Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/474603
Title: Study of mutations in rpo b gene in rifampicin resistant mycobacterium tuberculosis isolates from doda region of jammu and kashmir
Researcher: Akhtar Sameera
Guide(s): kaur Amandeep
Keywords: Life Sciences
Microbiology
University: Adesh University
Completed Date: 2023
Abstract: newline newline The current prospective study aimed to investigate mutations in rpo-B gene in Rifampicin resistant Mycobacterium tuberculosis isolates from Doda region of Jammu and Kashmir. It was observed that, out of 3600 samples processed the specificity of Ziehl- Neelsen (ZN) staining was lower as compared to other methods as 233 patients were found positive using CBNAAT and 203 were found positive with ZN Staining. There were 203 (87.12%) positive cases and 30 (12.88%) negative cases. From both ZN staining and CBNAAT, it was confirmed that mostly positive cases in males were in the age group of 21-90 years while for females, it was 21-80 years. In common for both sexes, maximum TB positivity was seen for 51-60 years (64; 27.46%) and 21-30 years (63; 27.3%). After analysing for rifampicin resistance from 233 pulmonary tuberculosis patients, only 8 patients showed positive results where 2 were from the age group of 11-30 years (25%), 4 from 31-50 years newline(50%) and 2 were above 50 (25%). It was found that 128 (54.9%) males and 105 (45%) females were positive for tuberculosis. For rifampicin resistance also, there were more male patients (n=5) (62.5%) than female patients (n=3) (37.5%). This study is conducted for the first time in Doda region to detect mutations (81bp) against rifampicin via CBNAAT which lied within the hot spot region of 81bp RRDR of rpo-B gene of 08 M. tuberculosis clinical isolates, although codon regions remained similar to already reported ones (516, 526, 531) in tuberculosis strains obtained from MDR TB positive patients. newlineThis study will open new horizons for early detection and improvement of drug treatment regimens to make it more effective to treat the drug resistance in TB. newline
Pagination: i - xvi, 1 - 142
URI: http://hdl.handle.net/10603/474603
Appears in Departments:Department of Interdisciplinary Biomedical Research

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02 - preliminary pages.pdfAttached File223.36 kBAdobe PDFView/Open
03 - table of contents.pdf486.74 kBAdobe PDFView/Open
04 - abstract.pdf14.69 kBAdobe PDFView/Open
05 - chapter 1.pdf316.14 kBAdobe PDFView/Open
06 - chapter 2.pdf552.54 kBAdobe PDFView/Open
07 - chapter 3.pdf874.26 kBAdobe PDFView/Open
08 - chapter 4.pdf1.07 MBAdobe PDFView/Open
09 - chapter 5.pdf375.28 kBAdobe PDFView/Open
10 - summary.pdf302.09 kBAdobe PDFView/Open
11 - refrences.pdf504.97 kBAdobe PDFView/Open
12 - appendix a.pdf465.75 kBAdobe PDFView/Open
13 - appendix b.pdf439.49 kBAdobe PDFView/Open
14 - master chart.pdf631.36 kBAdobe PDFView/Open
1 - title page.pdf192.02 kBAdobe PDFView/Open
80_recommendation.pdf250.67 kBAdobe PDFView/Open
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