Angkana ChaiprasertTherdsak PrammanananNipa TingtoyPreeyawis Na-UbolSomboon SrimuangKittipan SamerpitakWatcharin RangsipanuratnMahidol UniversityKhon Kaen UniversityHuachiew Chalermprakiet UniversityThailand National Center for Genetic Engineering and Biotechnology2018-08-202018-08-202006-12-01Southeast Asian Journal of Tropical Medicine and Public Health. Vol.37, No.3 (2006), 494-502012515622-s2.0-33845749105https://repository.li.mahidol.ac.th/handle/123456789/23465A rapid, inexpensive, simple, and accurate multiplex polymerase chain reaction (PCR) was developed in a single tube for identification of Mycobacterium tuberculosis. Assessment of sensitivity and specificity of simple PCR was performed with 116 strains of M. tuberculosis complex (MTC) and 144 strains of nontuberculous mycobacteria (NTM) compared with the biochemical method. Specific amplification of KS4, MTC-specific DNA fragment, was found in 98% (114/116) of MTC and not detected in 99% (143/144) of NTM. Amplification of the mtp40 gene revealed 95% sensitivity (100/105 strains of M. tuberculosis) and 77% specificity (not found in 119/155 mycobacterial strains). A multiplex PCR method based on the combination of KS4- and mrp40-derived primers was used for identification of M. tuberculosis. Crude DNA from slow growing mycobacteria with cream rough colonies that showed both 768-bp amplified product for KS4 and 396-bp for mtp40 was identified as M. tuberculosis whereas that from MTC gave only the 768-bp product.Mahidol UniversityMedicineArticleSCOPUS