Burden of baseline resistance of Mycobacterium tuberculosis to fluoroquinolones and second-line injectables in central India

被引:4
|
作者
Desikan, Prabha [1 ]
Panwalkar, Nikita [1 ]
Chaudhuri, Shreya [1 ]
Khan, Zeba [1 ]
Punde, Ram Prakash [1 ]
Pauranik, Ankur [1 ]
Mirza, Shaina Beg [1 ]
Ranjan, Rajeev [1 ]
Anand, Sridhar [2 ]
Sachdeva, K. S. [3 ]
机构
[1] Bhopal Mem Hosp & Res Ctr, Dept Microbiol, Natl Reference Lab, Bhopal 462038, India
[2] World Hlth Org, New Delhi, India
[3] Minist Hlth & Family Welf, Cent TB Div, New Delhi 110011, India
关键词
baseline resistance; central India; fluoroquinolones; Mycobacterium tuberculosis; revised national TB control programme; second-line injectable drugs; MUTATIONS; DRUG; PREVALENCE; KANAMYCIN; GYRB; RRS;
D O I
10.1093/trstmh/trz121
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Drug-resistant TB is a serious public health problem in India. Pre-existing resistance to fluoroquinolones (FQs) and second-line injectable drugs (SLIDs) in strains of Mycobacterium tuberculosis (MTB) resistant to rifampicin (RIF) and/or isoniazid (INH) contributes to treatment failures and consequent transmission of drug-resistant TB. A baseline assessment of resistance of MTB to FQs and SLIDs may help guide policies to further improve management of drug-resistant TB in India. This study aims to determine the prevalence of resistance to FQs and SLIDs among MTB strains having RIF and/or INH resistance in central India. Method: A total of 1032 smear positive sputum samples were subjected to line probe assay (GenoType MTBDRsl version 2) to test for resistance to FQs and SLIDs, according to the integrated diagnostic algorithm of the revised national TB control programme. Results: Of 1032 samples, 92 (8.91%) were not interpretable and hence excluded, 295 (31.38%) were resistant to FQs alone, 13 (1.38%) were resistant to SLIDs alone, 15 (1.59%) were resistant to both FQs as well as SLIDs and 617 (65.63%) were sensitive to both FQs and SLIDs. The most common mutations in gyrA and gyrB genes were observed at codons D94G and E540V, respectively. Mutations at codon A1401G in rrs genes and in the C-14 T region of eis genes were most frequently observed. Conclusion: High levels of FQ resistance points towards indiscriminate use of this class of drugs. Regulation for judicial use of FQs is an urgent requirement.
引用
收藏
页码:249 / 254
页数:6
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