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十年间对中国玉龙鼠疫疫源地的监测以及对分离株的分子分型和溯源。

Ten years of surveillance of the Yulong plague focus in China and the molecular typing and source tracing of the isolates.

机构信息

Yunnan Provincial Key Laboratory for Zoonosis Control and Prevention, Yunnan Institute for Endemic Disease Control and Prevention, Dali city of Yunnan province, China.

Lijiang Center for Disease Control and Prevention, Lijiang City of Yunnan province, China.

出版信息

PLoS Negl Trop Dis. 2018 Mar 30;12(3):e0006352. doi: 10.1371/journal.pntd.0006352. eCollection 2018 Mar.

Abstract

Plague, caused by Yersinia pestis, was classified as a reemerging infectious disease by the World Health Organization. The five human pneumonic plague cases in Yulong County in 2005 gave rise to the discovery of a Yulong plague focus in Yunnan province, China. Thereafter, continuous wild rodent plague (sylvatic plague) was identified as the main plague reservoir of this focus. In this study, the epizootics in Yulong focus were described, and three molecular typing methods, including the different region (DFR) analysis, clustered regularly interspaced short palindromic repeats (CRISPRs), and the multiple-locus variable number of tandem repeats (VNTR) analysis (MLVA) (14+12), were used for the molecular typing and source tracing of Y. pestis isolates in the Yulong plague focus. Simultaneously, several isolates from the vicinity of Yunnan were used as controls. The results showed that during the 10-year period from 2006 to 2016, an animal plague epidemic occurred in 6 of those years, and 5 villages underwent an animal plague epidemic within a 30-km2 area of the Yulong plague focus. Searching for dead mice was the most effective monitoring method in this plague focus. No positive sample has been found in 6937 captured live rodents thus far, suggesting that the virulence of strains in the Yulong plague focus is stronger and the survival time of mice is shorter after infection. Strains from Lijiang, Sichuan and Tibet were of the same complex based on a typing analysis of DFR and CRISPR. The genetic relationship of Y. pestis illustrated by MLVA "14+12" demonstrates that Tibet and Sichuan strains evolved from the strains 1.IN2 (Qinghai, 1970 and Tibet, 1976), and Lijiang strains are closer to Batang strains (Batang County in Sichuan province, 2011, Himalaya marmot plague foci) in terms of genetic or phylogenic relationships. In conclusion, we have a deeper understanding of this new plague focus throughout this study, which provides a basis for effective prevention and control.

摘要

鼠疫由鼠疫耶尔森菌引起,被世界卫生组织列为新发传染病。2005 年玉龙县发生的 5 例人间肺鼠疫病例导致在中国云南省发现了一个玉龙鼠疫疫源地。此后,连续的野生啮齿动物鼠疫(自然疫源性鼠疫)被确定为该疫源地的主要鼠疫储存库。在本研究中,描述了玉龙疫源地的动物鼠疫流行情况,并采用三种分子分型方法,包括不同区域(DFR)分析、成簇规律间隔短回文重复(CRISPRs)和多位点可变数目串联重复(VNTR)分析(MLVA)(14+12),对玉龙鼠疫疫源地的鼠疫耶尔森菌分离株进行了分子分型和溯源。同时,选择了云南周边的几个分离株作为对照。结果表明,在 2006 年至 2016 年的 10 年间,有 6 年发生了动物鼠疫流行,在玉龙鼠疫疫源地 30km2 范围内的 5 个村庄发生了动物鼠疫流行。在该鼠疫疫源地,搜索死鼠是最有效的监测方法。迄今为止,在 6937 只捕获的活鼠中未发现阳性样本,这表明玉龙鼠疫疫源地的菌株毒力更强,感染后老鼠的存活时间更短。丽江、四川和西藏的分离株在 DFR 和 CRISPR 分型分析中属于同一复合体。通过 MLVA“14+12”的遗传关系表明,西藏和四川的菌株来源于 1.IN2(青海,1970 年和西藏,1976 年)菌株,而丽江的菌株在遗传或系统发育关系上与四川巴塘的菌株(2011 年四川巴塘县喜马拉雅旱獭鼠疫疫源地)更为接近。总之,通过本研究,我们对这个新的鼠疫疫源地有了更深入的了解,为有效防控提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5c8/5895057/0609b3b54a74/pntd.0006352.g001.jpg

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