Rahman Masmudur M, Mohamed Mohamed R, Kim Manbok, Smallwood Sherin, McFadden Grant
Department of Molecular Genetics and Microbiology, College of Medicine, University of Florida, Gainesville, Florida, USA.
PLoS Pathog. 2009 Oct;5(10):e1000635. doi: 10.1371/journal.ppat.1000635. Epub 2009 Oct 23.
NF-kappaB and inflammasomes both play central roles in orchestrating anti-pathogen responses by rapidly inducing a variety of early-response cytokines and chemokines following infection. Myxoma virus (MYXV), a pathogenic poxvirus of rabbits, encodes a member of the cellular pyrin domain (PYD) superfamily, called M013. The viral M013 protein was previously shown to bind host ASC-1 protein and inhibit the cellular inflammasome complex that regulates the activation and secretion of caspase 1-regulated cytokines such as IL-1beta and IL-18. Here, we report that human THP-1 monocytic cells infected with a MYXV construct deleted for the M013L gene (vMyxM013-KO), in stark contrast to the parental MYXV, rapidly induce high levels of secreted pro-inflammatory cytokines like TNF, IL-6, and MCP-1, all of which are regulated by NF-kappaB. The induction of these NF-kappaB regulated cytokines following infection with vMyxM013-KO was also confirmed in vivo using THP-1 derived xenografts in NOD-SCID mice. vMyxM013-KO virus infection specifically induced the rapid phosphorylation of IKK and degradation of IkappaBalpha, which was followed by nuclear translocation of NF-kappaB/p65. Even in the absence of virus infection, transiently expressed M013 protein alone inhibited cellular NF-kappaB-mediated reporter gene expression and nuclear translocation of NF-kappaB/p65. Using protein/protein interaction analysis, we show that M013 protein also binds directly with cellular NF-kappaB1, suggesting a direct physical and functional linkage between NF-kappaB1 and ASC-1. We further demonstrate that inhibition of the inflammasome with a caspase-1 inhibitor did not prevent the induction of NF-kappaB regulated cytokines following infection with vMyxM013-KO virus, but did block the activation of IL-1beta. Thus, the poxviral M013 inhibitor exerts a dual immuno-subversive role in the simultaneous co-regulation of both the cellular inflammasome complex and NF-kappaB-mediated pro-inflammatory responses.
核因子κB(NF-κB)和炎性小体在感染后通过快速诱导多种早期反应细胞因子和趋化因子来协调抗病原体反应中均发挥核心作用。黏液瘤病毒(MYXV)是兔的一种致病性痘病毒,编码一种细胞含吡啉结构域(PYD)超家族成员,称为M013。病毒M013蛋白先前已被证明可结合宿主ASC-1蛋白并抑制调节半胱天冬酶1调节的细胞因子如IL-1β和IL-18的激活和分泌的细胞炎性小体复合物。在此,我们报告,与亲本MYXV形成鲜明对比的是,用缺失M013L基因的MYXV构建体(vMyxM013-KO)感染的人THP-1单核细胞会迅速诱导高水平的分泌型促炎细胞因子,如TNF、IL-6和MCP-1,所有这些细胞因子均受NF-κB调节。在NOD-SCID小鼠中使用THP-1衍生的异种移植瘤在体内也证实了感染vMyxM013-KO后这些受NF-κB调节的细胞因子的诱导。vMyxM013-KO病毒感染特异性诱导IKK的快速磷酸化和IkappaBα的降解,随后是NF-κB/p65的核转位。即使在没有病毒感染的情况下,单独瞬时表达的M013蛋白也会抑制细胞NF-κB介导的报告基因表达和NF-κB/p65的核转位。通过蛋白质/蛋白质相互作用分析,我们表明M013蛋白还直接与细胞NF-κB1结合,提示NF-κB1与ASC-1之间存在直接的物理和功能联系。我们进一步证明,用半胱天冬酶-1抑制剂抑制炎性小体并不能阻止感染vMyxM013-KO病毒后NF-κB调节的细胞因子的诱导,但确实会阻断IL-1β的激活。因此,痘病毒M013抑制剂在同时共同调节细胞炎性小体复合物和NF-κB介导的促炎反应中发挥双重免疫颠覆作用。