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瘟病毒中超级感染的排除或超级感染的增强——猪戊型肝炎病毒感染不依赖于ADAM17。

Exclusion of Superinfection or Enhancement of Superinfection in Pestiviruses-APPV Infection Is Not Dependent on ADAM17.

作者信息

Geranio Francesco, Affeldt Sebastian, Cechini Angelika, Barth Sandra, Reuscher Carina M, Riedel Christiane, Rümenapf Till, Lamp Benjamin

机构信息

Institute of Virology, Faculty of Veterinary Medicine, Justus-Liebig-University Giessen, Schubertstrasse 81, 35392 Giessen, Germany.

CIRI-Centre International de Recherche en Infectiologie, Université Lyon, Université Claude Bernard Lyon 1, Inserm, U1111, CNRS, UMR5308, ENS Lyon, 46 Allée d'Italie, 69007 Lyon, France.

出版信息

Viruses. 2024 Nov 26;16(12):1834. doi: 10.3390/v16121834.

DOI:10.3390/v16121834
PMID:39772144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11680174/
Abstract

Some viruses can suppress superinfections of their host cells by related or different virus species. The phenomenon of superinfection exclusion can be caused by inhibiting virus attachment, receptor binding and entry, by replication interference, or competition for host cell resources. Blocking attachment and entry not only prevents unproductive double infections but also stops newly produced virions from re-entering the cell post-exocytosis. In this study, we investigated the exclusion of superinfections between the different pestivirus species. Bovine and porcine cells pre-infected with non-cytopathogenic pestivirus strains were evaluated for susceptibility to subsequent superinfection using comparative titrations. Our findings revealed significant variation in exclusion potency depending on the pre- and superinfecting virus species, as well as the host cell species. Despite this variability, all tested classical pestivirus species reduced host cell susceptibility to subsequent infections, indicating a conserved entry mechanism. Unexpectedly, pre-infection with atypical porcine pestivirus (APPV) increased host cell susceptibility to classical pestiviruses. Further analysis showed that APPV can infect SK-6 cells independently of ADAM17, a critical attachment factor for the classical pestiviruses. These results indicate that APPV uses different binding and entry mechanisms than the other pestiviruses. The observed increase in the susceptibility of cells post-APPV infection warrants further investigation and could have practical implications, such as aiding challenging pestivirus isolation from diagnostic samples.

摘要

一些病毒可以抑制其宿主细胞被相关或不同病毒种类的超感染。超感染排除现象可由抑制病毒附着、受体结合和进入、复制干扰或对宿主细胞资源的竞争引起。阻断附着和进入不仅能防止无效的双重感染,还能阻止新产生的病毒粒子在胞吐后重新进入细胞。在本研究中,我们调查了不同瘟病毒种类之间的超感染排除情况。使用比较滴定法评估了预先感染非细胞病变性瘟病毒株的牛和猪细胞对后续超感染的敏感性。我们的研究结果显示,排除效力存在显著差异,这取决于预先感染和超感染的病毒种类以及宿主细胞种类。尽管存在这种变异性,但所有测试的经典瘟病毒种类都降低了宿主细胞对后续感染的敏感性,表明存在保守的进入机制。出乎意料的是,预先感染非典型猪瘟病毒(APPV)会增加宿主细胞对经典瘟病毒的敏感性。进一步分析表明,APPV可以独立于ADAM17感染SK-6细胞,ADAM17是经典瘟病毒的关键附着因子。这些结果表明,APPV使用的结合和进入机制与其他瘟病毒不同。观察到的APPV感染后细胞敏感性增加值得进一步研究,并且可能具有实际意义,例如有助于从诊断样本中分离具有挑战性的瘟病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3307/11680174/a48f16239fd8/viruses-16-01834-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3307/11680174/f9dedd278e03/viruses-16-01834-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3307/11680174/d8f281ad8247/viruses-16-01834-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3307/11680174/a48f16239fd8/viruses-16-01834-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3307/11680174/f9dedd278e03/viruses-16-01834-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3307/11680174/d8f281ad8247/viruses-16-01834-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3307/11680174/a48f16239fd8/viruses-16-01834-g003.jpg

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本文引用的文献

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Viruses. 2024 Oct 2;16(10):1564. doi: 10.3390/v16101564.
2
No evidence of spread of Linda pestivirus in the wild boar population in Southern Germany.在德国南部野猪种群中未发现琳达毕赤病毒的传播。
Virol J. 2024 Aug 30;21(1):205. doi: 10.1186/s12985-024-02476-x.
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Establishment of a superinfection exclusion method for pestivirus titration using a recombinant reporter pestiviruses.建立一种基于重组报告性瘟病毒的瘟病毒滴定的超强感染排除法。
J Vet Med Sci. 2024 Apr 1;86(4):389-395. doi: 10.1292/jvms.24-0005. Epub 2024 Feb 14.
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Host Cell Receptors Implicated in the Cellular Tropism of BVDV.宿主细胞受体参与 BVDV 的细胞嗜性。
Viruses. 2022 Oct 20;14(10):2302. doi: 10.3390/v14102302.
5
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6
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Viruses. 2022 Feb 13;14(2):381. doi: 10.3390/v14020381.
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Fifty Shades of E: Innate Immune Evasion by the Viral Endonucleases of All Pestivirus Species.所有瘟病毒种的病毒核酸内切酶对固有免疫系统的 50 种逃避策略。
Viruses. 2022 Jan 27;14(2):265. doi: 10.3390/v14020265.
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