Vaccinia virus 15-kilodalton (A14L) protein is essential for assembly and attachment of viral crescents to virosomes

Journal of Virology

Volumn 72, Issue 2, 1998, Pages 1287-1296

  Rodríguez, Juan Ramón ^a   Risco, Cristina ^a   Carrascosa, José L ^a   Esteban, Mariano ^a   Rodríguez, Dolores ^a  

^a CENTRO NACIONAL DE BIOTECNOLOGÍA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT;

ARTICLE; BIOGENESIS; CONTROLLED STUDY; ESCHERICHIA COLI; HELA CELL; HUMAN; HUMAN CELL; NONHUMAN; PRIORITY JOURNAL; VACCINIA VIRUS; VIRUS ASSEMBLY; VIRUS GENE; VIRUS MUTANT; VIRUS RECOMBINANT;

EID: 2642646234     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/jvi.72.2.1287-1296.1998     Document Type: Article

References (52)

1. Blasco, R., and B. Moss. 1991. Extracellular vaccinia virus formation and cell-to-cell virus transmission are prevented by deletion of the gene encoding the 37,000-dalton outer envelope protein. J. Virol. 65:5910-5920.
2. Blasco, R., J. R. Sisler, and B. Moss. 1993. Dissociation of progeny vaccinia virus from the cell membrane is regulated by a viral envelope glycoprotein: effect of a point mutation in the lectin homology domain of the A34R gene. J. Virol. 67:3319-3125.
3. Cudmore, S., R. Blasco, R. Vincentelli, M. Esteban, B. Sodeik, G. Griffiths, and J. Krijnse Locker. 1996. A vaccinia virus core protein, p39, is membrane associated. J. Virol. 70:6909-6921.
4. Dales, S., and L. Siminovitch. 1961. The development of vaccinia virus in Earles L strain cells as examined by electron microscopy. J. Biophys. Biochem. Cytol. 10:475-503.
5. Dales, S., and B. G. T. Pogo. 1981. Biology of poxviruses. Virology monographs, vol. 18. Springer-Verlag, New York, N.Y.
6. Demkowicz, W. E., J. S. Maa, and M. Esteban. 1992. Identification and characterization of vaccinia virus genes encoding proteins that are highly antigenic in animals and are immunodominant in vaccinated humans. J. Virol. 66:386-398.
7. Duncan, S. A., and G. L. Smith. 1992. Identification and characterization of an extracellular envelope glycoprotein affecting vaccinia virus egress. J. Virol. 66:1610-1621.
8. Engelstad, M., and G. L. Smith. 1993. The vaccinia virus 42-KDa envelope protein is required for the envelopment and egress of extracellular virus and for virus virulence. Virology 194:627-637.
9. Franke, C. A., E. M. Wilson, and D. E. Hruby. 1990. Use of a cell-free system to identify the vaccinia virus L1R gene product as the major late myristylated virion protein M25. J. Virol. 64:5988-5996.
10. Fuerst, J. R., M. P. Fernández, and B. Moss. 1989. Transfer of the inducible lac repressor/operator system from Escherichia coli to a vaccinia virus expression vector. Proc. Natl. Acad. Sci. USA 86:2549-2553.
11. Grimley, P. M., E. N. Rosemblum, S. J. Mims, and B. Moss. 1970. Interruption by rifampicin of an early stage in vaccinia virus morphogenesis: accumulation of membranes which are precursors of virus envelopes. J. Virol. 6:519-533.
12. Hiller, G., and K. Weber. 1985. Golgi-derived membranes that contain an acylated viral polypeptide are used for vaccinia virus envelopment. J. Virol. 55:651-659.
13. Ichihashi, Y., S. Matsumoto, and S. Dales. 1971. Biogenesis of poxviruses: role of A-type inclusions and host cell membranes in virus dissemination. Virology 46:507-532.
14. Krijnse-Locker, J., S. Schleich, D. Rodríguez, B. Goud, E. J. Snijder, and G. Griffiths. 1996. The role of a 21kDa viral membrane protein in the assembly of vaccinia virus from the intermediate compartment. J. Biol. Chem. 271: 14950-14958.
15. Liu, K., R. Rollins, and P. Traktman. Submitted for publication.
16. Maa, J-S., J. F. Rodríguez, and M. Esteban. 1990. Structural and functional characterization of a cell surface binding protein of vaccinia virus. J. Biol. Chem. 265:1569-1577.
17. McIntosh, A. A., and G. L. Smith. 1996. Vaccinia virus glycoprotein A34R is required for infectivity of extracellular enveloped virus. J. Virol. 70:272-281.
18. McNulty-Kowalczyk, A., and E. Paoletti. 1993. Mutations in ORF D13L and other genetic loci alter the rifampicin phenotype of vaccinia virus. Virology 194:638-646.
19. Moss, B., and E. N. Rosenblum. 1973. Protein cleavage and poxvirus morphogenesis: tryptic peptide analysis of core precursors accumulated by blocking assembly with rifampicin. J. Mol. Biol. 81:267-269.
20. Moss, B. 1990. Poxviridae and their replication, p. 2079-2111. In B. N. Fields and D. M. Knipe (ed.), Virology, 2nd ed. Raven Press, New York, N.Y.
21. Nagayama, A., B. G. T. Pogo, and S. Dales. 1970. Biogenesis of vaccinia virus: separation of early stages from maturation by means of rifampicin. Virology 4:1039-1051.
22. Niles, E. G., and J. Seto. 1988. Vaccinia virus gene D8 encodes a virion transmembrane protein. J. Virol. 62:3772-3778.
23. Parkinson, J. E., and G. L. Smith. 1994. Vaccinia virus gene A36R encodes a Mr 43-50 K protein on the surface of extracellular enveloped virus. Virology 204:376-390.
24. Payne, L. G. 1978. Polypeptide composition of extracellular enveloped vaccinia virus. J. Virol. 27:28-37.
25. Payne, L. G. 1992. Characterization of vaccinia virus glycoproteins by monoclonal antibody precipitation. Virology 187:251-260.
26. Ravanello, M. P., and D. Hruby. 1994. Characterization of the vaccinia virus L1R myristyl protein as a component of the intracellular virion envelope. J. Gen. Virol. 75:1479-1483.
27. Ravanello, M. P., and D. Hruby. 1994. Conditional lethal expression of the vaccinia virus L1R myristylated protein reveals a role in virion assembly. J. Virol. 68:6401-6410.
28. Rodríguez, D., J. R. Rodríguez, and M. Estcban. 1992. Insertional inactivation of the vaccinia virus 32-kDa gene is associated with attenuation in mice and reduction of viral gene expression in polarized epithelial cells. J. Virol. 66:183-189.
29. Rodríguez, D., J. R. Rodríguez, and M. Esteban. 1993. The vaccinia virus 14-kilodalton fusion protein forms a stable complex with the processed protein encoded by the vaccinia virus A17L gene. J. Virol. 67:3435-3440.
30. Rodriguez, D., M. Esteban, and J. R. Rodriguez. 1995. Vaccinia virus A17L gene product is essential for an early step in virion morphogenesis. J. Virol. 69:4640-4648.
31. Rodríguez, D., C. Risco, J. R. Rodríguez, J. L. Carrascosa, and M. Esteban. 1996. Inducible expression of vaccinia virus A17L gene provides a synchronized system to follow sorting of viral proteins during morphogenesis. J. Virol. 70:7641-7653.
32. Rodríguez, J. F., R. Janezko, and M. Esteban. 1985. Isolation and characterization of neutralizing monoclonal antibodies to vaccinia virus. J. Virol. 56:482-488.
33. Rodríguez, J. F., and M. Esteban. 1987. Mapping and nucleotide sequence of the vaccinia virus gene that encodes a 14-kilodalton fusion protein. J. Virol. 61:3550-3554.
34. Rodríguez, J. F., and G. L. Smith. 1990. Inducible gene expression from vaccinia virus vectors. Virology 177:239-250.
35. Rodríguez, J. F., and G. L. Smith. 1990. IPTG-dependent vaccinia virus: identification of a virus protein enabling virion envelopment by Golgi membrane and egress. Nucleic Acids Res. 18:5347-5351.
36. Rodríguez, J. R., C. Risco, J. L. Carrascosa, M. Esteban, and D. Rodríguez. 1997. Characterization of early stages in vaccinia virus membrane biogenesis: implication of the 21-kDa and a newly identified 15-kDa envelope protein. J. Virol. 71:1821-1833.
37. Salmons, T., A. Kuhn, S. Schleich, J. R. Rodríguez, D. Rodríguez, M. Esteban, G. Griffiths, and J. Krijnse Locker. 1997. Vaccinia virus membrane proteins P8 and P16 are cotranslationally inserted into the rough endoplasmic reticulum and retained in the intermediate compartment. J. Virol. 71: 7404-7420.
38. Schmelz, M., B. Sodeik, M. Ericsson, E. J. Wolffe, H. Shida, G. Hiller, and G. Griffiths. 1994. Assembly of vaccinia virus: the second wrapping cisterna is derived from the trans-Golgi network. J. Virol. 68:130-147.
39. r protein confers resistance to an inhibitor of virus envelopment and release. J. Virol. 65:3435-3442.
40. Sodeik, B., R. W. Doms, M. Ericsson, G. Hiller, C. E. Machamer, W. van't Hof, G. van Meer, B. Moss, and G. Griffiths. 1993. Assembly of vaccinia virus: role of the intermediate compartment between the endoplasmic reticulum and the Golgi stacks. J. Cell Biol. 121:521-541.
41. Sodeik, B., G. Griffiths, M. Ericsson, B. Moss, and R. W. Doms. 1994. Assembly of vaccinia virus: effects of rifampin on the intracellular distribution of viral protein p65. J. Virol. 68:1103-1114.
42. Stern, W., and S. Dales. 1974. Biogenesis of vaccinia: concerning the origin of the envelope phospholipids. Virology 62:293-306.
43. Takahashi, T., M. Oie, and Y. Ichihashi. 1994. N-terminal amino acid sequences of vaccinia virus structural proteins. Virology 202:844-852.
44. Tartaglia, J., and E. Paoletti. 1985. Physical mapping and DNA sequence analysis of the rifampin resistance locus in vaccinia virus. Virology 147:394-404.
45. Traktman, P., A. Caligiuri, S. A. Jesty, and U. Sankar. 1995. Temperature-sensitive mutants with lesions in the vaccinia virus F10 kinase undergo arrest at the earliest stage of virion morphogenesis. J. Virol. 69:6581-6587.
46. VanSlyke, J. K., P. Lee, E. M. Wilson, and D. E. Hruby. 1993. Isolation and analysis of vaccinia virus previrions. Virus Genes 7:311-324.
47. Wang, S., and S. Shuman. 1995. Vaccinia virus morphogenesis is blocked by temperature-sensitive mutations in the F10 gene, which encodes protein kinase 2. J. Virol. 69:6376-6388.
48. Wilcock, D., and G. L. Smith. 1994. Vaccinia virus core protein VP8 is required for virus infectivity, but not for core protein processing or for INV and EEV formation. Virology 202:294-304.
49. Wolffe, E. J., S. N. Isaacs, and B. Moss. 1993. Deletion of the vaccinia virus B5R gene encoding a 42-kilodalton membrane glycoprotein inhibits extracellular virus envelope formation and dissemination. J. Virol. 67:4732-4741.
50. Wolffe, E. J., D. M. Moore, P. J. Peters, and B. Moss. 1996. Vaccinia virus A17L open reading frame encodes an essential component of nascent viral membranes that is required to initiate morphogenesis. J. Virol. 70:2797-2808.
51. Zhang, Y., and B. Moss. 1991. Vaccinia virus morphogenesis is interrupted when expression of the gene encoding an 11-kilodalton phosphorylated protein is prevented by the Escherichia coli lac repressor. J. Virol. 65:6101-6110.
52. Zhang, Y., and B. Moss. 1992. Immature viral envelope formation is interrupted at the same stage by lac operator-mediated repression of the vaccinia virus D13L gene and by the drug rifampicin. Virology 187:643-653.