Co-occurring microflora and mucin drive Pseudomonas aeruginosa diversification and pathoadaptation

Author:

Bottery Michael J12,Johansen Helle Krogh3456,Pitchford Jon W78,Friman Ville-Petri79

Affiliation:

1. Division of Evolution Infection and Genomics , School of Biological Sciences, , Manchester M13 9PL , United Kingdom

2. University of Manchester , School of Biological Sciences, , Manchester M13 9PL , United Kingdom

3. The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark , 2800 Kongens Lyngby , Denmark

4. Department of Clinical Microbiology, Rigshospitalet, Copenhagen University Hospital , Copenhagen 9301 , Denmark

5. Department of Clinical Medicine , Faculty of Health and Medical Sciences, , Copenhagen 2200 , Denmark

6. University of Copenhagen , Faculty of Health and Medical Sciences, , Copenhagen 2200 , Denmark

7. Department of Biology, University of York , Wentworth Way, York YO10 5DD , United Kingdom

8. Department of Mathematics, University of York , Heslington, York YO10 5DD , United Kingdom

9. Department of Microbiology, University of Helsinki , Helsinki 00014 , Finland

Abstract

Abstract While several environmental factors contribute to the evolutionary diversification of the pathogenic bacterium Pseudomonas aeruginosa during cystic fibrosis lung infections, relatively little is known about the impact of the surrounding microbiota. By using in vitro experimental evolution, we show that the presence of Stenotrophomonas maltophilia, Staphylococcus aureus, or them both, prevent the evolution of loss of virulence, which repeatedly occurs in the absence of these species due to mutations in regulators of the Pseudomonas Quinolone Signal quorum sensing system, vqsM and pqsR. Moreover, the strength of the effect of co-occurring species is attenuated through changes in the physical environment by the addition of mucin, resulting in selection for phenotypes resembling those evolved in the absence of the co-occurring species. Together, our findings show that variation in mucosal environment and the surrounding polymicrobial environment can determine the evolutionary trajectory of P. aeruginosa, partly explaining its diversification and pathoadaptation from acute to chronic phenotype during cystic fibrosis lung infections.

Funder

Wellcome Trust

Centre for Future Health

University of York

Sir Henry Wellcome Postdoctoral Fellowship

Publisher

Oxford University Press (OUP)

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