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图潘病毒如何降解其变形虫宿主的核糖体RNA?核糖核酸酶T2的作用路径。

How Tupanvirus Degrades the Ribosomal RNA of Its Amoebal Host? The Ribonuclease T2 Track.

作者信息

Rolland Clara, La Scola Bernard, Levasseur Anthony

机构信息

Aix-Marseille Université, UMR MEPHI (Microbes, Evolution, Phylogeny and Infections), IRD, APHM, Faculté de Médecine, Marseille, France.

IHU Méditerranée Infection, Marseille, France.

出版信息

Front Microbiol. 2020 Jul 28;11:1691. doi: 10.3389/fmicb.2020.01691. eCollection 2020.

DOI:10.3389/fmicb.2020.01691
PMID:32849355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7399046/
Abstract

Tupanviruses are giant viruses recently discovered in Brazil from extreme environments: (TPV-SL) and (TPV-DO). Unexpected features in Tupanviruses is the cytotoxic effect observed during infection, where the virus degrades the ribosomal RNA (rRNA) of its amoebal host. Interestingly, only TPV-SL causes this rRNA shutdown. We performed a genomic comparison of the two strains to determine potential modifications explaining the absence of rRNA degradation by TPV-DO. Whole genome comparisons were performed as well as more in-depth analysis at the gene level. We also calculated selective pressure on the orthologous genes between the two viruses. Our computational and evolutionary investigations revealed a potential target: a ribonuclease T2. These enzymes are known to be involved in cellular RNA catabolism such as in lysosomal degradation of rRNA. Our results suggest a functional ribonuclease localized in acid compartment closely related to ribonuclease T2 from eukaryotes. Silencing of the RNAse T2 gene of TPV-SL abolished its rRNA shutdown ability thereby correlating assumption to the experimental evidence. In conclusion, all our results pointed to RNAse T2 as a target for explaining the difference for rRNA degradation ability between both strains.

摘要

土潘病毒是最近在巴西从极端环境中发现的巨型病毒

(TPV-SL)和(TPV-DO)。土潘病毒的意外特征是在感染过程中观察到的细胞毒性作用,即病毒降解其变形虫宿主的核糖体RNA(rRNA)。有趣的是,只有TPV-SL会导致这种rRNA关闭。我们对这两种毒株进行了基因组比较,以确定能够解释TPV-DO不存在rRNA降解现象的潜在修饰。我们进行了全基因组比较以及在基因水平上更深入的分析。我们还计算了两种病毒直系同源基因上的选择压力。我们的计算和进化研究揭示了一个潜在靶点:一种核糖核酸酶T2。已知这些酶参与细胞RNA分解代谢,如rRNA的溶酶体降解。我们的结果表明,一种功能性核糖核酸酶定位于与真核生物核糖核酸酶T2密切相关的酸性区室中。TPV-SL的RNAse T2基因沉默消除了其rRNA关闭能力,从而将假设与实验证据联系起来。总之,我们所有的结果都表明RNAse T2是解释两种毒株rRNA降解能力差异的一个靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/615dcf5a4ab2/fmicb-11-01691-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/41574ebd7b5a/fmicb-11-01691-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/5448204752ea/fmicb-11-01691-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/503669dbffd1/fmicb-11-01691-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/c4e6f1df2030/fmicb-11-01691-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/cb0b7993b3f3/fmicb-11-01691-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/f24508d43905/fmicb-11-01691-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/615dcf5a4ab2/fmicb-11-01691-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/41574ebd7b5a/fmicb-11-01691-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/5448204752ea/fmicb-11-01691-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/503669dbffd1/fmicb-11-01691-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/c4e6f1df2030/fmicb-11-01691-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/cb0b7993b3f3/fmicb-11-01691-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/f24508d43905/fmicb-11-01691-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c7/7399046/615dcf5a4ab2/fmicb-11-01691-g007.jpg

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