马来西亚登嘉楼某三级医院分离的耐碳青霉烯类和耐多粘菌素鲍曼不动杆菌的流行及遗传特征

ISRN Microbiology Pub Date : 2014-03-19 eCollection Date: 2014-01-01 DOI:10.1155/2014/953417
Soo-Sum Lean, Zarizal Suhaili, Salwani Ismail, Nor Iza A Rahman, Norlela Othman, Fatimah Haslina Abdullah, Zakaria Jusoh, Chew Chieng Yeo, Kwai-Lin Thong
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引用次数: 58

摘要

鲍曼不动杆菌引起的医院感染由于其对大多数抗菌素的耐药性增加而引起高度关注。在这项研究中,分析了马来西亚登嘉楼主要三级医院的54株非重复分离鲍曼不动杆菌的抗生素谱和基因型。在54株分离株中,39株(72.2%)为多药耐药(MDR)和碳青霉烯类耐药,而14株(25.9%)被归类为广泛耐药(XDR),并对多粘菌素B(“最后手段”药物)产生额外耐药。脉冲场凝胶电泳分析表明,耐多粘菌素菌株具有遗传多样性,而耐碳青霉烯菌株具有克隆亲缘关系。进一步研究了14株XDR菌株介导多粘菌素耐药性的基因pmrCAB和脂多糖生物合成基因lpxA、lpxC、lpxD和lpsB的突变。14株pmrA均存在P102H突变,pmrC和pmrB均未发现突变。在lpxA中未检测到突变,但每个耐多粘菌素分离物在lpxD中有2-4个氨基酸取代,在lpxC中有1-2个氨基酸取代。8株耐药菌株在lpsB中也显示出独特的H181Y突变。多粘菌素耐药程度值得关注,这里发现的新突变值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prevalence and Genetic Characterization of Carbapenem- and Polymyxin-Resistant Acinetobacter baumannii Isolated from a Tertiary Hospital in Terengganu, Malaysia.

Prevalence and Genetic Characterization of Carbapenem- and Polymyxin-Resistant Acinetobacter baumannii Isolated from a Tertiary Hospital in Terengganu, Malaysia.

Nosocomial infection caused by Acinetobacter baumannii is of great concern due to its increasing resistance to most antimicrobials. In this study, 54 nonrepeat isolates of A. baumannii from the main tertiary hospital in Terengganu, Malaysia, were analyzed for their antibiograms and genotypes. Out of the 54 isolates, 39 (72.2%) were multidrug resistant (MDR) and resistant to carbapenems whereas 14 (25.9%) were categorized as extensive drug resistant (XDR) with additional resistance to polymyxin B, the drug of "last resort." Pulsed-field gel electrophoresis analyses showed that the polymyxin-resistant isolates were genetically diverse while the carbapenem-resistant isolates were clonally related. The 14 XDR isolates were further investigated for mutations in genes known to mediate polymyxin resistance, namely, pmrCAB, and the lipopolysaccharide biosynthesis genes, lpxA, lpxC, lpxD, and lpsB. All 14 isolates had a P102H mutation in pmrA with no mutation detected in pmrC and pmrB. No mutation was detected in lpxA but each polymyxin-resistant isolate had 2-4 amino acid substitutions in lpxD and 1-2 substitutions in lpxC. Eight resistant isolates also displayed a unique H181Y mutation in lpsB. The extent of polymyxin resistance is of concern and the novel mutations discovered here warrant further investigations.

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