Literature DB >> 9717258

Interaction of vaccinia virus with the actin cytoskeleton.

M Way1.   

Abstract

Vaccinia virus infection results in large rearrangements of the host actin cytoskeleton including the formation of actin tails that are strikingly similar to those seen in Listeria, Shigella and Rickettsia infections. Using actin polymerization as the driving force the intracellular enveloped form of the vaccinia virus (IEV) is propelled on the tip of actin tails at a speed of 2.8 microns/min, both intra- and intercellularly. The similarities between the actin-based motility of the vaccinia virus, Listeria, Shigella and Rickettsia suggest that intracellular pathogens have developed a common strategy to exploit the actin cytoskeleton of the host to facilitate their intercellular spread. This review focuses on our current understanding of the interactions between the vaccinia virus and the actin cytoskeleton.

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Year:  1998        PMID: 9717258     DOI: 10.1007/BF02818616

Source DB:  PubMed          Journal:  Folia Microbiol (Praha)        ISSN: 0015-5632            Impact factor:   2.629


  60 in total

1.  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.

Authors:  R Blasco; B Moss
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

Review 2.  Actin and cell pathogenesis.

Authors:  S Higley; M Way
Journal:  Curr Opin Cell Biol       Date:  1997-02       Impact factor: 8.382

3.  Interaction of assembled progeny pox viruses with the cellular cytoskeleton.

Authors:  G Hiller; K Weber; L Schneider; C Parajsz; C Jungwirth
Journal:  Virology       Date:  1979-10-15       Impact factor: 3.616

4.  Drosophila kelch is an oligomeric ring canal actin organizer.

Authors:  D N Robinson; L Cooley
Journal:  J Cell Biol       Date:  1997-08-25       Impact factor: 10.539

5.  The tandem repeat domain in the Listeria monocytogenes ActA protein controls the rate of actin-based motility, the percentage of moving bacteria, and the localization of vasodilator-stimulated phosphoprotein and profilin.

Authors:  G A Smith; J A Theriot; D A Portnoy
Journal:  J Cell Biol       Date:  1996-11       Impact factor: 10.539

6.  Interaction of frog virus 3 with the cytomatrix. III. Role of microfilaments in virus release.

Authors:  K G Murti; M Chen; R Goorha
Journal:  Virology       Date:  1985-04-30       Impact factor: 3.616

7.  Vaccinia virus morphogenesis is interrupted when expression of the gene encoding an 11-kilodalton phosphorylated protein is prevented by the Escherichia coli lac repressor.

Authors:  Y F Zhang; B Moss
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

8.  Assembly of vaccinia virus: the second wrapping cisterna is derived from the trans Golgi network.

Authors:  M Schmelz; B Sodeik; M Ericsson; E J Wolffe; H Shida; G Hiller; G Griffiths
Journal:  J Virol       Date:  1994-01       Impact factor: 5.103

9.  One hundred base pairs of 5' flanking sequence of a vaccinia virus late gene are sufficient to temporally regulate late transcription.

Authors:  C Bertholet; R Drillien; R Wittek
Journal:  Proc Natl Acad Sci U S A       Date:  1985-04       Impact factor: 11.205

10.  Cytochalasin B inhibits the maturation of measles virus.

Authors:  K C Stallcup; C S Raine; B N Fields
Journal:  Virology       Date:  1983-01-15       Impact factor: 3.616

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  2 in total

1.  Ultrastructure of Rickettsia rickettsii actin tails and localization of cytoskeletal proteins.

Authors:  L S Van Kirk; S F Hayes; R A Heinzen
Journal:  Infect Immun       Date:  2000-08       Impact factor: 3.441

Review 2.  A meeting of good friends: when the cell biology of prokaryotes and eukaryotes meet.

Authors:  P Sebo
Journal:  Folia Microbiol (Praha)       Date:  1998       Impact factor: 2.629

  2 in total

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