Bovine herpesvirus 4 infects differentiated neuronal cells in culture and establish persistent infection upon selection

References

• Asano A, Inoshima Y, Murakami K, Iketani Y, Yamamoto Y, Sentsui H. 2003. Latency and persistence of bovine herpesvirus type 4, strain b11–41, in bovine nervous tissues. J Vet Med Sci. 65: 87–93. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Ballestas M E, Chatis P A, Kaye K M. 1999. Efficient persistence of extrachromosomal KSHV DNA mediated by latency-associated nuclear antigen. Science. 284: 641–644. [CROSSREF], [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Bartha A, Fadol A M, Liebermann H, Ludwig H, Mohanty S B, Osorio F A, Reed D E, Storz J, Straub O C, Van der, Maaten M J, Wellermans G. 1987. Problems concerning the taxonomy of the “Movar-Type” bovine herpesvirus. Intervirology. 28: 1–7. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Ceserman E, Moore P S, Rao P H, Inghirami G, Knowles D M, Chang Y. 1995. In vitro establishment and characterization of two aquired immunodeficiency syndrome-related lymphoma cell lines (BC-1 and BC-2) containing Kaposi's sarcoma-associated herpesvirus-like (KSHV) DNA sequences. Blood. 86: 2708–2714
   Google Scholar
• Decker L L, Shankar P, Khan G, Freeman R B, Dezube B J, Lieberman J, Thorley-Lawson D A. 1996. The Kaposi sarcoma-associated herpesvirus (KSHV) is present as an intact latent genome in KS tissue but replicates in the peripheral blood mononuclear cells of KS patients. J Exp Med. 184: 283–288. [CROSSREF], [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Dollard S C, Broker T R, Chow L T. 1993. Regulation of the human papillomavirus type 11 E6 promoter by viral and host transcription factors in primary human keratinocytes. J Virol. 67: 1721–1726. [PUBMED], [INFOTRIEVE]
   PubMedGoogle Scholar
• Donofrio G, Cavirani S, Taddei S, van, Santen V L. 2002. Bovine herpesvirus 4 as a gene delivery vector. J Virol Methods. 101: 49–61. [CROSSREF], [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Donofrio G, Cavirani S, van, Santen V L. 2000. Establishment of a cell line persistently infected with bovine herpesvirus 4 using a recombinant virus. J Gen Virol. 81: 1807–1814. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Donofrio G, Galli C, Lazzari G, van, Santen V L, Cavirani S, Flammini C F. 2003. Interaction of a green recombinant Bovine herpesvirus 4 with in vitro-produced bovine embryos. Vet Res Commun. 27: 415–424. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Dubuisson J, Thiry E, Bublot M, Thomas I, van, Bressem M F, Coignoul F, Pastoret P P. 1989. Experimental infection of bulls with a genital isolate of bovine herpesvirus-4 and reactivation of latent virus with dexamethasone. Vet Microbiol. 21: 97–114. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Dutko F J, Oldstone M B. 1981. Cytomegalovirus causes a latent infection in undifferentiated cells and is activated by induction of cell differentiation. J Exp Med. 154: 1636–1651. [CROSSREF], [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Egyed L, Bartha A. 1998. PCR studies on the potential sites for latency of BHV-4 in calves. Vet Res Commun. 22: 209–216. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Flore O, Rafii S, Ely S, O'Leary J J, Hyjek E M, Cesarman E. 1998. Transformation of primary human endothelial cells by Kaposi's sarcoma-associated herpesvirus. Nature. 394: 588–592. [CROSSREF], [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Guetta E, Ron D, Tal J. 1986. Development-dependent replication of minute virus of mice in differentiated mouse testicular cell lines. J Gen Virol. 67: 2549–2554. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Jung J U, Choi J K, Ensser A, Biesinger B. 1999. Herpesvirus saimiri as a model for gammaherpesvirus oncogenesis. Sem Cancer Biol. 9: 231–239. [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Keilbaugh S A, Prusoff W H, Simpson M V. 1991. The PC12 cell as a model for studies of the mechanism of induction of peripheral neuropathy by anti-HIV-I dideoxynucleoside analogs. Biochem Pharmacol. 42: R5–R8. [CROSSREF], [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Kieff E. 1996. Epstein-Barr virus and its replication. Fundamental virology, 3rd ed, Fields B N, Knipe D M, Howley P M, Philadelphia, Lippencott-Raven. pp 1109–1162
   Google Scholar
• Krogman L A, McAdaragh J P. 1982. Recrudescence of bovine herpesvirus-5 in experimentally infected calves. Am J Vet Res. 43: 336–338. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Kung S H, Medveczky P G. 1996. Identification of a herpesvirus Saimiri cis-acting DNA fragment that permits stable replication of episomes in transformed T cells. J Virol. 70: 1738–1744. [PUBMED], [INFOTRIEVE]
   PubMedGoogle Scholar
• Lin T M, Shi G Y, Tsai C F, Janny Su H, Leon Guo YL, Wu H L. 1997. Susceptibility of endothelial cells to bovine herpesvirus type 4 (BHV-4). J Virol Methods. 63: 219–225. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Lomonte P, Bublot M., van, Santen V L, Keil G, Pastoret P P, Thiry E. 1996. Bovine herpesvirus 4: genomic organization and relationship with two other gammaherpesviruses, Epstein-Barr virus and herpesvirus saimiri. Vet Microbiol. 53: 79–89. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Lopez O J, Galeota J A, Osorio F A. 1996. Bovine herpesvirus type-4 (BHV-4) persistently infects cells of the marginal zone of spleen in cattle. Microb Pathogen. 21: 47–58. [CROSSREF]
   Google Scholar
• Lupton S, Levine A J. 1985. Mapping genetic elements of Epstein-Barr virus that facilitate extrachromosomal persistence of Epstein-Barr virus-derived plasmids in human cells. Mol Cell Biol. 5: 2533–2542. [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Maniatis T, Fritsch E F, Sambrook J. 1989; Molecular Cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, New York
   Google Scholar
• Mettenleiter T C. 1989. Glycoprotein gIII deletion mutants of pseudorabies virus are impaired in virus entry. Virology. 171: 623–625. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Miller G. 1990. Epstein-Barr virus. Virology, Fields B N, Knipe D N, Chanock R M, Hirsch M S, Melnick J L, Monath T P, Roizman B, Raven Press, New York. pp. 1921–1958
   Google Scholar
• Miller G, Heston L, Grogan E, Gradoville L, Rigsby M, Sun R, Shedd D, Kushnaryov V M, Grossberg S, Chang Y. 1997. Selective switch between latency and lytic replication of Kaposi's sarcoma herpesvirus and Epstein-Barr virus in dually infected body cavity lymphoma cells. J Virol. 71: 314–324. [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Moses A V, Fish K N, Ruhl R, Smith P P, Strussenberg J G, Zhu L, Chandran B, Nelson J A. 1999. Long-term infection and transformation of dermal microvascular endothelial cells by human herpesvirus 8. J Virol. 73: 6892–6902. [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Naeem K, Caywood D D, Goyal S M, Werdin R E, Murtaugh M P. 1993. Persistence of bovid herpesvirus-4 in experimentally inoculated pregnant rabbits. Microbiologica. 16: 87–94. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Nagatsu T, Nakano T, Kato H, Higashida H. 1981. Expression of A and B types of monoamine oxidase in neuroblastoma hybrid cells. Neurochem Int. 3: 137–142. [CROSSREF]
   Google Scholar
• Nilsson K. 1979. The nature of lymphoid cell lines and their relationship to the virus. The Epstein-Barr virus, Epstein M A, Achong B G, Berlin, Springer-Verlag. pp 225–281
   Google Scholar
• Osorio F A, Reed D E. 1983. Experimental inoculation of cattle with bovine herpesvirus-4: evidience for a lymphoid-associated persistent infection. Am J Vet Res. 44: 975–980. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Osorio F A, Reed D E, Rock D L. 1982. Experimental infection of rabbits with bovine herpesvirus-4: acute and persistent infection. Vet Microbiol. 7: 503–513. [CROSSREF], [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Osorio F A, Rock D L, Reed D E. 1985. Studies on the pathogenesis of a bovine cytomegalo-like virus in an experimental host. J Gen Virol. 66: 1941–1951. [PUBMED], [INFOTRIEVE]
   Google Scholar
• Peterson R B, Goyal S M. 1988. Propagation and quantitation of animal herpesviruses in eight cell culture systems. Comp Immunol Microbiol Infect Dis. 11: 93–98. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Tan J, Town T, Mori T, Obregon D, Wu Y, Del le, Donne A, Rojiani A, Crawford F, Flavell R A, Mullan M. 2002. CD40 is expressed and functional on neuronal cells. EMBO J. 21: 643–652. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Thiry E, Bublot M, Dubuisson J, Pastoret P P. 1989. Bovine herpesvirus-4 (BHV-4) infections of cattle. Herpesvirus diseases of cattle, horses, and pigs, Wittmann G, Boston, Kluwer Academic Publishers. pp 96–115
   Google Scholar
• Truman D, Ludwig H, Storz J. 1986. Bovine herpesvirus type 4: studies on the biology and spread in cattle herds and in insemination bulls. J Vet Med B. 33: 485–501
   Google Scholar
• Usherwood E J, Stewart J P, Nash A A. 1996. Characterization of tumor cell lines derived from murine gammaherpesvirus-68-infected mice. J Virol. 70: 6516–6518. [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Wirth J J, Amalfitano A, Gross R, Oldstone M B, Fluck M M. 1992. Organ- and age-specific replication of polyomavirus in mice. J Virol. 66: 3278–3286. [PUBMED], [INFOTRIEVE]
   PubMedGoogle Scholar
• Yamamoto Y, Murakami K, Inoshima Y, Nakane T, Saika K, Sentsui H. 2000. Characterization of a bovine herpesvirus type 4 isolated from the spinal cord of a cow with astasia. Arch Virol. 145: 2363–2370. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar
• Yates J, Warren N, Reisman D, Sugden B. 1984. A cis-acting element from the Epstein-Barr viral genome that permits stable replication of recombinant plasmids in latently infected cells. Proc Nat Acad Sci U S A. 81: 3806–3810
   PubMed Web of Science ®Google Scholar
• Yates J L, Warren N, Sugden B. 1985. Stable replication of plasmids derived from Epstein-Barr virus in various mammalian cells. Nature. 313: 812–815. [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Zimmermann W, Broll H, Ehlers B, Buhk H J, Rosenthal A, Goltz M. 2001. Genome sequence of bovine herpesvirus 4, a bovine rhadinovirus, and identification of an origin of DNA replication. J Virol. 75: 1186–1194. [CROSSREF], [PUBMED], [INFOTRIEVE]
   Google Scholar