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食源性病原体肠炎沙门氏菌亚种的突变和转录错误率。

Rates of Mutations and Transcript Errors in the Foodborne Pathogen Salmonella enterica subsp. enterica.

机构信息

Institute of Evolution and Marine Biodiversity, KLMME, Ocean University of China, 5 Yushan Road, Qingdao, Shandong Province 266003, China.

Laboratory for Marine Biology and Biotechnology, Qingdao Pilot National Laboratory for Marine Science and Technology, Qingdao 266237, China.

出版信息

Mol Biol Evol. 2022 Apr 10;39(4). doi: 10.1093/molbev/msac081.

DOI:10.1093/molbev/msac081
PMID:35446958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9040049/
Abstract

Because errors at the DNA level power pathogen evolution, a systematic understanding of the rate and molecular spectra of mutations could guide the avoidance and treatment of infectious diseases. We thus accumulated tens of thousands of spontaneous mutations in 768 repeatedly bottlenecked lineages of 18 strains from various geographical sites, temporal spread, and genetic backgrounds. Entailing over ∼1.36 million generations, the resultant data yield an average mutation rate of ∼0.0005 per genome per generation, with a significant within-species variation. This is one of the lowest bacterial mutation rates reported, giving direct support for a high genome stability in this pathogen resulting from high DNA-mismatch-repair efficiency and replication-machinery fidelity. Pathogenicity genes do not exhibit an accelerated mutation rate, and thus, elevated mutation rates may not be the major determinant for the diversification of toxin and secretion systems. Intriguingly, a low error rate at the transcript level is not observed, suggesting distinct fidelity of the replication and transcription machinery. This study urges more attention on the most basic evolutionary processes of even the best-known human pathogens and deepens the understanding of their genome evolution.

摘要

由于 DNA 水平的错误推动了病原体的进化,因此系统地了解突变的速率和分子谱可以指导传染病的预防和治疗。因此,我们在 18 株来自不同地理区域、时间传播和遗传背景的菌株中,对 768 个重复瓶颈谱系进行了数万次自发突变的积累。这些数据包含了超过 136 万个世代,平均每个基因组每代的突变率约为 0.0005,存在显著的种内变异。这是报道的最低细菌突变率之一,直接支持了该病原体的高基因组稳定性,这是由于其具有高 DNA 错配修复效率和复制机制保真度。致病性基因没有表现出加速的突变率,因此,突变率的提高可能不是毒素和分泌系统多样化的主要决定因素。有趣的是,在转录水平上并没有观察到低错误率,这表明复制和转录机制的保真度不同。这项研究促使人们更加关注即使是最知名的人类病原体的最基本的进化过程,并加深了对它们基因组进化的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/9040049/ca0a2db05dc4/msac081f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/9040049/a6faffc5dea5/msac081f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/9040049/ae0b66069cf0/msac081f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/9040049/ca0a2db05dc4/msac081f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/9040049/a6faffc5dea5/msac081f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/9040049/ae0b66069cf0/msac081f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/9040049/ca0a2db05dc4/msac081f3.jpg

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