Fast test for assessing the susceptibility of Mycobacterium tuberculosis to isoniazid and rifampin by real-time PCR

Memórias do Instituto Oswaldo Cruz

Maria Gisele Gonçalves²  Lucila Okuyama Fukasawa²  Rosangela Siqueira Oliveira¹  Maristela Marques Salgado²  Lee H Harrison¹  Kathleen A Shutt¹  Claudio Tavares Sacchi² 

[1] ,Instituto Adolfo Lutz Centro de Imunologia São Paulo SP ,Brasil

关键词: Mycobacterium tuberculosis;    RT-PCR;    drug resistance;    INH;    RIF;   

DOI  :  10.1590/S0074-02762012000700011

来源: SciELO

【 摘 要 】

Mycobacterium tuberculosis is the bacterium that causes tuberculosis (TB), a leading cause of death from infectious disease worldwide. Rapid diagnosis of resistant strains is important for the control of TB. Real-time polymerase chain reaction (RT-PCR) assays may detect all of the mutations that occur in the M. tuberculosis 81-bp core region of the rpoB gene, which is responsible for resistance to rifampin (RIF) and codon 315 of the katG gene and the inhA ribosomal binding site, which are responsible for isoniazid (INH). The goal of this study was to assess the performance of RT-PCR compared to traditional culture-based methods for determining the drug susceptibility of M. tuberculosis. BACTEC TM MGIT TM 960 was used as the gold standard method for phenotypic drug susceptibility testing. Susceptibilities to INH and RIF were also determined by genotyping of katG, inhA and rpoB genes. RT-PCR based on molecular beacons probes was used to detect specific point mutations associated with resistance. The sensitivities of RT-PCR in detecting INH resistance using katG and inhA targets individually were 55% and 25%, respectively and 73% when combined. The sensitivity of the RT-PCR assay in detecting RIF resistance was 99%. The median time to complete the RT-PCR assay was three-four hours. The specificities for tests were both 100%. Our results confirm that RT-PCR can detect INH and RIF resistance in less than four hours with high sensitivity.

【 授权许可】

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