dc.contributor.authorMcElroy, Kerensa E.
dc.contributor.authorHui, Janice G. K.
dc.contributor.authorWoo, Jerry K. K.
dc.contributor.authorLuk, Alison W. S.
dc.contributor.authorWebb, Jeremy S.
dc.contributor.authorKjelleberg, Staffan
dc.contributor.authorRice, Scott A.
dc.contributor.authorThomas, Torsten
dc.date.accessioned2014-06-03T03:44:03Z
dc.date.available2014-06-03T03:44:03Z
dc.date.copyright2014en_US
dc.date.issued2014
dc.identifier.citationMcElroy, K. E., Hui, J. G. K., Woo, J. K. K., Luk, A. W. S., Webb, J. S., Kjelleberg, S., et al. (2014). Strain-specific parallel evolution drives short-term diversification during Pseudomonas aeruginosa biofilm formation. Proceedings of the National Academy of Sciences, 111(14), E1419-E1427.en_US
dc.identifier.issn1091-6490en_US
dc.identifier.urihttp://hdl.handle.net/10220/19521
dc.description.abstractGeneration of genetic diversity is a prerequisite for bacterial evolution and adaptation. Short-term diversification and selection within populations is, however, largely uncharacterised, as existing studies typically focus on fixed substitutions. Here, we use whole-genome deep-sequencing to capture the spectrum of mutations arising during biofilm development for two Pseudomonas aeruginosa strains. This approach identified single nucleotide variants with frequencies from 0.5% to 98.0% and showed that the clinical strain 18A exhibits greater genetic diversification than the type strain PA01, despite its lower per base mutation rate. Mutations were found to be strain specific: the mucoid strain 18A experienced mutations in alginate production genes and a c-di-GMP regulator gene; while PA01 acquired mutations in PilT and PilY1, possibly in response to a rapid expansion of a lytic Pf4 bacteriophage, which may use type IV pili for infection. The Pf4 population diversified with an evolutionary rate of 2.43 × 10−3 substitutions per site per day, which is comparable to single-stranded RNA viruses. Extensive within-strain parallel evolution, often involving identical nucleotides, was also observed indicating that mutation supply is not limiting, which was contrasted by an almost complete lack of noncoding and synonymous mutations. Taken together, these results suggest that the majority of the P. aeruginosa genome is constrained by negative selection, with strong positive selection acting on an accessory subset of genes that facilitate adaptation to the biofilm lifecycle. Long-term bacterial evolution is known to proceed via few, nonsynonymous, positively selected mutations, and here we show that similar dynamics govern short-term, within-population bacterial diversification.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesProceedings of the national academy of sciencesen_US
dc.rights© The Author(s). This paper was published in Proceedings of the National Academy of Sciences and is made available as an electronic reprint (preprint) with permission of the Author(s). The paper can be found at the following official DOI: http://dx.doi.org/10.1073/pnas.1314340111.  One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.en_US
dc.subjectDRNTU::Science::Biological sciences::Evolution
dc.titleStrain-specific parallel evolution drives short-term diversification during Pseudomonas aeruginosa biofilm formationen_US
dc.typeJournal Article
dc.identifier.doihttp://dx.doi.org/10.1073/pnas.1314340111
dc.description.versionPublished versionen_US


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