Abstract
The 5'- and 3'-terminal sequences of the genomic RNA from classical swine fever virus (CSFV) were determined, and the resulting information was used for construction of full-length CSFV cDNA clones. After transfection of in vitro-transcribed RNA derived from a cDNA construct, infectious CSFV was recovered from porcine cells. To confirm the de novo generation of infectious CSFV from cloned DNA, a genetically tagged CSFV was constructed. In comparison with parental CSFV, the recombinant viruses were retarded in growth by about 1 order of magnitude. Introduction of a deletion by exchange of part of the full-length construct for corresponding cDNA fragments derived from the genomes of cytopathogenic CSFV defective interfering particles (DIs) (G. Meyers and H.-J. Thiel, J. Virol. 69:3683-3689. 1995) resulted in recovery of cytopathogenic DIs in the DI genomes is responsible for their cytopathogenicity. The established system will allow novel approaches to analysis of pestiviral molecular biology and in particular to elucidation of the molecular basis of attenuation and cytopathogenicity of these viruses.
Full Text
The Full Text of this article is available as a PDF (436.1 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Boyer J. C., Haenni A. L. Infectious transcripts and cDNA clones of RNA viruses. Virology. 1994 Feb;198(2):415–426. doi: 10.1006/viro.1994.1053. [DOI] [PubMed] [Google Scholar]
- Brock K. V., Deng R., Riblet S. M. Nucleotide sequencing of 5' and 3' termini of bovine viral diarrhea virus by RNA ligation and PCR. J Virol Methods. 1992 Jul;38(1):39–46. doi: 10.1016/0166-0934(92)90167-c. [DOI] [PubMed] [Google Scholar]
- Cao X., Wimmer E. Intragenomic complementation of a 3AB mutant in dicistronic polioviruses. Virology. 1995 Jun 1;209(2):315–326. doi: 10.1006/viro.1995.1263. [DOI] [PubMed] [Google Scholar]
- Conzelmann K. K., Cox J. H., Schneider L. G., Thiel H. J. Molecular cloning and complete nucleotide sequence of the attenuated rabies virus SAD B19. Virology. 1990 Apr;175(2):485–499. doi: 10.1016/0042-6822(90)90433-r. [DOI] [PubMed] [Google Scholar]
- Corapi W. V., French T. W., Dubovi E. J. Severe thrombocytopenia in young calves experimentally infected with noncytopathic bovine viral diarrhea virus. J Virol. 1989 Sep;63(9):3934–3943. doi: 10.1128/jvi.63.9.3934-3943.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- De Moerlooze L., Desport M., Renard A., Lecomte C., Brownlie J., Martial J. A. The coding region for the 54-kDa protein of several pestiviruses lacks host insertions but reveals a "zinc finger-like" domain. Virology. 1990 Aug;177(2):812–815. doi: 10.1016/0042-6822(90)90555-6. [DOI] [PubMed] [Google Scholar]
- Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GILLESPIE J. H., SHEFFY B. E., BAKER J. A. Propagation of hog cholera virus in tissue culture. Proc Soc Exp Biol Med. 1960 Dec;105:679–681. doi: 10.3181/00379727-105-26215. [DOI] [PubMed] [Google Scholar]
- Kandolf R., Hofschneider P. H. Molecular cloning of the genome of a cardiotropic Coxsackie B3 virus: full-length reverse-transcribed recombinant cDNA generates infectious virus in mammalian cells. Proc Natl Acad Sci U S A. 1985 Jul;82(14):4818–4822. doi: 10.1073/pnas.82.14.4818. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kean K. M., Wychowski C., Kopecka H., Girard M. Highly infectious plasmids carrying poliovirus cDNA are capable of replication in transfected simian cells. J Virol. 1986 Aug;59(2):490–493. doi: 10.1128/jvi.59.2.490-493.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klump W. M., Bergmann I., Müller B. C., Ameis D., Kandolf R. Complete nucleotide sequence of infectious Coxsackievirus B3 cDNA: two initial 5' uridine residues are regained during plus-strand RNA synthesis. J Virol. 1990 Apr;64(4):1573–1583. doi: 10.1128/jvi.64.4.1573-1583.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kunkel T. A., Roberts J. D., Zakour R. A. Rapid and efficient site-specific mutagenesis without phenotypic selection. Methods Enzymol. 1987;154:367–382. doi: 10.1016/0076-6879(87)54085-x. [DOI] [PubMed] [Google Scholar]
- Lai C. J., Zhao B. T., Hori H., Bray M. Infectious RNA transcribed from stably cloned full-length cDNA of dengue type 4 virus. Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5139–5143. doi: 10.1073/pnas.88.12.5139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mandl C. W., Heinz F. X., Puchhammer-Stöckl E., Kunz C. Sequencing the termini of capped viral RNA by 5'-3' ligation and PCR. Biotechniques. 1991 Apr;10(4):484–486. [PubMed] [Google Scholar]
- Meyers G., Rümenapf T., Thiel H. J. Molecular cloning and nucleotide sequence of the genome of hog cholera virus. Virology. 1989 Aug;171(2):555–567. doi: 10.1016/0042-6822(89)90625-9. [DOI] [PubMed] [Google Scholar]
- Meyers G., Rümenapf T., Thiel H. J. Ubiquitin in a togavirus. Nature. 1989 Oct 12;341(6242):491–491. doi: 10.1038/341491a0. [DOI] [PubMed] [Google Scholar]
- Meyers G., Tautz N., Dubovi E. J., Thiel H. J. Viral cytopathogenicity correlated with integration of ubiquitin-coding sequences. Virology. 1991 Feb;180(2):602–616. doi: 10.1016/0042-6822(91)90074-L. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meyers G., Tautz N., Stark R., Brownlie J., Dubovi E. J., Collett M. S., Thiel H. J. Rearrangement of viral sequences in cytopathogenic pestiviruses. Virology. 1992 Nov;191(1):368–386. doi: 10.1016/0042-6822(92)90199-Y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meyers G., Thiel H. J. Cytopathogenicity of classical swine fever virus caused by defective interfering particles. J Virol. 1995 Jun;69(6):3683–3689. doi: 10.1128/jvi.69.6.3683-3689.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moennig V., Plagemann P. G. The pestiviruses. Adv Virus Res. 1992;41:53–98. doi: 10.1016/s0065-3527(08)60035-4. [DOI] [PubMed] [Google Scholar]
- Omata T., Kohara M., Sakai Y., Kameda A., Imura N., Nomoto A. Cloned infectious complementary DNA of the poliovirus Sabin 1 genome: biochemical and biological properties of the recovered virus. Gene. 1984 Dec;32(1-2):1–10. doi: 10.1016/0378-1119(84)90026-x. [DOI] [PubMed] [Google Scholar]
- Pellerin C., van den Hurk J., Lecomte J., Tijssen P. Identification of a new group of bovine viral diarrhea virus strains associated with severe outbreaks and high mortalities. Virology. 1994 Sep;203(2):260–268. doi: 10.1006/viro.1994.1483. [DOI] [PubMed] [Google Scholar]
- Pocock D. H., Howard C. J., Clarke M. C., Brownlie J. Variation in the intracellular polypeptide profiles from different isolates of bovine virus diarrhoea virus. Arch Virol. 1987;94(1-2):43–53. doi: 10.1007/BF01313724. [DOI] [PubMed] [Google Scholar]
- Purchio A. F., Larson R., Collett M. S. Characterization of bovine viral diarrhea virus proteins. J Virol. 1984 May;50(2):666–669. doi: 10.1128/jvi.50.2.666-669.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qi F., Ridpath J. F., Lewis T., Bolin S. R., Berry E. S. Analysis of the bovine viral diarrhea virus genome for possible cellular insertions. Virology. 1992 Jul;189(1):285–292. doi: 10.1016/0042-6822(92)90704-s. [DOI] [PubMed] [Google Scholar]
- Racaniello V. R., Baltimore D. Cloned poliovirus complementary DNA is infectious in mammalian cells. Science. 1981 Nov 20;214(4523):916–919. doi: 10.1126/science.6272391. [DOI] [PubMed] [Google Scholar]
- Rebhun W. C., French T. W., Perdrizet J. A., Dubovi E. J., Dill S. G., Karcher L. F. Thrombocytopenia associated with acute bovine virus diarrhea infection in cattle. J Vet Intern Med. 1989 Jan-Mar;3(1):42–46. doi: 10.1111/j.1939-1676.1989.tb00327.x. [DOI] [PubMed] [Google Scholar]
- Rice C. M., Grakoui A., Galler R., Chambers T. J. Transcription of infectious yellow fever RNA from full-length cDNA templates produced by in vitro ligation. New Biol. 1989 Dec;1(3):285–296. [PubMed] [Google Scholar]
- Rümenapf T., Meyers G., Stark R., Thiel H. J. Hog cholera virus--characterization of specific antiserum and identification of cDNA clones. Virology. 1989 Jul;171(1):18–27. doi: 10.1016/0042-6822(89)90506-0. [DOI] [PubMed] [Google Scholar]
- Schnell M. J., Mebatsion T., Conzelmann K. K. Infectious rabies viruses from cloned cDNA. EMBO J. 1994 Sep 15;13(18):4195–4203. doi: 10.1002/j.1460-2075.1994.tb06739.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Semler B. L., Dorner A. J., Wimmer E. Production of infectious poliovirus from cloned cDNA is dramatically increased by SV40 transcription and replication signals. Nucleic Acids Res. 1984 Jun 25;12(12):5123–5141. doi: 10.1093/nar/12.12.5123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sumiyoshi H., Hoke C. H., Trent D. W. Infectious Japanese encephalitis virus RNA can be synthesized from in vitro-ligated cDNA templates. J Virol. 1992 Sep;66(9):5425–5431. doi: 10.1128/jvi.66.9.5425-5431.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tautz N., Meyers G., Thiel H. J. Processing of poly-ubiquitin in the polyprotein of an RNA virus. Virology. 1993 Nov;197(1):74–85. doi: 10.1006/viro.1993.1568. [DOI] [PubMed] [Google Scholar]
- Tautz N., Thiel H. J., Dubovi E. J., Meyers G. Pathogenesis of mucosal disease: a cytopathogenic pestivirus generated by an internal deletion. J Virol. 1994 May;68(5):3289–3297. doi: 10.1128/jvi.68.5.3289-3297.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsukiyama-Kohara K., Iizuka N., Kohara M., Nomoto A. Internal ribosome entry site within hepatitis C virus RNA. J Virol. 1992 Mar;66(3):1476–1483. doi: 10.1128/jvi.66.3.1476-1483.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang C., Sarnow P., Siddiqui A. Translation of human hepatitis C virus RNA in cultured cells is mediated by an internal ribosome-binding mechanism. J Virol. 1993 Jun;67(6):3338–3344. doi: 10.1128/jvi.67.6.3338-3344.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weiland E., Ahl R., Stark R., Weiland F., Thiel H. J. A second envelope glycoprotein mediates neutralization of a pestivirus, hog cholera virus. J Virol. 1992 Jun;66(6):3677–3682. doi: 10.1128/jvi.66.6.3677-3682.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weiland E., Stark R., Haas B., Rümenapf T., Meyers G., Thiel H. J. Pestivirus glycoprotein which induces neutralizing antibodies forms part of a disulfide-linked heterodimer. J Virol. 1990 Aug;64(8):3563–3569. doi: 10.1128/jvi.64.8.3563-3569.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yamaya J., Yoshioka M., Meshi T., Okada Y., Ohno T. Expression of tobacco mosaic virus RNA in transgenic plants. Mol Gen Genet. 1988 Mar;211(3):520–525. doi: 10.1007/BF00425710. [DOI] [PubMed] [Google Scholar]
- van der Werf S., Bradley J., Wimmer E., Studier F. W., Dunn J. J. Synthesis of infectious poliovirus RNA by purified T7 RNA polymerase. Proc Natl Acad Sci U S A. 1986 Apr;83(8):2330–2334. doi: 10.1073/pnas.83.8.2330. [DOI] [PMC free article] [PubMed] [Google Scholar]