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The ins and outs of Mycobacterium tuberculosis drug susceptibility testing

期刊

CLINICAL MICROBIOLOGY AND INFECTION
卷 17, 期 8, 页码 1128-1134

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1469-0691.2011.03551.x

关键词

Molecular mechanisms; resistance; susceptibility testing; treatment; tuberculosis

资金

  1. German Research Council
  2. Bundesministerium fur Forschung und Technologie (Germany)
  3. European Commission
  4. Swiss National Research Foundation
  5. Bundesamt fur Gesundheit (Switzerland)
  6. University of Zurich
  7. Niedersachsischer Verein zur Bekampfung der Tuberkulose (Germany)
  8. UBS Optimus Foundation (Switzerland)

向作者/读者索取更多资源

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.

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