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CD74 与肠道病毒 D68 蛋白相互作用抑制病毒复制。

CD74 Interacts with Proteins of Enterovirus D68 To Inhibit Virus Replication.

机构信息

NHC Key Laboratory of System Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.

Key Laboratory of Respiratory Disease Pathogenomics, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.

出版信息

Microbiol Spectr. 2023 Aug 17;11(4):e0080123. doi: 10.1128/spectrum.00801-23. Epub 2023 Jul 6.

Abstract

Enterovirus D68 (EV-D68) is a member of the species D in the genus of the family . As an emerging non-polio enterovirus, EV-D68 is widely spread all over the world and causes severe neurological and respiratory illnesses. Although the intrinsic restriction factors in the cell provide a frontline defense, the molecular nature of virus-host interactions remains elusive. Here, we provide evidence that the major histocompatibility complex class II chaperone, CD74, inhibits EV-D68 replication in infected cells by interacting with the second hydrophobic region of 2B protein, while EV-D68 attenuates the antiviral role of CD74 through 3C cleavage. 3C cleaves CD74 at Gln-125. The equilibrium between CD74 and EV-D68 3C determines the outcome of viral infection. As an emerging non-polio enterovirus, EV-D68 is widely spread all over the world and causes severe neurological and respiratory illnesses. Here, we report that CD74 inhibits viral replication in infected cells by targeting 2B protein of EV-D68, while EV-D68 attenuates the antiviral role of CD74 through 3C cleavage. The equilibrium between CD74 and EV-D68 3C determines the outcome of viral infection.

摘要

肠道病毒 D68(EV-D68)是 科 属 种 D 的成员。作为一种新兴的非脊髓灰质炎肠道病毒,EV-D68 广泛分布于世界各地,引起严重的神经和呼吸道疾病。尽管细胞内的固有限制因素提供了一线防御,但病毒-宿主相互作用的分子性质仍然难以捉摸。在这里,我们提供的证据表明,主要组织相容性复合体 II 伴侣 CD74 通过与 2B 蛋白的第二个疏水区相互作用,抑制感染细胞中的 EV-D68 复制,而 EV-D68 通过 3C 切割来减弱 CD74 的抗病毒作用。3C 在 Gln-125 处切割 CD74。CD74 和 EV-D68 3C 之间的平衡决定了病毒感染的结果。作为一种新兴的非脊髓灰质炎肠道病毒,EV-D68 广泛分布于世界各地,引起严重的神经和呼吸道疾病。在这里,我们报告 CD74 通过靶向 EV-D68 的 2B 蛋白抑制感染细胞中的病毒复制,而 EV-D68 通过 3C 切割来减弱 CD74 的抗病毒作用。CD74 和 EV-D68 3C 之间的平衡决定了病毒感染的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0850/10434063/4ba1a65e84b8/spectrum.00801-23-f001.jpg

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