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Improved rapid molecular diagnosis of multidrug-resistant tuberculosis using a new reverse hybridization assay, REBA MTB-MDR

Authors
 Hyeeun Bang ; Sangjung Park ; Hyeyoung Lee ; Sang-Nae Cho ; Clifton E. Barry, III ; Laura E. Via ; Isdore Chola Shamputa ; Taeksun Song ; Dae Yoon Kim ; Eunjin Cho ; Hyunwoo Jin ; Joohwan Hwang 
Citation
 Journal of Medical Microbiology, Vol.60(pt 10) : 1447~1454, 2011 
Journal Title
 Journal of Medical Microbiology 
ISSN
 0022-2615 
Issue Date
2011
Abstract
Rapid diagnosis of multidrug-resistant tuberculosis (MDR-TB) is essential for the prompt initiation of effective second-line therapy to improve treatment outcome and limit transmission of this obstinate disease. A variety of molecular methods that enable the rapid detection of mutations implicated in MDR-TB have been developed. The sensitivity of the methods is dependent, in principle, on the repertoire of mutations being detected, which is typically limited to mutations in the genes rpoB, katG and the promoter region of inhA. In this study, a new reverse hybridization assay, REBA MTB-MDR (M&D), that probes mutations in the oxyR-ahpC intergenic region, in addition to those in rpoB, katG and the inhA promoter region, was evaluated. A set of 240 Mycobacterium tuberculosis clinical isolates from patients receiving retreatment regimens was subjected to conventional phenotypic drug-susceptibility testing (DST) and the REBA MTB-MDR assay. The nucleotide sequences of the loci known to be involved in drug resistance were determined for comparison. In brief, the results showed that the REBA MTB-MDR assay efficiently recognized nucleotide changes in the oxyR-ahpC intergenic region as well as those in rpoB, katG and the inhA promoter region with higher sensitivity, resulting in an 81.0 % detection rate for isoniazid resistance. Inclusion of the oxyR-ahpC intergenic region in the REBA MTB-MDR assay improved the overall sensitivity of molecular DST for MDR-TB from 73.1 to 79.9 %.
URI
http://ir.ymlib.yonsei.ac.kr/handle/22282913/93920
DOI
10.1099/jmm.0.032292-0
Appears in Collections:
1. 연구논문 > 1. College of Medicine > Dept. of Microbiology
Yonsei Authors
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