dc.contributor.author	Adhikari, Bal Ram
dc.date.accessioned	2022-03-04T05:22:56Z
dc.date.available	2022-03-04T05:22:56Z
dc.date.issued	2007
dc.description.abstract	Most first line anti-tuberculosis drugs have less in vitro activity against M. avium, M.intracellularand M. kansasii. Therefore rapid species identification and proper use of drugs are key requirements for the effective treatment and case management of tuberculosis as well as Mycobacterium avium complex-pulmonary disease (MAC-PD)and Mycobacterium kansasii-pulmonary disease (MK-PD). The development and evaluation of new diagnostic technique, which can diagnose causative agent in simple and rapid way, is the necessity of this century. Loop-Mediated Isoth rmalAmplification (LAMP) provides new possibilities of above requirements for directdetection of M. tuberculosis, M. avium complexandM.kansasiiin sputum samples. This study was carried out from October 2005 to September 2006. A total of 190 (129from 43 new suspected pulmonary tuberculosis patients and 61 from 61 follow uppatients) sputum samples were included in this study. All these samples were further processed for flurochrome staining but only 130(69 from new suspected pulmonary tuberculosis patients and 61 from follow up patients) sputum specimens were subjectedto culture and LAMP. Thus 130 sputum specimens were included in this study to compare them with microscopy, culture and LAMP. Among them 50(38.46%) werefound to be positive by flurochrome staining, culture and LAMP. Similarly 48(36.92%)samples were negative by all diagnostic methods. 1(0.77%) microscopy and culture positive sample was negative by LAMP. Similarly 3(2.31%) microscopy and LAMP positive cases were negative by culture. 3(2.31%) culture positive cases were negative by both Microscopy and LAMP. 8(6.16%) culture negative cases were positive by LAMP where as 17(13.07%) Microscopy negative samples were positive by culture and LAMP. Out of 78(100%) total LAMP positive cases, 76(97.44%) were positive with M.tuberculosis primer and remaining 2(2.56%) were positive with M. intracellular primer.None of the M. aviumand M. kansasii cases were found from the samples that were included in this study. While comparing the LAMP results with gold standard culture, the sensitivity,specificity, predictive value of positive test, predictive value of negative test, percentage of false negative and percentage of false positive of LAMP were found to be 94.36%,81.36%, 85.90%, 92.31%, 5.63% and 18.64% respectively. Similarly, LAMP had sensitivity 98.14% and specificity 67.11% while compare with microscopy. Therefore, LAMP is sensitive and specific molecular technique, which can be used effectively for the diagnosis of clinically, microscopically, and culturally confusing cases thus facilitating the effective treatment and case management of tuberculosis and other atypical my cobacterial infection. Due to its easy operation and rapid amplification efficiency, it can be used in well-equipped laboratories for clinical use if sample preparation, nucleic acid extraction and cross-contamination controls are addressed. Key words: M. tuberculosis, M aviumcomplex, M. kansasii, LAMP, TB, MAC-PD,MK-PD, Sputum	en_US
dc.identifier.uri	https://hdl.handle.net/20.500.14540/8696
dc.language.iso	en_US	en_US
dc.publisher	Department of Microbiology	en_US
dc.subject	M. tuberculosis	en_US
dc.subject	M aviumcomplex	en_US
dc.subject	TB	en_US
dc.subject	Sputum	en_US
dc.title	Use of Loop-Mediated Isothermal Amplification (Lamp) for Direct Detection of Mycobacterium in Sputum	en_US
dc.type	Thesis	en_US
local.academic.level	Masters	en_US
local.institute.title	Central Department of Microbiology	en_US

Use of Loop-Mediated Isothermal Amplification (Lamp) for Direct Detection of Mycobacterium in Sputum

Files

Original bundle

License bundle

Collections