High frequency of ofloxacin resistance patterns of Mycobacterium leprae from India: An indication to revisit second line anti-leprosy treatment regimen.


Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 27 06 2023
revised: 11 09 2023
accepted: 10 10 2023
medline: 4 12 2023
pubmed: 19 10 2023
entrez: 18 10 2023
Statut: ppublish

Résumé

Drug resistance in leprosy is an emerging concern, leading to treatment failures, recurrences, and potential spread of resistant Mycobacterium leprae in the community. In this study, we aimed to assess drug resistance prevalence and patterns amongst leprosy patients at a tertiary care referral hospital in India. Mutations in drug resistance determining regions for dapsone, rifampicin, and ofloxacin of the M. leprae genome in DNA extracted from skin biopsies of 136 leprosy patients (treatment-naive = 67, with persistent skin lesions = 35, with recurrence = 34) were analysed by polymerase chain reaction followed by Sanger sequencing. Wild-type strain (Thai-53) was used as a reference strain. Resistance mutations were identified in a total of 23 patients, constituting 16.9% of the cohort. Within this subset of 23 cases, resistance to ofloxacin was observed in 17 individuals (12.5%), while resistance to both dapsone and rifampicin was detected in three patients each (2.2% for both). The occurrence of ofloxacin resistance showed minimal disparity between recurrent and treatment-naive cases, at 17.6% and 16.4%, respectively. Dapsone resistance emerged in two treatment-naive cases and one case with persistent skin lesions. Notably, none of the treatment-naive cases or those with recurrence/relapse exhibited rifampicin resistance. Subsequently, no statistically significant correlation was identified between other clinical variables and the presence of antimicrobial resistance. The occurrence of resistance to the current multidrug therapy regimen (specifically dapsone and rifampicin) and to ofloxacin, a secondary antileprosy medication in M. leprae, represents a concerning scenario. This calls for an expansion towards bactericidal drug options and the establishment of robust surveillance for drug resistance in countries burdened with high leprosy rates. Moreover, the introduction of stringent antimicrobial stewardship initiatives is imperative. As a single centre study, it represents a limited, cross-sectional view of the real situation in the field.

Identifiants

pubmed: 37852372
pii: S2213-7165(23)00175-3
doi: 10.1016/j.jgar.2023.10.006
pii:
doi:

Substances chimiques

Rifampin VJT6J7R4TR
Leprostatic Agents 0
Ofloxacin A4P49JAZ9H
Dapsone 8W5C518302

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

262-267

Informations de copyright

Copyright © 2023. Published by Elsevier Ltd.

Auteurs

Seema Chhabra (S)

Department of Immunopathology, Postgraduate Institute of Medical Education and Research (PGIMER), Sector-12, Chandigarh, India. Electronic address: drseemachhabra@gmail.com.

Tarun Narang (T)

Department of Dermatology, Venereology & Leprology, PGIMER, Sector-12, Chandigarh, India. Electronic address: narangtarun@yahoo.co.in.

Smrity Sahu (S)

Department of Immunopathology, Postgraduate Institute of Medical Education and Research (PGIMER), Sector-12, Chandigarh, India.

Keshav Sharma (K)

Department of Immunopathology, Postgraduate Institute of Medical Education and Research (PGIMER), Sector-12, Chandigarh, India.

Shilpa Shilpa (S)

Department of Dermatology, Venereology & Leprology, PGIMER, Sector-12, Chandigarh, India.

Ayush Sharma (A)

Department of Immunopathology, Postgraduate Institute of Medical Education and Research (PGIMER), Sector-12, Chandigarh, India.

Sejal Jain (S)

Department of Dermatology, Venereology & Leprology, PGIMER, Sector-12, Chandigarh, India.

Itu Singh (I)

Stanley Browne Laboratory, The Leprosy Mission Community Hospital, Nand Nagari, New Delhi.

Rakesh Yadav (R)

Department of Medical Microbiology, PGIMER, Sector-12, Chandigarh, India.

Manjot Kaur (M)

Department of Medical Microbiology, PGIMER, Sector-12, Chandigarh, India.

Rahul Sharma (R)

Stanley Browne Laboratory, The Leprosy Mission Community Hospital, Nand Nagari, New Delhi.

Mohd Nadeem (M)

Stanley Browne Laboratory, The Leprosy Mission Community Hospital, Nand Nagari, New Delhi.

Pragati Pandey (P)

Department of Dermatology, Venereology & Leprology, PGIMER, Sector-12, Chandigarh, India.

Ranjana W Minz (RW)

Department of Immunopathology, Postgraduate Institute of Medical Education and Research (PGIMER), Sector-12, Chandigarh, India.

Sunil Dogra (S)

Department of Dermatology, Venereology & Leprology, PGIMER, Sector-12, Chandigarh, India. Electronic address: sundogra@hotmail.com.

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