The longest micron; transporting poxviruses out of the cell

Cellular Microbiology

Volumn 7, Issue 11, 2005, Pages 1531-1538

  Ward, Brian M ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

KINESIN;

CELL INTERACTION; CELL MATURATION; CELL TRANSPORT; CONTROLLED STUDY; INTRACELLULAR MEMBRANE; MICRONUCLEUS; MICROTUBULE; MORPHOGENESIS; NONHUMAN; POXVIRUS; PRIORITY JOURNAL; PROGENY; SHORT SURVEY; VIRION; VIRUS INFECTION;

HUMANS; KINESIN; MICROTUBULES; ORTHOPOXVIRUS; VIRION;

POXVIRIDAE;

EID: 27244438010     PISSN: 14625814     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1462-5822.2005.00614.x     Document Type: Short Survey

References (66)

1. Alberts, B. (2002) Molecular Biology of the Cell. New York: Garland Science.
2. Blasco, R., Sisler, J.R., and Moss, B. (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: 3319-3325.
3. Cudmore, S., Cossart, P., Griffiths, G., and Way, M. (1995) Actin-based motility of vaccinia virus. Nature 378: 636-638.
4. Duncan, S.A., and Smith, G.L. (1992) Identification and characterization of an extracellular envelope glycoprotein affecting vaccinia virus egress. J Virol 66: 1610-1621.
5. van Eijl, H., Hollinshead, M., and Smith, G.L. (2000) The vaccinia virus A36R protein is a type Ib membrane protein present on intracellular but not extracellular enveloped virus particles. Virology 271: 26-36.
6. van Eijl, H., Hollinshead, M., Rodger, G., Zhang, W.H., and Smith, G.L. (2002) The vaccinia virus F12L protein is associated with intracellular enveloped virus particles and is required for their egress to the cell surface. J Gen Virol 83: 195-207.
7. Engelstad, M., and Smith, G.L. (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.
8. Engelstad, M., Howard, S.T., and Smith, G.L. (1992) A constitutively expressed vaccinia gene encodes a 42-kDa glycoprotein related to complement control factors that forms part of the extracellular virus envelope. Virology 188: 801-810.
9. Frischknecht, F., Cudmore, S., Moreau, V., Reckmann, I., Rottger, S., and Way, M. (1999a) Tyrosine phosphorylation is required for actin-based motility of vaccinia but not Listeria or Shigella. Curr Biol 9: 89-92.
10. Frischknecht, F., Moreau, V., Rottger, S., Gonfloni, S., Reckmann, I., Superti-Furga, G., and Way, M. (1999b) Actin-based motility of vaccinia virus mimics receptor tyrosine kinase signalling. Nature 401: 926-929.
11. Geada, M.M., Galindo, I., Lorenzo, M.M., Perdiguero, B., and Blasco, R. (2001) Movements of vaccinia virus intracellular enveloped virions with GFP tagged to the F13L envelope protein. J Gen Virol 82: 2747-2760.
12. Grosenbach, D.W., Ulaeto, D.O., and Hruby, D.E. (1997) Palmitylation of the vaccinia virus 37-kDa major envelope antigen. Identification of a conserved acceptor motif and biological relevance. J Biol Chem 272: 1956-1964.
13. Hiller, G., and Weber, K. (1985) Golgi-derived membranes that contain an acylated viral polypeptide are used for vaccinia virus envelopment. J Virol 55: 651-659.
14. Hiller, G., Weber, K., Schneider, L., Parajsz, C., and Jungwirth, C. (1979) Interaction of assembled progeny pox viruses with the cellular cytoskeleton. Virology 98: 142-153.
15. Hiller, G., Jungwirth, C., and Weber, K. (1981) Fluorescence microscopical analysis of the life cycle of vaccinia virus in chick embryo fibroblasts. Virus-cytoskeleton interactions. Exp Cell Res 132: 81-87.
16. Hirokawa, N., and Takemura, R. (2005) Molecular motors and mechanisms of directional transport in neurons. Nat Rev Neurosci 6: 201-214.
17. Hirokawa, N., Pfister, K.K., Yorifuji, H., Wagner, M.C., Brady, S.T., and Bloom, G.S. (1989) Submolecular domains of bovine brain kinesin identified by electron microscopy and monoclonal antibody decoration. Cell 56: 867-878.
18. Hirt, P., Hiller, G., and Wittek, R. (1986) Localization and fine structure of a vaccinia virus gene encoding an envelope antigen. J Virol 58: 757-764.
19. Hisanaga, S., Murofushi, H., Okuhara, K., Sato, R., Masuda, Y., Sakai, H., and Hirokawa, N. (1989) The molecular structure of adrenal medulla kinesin. Cell Motil Cytoskeleton 12: 264-272.
20. Hollinshead, M., Rodger, G., Van Eijl, H., Law, M., Hollinshead, R., Vaux, D.J., and Smith, G.L. (2001) Vaccinia virus utilizes microtubules for movement to the cell surface. J Cell Biol 154: 389-402.
21. Husain, M., and Moss, B. (2002) Similarities in the induction of post-Golgi vesicles by the vaccinia virus F13L protein and phospholipase D. J Virol 76: 7777-7789.
22. Ichihashi, Y., Matsumoto, S., and Dales, S. (1971) Biogenesis of poxviruses: role of A-type inclusions and host cell membranes in virus dissemination. Virology 46: 507-532.
23. Isaacs, S.N., Wolffe, E.J., Payne, L.G., and Moss, B. (1992) Characterization of a vaccinia virus-encoded 42-kilodalton class I membrane glycoprotein component of the extracellular virus envelope. J Virol 66: 7217-7224.
24. Koonin, E.V. (1996) A duplicated catalytic motif in a new superfamily of phosphohydrolases and phospholipid synthases that includes poxvirus envelope proteins. Trends Biochem Sci 21: 242-243.
25. McIntosh, A.A., and Smith, G.L. (1996) Vaccinia virus glycoprotein A34R is required for infectivity of extracellular enveloped virus. J Virol 70: 272-281.
26. Mallik, R., and Gross, S.P. (2004) Molecular motors: strategies to get along. Curr Biol 14: R971-R982.
27. Miki, H., Setou, M., Kaneshiro, K., and Hirokawa, N. (2001) All kinesin superfamily protein, KIF, genes in mouse and human. Proc Natl Acad Sci USA 98: 7004-7011.
28. Moreau, V., Frischknecht, F., Reckmann, I., Vincentelli, R., Rabut, G., Stewart, D., and Way, M. (2000) A complex of N-WASP and WIP integrates signalling cascades that lead to actin polymerization. Nat Cell Biol 2: 441-448.
29. Morgan, C. (1976) Vaccinia virus reexamined: development and release. Virology 73: 43-58.
30. Moss, B. (2001) Poxviridae: the viruses and their replication. In Fields Virology. Fields, B.N., Knipe, D.M., and Howley, P.M. (eds). Philadelphia, PA: Lippincott-Raven Publishers, pp. 2849-2883.
31. Newsome, T.P., Scaplehorn, N., and Way, M. (2004) SRC mediates a switch from microtubule- to actin-based motility of vaccinia virus. Science 306: 124-129.
32. Parkinson, J.E., and Smith, G.L. (1994) Vaccinia virus gene A36R encodes a Mr 43-50 K protein on the surface of extacellular enveloped virus. Virology 204: 376-390.
33. Pfister, K.K. (2005) Dynein cargo gets its groove back. Structure (Camb) 13: 172-173.
34. Ploubidou, A., Moreau, V., Ashman, K., Reckmann, I., Gonzalez, C., and Way, M. (2000) Vaccinia virus infection disrupts microtubule organization and centrosome function. EMBO J 19: 3932-3944.
35. Rietdorf, J., Ploubidou, A., Reckmann, I., Holmstrom, A., Frischknecht, F., Zettl, M., et al. (2001) Kinesin-dependent movement on microtubules precedes actin-based motility of vaccinia virus. Nat Cell Biol 3: 992-1000.
36. Roper, R.L., and Moss, B. (1999) Envelope formation is blocked by mutation of a sequence related to the HKD phospholipid metabolism motif in the vaccinia virus F13L protein. J Virol 73: 1108-1117.
37. Roper, R.L., Payne, L.G., and Moss, B. (1996) Extracellular vaccinia virus envelope glycoprotein encoded by the A33R gene. J Virol 70: 3753-3762.
38. Roper, R.L., Wolffe, E.J., Weisberg, A., and Moss, B. (1998) The envelope protein encoded by the A33R gene is required for formation of actin-containing microvilli and efficient cell-to-cell spread of vaccinia virus. J Virol 72: 4192-4204.
39. Rottger, S., Frischknecht, F., Reckmann, I., Smith, G.L., and Way, M. (1999) Interactions between vaccinia virus IEV membrane proteins and their roles in IEV assembly and actin tail formation. J Virol 73: 2863-2875.
40. Sanderson, C.M., Frischknecht, F., Way, M., Hollinshead, M., and Smith, G.L. (1998) Roles of vaccinia virus EEV-specific proteins in intracellular actin tail formation and low pH-induced cell-cell fusion. J Gen Virol 79: 1415-1425.
41. Sanderson, C.M., Hollinshead, M., and Smith, G.L. (2000) The vaccinia virus A27L protein is needed for the microtubule-dependent transport of intracellular mature virus particles. J Gen Virol 81: 47-58.
42. Scaplehorn, N., Holmstrom, A., Moreau, V., Frischknecht, F., Reckmann, I., and Way, M. (2002) Grb2 and Nck act cooperatively to promote actin-based motility of vaccinia virus. Curr Biol 12: 740-745.
43. Schliwa, M., and Woehlke, G. (2001) Molecular motors. Switching on kinesin. Nature 411: 424-425.
44. Schliwa, M., and Woehlke, G. (2003) Molecular motors. Nature 422: 759-765.
45. Schmelz, M., Sodeik, B., Ericsson, M., Wolffe, E.J., Shida, H., Hiller, G., and Griffiths, G. (1994) Assembly of vaccinia virus: the second wrapping cisterna is derived from the trans Golgi network. J Virol 68: 130-147.
46. Shida, H. (1986) Nucleotide sequence of the vaccinia virus hemagglutinin gene. Virology 150: 451-462.
47. Smith, G.L., and Law, M. (2004) The exit of vaccinia virus from infected cells. Virus Res 106: 189-197.
48. Sodeik, B. (2000) Mechanisms of viral transport in the cytoplasm. Trends Microbiol 8: 465-472.
49. Stokes, G.V. (1976) High-voltage electron microscope study of the release of vaccinia virus from whole cells. J Virol 18: 636-643.
50. Sung, T.C., Roper, R.L., Zhang, Y., Rudge, S.A., Temel, R., Hammond, S.M., et al. (1997) Mutagenesis of phospholipase D defines a superfamily including a trans-Golgi viral protein required for poxvirus pathogenicity. EMBO J 16: 4519-4530.
51. Tooze, J., Hollinshead, M., Reis, B., Radsak, K., and Kern, H. (1993) Progeny vaccinia and human cytomegalovirus particles utilize early endosomal cisternae for their envelopes. Eur J Cell Biol 60: 163-178.
52. Vale, R.D. (2003) The molecular motor toolbox for intracellular transport. Cell 112: 467-480.
53. Vazquez, M.I., Rivas, G., Cregut, D., Serrano, L., and Esteban, M. (1998) The vaccinia virus 14-kilodalton (A27L) fusion protein forms a triple coiled-coil structure and interacts with the 21-kilodalton (A17L) virus membrane protein through a C-terminal alpha-helix. J Virol 72: 10126-10137.
54. Verhey, K.J., Lizotte, D.L., Abramson, T., Barenboim, L., Schnapp, B.J., and Rapoport, T.A. (1998) Light chain-dependent regulation of kinesin's interaction with microtubules. J Cell Biol 143: 1053-1066.
55. Walker, R.A., Salmon, E.D., and Endow, S.A. (1990) The Drosophila claret segregation protein is a minus-end directed motor molecule. Nature 347: 780-782.
56. Ward, B.M. (2005) Visualization and characterization of the intracellular movement of vaccinia virus intracellular mature virions. J Virol 79: 4755-4763.
57. Ward, B.M., and Moss, B. (2001a) Vaccinia virus intracellular movement is associated with microtubules and independent of actin tails. J Virol 75: 11651-11663.
58. Ward, B.M., and Moss, B. (2001b) Visualization of intracellular movement of vaccinia virus virions containing a green fluorescent protein-B5R membrane protein chimera. J Virol 75: 4802-4813.
59. Ward, B.M., and Moss, B. (2004) Vaccinia virus A36R membrane protein provides a direct link between intracellular enveloped virions and the microtubule motor kinesin. J Virol 78: 2486-2493.
60. Ward, B.M., Weisberg, A.S., and Moss, B. (2003) Mapping and functional analysis of interaction sites within the cytoplasmic domains of the vaccinia virus A33R and A36R envelope proteins. J Virol 77: 4113-4126.
61. Wolffe, E.J., Isaacs, S.N., and Moss, B. (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. (Published erratum: J Virol 1993, 67: 5709-5711).
62. Wolffe, E.J., Katz, E., Weisberg, A., and Moss, B. (1997) The A34R glycoprotein gene is required for induction of specialized actin-containing microvilli and efficient cell-to-cell transmission of vaccinia virus. J Virol 71: 3904-3915.
63. Wolffe, E.J., Weisberg, A.S., and Moss, B. (1998) Role for the vaccinia virus A36R outer envelope protein in the formation of virus-tipped actin-containing microvilli and cell-to-cell virus spread. Virology 244: 20-26.
64. Wolffe, E.J., Weisberg, A.S., and Moss, B. (2001) The vaccinia virus A33R protein provides a chaperone function for viral membrane localization and tyrosine phosphorylation of the A36R protein. J Virol 75: 303-310.
65. Zettl, M., and Way, M. (2002) The WH1 and EVH1 domains of WASP and Ena/VASP family members bind distinct sequence motifs. Curr Biol 12: 1617-1622.
66. Zhang, W.H., Wilcock, D., and Smith, G.L. (2000) Vaccinia virus F12L protein is required for actin tail formation, normal plaque size, and virulence. J Virol 74: 11654-11662.