Morphogenesis of a highly replicative EGFPVP22 recombinant Marek's disease virus in cell culture

Journal of Virology

Volumn 81, Issue 22, 2007, Pages 12348-12359

  Denesvre, C ^a   Blondeau, C ^a   Lemesle, M ^c   Le Vern, Y ^b   Vautherot, D ^a   Roingeard, P ^c   Vautherot, J F ^a  

^a UR1282   (France)

^b CEMAGREF   (France)

^c UNIVERSITÉ DE TOURS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ENHANCED GREEN FLUORESCENT PROTEIN; MAJOR TEGUMENT PROTEIN; UNCLASSIFIED DRUG; VIRUS PROTEIN; VIRUS PROTEIN VP22;

ARTICLE; AVIAN LYMPHOMATOSIS HERPETOVIRUS; BAC20 VIRUS; CELL SELECTION; CELL SPREADING; CELL ULTRASTRUCTURE; CYTOMETRY; EXOCYTOSIS; IMMUNOFLUORESCENCE MICROSCOPY; MAREK DISEASE VIRUS EGFPVP22; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; TRANSMISSION ELECTRON MICROSCOPY; VIRUS CAPSID; VIRUS CULTURE; VIRUS ENVELOPE; VIRUS INFECTIVITY; VIRUS MORPHOGENESIS; VIRUS MORPHOLOGY; VIRUS MUTANT; VIRUS NUCLEOCAPSID; VIRUS RECOMBINANT; VIRUS REPLICATION;

ANIMALS; CELLS, CULTURED; CHICK EMBRYO; CYTOPLASM; GREEN FLUORESCENT PROTEINS; MARDIVIRUS; MICROSCOPY, ELECTRON, TRANSMISSION; MORPHOGENESIS; RECOMBINANT FUSION PROTEINS; VIRAL PROTEINS; VIRUS REPLICATION;

GALLID HERPESVIRUS 2; MIRIDAE;

EID: 36048973358     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.01177-07     Document Type: Article

References (50)

1. Biggs, P. M. 2001. The history and biology of Marek's disease virus. Curr. Top. Microbiol. Immunol. 255:1-24.
2. Biggs, P. M., and L. N. Payne. 1967. Studies on Marek's disease. 1. Experimental transmission. J. Natl. Cancer Inst. 39:267-280.
3. Blondeau, C., N. Chbab, C. Beaumont, K. Courvoisier, N. Osterrieder, J.-F. Vautherot, and C. Denesvre. 2007. A full UL13 open reading frame in Marek's disease virus (MDV) is dispensable for tumor formation and feather follicle tropism and cannot restore horizontal virus transmission of rRB-1B in vivo. Vet. Res. (Paris) 38:419-433.
4. Bublot, M., and J. M. Sharma. 2004. Vaccination against Marek's disease, p. 168-185. In F. Davison and V. K. Nair (ed.), Marek's disease. An evolving problem. Elsevier Academic Press, Compton, United Kingdom.
5. Calnek, B. W., H. K. Adldinger, and D. E. Kahn. 1970. Feather follicle epithelium: a source of enveloped and infectious cell-free herpesvirus from Marek's disease. Avian Dis. 14:219-233.
6. Campadelli-Fiume, G., F. Farabegoli, S. Di Gaeta, and B. Roizman. 1991. Origin of unenveloped capsids in the cytoplasm of cells infected with herpes simplex virus 1. J. Virol. 65:1589-1595.
7. Campadelli-Fiume, G., and T. Gianni. 2006. HSV glycoproteins and their roles in virus entry and egress, p. 135-156. In R. M. Sandri-Goldin (ed.), Alpha herpesviruses. Caister Academic Press, Norfolk, United Kingdom.
8. Campadelli-Fiume, G., and B. Roizman. 2006. The egress of herpesviruses from cells: the unanswered questions. J. Virol. 80:6716-6717. (Letter.)
9. Cho, K.-O., K. Ohashi, and M. Onuma. 1999. Electron microscopic and immunohistochemical localization of Marek's disease (MD) herpesvirus particles in MD skin lymphomas. Vet. Pathol. 36:314-320.
10. Churchill, A. E., and P. M. Biggs. 1967. Agent of Marek's disease in tissue culture. Nature 215:528-530.
11. Cilloniz, C., W. Jackson, C. Grose, D. Czechowski, J. Hay, and W. T. Ruyechan. 2007. The varicella-zoster virus (VZV) ORF9 protein interacts with the IE62 major VZV transactivator. J. Virol. 81:761-774.
12. Coudert, F., and L. Cauchy. 1975. Virus replication and cell modifications in organ cultures of tumor tissue from chickens with Marek's disease. J. Natl. Cancer Inst. 55:47-51.
13. del Rio, T., T. H. Ch'ng, E. A. Flood, S. P. Gross, and L. W. Enquist. 2005. Heterogeneity of a fluorescent tegument component in single Pseudorabies virus virions and enveloped axonal assemblies. J. Virol. 79:3903-3919.
14. del Rio, T., H. C. Werner, and L. W. Enquist. 2002. The Pseudorabies virus VP22 homologue (UL49) is dispensable for virus growth in vitro and has no effect on virulence and neuronal spread in rodents. J. Virol. 76:774-782.
15. Dorange, F., S. El Mehdaoui, C. Pichon, P. Coursaget, and J. F. Vautherot. 2000. Marek's disease virus (MDV) homologues of herpes simplex virus type 1 UL49 (VP22) and UL48 (VP16) genes: high-level expression and characterization of MDV-1 VP22 and VP16. J. Gen. Virol. 81:2219-2230.
16. Dorange, F., B. K. Tischer, J. F. Vautherot, and N. Osterrieder. 2002. Characterization of Marek's disease virus serotype 1 (MDV-1) deletion mutants that lack UL46 to UL49 genes: MDV-1 UL49, encoding VP22, is indispensable for virus growth. J. Virol. 76:1959-1970.
17. Duffy, C., J. H. LaVail, A. N. Tauscher, E. G. Wills, J. A. Blaho, and J. D. Baines. 2006. Characterization of a UL49-null mutant: VP22 of herpes simplex virus type 1 facilitates viral spread in cultured cells and the mouse cornea. J. Virol. 80:8664-8675.
18. Elliott, G., W. Hafezi, A. Whiteley, and E. Bernard. 2005. Deletion of the herpes simplex virus VP22-encoding gene (UL49) alters the expression, localization, and virion incorporation of ICPO. J. Virol. 79:9735-9745.
19. Elliott, G., and P. O'Hare. 1999. Live-cell analysis of a green fluorescent protein-tagged herpes simplex virus infection. J. Virol. 73:4110-4119.
20. Enquist, L. W., P. J. Husak, B. W. Banfield, and G. A. Smith. 1998. Infection and spread of alphaherpesviruses in the nervous system. Adv. Virus Res. 51:237-347.
21. Fuchs, W., H. Granzow, and T. C. Mettenleiter. 2003. A Pseudorabies virus recombinant simultaneously lacking the major tegument proteins encoded by the UL46, UL47, UL48, and UL49 genes is viable in cultured cells. J. Virol. 77:12891-12900.
22. Granzow, H., B. G. Klupp, W. Fuchs, J. Veits, N. Osterrieder, and T. C. Mettenleiter. 2001. Egress of alphaherpesviruses: comparative ultrastructural study. J. Virol. 75:3675-3684.
23. Granzow, H., B. G. Klupp, and T. C. Mettenleiter. 2004. The Pseudorabies virus US3 protein is a component of primary and of mature virions. J. Virol. 78:1314-1323.
24. Granzow, H., F. Weiland, A. Jöns, B. G. Klupp, A. Karger, and T. C. Mettenleiter. 1997. Ultrastructural analysis of the replication cycle of Pseudorabies virus in cell culture: a reassessment. J. Virol. 71:2072-2082.
25. Harson, R., and C. Grose. 1995. Egress of varicella-zoster virus from the melanoma cell: a tropism for the melanocyte. J. Virol. 69:4994-5010.
26. Igakura, T., J. C. Stinchcombe, P. K. Goon, G. P. Taylor, J. N. Weber, G. M. Griffiths, Y. Tanaka, M. Osame, and C. R. Bangham. 2003. Spread of HTLV-I between lymphocytes by virus-induced polarization of the cytoskeleton. Science 299:1713-1716.
27. Johnson, D. C., and M. T. Huber. 2002. Directed egress of animal viruses promotes cell-to-cell spread. J. Virol. 76:1-8.
28. Johnson, E. A., C. N. Burke, T. N. Fredrickson, and R. A. DiCapua. 1975. Morphogenesis of Marek's disease virus in feather follicle epithelium. J. Natl. Cancer Inst. 55:89-99.
29. Kaether, C., and H. H. Gerdes. 1995. Visualization of protein transport along the secretory pathway using green fluorescent protein. FEBS Lett. 369:267-271.
30. Kingston, E. 2001. Introduction of DNA into mammalian cells, p. 9.0.1-9.1.11. In F. M. Ausubel, R. Brent, R. E. Kingston, D. D. Moore, J. G. Seidman, J. A. Smith, and K. Struhl (ed.), Current protocols in molecular biology, vol. 1. John Wiley & Sons, Inc., Boston, MA.
31. Leuzinger, H., U. Ziegler, E. M. Schraner, C. Fraefel, D. L. Glauser, I. Heid, M. Ackermann, M. Mueller, and P. Wild. 2005. Herpes simplex virus 1 envelopment follows two diverse pathways. J. Virol. 79:13047-13059.
32. Liang, X., B. Chow, Y. Li, C. Raggo, D. Yoo, S. Attah-Poku, and L. A. Babiuk. 1995. Characterization of bovine herpesvirus 1 UL49 homolog gene and product: bovine herpesvirus 1 UL49 homolog is dispensable for virus growth. J. Virol. 69:3863-3867.
33. Matlin, K. S., and K. Simons. 1983. Reduced temperature prevents transfer of a membrane glycoprotein to the cell surface but does not prevent terminal glycosylation. Cell 34:233-243.
34. Mettenleiter, T. C. 2004. Budding events in herpesvirus morphogenesis. Virus Res. 106:167-180.
35. Mettenleiter, T. C. 2002. Herpesvirus assembly and egress. J. Virol. 76:1537-1547.
36. Mettenleiter, T. C., and T. Minson. 2006. Egress of alphaherpesviruses. J. Virol. 80:1610-1611. (Letter.)
37. Mettenleiter, T. C., and T. Minson. 2006. The egress of herpesviruses from cells: the unanswered questions. J. Virol. 80:6718-6719. (Authors' reply to letter.)
38. Nazerian, K., and B. R. Burmester. 1968. Electron microscopy of a herpes virus associated with the agent of Marek's disease in cell culture. Cancer Res. 28:2454-2462.
39. Nazerian, K., J. J. Solomon, R. L. Witter, and B. R. Burmester. 1968. Studies on the etiology of Marek's disease. 11. Finding of a herpesvirus in cell culture. Proc. Soc. Exp. Biol. Med. 127:177-182.
40. Nazerian, K., and R. L. Witter. 1975. Properties of a chicken lymphoblastoid cell line from Marek's disease tumor. J. Natl. Cancer Inst. 54:453-458.
41. Parcells, M. S., A. S. Anderson, J. L. Cantello, and R. W. Morgan. 1994. Characterization of Marek's disease virus insertion and deletion mutants that lack US1 (ICP22 homolog), US10, and/or US2 and neighboring short-component open reading frames. J. Virol. 68:8239-8253.
42. Patient, R., C. Hourioux, P. Y. Sizaret, S. Trassard, C. Sureau, and P. Roingeard. 2007. Hepatitis B virus subviral envelope particle morphogenesis and intracellular trafficking. J. Virol. 81:3842-3851.
43. S3.5 protein kinases of herpes simplex virus 1 differ with respect to their functions in blocking apoptosis and in virion maturation and egress. J. Virol. 80:3752-3764.
44. Roizman, B., and A. E. Sears. 1996. Herpes simplex viruses and their replication, p. 1043-1107. In B. N. Fields, D. M. Knipe, and P. M. Howley (ed.), Fundamental virology, third ed. Lippincott-Raven Publishers, Philadelphia, PA.
45. Schumacher, D., B. K. Tischer, W. Fuchs, and N. Osterrieder. 2000. Reconstitution of Marek's disease virus serotype 1 (MDV-1) from DNA cloned as a bacterial artificial chromosome and characterization of a glycoprotein B-negative MDV-1 mutant. J. Virol. 74:11088-11098.
46. S3 orthologue of Marek's disease virus is required for efficient de-envelopment of perinuclear virions and involved in actin stress fiber breakdown. J. Virol. 79:3987-3997.
47. Sinzger, C., J. Knapp, K. Schmidt, M. Kahl, and G. Jahn. 1999. A simple and rapid method for preparation of viral DNA from cell associated cytomegalovirus. J. Virol. Methods 81:115-122.
48. Wild, P. 2006. Egress of alphaherpesviruses. J. Virol. 80:1611-1612. (Author's reply to letter.)
49. Wild, P. 2006. The egress of herpesviruses from cells: the unanswered questions. J. Virol. 80:6717-6718. (Author's reply to letter.)
50. Wild, P., M. Engels, C. Senn, K. Tobler, U. Ziegler, E. M. Schraner, E. Loepfe, M. Ackermann, M. Mueller, and P. Walther. 2005. Impairment of nuclear pores in bovine herpesvirus 1-infected MDBK cells. J. Virol. 79:1071-1083.