A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.

Streptomycin is considered to be one of the effective antibiotics for the treatment of plague. In order to investigate the streptomycin resistance of Y. pestis in China, we evaluated streptomycin susceptibility of 536 Y. pestis strains in China in vitro using the minimal inhibitory concentration (MI...

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Main Authors: Ruixia Dai, Jian He, Xi Zha, Yiting Wang, Xuefei Zhang, He Gao, Xiaoyan Yang, Juan Li, Youquan Xin, Yumeng Wang, Sheng Li, Juan Jin, Qi Zhang, Jixiang Bai, Yao Peng, Hailian Wu, Qingwen Zhang, Baiqing Wei, Jianguo Xu, Wei Li
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-04-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://doi.org/10.1371/journal.pntd.0009324
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spelling doaj-051f358f5cbb4eb1abec3fe300952d122021-07-30T04:32:38ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352021-04-01154e000932410.1371/journal.pntd.0009324A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.Ruixia DaiJian HeXi ZhaYiting WangXuefei ZhangHe GaoXiaoyan YangJuan LiYouquan XinYumeng WangSheng LiJuan JinQi ZhangJixiang BaiYao PengHailian WuQingwen ZhangBaiqing WeiJianguo XuWei LiStreptomycin is considered to be one of the effective antibiotics for the treatment of plague. In order to investigate the streptomycin resistance of Y. pestis in China, we evaluated streptomycin susceptibility of 536 Y. pestis strains in China in vitro using the minimal inhibitory concentration (MIC) and screened streptomycin resistance-associated genes (strA and strB) by PCR method. A clinical Y. pestis isolate (S19960127) exhibited high-level resistance to streptomycin (the MIC was 4,096 mg/L). The strain (biovar antiqua) was isolated from a pneumonic plague outbreak in 1996 in Tibet Autonomous Region, China, belonging to the Marmota himalayana Qinghai-Tibet Plateau plague focus. In contrast to previously reported streptomycin resistance mediated by conjugative plasmids, the genome sequencing and allelic replacement experiments demonstrated that an rpsL gene (ribosomal protein S12) mutation with substitution of amino-acid 43 (K43R) was responsible for the high-level resistance to streptomycin in strain S19960127, which is consistent with the mutation reported in some streptomycin-resistant Mycobacterium tuberculosis strains. Streptomycin is used as the first-line treatment against plague in many countries. The emergence of streptomycin resistance in Y. pestis represents a critical public health problem. So streptomycin susceptibility monitoring of Y. pestis isolates should not only include plasmid-mediated resistance but also include the ribosomal protein S12 gene (rpsL) mutation, especially when treatment failure is suspected due to antibiotic resistance.https://doi.org/10.1371/journal.pntd.0009324
collection DOAJ
language English
format Article
sources DOAJ
author Ruixia Dai
Jian He
Xi Zha
Yiting Wang
Xuefei Zhang
He Gao
Xiaoyan Yang
Juan Li
Youquan Xin
Yumeng Wang
Sheng Li
Juan Jin
Qi Zhang
Jixiang Bai
Yao Peng
Hailian Wu
Qingwen Zhang
Baiqing Wei
Jianguo Xu
Wei Li
spellingShingle Ruixia Dai
Jian He
Xi Zha
Yiting Wang
Xuefei Zhang
He Gao
Xiaoyan Yang
Juan Li
Youquan Xin
Yumeng Wang
Sheng Li
Juan Jin
Qi Zhang
Jixiang Bai
Yao Peng
Hailian Wu
Qingwen Zhang
Baiqing Wei
Jianguo Xu
Wei Li
A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.
PLoS Neglected Tropical Diseases
author_facet Ruixia Dai
Jian He
Xi Zha
Yiting Wang
Xuefei Zhang
He Gao
Xiaoyan Yang
Juan Li
Youquan Xin
Yumeng Wang
Sheng Li
Juan Jin
Qi Zhang
Jixiang Bai
Yao Peng
Hailian Wu
Qingwen Zhang
Baiqing Wei
Jianguo Xu
Wei Li
author_sort Ruixia Dai
title A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.
title_short A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.
title_full A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.
title_fullStr A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.
title_full_unstemmed A novel mechanism of streptomycin resistance in Yersinia pestis: Mutation in the rpsL gene.
title_sort novel mechanism of streptomycin resistance in yersinia pestis: mutation in the rpsl gene.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2021-04-01
description Streptomycin is considered to be one of the effective antibiotics for the treatment of plague. In order to investigate the streptomycin resistance of Y. pestis in China, we evaluated streptomycin susceptibility of 536 Y. pestis strains in China in vitro using the minimal inhibitory concentration (MIC) and screened streptomycin resistance-associated genes (strA and strB) by PCR method. A clinical Y. pestis isolate (S19960127) exhibited high-level resistance to streptomycin (the MIC was 4,096 mg/L). The strain (biovar antiqua) was isolated from a pneumonic plague outbreak in 1996 in Tibet Autonomous Region, China, belonging to the Marmota himalayana Qinghai-Tibet Plateau plague focus. In contrast to previously reported streptomycin resistance mediated by conjugative plasmids, the genome sequencing and allelic replacement experiments demonstrated that an rpsL gene (ribosomal protein S12) mutation with substitution of amino-acid 43 (K43R) was responsible for the high-level resistance to streptomycin in strain S19960127, which is consistent with the mutation reported in some streptomycin-resistant Mycobacterium tuberculosis strains. Streptomycin is used as the first-line treatment against plague in many countries. The emergence of streptomycin resistance in Y. pestis represents a critical public health problem. So streptomycin susceptibility monitoring of Y. pestis isolates should not only include plasmid-mediated resistance but also include the ribosomal protein S12 gene (rpsL) mutation, especially when treatment failure is suspected due to antibiotic resistance.
url https://doi.org/10.1371/journal.pntd.0009324
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