A third distinct tumor necrosis factor receptor of orthopoxviruses

被引:101
作者
Loparev, VN
Parsons, JM
Knight, JC
Panus, JF
Ray, CA
Buller, RHL
Pickup, DJ
Esposito, JJ
机构
[1] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, Div Viral & Rickettsial Dis,Poxvirus Sect, Viral Exanthems & Herpesvirus Branch, Atlanta, GA 30333 USA
[2] St Louis Univ, Dept Mol Biol & Immunol, St Louis, MO 63104 USA
[3] Duke Univ, Dept Microbiol, Durham, NC 27710 USA
关键词
D O I
10.1073/pnas.95.7.3786
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cowpox virus Brighten red strain (CPV) contains a gene, crmD, which encodes a 320-aa tumor necrosis factor receptor (TNFR) of 44% and 22% identity, respectively, to the CPV TNFR-like proteins, cytokine response modifiers (crm) CrmB and CrmC, The crmD gene was interrupted in three other cowpox strains examined and absent in various other orthopoxviruses; however, four strains of ectromelia virus (ECT) examined contained an intact crmD (97% identity to CPV crmD) and lacked cognates of crmB and crmC, The protein, CrmD, contains a transport signal; a 151-aa cysteine-rich region with 21 cysteines that align with human TNFRII ligand-binding region cysteines; and C-terminal region sequences that are highly diverged from cellular TNFR C-terminal region sequences involved in signal transduction, Bacterial maltose binding proteins containing the CPV or ECT CrmD cysteine rich region bound TNF and lymphotoxin-alpha (LT alpha) and blocked their in vitro cytolytic activity, Secreted viral CrmD bound TNF and LT alpha and was detectable after the early stage of replication, using nonreducing conditions, as 60- to 70-kDa predominant and 90- to 250-kDa minor disulfide-linked complexes that were able to be reduced to a 46-kDa form and deglycosylated to a 38-kDa protein, Cells infected with CPV produced extremely low amounts of CrmD compared with ECT, Possessing up to three TNFRs, including CrmD, which is secreted as disulfide-linked complexes in varied amounts by CPV and ECT, likely enhances the dynamics of the immune modulating mechanisms of orthopoxviruses.
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页码:3786 / 3791
页数:6
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