Drug resistance and epidemiological success of modern Mycobacterium tuberculosis lineages in western India.

drug resistance lineage transmission tuberculosis whole genome sequencing

Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
31 May 2024
Historique:
received: 11 08 2023
revised: 24 04 2024
accepted: 03 05 2024
medline: 31 5 2024
pubmed: 31 5 2024
entrez: 31 5 2024
Statut: aheadofprint

Résumé

Transmission is contributing to the slow decline of tuberculosis (TB) incidence globally. Drivers of TB transmission in India, the country estimated to carry a quarter of the World's burden, are not well studied. We conducted a genomic epidemiology study to compare epidemiological success, host factors and drug resistance (DR) among the four major Mycobacterium tuberculosis (Mtb) lineages (L1-4) circulating in Pune, India. We performed whole-genome sequencing (WGS) of Mtb sputum culture-positive isolates from participants in two prospective cohort studies and predicted genotypic susceptibility using a validated random forest model. We used maximum likelihood estimation to build phylogenies. We compared lineage specific phylogenetic and time-scaled metrics to assess epidemiological success. Of the 642 isolates that underwent WGS, 612 met sequence quality criteria. Most isolates belonged to L3 (44.6%). The majority (61.1%) of multidrug-resistant isolates belonged to L2 (P < 0.001). In molecular dating, L2 demonstrated a higher rate and more recent resistance acquisition. We measured higher clustering, and time-scaled haplotypic density (THD) for L4 and L2 compared to L3 and/or L1 suggesting higher epidemiological success. L4 demonstrated higher THD and clustering (OR 5.1 (95% CI 2.3-12.3) in multivariate models controlling for host factors and DR. L2 shows a higher frequency of DR and both L2 and L4 demonstrate evidence of higher epidemiological success than L3 or L1 in the study setting. Our findings highlight the need for contact tracing around TB cases, and heightened surveillance of TB DR in India.

Sections du résumé

BACKGROUND BACKGROUND
Transmission is contributing to the slow decline of tuberculosis (TB) incidence globally. Drivers of TB transmission in India, the country estimated to carry a quarter of the World's burden, are not well studied. We conducted a genomic epidemiology study to compare epidemiological success, host factors and drug resistance (DR) among the four major Mycobacterium tuberculosis (Mtb) lineages (L1-4) circulating in Pune, India.
METHODS METHODS
We performed whole-genome sequencing (WGS) of Mtb sputum culture-positive isolates from participants in two prospective cohort studies and predicted genotypic susceptibility using a validated random forest model. We used maximum likelihood estimation to build phylogenies. We compared lineage specific phylogenetic and time-scaled metrics to assess epidemiological success.
RESULTS RESULTS
Of the 642 isolates that underwent WGS, 612 met sequence quality criteria. Most isolates belonged to L3 (44.6%). The majority (61.1%) of multidrug-resistant isolates belonged to L2 (P < 0.001). In molecular dating, L2 demonstrated a higher rate and more recent resistance acquisition. We measured higher clustering, and time-scaled haplotypic density (THD) for L4 and L2 compared to L3 and/or L1 suggesting higher epidemiological success. L4 demonstrated higher THD and clustering (OR 5.1 (95% CI 2.3-12.3) in multivariate models controlling for host factors and DR.
CONCLUSION CONCLUSIONS
L2 shows a higher frequency of DR and both L2 and L4 demonstrate evidence of higher epidemiological success than L3 or L1 in the study setting. Our findings highlight the need for contact tracing around TB cases, and heightened surveillance of TB DR in India.

Identifiants

pubmed: 38819323
pii: 7685855
doi: 10.1093/infdis/jiae240
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Published by Oxford University Press on behalf of Infectious Diseases Society of America 2024.

Auteurs

Avika Dixit (A)

Division of Infectious Diseases, Boston Children's Hospital, Boston MA, USA.
Department of Biomedical Informatics, Harvard Medical School, Boston MA, USA.

Yasha Ektefaie (Y)

Department of Biomedical Informatics, Harvard Medical School, Boston MA, USA.

Anju Kagal (A)

Byramjee-Jeejeebhoy Government Medical College, Pune, India.

Luca Freschi (L)

Department of Biomedical Informatics, Harvard Medical School, Boston MA, USA.

Rajesh Karyakarte (R)

Byramjee-Jeejeebhoy Government Medical College, Pune, India.

Rahul Lokhande (R)

Byramjee-Jeejeebhoy Government Medical College, Pune, India.

Matthias Groschel (M)

Department of Biomedical Informatics, Harvard Medical School, Boston MA, USA.

Jeffrey A Tornheim (JA)

Center for Clinical Global Health Education, Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Center for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Nikhil Gupte (N)

Center for Clinical Global Health Education, Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Byramjee-Jeejeebhoy Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Johns Hopkins India, Pune, India.

Neeta N Pradhan (NN)

Byramjee-Jeejeebhoy Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Johns Hopkins India, Pune, India.

Mandar S Paradkar (MS)

Byramjee-Jeejeebhoy Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Johns Hopkins India, Pune, India.

Sona Deshmukh (S)

Byramjee-Jeejeebhoy Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Johns Hopkins India, Pune, India.

Dileep Kadam (D)

Byramjee-Jeejeebhoy Government Medical College, Pune, India.

Marco Schito (M)

Critical Path Institute, Tucson, AZ, USA.

David M Engelthaler (DM)

Translational Genomics Research Institute, Flagstaff, AZ, USA.

Amita Gupta (A)

Center for Clinical Global Health Education, Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of International Health, Johns Hopkins Bloomberg School of Public Heath, Baltimore, MD, USA.

Jonathan Golub (J)

Center for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Vidya Mave (V)

Center for Clinical Global Health Education, Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Byramjee-Jeejeebhoy Medical College-Johns Hopkins University Clinical Research Site, Pune, India.
Johns Hopkins India, Pune, India.

Maha Farhat (M)

Department of Biomedical Informatics, Harvard Medical School, Boston MA, USA.
Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Boston, MA, USA.

Classifications MeSH