The ins and outs of Mycobacterium tuberculosis drug susceptibility testing

被引:88
作者
Boettger, E. C. [1 ]
机构
[1] Univ Zurich, Inst Med Mikrobiol, CH-8006 Zurich, Switzerland
基金
新加坡国家研究基金会;
关键词
Molecular mechanisms; resistance; susceptibility testing; treatment; tuberculosis; 16S RIBOSOMAL-RNA; MULTIDRUG-RESISTANT TUBERCULOSIS; STREPTOMYCIN RESISTANCE; ISONIAZID-RESISTANT; MUTATIONS; KANAMYCIN; GENE; RIFAMPICIN; INHA; KATG;
D O I
10.1111/j.1469-0691.2011.03551.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Drug susceptibility testing of Mycobacterium tuberculosis in the diagnostic laboratory classifies clinical isolates as either drug-'resistant' or drug-'susceptible', on the basis of their ability to grow in the presence of a 'critical concentration' of the test compound. From knowledge of the mechanisms that underlie drug resistance, it has become evident that drug resistance in M. tuberculosis is quite heterogeneous and involves low-level, moderate-level and high-level drug resistance phenotypes. Different mutations are associated with different levels of phenotypic resistance, and the acquisition of a genetic alteration leading to a decrease in drug susceptibility does not inevitably exclude the affected compound from treatment regimens. As a result, the simple categorization of clinical M. tuberculosis isolates as 'resistant' on the basis of susceptibility testing at 'critical concentrations' may need to be revised and supplemented by quantitative measures of resistance testing to reflect the biological complexity of drug resistance, with the view of optimally exploiting the compounds available for treatment.
引用
收藏
页码:1128 / 1134
页数:7
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