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Abstract(s)
Proteins secreted to the extracellular environment or to the periphery of the cell envelope, the secretome, play essential
roles in foraging, antagonistic and mutualistic interactions. We hypothesize that arms races, genetic conflicts and varying
selective pressures should lead to the rapid change of sequences and gene repertoires of the secretome. The analysis of 42
bacterial pan-genomes shows that secreted, and especially extracellular proteins, are predominantly encoded in the
accessory genome, i.e. among genes not ubiquitous within the clade. Genes encoding outer membrane proteins might
engage more frequently in intra-chromosomal gene conversion because they are more often in multi-genic families. The
gene sequences encoding the secretome evolve faster than the rest of the genome and in particular at non-synonymous
positions. Cell wall proteins in Firmicutes evolve particularly fast when compared with outer membrane proteins of
Proteobacteria. Virulence factors are over-represented in the secretome, notably in outer membrane proteins, but cell
localization explains more of the variance in substitution rates and gene repertoires than sequence homology to known
virulence factors. Accordingly, the repertoires and sequences of the genes encoding the secretome change fast in the clades
of obligatory and facultative pathogens and also in the clades of mutualists and free-living bacteria. Our study shows that
cell localization shapes genome evolution. In agreement with our hypothesis, the repertoires and the sequences of genes
encoding secreted proteins evolve fast. The particularly rapid change of extracellular proteins suggests that these public
goods are key players in bacterial adaptation.
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PLoS ONE