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科威特医院中高水平氨基糖苷类耐药肠球菌的特征分析

Characterization of high-level aminoglycoside-resistant enterococci in Kuwait hospitals.

作者信息

Udo E E, Al-Sweih N, John P, Jacob L E, Mohanakrishnan S

机构信息

Department of Microbiology, Faculty of Medicine, Kuwait University, Safat 13110, Kuwait.

出版信息

Microb Drug Resist. 2004 Summer;10(2):139-45. doi: 10.1089/1076629041310037.

Abstract

This study investigated the distribution of genes for aminoglycoside-modifying enzymes (AME) and the genetic relatedness of high-level aminoglycoside-resistant enterococci isolated in Kuwait hospitals. A total of 117 enterococci, consisting of 109 Enterococcus faecalis, seven Enterococcus faecium, and one Enterococcus casseliflavus were studied. The MICs of gentamicin, kanamycin, amikacin, tobramycin, and streptomycin were determined by agar dilution and the genes encoding the AAC(6')- APH(2"), ANT(4'), APH(3'), APH (2")-Ib, APH (2")-Ic, APH (2")-Id, and ANT(6) enzymes were amplified by PCR. They were typed by pulsed-field gel electrophoresis (PFGE). Filter mating was used to transfer gentamicin resistance determinants. They were all resistant to kanamycin (MIC 2000 mg/L). Fifty-five isolates were resistant to gentamicin (MIC 500 mg/L), 72 were resistant to tobramycin (MIC 64 mg/L), 115 were resistant to amikacin (MIC 64 mg/L), and 97 were resistant to streptomycin (MIC 1000 mg/L). The aac(6')-Ie-aph(2")-Ia was detected in all isolates with gentamicin MIC 500 mg/L and in 15 isolates with gentamicin MIC 256 mg/L. The aph(3')-IIIa gene was detected in 101 isolates, whereas the ant(6')-Ia gene was detected in 85 of the 97 streptomycin-resistant isolates with MIC 1000 mg/L. The aac(6')-Ii gene was detected only in the seven E. faecium isolates. None of them contained ant(4')-Ia, aph(2")-Ib, aph(2")-Ic and aph(2")-Id. PFGE revealed heterogeneous patterns with no dominant clone. The results demonstrated that AME are common in aminoglycoside-resistant enterococci isolated in Kuwait. However, the absence of a dominant clone suggests that they acquired high-level aminoglycoside independently.

摘要

本研究调查了科威特医院分离出的高水平氨基糖苷类耐药肠球菌中氨基糖苷类修饰酶(AME)基因的分布及遗传相关性。共研究了117株肠球菌,其中包括109株粪肠球菌、7株屎肠球菌和1株格氏肠球菌。通过琼脂稀释法测定庆大霉素、卡那霉素、阿米卡星、妥布霉素和链霉素的最低抑菌浓度(MIC),并通过聚合酶链反应(PCR)扩增编码AAC(6')-APH(2")、ANT(4')、APH(3')、APH (2")-Ib、APH (2")-Ic、APH (2")-Id和ANT(6)酶的基因。采用脉冲场凝胶电泳(PFGE)对其进行分型。通过滤膜交配法转移庆大霉素耐药决定簇。所有菌株均对卡那霉素耐药(MIC为2000mg/L)。55株对庆大霉素耐药(MIC为500mg/L),72株对妥布霉素耐药(MIC为64mg/L),115株对阿米卡星耐药(MIC为64mg/L),97株对链霉素耐药(MIC为1000mg/L)。在所有庆大霉素MIC为500mg/L的菌株以及15株庆大霉素MIC为256mg/L的菌株中检测到aac(6')-Ie-aph(2")-Ia。在101株菌株中检测到aph(3')-IIIa基因,而在97株MIC为1000mg/L的链霉素耐药菌株中的85株中检测到ant(6')-Ia基因。仅在7株屎肠球菌菌株中检测到aac(6')-Ii基因。它们均未含有ant(4')-Ia、aph(2")-Ib、aph(2")-Ic和aph(2")-Id。PFGE显示出异质性模式,无优势克隆。结果表明,AME在科威特分离出的氨基糖苷类耐药肠球菌中很常见。然而,缺乏优势克隆表明它们是独立获得高水平氨基糖苷类耐药性的。

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