Patent application title: INFECTIOUS CLONES
Luis Enjuanes Sanchez (Madrid, ES)
Consejo Superior De Investigaciones Cientificas
IPC8 Class: AA61K39215FI
Class name: Drug, bio-affecting and body treating compositions antigen, epitope, or other immunospecific immunoeffector (e.g., immunospecific vaccine, immunospecific stimulator of cell-mediated immunity, immunospecific tolerogen, immunospecific immunosuppressor, etc.) recombinant virus encoding one or more heterologous proteins or fragments thereof
Publication date: 2011-06-16
Patent application number: 20110142879
Methods of preparing a DNA comprising sequences derived from the genomic
RNA (gRNA) of a coronavirus are provided, comprising cloning under the
expression of a promoter a coronavirus interfering defective genome into
a bacterial artificial chromosome (BAC) and reinserting into said genome
the deleted sequences within the defective genome, wherein said sequences
have a homology of at least 60% to the natural sequence of the virus,
wherein said sequences code for an RNA-dependent RNA polymerase and at
least one structural or non-structural protein, and wherein a fragment of
said DNA is capable of being transcribed into RNA and assembeld to a
virion. Also provided are infective clones, recombinant viral vectors,
75. A method of preparing a DNA comprising sequences derived from the genomic RNA (gRNA) of a coronavirus comprising: cloning under the expression of a promoter a coronavirus interfering defective genome into a bacterial artificial chromosome (BAC); and re-inserting into said genome the deleted sequences within the defective genome wherein said sequences have a homology of at least 60% to the natural sequence of the virus, wherein said sequences code for an RNA-dependent RNA polymerase and at least one structural or non-structural protein, and wherein a fragment of said DNA is capable of being transcribed into RNA and assembled to a virion.
76. The method according to claim 75, wherein sequences within the viral genome which are toxic for the bacteria into which it is to be cloned are identified before re-insertion into said DNA.
77. The method according to claim 76, wherein the toxic sequences within the viral genome are the last sequences to be re-inserted when completing the genome.
78. The method according to claim 75, wherein an infective clone is obtained which comprises a full-length copy of complementary DNA (cDNA) to the gRNA of a coronavirus cloned under a transcriptional regulatory sequence, said method further comprising: constructing the full-length cDNA from the gRNA of a coronarivus; and joining the transcriptional-regulatory elements to said full-length cDNA.
79. The method according to claim 78, wherein construction of the full-length cDNA of the gRNA of a coronavirus comprises: cloning an interfering defective genome derived from said coronavirus under a promoter of expression in a BAC; completing the deletions of said interfering defective genome by regenerating the deleted sequences with respect to the infective gRNA; identifying the sequences in the coronavirus which are toxic for the bacteria in which it is going to be cloned; removing said toxic sequences; and inserting said toxic sequences just before effecting the transfection in eukaryotic cells to obtain the cDNA clone corresponding to the gRNA of the coronavirus.
80. An infective clone comprising a full-length copy of complementary DNA (cDNA) to the genomic RNA (gRNA) of a coronavirus cloned under a transcription-regulatory sequence, wherein said infective cDNA is cloned in a bacterial artificial chromosome (BAC).
81. The infective clone according to claim 80, wherein said coronavirus is an isolate of the porcine transmissible gastroenteritis virus (TGEV).
82. The infective clone according to claim 80, wherein the promoter employed is the immediately early (IE) promoter of expression of cytomegalovirus (CMV).
83. The infective clone according to claim 80, wherein said full-length cDNA is flanked at the 3' end by a poly(A) tail, the ribozyme of the hepatitis delta virus (HDV), and the termination and polyadenylation sequences of bovine growth hormone (BGH).
84. The infective clone according to claim 80, wherein said infective cDNA is obtainable from the BAC of E. coli deposited under CECT 5265 at the Spanish Collection of Type Cultures.
85. E. coli deposited under CECT 5265 at the Spanish Collection of Type Cultures.
86. A recombinant viral vector comprising an infective clone according to claim 80 modified to contain a heterologous nucleic acid inserted into said infective clone under conditions that allow said heterologous nucleic acid to be expressed.
87. The recombinant viral vector according to claim 86, wherein said heterologous nucleic acid is selected between a gene and a gene fragment that codes a gene product of interest.
88. A vaccine for protecting an animal against the infection caused by an infectious agent comprising at least one recombinant viral vector according to claim 86, wherein said viral vector expresses either at least one antigen suitable for inducing an immune response against said infectious agent or an antibody that provides protection against said infectious agent.
89. The vaccine according to claim 88, further comprising a pharmaceutically-acceptable excipient.
90. The vaccine according to claim 88, wherein said viral vector expresses at least one antigen capable of inducing a systemic immune response and/or an immune response in mucous membranes against different infectious agents that propagate in respiratory or intestinal mucous membranes.
91. The vaccine according to claim 88, wherein the vaccine is a multivalent vaccine for protection against the infection caused by more than one infectious agent.
92. The multivalent vaccine according to claim 91, further comprising independent recombinant viral vectors for mixing and joint inoculation, wherein said recombinant viral vectors each express at least one different antigen or a different antibody.
CROSS-REFERENCE TO RELATED APPLICATIONS
 This application is a divisional application of U.S. patent application Ser. No. 12/285,213, filed on Sep. 30, 2008, which is a continuation application of U.S. patent application Ser. No. 10/148,669, filed on Jun. 3, 2002, now U.S. Pat. No. 7,445,928, issued on Nov. 4, 2007, which is a U.S. National Stage application pursuant to 35 U.S.C. §371 of International Patent Application No. PCT/EP00/12063, filed on Nov. 30, 2000, and published as WO 01/39797 on Jun. 7, 2001 which claims priority to Spanish Patent Application No. 9902673, filed on Dec. 3, 1999, the contents of which are incorporated herein by reference in their entireties for all purposes.
FIELD OF THE INVENTION
 This invention relates to methods of preparing a DNA or an RNA, nucleic acids obtainable by this method and their use as vaccines and for gene therapy.
BACKGROUND OF THE INVENTION
 Advances in recombinant DNA technology have led to progress in the development of gene transfer between organisms. At this time, numerous efforts are being made to produce chemical, pharmaceutical, and biological products of economic and commercial interest through the use of gene transfer techniques.
 One of the key elements in genetic manipulation of both prokaryotic and eukaryotic cells is the development of vectors and vector-host systems. In general, a vector is a nucleic acid molecule capable of replicating or expressing in a host cell. A vector-host system can be defined as a host cell that bears a vector and allows the genetic information it contains to be replicated and expressed.
 Vectors have been developed from viruses with both DNA and RNA genomes. Viral vectors derived from DNA viruses that replicate in the nucleus of the host cell have the drawback of being able to integrate into the genome of said cell, so they are generally not very safe. In contrast, viral vectors derived from RNA viruses, which replicate in the cytoplasm of the host cell, are safer than those based on DNA viruses, since the replication occurs through RNA outside the nucleus. These vectors are thus very unlikely to integrate into the host cell's genome.
 cDNA clones have been obtained from single-chain RNA viruses with positive polarity [ssRNA(+)], for example, picornavirus (Racaniello & Baltimore, 1981); bromovirus (Ahlquist et al., 1984); alphavirus, a genus that includes the Sindbis virus; Semliki Forest virus (SFV) and the Venezuelan equine encephalitis virus (VEE) (Rice et al., 1987; Liljestrom and Garoff, 1991; Frolov et al., 1996; Smerdou and Liljestrom, 1999); flavivirus and pestivirus (Rice and Strauss, 1981; Lai et al., 1991; Rice et al., 1989); and viruses of the Astroviridae family (Geigenmuller et al., 1997). Likewise, vectors for the expression of heterologous genes have been developed from clones of DNA complementary to the genome of ssRNA(+) virus, for example alphavirus, including the Sindbis virus, Semliki Forest virus (SFV), and the Venezuelan equine encephalitis (VEE) virus (Frolov et al., 1996; Liljestrom, 1994; Pushko et al., 1997). However, all methods of preparing recombinant viruses starting from RNA viruses are still complicated by the fact that most of the viruses comprise sequences which are toxic for bacteria. Preparing a cDNA of the viral RNA and subcloning of the cDNA in bacteria therefore often leads to deletion or rearangement of the DNA sequences in the bacterial host. For this purpose most of the commonly used subcloning and expression vectors cannot be used for preparation of large DNA sections derived from recombinant RNA viruses. However, obtaining vectors, which can carry long foreign DNA sequences is required for a number of aspects in the development of pharmaceuticals, specifically vaccines.
 The coronaviruses are ssRNA(+) viruses that present the largest known genome for an RNA virus, with a length comprised between about 25 and 31 kilobases (kb) (Siddell, 1995; Lai & Cavanagh, 1997; Enjuanes et al., 1998). During infection by coronavirus, the genomic. RNA (gRNA) replicates and a set of subgenomic RNAs (sgRNA) of positive and negative polarity is synthesized (Sethna et al., 1989; Sawicki and Sawicki, 1990; van der Most & Spaan, 1995). The synthesis of the sgRNAs is an RNA-dependent process that occurs in the cytoplasm of the infected cell, although its precise mechanism is still not exactly known.
 The construction of cDNAs that code defective interfering (DI) genomes (deletion mutants that require the presence of a complementing virus for their replication and transcription) of some coronaviruses, such as the murine hepatitis virus (MHV), infectious bronchitis virus (IBV), bovine coronavirus (BCV) (Chang et al., 1994), and porcine gastroenteritis virus (TGEV) (Spanish Patent Application P9600620; Mendez et al., 1996; Izeta et al., 1999; Sanchez et al., 1999) has been described. However, the construction of a cDNA clone that codes a complete genome of a coronavirus has not been possible due to the large size of and the toxic sequences within the coronavirus genome.
 In summary, although a large number of viral vectors have been developed to replicate and express heterologous nucleic acids in host cells, the majority of the known vectors for expression of heterologous genes are not well suited for subcloning of RNA viruses. Further, the viral vectors so obtained present drawbacks due to lack of species specificity and target organ or tissue limitation and to their limited capacity for cloning, which restricts the possibilities of use in both basic and applied research.
 Hence there is a need for methods to develop new vectors for expression of heterologous genes that can overcome the aforesaid problems. In particular, it would be advantagous to have large vectors for expression of heterologous genes with a high level of safety and cloning capacity, which can be designed so that their species specificity and tropism can be controlled.
SUMMARY OF THE INVENTION
 According to the present invention the above problems are solved by a method of preparing a DNA comprising steps, wherein  (a) a DNA comprising a full length copy of the genomic RNA (gRNA) of an RNA virus; or  (b) a DNA comprising one or several fragments of a gRNA of an RNA virus, which fragments code for an RNA dependent RNA polymerase and at least one structural or non-structural protein; or  (c) a DNA having a homology of at least 60% to the sequences of (a) or (b); is cloned into a bacterial artificial chromosome (BAC).
 Surprisingly, the present inventors found that the problems encountered by the prior art methods to subclone and express large DNA sequences derived from viral gRNA can be overcome by using BACs as a cloning vector. The use of BACs has the particular advantage that these vectors are present in bacteria in a number of one or two copies per cell, which considerably limits the toxicity and reduces the possibilities of interplasmid recombinantion.
 The invention further provides methods of preparing a viral RNA or a virion comprising steps, wherein a DNA is prepared according to one of the above methods, the DNA is expressed and the viral RNA or the virion is isolated. Further, methods of preparing pharmaceuticals, specifically vaccines comprising the steps of the above methods to prepare a DNA are disclosed.
 According to another aspect of the present invention provides a DNA comprising sequences derived from the genomic RNA (gRNA) of a coronavirus which sequences have a homology of at least 60% to the natural sequence of the coronavirus and code for an RNA dependent RNA polymerase and at least one structural or non-structural protein, wherein a fragment of said DNA is capable of being transcribed into RNA and which RNA can be assembled to a virion. The present invention also encompasses methods of preparing respective DNAs.
 The present invention further provides vectors, more specifically bacterial artificial chromosomes (BACs) comprising respective nucleic acids. According to a further embodiment the present invention is directed to host cells and infectious, attenuated or inactivated virions comprising the DNAs or RNAs of the present invention.
 The invention also provides pharmaceutical preparations, such as mono- or multivalent vaccines comprising nucleic acids, vectors, host cells or virions of the present invention.
 Finally, the present invention provides methods for producing a virion or a viral RNA comprising steps, wherein a DNA according to the present invention is transcribed and the virions or viral RNAs are recovered, as well as viral RNAs obtainable by this method.
BRIEF DESCRIPTION OF THE FIGURES
 FIG. 1 shows the construction of a cDNA clone that codes an infective RNA of TGEV. FIG. 1A shows the genetic structure of the TGEV, with the names of the genes indicated by letters and numbers (1a, 1b, S, 3a, 3b, E, M, N, and 7). FIG. 1B shows the cDNA-cloning strategy, which consisted in completing the DI-C genome. Deletions Δ1, Δ2, and Δ3 that have been completed to reestablish the full length of the cDNA are indicated. The numbers located beneath the structure of the DI-C genome indicate the nucleotides that flank each deletion in said DI-C genome. FIG. 1C shows the four cDNA fragments constructed to complete deletion Δ1 and the position of the principal restriction sites used during joining. The insertion of fragment Δ1 produced an increase in the toxicity of the cDNA.
 FIG. 2 shows the structure of the pBeloBAC plasmid (Wang et al., 1997) used in cloning the infective cDNA of TGEV. The pBeloBAC plasmid was provided by H. Shizuya and M. Simon (California Institute of Technology) and includes 7,507 base pairs (bp) that contain the replication origin of the F factor of E. coli (oriS), the genes necessary to keep one single copy of the plasmid per cell (parA, parB, parC, and repE), and the chloramphenicol-resistance gene (CMr). The positions of the T7 and SP6 promoters and of the unique restriction sites are indicated. CosN: site cosN of lambda to facilitate the construction of the pBAC plasmid; lac Z: β-galactosidase gene. Sequence loxP used during the generation of the plasmid is also indicated.
 FIG. 3 shows the structure of the basic plasmids used in the construction of TGEV cDNA. The pBAC-TcDNA.sup.ΔClaI plasmid contains all the information of the TGEV RNA except for one ClaI-ClaI fragment of 5,198 bp. The cDNA was cloned under the immediately early (IE) promoter of expression of cytomegalovirus (CMV) and is flanked at the 3'-end by a poly(A) tail with 24 residues of A, the ribozyme of the hepatitis delta virus (HDV), and the termination and polyadenylation sequences of bovine growth hormone (BGH). The pBAC-B+C+D5' plasmid contains the ClaI-ClaI fragment required to complete the pBAC-TcDNA.sup.ΔClaI until the cDNA is full length. The pBAC-TcDNAFL plasmid contains the full-length cDNA of TGEV. SAP: shrimp alkaline phosphatase.
 FIG. 4 shows the differences in the nucleotide sequence of the S gene of the clones of TGEV PUR46-MAD (MAD) (SEQ ID NOs: 8 & 9) and C11 (SEQ ID NOs: 6 & 7). The numbers indicate the positions of the substituted nucleotides, considering as nucleotide one of each gene the A of the initiating codon. The letters within the bars indicate the corresponding nucleotide in the position indicated. The letters located beneath the bars indicate the amino acid (aa) substitutions coded by the nucleotides that are around the indicated position. Δ6 nt indicates a 6-nucleotide deletion. The arrow indicates the position of the termination codon of the S gene.
 FIG. 5 shows the strategy followed to rescue the infective TGEV from the full-length TGEV cDNA. The pBAC-TcDNAFL plasmid was transfected to ST cells (pig testicle cells), and 48 h after transfection, the supernatant was used to infect new ST cells. The virus was passed at the times indicated. At each passage, aliquots of supernatant and of cellular monolayer were collected for virus titration and isolation of RNA for RT-PCR analysis, respectively. vgRNA: full-length viral RNA.
 FIG. 6 shows the cytopathic effect (CPE) produced by the TGEV cDNA in the transfected ST cells. The absence of CPE in non-transfected (control) ST cells (FIG. 6A) and the CPE observed 14 and 20 h after transfection with pBAC-TcDNAFL in ST cells are shown (FIGS. 6B and 6C, respectively).
 FIG. 7 shows the evolution of the viral titer with the passage. A graph representing the viral titer in the supernatant of two series of cellular monolayers (1 and 2) at different passages after transfection with pBAC-TcDNAFL is shown. Mock 1 and 2 refer to nontransfected ST cells. TcDNA 1 and 2 refer to ST cells transfected with pBAC-TcDNAFL.
 FIG. 8 shows the results of the analysis of the sequence of the virus recovered after transfecting ST cells with pBAC-TcDNAFL. The structure of the TGEV genome is indicated at the top of the figure. Likewise, the differences in the sequence of nucleotides (genetic markers) between the virus recovered from the pBAC-TcDNAFL (TcDNA) plasmid, and TGEV clones C8 and C11 are indicated. The positions of the differences between the nucleotides are indicated by the numbers located over the bar. The cDNA sequences of the TcDNA virus and of clone C11 were determined by sequencing the fragments obtained by RT-PCR (reverse-transcription and polymerase chain reaction). The sequence of clone C8 is being sent for publication (Penzes et al., 1999) and is included at the end of this patent. The restriction patterns are shown with ClaI and DraIII of the fragments obtained by RT-PCR that include nucleotides 18,997 and 20,990 of the TcDNA and C8 viruses. The restriction patterns show the presence or absence of ClaI and DraIII sites in the cDNA of these viruses. The result of this analysis indicated that the TcDNA virus recovered had the S-gene sequence expected for isolate C11. MWM: molecular weight markers.
 FIG. 9 shows the results of the RT-PCR analysis of the virus recovered. The viral RNA was expressed under the control of the CMV promoter recognized by the cellular polymerase pol II. In principle, this RNA could undergo splicing during its transport to the cytoplasm. To study whether this was the case, the sites of the RNA with a high probability of splicing were determined using a program for predicting splicing sites in sequences of human DNA (Version 18.104.22.168, Department of Cell Biology, Baylor College of Medicine) (Solovyev et al., 1994). The potential splicing site with maximum probability of cut had the donor site at nt 7,243 and the receiver at nt 7,570 (FIG. 9A). To study whether this domain had undergone splicing, a RT-PCR fragment flanked by nt 7,078 and nt 7,802 (FIG. 9B) was prepared from RNA of passages 0 and 2 of nontransfected cultures (control), or from ST cells transfected with TcDNA with the ClaI fragment in reverse orientation (TcDNAFL(-ΔClaI)RS ), or in the correct orientation (TcDNAFL), and the products resulting from the RT-PCR were analyzed in agarose gels. The results obtained are shown in FIGS. 9C (passage 0) and 9D (passage 2).
 FIG. 10 shows the results of the immunofluorescence analysis of the virus produced in cultures of ST cells transfected with TcDNA. Staining for immunofluorescence was done with antibodies specific for the TGEV PUR46-MAD isolate, and for the virus recovered after transfection with the pBAC-TcDNAFLplasmid. For this, TGEV-specific monoclonal antibodies were used which bind to both isolates or only to PUR46-MAD (Sanchez et al., 1990). The result confirmed that the TcDNA virus had the expected antigenicity. The specific polyclonal antiserum for TGEV bound to both viruses, but not to the uninfected cultures, and only the expected monoclonal antibodies specific for the S (ID.B12 and 6A.C3), M (3B.B3), and N (3B.D8) proteins bound to the TcDNA virus (Sanchez et al., 1999).
 FIG. 11 (SEQ ID NOs: 10-15) shows the expression of GUS under different transcription-regulatory sequences (TRSs) that vary flanking region 5' of the intergenic (IG) sequence. In FIG. 11A, minigenome M39 was cloned under the control of the CMV promoter. Inserted into this minigenome was a multiple cloning sequence (PL1, 5'-CCTAGGATTTAAATCCTAAGG-3'; SEQ ID NO:2) and the transcription unit formed by the selected transcription-regulating sequences (TRS), another multiple cloning sequence (PL2, 5'-GCGGCCGCGCCGGCGAGGCCTGTCGAC-3'; SEQ ID NO:3; or PL3, 5'-GTCGAC-3'; SEQ ID NO:4), sequences with the structure of a Kozak (Kz) domain, the 5-glucuronidase (GUS) gene, and another multiple cloning site (PL4, 5'-GCTAGCCCAGGCGCGCGGTACC-3'; SEQ ID NO:5). These sequences 1were flanked at the 3'-end by the 3'-sequence of minigenome M39, the HDV ribozyme, and the termination and polyadenylation sequences of BGH. The TRSs had a different number (0, -3, -8, and -88) of nucleotides at the 5'-end of the IG sequence (CUAAAC), and came from the N, S, or M genes, as indicated. ST cells were transfected with the different plasmids, were infected with the complementing virus (PUR46-MAD), and the supernatants were passed 6 times. The GUS activity in the infected cells was determined by means of the protocol described by Izeta (Izeta et al., 1999). The results obtained by relating the GUS activity to the passage number are collected in FIG. 11B. It should be noted that CTAAAC and CUAAC have the same meaning for the purpose of this patent. The first represents the sequence of the DNA and the second that of the corresponding RNA.
 FIG. 12 (SEQ ID NOs: 16-24) shows the expression of GUS under different TRSs that vary in the 3'-flanking region of the IG sequence (see FIG. 11A). Using this transcription unit with the 5'-flanking region corresponding to the -88 nt of the N gene of TGEV plus the IG sequence (CUAAAC), the 3'-flanking sequences were modified. These sequences corresponded to those of the different TGEV genes (S, 3a, 3b, E, M, N, and 7), as is indicated in FIG. 12A. In two cases, 3'-sequences were replaced by others that contained a restriction site (SalI) and an optimized Kozak sequence (Kz), or by a sequence identical to the one that follows the first IG sequence located following the leader of the viral genome. The activity of GUS in the infected cells was determined by means of the protocol described above (Izeta et al., 1999). cL12 indicates a sequence of 12 nucleotides identical to that of 3'-end of the "leader" sequence of the TGEV genome (see the virus sequence indicated at the end). The results obtained by relating the expression of GUS to the passage number are collected in FIG. 12B.
 FIG. 13 shows the effect of the site of insertion of the module of expression in the minigenome over the levels of GUS expression. The GUS transcription unit, containing -88 nt of the N gene flanking the 5'-end of the IG sequence (CUAAAC), and the Kz sequences flanking the 3'-end (see FIG. 12A), was inserted into four single restriction sites in minigenome M39 (FIG. 13A) to determine if all these sites were equally permissive for the expression of the heterologous gene. ST cells were transfected with these plasmids and infected with the complementing virus (PUR46-MAD). The GUS activity in the infected cells was determined at passage 0 (P0) following the protocol described above (Izeta et al., 1999). The results obtained are collected in FIG. 13B.
 FIG. 14 (SEQ ID NO: 1) shows the consensus sequence of the PUR46-MAD isolate of TGEV.
DETAILED DESCRIPTION OF THE INVENTION
 According to the present invention methods of preparing a DNA are provided, which comprise steps, wherein  (a) a DNA comprising a full length copy of the genomic RNA (gRNA) of an RNA virus; or  (b) a DNA comprising one or several fragments of a gRNA of an
 RNA virus, which fragments code for an RNA dependent RNA polymerase and at least one structural or non-structural protein; or  (c) a DNA having a homology of at least 60% to the sequences of (a) or (b); is cloned into a bacterial artificial chromosome (BAC).
 According to the present application a "bacterial artificial chromosome" is a DNA sequence which comprises the sequence of the F factor. Plasmids containing this sequences, so-called F plasmids, are capable of stably maintaining heterologous sequences longer than 300 Kb in low copy number (one or two copies per cell). Respective BACs are known in the art (Shizuya et al., 1992).
 According to the present invention the DNA cloned into the BAC has a homology of at least 60%, preferably 75% and more preferably 85 or 95%, to a natural sequence of an RNA virus. Sequence homology is preferably determined using the Clustal computer program available from the European Bioinformatics Institute (EBI).
 According to the methods of the present invention the DNA cloned into the BAC may further comprise sequences coding for several or all except one of the structural or non-structural proteins of the virus.
 In a preferred embodiment of the present invention the DNA cloned into the BAC further comprises sequences encoding one or several heterologous gene. According to the present application a gene is characterized as a "heterologous gene" if it is not derived from the virus which was used as a source for the genes encoding the RNA dependent RNA polymerase and the structural or non-structural protein. A "heterologous gene" thus also refers to genes derived from one type of virus and expressed in a vector comprising sequences derived from another type of virus. Any heterologous gene of interest can be inserted into the nucleic acids of the present invention. The insertion of genes encoding one or several peptides or proteins which are recognised as an antigen from an infectious agent by the immune system of a mammal is especially preferred. Alternatively, the method of the present invention may be performed using heterologous genes encoding at least one molecule interfering with the replication of an infectious agent or an antibody providing protection against an infectious agent. The heterologous sequences may contain sequences encoding an immune modulator, a cytokine, an immonenhancer and/or an anti-inflammatory compound.
 The method of the present invention may be performed using a DNA for cloning into a BAC that has any size. However, specific advantages over the known methods to prepare subcloned DNA from viral are obtained, if large sequences are used. The DNA cloned into the BAC may thus comprise a length of at least 5 Kb, wherein DNA with a size of at least 15, 25 or 30 Kb is specifically preferred.
 According to specifically preferred embodiments of the present invention methods are provided, wherein the BAC comprises a sequence controlling the transcription of the DNA cloned into the BAC. This will allow transcription of the viral RNA and thus enable expression of the virus. Any sequence controlling transcription known in the art maybe used for this purpose, including sequences driving the expression of genes derived from DNA or RNA genomes. The use of the immediately early (IE) promoter of cytomegalovirus (CMV) is preferred.
 The DNA cloned into the BAC may also be flanked at the 3'-end by a poly (A) tail. The nucleic acid may comprise termination and/or polyadenylation sequences of bovine growth hormone (BGH). Additionally or alternatively, the nucleic acids may comprise sequences encoding a ribozyme, for example the ribozyme of the hepatitis δ virus (HDV).
 Additional advantages may be achieved if at least one of the genes of the virus has been modified by substituting, deleting or adding nucleotides. For example the gene controlling tropism of the virus may be modified to obtain viruses with altered tropism. Alternativly, the gene controlling tropism of the virus has been substituted with the respective gene of another virus. The modification is preferably performed in the S, M and/or N genes of the virus.
 In a preferred embodiment of the present invention a method is provided, wherein the DNA cloned into the BAC is capable of being transcribed into RNA which RNA can be assembled to an virion. The virion may be an infectious, attenuated, replication defective or inactivated virus.
 Any RNA virus may be used in the methods of the invention. The virus can for example be a picornavirus, flavivirus, togavirus, coronavirus, toroviruses, arterivurses, calcivirus, rhabdovirus, paramixovirus, Filovirus, bornavirus, orthomyxovirus, bunyavirus, arenavirus or reovirus. The use of viruses naturally having a plus strand genome is preferred.
 Additionally, the present invention provides methods of preparing a viral RNA or a virion comprising steps, wherein a DNA is prepared according to one of above methods, the DNA is expressed in a suitable host cell and the viral RNA or the virion is isolated from that host cell. Any of methods for isolating viruses from the cell culture known in the art may be used. Alternatively, methods of preparing a viral RNA or a virion are disclosed, wherein the DNA of the present invention is transcribed or translated using chemicals, biological reagents and/or cell extracts and the viral RNA or the virion is subsequently isolated. For certain embodiments, the virus may subsequently be inactivated or killed.
 The invention also provides methods for preparing a pharmaceutical composition comprising steps, wherein a DNA, a viral RNA or a virion is prepared according to one of the above methods and is subsequently mixed with a pharmaceutically acceptable adjuvants and/or carrier. A large number of adjuvans and carriers and diluents are known in the prior art and may be used in accordance with the present invention. The pharmaceutical is preferably a vaccine for protecting humans or animals against an infectious disease. The pharmaceutical can advantageously also be used for gene therapy.
 The present invention further provides for the first time a DNA comprising sequences derived from the genomic RNA (gRNA) of a coronavirus which sequences have a homology of at least 60% to the natural sequence of the coronavirus and code for an RNA dependent RNA polymerase and at least one structural or non-structural protein, wherein a fragment of said DNA is capable of being transcribed into RNA which can be assembled to a virion.
 According to the present invention the term "sequence derived from a coronavirus" is used to refer to a nucleic acid sequence which has a homology of at least 60%, preferably 75% and more preferably 85 or 95%, to a natural sequence of a coronavirus. Sequence homology can be determined using the Clustal computer program available from the European Bioinformatics Institute (EBI).
 The term "coronavirus" is used according to the present invention to refer to a group of viruses having a single molecule of linear, positive sense, ssRNA of 25 to 33 Kb. These viruses usually contain 7 to 10 structural genes, i.e. genes encoding proteins that determine the viral structure. These genes are typically arranged in the viral genome in the order of 5' replicase-(hemagglutinin-esterase)-spike-envelope-membrane-nucleoprotein-- 3'. Additionally the viral genome may comprise a number of non-structural genes which encode a nested set of mRNAs with a common 3' end and are largely non-essential.
 The term "capable of being transcribed into RNA which can be assembled into a virion" is used to characterize a DNA sequence, which--once introduced into a suitable host cell--will be transcribed into RNA and generate virions. The virions are preferably infectious viruses, but may also be inactivated, attenuated or replication defective viruses comprising said RNA. Preferably all the information necessary for expression of the virion is encoded by the DNA sequence of the present invention.
 The nucleic acids of the present invention may further comprise a sequence encoding one or several heterologous genes of interest. According to the present invention a gene is characterized as a "heterologous gene" if it is not derived from the coronavirus which was used as a source for the genes encoding the RNA dependent RNA polymerase and the structural or non-structural protein. A "heterologous gene" thus also refers to genes derived from one type of coronavirus and expressed in a vector comprising sequences derived from another type of coronavirus. Any heterologous gene of interest can be inserted into the nucleic acids of the present invention. The insertion of genes encoding peptides or proteins which are recognised as an antigen from an infectious agent by the immune system of a mammal is especially preferred. The heterologous gene may thus encode at least one antigen suitable for inducing an immune response against an infectious agent, at least one molecule interfering with the replication of an infectious agent or an antibody providing protection against an infectious agent. Alternatively or additionally, the heterologous gene may encode an immune modulator, a cytokine, an immonenhancer or an anti-inflammatory compound.
 The fragment of the DNA according to the present invention which is transcribed into RNA preferably has a size of at least 25 Kb. Fragments with a size of at least 30 Kb are especially preferred.
 According to a preferred embodiment of the present invention the DNA further comprises sequences derived from a coronavirus coding for several or all except one of the structural or non-structural proteins of a coronavirus. Alternatively, the DNA of the present invention further comprises sequences coding for all of the structural or non-structural proteins of a coronavirus.
 According to a further embodiment, the nucleic acids of the present invention comprise a sequence controlling the transcription of a sequence derived from a coronavirus gRNA. Any sequence controlling transcription known in the art may be used for this purpose, including sequences driving the expression of genes derived from DNA or RNA genomes. The use of the immediately early (IE) promoter of cytomegalovirus (CMV) is preferred.
 The nucleic acid according to the present invention may also be flanked at the 3'-end by a poly(A)tail. The nucleic acid may comprise termination and/or polyadenylation sequences of bovine growth hormone (BGH). Additionally or alternatively, the nucleic acids may comprise sequences encoding a ribozyme, for example the ribozyme of the hepatitis δ virus (HDV).
 The nucleic acids of the present invention may comprise sequences derived from any coronavirus, for example derived from an isolate of the porcine transmissible gastroenteritis virus (TGEV), murine hepatitits virus (MHV), infectious bronchitis virus (IBV), bovine coronavirus (BoCV), canine coronavirus (CCoV), feline coronavirus (FcoV) or human coronavirus. According to a preferred embodiment the nucleic acid is derived from a transmissable gastroenteritis virus.
 According to a further embodiment of the present invention, the DNAs of the present invention are part of a plasmid, preferably part of a bacterial artificial chromosome (BAC).
 The present invention further provides host cells comprising respective nucleic acids or vectors. The host cells may be eucaryotes or procaryotes. Alternatively, the present invention provides virions comprising a nucleic acid according the present invention. Respective virions may for example be isolated from cell cultures transfected or infected with the nucleic acids of the present invention.
 According to a further embodiment, the present invention provides methods for producing a virion or a viral RNA comprising steps, wherein a DNA of the present invention is introduced into a host cell, host cells containing the DNA are cultivated under conditions allowing the expression thereof and the virion or viral RNA is recovered. Additionally, methods for producing a virion or a viral RNA are provided, wherein a DNA of the present invention is mixed in vitro with chemicals, biological reagents and/or cell extracts under conditions allowing the expression of the DNA and the virion or viral RNA is recovered. The present invention also encompasses the virions and viral RNAs obtainable by either of the above methods. RNAs and virions carrying a heterologous gene are preferred. The viruses so obtained may have the form of an infectious, attenuated, replication defective or inactivated virus.
 The virus may comprise modified genes, for example a modified S, N or M gene. In a specific embodiment of the present invention the modification of the S, N or M gene gives raise to an attenuated virus or a virus with altered tropism.
 According to a further embodiment the invention provides a pharmaceutical preparation comprising nucleic acids, host cells or virions according to the present invention. According to a preferred embodiment the pharmaceutical preparation is a vaccine capable of protecting an animal against diseases caused by an infectious agent. The vaccine may for example comprise sequences of at least one antigen suitable for inducing an immune response against the infectious agent or an antibody providing protection against said infectious agent. The vaccine may comprise a DNA expressing at least one molecule interfering with the replication of the infectious agent. Alternatively the vaccine may comprise a vector expressing at least one antigen capable of inducing a systemic immune response and/or an immune response in mucous membranes against different infectious agents that propagate in respiratory, intestinal mucous membranes or in other tissues. The vaccine may also be a multivalent vaccine capable of protecting an animal against the infection caused by more than one infectious agent, that comprises more than one nucleic acid of the present invention each of which expresses an antigen capable of inducing an immune response against each of said infectious agents, or antibodies that provide protection against each one of said infectious agents or other molecules that interfere with the replication of any infectious agent.
 The vaccines of the present invention may further comprise any of the pharmaceutically acceptable carriers or diluents known in the state of the art.
 The present invention further provides methods for preparing a DNA of the present invention comprising steps, wherein an interfering defective genome derived from a coronavirus is cloned under the expression of a promotor into a BAC vector and the deletions within the defective genome are re-inserted. The method may further comprise steps, wherein toxic sequences within the viral genome are identified before re-insertion into the remaining genomic DNA. Preferably, the toxic sequences within the viral genome are the last sequences to be re-inserted before completing the genome. According to the present invention this method is suitable to yield infectious clones of coronaviruses which are stable in bacteria for at least 80 generations and thus provides a very efficient cloning vector.
 The present invention provides the development of infective clones of cDNA derived from coronavirus (Almazan et al., 2000), as well as vectors constructed from said infective clones that also include heterologous nucleic acid sequences inserted into said clones. The infective clones and vectors provided by this invention have numerous applications in both basic and applied research, as well as a high cloning capacity, and can be designed in such a way that their species specificity and tropism can be easily controlled.
 This patent describes the development of a method that makes it possible to obtain, for the first time in the history of coronavirus, a full-length infective cDNA clone that codes the genome of a coronavirus (Almazan et al., 2000).
 A new vector or system of expression of heterologous nucleic acids based on a coronavirus generated from an infective cDNA clone that codes the genomic RNA (gRNA) of a coronavirus has been developed. In one particular realization of this invention, the coronavirus is the porcine transmissible gastroenteritis virus (TGEV).
 The new system of expression can be used in basic or applied research, for example, to obtain products of interest (proteins, enzymes, antibodies, etc.), as a vaccinal vector, or in gene therapy in both humans and animals. The infective coronavirus obtained from the infective cDNA clone can be manipulated by conventional genetic engineering techniques so that new genes can be introduced into the genome of the coronavirus, and so that these genes can be expressed in a tissue- and species-specific manner to induce an immune response or for gene therapy. In addition, the expression has been optimized by the selection of new transcription-regulating sequences (TRS) that make it possible to increase the levels of expression more than a hundredfold.
 The vectors derived from coronavirus, particularly TGEV, present several advantages for the induction of immunity in mucous membranes with respect to other systems of expression that do not replicate in them: (i) TGEV infects intestinal and respiratory mucous membranes (Enjuanes and Van der Zeijst, 1995), that is, the best sites for induction of secretory immunity; (ii) its tropism can be controlled by modifying the S (spike) gene (Ballesteros et al., 1997); (iii) there are nonpathogenic strains for the development of systems of expression that depend on complementing virus (Sanchez et al., 1992); and (iv) coronaviruses are cytoplasmic RNA viruses that replicate without passing through an intermediate DNA stage (Lai and Cavanagh, 1997), making its integration into the cellular chromosome practically impossible.
 The procedure that has made it possible to recover an infective coronavirus from a cDNA that codes the gRNA of a coronavirus includes the following strategies:  (i) expression of the RNA of the coronavirus under the control of an appropriate promoter;  (ii) cloning of the genome of the coronavirus in bacterial artificial chromosomes (BACs);  (iii) identification of the sequences of cDNA of the coronavirus that are directly or indirectly toxic to bacteria;  (iv) identification of the precise order of joining of the components of the cDNA that codes an infective RNA of coronavirus (promoters, transcription-termination sequences, polyadenylation sequences, ribozymes, etc.); and  (v) identification of a group of technologies and processes (conditions for the growth of BACs, modifications to the purification process of BAC DNA, transformation techniques, etc.) that, in combination, allow the efficient rescue of an infective coronavirus of a cDNA.
 The promoter plays an important role in increasing the expression of viral RNA in the nucleus, where it is synthesized, to be transported to the cytoplasm later on.
 The use of BACs constitutes one of the key points of the procedure of the invention. As is known, cloning of eukaryotic sequences in bacterial plasmids is often impossible due to the toxicity of the exogenous sequences for bacteria. In these cases, the bacteria usually eliminate toxicity by modifying the introduced sequences. Nevertheless, in the strategy followed in this case, to avoid the possible toxicity of these viral sequences, the necessary clonings were carried out to obtain a complete cDNA of the coronavirus in BACs. These plasmids appear in only one copy or a maximum of two per cell, considerably limiting their toxicity and reducing the possibilities of interplasmid recombination.
 Through the identification of the bacteriotoxic cDNA sequences of the coronavirus, the construction of the cDNA that codes the complete genome of a coronavirus can be completed, with the exception of the toxic sequences, which are added in the last step of construction of the complete genome, that is, just before transfection in eukaryotic cells, avoiding their modification by the bacteria.
 One object of the present invention therefore consists in an infective double-chain cDNA clone that codes the gRNA of a coronavirus, as well as the procedure for obtaining it.
 An additional object of this invention consists in a set of recombinant viral vectors that comprises said infective clone and sequences of heterologous nucleic acids inserted into said infective clone.
 An additional object of this invention consists in a method for producing a recombinant coronavirus that comprises the introduction of said infective clone into a host cell, the culture of the transformed cell in conditions that allow the replication of the infective clone and production of the recombinant coronavirus, and recovering the recombinant coronavirus from the culture.
 Another object of this invention consists in a method for producing a modified recombinant coronavirus that comprises introducing the recombinant viral vector into a host cell, cultivating it in conditions that allow the viral vector to replicate and the modified recombinant coronavirus to be produced, and recovering the modified recombinant coronavirus from the culture. Another object of this invention consists in a method for producing a product of interest that comprises cultivating a host cell that contains said recombinant viral vector in conditions that allow the expression of the sequence of heterologous DNA.
 Cells containing the aforementioned infective clones or recombinant viral vector constitute another object of the present invention.
 Another object of this invention consists in a set of vaccines that protect animals against infections caused by infectious agents. These vaccines comprise infective vectors that express at least one antigen adequate for inducing an immune response against each infective agent, or at least one antibody that provides protection against said infective agent, along with a pharmaceutically acceptable excipient. The vaccines can be mono- or multivalent, depending on whether the vectors express one or more antigens capable of inducing an immune response to one or more infectious agents, or, alternatively, one or more antibodies that provide protection against one or more infectious agents.
 Another object provided by this invention comprises a method of animal immunization that consists in the administration of said vaccine.
 The invention provides a cDNA clone that codes the infective RNA of a coronavirus, henceforth the infective clone of the invention, which comprises: (1) a copy of the complementary DNA (cDNA) to the infective genomic RNA (gRNA) of a coronavirus or the viral RNA itself; and (2) an expression module for an additional gene, which includes optimized transcription-promoting sequences.
 In one particular realization of this invention, the coronavirus is a TGEV isolate, in particular, the PUR46-MAD isolate (Sanchez et al., 1990), modified by the replacement of the S gene of this virus by the S gene of the clone C11 TGEV isolate or the S gene of a canine or human coronavirus.
 The transcription-promoting sequence, or promoter, is an RNA sequence located at the 5'-terminal end of each messenger RNA (mRNA) of coronavirus, to which the viral polymerase RNA binds to begin the transcription of the messenger RNA (mRNA). In a particular and preferred embodiment the viral genome is expressed from a cDNA using the IE promoter of CMV, due to the high level of expression obtained using this promoter (Dubensky et al., 1996), and to previous results obtained in our laboratory that indicated that large defective genomes (9.7 kb and 15 kb) derived from the TGEV coronavirus expressed RNAs that did not undergo splicing during their transport from the nucleus, where they are synthesized, to the cytoplasm.
 The infective clone of the invention also contains a transcription termination sequence and a polyadenylation signal such as that coming from the BGH gene. These termination sequences have to be placed at the 3'-end of the poly(A) tail. In one particular realization, the infective clone of the invention contains a poly(A) tail of 24 residues of A and the termination and polyadenylation sequences of the BGH separated from the poly(A) tail by the sequence of the HDV ribozyme.
 The plasmid into which the infective cDNA of the virus has been inserted is a DNA molecule that possesses a replication origin, and is therefore potentially capable of replicating in a suitable cell. The plasmid used is a replicon adequate for maintaining and amplifying the infective clone of the invention in an adequate host cell such as a bacterium, for example, Escherichia coli. The replicon generally carries a gene of resistance to antibiotics that allows the selection of the cells that carry it (for example, cat).
 In Example 1, the construction of an infective clone of TGEV under the control of the IE promoter of CMV is described. The 3'-end of the cDNA appears flanked by a 24 nt poly(A) sequence, the HDV ribozyme, and the transcription termination sequence of the BGH.
 The procedure for obtaining the infective clone of the invention comprises constructing the full-length cDNA from the gRNA of a coronavirus and joining the transcription-regulating elements.
 The cDNA that codes the infective gRNA of a coronavirus was obtained from a DI genome derived from a coronavirus cloned as a cDNA under the control of an appropriate promoter in a BAC, for the purpose of increasing the cDNA's stability. Then the bacteriotoxic sequences were identified and, for the purpose of eliminating that toxicity, said toxic sequences were removed and inserted at the end of the construction of the complete genome, just before transfection in eukaryotic cells. The viral progeny can be reconstituted by means of transfection of the BAC plasmid that contains the coronavirus genome in eukaryotic cells that support viral replication.
 The transcription-regulating elements are joined by means of conventional techniques (Maniatis et al., 1989).
 The infective clone of the invention can be manipulated by conventional genetic engineering techniques to insert at least one sequence of a heterologous nucleic acid that codes a determined activity, under the control of the promoter that is present in the infective clone and of the regulating sequences contained in the resulting expression vector.
 The infective clone of the invention presents numerous applications; for example, it can be used both in basic research, for example, to study the mechanism of replication and transcription of coronaviruses, and in applied research, for example, in the development of efficient systems of expression of products of interest (proteins, enzymes, antibodies, etc.).
 Appropriate cells can be transformed from the infective cDNA clone of the invention, and the virions obtained containing the complete genome of the coronavirus can be recovered. Therefore, the invention moreover provides a method for producing a recombinant coronavirus that comprises the introduction of an infective cDNA of the invention into a host cell, the culture of said cell under conditions that allow the expression and replication of the infective clone and the recovery of the virions obtained from the recombinant coronavirus, which contain the infective genome of the coronavirus. The infective clone of the invention can be introduced into the host cell in various ways, for example by transfection of the host cell with an RNA transcribed in vitro from an infective clone of the invention, or by infecting the host cell with the infective cDNA clone of the invention. Said host cells that contain the infective clone of the invention constitute an additional object of the present invention.
 The invention also provides a set of recombinant viral vectors derived from an infective clone of the invention, henceforth viral vectors of the invention. The viral vectors of the invention comprise an infective cDNA clone of the invention modified to contain a heterologous nucleic acid inserted into said infective clone under conditions that allow said heterologous nucleic acid to be expressed.
 The term "nucleic acid," as it is used in this description, includes genes or gene fragments as well as, in general, any molecule of DNA or RNA.
 In the sense used in this description, the term "heterologous" applied to a nucleic acid refers to a nucleic acid sequence that is not normally present in the vector used to introduce the heterologous nucleic acid into a host cell.
 The heterologous nucleic acid that can contain the viral vector of the invention can be a gene or fragment that codes a protein, a peptide, an epitope, or any gene product of interest (such as antibodies, enzymes, etc.). The heterologous nucleic acid can be inserted into the infective clone of the invention by means of conventional genetic engineering techniques in any appropriate region of the cDNA, for example, after ORF 1b or between genes N and 7, following the initiator codon (AUG), and in reading frame with that gene; or, alternatively, in the zones corresponding to other ORFs. In the construction of the viral vector of the invention, it is essential that the insertion of the heterologous nucleic acid not interfere with any of the basic viral functions.
 The viral vector of the invention can express one or more activities. In this latter case, the viral vector will include as many sequences of heterologous nucleic acid as activities to be expressed, preceded by one or several promoters, or by a promoter and various ribosome recognition sites (IRES, internal ribosome entry sites), or by various promoters and one ribosome recognition site.
 Therefore, the invention provides a method for producing a product of interest that comprises cultivating a host cell that contains a viral vector of the invention under conditions that allow the heterologous nucleic acid to be expressed and the product of interest to be recovered. Said host cells that contain the viral vector of the invention constitute an additional object of the present invention.
 The viral vector of the invention can be designed so that its species specificity and tropism can be easily controlled. Due to these characteristics, a very interesting application of the viral vectors of the invention is their use in gene therapy as a vector of the gene of interest, or as a vaccinal vector to induce immune responses against different pathogens.
 The invention furthermore provides vaccines, capable of protecting an animal against the infection caused by an infectious agent, that comprise (i) at least one viral vector of the invention that expresses at least one antigen suitable for inducing an immune response against said infectious agent, or an antibody that provides protection against said infectious agent, along with, optionally, (ii) a pharmaceutically acceptable excipient.
 In the sense used in this description, "inducing protection" should be understood as the immune response of the receiving organism (animal to be immunized) induced by the viral vector of the invention, through suitable mechanisms such as that induced by substances that potentiate cellular response (interleukins, interferons, etc.), cellular necrosis factors, and similar substances that protect the animal from infections caused by infectious agents.
 Included under the term "animal" are all animals of any species, preferably mammals, including man.
 The term "infectious agent" in the sense used in this description includes any viral, bacterial, fungal, parasitic, or other infective agent that can infect an animal and cause it a pathology.
 In one particular realization, the vaccine provided by this invention comprises at least one viral vector of the invention that expresses at least one antigen capable of inducing a systemic immune response and/or an immune response in mucous membranes against different infectious agents that propagate in respiratory or intestinal mucous membranes. The vectors of the invention are quite suitable to induce immunity in mucous membranes as well as lactogenic immunity, which is of special interest in protecting newborns against intestinal tract infections.
 In another particular realization, the vaccine provided by this invention comprises at least one viral vector of the invention that expresses at least one gene that codes for the light and heavy chains of an antibody of any isotype (for example, IgG1, IgA, etc.) that protects against an infectious agent.
 Species specificity can be controlled so that the viral vector may express the S protein of the envelope of a coronavirus that infects the desired species (man, dog, cat, pig, etc.), suitable to be recognized by the cellular receptors of the corresponding species.
 The vaccines provided by this invention can be monovalent or multivalent, depending on whether the viral vectors of the invention express one or more antigens capable of inducing an immune response to one or more infectious agents, or one or more antibodies that provide protection against one or more infectious agents.
 In a particular realization of this invention, monovalent vaccines capable of protecting man, pigs, dogs and cats against different infectious human, porcine, canine, and feline agents are provided, and tropism is controlled by expressing the S glycoprotein of the coronavirus with the desired species specificity.
 The monovalent vaccines against porcine infectious agents can contain a vector that expresses an antigen selected from the group consisting essentially of antigens of the following porcine pathogens: Actinobacillus pleuropneumoniae, Actinobacillus suis, Haemophilus parasuis, porcine parvovirus, Leptospira, Escherichia coli, Erysipelotrix rhusiopathiae, Pasteurella multocida, Bordetella bronchiseptica, Clostridium sp., Serpulina hydiosenteriae, Mycoplasma hyopneumoniae, porcine epidemic diarrhea virus (PEDV), porcine respiratory coronavirus, rotavirus, or against the pathogens that cause porcine respiratory and reproductive syndrome, Aujeszky's disease (pseudorabies), swine influenza, or transmissible gastroenteritis, and the etiological agent of atrophic rhinitis and proliferative ileitis. The monovalent vaccines against canine infectious agents can contain an expression vector that expresses an antigen selected from the group essentially consisting of antigens of the following canine pathogens: canine herpes viruses, types 1 and 2 canine adenovirus, types 1 and 2 canine parvovirus, canine reovirus, canine rotavirus, canine coronavirus, canine parainfluenza virus, canine influenza virus, distemper virus, rabies virus, retrovirus, and canine calicivirus.
 The monovalent vaccines against feline infectious agents can contain an expression vector that expresses an antigen selected from the group essentially consisting of antigens of the following feline pathogens: cat calicivirus, feline immunodeficiency virus, feline herpes viruses, feline panleukopenia virus, feline reovirus, feline rotavirus, feline coronavirus, cat infectious peritonitis virus, rabies virus, feline Chlamydia psittaci, and feline leukemia virus.
 The vectors can express an antibody that provides protection against an infectious agent, for example, a porcine, canine or feline infectious agent such as those cited above. In one particular realization, the vector expresses the recombinant monoclonal antibody identified as 6A.C3, which neutralizes TGEV, expressed with isotypes IgG1 or IgA, in which the constant part of the immunoglobulin is of porcine origin, or neutralizing antibodies for human and porcine rotaviruses.
 As the excipient, a diluent such as physiological saline or other similar saline solutions can be used. Likewise, these vaccines can also contain an adjuvant from those usually used in the formulation of both aqueous vaccines, such as aluminum hydroxide, QuilA, suspensions of alumina gels and the like, and oily vaccines based on mineral oils, glycerides, fatty acid derivatives, and their mixtures.
 The vaccines of the present invention can also contain cell-response-potentiating (CRP) substances, that is, substances that potentiate subpopulations of helper T-cells (Th1 and Th2) such as interleukin-1 (IL-1), IL-2, IL-4, IL-5, IL-6, IL-12, gamma-IFN (gamma-interferon), cellular necrosis factor, and similar substances that could theoretically provoke cellular immunity in vaccinated animals. These CRP substances could be used in vaccine formulations with aqueous or oily adjuvants. Another type of adjuvants that modulate and immunostimulate cellular response can also be used, such as MDP (muramyl dipeptide), ISCOM (Immunostimulant Complex), or liposomes.
 The invention provides multivalent vaccines capable of preventing and protecting animals from infections caused by different infectious agents. These multivalent vaccines can be prepared from viral vectors of the invention into which the different sequences that code the corresponding antigens have been inserted in the same recombinant vector, or by constructing independent recombinant vectors that would later be mixed for joint inoculation. Therefore, these multivalent vaccines comprise a viral vector that contains more than one sequence of heterologous nucleic acids that code for more than one antigen or, alternatively, different viral vectors, each of which expresses at least one different antigen.
 Analogously, multivalent vaccines that comprise multivalent vectors can be prepared using sequences that code antibodies that protect against infectious agents, instead of sequences that code the antigens.
 In one particular realization of this invention, vaccines capable of immunizing humans, pigs, dogs, and cats against different porcine, canine and feline infectious agents, respectively, are provided. For this, the viral vectors contained in the vaccine must express different antigens of the human, porcine, canine or feline pathogens mentioned above or others.
 The vaccines of this invention can be presented in liquid or lyophilized form and can be prepared by suspending the recombinant systems in the excipient. If said systems were in lyophilized form, the excipient itself could be the reconstituting substance.
 Alternatively, the vaccines provided by this invention can be used in combination with other conventional vaccines, either forming part of them or as a diluent or lyophilized fraction to be diluted with other conventional or recombinant vaccines.
 The vaccines provided by this invention can be administered to the animal orally, nasally, subcutaneously, intradermally, intraperitoneally, intramuscularly, or by aerosol.
 The invention also provides a method for the immunization of animals, in particular pigs, dogs and cats, against one or various infectious agents simultaneously, that comprises the oral, nasal, subcutaneous, intradermal, intraperitoneal, intramuscular, or aerosol administration (or combinations thereof) of a vaccine that contains an immunologically efficacious quantity of a recombinant system provided by this invention.
 In addition, the invention also provides a method for protecting newborn animals against infectious agents that infect said animals, consisting in the oral, nasal, subcutaneous, intradermal, intraperitoneal, intramuscular, or aerosol administration (or combinations thereof) of a vaccine of those provided by this invention to mothers before or during the gestation period, or to their offspring.
 The invention is illustrated by the following examples, which describe in detail the obtainment of infective clones and the construction of the viral vectors of the invention. These examples should not be considered as limiting the scope of the invention, but as illustrating it. In said example, the transformation and growth of bacteria, DNA purification, sequence analysis, and the assay to evaluate the stability of the plasmids were carried out according to the methodology described below.
 Transformation of Bacteria
 All of the plasmids were electroporated in the E. coli DH10B strain (Gibco BRL), introducing slight modifications to previously described protocols (Shizuya et al., 1992). For each transformation, 2 μL of the ligation and 50 μL of competent bacteria were mixed in 0.2-cm dishes (BioRad) and electroporated at 200 Ω, 2.5 kV, and 25 μF. Then, 1 mL of SOC medium (Maniatis et al., 1989) was added at each transformation, the cells were incubated a 37° C. for 45 min, and finally, the recombinant colonies were detected on plates of LB SOC media (Maniatis et al., 1989) with 12.5 μg/mL of chloramphenicol.
 Growth Conditions of the Bacteria
 The bacteria containing the original plasmids, in which the incomplete genome of TGEV was cloned (FIG. 3), were grown at 37° C., showing normal growth kinetics. On the other hand, the BAC that contained the complete cDNA was grown at 30° C. for the purpose of minimizing instability as much as possible. Even so, the size of the colonies was reduced and incubation periods of up to 24 h were necessary to achieve normal colony sizes.
 Purification of DNA
 The protocol described by Woo (Woo et al., 1994) was followed, with slight modifications. From a single colony, 4 L of LB were inoculated with chloramphenicol (12.5 μg/ml). After an incubation period of 18 h at 30° C., the bacteria were collected by centrifugation at 6,000 G, and the plasmid was purified using the Qiagen Plasmid Maxipreparations kit according to the manufacturer's recommendations. By means of this procedure, it was observed that the plasmid DNA obtained was contaminated with bacterial DNA. To eliminate the contaminating bacterial DNA, the plasmidic DNA was purified by means of centrifugation at 55,000 rpm for 16 h on a CsCl gradient. The yield obtained was between 15 and 30 μg/L, depending on the size of the plasmid.
 Sequence Analysis
 The DNA was sequenced in an automatic sequencer (373 DNA Sequencer, Applied Biosystems) using dideoxynucleotides marked with fluorochromes and a temperature-resistant polymerase (Perkin Elmer). The reagents were obtained by way of a kit (ABI PRISM Dye Terminator Cycle Sequencing Ready Reaction Kit) from the Applied Biosystems company. The thermocycler used to perform the sequencing reactions was a "GeneAmpPCR System 9600" (Perkin Elmer).
 The joining of the sequences and their comparison with the consensus sequence of the TGEV were carried out using the SeqMan II and Align (DNASTAR) programs, respectively. No differences in relation to the consent sequence were detected.
 Stability of the Plasmids
 From the original glycerolates, the bacteria that contained recombinant pBeloBAC11 plasmids were grown in 20 mL of LB with chloramphenicol (12.5 μg/mL) for 16 h at 30° C. and 37° C. This material was considered passage 0. The bacteria were diluted 106 times and grown at 30° C. and 37° C. for 16 h. Serial passages were realized during eight consecutive days (each passage represents approximately 20 generations). The plasmid DNA was purified by Miniprep at passages 0 and 8 (160 generations) and analyzed with restriction endonucleases. The two plasmids that contained part of the genome of TGEV were highly stable, whereas the plasmid that contained the complete genome of TGEV showed a certain instability after 40 generations (at this point approximately 80% of the DNA presented the correct restriction pattern).
 Construction of a Recombinant Vector based on a Clone of Infective cDNA Derived from TGEV
 1.1 Generation of an Infective cDNA of TGEV
 For the purpose of obtaining a cDNA that coded for the complete TGEV genome, we originally started with a cDNA that coded for the defective DI-C genome (Mendez et al., 1996). This cDNA, with an approximate length of one third of the TGEV genome, was cloned in the low-copy pACNR1180 plasmid (Ruggli et al., 1996) and its sequence was determined. The cDNA that coded the defective genome was efficiently rescued (replicated and packaged) with the help of a complementing virus (Mendez et al., 1996; Izeta et al., 1999).
 The DI-C genome presents three deletions (Δ1, Δ2, and Δ3) of approximately 10, 1 and 8 kilobases (kb), at ORFs 1a, 1b, and between genes S and 7, respectively (see FIG. 1). The strategy followed to complete the sequence of a cDNA that would code for an infective TGEV genome was to incorporate, step by step, the sequences deleted in the DI-C genome, analyzing the bacteriotoxicity of the new generated constructions. This aspect is very important, since it is widely documented in the scientific literature that recombinant plasmids presenting cDNAs of RNA virus generally grew poorly and were unstable (Boyer and Haenni, 1994; Rice et al., 1989; Mandl et al., 1997).
 The first deletion to be completed was deletion Δ2, of 1 kb, of ORF 1b, yielding a stable recombinant plasmid. The sequence that lacked ORF la was introduced by cloning cDNA fragments A, B, C, and D (FIG. 1) (Almazan et al., 2000) in such a way that all the information required for the gene of the replicase would be complete. The recombinant plasmid obtained was unstable in the bacteria, generating new plasmids that had incorporated additions and deletions in fragment B (Almazan et al., 2000). Interestingly, the elimination of a 5,198 by ClaI-ClaI restriction fragment that encompassed the region of the genome comprised between nucleotides 4,417 and 9,615 (Penzes et al., 1999) yielded a relatively stable plasmid in the E. coli DH10B strain. Later, the sequence of deletion Δ3 was added by cloning all the genetic information for the structural and nonstructural proteins of the 3'-end of the TGEV genome (FIG. 1).
 For the purpose of incrementing the stability of the TGEV cDNA, it was decided that it would be subcloned in BAC using the pBeloBAC11 plasmid (Kim et al., 1992) (see FIG. 2). The pBeloBAC11 plasmid was a generous gift from H. Shizuya and M. Simon (California Institute of Technology). The plasmid, 7,507 by in size, includes the replication origin of the F factor from parB, parC, E. coli (oriS) and the genes necessary to keep a single copy of the plasmid per cell (parA, and repE). The plasmid also presents the gene of resistance to chloramphenicol (cat) as a selection marker. The cDNA was cloned under the control of the IE promoter of CMV, due to the high level of expression obtained using this promoter (Dubensky et al., 1996) and to previous results obtained in our laboratory, indicating that large (9.7 kb and 15 kb) defective genomes derived from TGEV expressed RNAs that did not undergo splicing during transport from the nucleus, where they are synthesized, to the cytoplasm (Izeta et al., 1999; Penzes et al., 1999; Almazan et al., 2000). The generated TGEV cDNA (pBAC-TcDNA-ΔClaI) contained the information for the genes of the replicase, with the exception of the deleted 5,198 by ClaI fragment, and all the information of the structural and nonstructural genes. The 3'-end of the cDNA appears flanked by a 24 nt polyA sequence, the HDV ribozyme, and the transcription termination sequence of BGH (Izeta et al., 1999). On the other hand, the ClaI fragment necessary to generate a complete genome of TGEV was cloned in BAC, generating the plasmid pBAC-B+C+D5', which contained the region of the TGEV genome between 4,310 and 9,758 (see FIG. 3). Both plasmids were grown in the E. coli DH10B strain and sequenced in their entirety. The sequence obtained was identical to the consent sequence of the PUR46-MAD isolate of TGEV provided at the end of this document (SEQ ID NO: 1), with the exception of two replacements in the positions of nucleotides 6,752 (A=>G, silent) and 18,997 (T=>C, silent), and the changes in the S gene of the PUR46-MAD that has been replaced by the D gene of isolate C11 (these changes are indicated in FIG. 4).
 Furthermore, for the purpose of generating a cDNA that would code a virulent TGEV, the S gene of the PUR46-MAD isolate, which replicates at highs levels in the respiratory tract (>106 PFU/g of tissue) and at low levels in the intestinal tract (<103 PFU/mL), was completely replaced by the S gene of TGEV clone 11, henceforth C11, which replicates with elevated titers both in the respiratory tract (<106 PFU/mL) and in the intestinal tract (<106 PFU/mL) (Sanchez et al., 1999). The S gene of C11 presents 14 nucleotides that differ from the S gene of the PUR46-MAD isolate, plus a 6 nt insertion at the 5'-end of the S gene (see FIG. 4) (Sanchez et al., 1999). Previous results in our laboratory (Sanchez et al., 1999) showed that mutants generated by directed recombination, in which the S gene of the PUR46-MAD isolate of the TGEV was replaced with the S gene of the C11 intestinal isolate, acquired intestinal tropism and increased virulence, unlike the natural PUR46-MAD isolate of the TGEV that replicates very little or not at all in the intestinal tracts of infected pigs. A cDNA was constructed from the PUR46-MAD isolate of TGEV with the S gene of the intestinal isolate C11, by means of cloning of the 5,198 by ClaI-ClaI fragment, obtained from the pBAC-B+C+D5' plasmid, in the pBAC-TcDNA.sup.-ΔClaI plasmid, to generate the pBAC-TcDNAFL plasmid that contains the cDNA that codes for the complete TGEV genome (FIG. 3).
 The stability in bacteria of the plasmids used in the construction of the clone of infective cDNA (pBAC-TcDNA.sup.-ΔClaI and pBAC-ClaIF), as well as the plasmid that contains the complete cDNA (pBAC-TcDNAFL), was analyzed after being grown in E. coli for 160 generations. The stability was analyzed by means of digestion with restriction enzymes of the purified DNAs. No deletions or insertions were detected, although the presence of minor changes not detected by the analysis technique used cannot be ruled out in the case of the pBAC-TcDNA.sup.-ΔClaI plasmid and the pBAC-B+C+D5' plasmid. In the case of the pBAC-TcDNA plasmid, which contains the complete genome of TGEV, a certain instability was detected after 40 generations (at this point approximately 80% of the DNA presented the correct restriction pattern). This slight instability, however, does not represent an obstacle to the rescue of the infective virus, since 20 generations (4 L of culture) of bacterial growth are sufficient to generate a quantity of plasmid DNA that allows the virus to be rescued.
 1.2 Rescue of an Infective TGEV from a cDNA that Codes for the Complete Genome
 ST cells were transfected with the pBAC-TcDNAFL plasmid. At 48 h posttransfection, the supernatant of the culture was collected and passed into ST cells six times (see FIG. 5). Starting at passage 2, at 14 h postinfection, the cytopathic effect became apparent, extending later, at 20 h postinfection, to practically all of these cells that formed the monolayer (see FIG. 6). On the other hand, the titer of rescued virus increased rapidly with the passages, reaching values on the order of 108 PFU/mL as of passage 3 (see FIG. 7). The experiment was repeated five times, and in all cases, infective virus with similar titers were recovered, whereas, in the case of nontransfected ST cells or ST cells transfected with a similar plasmid, where the ClaI-ClaI fragment was found in the opposite orientation, virus was never recovered.
 For the purpose of eliminating the possibility that the virus obtained was the product of contamination, the sequence at positions 6,752 and 18,997 was determined by means of sequencing of cDNA fragments amplified by RT-PCR using the genomic RNA of the rescued virus as a template. The analysis of the sequence determined that the nucleotides in positions 6,752 and 18,997 were those present in the cDNA. Furthermore, the rescued virus presented, in the cDNA sequence of the S gene, a restriction site DraIII at position 20,990, as was expected for the S gene of C11 (FIG. 8). The presence of these three genetic markers confirmed that the isolated virus came from the cDNA.
 In a more in-depth characterization of the virus generated, a comparative analysis was made by immunofluorescence of infected cells with the virus recovered (TcDNA) after transfection with the pBAC-TcDNAFL plasmid or cells infected with the PUR46-MAD isolate of the TGEV. For this, specific polyclonal and monoclonal antibodies that recognized both the C11 isolate and the PUR46-MAD isolate, or only the latter, were used (see FIG. 10). The results obtained confirmed the antigenicity expected for the new TcDNA virus. The polyclonal antibody specific for TGEV, the expected specific monoclonal of the S protein (ID.B12 and 6A.C3), as well as the specific monoclonal of the M (3B.B3) and N (3B.D8) proteins recognized both the TcDNA and the PUR46-MAD. The data obtained indicated that the virus generated presented the M and N proteins of the PUR46-MAD isolate and the S protein of the C11 isolate, as had been designed in the original cDNA.
 1.3 In Vivo Infectivity and Virulence
 For the purpose of analyzing the in vivo infectivity of the TcDNA virus, a group of five newborn pigs was inoculated with virus cloned from passage 6, and mortality was analyzed. The five inoculated pigs died 3 to 4 days postinoculation, indicating that the TcDNA virus was virulent. In contrast, two pigs inoculated only with the diluent of the virus and maintained in the same conditions did not suffer alterations.
 1.4 Optimization of the Levels of Expression by Modification of the Transcription-Regulating Sequences
 RNA synthesis in coronavirus takes place by means of an RNA-dependent process, in which the mRNAs are transcribed from templates with negative polarity. In the TGEV, a conserved consensus sequence, CUAAAC, appears, which is located just in front of the majority of the genes. These sequences represent signals for the transcription of the subgenomic mRNAs. In coronavirus, there are between six and eight types of mRNAs with variable sizes, depending on the type of coronavirus and of the host. The largest corresponds to the genomic RNA, which in turn serves as mRNA for ORFs 1a and 1b. The rest of the mRNAs correspond to subgenomic mRNAs. These RNAs are denominated mRNA 1 to 7, in decreasing size order. On the other hand, some mRNAs that have been discovered after the set of originally described mRNAs have been denominated with the name of the corresponding mRNA, a dash, and a number, e.g., mRNA 2-1. The mRNAs present a coterminal structure in relation to the structure of the genomic RNA. With the exception of the smallest mRNA, the rest are structurally polycistronic, while, in general, only the ORF located closest to 5' is translated.
 The efficiency in the expression of a marker gene (GUS) has been studied using different sequences flanking the 5'-terminal of the minimal intergenic (IG) sequence CUAAAC (FIG. 11), different sequences flanking the 3'-terminal of the IG sequence (FIG. 12), and various insertion sites (FIG. 13). The results obtained (FIGS. 11 to 13) indicated that optimal expression was achieved with a TRS consisting of: (i) the -88 nt flanking the consent sequence for the N gene of TGEV; (ii) the IG sequence; and (iii) the 3'-flanking sequence of the IG sequence of the S gene. Furthermore, in agreement with the results obtained in relationship to the point of insertion of the heterologous gene, the greatest levels of expression were achieved when the heterologous gene was located at the 3'-end of the genome. A TRS such as that described allows the GUS to be expressed at levels between 2 and 8 pg per 106 cells.
 1.5 Tissue Specificity of the System of Expression
 Many pathogens enter the host through the mucous membranes. To prevent this type of infections, it is important to develop systems of expression that allow the induction of high levels of secretory immunity. This can be achieved fundamentally through the administration of antigens in the lymph nodes associated with the respiratory and intestinal tract. To achieve this goal, and in general to direct the expression of a gene at the tissue of interest, the molecular bases of the tropism of TGEV have been studied. These studies have showed that the tissue specificity of TGEV can be modified by the construction of recombinant viruses containing the S gene of coronavirus with the desired tropism (Ballesteros et al., 1997; Sanchez et al., 1999). This information makes it possible to construct systems of expression based on cDNA genomes of coronavirus with respiratory or intestinal tropism.
 1.6 Expression of the Viral Antigen Coded by the ORF5 of PRRSV Using Infective cDNA
 For the purpose of optimizing the levels of expression of heterologous genes, constructions were made from a vector of interchangeable modules flanked by cloning sequences that facilitate the exchange of TRSs and heterologous genes within the vector. The construction, which included ORF 5 of the PRRSV (Porcine respiratory and reproductive syndrome virus) flanked at the 5'-end by the minimal IGS consensus sequence (CUAAAC) preceded by the -88 nts flanking the gene of the viral nucleocapsid (N), and at the 3' -end by restriction site SalI (GTCGAC) and a sequence analogous to that of Kozak (AC)GACC, yielded an optimal expression (about 10 μg/106 cells). In principle, these levels of expression of the heterologous gene are more than sufficient to induce an immune response. The heterologous gene was inserted into the position previously occupied by genes 3a and 3b of the virus, which are dispensable.
 1.7 Induction of an Immune Response in Swine to an Antigen Expressed with the cDNA Derived Virus Vector
 Using the same type of virus vector derived from the cDNA and the TRSs described above, the gene encoding the green fluorescent protein (GFP) was expressed at high levels (20 μg of protein per million of cells in swine testis, ST, cells). The expression levels were stable for more than 20 passages in cell culture. Furthermore, a set of swine were immunized with the live virus vector, that was administered by the oral, intra-nasal and intragastric routes and a strong humoral immune response was detected against both the virus vector and the GFP. Interestingly, no secondary effect was observed in the inoculated animals after the administration of three doses of the virus vector.
 1.8 Construction of a Safe Virus Vector that Expresses the Foreign Gene Without Leading to the Generation of an Infectious Virus.
 To design vector for humans, biosafety is a priority. To achieve this goal, three types of safety guards are being engineered in the vector. Two of these are based on the deletion of two virus components, mapping at different positions of the virus genome, essential for the replication of the virus. These components are being provided in trans by a packaging cell line. This cell (Baby Hamster Kidney, BHK) expresses the missing TGEV genes encoding essential structural proteins of the virus (the envelope E and the membrane M proteins). The third safety guard is the relocation of the packaging signal of the virus genome, in such a way that the recovery of an infectious virus by recombination is prevented, leading to the generation of a suicide vector that efficiently expresses the heterologous genes but that is unable to propagate even to the closest neighbor cell.
 With the design of the new vector for use in humans, we are not producing a new virus that could be propagated within the human species, since this vector can not be transmitted from cell to cell in human beings. The vector is based on a replication defective virus. It can only be grown in the vaccine factory by using packaging cells complementing the deletions of the virus. These safety guards represent novel procedures in the engineering of coronaviruses. The recombinant virus with a new tropism will be replication competent at least in feline cells, since these cells replicate human, porcine, canine and feline coronaviruses.
 Deposition of Microorganisms:
 The bacterium derived from Escherichia coli, carrying the plasmid with the infective clone of the invention, identified as Escherichia coli pBAC-TcDNAFL, has been deposited with the Spanish Collection of Type Cultures (CECT), Burjassot (Valencia), on Nov. 24, 1999, under registration number CECT 5265.
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15128588DNAPorcine Transmissible Gastroenteritis V 1acttttaaag taaagtgagt gtagcgtggc tatatctctt cttttacttt aactagcctt 60gtgctagatt ttgtcttcgg acaccaactc gaactaaacg aaatatttgt ctttctatga 120aatcatagag gacaagcgtt gattatttcc attcagtttg gcaatcactc cttggaacgg 180ggttgagcga acggtgcagt agggttccgt ccctatttcg taagtcgcct agtagtagcg 240agtgcggttc cgcccgtaca acgttgggta gaccgggttc cgtcctgtga tctccctcgc 300cggccgccag gagaatgagt tccaaacaat tcaagatcct tgttaatgag gactatcaag 360tcaacgtgcc tagtcttcct attcgtgacg tgttacagga aattaagtac tgctaccgta 420atggatttga gggctatgtt ttcgtaccag aatactgtcg tgacctagtt gattgcgatc 480gtaaggatca ctacgtcatt ggtgttcttg gtaacggagt aagtgatctt aaacctgttc 540ttcttaccga accctccgtc atgttgcaag gctttattgt tagagctaac tgcaatggcg 600ttcttgagga ctttgacctt aaaattgctc gcactggcag aggtgccata tatgttgatc 660aatacatgtg tggtgctgat ggaaaaccag tcattgaagg cgattttaag gactacttcg 720gtgatgaaga catcattgaa tttgaaggag aggagtacca ttgcgcttgg acaactgtgc 780gcgatgagaa accgctgaat cagcaaactc tctttaccat 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taatggtgtg aaagtagttt gtgatggctg caaaggtttt gctaaccaac 2580tttcaaaagg ttacaacaag ctctgtaatg cggctcgcaa tgatattgag atcggtggta 2640taccattttc cacttttaaa acacctacaa atacttttat tgaaatgaca gatgctatct 2700attcagttat tgaacaaggt aaggcattat cctttagaga tgctgatgtg ccagttgtag 2760acaatggtac catttctact gctgattggt ctgaacccat tctgcttgaa cctgctgaat 2820atgtaaaacc aaagaacaat ggtaatgtca ttgttattgc aggttataca ttttataaag 2880atgaggatga acatttttat ccttatggtt ttggtaaaat tgtgcagaga atgtataata 2940aaatgggtgg tggtgacaaa actgtctcat tttcagaaga agtagatgtt caagaaattg 3000cacctgttac acgtgttaaa cttgaattcg aatttgacaa tgaaattgta actggtgttc 3060ttgaacgggc tattggtact agatacaaat ttactggtac aacttgggaa gaatttgaag 3120agtctatttc tgaagaactc gatgcaatct ttgatactct agcaaaccaa ggtgtcgaac 3180ttgaaggtta cttcatttat gacacttgtg gtggctttga tataaaaaat ccagatggta 3240ttatgatctc tcagtatgat atcaatatta ctgctgatga aaaatcagaa gttagtgcat 3300caagtgaaga agaagaagtt gaatctgttg aagaagatcc tgagaatgaa attgtagaag 3360catctgaagg tgctgaaggg acttcttctc aagaagaggt tgaaacagta gaagttgcag 3420atattacttc tacagaagaa gatgttgaca ttgttgaagt atctgctaaa gatgaccctt 3480gggctgcagc tgttgatgta caagaagctg aacaatttaa tccttctcta ccacctttca 3540agacaacgaa tctcaacgga aaaattatcc ttaagcaagg ggataataat tgttggataa 3600atgcttgttg ctatcagctt caggcctttg attttttcaa caatgaagct tgggagaaat 3660ttaagaaagg tgatgtcatg gactttgtaa acctttgtta tgcagcaaca acactagcaa 3720gaggtcattc tggtgatgca gagtatcttc ttgaacttat gctcaatgat tatagcacag 3780ccaagatagt acttgcagct aagtgtggtt gtggtgaaaa agaaattgtt ttggaaagag 3840ctgtttttaa actcacccca cttaaggaga gttttaatta tggtgtttgt ggtgactgca 3900tgcaagttaa cacctgtaga tttttaagtg ttgaaggctc tggtgttttt gttcatgaca 3960tattaagcaa gcaaacgcca gaagctatgt ttgttgtcaa acctgttatg catgcagttt 4020acactggcac aactcaaaat ggccattaca tggttgatga tattgaacac ggttattgtg 4080tagatggtat gggtattaaa ccacttaaga aacggtgtta tacatccaca ttgttcatta 4140atgccaatgt aatgactaga gctgaaaaac caaaacaaga gtttaaagtt gaaaaagtag 4200aacagcaacc gatagtggag gaaaacaaat cctctattga aaaagaggaa attcaaagtc 4260ctaaaaacga tgaccttata cttccatttt acaaagctgg taaactttcc ttttatcagg 4320gtgctttgga tgttttgatc aatttcttgg aacctgatgt tattgttaat gctgctaatg 4380gtgatcttaa acacatgggt ggtgtcgcaa gagccatcga tgttttcact ggtggcaaat 4440taacagaacg ttctaaggat tatcttaaaa agaacaaatc tattgctcct ggtaatgctg 4500ttttctttga aaatgtcatt gagcatctta gtgttttgaa tgcagttgga ccacgtaatg 4560gtgacagccg agttgaagcc aaactttgta atgtttacaa agcaattgca aagtgtgaag 4620gaaaaatatt aacaccactt attagtgttg gtatctttaa tgttagactt gaaacatcat 4680tgcagtgctt acttaagact gtgaatgaca ggggattgaa tgtcttcgta tacactgacc 4740aggagaggca aactattgag aatttcttct cttgttctat ccctgtcaat gttactgagg 4800ataatgttaa ccatgaacgt gtgtctgttt cttttgacaa aacatacggt gaacagctta 4860agggcaccgt tgtcatcaaa gacaaagatg ttacaaacca gttgcctagc gcttttgatg 4920ttggtcaaaa agttattaag gctattgata tagattggca agctcattat ggtttccgtg 4980atgctgctgc ttttagcgct agtagtcatg atgcttataa atttgaagtt gttacacata 5040gcaatttcat tgtgcataag cagactgaca acaactgttg gattaatgca atttgtcttg 5100cattacagag actcaagcca cagtggaaat ttcctggtgt tagaggtctc tggaatgaat 5160ttcttgagcg taaaacacaa ggttttgtac atatgttgta tcacatttct ggagtaaaga 5220aaggtgagcc aggtgatgct gaattaatgc tgcataaact tggtgacttg atggacaatg 5280attgtgaaat cattgtcaca cacactacag catgtgacaa gtgcgcaaaa gtagaaaagt 5340ttgttggacc agtggtagca gcacctcttg caattcatgg cactgacgaa acatgtgtgc 5400atggcgttag tgtcaatgtc aaagtcaccc aaattaaggg cactgttgct attacttctt 5460tgattggtcc tattattgga gaagtactag aagcaactgg ttatatttgt tatagcggtt 5520ctaacaggaa tggtcattac acctattacg ataaccgtaa tggattagtg gttgatgcag 5580aaaaggctta ccattttaat agagacttat tacaggtcac aacagctatt gcaagtaatt 5640tcgttgtcaa gaaaccacaa gcagaggaaa gacctaagaa ttgtgctttt aacaaagttg 5700cagcatctcc taagattgta caagaacaaa aattgttggc tattgaaagt ggtgctaact 5760atgctcttac tgaatttgga agatatgctg acatgttctt tatggctgga gataaaattc 5820ttaggttgct gcttgaagtc tttaaatatt tgctggtttt atttatgtgt cttagaagta 5880ctaagatgcc taaagttaaa gtcaaaccac ctcttgcatt taaagatttt ggtgctaagg 5940tcagaacgct caattacatg agacaattga acaaaccctc tgtctggcgt tacgcaaaac 6000tagttttatt gttgatagca atatataatt tcttttattt gtttgtcagt ataccagtag 6060tgcataaatt aacatgtaac ggtgctgtac aggcatataa aaattctagt tttataaagt 6120ctgcagtctg tggcaactct attttatgca aagcctgttt ggcttcttat gatgagttgg 6180ctgattttca acatctccaa gttacttggg atttcaaatc tgacccacta tggaacagac 6240tggtacaatt gtcttacttt gcattcttgg ctgtttttgg taataactat gttaggtgtt 6300ttcttatgta ttttgtatct cagtacctca acctttggct ttcttatttt ggttatgtag 6360agtacagttg gtttttgcat gttgtcaact ttgaatccat ctcagctgag tttgtgatcg 6420tagttatagt ggttaaggca gttctcgccc ttaaacatat tgttttcgca tgctcaaacc 6480cgtcttgcaa aacgtgctct aggactgcaa ggcagacacg tattcctatt caagttgttg 6540ttaatggttc aatgaagact gtttatgttc atgctaatgg tactggtaaa ttctgcaaga 6600aacacaattt ttattgtaag aactgtgatt cttatggctt tgaaaacaca ttcatctgtg 6660acgaaattgt acgtgatctc agtaatagtg ttaaacaaac tgtttacgcc actgatagat 6720ctcatcaaga agtcacaaaa gttgaatgtt cagatggctt ttacagattt tatgttggtg 6780atgaattcac ttcatatgac tatgatgtaa aacacaagaa atacagtagt caagaggttc 6840tcaagagcat gctcttgctt gatgacttca ttgtgtacag tccatctggt tctgctcttg 6900caaatgttag aaatgcctgt gtttactttt cacaacttat tggtaagcct attaagattg 6960ttaacagtga tttgcttgaa gacctctctg tagattttaa aggggcactt tttaatgcta 7020aaaagaatgt aattaagaat tctttcaatg ttgatgtctc agaatgcaaa aatcttgacg 7080aatgttacag ggcttgcaat cttaatgttt cattttctac atttgaaatg gctgtcaaca 7140atgctcatag gtttggtatt ctgattactg atcgttcttt taacaatttc tggccatcaa 7200aagttaagcc tggttcatct ggtgtgtcgg ccatggacat tggtaagtgt atgacttctg 7260atgctaagat tgttaatgct aaagttttaa ctcaacgtgg taaaagtgtt gtttggctta 7320gccaggattt tgctgcactt agctcaactg ctcagaaagt tttggttaaa acttttgtag 7380aagaaggtgt caacttttca ctcacattta atgctgtagg ttcagatgat gatcttcctt 7440atgaaagatt cactgaatct gtgtctccaa aaagtggttc aggctttttc gatgtaatta 7500cacagcttaa acaaattgtg attttggttt ttgtttttat ctttatttgt ggtttgtgct 7560ctgtttacag tgttgctaca cagtcctaca ttgaatctgc tgaaggctat gactacatgg 7620ttattaagaa tggaattgtt caaccttttg acgataccat ttcatgtgtt cataacactt 7680ataaaggatt cggtgactgg tttaaagcta agtatggttt tatccctact tttggtaaat 7740catgtccaat tgttgtagga actgtttttg atcttgaaaa tatgagacca attcctgacg 7800tgcctgcata tgtttctatt gtgggtagat ctcttgtttt cgctattaat gctgcttttg 7860gtgttactaa tatgtgctat gatcatactg gcaatgcagt tagtaaggac tcttactttg 7920atacttgtgt gtttaatact gcgtgcacca ctcttacagg tcttggtggt acaattgtat 7980attgtgcaaa gcaaggttta gttgaaggtg ctaagctcta tagtgatctt atgccagact 8040attattatga gcatgctagt ggtaacatgg ttaaattgcc agcaattatt agaggacttg 8100gtctacgttt tgtgaaaaca caggctacaa cttattgtag agtgggagag tgcattgata 8160gtaaagctgg tttttgcttt ggtggcgata actggtttgt ctacgacaat gagtttggca 8220atggatacat ctgtggtaat tctgtgctag gattctttaa gaatgtcttc aaactcttta 8280actctaacat gtctgtggta gctacatctg gtgcgatgct tgttaacatt attattgcat 8340gcttagctat tgcaatgtgt tatggtgttc ttaagtttaa gaagattttt ggtgattgta 8400ctttcctcat tgttatgatc attgtcaccc ttgttgtgaa caatgtgtct tattttgtca 8460ctcaaaacac gttctttatg atcatctacg ccattgttta ctattttata acaagaaaac 8520ttgcataccc aggcattctt gatgctgggt ttattattgc ttatattaat atggctccat 8580ggtacgtgat taccgcatat atcctagttt tcctctatga ctcactccct tcactgttta 8640aacttaaagt ttcaacaaat ctttttgaag gtgataaatt tgtgggtaac tttgaatctg 8700ctgctatggg tacttttgtt attgacatgc gttcatatga aactattgtt aattctactt 8760ctattgctag aattaaatca tatgctaaca gcttcaataa atataagtac tacacaggtt 8820caatgggaga agctgactac agaatggctt gctatgctca tcttggtaaa gctcttatgg 8880actattctgt taatagaaca gacatgcttt acacacctcc tactgttagt gttaattcta 8940cacttcagtc aggtttgcgg aaaatggcac agcctagtgg tcttgtagag ccttgcattg 9000taagagtttc ctatggtaac aatgtgctta atggtttatg gttaggagat gaagtcattt 9060gccctagaca tgttattgct agtgatacca cacgtgttat caactatgaa aatgaaatgt 9120ctagtgtgag acttcacaac ttttcagttt ctaagaataa tgtgtttttg ggtgttgtgt 9180ctgccagata taagggtgtg aatcttgtac ttaaagtcaa ccaggttaat cctaacacac 9240cagaacataa atttaagtct attaaagctg gtgaaagttt taacattctt gcttgttatg 9300aaggatgtcc tggcagtgtt tatggtgtca acatgagaag tcaaggtacc attaaaggat 9360cttttatagc tggtacttgt ggatcagtag gttatgtgtt agaaaatgga attctctatt 9420ttgtatacat gcatcactta gaacttggaa atggctcgca tgttggttcc aattttgaag 9480gagaaatgta cggtggttat gaagatcaac ctagcatgca attggaaggt actaatgtca 9540tgtcatcaga taatgtggtt gcattcctat atgctgcact tatcaatggt gaaaggtggt 9600ttgttacaaa cacatcgatg tcattagaat catacaatac atgggccaaa actaacagtt 9660tcacagaact ttcttcaact gatgctttta gcatgttggc tgcaaaaact ggtcaaagtg 9720ttgagaaatt actagatagc atcgtaagac tcaacaaggg ttttggaggt cgtactatac 9780tttcttatgg ctcattgtgt gacgagttca ctccaactga agtcataagg caaatgtatg 9840gtgtaaatct tcaggctggt aaagtaaaat ctttcttcta ccctattatg actgcaatga 9900caattctctt tgccttttgg cttgaattct ttatgtacac acccttcact tggattaatc 9960caacttttgt tagcattgta ttggctgtta caactttgat ctcgacggtt tttgtctctg 10020gcatcaaaca taagatgttg ttctttatgt cttttgtcct tcctagtgtt atccttgtga 10080cagcacacaa tttgttctgg gacttttctt actatgaaag tcttcagtca attgttgaga 10140atactaacac tatgtttttg cctgttgaca tgcaaggtgt catgctcaca gtgttttgct 10200ttattgtctt tgttacatat agtgttagat tcttcacttg caaacaatca tggttctcac 10260ttgctgtgac aactattctt gtgatcttta acatggttaa aatctttgga acatctgatg 10320aaccatggac tgaaaaccaa attgctttct gctttgtgaa catgcttact atgattgtca 10380gtcttactac aaaggattgg atggttgtca ttgcatcata cagaattgca tattatattg 10440ttgtatgtgt aatgccatct gcttttgtat ctgactttgg gtttatgaag tgtattagca 10500ttgtttacat ggcgtgcggt tatttgtttt gttgctatta tggcattctt tattgggtta 10560acagatttac atgcatgact tgtggtgttt atcaattcac tgtgtctgca gctgaactta 10620aatacatgac cgctaacaac ctttctgcac ctaagaacgc atatgacgct atgattctta 10680gtgctaaatt gattggtgtt ggaggtaaga gaaacatcaa aatttcaact gtacagtcaa 10740aacttacaga gatgaaatgt accaatgttg tcttgcttgg tcttttatct aaaatgcatg 10800tcgagtctaa ctcaaaagag tggaactatt gtgttggact acacaatgag ataaaccttt 10860gtgacgatcc tgaaatcgtt cttgagaaac tgttagctct tattgcattc ttcttgtcca 10920aacataacac ttgtgacctt agcgaactta ttgaatcata ctttgagaac accaccatac 10980tccagagtgt ggcttcagct tatgctgcat tgcctagctg gattgcactt gaaaaagctc 11040gcgctgatct tgaagaggct aagaaaaatg atgttagccc tcaaattttg aagcagctta 11100ctaaagcatt taacattgcc aagagtgatt ttgagcgcga agcatcagtg caaaagaaac 11160tcgacaaaat ggctgagcag gctgcagcta gtatgtataa agaagcacga gctgtggaca 11220gaaagtcaaa gattgtttct gctatgcata gcctactttt tggtatgctt aagaaacttg 11280atatgtccag tgtcaacact attattgacc aggctcgtaa tggtgttcta cctttaagta 11340tcattccagc tgcatcagct acaagacttg ttgttattac acctagcctt gaagtgtttt 11400ccaagattag gcaagaaaac aatgttcatt atgctggtgc tatttggact attgttgaag 11460ttaaagatgc taatggttca catgtacatc ttaaggaagt caccgctgct aatgaattaa 11520accttacttg gccattgagc attacttgtg agagaaccac aaagcttcag aacaatgaaa 11580ttatgccagg taaacttaaa gaaagagctg tcagagcgtc agcaactctt gatggtgaag 11640ctttcggcag tggaaaggct cttatggcat ctgaaagtgg aaaaagcttt atgtatgcat 11700ttatagcctc agacaacaat cttaagtatg ttaagtggga gagcaataat gatattatac 11760ctattgaact tgaagctcca ttgcgtttct atgttgacgg cgctaatggt cctgaagtca 11820agtatttgta ttttgtcaag aatttaaaca ctcttagacg tggtgccgtt cttggttata 11880tcggtgcaac agttcgtctg caagctggta aacccactga acatccatct aacagtagtt 11940tattgacatt gtgtgctttt tcacctgatc ctgctaaagc atatgttgat gctgttaaga 12000gaggcatgca accagttaat aactgtgtaa aaatgctctc aaatggtgct ggtaatggta 12060tggctgttac aaacggtgtc gaagctaaca cacaacagga ctcttatggt ggtgcttcag 12120tttgtattta ttgcagatgc catgttgaac atcctgctat tgatggatta tgccgctaca 12180aaggtaagtt cgtgcaaata ccaactggca cacaagatcc aattcggttc tgtattgaaa 12240atgaagtttg tgttgtctgt ggttgttggc ttaacaatgg ttgcatgtgc gatcgtactt 12300ctatgcagag ttttactgtt gatcaaagtt atttaaacga gtgcggggtt ctagtgcagc 12360tcgactagaa ccctgcaatg gtactgatcc agaccatgtt agtagagctt ttgacatcta 12420caacaaagat gttgcgtgta ttggtaaatt ccttaagacg aattgttcaa gatttaggaa 12480tttggacaaa catgatgcct actacattgt caaacgttgt acaaagaccg ttatggacca 12540tgagcaagtc tgttataacg atcttaaaga ttctggtgct gttgctgagc atgacttctt 12600cacatataaa gagggtagat gtgagttcgg taatgttgca cgtaggaatc ttacaaagta 12660cacaatgatg gatctttgtt acgctatcag aaattttgat gaaaagaact gtgaagttct 12720caaagaaata ctcgtgacag taggtgcttg cactgaagaa ttctttgaaa ataaagattg 12780gtttgatcca gttgaaaatg aagccataca tgaagtttat gcaaaacttg gacccattgt 12840agccaatgct atgcttaaat gtgttgcttt ttgcgatgcg atagtggaaa aaggctatat 12900aggtgttata acacttgaca accaagatct taatggcaat ttctacgatt tcggcgattt 12960cgtgaagact gctccgggtt ttggttgcgc ttgtgttaca tcatattatt cttatatgat 13020gcctttaatg gggatgactt catgcttaga gtctgaaaac tttgtgaaaa gtgacatcta 13080tggttctgat tataagcagt atgatttact agcttatgat tttaccgaac ataaggagta 13140ccttttccaa aaatacttta agtactggga tcgcacatat cacccaaatt gttctgattg 13200tactagtgac gagtgtatta ttcattgtgc taattttaac acattgtttt ctatgacaat 13260accaatgaca gcttttggac cacttgtccg taaagttcat attgatggtg taccagtagt 13320tgttactgca ggttaccatt tcaaacaact tggtatagta tggaatcttg atgtaaaatt 13380agacacaatg aagttgagca tgactgatct tcttagattt gtcacagatc caacacttct 13440tgtagcatca agccctgcac ttttagacca gcgtactgtc tgtttctcca ttgcagcttt 13500gagtactggt attacatatc agacagtaaa accaggtcac tttaacaaag atttctacga 13560tttcataaca gagcgtggat tctttgaaga gggatctgag ttaacattaa aacatttttt 13620ctttgcacag ggtggtgaag ctgctatgac agacttcaat tattatcgct acaatagagt 13680cacagtactt gatatttgcc aagctcaatt tgtttacaaa atagttggca agtattttga 13740atgttatgac ggtgggtgca ttaatgctcg tgaagttgtt gttacaaact atgacaagag 13800tgctggctat cctttgaaca aatttggtaa agctagactt tactacgaaa ctctttcata 13860tgaagagcag gatgcacttt ttgctttaac aaagagaaat gttttaccca caatgactca 13920aatgaatttg aaatacgcta tttctggtaa ggcaagagct cgtacagtag gaggagtttc 13980acttctttct accatgacta cgagacaata tcatcagaag catttgaagt caattgctgc 14040aacacgcaat gctactgtgg tcattggttc aaccaagttt tatggtggtt gggacaatat 14100gcttaaaaat ttaatgcgtg atgttgataa tggttgtttg atgggatggg actatcctaa 14160gtgtgaccgt gctttaccta atatgattag aatggcttct gccatgatat taggttctaa 14220gcatgttggt tgttgtacac ataatgatag gttctaccgc ctctccaatg agttagctca 14280agtactcaca gaagttgtgc attgcacagg tggtttttat tttaaacctg gtggtacaac 14340tagcggtgat ggtactacag catatgctaa ctctgctttt aacatctttc aagctgtttc 14400tgctaatgtt aataagcttt tgggggttga ttcaaacgct tgtaacaacg ttacagtaaa 14460atccatacaa cgtaaaattt acgataattg ttatcgtagt agcagcattg atgaagaatt 14520tgttgttgag tactttagtt atttgagaaa acacttttct atgatgattt tatctgatga 14580tggagttgtg tgctacaaca aagattatgc ggatttaggt tatgtagctg acattaatgc 14640ttttaaagca acactttatt accagaataa cgtctttatg tccacttcta agtgttgggt 14700agaaccagat cttagtgttg gaccacatga attttgttca cagcatacat tgcagattgt 14760tgggcctgat ggagactact atcttcccta tccagacccg tccagaattt tatcagctgg 14820tgtgtttgtt gatgacatag ttaaaacaga caatgttatt atgttagaac gttacgtgtc 14880attggctatt gacgcatacc cgctcacaaa acaccctaag cctgcttatc aaaaagtgtt 14940ttacactcta ctagattggg ttaaacatct acagaaaaat ttgaatgcag gtgttcttga 15000ttcgttttca gtgacaatgt
tagaggaagg tcaagataag ttctggagtg aagagtttta 15060cgctagcctc tatgaaaagt ccactgtctt gcaagctgca ggcatgtgtg tagtatgtgg 15120ttcgcaaact gtacttcgtt gtggagactg tcttaggaga ccacttttat gcacgaaatg 15180tgcttacgac catgttatgg gaacaaagca taaattcatt atgtctatca caccatatgt 15240gtgtagtttt aatggttgta atgtcaatga tgttacaaag ttgtttttag gtggtcttag 15300ttattattgt atgaaccaca aaccacagtt gtcattccca ctctgtgcta atggcaacgt 15360ttttggtcta tataaaagta gtgcagtcgg ctcagaggct gttgaagatt tcaacaaact 15420tgcagtttct gactggacta atgtagaaga ctacaaactt gctaacaatg tcaaggaatc 15480tctgaaaatt ttcgctgctg aaactgtgaa agctaaggag gagtctgtta aatctgaata 15540tgcttatgct gtattaaagg aggttatcgg ccctaaggaa attgtactcc aatgggaagc 15600ttctaagact aagcctccac ttaacagaaa ttcagttttc acgtgttttc agataagtaa 15660ggatactaaa attcaattag gtgaatttgt gtttgagcaa tctgagtacg gtagtgattc 15720tgtttattac aagagcacga gtacttacaa attgacacca ggtatgattt ttgtgttgac 15780ttctcataat gtgagtcctc ttaaagctcc aattttagtc aaccaagaaa agtacaatac 15840catatctaag ctctatcctg tctttaatat agcggaggcc tataatacac tggttcctta 15900ctaccaaatg ataggtaagc aaaaatttac aactatccaa ggtcctcctg gtagcggtaa 15960atctcattgt gttataggtt tgggtttgta ttaccctcag gcgagaatag tctacactgc 16020atgttctcat gcggctgtag acgctttatg tgaaaaagca gccaaaaact tcaatgttga 16080tagatgttca aggataatac ctcaaagaat cagagttgat tgttacacag gctttaagcc 16140taataacacc aatgcgcagt acttgttttg tactgttaat gctctaccag aagcaagttg 16200tgacattgtt gtagttgatg aggtctctat gtgtactaat tatgatctta gtgtcataaa 16260tagccgactg agttacaaac atattgttta tgttggagac ccacagcagc taccagctcc 16320tagaactttg attaataagg gtgtacttca accgcaggat tacaatgttg taaccaaaag 16380aatgtgcaca ctaggacctg atgtcttttt gcataaatgt tacaggtgcc cagctgaaat 16440tgttaagaca gtctctgcac ttgtttatga aaataaattt gtacctgtca acccagaatc 16500aaagcagtgc ttcaaaatgt ttgtaaaagg tcaggttcag attgagtcta actcttctat 16560aaacaacaag caactagagg ttgtcaaggc ctttttagca cataatccaa aatggcgtaa 16620agctgttttc atctcaccct ataatagtca aaattatgtt gctcggcgtc ttcttggttt 16680gcaaacgcaa actgtggatt ccgctcaggg tagtgagtat gattacgtca tctacacaca 16740gacctccgat acacagcatg ctactaatgt taacagattt aatgttgcca ttacgagagc 16800aaaggttggt atactttgta tcatgtgtga tagaactatg tatgagaatc ttgatttcta 16860tgaactcaaa gattcaaaga ttggtttaca agcaaaacct gaaacttgtg gtttatttaa 16920agattgttcg aagagcgaac aatacatacc acctgcttat gcaacgacat atatgagctt 16980atctgataat tttaagacaa gtgatggttt agctgttaac atcggtacaa aagatgttaa 17040atatgctaat gtcatctcat atatgggatt caggtttgaa gccaacatac caggctatca 17100cacactattc tgcacgcgag attttgctat gcgtaatgtt agagcatggc ttgggtttga 17160cgttgaaggt gcacatgtct gtggtgataa tgttggaact aatgtaccat tacagctggg 17220tttctcaaac ggtgtggatt ttgtagtgca aactgaagga tgtgttatta ctgaaaaagg 17280taatagcatt gaggttgtaa aagcacgagc accaccaggt gagcaatttg cacacttgat 17340tccgcttatg agaaagggtc aaccttggca cattgttaga cgccgtatag tgcagatggt 17400ctgtgactat tttgatggct tatcagacat tctgatcttt gtgctttggg ctggtggtct 17460tgaacttaca actatgagat actttgttaa aattggaaga ccacaaaaat gtgaatgcgg 17520caaaagtgca acttgttata gtagctctca atctgtttat gcttgcttca agcatgcatt 17580aggatgtgat tatttatata acccttactg cattgacata cagcaatggg gttacacagg 17640atctttgagc atgaatcatc atgaagtttg caacattcat agaaatgagc atgtagctag 17700tggtgatgct atcatgacta gatgtctcgc tatacatgac tgttttgtca aacgtgttga 17760ttggtcaatt gtgtaccctt ttattgacaa tgaagaaaag atcaataaag ctggtcgcat 17820agtgcagtca catgtcatga aagctgctct gaagattttt aatcctgctg caattcacga 17880tgtgggtaat ccaaaaggca tccgttgtgc tacaacacca ataccatggt tttgttatga 17940tcgtgatcct attaataaca atgttagatg tctggattat gactatatgg tacatggtca 18000aatgaatggt cttatgttat tttggaactg taatgtagac atgtacccag agttttcaat 18060tgtttgtaga tttgatactc gcactcgctc taaattgtct ttagaaggtt gtaatggtgg 18120tgcattgtat gttaataacc atgctttcca cacaccagct tatgatagaa gagcttttgc 18180taagcttaaa cctatgccat tcttttacta tgatgatagt aattgtgaac ttgttgatgg 18240gcaacctaat tatgtaccac ttaagtcaaa tgtttgcata acaaaatgca acattggtgg 18300tgctgtctgc aagaagcatg ctgctcttta cagagcgtat gttgaggatt acaacatttt 18360tatgcaggct ggttttacaa tatggtgtcc tcaaaacttt gacacctata tgctttggca 18420tggttttgtt aatagcaaag cacttcagag tctagaaaat gtggctttta atatcgttaa 18480gaaaggtgcc ttcaccggtt taaaaggtga cttaccaact gctgttattg ctgacaaaat 18540aatggtaaga gatggaccta ctgacaaatg tatttttaca aataagacta gtttacctac 18600aaatgtagct tttgagttat atgcaaaacg caaacttgga ctcacacctc cattaacaat 18660acttaggaat ttaggtgttg tcgcaacata taagtttgtg ttgtgggatt atgaagctga 18720acgtcctttc tcaaatttca ctaagcaagt gtgttcctac actgatcttg atagtgaagt 18780tgtaacatgt tttgataata gtattgctgg ttcttttgag cgttttacta ctacaagaga 18840tgcagtgctt atttctaata acgctgtgaa agggcttagt gccattaaat tacaatatgg 18900ccttttgaat gatctacctg taagtactgt tggaaataaa cctgtcacat ggtatatcta 18960tgtgcgcaag aatggtgagt acgtcgaaca aatcgatagt tactatacac agggacgtac 19020ttttgaaacc ttcaaacctc gtagtacaat ggaagaagat tttcttagta tggatactac 19080actcttcatc caaaagtatg gtcttgagga ttatggtttt gaacacgttg tatttggaga 19140tgtctctaaa actaccattg gtggtatgca tcttcttata tcgcaagtgc gccttgcaaa 19200aatgggtttg ttttccgttc aagaatttat gaataattct gacagtacac tgaaaagttg 19260ttgtattaca tatgctgatg atccatcttc taagaatgtg tgcacttata tggacatact 19320cttggacgat tttgtgacta tcattaagag cttagatctt aatgttgtgt ccaaagttgt 19380ggatgtcatt gtagattgta aggcatggag atggatgttg tggtgtgaga attcacatat 19440taaaaccttc tatccacaac tccaatctgc tgaatggaat cccggctata gcatgcctac 19500actgtacaaa atccagcgta tgtgtctcga acggtgtaat ctctacaatt atggtgcaca 19560agtgaaatta cctgtaggca ttactactaa gttcgttaag tatactcagt tgtgtcaata 19620ccttaacact actacattgt gtgtaccaca caaaatgcgt gtattgcatt taggagctgc 19680tggtgcatct ggtgttgctc ctggtagtac tgtattaaga agatggttac cagatgatgc 19740catattggtt gataatgatt tgagagatta cgtttccgac gcagacttca gtgttacagg 19800tgattgtact agtctttaca tcgaagacaa gtttgatttg ctcgtctctg atttatatga 19860tggctccaca aaatcaattg acggtgaaaa cacgtcgaaa gatggtttct ttacttatat 19920taatggtttc attaaagaga aactgtcact tggtggatct gttgccatta aaatcacgga 19980atttagttgg aataaagatt tatatgaatt gattcaaaga tttgagtatt ggactgtgtt 20040ttgtacaagt gttaacacgt catcatcaga aggctttctg attggtatta actacttagg 20100accatactgt gacaaagcaa tagtagatgg aaatataatg catgccaatt atatattttg 20160gagaaactct acaattatgg ctctatcaca taactcagtc ctagacactc ctaaattcaa 20220gtgtcgttgt aacaacgcac ttattgttaa tttaaaagaa aaagaattga atgaaatggt 20280cattggatta ctaaggaagg gtaagttgct cattagaaat aatggtaagt tactaaactt 20340tggtaaccac ttcgttaaca caccatgaaa aaactatttg tggttttggt cgtaatgcca 20400ttgatttatg gagacaattt tccttgttct aaattgacta atagaactat aggcaaccag 20460tggaatctca ttgaaacctt ccttctaaac tatagtagta ggttaccacc taattcagat 20520gtggtgttag gtgattattt tcctactgta caaccttggt ttaattgcat tcgcaatgat 20580agtaatgacc tttatgttac actggaaaat cttaaagcat tgtattggga ttatgctaca 20640gaaaatatca cttggaatca cagacaacgg ttaaacgtag tcgttaatgg atacccatac 20700tccatcacag ttacaacaac ccgcaatttt aattctgctg aaggtgctat tatatgcatt 20760tgtaagggct caccacctac taccaccaca gaatctagtt tgacttgcaa ttggggtagt 20820gagtgcaggt taaaccataa gttccctata tgtccttcta attcagaggc aaattgtggt 20880aatatgctgt atggcctaca atggtttgca gatgaggttg ttgcttattt acatggtgct 20940agttaccgta ttagttttga aaatcaatgg tctggcactg tcacatttgg tgatatgcgt 21000gcgacaacat tagaagtcgc tggcacgctt gtagaccttt ggtggtttaa tcctgtttat 21060gatgtcagtt attatagggt taataataaa aatggtacta ccgtagtttc caattgcact 21120gatcaatgtg ctagttatgt ggctaatgtt tttactacac agccaggagg ttttatacca 21180tcagatttta gttttaataa ttggttcctt ctaactaata gctccacgtt ggttagtggt 21240aaattagtta ccaaacagcc gttattagtt aattgcttat ggccagtccc tagctttgaa 21300gaagcagctt ctacattttg ttttgagggt gctggctttg atcaatgtaa tggtgctgtt 21360ttaaataata ctgtagacgt cattaggttc aaccttaatt ttactacaaa tgtacaatca 21420ggtaagggtg ccacagtgtt ttcattgaac acaacgggtg gtgtcactct tgaaatttca 21480tgttatacag tgagtgactc gagctttttc agttacggtg aaattccgtt cggcgtaact 21540gatggaccac ggtactgtta cgtacactat aatggcacag ctcttaagta tttaggaaca 21600ttaccaccta gtgtcaagga gattgctatt agtaagtggg gccattttta tattaatggt 21660tacaatttct ttagcacatt tcctattgat tgtatatctt ttaatttgac cactggtgat 21720agtgacgttt tctggacaat agcttacaca tcgtacactg aagcattagt acaagttgaa 21780aacacagcta ttacaaaggt gacgtattgt aatagtcacg ttaataacat taaatgctct 21840caaattactg ctaatttgaa taatggattt tatcctgttt cttcaagtga agttggtctt 21900gtcaataaga gtgttgtgtt actacctagc ttttacacac ataccattgt taacataact 21960attggtcttg gtatgaagcg tagtggttat ggtcaaccca tagcctcaac attaagtaac 22020atcacactac caatgcagga tcacaacacc gatgtgtact gtattcgttc tgaccaattt 22080tcagtttatg ttcattctac ttgcaaaagt gctttatggg acaatatttt taagcgaaac 22140tgcacggacg ttttagatgc cacagctgtt ataaaaactg gtacttgtcc tttctcattt 22200gataaattga acaattactt aacttttaac aagttctgtt tgtcgttgag tcctgttggt 22260gctaattgta agtttgatgt agctgcccgt acaagaacca atgagcaggt tgttagaagt 22320ttgtatgtaa tatatgaaga aggagacaac atagtgggtg taccgtctga taatagtggt 22380gtgcacgatt tgtcagtgct acacctagat tcctgcacag attacaatat atatggtaga 22440actggtgttg gtattattag acaaactaac aggacgctac ttagtggctt atattacaca 22500tcactatcag gtgatttgtt aggttttaaa aatgttagtg atggtgtcat ctactctgta 22560acgccatgtg atgtaagcgc acaagcagct gttattgatg gtaccatagt tggggctatc 22620acttccatta acagtgaact gttaggtcta acacattgga caacaacacc taatttttat 22680tactactcta tatataatta cacaaatgat aggactcgtg gcactgcaat tgacagtaat 22740gatgttgatt gtgaacctgt cataacctat tctaacatag gtgtttgtaa aaatggtgct 22800tttgttttta ttaacgtcac acattctgat ggagacgtgc aaccaattag cactggtaat 22860gtcacgatac ctacaaactt taccatatcc gtgcaagtcg aatatattca ggtttacact 22920acaccagtgt caatagactg ttcaagatat gtttgtaatg gtaaccctag gtgtaacaaa 22980ttgttaacac aatacgtttc tgcatgtcaa actattgagc aagcacttgc aatgggtgcc 23040agacttgaaa acatggaggt tgattccatg ttgtttgttt ctgaaaatgc ccttaaattg 23100gcatctgttg aagcattcaa tagttcagaa actttagacc ctatttacaa agaatggcct 23160aatataggtg gttcttggct agaaggtcta aaatacatac ttccgtccca taatagcaaa 23220cgtaagtatc gttcagctat agaggacttg ctttttgata aggttgtaac atctggttta 23280ggtacagttg atgaagatta taaacgttgt acaggtggtt atgacatagc tgacttagta 23340tgtgctcaat actataatgg catcatggtg ctacctggtg tggctaatgc tgacaaaatg 23400actatgtaca cagcatccct tgcaggtggt ataacattag gtgcacttgg tggaggcgcc 23460gtggctatac cttttgcagt agcagttcag gctagactta attatgttgc tctacaaact 23520gatgtattga acaaaaacca gcagattctg gctagtgctt tcaatcaagc tattggtaac 23580attacacagt catttggtaa ggttaatgat gctatacatc aaacatcacg aggtcttgct 23640actgttgcta aagcattggc aaaagtgcaa gatgttgtca acatacaagg gcaagcttta 23700agccacctaa cagtacaatt gcaaaataat ttccaagcca ttagtagttc tattagtgac 23760atttataata ggcttgacga attgagtgct gatgcacaag ttgacaggct gatcacagga 23820agacttacag cacttaatgc atttgtgtct cagactctaa ccagacaagc ggaggttagg 23880gctagtagac aacttgccaa agacaaggtt aatgaatgcg ttaggtctca gtctcagaga 23940ttcggattct gtggtaatgg tacacatttg ttttcactcg caaatgcagc accaaatggc 24000atgattttct ttcacacagt gctattacca acggcttatg aaactgtgac tgcttggcca 24060ggtatttgtg cttcagatgg tgatcgcact tttggacttg tcgttaaaga tgtccagttg 24120actttgtttc gtaatctaga tgacaagttc tatttgaccc ccagaactat gtatcagcct 24180agagttgcaa ctagttctga ctttgttcaa attgaagggt gcgatgtgct gtttgttaat 24240gcaactgtaa gtgatttgcc tagtattata cctgattata ttgatattaa tcagactgtt 24300caagacatat tagaaaattt tagaccaaat tggactgtac ctgagttgac atttgacatt 24360tttaacgcaa cctatttaaa cctgactggt gaaattgatg acttagaatt taggtcagaa 24420aagctacata acaccactgt agaacttgcc attctcattg acaacattaa caatacatta 24480gtcaatcttg aatggctcaa tagaattgaa acctatgtaa aatggccttg gtatgtgtgg 24540ctactaatag gcttagtagt aatattttgc ataccattac tgctattttg ctgttgtagt 24600acaggttgct gtggatgcat aggttgttta ggaagttgtt gtcactctat atgtagtaga 24660agacaatttg aaaattacga accaattgaa aaagtgcacg tccattaaat ttaaaatgtt 24720aattctatca tctgctataa tagcagttgt ttctgctaga gaattttgtt aaggatgatg 24780aataaagtct ttaagaacta aacttacgag tcattacagg tcctgtatgg acattgtcaa 24840atccatttac acatccgtag atgctgtact tgacgaactt gattgtgcat actttgctgt 24900aactcttaaa gtagaattta agactggtaa attacttgtg tgtataggtt ttggtgacac 24960acttcttgct gctaaggata aagcatatgc taagcttggt ctctccatta ttgaagaagt 25020caatagtcat atagttgttt aatatcatta aacacacaaa acccaaagca ttaagtgtta 25080caaaacaatt aaagagagat tatagaaaaa ctgtcattct aaattccatg cgaaaatgat 25140tggtggactt tttcttagta ctctgagttt tgtaattgtt agtaaccatt ctattgttaa 25200taacacagca aatgtgcatc atatacaaca agaacgtgtt atagtacaac agcatcatgt 25260tgttagtgct agaacacaaa actattaccc agagttcagc atcgctgtac tctttgtatc 25320ttttctagct ttgtaccgta gtacaaactt taagacgtgt gtcggcatct taatgtttaa 25380gattttatca atgacacttt taggacctat gcttatagca tatggttact acattgatgg 25440cattgttaca acaactgtct tatctttaag atttgtctac ttagcatact tttggtatgt 25500taatagtagg tttgaattta ttttatacaa tacaacgaca ctcatgtttg tacatggcag 25560agctgcaccg tttatgagaa gttctcacag ctctatttat gtcacattgt atggtggcat 25620aaattatatg tttgtgaatg acctcacgtt gcattttgta gaccctatgc ttgtaagcat 25680agcaatacgt ggcttagctc atgctgatct aactgtagtt agagcagttg aacttctcaa 25740tggtgatttt atttatgtat tttcacagga gcccgtagtc ggtgtttaca atgcagcctt 25800ttctcaggcg gttctaaacg aaattgactt aaaagaagaa gaagaagacc atacctatga 25860cgtttcctag ggcattgact gtcatagatg acaatggaat ggtcattaac atcattttct 25920ggttcctgtt gataattata ttgatattac tttcaatagc attgctaaat ataattaagc 25980tatgcatggt gtgttgcaat ttaggaagga cagttattat tgttccagcg caacatgctt 26040acgatgccta taagaatttt atgcgaatta aagcatacaa ccccgatgga gcactccttg 26100cttgaactaa acaaaatgaa gattttgtta atattagcgt gtgtgattgc atgcgcatgt 26160ggagaacgct attgtgctat gaaatccgat acagatttgt catgtcgcaa tagtacagcg 26220tctgattgtg agtcatgctt caacggaggc gatcttattt ggcatcttgc aaactggaac 26280ttcagctggt ctataatatt gatcgttttt ataactgtgc tacaatatgg aagacctcaa 26340ttcagctggt tcgtgtatgg cattaaaatg cttataatgt ggctattatg gcccgttgtt 26400ttggctctta cgatttttaa tgcatactcg gaataccaag tgtccagata tgtaatgttc 26460ggctttagta ttgcaggtgc aattgttaca tttgtactct ggattatgta ttttgtaaga 26520tccattcagt tgtacagaag gactaagtct tggtggtctt tcaaccctga aactaaagca 26580attctttgcg ttagtgcatt aggaagaagc tatgtgcttc ctctcgaagg tgtgccaact 26640ggtgtcactc taactttgct ttcagggaat ttgtacgctg aagggttcaa aattgcaggt 26700ggtatgaaca tcgacaattt accaaaatac gtaatggttg cattacctag caggactatt 26760gtctacacac ttgttggcaa gaagttgaaa gcaagtagtg cgactggatg ggcttactat 26820gtaaaatcta aagctggtga ttactcaaca gaggcaagaa ctgataattt gagtgagcaa 26880gaaaaattat tacatatggt ataactaaac ttctaaatgg ccaaccaggg acaacgtgtc 26940agttggggag atgaatctac caaaacacgt ggtcgttcca attcccgtgg tcggaagaat 27000aataacatac ctctttcatt cttcaacccc ataaccctcc aacaaggttc aaaattttgg 27060aacttatgtc cgagagactt tgtacccaaa ggaataggta acagggatca acagattggt 27120tattggaata gacaaactcg ctatcgcatg gtgaagggcc aacgtaaaga gcttcctgaa 27180aggtggttct tctactactt aggtactgga cctcatgcag atgccaaatt taaagataaa 27240ttagatggag ttgtctgggt tgccaaggat ggtgccatga acaaaccaac cacgcttggt 27300agtcgtggtg ctaataatga atccaaagct ttgaaattcg atggtaaagt gccaggcgaa 27360tttcaacttg aagttaatca atcaagagac aattcaaggt cacgctctca atctagatct 27420cggtctagaa atagatctca atctagaggc aggcaacaat tcaataacaa gaaggatgac 27480agtgtagaac aagctgttct tgccgcactt aaaaagttag gtgttgacac agaaaaacaa 27540cagcaacgct ctcgttctaa atctaaagaa cgtagtaact ctaagacaag agatactaca 27600cctaagaatg aaaacaaaca cacctggaag agaactgcag gtaaaggtga tgtgacaaga 27660ttttatggag ctagaagcag ttcagccaat tttggtgaca ctgacctcgt tgccaatggg 27720agcagtgcca agcattaccc acaactggct gaatgtgttc catctgtgtc tagcattctg 27780tttggaagct attggacttc aaaggaagat ggcgaccaga tagaagtcac gttcacacac 27840aaataccact tgccaaagga tgatcctaag actggacaat tccttcagca gattaatgcc 27900tatgctcgtc catcagaagt ggcaaaagaa cagagaaaaa gaaaatctcg ttctaaatct 27960gcagaaaggt cagagcaaga tgtggtacct gatgcattaa tagaaaatta tacagatgtg 28020tttgatgaca cacaggttga gataattgat gaggtaacga actaaacgag atgctcgtct 28080tcctccatgc tgtatttatt acagttttaa tcttactact aattggtaga ctccaattat 28140tagaaagact attacttaat cactctttca atcttaaaac tgtcaatgac tttaatatct 28200tatataggag tttagcagaa accagattac taaaagtggt gcttcgagta atctttctag 28260tcttactagg attttgctgc tacagattgt tagtcacatt aatgtaaggc aacccgatgt 28320ctaaaactgg tttttccgag gaattactgg tcatcgcgct gtctactctt gtacagaatg 28380gtaagcacgt gtaataggag gtacaagcaa ccctattgca tattaggaag tttagatttg 28440atttggcaat gctagattta gtaatttaga gaagtttaaa gatccgctac gacgagccaa 28500caatggaaga gctaacgtct ggatctagtg attgtttaaa atgtaaaatt gtttgaaaat 28560tttccttttg atagtgatac aaaaaaaa 28588221DNAPorcine Transmissible Gastroenteritis V 2cctaggattt aaatcctaag g 21327DNAPorcine Transmissible Gastroenteritis V 3gcggccgcgc cggcgaggcc tgtcgac 2746DNAPorcine Transmissible Gastroenteritis V 4gtcgac 6522DNAPorcine Transmissible Gastroenteritis V 5gctagcccag gcgcgcggta cc 22611DNAPorcine Transmissible Gastroenteritis Vmisc_feature(4)...(5)between nucleotides 4 & 5 is a gap of unknown length 6ctatggtata a 11711DNAPorcine Transmissible Gastroenteritis Vmisc_feature(4)...(5)between nucleotides 4 & 5 is a gap of unknown length 7aatgtaagtt a 11811DNAPorcine Transmissible Gastroenteritis Vmisc_feature(4)...(5)between nucleotides 4 & 5 is a gap of unknown length 8atttgcttga a 11911DNAPorcine Transmissible Gastroenteritis Vmisc_feature(4)...(5)between nucleotides 4 & 5 is a gap of unknown length 9ctatggtata a 111025DNAPorcine Transmissible Gastroenteritis V 10tttggtaaca cttcgttaac acacc 251123DNAPorcine Transmissible Gastroenteritis V 11ttacgagtca ttacaggtcc tgt 231224DNAPorcine Transmissible Gastroenteritis V 12tttaagacgt gtgtcggcat ctta 241337DNAPorcine Transmissible
Gastroenteritis V 13gaaattgact taaaagaaga agaagaagac catacct 371410DNAPorcine Transmissible Gastroenteritis V 14gtcgacgacc 101512DNAPorcine Transmissible Gastroenteritis V 15gaaatatttg tc 12
Patent applications by Luis Enjuanes Sanchez, Madrid ES
Patent applications by Consejo Superior De Investigaciones Cientificas
Patent applications in class Recombinant virus encoding one or more heterologous proteins or fragments thereof
Patent applications in all subclasses Recombinant virus encoding one or more heterologous proteins or fragments thereof