact 3180cagcagagat agtattgaac caactatgcg tgaggttctt tggactcgac ctggactccg 3240gtctattttc tgcacccact gttccgttat ccattaggaa taatcactgg gataattccc 3300cgtcgcctaa catgtacggg ttgaataaag aagtggtccg ccagctctcc cgcaggtacc 3360cacaactgcc tcgagcagtt gccaccggaa gagtctatga catgaacact ggcacgctgc 3420gcaattatga tccgcgcata aatctagtac ctgtgaacag aagactgcct catgctttag 3480tcctccacca taatgaacac ccacagagtg acttttcttc attcgtcagc aaactgaagg 3540gcagaactgt cttggtggtc ggggagaagt tgtccgtccc aggcaaaaag gtcgactggt 3600tgtcagacca gcctgaggct acctttagag ctcggctgga tttaggtatc ccaggtgacg 3660tgcccaaata cgacattgta tttattaacg tgaggactcc atataaatac catcattatc 3720agcagtgtga agaccacgcc attaagctta gtatgttgac caagaaagct tgtctgcatt 3780tgaatcccgg cggaacctgc gtcagcatag gttatggtta cgctgacagg gccagcgaga 3840gcatcattgg tgctatagcg cggcagttca agttctcccg ggtatgcaaa ccgaaatcct 3900cacatgaaga gacagaagta ctgtttgtat tcattgggta cgatcgcaag gcccgtacgc 3960acaatcctta caagctttca tctaccttga ccaacatcta tacaggttcc agactccacg 4020aagccggatg cgcaccctca tatcatgtgg tgcgagggga tattgccacg gccaccgaag 4080gagtgatcat aaatgctgct aacagcaaag gacaacctgg cggaggggtg tgcggagcgc 4140tgtataagaa attcccggaa agcttcgatt tacagccgat cgaagtagga aaagcgcgac 4200tggtcaaagg tgcagctaaa catatcattc atgccgtagg accaaacttc aacaaagttt 4260cggaagttga aggggacaaa cagttggcag aggcttatga gtccatcgct aaaattgtca 4320acgataacaa ttacaagtca gtagcgattc cactgttgtc caccggcatc ttttccggga 4380acaaagatcg actaacccaa tcattgaacc atttgctgac agctttagac accactgatg 4440cagatgtagc catatactgc agggacaaga aatgggaaat gactctcaag gaagcagtgg 4500ctaggagaga agcagtggag gagatatgca tatcagacga ctcttcggtg acagaaccgg 4560atgcagagct ggtgagggta catccgaaga gttctttggc tggaaggaag ggctacagca 4620caagtgatgg caagactttc tcatatttgg aagggaccaa atttcaccag gcggccaagg 4680atatagcaga aattaatgcc atgtggccag ttgcaacgga ggccaatgag caagtatgca 4740tgtatatcct cggtgaaagc atgagcagca ttaggtcgaa atgccccgtc gaggagtcgg 4800aagcctccac accacctagc acgctgcctt gcttgtgcat ccatgctatg actccagaaa 4860gagtacaacg cctaaaagcc tcacgtccag aacaaattac tgtgtgctca tcctttccat 4920tgccgaagta tagaatcact ggtgtgcaga agatccagtg ctcccagcct atactgttct 4980caccgaaggt gcctgcgtac attcatccac ggaagtacct cgtggaaaca ccaccggtag 5040aagagactcc ggagtcgccg gcagagaacc aatccacaga ggggacacct gaacaaccag 5100cacttgtaaa cgtggatgca accaggacta gaatgcctga accgatcatc attgaagagg 5160aagaagagga tagtataagt ttgctgtcag acggcccgac ccaccaggtg ctgcaagtcg 5220aggcagacat tcacgggtcg ccttctgtat ccagctcatc ctggtccatt cctcatgcat 5280ccgactttga tgtggacagc ttatccatcc ttgacaccct ggatggagct agcgtgacca 5340gcggggcagt gtcagccgag actaactcct acttcgcaag gagcatggag tttcgggcgc 5400gaccggtgcc tgcgcctcga accgtattca ggaaccctcc acatcccgca ccgcgcacaa 5460gaacaccgcc acttgcacac agcagggcca gctcgagaac tagcctagtt tccaccccgc 5520caggcgtgaa tagggtgatt actagagagg agctcgaggc gcttaccccg tcccgcgctc 5580ctagcaggtc ggcctcaaga actagcctgg tctctaaccc gccaggcgta aatagggtga 5640ttacaagaga ggagtttgag gcgttcgtag cacaacaaca atgacggttt gacgcgggtg 5700catacatctt ttcctccgat accggtcaag ggcatttaca acaaaaatca gtaaggcaaa 5760cggtgttatc cgaagtggtg ttggagagga ccgaattgga gatttcgtat gccccgcgcc 5820tcgaccagga aaaagaagaa ctactacgca agaaattaca gctgaatccc acacctgcta 5880acagaagcag ataccagtcc aggagggtgg agaatatgaa agccataaca gctagacgta 5940ttctgcaagg cctagggcat tatttgaagg cagaaggaaa agtggagtgc tatcgaaccc 6000tgcatcctgt tcctttgtat tcatctagtg tgaatcgtgc tttttcaagc cccaaggtcg 6060cagtggaagc ctgcaatgcc atgctgaaag aaaattttcc gactgtagct tcctactgta 6120ttattccaga gtacgatgcc tatctggaca tggttgacgg cgcttcttgt tgcttagaca 6180ctgccagttt ttgccctgcg aagctgcgca gctttccaaa gaaacactcc tatttggaac 6240ccacaatacg gtcggcagtg ccatcagcga ttcagaacac gctccagaac gtcctggcag 6300ctgccacaaa aagaaattgc aacgtcacgc aaatgagaga attgcccgta ttggattcgg 6360ctgcctttaa tgtggaatgc ttcaagaaat atgcgtgcaa taatgaatat tgggaaacgt 6420ttaaagaaaa ccccatcagg cttactgaag aaaatgtggt aaattacatt actaaattaa 6480aaggaccaaa agctgctgct ctttttgcga agacacataa tttgaatatg ttacaggaca 6540taccaatgga caggtttgta atggacttaa agagggacgt gaaagtgact ccaggaacaa 6600aacatactga agaacggccc aaggtacagg tgattcaggc tgccgatcca ctagcgacag 6660cggatctgtg cggaatccac cgggagttgg ttaggagatt aaatgctgtc ctgcttccga 6720acatccatac actgtttgac atgtcggctg aagactttga cgctattatt gccgagcatt 6780tccagcctgg ggactgtgta ctggaaactg acattgcgtc gtttgataaa agtgaggacg 6840acgccatggc tctgaccgcg ttaatgattc tggaagacct aggagtggac gcagagctgt 6900tgacgctgat tgaggcggct ttcggcgaaa tatcatcaat acatttgccc accaaaacta 6960aatttaaatt cggagccatg atgaaatccg gaatgttcct cacactgttt gtgaacacag 7020tcatcaacat cgtaatcgca agcagagtgt taagagagcg gctaaccgga tcaccatgtg 7080cagcattcat tggagatgac aatatcgtga aaggagtcaa atctgacaaa ttaatggcag 7140acaggtgcgc cacttggttg aacatggaag tcaagatcat agacgccgtg gtgggcgaga 7200aagcgcccta tttttgtgga gggtttatct tgtgtgactc cgtgaccggc acagcgtgcc 7260gtgtggcaga ccccctaaaa aggctgttta agcttggcaa acccctggca gtagacgatg 7320aacatgacga tgacaggaga agggcattac acgaagagtc aacacgctgg aatcgagtgg 7380gaattcttcc agagctgtgt aaggcagtag aatcaaggta tgaaaccgta ggaacttcca 7440tcatagttat ggccatgact actctagcta gcagtgttaa atcattcagc tacctgagag 7500gggcccctat aactctctac ggctaacctg aatggactac gacatagtct agtccgccaa 7560gatgttcccg ttccaaccaa tgtatccgat gcagccaatg ccctatcgta acccgttcgc 7620ggccccgcgc aggccctggt tccccagaac cgaccctttt ctggcgatgc aggtgcagga 7680attaacccgc tcgatggcta acctgacgtt caagcaacgc cgggacgcgc cacctgaggg 7740gccacctgct aagaaaccta agagggaggc cccgcaaaag caaaaagggg gaggccaagg 7800gaagaagaag aagaaccagg ggaagaagaa ggccaagacg gggccgccta atccgaaggc 7860acagagtgga aacaagaaga agcccaacaa gaaaccaggc aagagacagc gcatggtcat 7920gaaattggaa tctgacaaga cattcccaat tatgctggaa gggaagatta acggctacgc 7980ttgcgtggtc ggagggaagt tattcaggcc gatgcacgtg gaaggcaaga tcgacaacga 8040cgttctggcc gcacttaaga cgaagaaagc atccaaatat gatcttgagt atgcagatgt 8100gccacagaac atgcgggccg atacattcaa gtacacccat gagaagcccc aaggctatta 8160cagctggcat catggagcag tccaatatga aaatgggcgt ttcacggtgc caaaaggagt 8220tggggccaag ggagacagcg gaagacccat tctggataat cagggacggg tggtcgctat 8280tgtgctggga ggtgtgaatg aaggatctag gacagccctt tcagtcgtca tgtggaacga 8340gaagggagta actgtgaagt atactccgga gaactgcgag caatggtcac tagtgaccac 8400tatgtgcctg ctcgccaatg tgacgttccc atgtgccgaa ccaccaattt gctacgacag 8460aaaaccagca gagactttgg ccatgctcag cgttaacgtt gacaacccgg gctacgatga 8520gctgctggaa gcagctgtta agtgccccgg aagaaaaagg agatctaccg aggagctgtt 8580taaggagtat aagctaacgc gcccttacat ggccagatgc atcagatgtg ccgttgggag 8640ctgccatagt ccaatagcaa ttgaggcagt gaagagcgac gggcacgacg gctatgttag 8700acttcagact tcctcgcagt atggcctgga ttcctctggc aacttaaagg gaaggactat 8760gcggtatgat atgcacggga ccattgaaga gataccacta catcaagtgt cactccacac 8820atctcgcccg tgtcacattg tggatgggca tggttatttt ctgcttgcta ggtgcccggc 8880aggggactcc atcaccatgg aatttaagaa aggttcagtc acacactcct gctcagtgcc 8940gtatgaagtg aaatttaatc ctgtaggcag agaactctac actcatccac cagaacacgg 9000agcagagcaa gcgtgccaag tctacgcgca cgatgcacag aacagaggag cttatgtcga 9060gatgcacctc ccgggctcag aagtggacag cagtttgatt tccttgagcg gcagttcagt 9120caccgtgaca cctcctgtcg ggactagcgc cttggtgaaa tgcaagtgcg gcggcacaaa 9180gatctccgaa accatcaaca aggcaaaaca gttcagccag tgcacaaaga aggagcagtg 9240cagagcatat cgactgcaga atgacaagtg ggtgtataat tctgacaaac tgcccaaagc 9300agcgggagcc accctaaaag gaaaactaca cgtcccgttc ttgctggcag acggcaaatg 9360caccgtgcct ctagcaccgg aacctatgat aaccttcggt ttccgatcag tgtcactgaa 9420actgcaccct aagaatccca catatctgac cactcgccaa cttgctgatg agcctcatta 9480cacgcacgag ctcatatctg aaccagctgt taggaatttt accgtcactg aaaaggggtg 9540ggagtttgta tggggaaacc atccgccgaa aaggttttgg gcacaggaaa cagcacccgg 9600aaatccacat gggctgccac atgaggtgat aactcattat taccacagat accctatgtc 9660caccatcctg ggtttgtcaa tttgcgccgc cattgtaacc gtttccgttg cagcgtccac 9720ctggctgttt tgcaaatcca gagtttcgtg cctaactcct taccggctaa cacctaacgc 9780caggatgccg ctttgcctgg ccgtgctttg ctgcgcccgc actgcccggg ccgagaccac 9840ctgggagtcc ttggatcacc tatggaacaa taaccaacag atgttctgga ttcaattgct 9900gatccctctg gccgccttga ttgtagtgac tcgcctgctc aagtgcgtgt gctgtgtagt 9960gcctttttta gtcgtggccg gcgccgcagg cgccggcgcc tacgagcacg cgaccacgat 10020gccgagccaa gcgggaatct cgtataacac catagtcaac agagcaggct acgcgccact 10080ccctatcagc ataacaccaa caaagatcaa gctgataccc acagtgaact tggagtacgt 10140cacctgccac tacaaaacag gaatggattc accagccatc aaatgctgcg gatctcagga 10200atgtactcca actaacaggc ctgatgaaca gtgcaaagtc ttcacagggg tttacccgtt 10260catgtgggga ggtgcatatt gcttttgcga cactgagaat actcaggtca gcaaggccta 10320cgtaatgaaa tctgacgact gccttgcgga tcatgctgaa gcatacaaag cgcacacagc 10380ctcagtgcag gcgttcctca acatcacagt gggggaacac tctattgtga ccaccgtgta 10440tgtgaatgga gaaactcctg tgaacttcaa tggggtcaaa ctaactgcag gtccactttc 10500cacagcttgg acaccctttg acagaaaaat cgtgcagtat gccggggaga tctataatta 10560cgattttcct gagtatgggg caggacaacc aggagcattt ggagacatac aatccagaac 10620agtctcaagc tcagatctgt atgccaatac caacctagtg ctgcagagac ccaaagcagg 10680agcgatccat gtgccataca ctcaggcacc atcgggtttt gagcaatgga agaaagataa 10740agctccgtca ttgaaattca ccgccccttt cggatgcgaa atatatacaa accccattcg 10800cgccgaaaat tgtgctgtag ggtcaattcc attagccttt gacattcccg acgccttgtt 10860caccagggtg tcagaaacac cgacactttc agcggccgaa tgcactctta acgagtgcgt 10920gtattcatcc gactttggcg ggatcgccac ggtcaagtat tcggccagca agtcaggcaa 10980gtgcgcagtc catgtgccat cagggactgc taccctaaaa gaagcagcag tcgagctaac 11040cgagcaaggg tcggcgacca ttcatttctc gaccgcaaat atccacccgg agttcaggct 11100ccaaatatgc acatcatatg tcacgtgcaa aggtgattgt caccccccga aagaccacat 11160tgtgacacac ccccagtatc acgcccaaac atttacagcc gcggtgtcaa aaaccgcgtg 11220gacgtggtta acatccctgc tgggaggatc ggccgtaatt attataattg gcttagtgct 11280ggctactatt gtggccatgt acgtgctgac caaccagaaa cataattgaa catagcagca 11340attggcaagc tgcttatata gaacttgcgg cgattggcat gccgctttaa aattttattt 11400tattttcttt tcttttccga atcggatttt gtttttaata tttc 11444220DNAArtificial SequencePrimer 2aatgctagag cguutucgca 20320DNAArtificial SequencePrimer 3aatgctagag cguutucgca 20417DNAArtificial SequencePrimer 4gctagagcgu utucgca 17517DNAArtificial SequencePrimer 5tgcgaagggu acgtcgt 17616DNAArtificial SequencePrimer 6tgugtgacca gaugac 16720DNAArtificial SequencePrimer 7aatgctagag cgttttcgca 20820DNAArtificial SequencePrimer 8aatgctagag cgttttcgca 20917DNAArtificial SequencePrimer 9gctagagcgt tttcgca 171014DNAArtificial SequencePrimer 10tgcgaagggt acgt 141117DNAArtificial SequencePrimer 11tgcgaagggt acgtcgt 171216DNAArtificial SequencePrimer 12tgtgtgacca gatgac 161321DNAArtificial SequencePrimer 13taatgctaga gcguutucgc a 211421DNAArtificial SequencePrimer 14taatgctaga gcguutucgc a 211521DNAArtificial SequencePrimer 15taatgctaga gcguutucgc a 211618DNAArtificial SequencePrimer 16tgctagagcg uutucgca 181715DNAArtificial SequencePrimer 17ttgcgaaggg uacgt 151818DNAArtificial SequencePrimer 18ttgcgaaggg uacgtcgt 181918DNAArtificial SequencePrimer 19ttgcgaaggg uacgtcgt 182017DNAArtificial SequencePrimer 20ttgugtgacc agaugac 172128DNAArtificial SequencePrimer 21tccatgctaa tgctagagcg ttttcgca 282224DNAArtificial SequencePrimer 22tgtcagttgc gaagggtacg tcgt 242321DNAArtificial SequencePrimer 23taatgctaga gcgttttcgc a 212418DNAArtificial SequencePrimer 24ttgcgaaggg tacgtcgt 182523DNAArtificial SequencePrimer 25uccaatgcta gagcgttttc gca 232620DNAArtificial SequencePrimer 26ucctgcgaag ggtacgtcgt 202724DNAArtificial SequencePrimer 27uccuaatgct agagcgtttt cgca 242821DNAArtificial SequencePrimer 28uccutgcgaa gggtacgtcg t 212925DNAArtificial SequencePrimer 29uccuuaatgc tagagcgttt tcgca 253022DNAArtificial SequencePrimer 30uccuutgcga agggtacgtc gt 223126DNAArtificial SequencePrimer 31tccttcaatg ctagagcgtt ttcgca 263223DNAArtificial SequencePrimer 32tccttctgcg aagggtacgt cgt 233328DNAArtificial SequencePrimer 33tgccagctac actgtgcgac cagatgac 283424DNAArtificial SequencePrimer 34tattgtcagt tgcgaagggt acgt 243524DNAArtificial SequencePrimer 35tattgtcagt tgcgacgggt acgt 243626DNAArtificial SequencePrimer 36tctatagtca gttgcgacgg gtacgt 263731DNAArtificial SequencePrimer 37tgtcagctac attgtgtgac caaatgactg g 313831DNAArtificial SequencePrimer 38taccagccac actttgcgat cagatgacag g 313928DNAArtificial SequencePrimer 39tccatgctaa cgccagagcg ttttcgca 284028DNAArtificial SequencePrimer 40tccatgctaa cgccagagcg ttttcgca 284125DNAArtificial SequencePrimer 41tgacgtagac ccccagagtc
cgttt 254227DNAArtificial SequencePrimer 42tggcgctatg atgaaatctg gaatgtt 274327DNAArtificial SequencePrimer 43tggcgctatg atgaaatctg gaatgtt 274424DNAArtificial SequencePrimer 44tgccttcatc ggcgatgaca acat 244531DNAArtificial SequencePrimer 45tgtcggccga ggattttgat gctatcatag c 314627DNAArtificial SequencePrimer 46tgcggtaccg tcaccatttc agaacac 274720DNAArtificial SequencePrimer 47gcacttccaa uguccaggat 204820DNAArtificial SequencePrimer 48gcacttccaa uguctaggat 204917DNAArtificial SequencePrimer 49ggcgcacutc caauguc 175020DNAArtificial SequencePrimer 50ttgcagcaca agaatccctc 205114DNAArtificial SequencePrimer 51tgguugagcc caac 145220DNAArtificial SequencePrimer 52gcacttccaa tgtccaggat 205320DNAArtificial SequencePrimer 53gcacttccaa tgtctaggat 205417DNAArtificial SequencePrimer 54ggcgcacttc caatgtc 175520DNAArtificial SequencePrimer 55ttgcagcaca agaatccctc 205620DNAArtificial SequencePrimer 56ttgcagcaca agaatccctc 205714DNAArtificial SequencePrimer 57tggttgagcc caac 145821DNAArtificial SequencePrimer 58tgcacttcca auguccagga t 215921DNAArtificial SequencePrimer 59tgcacttcca auguccagga t 216021DNAArtificial SequencePrimer 60tgcacttcca auguctagga t 216118DNAArtificial SequencePrimer 61tggcgcacut ccaauguc 186221DNAArtificial SequencePrimer 62tttgcagcac aagaatccct c 216321DNAArtificial SequencePrimer 63tttgcagcac aagaatccct c 216421DNAArtificial SequencePrimer 64tttgcagcac aagaatccct c 216515DNAArtificial SequencePrimer 65ttgguugagc ccaac 156624DNAArtificial SequencePrimer 66tggcgcactt ccaatgtcca ggat 246729DNAArtificial SequencePrimer 67tctgtcactt tgcagcacaa gaatccctc 296821DNAArtificial SequencePrimer 68tgcacttcca atgtccagga t 216921DNAArtificial SequencePrimer 69tttgcagcac aagaatccct c 217023DNAArtificial SequencePrimer 70uccgcacttc caatgtccag gat 237123DNAArtificial SequencePrimer 71uccttgcagc acaagaatcc ctc 237224DNAArtificial SequencePrimer 72uccugcactt ccaatgtcca ggat 247324DNAArtificial SequencePrimer 73uccuttgcag cacaagaatc cctc 247425DNAArtificial SequencePrimer 74uccuugcact tccaatgtcc aggat 257525DNAArtificial SequencePrimer 75uccuuttgca gcacaagaat ccctc 257626DNAArtificial SequencePrimer 76tccttcgcac ttccaatgtc caggat 267726DNAArtificial SequencePrimer 77tccttcttgc agcacaagaa tccctc 267828DNAArtificial SequencePrimer 78tgacgactat ccgctggttg agcccaac 287927DNAArtificial SequencePrimer 79tgtcactttg caacacaaga atccctc 278027DNAArtificial SequencePrimer 80tgtcactttg caacacaaga atccctc 278127DNAArtificial SequencePrimer 81tgtcactttg cagcacaaga atccctc 278228DNAArtificial SequencePrimer 82tgacgactat ccgctggttg agcccaac 288328DNAArtificial SequencePrimer 83tgacgactat ccgctggttg agcccaac 288427DNAArtificial SequencePrimer 84tgctggtgca cttccaatat ccaggat 278524DNAArtificial SequencePrimer 85tgccggtgcg ctgcctatgt ccaa 248625DNAArtificial SequencePrimer 86tcgctctggc attagcatgg tcatt 258724DNAArtificial SequencePrimer 87tatgttgtcg tcgccgatga acgc 248824DNAArtificial SequencePrimer 88tacgatgttg tcgtcgccga tgaa 248925DNAArtificial SequencePrimer 89tccaagtggc gcacctgtct gccat 259026DNAArtificial SequencePrimer 90tcatcttggc ttttgtcaaa ggaggc 269130DNAArtificial SequencePrimer 91tggtagttct ctcatttgtg tgacgttgca 30924108DNAArtificial SequenceCalibrant sequence pVIR001 92agcgcccaat acgcaaaccg cctctccccg cgcgttggcc gattcattaa tgcagctggc 60acgacaggtt tcccgactgg aaagcgggca gtgagcgcaa cgcaattaat gtgagttagc 120tcactcatta ggcaccccag gctttacact ttatgcttcc ggctcgtatg ttgtgtggaa 180ttgtgagcgg ataacaattt cacacaggaa acagctatga ccatgattac gccaagctat 240ttaggtgacg cgttagaata ctcaagctat gcatcaagct tggtaccgag ctcggatcca 300ctagtaacgg ccgccagtgt gctggaattc aggactcaag ctggagtgtg gaatgcatgc 360ttattcacat acaaactacc accatcacag cctggtaagt tcaagtttga caagactctt 420gaacctacac acaattgcat tggctgggta acgatcaacg ttacaattcc aaaacaaaca 480aacaccatca gtgaatttat cctctgtcac attttggata atcccaaccc ataaggtgtg 540gagtttctac atcactgtaa atttaacata ttatgccagc caccgtaaaa cttgcttgtt 600ccatgacgac tatgcgctgg ttgagcccaa ccagcagttt ttgcgcgtcg tccgcactga 660cttgccagta tgccagtcat ttggtcacac aatgtagctg ggtctgtcac tttgcagcac 720aagaatccct cgcggtgcat cgtagcagca tagcctgaag gcttcccata caggcctgga 780agctattctt ttaacgacgt acccgtcgca actaactata ctgcgggcgg gcgcacttcc 840aatgtcaagg atcgtgtcgg atgggtccac ctccgttcag ttttgaagcc agatgcgaaa 900acgctctggc attagcatgg tcattttgtc ctgaattctg cagatatcca tcacactggc 960ggccgctcga gcatgcatct agagggccca attcgcccta tagtgagtcg tattacaatt 1020cactggccgt cgttttacaa cgtcgtgact gggaaaaccc tggcgttacc caacttaatc 1080gccttgcagc acatccccct ttcgccagct ggcgtaatag cgaagaggcc cgcaccgatc 1140gcccttccca acagttgcgc agcctatacg tacggcagtt taaggtttac acctataaaa 1200gagagagccg ttatcgtctg tttgtggatg tacagagtga tattattgac acgccggggc 1260gacggatggt gatccccctg gccagtgcac gtctgctgtc agataaagtc tcccgtgaac 1320tttacccggt ggtgcatatc ggggatgaaa gctggcgcat gatgaccacc gatatggcca 1380gtgtgccggt ctccgttatc ggggaagaag tggctgatct cagccaccgc gaaaatgaca 1440tcaaaaacgc cattaacctg atgttctggg gaatataaat gtcaggcatg agattatcaa 1500aaaggatctt cacctagatc cttttcacgt agaaagccag tccgcagaaa cggtgctgac 1560cccggatgaa tgtcagctac tgggctatct ggacaaggga aaacgcaagc gcaaagagaa 1620agcaggtagc ttgcagtggg cttacatggc gatagctaga ctgggcggtt ttatggacag 1680caagcgaacc ggaattgcca gctggggcgc cctctggtaa ggttgggaag ccctgcaaag 1740taaactggat ggctttcttg ccgccaagga tctgatggcg caggggatca agctctgatc 1800aagagacagg atgaggatcg tttcgcatga ttgaacaaga tggattgcac gcaggttctc 1860cggccgcttg ggtggagagg ctattcggct atgactgggc acaacagaca atcggctgct 1920ctgatgccgc cgtgttccgg ctgtcagcgc aggggcgccc ggttcttttt gtcaagaccg 1980acctgtccgg tgccctgaat gaactgcaag acgaggcagc gcggctatcg tggctggcca 2040cgacgggcgt tccttgcgca gctgtgctcg acgttgtcac tgaagcggga agggactggc 2100tgctattggg cgaagtgccg gggcaggatc tcctgtcatc tcaccttgct cctgccgaga 2160aagtatccat catggctgat gcaatgcggc ggctgcatac gcttgatccg gctacctgcc 2220cattcgacca ccaagcgaaa catcgcatcg agcgagcacg tactcggatg gaagccggtc 2280ttgtcgatca ggatgatctg gacgaagagc atcaggggct cgcgccagcc gaactgttcg 2340ccaggctcaa ggcgagcatg cccgacggcg aggatctcgt cgtgacccat ggcgatgcct 2400gcttgccgaa tatcatggtg gaaaatggcc gcttttctgg attcatcgac tgtggccggc 2460tgggtgtggc ggaccgctat caggacatag cgttggctac ccgtgatatt gctgaagagc 2520ttggcggcga atgggctgac cgcttcctcg tgctttacgg tatcgccgct cccgattcgc 2580agcgcatcgc cttctatcgc cttcttgacg agttcttctg aattattaac gcttacaatt 2640tcctgatgcg gtattttctc cttacgcatc tgtgcggtat ttcacaccgc atcaggtggc 2700acttttcggg gaaatgtgcg cggaacccct atttgtttat ttttctaaat acattcaaat 2760atgtatccgc tcatgagaca ataaccctga taaatgcttc aataatagca cgtgaggagg 2820gccaccatgg ccaagttgac cagtgccgtt ccggtgctca ccgcgcgcga cgtcgccgga 2880gcggtcgagt tctggaccga ccggctcggg ttctcccggg acttcgtgga ggacgacttc 2940gccggtgtgg tccgggacga cgtgaccctg ttcatcagcg cggtccagga ccaggtggtg 3000ccggacaaca ccctggcctg ggtgtgggtg cgcggcctgg acgagctgta cgccgagtgg 3060tcggaggtcg tgtccacgaa cttccgggac gcctccgggc cggccatgac cgagatcggc 3120gagcagccgt gggggcggga gttcgccctg cgcgacccgg ccggcaactg cgtgcacttc 3180gtggccgagg agcaggactg acacgtgcta aaacttcatt tttaatttaa aaggatctag 3240gtgaagatcc tttttgataa tctcatgacc aaaatccctt aacgtgagtt ttcgttccac 3300tgagcgtcag accccgtaga aaagatcaaa ggatcttctt gagatccttt ttttctgcgc 3360gtaatctgct gcttgcaaac aaaaaaacca ccgctaccag cggtggtttg tttgccggat 3420caagagctac caactctttt tccgaaggta actggcttca gcagagcgca gataccaaat 3480actgttcttc tagtgtagcc gtagttaggc caccacttca agaactctgt agcaccgcct 3540acatacctcg ctctgctaat cctgttacca gtggctgctg ccagtggcga taagtcgtgt 3600cttaccgggt tggactcaag acgatagtta ccggataagg cgcagcggtc gggctgaacg 3660gggggttcgt gcacacagcc cagcttggag cgaacgacct acaccgaact gagataccta 3720cagcgtgagc tatgagaaag cgccacgctt cccgaaggga gaaaggcgga caggtatccg 3780gtaagcggca gggtcggaac aggagagcgc acgagggagc ttccaggggg aaacgcctgg 3840tatctttata gtcctgtcgg gtttcgccac ctctgacttg agcgtcgatt tttgtgatgc 3900tcgtcagggg ggcggagcct atggaaaaac gccagcaacg cggccttttt acggttcctg 3960gccttttgct ggccttttgc tcacatgttc tttcctgcgt tatcccctga ttctgtggat 4020aaccgtatta ccgcctttga gtgagctgat accgctcgcc gcagccgaac gaccgagcgc 4080agcgagtcag tgagcgagga agcggaag 41089317DNAArtificial SequencePrimer 93gctagagcgt tttcgca 17
Patent applications by Mark W. Eshoo, Solana Beach, CA US
Patent applications by Rangarajan Sampath, San Diego, CA US
Patent applications by Thomas A. Hall, Oceanside, CA US
Patent applications by IBIS BIOSCIENCES, INC.
Patent applications in class Involving virus or bacteriophage
Patent applications in all subclasses Involving virus or bacteriophage