Whole-Genome Sequencing of Mycobacterium tuberculosis Provides Insight into the Evolution and Genetic Composition of Drug-Resistant Tuberculosis in Belarus

Author:

Wollenberg Kurt R.1,Desjardins Christopher A.2,Zalutskaya Aksana3,Slodovnikova Vervara3,Oler Andrew J.1,Quiñones Mariam1,Abeel Thomas2,Chapman Sinead B.2,Tartakovsky Michael1,Gabrielian Andrei1,Hoffner Sven4,Skrahin Aliaksandr5,Birren Bruce W.2,Rosenthal Alexander1,Skrahina Alena3,Earl Ashlee M.2

Affiliation:

1. Office of Cyber Infrastructure & Computational Biology, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, Maryland, USA

2. The Broad Institute of MIT & Harvard, Cambridge, Massachusetts, USA

3. Republican Scientific and Practical Centre for Pulmonology and Tuberculosis, Minsk, Belarus

4. Department of Microbiology, The Public Health Agency of Sweden, Solna, Sweden

5. Belarusian State Medical University, Minsk, Belarus

Abstract

ABSTRACT The emergence and spread of drug-resistant Mycobacterium tuberculosis (DR-TB) are critical global health issues. Eastern Europe has some of the highest incidences of DR-TB, particularly multidrug-resistant (MDR) and extensively drug-resistant (XDR) TB. To better understand the genetic composition and evolution of MDR- and XDR-TB in the region, we sequenced and analyzed the genomes of 138 M. tuberculosis isolates from 97 patients sampled between 2010 and 2013 in Minsk, Belarus. MDR and XDR-TB isolates were significantly more likely to belong to the Beijing lineage than to the Euro-American lineage, and known resistance-conferring loci accounted for the majority of phenotypic resistance to first- and second-line drugs in MDR and XDR-TB. Using a phylogenomic approach, we estimated that the majority of MDR-TB was due to the recent transmission of already-resistant M. tuberculosis strains rather than repeated de novo evolution of resistance within patients, while XDR-TB was acquired through both routes. Longitudinal sampling of M. tuberculosis from 34 patients with treatment failure showed that most strains persisted genetically unchanged during treatment or acquired resistance to fluoroquinolones. HIV+ patients were significantly more likely to have multiple infections over time than HIV− patients, highlighting a specific need for careful infection control in these patients. These data provide a better understanding of the genomic composition, transmission, and evolution of MDR- and XDR-TB in Belarus and will enable improved diagnostics, treatment protocols, and prognostic decision-making.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference23 articles.

1. World Health Organization. 2015. Global tuberculosis report. World Health Organization Geneva Switzerland. https://www.health-e.org.za/wp-content/uploads/2015/10/Global-TB-Report-2015-FINAL-2.pdf.

2. World Health Organization. 2008. Guidelines for the programmatic management of drug-resistant tuberculosis. World Health Organization, Geneva, Switzerland.

3. Multidrug-resistant Myobacterium tuberculosis caused by the Beijing genotype and a specific T1 genotype clone (SIT No. 266) is widely transmitted in Minsk

4. Multidrug-resistant tuberculosis in Belarus: the size of the problem and associated risk factors

5. Drug resistance-related mutations in multidrug-resistant Mycobacterium tuberculosis isolates from diverse geographical regions

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