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Integrative analysis of fitness and metabolic effects of plasmids in Pseudomonas aeruginosa PAO1

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posted on 2018-06-04, 15:03 authored by Alvaro San-Millan, Macarena Toll-Riera, Qin Qi, Alex Betts, Richard J. Hopkinson, James McCullagh, R. Craig MacLean
Horizontal gene transfer (HGT) mediated by the spread of plasmids fuels evolution in prokaryotes. Although plasmids provide bacteria with new adaptive genes, they also produce physiological alterations that often translate into a reduction in bacterial fitness. The fitness costs associated with plasmids represent an important limit to plasmid maintenance in bacterial communities, but their molecular origins remain largely unknown. In this work we combine phenomics, transcriptomics and metabolomics to study the fitness effects produced by a collection of diverse plasmids in the opportunistic pathogen P. aeruginosa PAO1. Using this approach, we scan the physiological changes imposed by plasmids and test the generality of some main mechanisms that have been proposed to explain the cost of HGT, including increased biosynthetic burden, reduced translational efficiency, and impaired chromosomal replication. Our results suggest that the fitness effects of plasmids have a complex origin, since none of these mechanisms could individually provide a general explanation for the cost of plasmid carriage. Interestingly, our results also showed that plasmids alter the expression of a common set of metabolic genes in PAO1, and produce convergent changes in host cell metabolism. These surprising results suggest that there is a common metabolic response to plasmids in P. aeruginosa PAO1.

Funding

This work was supported by funding from the European Research Council under the European Union’s Seventh Framework Programme (FP7/2007-2013)/ERC grant (StG-2011-281591). Work in ASM lab was supported by the Instituto de Salud Carlos III (Plan Estatal de I+D+i 2013-2016): grants CP15-00012, PI16-00860, and CIBER (CB06/02/0053), co-financed by the European Development Regional Fund ‘‘A way to achieve Europe’’ (ERDF). RCM is supported by a Wellcome Trust Senior Research Fellowship (WT106918AIA). ASM is supported by a Miguel Servet Fellowship from the Instituto de Salud Carlos III (MS15/00012) co-financed by The European Social Fund "Investing in your future" (ESF) and ERDF. MT-R is supported by the Ambizione program of the Swiss National Science Foundation (PZ00P3_161545 to M.T-R.). RJH acknowledges a William R. Miller Junior Research Fellowship, St. Edmund Hall, Oxford, UK. ASM and RJH thank Pembroke College MCR, Oxford, UK, for promoting interdisciplinary research through football. We thank the Oxford Genomics Center at the Wellcome Trust Centre for Human Genetics funded by Wellcome Trust grant reference 090532/Z/09/Z and Medical Research Council Hub grant no. G0900747 91070 for generation of the high449 throughput sequencing data. We thank Stephen P. Diggle for kindly providing us with the QS reporter PAO1 strain PlasB::lux.

History

Citation

ISME Journal, 2018

Author affiliation

/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry

Version

  • VoR (Version of Record)

Published in

ISME Journal

Publisher

Nature Publishing Group for International Society for Microbial Ecology

issn

1751-7362

eissn

1751-7370

Acceptance date

2018-05-25

Copyright date

2018

Available date

2018-09-06

Publisher version

https://www.nature.com/articles/s41396-018-0224-8

Notes

The online version of this article (https://doi.org/10.1038/s41396-018-0224-8) contains supplementary material, which is available to authorized users.

Language

en

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