Publication: Distribution of rpoB mutations among multidrug-resistant Mycobacterium tuberculosis (MDRTB) strains from Thailand and development of a rapid method for mutation detection
Issued Date
2008-01-01
Resource Type
ISSN
14690691
1198743X
1198743X
Other identifier(s)
2-s2.0-41949099041
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Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Clinical Microbiology and Infection. Vol.14, No.5 (2008), 446-453
Suggested Citation
T. Prammananan, W. Cheunoy, D. Taechamahapun, J. Yorsangsukkamol, S. Phunpruch, P. Phdarat, M. Leechawengwong, A. Chaiprasert Distribution of rpoB mutations among multidrug-resistant Mycobacterium tuberculosis (MDRTB) strains from Thailand and development of a rapid method for mutation detection. Clinical Microbiology and Infection. Vol.14, No.5 (2008), 446-453. doi:10.1111/j.1469-0691.2008.01951.x Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/19842
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Title
Distribution of rpoB mutations among multidrug-resistant Mycobacterium tuberculosis (MDRTB) strains from Thailand and development of a rapid method for mutation detection
Abstract
Since rifampicin resistance is a surrogate marker for multidrug-resistant Mycobacterium tuberculosis (MDRTB), the present study aimed to investigate rpoB mutations conferring rifampicin resistance in M. tuberculosis strains from Thailand, and to develop a rapid, inexpensive and simple PCR-based method for rapid detection of MDRTB. Overall, 267 M. tuberculosis isolates, including 143 MDRTB isolates, were investigated. Isolates of the Beijing strain predominated among the MDRTB isolates (79.1%), but accounted for only 45.5% of the susceptible isolates. Mutations in the rpoB gene were found most commonly at codons 531, 526 and 516 (58%, 25.2% and 9.1%, respectively). A multiplex allele-specific PCR was developed and tested with 216 clinical isolates. In comparison with the proportion method, the method showed 94.2% sensitivity and 100% specificity, and had a 100% positive predictive value and a 95% negative predictive value, which suggested that this method could be useful for screening for MDRTB, particularly in resource-limited countries. © 2008 European Society of Clinical Microbiology and Infectious Diseases.