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非洲猪瘟病毒分子生物学及宿主相互作用的进展为防控提供了新工具。

Advances in African swine fever virus molecular biology and host interactions contributing to new tools for control.

作者信息

Dixon Linda K

机构信息

The Pirbright Institute, Pirbright, Woking, Surrey, United Kingdom.

出版信息

J Virol. 2025 Jun 17;99(6):e0093224. doi: 10.1128/jvi.00932-24. Epub 2025 May 9.

Abstract

African swine fever virus (ASFV) causes a frequently fatal hemorrhagic disease in domestic pigs and wild boar. The spread from Africa to Georgia in 2007 initiated a pandemic affecting many European and most Asian countries. This has had a very high socio-economic impact and threatens global food security. The virus is a large, complex, cytoplasmic DNA virus, the only member of the family and codes for 170-190 proteins. Many of these have unknown functions and do not resemble other viruses or host proteins. This complexity has hindered the development of vaccines and other tools for control. The intensity of research has increased since the spread of ASFV in Europe and Asia, leading to rapid advances in knowledge. This review summarizes recent research, including the determination by cryogenic electron microscopy of the virus capsid structure and virion proteome. Novel information on the virus replication cycle, including mechanisms of virus entry into cells and the identification of host endosomal proteins important for entry, is summarized. Multiple, novel virus immune evasion proteins and their targets in the type I interferon response and inflammation pathways have been identified. The potential for the application of this knowledge to developing novel control tools, including modified live vaccines and other interventions targeting critical virus processes or host interactions, is discussed.

摘要

非洲猪瘟病毒(ASFV)在家猪和野猪中引发一种常具致命性的出血性疾病。2007年该病毒从非洲传播至格鲁吉亚,引发了一场波及许多欧洲国家和多数亚洲国家的大流行。这造成了极高的社会经济影响,并威胁到全球粮食安全。该病毒是一种大型、复杂的细胞质DNA病毒,是该病毒科的唯一成员,编码170 - 190种蛋白质。其中许多蛋白质功能未知,且与其他病毒或宿主蛋白质不同。这种复杂性阻碍了疫苗及其他防控工具的研发。自ASFV在欧洲和亚洲传播以来,研究力度加大,知识取得快速进展。本综述总结了近期研究,包括通过低温电子显微镜确定病毒衣壳结构和病毒粒子蛋白质组。总结了关于病毒复制周期的新信息,包括病毒进入细胞的机制以及对病毒进入重要的宿主内体蛋白的鉴定。已鉴定出多种新型病毒免疫逃避蛋白及其在I型干扰素反应和炎症途径中的靶点。讨论了将这些知识应用于开发新型防控工具的潜力,包括改良活疫苗和其他针对关键病毒过程或宿主相互作用的干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35c7/12172490/fb9aded37c03/jvi.00932-24.f001.jpg

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