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Phylogenomic and genomic analysis reveals unique and shared genetic signatures of Mycobacterium kansasii complex species

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posted on 2024-07-12, 09:30 authored by Edson Machado, Sidra Vasconcellos, Lia Gomes, Marcos Catanho, Jesus Ramos, Luciana de Carvalho, Telma Goldenberg, Margareth Dalcolmo, Paulo Redner, Paulo Caldas, Carlos CamposCarlos Campos, Maria Cristina Lourenço, Elena Lasunskaia, Vinicius Mussi, Lizania Spinasse, Solange Vinhas, Leen Rigouts, Sari Cogneau, Pim de Rijk, Christian Utpatel, Jarmila Kaustova, Tridia van der Laan, Han de Neeling, Nalin Rastogi, Klavdia Levina, Marge Kütt, Igor Mokrousov, Viacheslav Zhuravlev, Ndivhu Makhado, Manca Žolnir-Dovč, Vera Jankovic, Jacobus de Waard, Maria Sisco, Dick van Soolingen, Stefan Niemann, Bouke C. de Jong, Conor MeehanConor Meehan, Philip Suffys


Supplementary Material/Supporting data/code for Phylogenomic and genomic analysis reveals unique and shared genetic signatures of Mycobacterium kansasii complex species, as described on Microbial Genomics.

Species belonging to the Mycobacterium kansasii complex (MKC) are frequently isolated from humans and the environment and can cause serious diseases. The most common MKC infections are caused by the species M. kansasii (stricto sensu), leading to tuberculosis-like disease. However, a broad spectrum of virulence, antimicrobial resistance and pathogenicity of these non-tuberculous mycobacteria (NTM) are observed across the MKC. Many genomic aspects of the MKC that relate to these broad phenotypes are not well elucidated. Here, we performed genomic analyses from a collection of 665 MKC strains, isolated from environmental, animal and human sources. We inferred the MKC pangenome, mobilome, resistome, virulome and defense systems and show that the MKC species harbors unique and shared genomic signatures. High frequency of presence of prophages and different types of defense systems was observed. We found that the M. kansasii species splits into four lineages, of which three are lowly represented and mainly in Brazil, while one lineage is dominant and globally spread. Moreover, we show that four sub-lineages of this most distributed M. kansasii lineage emerged during the 20th century. Further analysis of the M. kansasii genomes revealed almost 300 regions of difference contributing to genomic diversity, as well as fixed mutations that may explain the M. kansasii's increased virulence and drug resistance.

Funding

Incorporating whole genome diversity into the clinical epidemiology of Mycobacterium tuberculosis

Academy of Medical Sciences

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306344/2021-1

307474/2020-8

310418/2016-0

207422/2014-1

26/201.115/2022

26/204.546/2021

26/210.877/2019

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