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The rapid diagnosis of isoniazid and rifampicin resistance in Mycobacterium tuberculosis--a molecular story. | LitMetric

The rapid diagnosis of isoniazid and rifampicin resistance in Mycobacterium tuberculosis--a molecular story.

J Med Microbiol

Mycobacterium Reference Unit, Public Health Laboratory Service, Dulwich Hospital, London.

Published: March 1998

AI Article Synopsis

  • Isoniazid and rifampicin resistance testing involves methods like resistance ratios and absolute concentration, but standardizing these methods is challenging.
  • The WHO is working to create standardized data on drug resistance, with broth-based methods being faster (7-14 days) compared to solid media, though some methods are costly and involve radioactive waste.
  • New techniques using mycobacteriophages and advanced molecular detection methods are emerging, but they rely on knowledge of specific genes and mutations, leaving some resistance mechanisms still unknown.

Article Abstract

Isoniazid and rifampicin resistance are assayed phenotypically by the resistance ratio, absolute concentration or proportion methods. Assay methods are often difficult to standardise and the World Health Organization (WHO) Global Programme on Drug Resistance is attempting to produce standardised drug resistance data worldwide. Broth-based methods are faster than solid media systems, and a commercial radiometric system, the Bactec 460, is arguably the fastest method and permits testing to be completed within 7-14 days; however, this method is expensive and requires disposal of radioactive material. Novel phenotypic methods that utilise mycobacteriophages have shown promise. Other molecular detection systems require knowledge of the genes encoding the drug target (the inhA/mabA, katG, oxyR and ahpC genes for isoniazid; rpoB for rifampicin) and the mutations producing resistance. These genotypic methods are limited in that not all resistance mechanisms are known, but advanced assays for rifampicin resistance that use gene sequencing, heteroduplex analysis, solid-phase hybridisation or single-strand conformation polymorphism analysis are becoming available.

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Source
http://dx.doi.org/10.1099/00222615-47-3-189DOI Listing

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