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首页> 外文期刊>Microbial drug resistance: MDR : Mechanisms, epidemiology, and disease >Alliance of Efflux Pumps with beta-Lactamases in Multidrug-Resistant Klebsiella pneumoniae Isolates
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Alliance of Efflux Pumps with beta-Lactamases in Multidrug-Resistant Klebsiella pneumoniae Isolates

机译:在多药抗性Klebsiella肺炎中的β-内酰胺酶中的Efflux泵联盟

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摘要

Nosocomial infections caused by Klebsiella pneumoniae are primarily characterized by a high prevalence of extended-spectrum beta-lactamases (ESBL's) and a soaring pace of carbapenemase dissemination. Availability of limited antimicrobial agents as a therapeutic option for multidrug-resistant bacteria raises an alarming concern. This study aimed at the molecular characterization of multidrug-resistant K. pneumoniae clinical isolates and studied the role of efflux pumps in beta-lactam resistance. Thirty-three isolates confirmed as ESBL-positive K. pneumoniae that harbored resistance genes to major classes of antibiotics. The results showed that CTX-M15 was the preeminent beta-lactamase along with carbapenemases in ESBL-positive isolates. However, the efficacy of different antibiotics varied in the presence of lactamase inhibitors and efflux pump inhibitors (EPIs). Those showing increased efficacy of antibiotics with EPI were further explored for the expression of efflux pump genes and expressed a significantly different level of efflux pumps. We found that an isolate had higher expression of kpnF (SMR family) and kdeA (MATE family) pump genes relative to RND family pump genes. No mutations were observed in the genes for porins. Together, the findings suggest that beta-lactamases are not the only single factor responsible for providing resistance against the existing beta-lactam drugs. Resistance may increase many folds by simultaneous expression of RND family (the most prominent family in Gram-negative bacteria) and other efflux pump family.
机译:Klebsiella肺炎引起的医院感染主要是延伸光谱β-内酰胺酶(ESBL的)的高普及和慢性碳癌溶解的速度。有限抗微生物剂作为多药物抗性细菌的治疗选择提高了令人惊叹的问题。本研究旨在抗抑制肺炎肝癌临床分离物的分子表征,并研究了β-内酰胺型抗缺口泵的作用。三十三个分离物确认为ESBL阳性K.肺炎,其抗抗生素患者抗生素。结果表明,CTX-M15是ESBL阳性分离株中的肽β-内酰胺酶以及Carbapenemase。然而,不同抗生素在内酰胺酶抑制剂和流出泵抑制剂(EPIS)存在下变化的疗效。表现出抗生素与EPI的效果增加的那些,用于表达外排泵基因,表达了显着不同的流出泵水平。我们发现,相对于RND族泵基因,分离物具有更高的KPNF(SMR系列)和KDEA(MATE系列)泵基因的表达。在孔林根基因中没有观察到突变。结果表明,β-内酰胺酶不是负责为现有β-内酰胺药物提供抗性的唯一单因素。通过同时表达RND家族(革兰氏阴性细菌中最突出的家庭)和其他流出泵系列,抗性可能会增加许多折叠。

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