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垂死复制:病毒生命周期、细胞死亡途径和免疫的协调。

Dying to replicate: the orchestration of the viral life cycle, cell death pathways, and immunity.

机构信息

Unité d'Immunologie des Cellules Dendritiques, Departement d'Immunologie, Institut Pasteur and Inserm U818, Paris France.

出版信息

Immunity. 2011 Oct 28;35(4):478-90. doi: 10.1016/j.immuni.2011.10.010.

Abstract

Manipulation of cell death pathways has been identified as a common feature of host-microbe interactions. We examine two examples: influenza A as a representative acute infection and cytomegalovirus as an example of chronic infection. From the perspective of viral entry, replication, and transmission, we identify points of interconnection with the host response to infection, namely the induction of host cell death, inflammation, and immunity. Following from this analysis, we argue that the evolution and fine-tuned regulation of death-associated genes may result from constant microbial pressure--past and present--that helped to support and coordinate cell death programs within the host. Interestingly, the delay in host cell death allows time for the virus to replicate while perturbations in cell death allow the host cell to initiate an immune response. This may represent a genetically encoded trade-off ensuring survival of both host and virus, or it may be a part of the complex agenda of infectious microbes.

摘要

细胞死亡途径的调控已被确定为宿主-微生物相互作用的共同特征。我们研究了两个例子:甲型流感作为一种代表急性感染,巨细胞病毒作为慢性感染的一个例子。从病毒进入、复制和传播的角度来看,我们确定了与宿主感染反应的连接点,即诱导宿主细胞死亡、炎症和免疫。在此分析的基础上,我们认为与死亡相关基因的进化和精细调控可能是由于过去和现在的微生物压力导致的,这些压力有助于支持和协调宿主内的细胞死亡程序。有趣的是,宿主细胞死亡的延迟为病毒复制提供了时间,而细胞死亡的干扰则使宿主细胞能够启动免疫反应。这可能代表着一种遗传编码的权衡,以确保宿主和病毒的生存,或者它可能是感染性微生物复杂议程的一部分。

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