临床微生物实验室双盘扩散法作为ESBL产生生物表型确认方法的局限性

Thass N, R. Vs
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引用次数: 0

摘要

近年来,世界范围内越来越多地报道了产生革兰氏阴性菌的扩展谱β-内酰胺酶(ESBL)。1扩展谱β-内酰胺酶能够通过水解青霉素类、第一代、第二代和第三代头孢菌素和氨曲南(但不包括头孢霉素或碳青霉烯类)使细菌产生耐药性。许多临床微生物学实验室使用双盘扩散法记录ESBLs,随后报告给临床医生。在常规微生物实验室进行ESBLs基因型检测是不可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Limitation of Double Disc Diffusion Method as a phenotypic confirmatory method for ESBL producing organisms in Clinical Microbiology Laboratory
In the recent years, Extended Spectrum β-lactamase (ESBL) producing gram negative bacteria are increasingly being reported worldwide .1 Extended spectrum β-lactamases are capable of conferring bacterial resistance to the penicillins, first, second, and third generation cephalosporins, and aztreonam (but not the cephamycins or carbapenems) by hydrolysis of these antibiotics. 2 Many Clinical Microbiology laboratories use double disc diffusion method to document ESBLs, which are subsequently reported to the clinicians. Performing genotypic tests for ESBLs in a routine microbiology laboratory is not feasible.
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