Rapid detection of Mycobacterium tuberculosis complex: PCR method using insertion sequence 6110

Rohani, M. and Khorshidi, A. and Moniri, R. and Torfeh, M. and Abddoshah, F. and Saffari, M. and Shajari, G. and Moosavi, G.A. (2009) Rapid detection of Mycobacterium tuberculosis complex: PCR method using insertion sequence 6110. Tehran University Medical Journal, 67 (3). pp. 173-177.

Full text not available from this repository.
Official URL: https://www.scopus.com/inward/record.uri?eid=2-s2....

Abstract

Background: Tuberculosis is an important cause of death in some countries. The world health organization estimates that if stronger measures are not taken up to control the prevalence of this disease, from 2000 to 2020 a billion people will be infected by the bacterium. According to time consuming of common detection methods of Mycobacterium tuberculosis such as culture, it is necessary to evaluate a rapid detection tests such as PCR. Rapid diagnosis of tuberculosis may have profound effects in patients' care According to importance of rapid detection and treatment of tuberculosis and for determine of sensitivity, specificity, positive predictive value and negative predictive value of PCR by using IS6110 this study was done in Kashan university of medical science. Methods: A total of 248 sputum samples from patients suspected of mycobacterial diseases were studied. DNA was extracted by boiling method. IS6110 PCR method by a specific pair of primers designed to amplify 123bp and 245bp sequences of the insertion sequence, 6110, in the M. tuberculosis genome was used to analyze sputum samples. Results: 32 out of 248 (12.9) of samples had positive culture. PCR yielded a sensitivity of 93.8 and specificity of 99.1 for the diagnosis of TB patients with TB confirmed by culture. There were two out of 32 (6.3) PCR-positive cases among the patients with non-TB disease. Conclusion: The findings of the present study indicate that Multiplex PCR may provide a faster method of detecting tuberculosis, thus enhancing diagnostic procedures and we conclude that the performance of an IS6110 PCR assay is valuable in the rapid diagnosis of tuberculosis.

Item Type: Article
Additional Information: cited By 3
Uncontrolled Keywords: DNA, article; bacterial genome; bacterium culture; bacterium detection; controlled study; diagnostic value; DNA denaturation; DNA extraction; gene insertion sequence; human; multiplex polymerase chain reaction; Mycobacterium tuberculosis; nonhuman; prediction; sensitivity and specificity; sputum analysis; tuberculosis
Subjects: Medicine
Immunology and Microbiology
Divisions: Faculty of Medicine > Basic Sciences > Department of Microbiology & Immunology
Depositing User: editor . 2
Date Deposited: 08 Jan 2017 16:37
Last Modified: 12 Mar 2017 13:42
URI: http://eprints.kaums.ac.ir/id/eprint/949

Actions (login required)

View Item View Item