The formation and function of extracellular enveloped vaccinia virus
- PMID: 12466468
- DOI: 10.1099/0022-1317-83-12-2915
The formation and function of extracellular enveloped vaccinia virus
Abstract
Vaccinia virus produces four different types of virion from each infected cell called intracellular mature virus (IMV), intracellular enveloped virus (IEV), cell-associated enveloped virus (CEV) and extracellular enveloped virus (EEV). These virions have different abundance, structure, location and roles in the virus life-cycle. Here, the formation and function of these virions are considered with emphasis on the EEV form and its precursors, IEV and CEV. IMV is the most abundant form of virus and is retained in cells until lysis; it is a robust, stable virion and is well suited to transmit infection between hosts. IEV is formed by wrapping of IMV with intracellular membranes, and is an intermediate between IMV and CEV/EEV that enables efficient virus dissemination to the cell surface on microtubules. CEV induces the formation of actin tails that drive CEV particles away from the cell and is important for cell-to-cell spread. Lastly, EEV mediates the long-range dissemination of virus in cell culture and, probably, in vivo. Seven virus-encoded proteins have been identified that are components of IEV, and five of them are present in CEV or EEV. The roles of these proteins in virus morphogenesis and dissemination, and as targets for neutralizing antibody are reviewed. The production of several different virus particles in the VV replication cycle represents a coordinated strategy to exploit cell biology to promote virus spread and to aid virus evasion of antibody and complement.
Similar articles
-
An investigation of incorporation of cellular antigens into vaccinia virus particles.J Gen Virol. 2002 Oct;83(Pt 10):2347-2359. doi: 10.1099/0022-1317-83-10-2347. J Gen Virol. 2002. PMID: 12237415
-
Replacing the SCR domains of vaccinia virus protein B5R with EGFP causes a reduction in plaque size and actin tail formation but enveloped virions are still transported to the cell surface.J Gen Virol. 2002 Feb;83(Pt 2):323-332. doi: 10.1099/0022-1317-83-2-323. J Gen Virol. 2002. PMID: 11807225
-
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. 2002 Jan;83(Pt 1):195-207. doi: 10.1099/0022-1317-83-1-195. J Gen Virol. 2002. PMID: 11752717
-
The exit of vaccinia virus from infected cells.Virus Res. 2004 Dec;106(2):189-97. doi: 10.1016/j.virusres.2004.08.015. Virus Res. 2004. PMID: 15567497 Review.
-
Extracellular enveloped vaccinia virus. Entry, egress, and evasion.Adv Exp Med Biol. 1998;440:395-414. Adv Exp Med Biol. 1998. PMID: 9782308 Review.
Cited by
-
Poxvirus cell entry: how many proteins does it take?Viruses. 2012 May;4(5):688-707. doi: 10.3390/v4050688. Epub 2012 Apr 27. Viruses. 2012. PMID: 22754644 Free PMC article. Review.
-
Modulation of the myxoma virus plaque phenotype by vaccinia virus protein F11.J Virol. 2012 Jul;86(13):7167-79. doi: 10.1128/JVI.06936-11. Epub 2012 Apr 18. J Virol. 2012. PMID: 22514354 Free PMC article.
-
Effect of the deletion of genes encoding proteins of the extracellular virion form of vaccinia virus on vaccine immunogenicity and protective effectiveness in the mouse model.PLoS One. 2013 Jun 13;8(6):e67984. doi: 10.1371/journal.pone.0067984. Print 2013. PLoS One. 2013. PMID: 23785523 Free PMC article.
-
Monkeypox virus: insights into pathogenesis and laboratory testing methods.3 Biotech. 2024 Mar;14(3):67. doi: 10.1007/s13205-024-03920-z. Epub 2024 Feb 12. 3 Biotech. 2024. PMID: 38357674 Review.
-
Molecular genetic analysis of orf virus: a poxvirus that has adapted to skin.Viruses. 2015 Mar 23;7(3):1505-39. doi: 10.3390/v7031505. Viruses. 2015. PMID: 25807056 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources