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Molecular Epidemiology and Polymorphism Analysis in Drug-Resistant Genes in M. tuberculosis Clinical Isolates from Western and Northern India.
Rana, Vibhuti; Singh, Nittu; Nikam, Chaitali; Kambli, Priti; Singh, Pravin K; Singh, Urmila; Jain, Amita; Rodrigues, Camilla; Sharma, Charu.
Afiliación
  • Rana V; CSIR- Institute of Microbial Technology, Chandigarh, 160036, India.
  • Singh N; CSIR- Institute of Microbial Technology, Chandigarh, 160036, India.
  • Nikam C; Department of Microbiology, P. D. Hinduja National Hospital and Medical Research Centre, Mumbai, 400016, Maharashtra, India.
  • Kambli P; Department of Microbiology, P. D. Hinduja National Hospital and Medical Research Centre, Mumbai, 400016, Maharashtra, India.
  • Singh PK; Department of Microbiology, King George Medical University, Lucknow, 226003, Uttar Pradesh, India.
  • Singh U; Department of Microbiology, King George Medical University, Lucknow, 226003, Uttar Pradesh, India.
  • Jain A; Department of Microbiology, King George Medical University, Lucknow, 226003, Uttar Pradesh, India.
  • Rodrigues C; Department of Microbiology, P. D. Hinduja National Hospital and Medical Research Centre, Mumbai, 400016, Maharashtra, India.
  • Sharma C; CSIR- Institute of Microbial Technology, Chandigarh, 160036, India.
Infect Drug Resist ; 15: 1717-1732, 2022.
Article en En | MEDLINE | ID: mdl-35422638
ABSTRACT

Introduction:

The mechanistic details of first line drug (FLD) resistance have been thoroughly explored but the genetic resistance mechanisms of second line injectables, which form the backbone of the combinatorial drug resistant tuberculosis therapy, are partially identified. This study aims to highlight the genetic and spoligotypic differences in the second line drug (SLD) resistant and sensitive Mycobacterium tuberculosis (Mtb) clinical isolates from Mumbai (Western India) and Lucknow (Northern India).

Methods:

The rrs, eis, whiB7, tlyA, gyrA and gyrB target loci were screened in 126 isolates and spoligotyped.

Results:

The novel mutations were observed in whiB7 loci (A43T, C44A, C47A, G48T, G59A and T152G in 5'-UTR; A42C, C253T and T270G in gene), tlyA (+CG200, G165A, C415G, and +G543) and gyrB (+G1359 and +A1429). Altogether, the rrs, eis, and whiB7 loci harbored mutations in ~86% and ~47% kanamycin resistant isolates from Mumbai and Lucknow, respectively. Mumbai strains displayed higher prevalence of mutations in gyrA (~85%) and gyrB loci (~13%) as compared to those from Lucknow (~69% and ~3.0%, respectively). Further, spoligotyping revealed that Beijing lineage is distributed equally amongst the drug resistant strains of Mumbai and Lucknow, but EAI-5 is existed at a higher level only in Mumbai. The lineages Manu2, CAS1-Delhi and T1 are more prevalent in Lucknow.

Conclusion:

Besides identifying novel mutations in whiB7, tlyA and gyrB target loci, our analyses unveiled a potential polymorphic and phylogeographical demarcation among two distinct regions.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies / Screening_studies Idioma: En Revista: Infect Drug Resist Año: 2022 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies / Screening_studies Idioma: En Revista: Infect Drug Resist Año: 2022 Tipo del documento: Article País de afiliación: India