Influenza A virus NS1 induces degradation of sphingosine 1-phosphate lyase to obstruct the host innate immune response

被引:10
|
作者
Wolf, Jennifer J. [1 ,2 ]
Xia, Chuan [1 ,2 ,5 ]
Studstill, Caleb J. [1 ,2 ]
Ngo, Hanh [1 ,2 ]
Brody, Steven L. [3 ]
Anderson, Paul E. [4 ]
Hahm, Bumsuk [1 ,2 ]
机构
[1] Univ Missouri, Dept Surg, Columbia, MO 65212 USA
[2] Univ Missouri, Dept Mol Microbiol & Immunol, Columbia, MO 65212 USA
[3] Washington Univ, Dept Med, Sch Med, St Louis, MO 63110 USA
[4] Univ Missouri, Lab Infect Dis Res, Columbia, MO 65212 USA
[5] Shandong Univ, State Key Lab Microbial Technol, Qingdao 266237, Peoples R China
关键词
Influenza virus; Sphingosine-1-phosphate lyase; Nonstructural protein 1; Type I interferon; Viral immune evasion; Ubiquitination; Protein degradation; SPHINGOSINE-1-PHOSPHATE LYASE; PROTEIN; INTERFERON; ACTIVATION; RESISTANCE; EPIDEMIOLOGY; INFECTIONS; INHIBITION; CISPLATIN; DISTINCT;
D O I
10.1016/j.virol.2021.02.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The type I interferon (IFN)-mediated innate immune response is one of the central obstacles influenza A virus (IAV) must overcome in order to successfully replicate within the host. We have previously shown that sphingosine 1-phosphate (S1P) lyase (SPL) enhances IKK?-mediated type I IFN responses. Here, we demonstrate that the nonstructural protein 1 (NS1) of IAV counteracts the SPL-mediated antiviral response by inducing degradation of SPL. SPL was ubiquitinated and downregulated upon IAV infection or NS1 expression, whereas NS1deficient IAV failed to elicit SPL ubiquitination or downregulation. Transiently overexpressed SPL increased phosphorylation of IKK?, resulting in enhanced expression of type I IFNs. However, this induction was markedly inhibited by IAV NS1. Collectively, this study reveals a novel strategy employed by IAV to subvert the type I IFN response, providing new insights into the interplay between IAV and host innate immunity.
引用
收藏
页码:67 / 75
页数:9
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