质粒上毒素-抗毒素系统与产生CTX-15的肺炎克雷伯菌ST11分离株持久性形成的关系

Q4 Immunology and Microbiology Journal of Bacteriology and Virology Pub Date : 2019-06-01 DOI:10.4167/JBV.2019.49.2.53
Eun Seon Chung, So Yeon Kim, K. Ko
{"title":"质粒上毒素-抗毒素系统与产生CTX-15的肺炎克雷伯菌ST11分离株持久性形成的关系","authors":"Eun Seon Chung, So Yeon Kim, K. Ko","doi":"10.4167/JBV.2019.49.2.53","DOIUrl":null,"url":null,"abstract":"We investigated the effect of toxin-antitoxin (TA) systems in bla CTX-M-15 -bearing plasmids of Klebsiella pneumoniae on persister formation. The persister formation rate was notably high in transconjugants in plasmids bearing TA system than the transconjugants in plasmids bearing no TA systems. Activation of relA and spoT expression was higher in transconjugants with plasmids bearing TA systems. Thus, TA systems in plasmids may contribute to the maintenance of bla CTX-M-15 -bearing plasmids and host survival via persister formation. Plasmids were obtained from four CTX-M-15-producing K. pneumoniae ST11 clinical isolates that were collected from patients in Hong Kong, Malaysia, India, and Thailand (HK02-026, M16-13, IN03-01, and TH02-34, respectively). Their whole plasmid sequences were determined previously (GenBank accession numbers, KY751926, KY751925, KY499796, and KY499797) (14). While TA genes, such as pemIK, mok-hok, and vagCD, were identified on the bla CTX-M-15 -bearing plasmids of HK02-026 and M16-13 (TA+), the bla CTX-M-15 -bearing plasmids of IN03-01 and TH02-34 had no TA genes (TA – ). Then, recovered plasmids were transferred to E. coli J53 cells, as described previously (6). In vitro antimicrobial susceptibility testing was performed by the broth microdilution method according to Clinical and Laboratory Standards Institute (CLSI) guidelines (15), and susceptibility was defined according to CLSI breakpoints. E. coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853 were used as control strains.","PeriodicalId":39739,"journal":{"name":"Journal of Bacteriology and Virology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4167/JBV.2019.49.2.53","citationCount":"0","resultStr":"{\"title\":\"Association Between Toxin-antitoxin Systems on Plasmids and Persister Formation in CTX-15-producing Klebsiella pneumoniae ST11 Isolates\",\"authors\":\"Eun Seon Chung, So Yeon Kim, K. Ko\",\"doi\":\"10.4167/JBV.2019.49.2.53\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We investigated the effect of toxin-antitoxin (TA) systems in bla CTX-M-15 -bearing plasmids of Klebsiella pneumoniae on persister formation. The persister formation rate was notably high in transconjugants in plasmids bearing TA system than the transconjugants in plasmids bearing no TA systems. Activation of relA and spoT expression was higher in transconjugants with plasmids bearing TA systems. Thus, TA systems in plasmids may contribute to the maintenance of bla CTX-M-15 -bearing plasmids and host survival via persister formation. Plasmids were obtained from four CTX-M-15-producing K. pneumoniae ST11 clinical isolates that were collected from patients in Hong Kong, Malaysia, India, and Thailand (HK02-026, M16-13, IN03-01, and TH02-34, respectively). Their whole plasmid sequences were determined previously (GenBank accession numbers, KY751926, KY751925, KY499796, and KY499797) (14). While TA genes, such as pemIK, mok-hok, and vagCD, were identified on the bla CTX-M-15 -bearing plasmids of HK02-026 and M16-13 (TA+), the bla CTX-M-15 -bearing plasmids of IN03-01 and TH02-34 had no TA genes (TA – ). Then, recovered plasmids were transferred to E. coli J53 cells, as described previously (6). In vitro antimicrobial susceptibility testing was performed by the broth microdilution method according to Clinical and Laboratory Standards Institute (CLSI) guidelines (15), and susceptibility was defined according to CLSI breakpoints. E. coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853 were used as control strains.\",\"PeriodicalId\":39739,\"journal\":{\"name\":\"Journal of Bacteriology and Virology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.4167/JBV.2019.49.2.53\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Bacteriology and Virology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4167/JBV.2019.49.2.53\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology and Virology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4167/JBV.2019.49.2.53","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 0

摘要

我们研究了携带肺炎克雷伯菌CTX-M-15的bla质粒中毒素-抗毒素(TA)系统对持久性细菌形成的影响。携带TA系统的质粒中的转偶联物中的持续物形成率显著高于不携带TA系统质粒中的跨偶联物。在具有携带TA系统的质粒的转导偶联物中,relA和spoT表达的激活更高。因此,质粒中的TA系统可能有助于维持携带bla CTX-M-15的质粒,并通过持续形成宿主存活。从香港、马来西亚、印度和泰国的患者中收集的四种产生CTX-M-15的肺炎克雷伯菌ST11临床分离株(分别为HK02-026、M16-13、IN03-01和TH02-34)获得质粒。它们的全质粒序列先前已确定(GenBank登录号,KY751926、KY751925、KY499796和KY499797)(14)。虽然在HK02-026和M16-13(TA+)的bla CTX-M-15携带质粒上鉴定了TA基因,如pemIK、mok-hok和vagCD,但IN03-01和TH02-34的bla CTX-M-15携带质粒没有TA基因(TA-)。然后,将回收的质粒转移到大肠杆菌J53细胞中,如前所述(6)。根据临床和实验室标准研究所(CLSI)指南(15),通过肉汤微量稀释法进行体外抗菌药敏试验,并根据CLSI断点定义药敏。使用大肠杆菌ATCC 25922和铜绿假单胞菌ATCC 27853作为对照菌株。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Association Between Toxin-antitoxin Systems on Plasmids and Persister Formation in CTX-15-producing Klebsiella pneumoniae ST11 Isolates
We investigated the effect of toxin-antitoxin (TA) systems in bla CTX-M-15 -bearing plasmids of Klebsiella pneumoniae on persister formation. The persister formation rate was notably high in transconjugants in plasmids bearing TA system than the transconjugants in plasmids bearing no TA systems. Activation of relA and spoT expression was higher in transconjugants with plasmids bearing TA systems. Thus, TA systems in plasmids may contribute to the maintenance of bla CTX-M-15 -bearing plasmids and host survival via persister formation. Plasmids were obtained from four CTX-M-15-producing K. pneumoniae ST11 clinical isolates that were collected from patients in Hong Kong, Malaysia, India, and Thailand (HK02-026, M16-13, IN03-01, and TH02-34, respectively). Their whole plasmid sequences were determined previously (GenBank accession numbers, KY751926, KY751925, KY499796, and KY499797) (14). While TA genes, such as pemIK, mok-hok, and vagCD, were identified on the bla CTX-M-15 -bearing plasmids of HK02-026 and M16-13 (TA+), the bla CTX-M-15 -bearing plasmids of IN03-01 and TH02-34 had no TA genes (TA – ). Then, recovered plasmids were transferred to E. coli J53 cells, as described previously (6). In vitro antimicrobial susceptibility testing was performed by the broth microdilution method according to Clinical and Laboratory Standards Institute (CLSI) guidelines (15), and susceptibility was defined according to CLSI breakpoints. E. coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853 were used as control strains.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Bacteriology and Virology
Journal of Bacteriology and Virology Immunology and Microbiology-Immunology
CiteScore
0.80
自引率
0.00%
发文量
16
期刊最新文献
Plazomicin—a New Aminoglycoside—for Treating Complicated Urinary Tract Infections Trends in Norovirus Distribution among the Children of Childcare Center Intestinal Organoid as a Research Platform for the Virus-host Interaction Distribution and Transmission of Enterobacteriaceae Clinical Isolates Co-resistant to Colistin and Carbapenem in Gangwon Province, South Korea Antiviral Activity of Flavonoids Against Non-polio Enteroviruses
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1