TY - JOUR
T1 - Phylogenomic and genomic analysis reveals unique and shared genetic signatures of Mycobacterium kansasii complex species
AU - Machado, Edson
AU - Vasconcellos, Sidra
AU - Gomes, Lia
AU - Catanho, Marcos
AU - Ramos, Jesus
AU - de Carvalho, Luciana
AU - Goldenberg, Telma
AU - Redner, Paulo
AU - Caldas, Paulo
AU - Campos, Carlos
AU - Dalcolmo, Margareth
AU - Lourenço, Maria Cristina
AU - Lasunskaia, Elena
AU - Mussi, Vinicius
AU - Spinassé, Lizania
AU - Vinhas, Solange
AU - Rigouts, Leen
AU - Cogneau, Sari
AU - de Rijk, Pim
AU - Utpatel, Christian
AU - Kaustova, Jarmila
AU - van der Laan, Tridia
AU - de Neeling, Han
AU - Rastogi, Nalin
AU - Levina, Klavdia
AU - Kütt, Marge
AU - Mokrousov, Igor
AU - Zhuravlev, Viacheslav
AU - Makhado, Ndivhu
AU - Žolnir-Dovč, Manca
AU - Jankovic, Vera
AU - de Waard, Jacobus
AU - Sisco, Maria Carolina
AU - van Soolingen, Dick
AU - Niemann, Stefan
AU - de Jong, Bouke C.
AU - Meehan, Conor J.
AU - Suffys, Philip
N1 - Publisher Copyright:
© 2024 The Authors.
PY - 2024
Y1 - 2024
N2 - 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 (sensu stricto), 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 defence systems and show that the MKC species harbours unique and shared genomic signatures. High frequency of presence of prophages and different types of defence systems were 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 twentieth 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.
AB - 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 (sensu stricto), 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 defence systems and show that the MKC species harbours unique and shared genomic signatures. High frequency of presence of prophages and different types of defence systems were 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 twentieth 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.
KW - Mycobacterium kansasii
KW - lineages
KW - pangenome
KW - phylogenomics
KW - virulence
UR - http://www.scopus.com/inward/record.url?scp=85199015988&partnerID=8YFLogxK
U2 - 10.1099/mgen.0.001266
DO - 10.1099/mgen.0.001266
M3 - Article
C2 - 39016539
AN - SCOPUS:85199015988
SN - 2057-5858
VL - 10
JO - Microbial genomics
JF - Microbial genomics
IS - 7
M1 - 001266
ER -