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
Eun Seon Chung, So Yeon Kim, K. Ko
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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。
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.
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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
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