2006年首尔和京畿道4家医院不动杆菌对碳青霉烯耐药机制及分子流行病学研究

K. Roh, Chang Ki Kim, J. Yum, D. Yong, S. Jeong, C. Lim, C. Lee, Yunjung Cho, Kyungwon Lee, Y. Chong
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引用次数: 3

摘要

背景:越来越多的不动杆菌耐多种药物,包括卡培尼姆,已经成为一个严重的问题。方法:于2006年5 - 11月收集临床分离的不动杆菌,对其碳青霉烯类药物的耐药模式、耐药机制及分子流行病学进行研究。采用CLSI纸片扩散法和琼脂稀释法进行抗菌药敏试验。用PCR法检测产生金属β-内酰胺酶和OXA碳青霉烯酶的异构体。根据OXA的类型和ISAba1的存在比较了对碳青霉烯的抗性和水解活性。采用脉冲场凝胶电泳(PFGE)测定流行病学特征。结果:亚胺培南不敏感率为10% ~ 67%。151株载blaOXA-51-like的分离株中,75株同时携带blaOXA-51-like和ISAba1, 25株同时携带blaOXA-51-like、blaOXA-23-like和ISAba1。blaOXA-51-like和携带isaba1的分离株的碳青霉烯类mic均高于仅携带blaOXA-51-like的分离株。携带blaoxa -23-like的分离株碳青霉烯类mic均高于携带blaOXA-51-like和ISAba1的分离株。blaOXA-51-like和携带isaba1的分离株以及blaOXA-51-like、blaOXA-23-like和携带isaba1的分离株对oxacillin和碳青霉烯类具有较高的水解活性。大部分菌株对虎环素敏感,所有菌株对粘菌素敏感。脉冲场凝胶电泳显示,曾多次爆发blaoxa -23样和blaoxa -51样阳性菌株。结论:产碳青霉烯酶的OXA和碳青霉烯烯烯酶不敏感的Acineto菌株普遍存在。blaoxa - haboring分离株的传播可能使碳青霉烯耐药不动杆菌感染的治疗变得困难,需要进一步的监测研究来防止碳青霉烯耐药的传播。(中华临床微生物学杂志2010;13:27-33)
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Carbapenem Resistance Mechanisms and Molecular Epidemiology of Acinetobacter spp. from Four Hospitals in Seoul and Gyeonggi Province in 2006
Background: Increasing numbers of Acinetobacter spp. resistant to multiple drugs, including carbape- nem, has been a serious problem. The aims of this study were to determine carbapenem resistance pat- terns and mechanisms, as well as to study the mo- lecular epidemiology of Acinetobacter spp. Methods: Clinical isolates of Acinetobacter spp. were collected from May to November in 2006. Antimicro- bial susceptibility testing was performed using CLSI disk diffusion and agar dilution methods. Metallo-β- lactamase- and OXA carbapenemase-producing iso- lates were detected by PCR. Carbapenem resistance and hydrolytic activities were compared according to OXA type and presence of ISAba1. Pulsed-field gel electrophoresis (PFGE) was performed to determine the epidemiologic features. Results: The imipenem non-susceptible rates were variable from 10% to 67%. Among 151 isolates car- rying blaOXA-51-like, 75 isolates carried both blaOXA-51-like and ISAba1, and 25 isolates had both blaOXA-51-like, blaOXA-23-like, and ISAba1. Carbapenem MICs of both blaOXA-51-like and ISAba1-carrying isolates were higher than those with blaOXA-51-like only. Carbapenem MICs of blaOXA-23-like-carrying isolates were higher than those with both blaOXA-51-like and ISAba1. Both blaOXA-51-like and ISAba1-carrying isolates and blaOXA-51-like, blaOXA-23-like, and ISAba1-carrying isolates demonstrated higher hydrolysis activities in oxacillin and carbapenems. Most of the tested isolates were susceptible to tige- cycline, and all of them were susceptible to colistin. Pulsed-field gel electrophoresis suggested that there had been several outbreaks of blaOXA-23-like and blaOXA-51-like-positive strains. Conclusion: Carbapenem non-susceptible Acineto- bacter isolates and OXA carbapenemase-producing isolates were prevalent. Dissemination of blaOXA-har- boring isolates may make it difficult to treat infections due to carbapenem-resistant Acinetobacter spp. Further surveillance studies are required to prevent the spread of carbapenem resistance. (Korean J Clin Microbiol 2010;13:27-33)
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