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Molecular Detection of Resistance Determinants

机译:抗性决定簇的分子检测

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摘要

The development of new antibiotics and the emergence of novel resistance mechanisms to counteract these drugs create a dynamic and challenging task for the clinical microbiology laboratory. The goal of antimicrobial resistance testing is to provide timely therapeutic options to guide the management of infectious diseases resulting from bacterial infections. Antimicrobial susceptibility has classically been determined using a variety of in vitro methods, such as disk diffusion, broth microdilution, and automated instrument-based methods. Using these methods, the reporting of MICs and interpretations can require 24 to 96 h after a pure culture of the suspected pathogen is obtained (6). Unfortunately, results obtained after 48 h are often of little clinical value and are unlikely to alter antimicrobial therapy. The extended turnaround associated with phenotypic antimicrobial resistance testing provides an opportunity for the use of alternative technologies capable of producing more timely results. The first reports in this supplement explore the manner in which the criteria for interpreting MICs are developed and the clinical relevance of antimicrobial susceptibility testing. In this report, we present an alternative to routine susceptibility testing and examine the role of molecular susceptibility testing now and in the future.
机译:新抗生素的开发和抵消这些药物的新型耐药机制的出现给临床微生物学实验室带来了充满挑战的动态任务。抗菌素耐药性测试的目的是提供及时的治疗选择,以指导细菌感染导致的传染病的处理。传统上,已使用多种体外方法(例如磁盘扩散法,肉汤微稀释法和基于仪器的自动化方法)确定了抗生素的敏感性。使用这些方法,在获得可疑病原体的纯培养后,可能需要24至96小时才能报告MIC和解释(6)。不幸的是,在48小时后获得的结果通常没有什么临床价值,并且不太可能改变抗微生物治疗。与表型抗药性测试相关的扩展周转提供了使用能够产生更及时结果的替代技术的机会。本增补中的第一份报告探讨了解释MIC的标准的开发方式以及抗微生物药敏试验的临床意义。在本报告中,我们提出了常规药敏试验的替代方法,并研究了分子药敏试验现在和将来的作用。

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