TY - JOUR KW - Adult KW - Age Factors KW - Aged KW - Base Sequence KW - Case-Control Studies KW - DNA, Bacterial KW - Female KW - Humans KW - Incidence KW - Iran KW - leprosy KW - Male KW - Middle Aged KW - Molecular Sequence Data KW - Mycobacterium tuberculosis KW - polymerase chain reaction KW - Sensitivity and Specificity KW - Sputum KW - Tuberculin Test KW - Tuberculosis AU - Rafi A AU - Feval F AB -
In this study of leprosy patients with putative tuberculosis, the polymerase chain reaction (PCR), one of the most reliable and sensitive molecular diagnostic methods, was carried out for the specific detection of Mycobacterium tuberculosis DNA. Sputum samples from 43 patients at Baba Baghi Leprosarium in Iran were tested. The DNA extraction method was based on the lysing and nuclease-inactivating properties of guanidinium thiocyanate (GuSCN) together with the nucleic acid binding properties of diatoms or silica particles. Primers for a 123-base pair (bp) fragment of the repetitive DNA sequence of M. tuberculosis were used for the PCR assay. The results of PCR were compared with direct microscopy and culture. In total, 14% of the patients in this study were found to be PCR positive for M. tuberculosis. No positive results were found by direct microscopy for acid fast bacilli (AFB) and culture. It was thought probable that the positive PCR results indicated the tuberculosis (TB) in such treated leprosy patients.
BT - The Southeast Asian journal of tropical medicine and public health C1 - http://www.ncbi.nlm.nih.gov/pubmed/8629055?dopt=Abstract DA - 1995 Jun IS - 2 J2 - Southeast Asian J. Trop. Med. Public Health LA - eng N2 -In this study of leprosy patients with putative tuberculosis, the polymerase chain reaction (PCR), one of the most reliable and sensitive molecular diagnostic methods, was carried out for the specific detection of Mycobacterium tuberculosis DNA. Sputum samples from 43 patients at Baba Baghi Leprosarium in Iran were tested. The DNA extraction method was based on the lysing and nuclease-inactivating properties of guanidinium thiocyanate (GuSCN) together with the nucleic acid binding properties of diatoms or silica particles. Primers for a 123-base pair (bp) fragment of the repetitive DNA sequence of M. tuberculosis were used for the PCR assay. The results of PCR were compared with direct microscopy and culture. In total, 14% of the patients in this study were found to be PCR positive for M. tuberculosis. No positive results were found by direct microscopy for acid fast bacilli (AFB) and culture. It was thought probable that the positive PCR results indicated the tuberculosis (TB) in such treated leprosy patients.
PY - 1995 SP - 253 EP - 7 T2 - The Southeast Asian journal of tropical medicine and public health TI - PCR to detect Mycobacterium tuberculosis DNA in sputum samples from treated leprosy patients with putative tuberculosis. VL - 26 SN - 0125-1562 ER -