| Literature DB >> 25804522 |
Jerónimo Rodríguez-Beltrán1, Jérôme Tourret2, Olivier Tenaillon3, Elena López4, Emmanuelle Bourdelier3, Coloma Costas1, Ivan Matic5, Erick Denamur3, Jesús Blázquez6.
Abstract
Homologous recombination promotes genetic diversity by facilitating the integration of foreign DNA and intrachromosomal gene shuffling. It has been hypothesized that if recombination is variable among strains, selection should favor higher recombination rates among pathogens, as they face additional selection pressures from host defenses. To test this hypothesis we have developed a plasmid-based method for estimating the rate of recombination independently of other factors such as DNA transfer, selective processes, and mutational interference. Our results with 160 human commensal and extraintestinal pathogenic Escherichia coli (ExPEC) isolates show that the recombinant frequencies are extremely diverse (ranging 9 orders of magnitude) and plastic (they are profoundly affected by growth in urine, a condition commonly encountered by ExPEC). We find that the frequency of recombination is biased by strain lifestyle, as ExPEC isolates display strikingly higher recombination rates than their commensal counterparts. Furthermore, the presence of virulence factors is positively associated with higher recombination frequencies. These results suggest selection for high homologous recombination capacity, which may result in a higher evolvability for pathogens compared with commensals.Entities:
Keywords: ExPEC; RecA; commensal; evolution; homologous recombination
Mesh:
Year: 2015 PMID: 25804522 DOI: 10.1093/molbev/msv072
Source DB: PubMed Journal: Mol Biol Evol ISSN: 0737-4038 Impact factor: 16.240