A rabbitpox virus serpin gene controls host range by inhibiting apoptosis in restrictive cells
- PMID: 7494278
- PMCID: PMC189710
- DOI: 10.1128/JVI.69.12.7688-7698.1995
A rabbitpox virus serpin gene controls host range by inhibiting apoptosis in restrictive cells
Abstract
Poxviruses are unique among viruses in encoding members of the serine proteinase inhibitor (serpin) superfamily. Orthopoxviruses contain three serpins, designated SPI-1, SPI-2, and SPI-3. SPI-1 encodes a 40-kDa protein that is required for the replication of rabbitpox virus (RPV) in PK-15 or A549 cells in culture (A. N. Ali, P. C. Turner, M. A. Brooks, and R. W. Moyer, Virology 202:305-314, 1994). Examination of nonpermissive human A549 cells infected with an RPV mutant disrupted in the SPI-1 gene (RPV delta SPI-1) suggests there are no gross defects in protein or DNA synthesis. The proteolytic processing of late viral structural proteins, a feature of orthopoxvirus infections associated with the maturation of virus particles, also appears relatively normal. However, very few mature virus particles of any kind are produced compared with the level found in infections with wild-type RPV. Morphological examination of RPV delta SPI-1-infected A549 cells, together with an observed fragmentation of cellular DNA, suggests that the host range defect is associated with the onset of apoptosis. Apoptosis is seen only in RPV delta SPI-1 infection of nonpermissive (A549 or PK-15) cells and is absent in all wild-type RPV infections and RPV delta SPI-2 mutant infections examined to date. Although the SPI-1 gene is expressed early, before DNA replication, the triggering apoptotic event occurs late in the infection, as RPV delta SPI-1-infected A549 cells do not undergo apoptosis when infections are carried out in the presence of cytosine arabinoside. While the SPI-2 (crmA) gene, when transfected into cells, has been shown to inhibit apoptosis, our experiments provide the first indication that a poxvirus serpin protein can inhibit apoptosis during a poxvirus infection.
Similar articles
-
Activation of caspases in pig kidney cells infected with wild-type and CrmA/SPI-2 mutants of cowpox and rabbitpox viruses.J Virol. 1998 May;72(5):3524-33. doi: 10.1128/JVI.72.5.3524-3533.1998. J Virol. 1998. PMID: 9557631 Free PMC article.
-
The SPI-1 gene of rabbitpox virus determines host range and is required for hemorrhagic pock formation.Virology. 1994 Jul;202(1):305-14. doi: 10.1006/viro.1994.1347. Virology. 1994. PMID: 8009842
-
Suppressors of a host range mutation in the rabbitpox virus serpin SPI-1 map to proteins essential for viral DNA replication.J Virol. 2005 Jul;79(14):9168-79. doi: 10.1128/JVI.79.14.9168-9179.2005. J Virol. 2005. PMID: 15994811 Free PMC article.
-
Vaccinia virus serpin-1 deletion mutant exhibits a host range defect characterized by low levels of intermediate and late mRNAs.Virology. 1999 Sep 30;262(2):298-311. doi: 10.1006/viro.1999.9884. Virology. 1999. PMID: 10502509
-
Serpins and regulation of cell death.Results Probl Cell Differ. 1998;24:63-89. doi: 10.1007/978-3-540-69185-3_4. Results Probl Cell Differ. 1998. PMID: 9949832 Review.
Cited by
-
Unraveling gene content variation across eukaryotic giant viruses based on network analyses and host associations.Virus Evol. 2021 Sep 16;7(2):veab081. doi: 10.1093/ve/veab081. eCollection 2021. Virus Evol. 2021. PMID: 34754514 Free PMC article.
-
Poxvirus tropism.Nat Rev Microbiol. 2005 Mar;3(3):201-13. doi: 10.1038/nrmicro1099. Nat Rev Microbiol. 2005. PMID: 15738948 Free PMC article. Review.
-
Murine serpin 2A is a redox-sensitive intracellular protein.Biochem J. 2003 Apr 1;371(Pt 1):165-73. doi: 10.1042/BJ20021567. Biochem J. 2003. PMID: 12470299 Free PMC article.
-
Characterization of a myxoma virus-encoded serpin-like protein with activity against interleukin-1 beta-converting enzyme.J Virol. 1996 Sep;70(9):5860-6. doi: 10.1128/JVI.70.9.5860-5866.1996. J Virol. 1996. PMID: 8709205 Free PMC article.
-
Analysis of the anti-apoptotic activity of four vaccinia virus proteins demonstrates that B13 is the most potent inhibitor in isolation and during viral infection.J Gen Virol. 2014 Dec;95(Pt 12):2757-2768. doi: 10.1099/vir.0.068833-0. Epub 2014 Aug 4. J Gen Virol. 2014. PMID: 25090990 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous