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Phylogeography and transmission of M. tuberculosis in Moldova: A prospective genomic analysis.
Yang, Chongguang; Sobkowiak, Benjamin; Naidu, Vijay; Codreanu, Alexandru; Ciobanu, Nelly; Gunasekera, Kenneth S; Chitwood, Melanie H; Alexandru, Sofia; Bivol, Stela; Russi, Marcus; Havumaki, Joshua; Cudahy, Patrick; Fosburgh, Heather; Allender, Christopher J; Centner, Heather; Engelthaler, David M; Menzies, Nicolas A; Warren, Joshua L; Crudu, Valeriu; Colijn, Caroline; Cohen, Ted.
Affiliation
  • Yang C; School of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, China.
  • Sobkowiak B; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Naidu V; Department of Mathematics, Simon Fraser University, Burnaby, Canada.
  • Codreanu A; Department of Mathematics, Simon Fraser University, Burnaby, Canada.
  • Ciobanu N; Phthisiopneumology Institute, Chisinau, Republic of Moldova.
  • Gunasekera KS; Phthisiopneumology Institute, Chisinau, Republic of Moldova.
  • Chitwood MH; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Alexandru S; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Bivol S; Phthisiopneumology Institute, Chisinau, Republic of Moldova.
  • Russi M; Center for Health Policies and Studies, Chisinau, Republic of Moldova.
  • Havumaki J; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Cudahy P; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Fosburgh H; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Allender CJ; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Centner H; Translational Genomics Research Institute, Flagstaff, Arizona, United States of America.
  • Engelthaler DM; Translational Genomics Research Institute, Flagstaff, Arizona, United States of America.
  • Menzies NA; Translational Genomics Research Institute, Flagstaff, Arizona, United States of America.
  • Warren JL; Department of Global Health and Population, and Center for Health Decision Science, Harvard TH Chan School of Public Health, Boston, Massachusetts, United States of America.
  • Crudu V; Department of Biostatistics, Yale School of Public Health, New Haven, Connecticut, United States of America.
  • Colijn C; Phthisiopneumology Institute, Chisinau, Republic of Moldova.
  • Cohen T; Department of Mathematics, Simon Fraser University, Burnaby, Canada.
PLoS Med ; 19(2): e1003933, 2022 02.
Article in En | MEDLINE | ID: mdl-35192619
ABSTRACT

BACKGROUND:

The incidence of multidrug-resistant tuberculosis (MDR-TB) remains critically high in countries of the former Soviet Union, where >20% of new cases and >50% of previously treated cases have resistance to rifampin and isoniazid. Transmission of resistant strains, as opposed to resistance selected through inadequate treatment of drug-susceptible tuberculosis (TB), is the main driver of incident MDR-TB in these countries. METHODS AND

FINDINGS:

We conducted a prospective, genomic analysis of all culture-positive TB cases diagnosed in 2018 and 2019 in the Republic of Moldova. We used phylogenetic methods to identify putative transmission clusters; spatial and demographic data were analyzed to further describe local transmission of Mycobacterium tuberculosis. Of 2,236 participants, 779 (36%) had MDR-TB, of whom 386 (50%) had never been treated previously for TB. Moreover, 92% of multidrug-resistant M. tuberculosis strains belonged to putative transmission clusters. Phylogenetic reconstruction identified 3 large clades that were comprised nearly uniformly of MDR-TB 2 of these clades were of Beijing lineage, and 1 of Ural lineage, and each had additional distinct clade-specific second-line drug resistance mutations and geographic distributions. Spatial and temporal proximity between pairs of cases within a cluster was associated with greater genomic similarity. Our study lasted for only 2 years, a relatively short duration compared with the natural history of TB, and, thus, the ability to infer the full extent of transmission is limited.

CONCLUSIONS:

The MDR-TB epidemic in Moldova is associated with the local transmission of multiple M. tuberculosis strains, including distinct clades of highly drug-resistant M. tuberculosis with varying geographic distributions and drug resistance profiles. This study demonstrates the role of comprehensive genomic surveillance for understanding the transmission of M. tuberculosis and highlights the urgency of interventions to interrupt transmission of highly drug-resistant M. tuberculosis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis / Tuberculosis, Multidrug-Resistant / Mycobacterium tuberculosis Type of study: Observational_studies / Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: PLoS Med Journal subject: MEDICINA Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis / Tuberculosis, Multidrug-Resistant / Mycobacterium tuberculosis Type of study: Observational_studies / Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: PLoS Med Journal subject: MEDICINA Year: 2022 Document type: Article Affiliation country:
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