Echovirus 11 infection induces pyroptotic cell death by facilitating NLRP3 inflammasome activation

炎症体 回声病毒 上睑下垂 目标2 半胱氨酸蛋白酶1 发病机制 Echo(通信协议) 生物 病毒 病毒学 免疫学 炎症 肠道病毒 计算机网络 计算机科学
作者
Chong Wang,Ruyi Yang,Fengxia Yang,Yang Han,Yujie Ren,Xiaobei Xiong,Xinyun Wang,Yidan Bi,Lijun Li,Yang Qiu,Yi Xu,Xi Zhou
出处
期刊:PLOS Pathogens [Public Library of Science]
卷期号:18 (8): e1010787-e1010787 被引量:6
标识
DOI:10.1371/journal.ppat.1010787
摘要

Echovirus 11 (ECHO 11) is a positive-strand RNA virus belonging to the genus Enterovirus of the family Picornaviridae . ECHO 11 infections can cause severe inflammatory illnesses in neonates, including severe acute hepatitis with coagulopathy. The activation of NLRP3 inflammasome is important for host defense against invading viruses, which also contributes to viral pathogenicity. However, whether and how ECHO 11 induces NLRP3 inflammasome activation remains unclear. In this study, we isolated a clinical strain of ECHO 11 from stools of an ECHO 11-infected newborn patient with necrotizing hepatitis. This virus shared 99.95% sequence identity with the previously published ECHO 11 sequence. The clinically isolated ECHO 11 can efficiently infect liver cells and strongly induces inflammation. Moreover, we showed that ECHO 11 induced IL-1β secretion and pyroptosis in cells and mouse bone marrow-derived macrophages (BMDMs). Furthermore, ECHO 11 infection triggered NLRP3 inflammasome activation, as evidenced by cleavages of GSDMD, pro-IL-1β and pro-caspase-1, and the release of LDH. ECHO 11 2B protein was required for NLRP3 inflammasome activation via interacting with NLRP3 to facilitate the inflammasome complex assembly. In vivo , expression of ECHO 11 2B also activated NLRP3 inflammasome in the murine liver. Besides, 2Bs of multiple EVs can also interact with NLRP3 and induce NLRP3 inflammasome activation. Together, our findings demonstrate a mechanism by which ECHO 11 induces inflammatory responses by activating NLRP3 inflammasome, providing novel insights into the pathogenesis of ECHO 11 infection.
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