| Literature DB >> 33926925 |
Josephine M Bryant1,2, Karen P Brown1,3, Sophie Burbaud1, Isobel Everall1,4, Juan M Belardinelli5, Daniela Rodriguez-Rincon1, Dorothy M Grogono1,3, Chelsea M Peterson5, Deepshikha Verma5, Ieuan E Evans1,3, Christopher Ruis1,2, Aaron Weimann1,2, Divya Arora1, Sony Malhotra6,7, Bridget Bannerman1,2, Charlotte Passemar1, Kerra Templeton8, Gordon MacGregor8, Kasim Jiwa9, Andrew J Fisher9, Tom L Blundell6, Diane J Ordway5, Mary Jackson5, Julian Parkhill10,11, R Andres Floto12,2,3.
Abstract
Although almost all mycobacterial species are saprophytic environmental organisms, a few, such as Mycobacterium tuberculosis, have evolved to cause transmissible human infection. By analyzing the recent emergence and spread of the environmental organism M. abscessus through the global cystic fibrosis population, we have defined key, generalizable steps involved in the pathogenic evolution of mycobacteria. We show that epigenetic modifiers, acquired through horizontal gene transfer, cause saltational increases in the pathogenic potential of specific environmental clones. Allopatric parallel evolution during chronic lung infection then promotes rapid increases in virulence through mutations in a discrete gene network; these mutations enhance growth within macrophages but impair fomite survival. As a consequence, we observe constrained pathogenic evolution while person-to-person transmission remains indirect, but postulate accelerated pathogenic adaptation once direct transmission is possible, as observed for M. tuberculosis Our findings indicate how key interventions, such as early treatment and cross-infection control, might restrict the spread of existing mycobacterial pathogens and prevent new, emergent ones.Entities:
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Year: 2021 PMID: 33926925 PMCID: PMC7611193 DOI: 10.1126/science.abb8699
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728