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巨型病毒的宿主-病毒相互作用及防御机制

Host-virus interactions and defense mechanisms for giant viruses.

作者信息

Chelkha Nisrine, Levasseur Anthony, La Scola Bernard, Colson Philippe

机构信息

Aix-Marseille University, Institut de Recherche pour le Développement (IRD), Assistance Publique - Hôpitaux de Marseille (AP-HM), Microbes Evolution Phylogeny and Infections (MEPHI), Marseille, France.

IHU Méditerranée Infection, Marseille, France.

出版信息

Ann N Y Acad Sci. 2020 Oct 8. doi: 10.1111/nyas.14469.

Abstract

Giant viruses, with virions larger than 200 nm and genomes larger than 340 kilobase pairs, modified the now outdated perception of the virosphere. With virions now reported reaching up to 1.5 μm in size and genomes of up to 2.5 Mb encoding components shared with cellular life forms, giant viruses exhibit a complexity similar to microbes, such as bacteria and archaea. Here, we review interactions of giant viruses with their hosts and defense strategies of giant viruses against their hosts and coinfecting microorganisms or virophages. We also searched by comparative genomics for homologies with proteins described or suspected to be involved in defense mechanisms. Our search reveals that natural immunity and apoptosis seem to be crucial components of the host defense against giant virus infection. Conversely, giant viruses possess methods of hijacking host functions to counteract cellular antiviral responses. In addition, giant viruses may encode other unique and complex pathways to manipulate the host machinery and eliminate other competing microorganisms. Notably, giant viruses have evolved defense mechanisms against their virophages and they might trigger defense systems against other viruses through sequence integration. We anticipate that comparative genomics may help identifying genes involved in defense strategies of both giant viruses and their hosts.

摘要

巨型病毒的病毒粒子大于200纳米,基因组大于340千碱基对,改变了如今已过时的病毒圈观念。如今报道的病毒粒子大小可达1.5微米,基因组大小可达2.5兆碱基,编码与细胞生命形式共有的成分,巨型病毒展现出与细菌和古菌等微生物相似的复杂性。在此,我们综述巨型病毒与其宿主的相互作用,以及巨型病毒针对其宿主、共感染的微生物或噬病毒体的防御策略。我们还通过比较基因组学搜索与已描述或疑似参与防御机制的蛋白质的同源性。我们的搜索结果显示,天然免疫和细胞凋亡似乎是宿主抵御巨型病毒感染的关键组成部分。相反,巨型病毒拥有劫持宿主功能以对抗细胞抗病毒反应的方法。此外,巨型病毒可能编码其他独特且复杂的途径来操纵宿主机制并清除其他竞争性微生物。值得注意的是,巨型病毒已经进化出针对其噬病毒体的防御机制,并且它们可能通过序列整合触发针对其他病毒的防御系统。我们预计比较基因组学可能有助于鉴定参与巨型病毒及其宿主防御策略的基因。

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