Historical variations in mutation rate in an epidemic pathogen, <i>Yersinia pestis</i>

Yujun Cui(BGI Group (China)), Chang Yu(BGI Group (China)), Yanfeng Yan(BGI Group (China)), Dongfang Li(BGI Group (China)), Yanjun Li(BGI Group (China)), Thibaut Jombart(Imperial College London), Lucy A. Weinert(University College London), Zuyun Wang(Qinghai Institute for Endemic Diease Prevention and Control), Zhaobiao Guo(Institute of Microbiology), Lizhi Xu(BGI Group (China)), Yujiang Zhang(Xinjiang Uygur Autonomous Region Disease Prevention and Control Center), Hancheng Zheng(BGI Group (China)), Nan Qin(BGI Group (China)), Xiao Xiao(Institute of Microbiology), Ming-Shou Wu(Yunnan Institute of Endemic Diseases Control and Prevention), Xiaoyi Wang(Institute of Microbiology), Dongsheng Zhou(Institute of Microbiology), Zhizhen Qi(Qinghai Institute for Endemic Diease Prevention and Control), Zongmin Du(Institute of Microbiology), Honglong Wu(BGI Group (China)), Xianwei Yang(BGI Group (China)), Hongzhi Cao(BGI Group (China)), Hu Wang(Qinghai Institute for Endemic Diease Prevention and Control), Jing Wang(BGI Group (China)), Shusen Yao(Beijing Center for Disease Prevention and Control), Alexander Rakin(Ludwig-Maximilians-Universität München), Yingrui Li(BGI Group (China)), Daniel Falush(University College Cork), François Balloux(University College London), Mark Achtman(University College Cork), Yajun Song(University College Cork), Jun Wang(BGI Group (China)), Ruifu Yang(BGI Group (China))
Proceedings of the National Academy of Sciences
December 27, 2012
Cited by 406Open Access
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Abstract

The genetic diversity of Yersinia pestis, the etiologic agent of plague, is extremely limited because of its recent origin coupled with a slow clock rate. Here we identified 2,326 SNPs from 133 genomes of Y. pestis strains that were isolated in China and elsewhere. These SNPs define the genealogy of Y. pestis since its most recent common ancestor. All but 28 of these SNPs represented mutations that happened only once within the genealogy, and they were distributed essentially at random among individual genes. Only seven genes contained a significant excess of nonsynonymous SNP, suggesting that the fixation of SNPs mainly arises via neutral processes, such as genetic drift, rather than Darwinian selection. However, the rate of fixation varies dramatically over the genealogy: the number of SNPs accumulated by different lineages was highly variable and the genealogy contains multiple polytomies, one of which resulted in four branches near the time of the Black Death. We suggest that demographic changes can affect the speed of evolution in epidemic pathogens even in the absence of natural selection, and hypothesize that neutral SNPs are fixed rapidly during intermittent epidemics and outbreaks.


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