Transmission Dynamics of a Mycobacterium tuberculosis Complex Outbreak in an Indigenous Population in the Colombian Amazon Region.


Journal

Microbiology spectrum
ISSN: 2165-0497
Titre abrégé: Microbiol Spectr
Pays: United States
ID NLM: 101634614

Informations de publication

Date de publication:
15 06 2023
Historique:
medline: 19 6 2023
pubmed: 24 5 2023
entrez: 24 5 2023
Statut: ppublish

Résumé

Whole genome sequencing (WGS) has become the main tool for studying the transmission of Mycobacterium tuberculosis complex (MTBC) strains; however, the clonal expansion of one strain often limits its application in local MTBC outbreaks. The use of an alternative reference genome and the inclusion of repetitive regions in the analysis could potentially increase the resolution, but the added value has not yet been defined. Here, we leveraged short and long WGS read data of a previously reported MTBC outbreak in the Colombian Amazon Region to analyze possible transmission chains among 74 patients in the indigenous setting of Puerto Nariño (March to October 2016). In total, 90.5% (67/74) of the patients were infected with one distinct MTBC strain belonging to lineage 4.3.3. Employing a reference genome from an outbreak strain and highly confident single nucleotide polymorphisms (SNPs) in repetitive genomic regions, e.g., the proline-glutamic acid/proline-proline-glutamic-acid (PE/PPE) gene family, increased the phylogenetic resolution compared to a classical H37Rv reference mapping approach. Specifically, the number of differentiating SNPs increased from 890 to 1,094, which resulted in a more granular transmission network as judged by an increasing number of individual nodes in a maximum parsimony tree, i.e., 5 versus 9 nodes. We also found in 29.9% (20/67) of the outbreak isolates, heterogenous alleles at phylogenetically informative sites, suggesting that these patients are infected with more than one clone. In conclusion, customized SNP calling thresholds and employment of a local reference genome for a mapping approach can improve the phylogenetic resolution in highly clonal MTBC populations and help elucidate within-host MTBC diversity.

Identifiants

pubmed: 37222610
doi: 10.1128/spectrum.05013-22
pmc: PMC10269451
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0501322

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Francy J Pérez-Llanos (FJ)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.

Viola Dreyer (V)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
German Center for Infection Research, Hamburg-Lübeck-Borstel-Riems, Germany.

Ivan Barilar (I)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
German Center for Infection Research, Hamburg-Lübeck-Borstel-Riems, Germany.

Christian Utpatel (C)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
German Center for Infection Research, Hamburg-Lübeck-Borstel-Riems, Germany.

Thomas A Kohl (TA)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
German Center for Infection Research, Hamburg-Lübeck-Borstel-Riems, Germany.

Martha Isabel Murcia (MI)

Grupo MICOBAC-UN, Departamento de Microbiología, Facultad de Medicina, Universidad Nacional de Colombia, Bogotá, Colombia.

Susanne Homolka (S)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.

Matthias Merker (M)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
German Center for Infection Research, Hamburg-Lübeck-Borstel-Riems, Germany.
Evolution of the Resistome, Research Center Borstel, Borstel, Germany.

Stefan Niemann (S)

Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
German Center for Infection Research, Hamburg-Lübeck-Borstel-Riems, Germany.

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Classifications MeSH