{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,7]],"date-time":"2026-07-07T13:19:49Z","timestamp":1783430389085,"version":"3.54.6"},"reference-count":28,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","license":[{"start":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T00:00:00Z","timestamp":1775001600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,4]]},"abstract":"<jats:sec>\n                    <jats:title>Background:<\/jats:title>\n                    <jats:p>\n                      Drug-resistant tuberculosis (TB), especially rifampicin-resistant and multidrug-resistant TB, remains a significant public health challenge worldwide. Rapid and accurate methods for molecular diagnostics, such as first-line line probe assay (FL-LPA), are recommended by the World Health Organization for early detection of Rif and isoniazid resistance. However, limited data are available comparing resistance patterns between extrapulmonary TB (EPTB) and pulmonary TB (PTB). This study aims to compare first-line anti-tubercular drug resistance patterns and molecular mutations associated with\n                      <jats:italic toggle=\"yes\">katG, rpoB,<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">inhA<\/jats:italic>\n                      genes between PTB and EPTB.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>\n                      This study was a prospective analysis of 471\n                      <jats:italic toggle=\"yes\">Mycobacterium tuberculosis<\/jats:italic>\n                      samples subjected to the FL-LPA or the genotype MTBDRplus for the detection of Rif, isoniazid, and multidrug resistance. Demographic, clinical, microbiological, and molecular resistance data were compared between PTB and EPTB isolates. Resistance-associated mutations in the\n                      <jats:italic toggle=\"yes\">rpoB<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">katG<\/jats:italic>\n                      , and\n                      <jats:italic toggle=\"yes\">inhA<\/jats:italic>\n                      genes were evaluated.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      PTB accounted for the majority of samples (94.1%), whereas EPTB constituted 5.9%. PTB patients were more likely to be male, while EPTB patients were more likely to be female. The majority of drug resistance, or 94.1% of all resistant patterns, was found in PTB samples. The most prevalent resistance profile, especially in PTB patients, was isoniazid mono-resistance (H), which was mostly linked to the\n                      <jats:italic toggle=\"yes\">katG<\/jats:italic>\n                      S315T mutation and indicated high-level isoniazid resistance. Canonical rpoB mutations in the rifampicin (Rif) resistance-determining region, such as S531 L, D516V, and H526 replacements, were the main cause of Rif resistance. In line with their paucibacillary character, EPTB cases showed decreased bacillary burden, lower smear positivity, and a narrow range of resistance-associated mutations. Both PTB and EPTB isolates had InhA promoter alterations linked to low-level isoniazid resistance.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>\n                      The study demonstrates a substantially higher burden of molecular drug resistance in PTB than in EPTB. The predominance of canonical\n                      <jats:italic toggle=\"yes\">rpoB<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">katG<\/jats:italic>\n                      mutations highlights ongoing transmission of drug-resistant strains, emphasizing the value of FL-LPA in the routine TB diagnosis. Globally, molecular drug susceptibility testing, including extrapulmonary specimens, remains essential to guide appropriate therapy and strengthen TB control efforts under national and global elimination programs.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/ijmy.ijmy_85_26","type":"journal-article","created":{"date-parts":[[2026,6,30]],"date-time":"2026-06-30T22:18:16Z","timestamp":1782857896000},"page":"104-114","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Genotypic Characterization of Drug Resistance-associated Mutations in Mycobacterium tuberculosis Using Line Probe Assays in Central India"],"prefix":"10.4103","volume":"15","author":[{"given":"Antisha","family":"Tiwari","sequence":"first","affiliation":[{"name":"Department of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, 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India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jitendra","family":"Singh","sequence":"additional","affiliation":[{"name":"Department of Translational Medicine, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sagar","family":"Khadanga","sequence":"additional","affiliation":[{"name":"Department of General Medicine and All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alkesh","family":"Khurana","sequence":"additional","affiliation":[{"name":"Department of Pulmonary Medicine, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shashank","family":"Purwar","sequence":"additional","affiliation":[{"name":"Department of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, 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