Genetic exchanges are more frequent in bacteria encoding capsules

PLoS Genet. 2018 Dec 21;14(12):e1007862. doi: 10.1371/journal.pgen.1007862. eCollection 2018 Dec.

Abstract

Capsules allow bacteria to colonize novel environments, to withstand numerous stresses, and to resist antibiotics. Yet, even though genetic exchanges with other cells should be adaptive under such circumstances, it has been suggested that capsules lower the rates of homologous recombination and horizontal gene transfer. We analysed over one hundred pan-genomes and thousands of bacterial genomes for the evidence of an association between genetic exchanges (or lack thereof) and the presence of a capsule system. We found that bacteria encoding capsules have larger pan-genomes, higher rates of horizontal gene transfer, and higher rates of homologous recombination in their core genomes. Accordingly, genomes encoding capsules have more plasmids, conjugative elements, transposases, prophages, and integrons. Furthermore, capsular loci are frequent in plasmids, and can be found in prophages. These results are valid for Bacteria, independently of their ability to be naturally transformable. Since we have shown previously that capsules are commonly present in nosocomial pathogens, we analysed their co-occurrence with antibiotic resistance genes. Genomes encoding capsules have more antibiotic resistance genes, especially those encoding efflux pumps, and they constitute the majority of the most worrisome nosocomial bacteria. We conclude that bacteria with capsule systems are more genetically diverse and have fast-evolving gene repertoires, which may further contribute to their success in colonizing novel niches such as humans under antibiotic therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria / classification
  • Bacteria / genetics*
  • Bacterial Capsules / genetics*
  • DNA Restriction-Modification Enzymes / genetics
  • Drug Resistance, Bacterial / genetics
  • Gene Transfer, Horizontal
  • Genome, Bacterial*
  • Homologous Recombination
  • Interspersed Repetitive Sequences
  • Phylogeny
  • Species Specificity

Substances

  • DNA Restriction-Modification Enzymes

Grants and funding

This work was supported by an FRM (Fondation pour la recherche médicale) grant [ARF20150934077] awarded to OR. JAMS is supported by an EU FP7 PRESTIGE grant [PRESTIGE-2017-1-0012]. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.