Analysis of Aminoglycoside Modifying Enzyme Genes Responsible for High-Level Aminoglycoside Resistance among Enterococcal Isolates.

IF 1.1 Q4 MICROBIOLOGY
Journal of Pathogens Pub Date : 2017-01-01 Epub Date: 2017-12-24 DOI:10.1155/2017/3256952
Vishal Shete, Naveen Grover, Mahadevan Kumar
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引用次数: 24

Abstract

Enzymatic modification results in high-level resistance to aminoglycoside (HLAR), which eliminates the synergistic bactericidal effect of combined exposure to a cell wall-active agent and an aminoglycoside. So aim of the study was to determine prevalence of HLAR enterococcal isolate and to study distribution of aminoglycoside modifying enzyme genes in them. A total of 100 nonrepeat isolates of enterococci from various clinical samples were analyzed. As per Clinical and Laboratory Standards Institute guidelines enterococci were screened for HLAR by Kirby-Bauer disc diffusion method. Minimum inhibitory concentration of all isolates for gentamicin and streptomycin was determined by E-test. Multiplex polymerase chain reaction (PCR) was carried out for HLAR enterococcal isolates to identify aminoglycoside modifying enzymes genes responsible for resistance. 60% isolates were found to be high-level gentamicin resistant (HLGR) whereas 45% isolates were found to be high-level streptomycin resistant (HLSR). By multiplex PCR 80% HLGR isolates carried bifunctional aminoglycoside modifying enzyme gene aac(6')-Ie-aph(2'')-Ia whereas 18 out of 45 high-level streptomycin resistant, that is, 40%, isolates carried aph(3')-IIIa. However, aph(2'')-Ib, aph(2'')-Ic, aph(2'')-Id, and ant(4')-Ia genes which encode other aminoglycosides modifying enzymes were not detected. Bifunctional aminoglycoside modifying enzyme gene aac(6')-Ie-aph(2'')-Ia is the predominant gene responsible for HLAR.

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肠球菌高水平氨基糖苷耐药氨基糖苷修饰酶基因分析。
酶修饰导致对氨基糖苷(HLAR)的高水平抗性,从而消除了联合暴露于细胞壁活性剂和氨基糖苷的协同杀菌作用。因此,本研究的目的是确定hla分离肠球菌的流行情况,并研究其氨基糖苷修饰酶基因的分布。对来自不同临床样本的100株非重复肠球菌进行了分析。根据临床和实验室标准协会的指导方针,采用Kirby-Bauer圆盘扩散法筛选肠球菌是否患有hla。采用e -法测定各菌株对庆大霉素和链霉素的最低抑菌浓度。采用多重聚合酶链反应(PCR)方法对分离的HLAR肠球菌进行耐药氨基糖苷修饰酶基因的鉴定。60%的分离株具有高度庆大霉素耐药(HLGR), 45%的分离株具有高度链霉素耐药(HLSR)。通过多重PCR, 80%的HLGR分离株携带双功能氨基糖苷修饰酶基因aac(6’)-Ie-aph(2’)-Ia,而45株高水平链霉素耐药株中有18株携带aph(3’)-IIIa,即40%。而编码其他氨基糖苷修饰酶的aph(2”)-Ib、aph(2”)-Ic、aph(2”)-Id和ant(4”)-Ia基因未检出。双功能氨基糖苷修饰酶基因aac(6’)-Ie-aph(2’)-Ia是导致hla的主要基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pathogens
Journal of Pathogens MICROBIOLOGY-
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审稿时长
15 weeks
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