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Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019
On 12 November 2019, one couple from the Sonid Left Qi (County) in the Inner Mongolia Autonomous Region was diagnosed with pneumonic plague in Beijing. The wife acquired the infection from her husband. Thereafter, two bubonic plague cases were identified in Inner Mongolia on November 16(th) and 24(t...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8362994/ https://www.ncbi.nlm.nih.gov/pubmed/34343197 http://dx.doi.org/10.1371/journal.pntd.0009558 |
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author | Li, Jianyun Wang, Yumeng Liu, Fang Shen, Xiaona Wang, Yiting Fan, Mengguang Peng, Yao Wang, Shuyi Feng, Yilan Zhang, Wen Lv, Yanning Zhang, Huijuan Lu, Xin Zhang, Enmin Wei, Jianchun Chen, Lijuan Kan, Biao Zhang, Zhongbing Xu, Jianguo Wang, Wenrui Li, Wei |
author_facet | Li, Jianyun Wang, Yumeng Liu, Fang Shen, Xiaona Wang, Yiting Fan, Mengguang Peng, Yao Wang, Shuyi Feng, Yilan Zhang, Wen Lv, Yanning Zhang, Huijuan Lu, Xin Zhang, Enmin Wei, Jianchun Chen, Lijuan Kan, Biao Zhang, Zhongbing Xu, Jianguo Wang, Wenrui Li, Wei |
author_sort | Li, Jianyun |
collection | PubMed |
description | On 12 November 2019, one couple from the Sonid Left Qi (County) in the Inner Mongolia Autonomous Region was diagnosed with pneumonic plague in Beijing. The wife acquired the infection from her husband. Thereafter, two bubonic plague cases were identified in Inner Mongolia on November 16(th) and 24(th). In this study, genome-wide single nucleotide polymorphism (SNP) analysis was used to identify the phylogenetic relationship of Yersinia pestis strains isolated in Inner Mongolia. Strains isolated from reservoirs in 2018 and 2019 in Inner Mongolia, together with the strain isolated from Patient C, were further clustered into 2.MED3m, and two novel lineages (2.MED3q, 2.MED3r) in the 2.MED3 population. According to the analysis of PCR-based molecular subtyping methods, such as the MLVA 14 scheme and seven SNP allele sequencing, Patients A/B and D were classified as 2.MED3m. In addition, strains from rodents living near the patients’ residences were clustered into the same lineage as patients. Such observations indicated that human plague cases originated from local reservoirs. Corresponding phylogenetic analysis also indicated that rodent plague strains in different areas in Inner Mongolia belong to different epizootics rather than being caused by spreading from the same epizootic in Meriones unguiculatus in 2019. |
format | Online Article Text |
id | pubmed-8362994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83629942021-08-14 Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019 Li, Jianyun Wang, Yumeng Liu, Fang Shen, Xiaona Wang, Yiting Fan, Mengguang Peng, Yao Wang, Shuyi Feng, Yilan Zhang, Wen Lv, Yanning Zhang, Huijuan Lu, Xin Zhang, Enmin Wei, Jianchun Chen, Lijuan Kan, Biao Zhang, Zhongbing Xu, Jianguo Wang, Wenrui Li, Wei PLoS Negl Trop Dis Research Article On 12 November 2019, one couple from the Sonid Left Qi (County) in the Inner Mongolia Autonomous Region was diagnosed with pneumonic plague in Beijing. The wife acquired the infection from her husband. Thereafter, two bubonic plague cases were identified in Inner Mongolia on November 16(th) and 24(th). In this study, genome-wide single nucleotide polymorphism (SNP) analysis was used to identify the phylogenetic relationship of Yersinia pestis strains isolated in Inner Mongolia. Strains isolated from reservoirs in 2018 and 2019 in Inner Mongolia, together with the strain isolated from Patient C, were further clustered into 2.MED3m, and two novel lineages (2.MED3q, 2.MED3r) in the 2.MED3 population. According to the analysis of PCR-based molecular subtyping methods, such as the MLVA 14 scheme and seven SNP allele sequencing, Patients A/B and D were classified as 2.MED3m. In addition, strains from rodents living near the patients’ residences were clustered into the same lineage as patients. Such observations indicated that human plague cases originated from local reservoirs. Corresponding phylogenetic analysis also indicated that rodent plague strains in different areas in Inner Mongolia belong to different epizootics rather than being caused by spreading from the same epizootic in Meriones unguiculatus in 2019. Public Library of Science 2021-08-03 /pmc/articles/PMC8362994/ /pubmed/34343197 http://dx.doi.org/10.1371/journal.pntd.0009558 Text en © 2021 Li et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Li, Jianyun Wang, Yumeng Liu, Fang Shen, Xiaona Wang, Yiting Fan, Mengguang Peng, Yao Wang, Shuyi Feng, Yilan Zhang, Wen Lv, Yanning Zhang, Huijuan Lu, Xin Zhang, Enmin Wei, Jianchun Chen, Lijuan Kan, Biao Zhang, Zhongbing Xu, Jianguo Wang, Wenrui Li, Wei Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019 |
title | Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019 |
title_full | Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019 |
title_fullStr | Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019 |
title_full_unstemmed | Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019 |
title_short | Genetic source tracking of human plague cases in Inner Mongolia-Beijing, 2019 |
title_sort | genetic source tracking of human plague cases in inner mongolia-beijing, 2019 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8362994/ https://www.ncbi.nlm.nih.gov/pubmed/34343197 http://dx.doi.org/10.1371/journal.pntd.0009558 |
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