Genotype–Phenotype Characterization of Serial Mycobacterium tuberculosis Isolates in Bedaquiline-Resistant Tuberculosis

Author:

Brown Tyler S12,Tang Linrui3ORCID,Omar Shaheed Vally45,Joseph Lavania4,Meintjes Graeme6,Maartens Gary67,Wasserman Sean68,Shah N Sarita9,Farhat Maha R10,Gandhi Neel R9,Ismail Nazir4,Brust James C M11,Mathema Barun3ORCID

Affiliation:

1. Section of Infectious Diseases, Boston University School of Medicine , Boston, Massachusetts , USA

2. Center for Communicable Disease Dynamics, Harvard T.H. Chan School of Public Health , Boston, Massachusetts , USA

3. Department of Epidemiology, Columbia University Mailman School of Public Health , New York, New York , USA

4. Centre for Tuberculosis, National Institute for Communicable Diseases , Johannesburg , South Africa

5. Department of Molecular Medicine & Hematology, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand , Johannesburg , South Africa

6. Wellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine, and Department of Medicine, University of Cape Town , Cape Town , South Africa

7. Division of Clinical Pharmacology, Department of Medicine, University of Cape Town , Cape Town , South Africa

8. Division of Infectious Diseases and HIV Medicine, Department of Medicine, University of Cape Town , Cape Town , South Africa

9. Departments of Epidemiology and Global Health and Medicine, Rollins School of Public Health and Emory School of Medicine , Atlanta, Georgia , USA

10. Department of Biomedical Informatics, Harvard Medical School , Boston, Massachusetts , USA

11. Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center , Bronx, New York , USA

Abstract

Abstract Background Emerging resistance to bedaquiline (BDQ) threatens to undermine advances in the treatment of drug-resistant tuberculosis (DRTB). Characterizing serial Mycobacterium tuberculosis (Mtb) isolates collected during BDQ-based treatment can provide insights into the etiologies of BDQ resistance in this important group of DRTB patients. Methods We measured mycobacteria growth indicator tube (MGIT)–based BDQ minimum inhibitory concentrations (MICs) of Mtb isolates collected from 195 individuals with no prior BDQ exposure who were receiving BDQ-based treatment for DRTB. We conducted whole-genome sequencing on serial Mtb isolates from all participants who had any isolate with a BDQ MIC >1 collected before or after starting treatment (95 total Mtb isolates from 24 participants). Results Sixteen of 24 participants had BDQ-resistant TB (MGIT MIC ≥4 µg/mL) and 8 had BDQ-intermediate infections (MGIT MIC = 2 µg/mL). Participants with pre-existing resistance outnumbered those with resistance acquired during treatment, and 8 of 24 participants had polyclonal infections. BDQ resistance was observed across multiple Mtb strain types and involved a diverse catalog of mmpR5 (Rv0678) mutations, but no mutations in atpE or pepQ. Nine pairs of participants shared genetically similar isolates separated by <5 single nucleotide polymorphisms, concerning for potential transmitted BDQ resistance. Conclusions BDQ-resistant TB can arise via multiple, overlapping processes, including transmission of strains with pre-existing resistance. Capturing the within-host diversity of these infections could potentially improve clinical diagnosis, population-level surveillance, and molecular diagnostic test development.

Funder

US Department of Health and Human Services

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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