DETEKSI MOLEKUL MUTASI GEN rpoB MYCOBACTERIUM TUBERCULOSIS PADA DAHAK DENGAN POLYMERASE CHAIN REACTION DAN SINGLE STRAND CONFORMATION POLYMORPHISM  

Oleh:

Notopuro, P B ; Nugraha, J. ; Notopuro, H

Jenis: Article from Journal - ilmiah nasional - terakreditasi DIKTI
Dalam koleksi: Indonesian Journal of Clinical Pathology and Medical Laboratory vol. 16 no. 02 (Mar. 2010), page 81-87.
Topik: MDR-TB; PCR-SSCp; Culture

Ketersediaan

Perpustakaan FK Nomor Panggil: I01.K.02 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

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Isi artikel

Tuberculosis is a chronic infectious disease which is found in the developing as well as the developed country. This disease is one of the community health problems which become the priority programs in the national as well as international health. In the last two decades, they can be found in the emergency tuberculosis problems that is related with the Multi Drug Resistance (MDR) Strain. The detection of rifampicin resistance in M. tuberculosis infection can help clinical laboratory to find the MDR strain. Related to th is problem the proportional culture method is still the gold standard for rifampicin resistance detection for M. tuberculosis infection. But this method needs 4-6 weeks to obtain the result, while its sensitivity is not very high. The development of the molecular detection for M. tuberculosis rifampicin resistance in a direct clinical specimen such as sputum, cerebrospinal fluid, etc. will give an improvement in the diagnosis, because it has an accurate, fast, sensitive and a specific result. Isolates from twenty six of M. tuberculosis derived from, the sputum of tuberculosis patients that have failed the tuberculosis treatment, were examined with the proportional culture method. In this study PCR-SSCP were used for the molecular detection of rifampicin resistancy using direct sputum samples. The proportional culture method was used as a gold standard for the rifampicin resistance detection. A set of primers was directed to conserve the region of rpoB gene of M. tubercuLosis. This RNA polymerase gene was encondes?, which is bound on rifampicin. A 157-bp fragment was amplified by PCR and analyzed by SSCP technique. The sensitivity of PCR-SSCP is 80% (high), its specificity is 95.2% (very high), the positive predictive value is 80% and the negative predictive value is 95.2%. Statistically there were no significant difference between the result of PCR-SSCP and the proportional culture method. Based on the study result, the molecular detection technique for rifampicin resistance on M. tuberculosis infection can be used as the screening device /means for Multi Drug Resistance Tuberculosis (MDR-TB), while the clinician waits the culure result.

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