Molecular detection of antimicrobial resistance

被引:305
作者
Fluit, AC [1 ]
Visser, MR [1 ]
Schmitz, FJ [1 ]
机构
[1] Univ Utrecht, Med Ctr, Eijkman Winkler Inst, NL-3508 GA Utrecht, Netherlands
关键词
D O I
10.1128/CMR.14.4.836-871.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The determination of antimicrobial susceptibility of a clinical isolate, especially with increasing resistance, is often crucial for the optimal antimicrobial therapy of infected patients. Nucleic acid-based assays for the detection of resistance may offer advantages over phenotypic assays. Examples are the detection of the methicillin resistance-encoding mecA gene in staphylococci, rifampin resistance in Mycobacterium tuberculosis, and the spread of resistance determinants across the globe. However, molecular assays for the detection of resistance have a number of limitations. New resistance mechanisms may be missed, and in some cases the number of different genes makes generating an assay too costly to compete with phenotypic assays. In addition, proper quality control for molecular assays poses a problem for many laboratories, and this results in questionable results at best. The development of new molecular techniques, e.g., PCR using molecular beacons and DNA chips, expands the possibilities for monitoring resistance. Although molecular techniques for the detection of antimicrobial resistance clearly are winning a place in routine diagnostics, phenotypic assays are still the method of choice for most resistance determinations. In this review, we describe the applications of molecular techniques for the detection of antimicrobial resistance and the current state of the art.
引用
收藏
页码:836 / 871
页数:36
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