Beschreibung:
<jats:p>Five hundred and thirty-four unrelated <jats:italic>
<jats:named-content content-type="species">
<jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://doi.org/10.1601/nm.2553" xlink:type="simple">Pseudomonas aeruginosa</jats:ext-link>
</jats:named-content>
</jats:italic> isolates from inanimate habitats, patients with cystic fibrosis (CF) and other human infections were sequenced in 19 genes that had been identified previously as the hot spots of genomic within-host evolution in serial isolates from 12 CF lungs. Amplicon sequencing confirmed a significantly higher sequence diversity of the 19 loci in <jats:italic>
<jats:named-content content-type="species">
<jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://doi.org/10.1601/nm.2553" xlink:type="simple">P. aeruginosa</jats:ext-link>
</jats:named-content>
</jats:italic> isolates from CF patients compared to those from other habitats, but this overrepresentation was mainly due to the larger share of synonymous substitutions. Correspondingly, non-synonymous substitutions were either rare (<jats:italic>gltT</jats:italic>, <jats:italic>lepA</jats:italic>, <jats:italic>ptsP</jats:italic>) or benign (<jats:italic>nuoL</jats:italic>, <jats:italic>fleR</jats:italic>, <jats:italic>pelF</jats:italic>) in some loci. Other loci, however, showed an accumulation of non-neutral coding variants. Strains from the CF habitat were often mutated at evolutionarily conserved positions in the elements of stringent response (RelA, SpoT), LPS (PagL), polyamine transport (SpuE, SpuF) and alginate biosynthesis (AlgG, AlgU). The strongest skew towards the CF lung habitat was seen for amino acid sequence variants in AlgG that clustered in the carbohydrate-binding/sugar hydrolysis domain. The master regulators of quorum sensing <jats:italic>lasR</jats:italic> and <jats:italic>rhlR</jats:italic> were frequent targets for coding variants in isolates from chronic and acute human infections. Unique variants in <jats:italic>lasR</jats:italic> showed strong evidence of positive selection indicated by <jats:italic>d</jats:italic>
<jats:sub>N</jats:sub>/<jats:italic>d</jats:italic>
<jats:sub>S</jats:sub> values of ~4. The <jats:italic>pelA</jats:italic> gene that encodes a multidomain enzyme involved in both the formation and dispersion of Pel biofilms carried the highest number of single-nucleotide variants among the 19 genes and was the only gene with a higher frequency of missense mutations in <jats:italic>
<jats:named-content content-type="species">
<jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://doi.org/10.1601/nm.2553" xlink:type="simple">P. aeruginosa</jats:ext-link>
</jats:named-content>
</jats:italic> strains from non-CF habitats than in isolates from CF airways. PelA protein variants are widely distributed in the <jats:italic>
<jats:named-content content-type="species">
<jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://doi.org/10.1601/nm.2553" xlink:type="simple">P. aeruginosa</jats:ext-link>
</jats:named-content>
</jats:italic> population. In conclusion, coding variants in a subset of the examined loci are indeed characteristic for the adaptation of <jats:italic>
<jats:named-content content-type="species">
<jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://doi.org/10.1601/nm.2553" xlink:type="simple">P. aeruginosa</jats:ext-link>
</jats:named-content>
</jats:italic> to the CF airways, but for other loci the elevated mutation rate is more indicative of infections in human habitats (<jats:italic>lasR, rhlR</jats:italic>) or global diversifying selection (<jats:italic>pelA</jats:italic>).</jats:p>