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Phenotypic and genotypic characterization of Mycobacterium tuberculosis pyrazinamide resistance—India, 2018–2020

Title: Phenotypic and genotypic characterization of Mycobacterium tuberculosis pyrazinamide resistance—India, 2018–2020
Authors: Sembulingam Tamilzhalagan; Evanslin Santus Justin; Ashok Selvaraj; Karthick Venkateswaran; Arun Kumar Sivakumar; Suganthi Chittibabu; Heather P. McLaughlin; Patrick K. Moonan; Jonathan P. Smith; Sakthi Suba; Mukesh Kumar Sathya Narayanan; Christine S. Ho; Nishant Kumar; Srikanth P. Tripathy; Siva K. Shanmugam; Patricia J. Hall-Eidson; Uma Devi Ranganathan
Source: Frontiers in Microbiology, Vol 15 (2025)
Publisher Information: Frontiers Media S.A.
Publication Year: 2025
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: tuberculosis; drug resistance; drug susceptibility testing; genetic mutations; whole genome sequencing; pyrazinamide; Microbiology; QR1-502
Description: Pyrazinamide (PZA) is a key first-line antituberculosis drug that plays an important role in eradicating persister Mycobacterium tuberculosis (TB) bacilli and shortening the duration of tuberculosis treatment. However, PZA-resistance is on the rise, particularly among persons with multidrug-resistant (MDR) tuberculosis. This nationwide study was conducted to explore the prevalence of mutations conferring PZA resistance, catalogue mutation diversity, investigate the associations of PZA resistance with specific lineages, examine co-resistance to 13 first- and second-line drugs, and evaluate the diagnostic accuracy of sequencing pncA and panD genes for predicting PZA resistance. Whole genome sequencing was performed on 2,207 M. tuberculosis isolates from 25 States and 4 Union Territories of India. The majority of phenotypically PZA-resistant isolates (77%) harbored 171 distinct mutations in pncA; however, a small number of mutations in panD, rpsA and clpC1 were also observed. A set of novel mutations associated PZA resistance was uncovered, along with an additional 143 PZA resistance-conferring mutations in pncA based on application of WHO-endorsed grading rules. PZA resistance was predominately observed in Lineage 2 and eight lineage-specific resistance markers were identified. Mutations distributed across pncA correlate to 94% of PZA resistance and were the predominant drivers of phenotypic resistance; evidence generated herein substantiates sequencing the entire gene and promoter for comprehensive genotypic-based prediction of PZA resistance. This work provides key insights into the scope of PZA-resistance in India, a high drug-resistant TB burden country, and can support the effectiveness of TB prevention and control efforts.
Document Type: article in journal/newspaper
Language: English
Relation: https://www.frontiersin.org/articles/10.3389/fmicb.2024.1515627/full; https://doaj.org/toc/1664-302X; https://doaj.org/article/49c82e9534f444f196c0b0ab2328da18
DOI: 10.3389/fmicb.2024.1515627
Availability: https://doi.org/10.3389/fmicb.2024.1515627; https://doaj.org/article/49c82e9534f444f196c0b0ab2328da18
Accession Number: edsbas.1FBF930B
Database: BASE