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The evolution of virulence inPseudomonas aeruginosaduring chronic wound infection
Author(s) -
Jelly Vanderwoude,
Derek Fleming,
Sheyda Azimi,
Urvish Trivedi,
Kendra P. Rumbaugh,
Stephen P. Diggle
Publication year - 2020
Publication title -
proceedings of the royal society b biological sciences
Language(s) - English
Resource type - Journals
eISSN - 1471-2954
pISSN - 0962-8452
DOI - 10.1098/rspb.2020.2272
Subject(s) - virulence , pseudomonas aeruginosa , biology , microbiology and biotechnology , human pathogen , pathogen , chronic infection , pathogenesis , chronic wound , gene , experimental evolution , genetics , bacteria , immunology , wound healing , immune system
Opportunistic pathogens are associated with a number of chronic human infections, yet the evolution of virulence in these organisms during chronic infection remains poorly understood. Here, we tested the evolution of virulence in the human opportunistic pathogenPseudomonas aeruginosa in a murine chronic wound model using a two-part serial passage and sepsis experiment, and found that virulence evolved in different directions in each line of evolution. We also assessedP. aeruginosa adaptation to a chronic wound after 42 days of evolution and found that morphological diversity in our evolved populations was limited compared with that previously described in cystic fibrosis (CF) infections. Using whole-genome sequencing, we found that genes previously implicated inP. aeruginosa pathogenesis (lasR ,pilR ,fleQ ,rpoN andpvcA ) contained mutations during the course of evolution in wounds, with selection occurring in parallel across all lines of evolution. Our findings highlight that: (i)P. aeruginosa heterogeneity may be less extensive in chronic wounds than in CF lungs; (ii) genes involved inP. aeruginosa pathogenesis acquire mutations during chronic wound infection; (iii) similar genetic adaptations are employed byP. aeruginosa across multiple infection environments; and (iv) current models of virulence may not adequately explain the diverging evolutionary trajectories observed in an opportunistic pathogen during chronic wound infection.

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