posted on 2018-06-04, 15:03authored byAlvaro 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
The online version of this article
(https://doi.org/10.1038/s41396-018-0224-8) contains supplementary
material, which is available to authorized users.