Biology of ovine adenovirus infection of nonpermissive cells

Journal of Virology

Volumn 76, Issue 21, 2002, Pages 10882-10893

  Kümin, Daniel ^a   Hofmann, Christian ^a   Rudolph, Michael ^a   Both, Gerald W ^a   Löser, Peter ^a  

^a DeveloGen AG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

VIRUS DNA;

ADENOVIRUS; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DNA REPLICATION; DNA VECTOR; GENE THERAPY; HUMAN; HUMAN ADENOVIRUS; HUMAN CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; SHEEP; VIRUS INFECTION; VIRUS ISOLATION; VIRUS REPLICATION;

ADENOVIRIDAE; ANIMALS; CELL LINE; DNA REPLICATION; DNA, VIRAL; HUMANS; MICE; RATS; RNA, VIRAL; SHEEP; TUMOR CELLS, CULTURED;

EID: 0036839209     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.76.21.10882-10893.2002     Document Type: Article

References (60)

1. Anderson, K. P., and D. F. Klessig. 1984. Altered mRNA splicing in monkey cells abortively infected with human adenovirus may be responsible for inefficient synthesis of the virion fiber polypeptide. Proc. Natl. Acad. Sci. USA 81:4023-4027.
2. Anderson, K. P., and D. F. Klessig. 1983. Posttranscriptional block to synthesis of a human adenovirus capsid protein in abortively infected monkey cells. J. Mol. Appl. Genet. 2:31-43.
3. Benko, M., and B. Harrach. 1998. A proposal for a new (third) genus within the family Adenoviridae. Arch. Virol. 143:829-837.
4. Bergelson, J. M., J. A. Cunningham, G. Droguett, E. A. Kurt-Jones, A. Krithivas, J. S. Hong, M. S. Horwitz, R. L. Crowell, and R. W. Finberg. 1997. Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5. Science 275:1320-1323.
5. Both, G. 2001. Xenogenic adenoviral vectors, p. 447-479. In D. Curiel and J. Douglas (ed.), Adenoviral vectors for gene therapy. Academic Press, New York, N.Y.
6. Boyle, D. B., A. D. Pye, R. Kocherhans, B. M. Adair, S. Vrati, and G. W. Both. 1994. Characterisation of Australian ovine adenovirus isolates. Vet. Microbiol. 41:281-291.
7. Cauthen, A. N., and K. R. Spindler. 1999. Novel expression of mouse adenovirus type I early region 3 gp11K at late times after infection. Virology 259:119-128.
8. Cepko, C. L., and P. A. Sharp. 1983. Aberrant distribution of human adenovirus type 2 late proteins in monkey kidney cells. J. Virol. 46:302-306.
9. Cichon, G., H. H. Schmidt, T. Benhidjeb, P. Loser, S. Ziemer, R. Haas, N. Grewe, F. Schnieders, J. Heeren, M. P. Manns, P. M. Schlag, and M. Strauss. 1999. Intravenous administration of recombinant adenoviruses causes thromboeytopenia anemia and erythroblastosis in rabbits. J. Gene Med. 1:360-371.
10. Cichon, G., and M. Strauss. 1998. Transient immunosuppression with 15-deoxyspergualin prolongs reporter gene expression and reduces humoral immune response after adenoviral gene transfer. Gene Ther. 5:85-90.
11. Dan, A., Z. Ruzsics, W. C. Russell, M. Benko, and B. Harrach. 1998. Analysis of the hexon gene sequence of bovine adenovirus type 4 provides further support for a new adenovirus genus (Atadenovirus). J. Gen. Virol. 79:1453-1460.
12. de Jong, R. N., and P. C. van der Vliet. 1999. Mechanism of DNA replication in eukaryotic cells: cellular host factors stimulating adenovirus DNA replication. Gene 236:1-12.
13. Doerfler, W. 1969. Nonproductive infection of baby hamster kidney cells (BHK21) with adenovirus type 12. Virology 38:587-606.
14. Eggerding, F. A., and W. C. Pierce. 1986. Molecular biology of adenovirus type 2 semipermissive infections. I. Viral growth and expression of viral replicative functions during restricted adenovirus infection. Virology 148:97-113.
15. Eron, L. 1975. Post-transcriptional restriction of human adenovirus expression in monkey cells. J. Virol. 15:1256-1261.
16. Harrach, B., and M. Benko. 1999. Phylogenetic analysis of adenovirus sequences-proof of the necessity of establishing a third genus in the Adenoviridae family, p. 309-339. In W. S. M. Wold (ed.), Adenovirus methods and protocols, vol. 21. Humana Press Inc., Totowa, N.J.
17. Harrach, B., B. M. Meehan, M. Benko, B. M. Adair, and D. Todd. 1997. Close phylogenetic relationship between egg drop syndrome virus, bovine adenovirus serotype 7, and ovine adenovirus strain 287. Virology 229:302-308.
18. Hofmann, C., P. Löser, G. Cichon, W. Arnold, G. W. Both, and M. Strauss. 1999. Ovine adenovirus vectors overcome preexisting humoral immunity against human adenoviruses in vivo. J. Virol. 73:6930-6936.
19. Hofmann, C., V. Sandig, G. Jennings, M. Rudolph, P. Schlag, and M. Strauss. 1995. Efficient gene transfer into human hepatocytes by baculovirus vectors. Proc. Natl. Acad. Sci. USA 92:10099-10103.
20. Hosel, M., J. Schroer, D. Webb, E. Jaroshevskaja, and W. Doerfler. 2001. Cellular and early viral factors in the interaction of adenovirus type 12 with hamster cells: the abortive response. Virus Res. 81:1-16.
21. Hosel, M., D. Webb, J. Schroer, B. Schmitz, and W. Doerfler. 2001. Overexpression of the adenovirus type 12 (Adl2) pTP or E1A gene facilitates Adl2 DNA replication in nonpermissive BHK21 hamster cells. J. Virol. 75:10041-10053.
22. Johnston, J. M., K. P. Anderson, and D. F. Klessig. 1985. Partial block to transcription of human adenovirus type 2 late genes in abortively infected monkey cells. J. Virol. 56:378-385.
23. Khatri, A., and G. W. Both. 1998. Identification of transcripts and promoter regions of ovine adenovirus OAV287. Virology 245:128-141.
24. Khatri, A., Z. Z. Xu, and G. W. Both. 1997. Gene expression by atypical recombinant ovine adenovirus vectors during abortive infection of human and animal cells in vitro. Virology 239:226-237.
25. Klessig, D. F., and C. W. Anderson. 1975. Block to multiplication of adenovirus serotype 2 in monkey cells. J. Virol. 16:1650-1668.
26. Klessig, D. F., and L. T. Chow. 1980. Incomplete splicing and deficient accumulation of the fiber messenger RNA in monkey cells infected by human adenovirus type 2. J. Mol. Biol. 139:221-242.
27. Klimkait, T., and W. Doerfler. 1985. Adenovirus types 2 and 5 functions elicit replication and late expression of adenovirus type 12 DNA in hamster cells. J. Virol. 55:466-474.
28. Klonjkowski, B., P. Gilardi-Hebenstreit, J. Hadchouel, V. Randrianarison, S. Boutin, P. Yeh, M. Perricaudet, and E. J. Kremer. 1997. A recombinant El-deleted canine adenoviral vector capable of transduction and expression of a transgene in human-derived cells and in vivo. Hum. Gene Ther. 8:2103-2115.
29. Kremer, E. J., S. Boutin, M. Chillon, and O. Danos. 2000. Canine adenovirus vectors: an alternative for adenovirus-mediated gene transfer. J. Virol. 74:505-512.
30. Lockett, L. J., and G. W. Both. 2002. Complementation of a defective human adenovirus by an otherwise incompatible ovine adenovirus recombinant carrying a functional E1A gene. Virology 294:333-341.
31. Löser, P., G. Cichon, G. S. Jennings, G. W. Both, and C. Hofmann. 1999. Ovine adenovirus vectors promote efficient gene delivery in vivo. Gene Ther. Mol. Biol. 4:33-43.
32. Löser P., M. Hillgenberg, W. Arnold, G. W. Both, and C. Hofmann. 2000. Ovine adenovirus vectors mediate efficient gene transfer to skeletal muscle. Gene Ther. 7:1491-1498.
33. Löser, P., A. Hüser, M. Hillgenberg, D. Kümin, G. W. Both, and C. Hofmann. 2002. Advances in the development of non-human viral DNA-vectors for gene delivery. Curr. Gene Ther. 2:161-171.
34. Löser, P., D. Kümin, M. Hillgenberg, G. W. Both, and C. Hofmann. 2001. Preparation of ovine adenovirus vectors. Methods Mol. Med. 69:415-426.
35. Lucher, L. A. 1995. Abortive adenovirus infection and host range determinants. Curr. Top. Microbiol. Immunol. 199:119-152.
36. Lucher, L. A., B. Khuntirat, J. Zhao, and P. C. Angeletti. 1992. Altered expression of adenovirus 12 DNA-binding protein but not DNA polymerase during abortive infection of hamster cells. Virology 189:187-195.
37. Maizel, J. V., Jr., D. O. White, and M. D. Scharff. 1968. The polypeptides of adenovirus. I. Evidence for multiple protein components in the virion and a comparison of types 2, 7A, and 12. Virology 36:115-125.
38. Michou, A. I., H. Lehrmann, M. Saltik and M. Cotten. 1999. Mutational analysis of the avian adenovirus CELO, which provides a basis for gene delivery vectors. J. Virol. 73:1399-1410.
39. Morral, N., W. O'Neal, K. Rice, M. Leland, J. Kaplan, P. A. Piedra, H. Zhou, R. J. Parks, R. Velji, E. Aguilar-Cordova, S. Wadsworth, F. L. Graham, S. Kochanek, K. D. Carey, and A. L. Beaudet. 1999. Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons. Proc. Natl. Acad. Sci. USA 96:12816-12821.
40. Morsy, M. A., M. Gu, S. Motzel, J. Zhao, J. Lin, Q. Su, H. Allen, L. Franlin, R. J. Parks, F. L. Graham, S. Kochanek, A. J. Bett, and C. T. Caskey. 1998. An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene. Proc. Natl Acad. Sci. USA 95:7866-7871.
41. Nakabayashi, H., K. Taketa, T. Yamane, M. Miyazaki, K. Miyano, and J. Sato. 1984. Phenotypical stability of a human hepatoma cell line, HuH-7, in long-term culture with chemically defined medium. Gann 75:151-158.
42. Nichols, W. W., D. G. Murphy, V. J. Cristofalo, L. H. Toji, A. E. Greene, and S. A. Dwight. 1977. Characterization of a new human diploid cell strain, IMR-90. Science 196:60-63.
43. Nicolas, J. C., C. S. Young, F. Suarez, M. Girard, and A. J. Levine. 1983. Detection, rescue, and mapping of mutations in the adenovirus DNA binding protein gene. Proc. Natl. Acad. Sci. USA 80:1674-1677.
44. Paul, D., M. Hohne, C. Pinkert, A. Piasecki, E. Ummelmann, and R. L. Brinster. 1988. Immortalized differentiated hepatocyte lines derived from transgenic mice harboring SV40 T-antigen genes. Exp. Cell Res. 175:354-362.
45. Pye, D. 1989. Cell lines for growth of sheep viruses. Aust. Vet. J. 66:231-232.
46. Quade, K. 1979. Transformation of mammalian cells by avian myelocytomatosis virus and avian erythroblastosis virus. Virology 98:461-465.
47. Rasmussen, U. B., M. Benchaibi, V. Meyer, Y. Schlesinger, and K. Schughart. 1999. Novel human gene transfer vectors: evaluation of wild-type and recombinant animal adenoviruses in human-derived cells. Hum. Gene Ther. 10:2587-2599.
48. Schiedner, G., N. Morral, R. J. Parks, Y. Wu, S. C. Koopmans, C. Langston, F. L. Graham, A. L. Beaudet, and S. Kochanek. 1998. Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity. Nat. Genet. 18:180-183.
49. Schiedner, G., B. Schmitz, and W. Doerfler. 1994. Late transcripts of adenovirus type 12 DNA are not translated in hamster cells expressing the El region of adenovirus type 5. J. Virol. 68:5476-5482.
50. Silverman, L., and D. F. Klessig. 1989. Characterization of the translational defect to fiber synthesis in monkey cells abortively infected with human adenovirus: role of ancillary leaders. J. Virol. 63:4376-4385.
51. Silverstein, G., and W. A. Strohl. 1986. Restricted replication f adenovirus type 2 in mouse Balb/3T3 cells. Arch. Virol. 87:241-264.
52. Steinwaerder, D. S., C. A. Carlson, and A. Lieber. 2000. DNA replication of first-generation adenovirus vectors in tumor cells. Hum. Gene Ther. 11:1933-1948.
53. Venktesh, A., F. Watt, Z. Z. Xu, and G. W. Both. 1998. Ovine adenovirus (OAV287) lacks a virus-associated RNA gene. J. Gen. Virol. 79:509-516.
54. Vrati, S., D. Boyle, R. Kocherhans, and G. W. Both. 1995. Sequence of ovine adenovirus homologs for 100K hexon assembly, 33K, pVIII, and fiber genes: early region E3 is not in the expected location. Virology 209:400-408.
55. Vrati, S., D. E. Brookes, D. B. Boyle, and G. W. Both. 1996. Nucleotide sequence of ovine adenovirus tripartite leader sequence and homologues of the IVa2, DNA polymerase and terminal proteins. Gene 177:35-41.
56. Vrati, S., D. E. Brookes, P. Strike, A. Khatri, D. B. Boyle, and G. W. Both. 1996. Unique genome arrangement of an ovine adenovirus: identification of new proteins and proteinase cleavage sites. Virology 220:186-199.
57. Wickham, T. J., P. Mathias, D. A. Cheresh, and G. R. Nemerow. 1993. Integrins αvβ3 and αavβ5 promote adenovirus internalization but not virus attachment. Cell 73:309-319.
58. Xu, Z. Z., and G. W. Both. 1998. Altered tropism of an ovine adenovirus carrying the fiber protein cell binding domain of human adenovirus type 5. Virology 248:156-163.
59. Xu, Z. Z., A. Hyatt, D. B. Boyle, and G. W. Both. 1997. Construction of ovine adenovirus recombinants by gene insertion or deletion of related terminal region sequences. Virology 230:62-71.
60. Xu, Z. Z., M. Nevels, E. S. MacAvoy, L. J. Lockett, D. Curiel, T. Dobner, and G. W. Both. 2000. An ovine adenovirus vector lacks transforming ability in cells that are transformed by AD5 E1A/B sequences. Virology 270:162-172.