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斯里兰卡产碳青霉烯酶肺炎克雷伯菌β-内酰胺类耐药的分子机制。

Molecular mechanisms of β-lactam resistance in carbapenemase-producing Klebsiella pneumoniae from Sri Lanka.

机构信息

School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Western Australia, Australia.

Department of Microbiology, University of Colombo, Colombo, Sri Lanka.

出版信息

J Med Microbiol. 2014 Aug;63(Pt 8):1087-1092. doi: 10.1099/jmm.0.076760-0. Epub 2014 May 22.

Abstract

Carbapenemases are increasingly important antimicrobial resistance determinants. Little is known about the carbapenem resistance mechanisms in Sri Lanka. We examined 22 carbapenem-resistant Klebsiella pneumoniae from Sri Lanka to determine their β-lactam resistance mechanisms. The predominant resistance mechanisms we detected in this study were OXA-181, NDM-1 carbapenemases and extended-spectrum β-lactamase CTX-M-15. All isolates were then genotyped by pulsed-field gel electrophoresis, variable-number tandem repeat sequence analysis and multilocus sequence typing, and seven distinct genotypes were observed. Five OXA-181-positive Klebsiella pneumoniae isolates were genotypically related to an isolate of Indian origin. Multilocus sequence typing found that these related isolates belong to ST-14, which has been associated with dissemination of OXA-181 from the Indian subcontinent. Other genotypes we discovered were ST-147 and ST-340, also associated with intercontinental spread of carbapenemases of suspected subcontinental origin. The major porin genes ompK35 and ompK36 from these isolates had insertions, deletions and substitutions. Some of these were exclusive to strains within single pulsotypes. We detected one ompK36 variant, ins AA134-135GD, in six ST-14- and six ST-147, blaOXA-181-positive isolates. This porin mutation was an independent predictor of high-level meropenem resistance in our entire Sri Lankan isolate collection (P=0.0030). Analysis of the Sri Lankan ST-14 and ST-147 ins AA134-135GD-positive isolates found ST-14 was more resistant to meropenem than other isolates (mean MIC: 32±0 µg ml(-1) and 20±9.47 µg ml(-1), respectively, P=0.0277). The likely international transmission of these carbapenem resistance determinants highlights the need for regional collaboration and prospective surveillance of carbapenem-resistant Enterobacteriaceae.

摘要

碳青霉烯酶是日益重要的抗菌药物耐药决定因素。关于斯里兰卡碳青霉烯类耐药机制知之甚少。我们检测了 22 株来自斯里兰卡的耐碳青霉烯类肺炎克雷伯菌,以确定其β-内酰胺类药物耐药机制。在本研究中,我们检测到的主要耐药机制是 OXA-181、NDM-1 碳青霉烯酶和超广谱β-内酰胺酶 CTX-M-15。然后,我们通过脉冲场凝胶电泳、可变数串联重复序列分析和多位点序列分型对所有分离株进行了基因分型,观察到 7 种不同的基因型。5 株 OXA-181 阳性肺炎克雷伯菌分离株与印度来源的分离株在基因型上具有亲缘关系。多位点序列分型发现,这些相关分离株属于 ST-14,该菌与 OXA-181 从印度次大陆的传播有关。我们发现的其他基因型为 ST-147 和 ST-340,也与亚大陆来源的碳青霉烯酶的洲际传播有关。这些分离株的主要孔蛋白基因 ompK35 和 ompK36 存在插入、缺失和替换。其中一些仅存在于单一脉冲群的菌株中。我们在 6 株 ST-14 和 6 株 ST-147、blaOXA-181 阳性分离株中检测到一种 ompK36 变体 ins AA134-135GD。在我们整个斯里兰卡分离株的集合中,这种孔蛋白突变是高水平美罗培南耐药的独立预测因子(P=0.0030)。对斯里兰卡 ST-14 和 ST-147 ins AA134-135GD 阳性分离株的分析发现,ST-14 对美罗培南的耐药性高于其他分离株(平均 MIC:32±0 µg ml(-1) 和 20±9.47 µg ml(-1),分别,P=0.0277)。这些碳青霉烯类耐药决定因素的可能国际传播突出表明需要进行区域合作和对耐碳青霉烯类肠杆菌科的前瞻性监测。

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