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猪瘟病毒通过诱导自噬/线粒体自噬靶向降解 RIPK3 来限制细胞坏死以维持感染。

CSFV restricts necroptosis to sustain infection by inducing autophagy/mitophagy-targeted degradation of RIPK3.

机构信息

College of Veterinary Medicine, South China Agricultural University , Guangzhou, China.

Agro-Biological Gene Research Center, Guangdong Academy of Agricultural Sciences, State Key Laboratory of Livestock and Poultry Breeding industry , Guangzhou, China.

出版信息

Microbiol Spectr. 2024 Jan 11;12(1):e0275823. doi: 10.1128/spectrum.02758-23. Epub 2023 Dec 15.

Abstract

CSFV infection in pigs causes persistent high fever, hemorrhagic necrotizing multi-organ inflammation, and high mortality, which seriously threatens the global swine industry. Cell death is an essential immune response of the host against pathogen invasion, and lymphopenia is the most typical clinical feature in the acute phase of CSFV infection, which affects the initial host antiviral immunity. As an "old" virus, CSFV has evolved mechanisms to evade host immune response after a long genetic evolution. Here, we show that necroptosis is a limiting host factor for CSFV infection and that CSFV-induced autophagy can subvert this host defense mechanism to promote its sustained replication. Our findings reveal a complex link between necroptosis and autophagy in the process of cell death, provide evidence supporting the important role for CSFV in counteracting host cell necrosis, and enrich our knowledge of pathogens that may subvert and evade this host defense.

摘要

猪瘟病毒(CSFV)感染可引起持续性高热、出血性坏死性多器官炎症和高死亡率,严重威胁全球养猪业。细胞死亡是宿主针对病原体入侵的必要免疫反应,而淋巴细胞减少是 CSFV 感染急性期最典型的临床特征,它会影响宿主抗病毒免疫的初始应答。作为一种“古老”的病毒,CSFV 在长期的遗传进化过程中已进化出逃避宿主免疫反应的机制。在这里,我们发现坏死性细胞凋亡是限制 CSFV 感染的宿主因素,而 CSFV 诱导的自噬可以颠覆这种宿主防御机制,从而促进其持续复制。我们的研究结果揭示了细胞死亡过程中坏死性细胞凋亡和自噬之间的复杂联系,为 CSFV 在拮抗宿主细胞坏死方面的重要作用提供了证据,并丰富了我们对可能颠覆和逃避这种宿主防御的病原体的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da4e/10782971/b349079faeb6/spectrum.02758-23.f001.jpg

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