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Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa
Nearly all bacteria produce narrow-spectrum antibiotics called bacteriocins. Studies have shown that bacteriocins can mediate microbial interactions, but the mechanisms underlying patterns of inhibition are less well understood. We assembled a spatially structured collection of isolates of Pseudomon...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735282/ https://www.ncbi.nlm.nih.gov/pubmed/33143580 http://dx.doi.org/10.1098/rspb.2020.1706 |
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author | Mojesky, Aubrey A. Remold, Susanna K. |
author_facet | Mojesky, Aubrey A. Remold, Susanna K. |
author_sort | Mojesky, Aubrey A. |
collection | PubMed |
description | Nearly all bacteria produce narrow-spectrum antibiotics called bacteriocins. Studies have shown that bacteriocins can mediate microbial interactions, but the mechanisms underlying patterns of inhibition are less well understood. We assembled a spatially structured collection of isolates of Pseudomonas aeruginosa from bathroom and kitchen sink drains in nine households. Growth inhibition of these P. aeruginosa by bacteriocins, known as pyocins in this species, was measured using pairwise inhibition assays. Carbon source usage of these isolates was measured, and genetic distance was estimated using multilocus sequencing. We found that as the distance between sites of isolation increased, there was a significantly higher probability of inhibition, and that pyocin inhibition and susceptibility vary greatly among isolates collected from different houses. We also detected support for other mechanisms influencing diversity: inhibition outcomes were influenced by the type of drain from which isolates were collected, and while we found no indication that carbon source utilization influences inhibition, inhibition was favoured at an intermediate genetic distance. Overall, these results suggest that the combined effects of dispersal limitation among sites and competitive exclusion within them maintain diversity in pyocin inhibition and susceptibility phenotypes, and that additional processes such as local adaptation and effects of phylogenetic distance could further contribute to spatial variability. |
format | Online Article Text |
id | pubmed-7735282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77352822020-12-28 Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa Mojesky, Aubrey A. Remold, Susanna K. Proc Biol Sci Evolution Nearly all bacteria produce narrow-spectrum antibiotics called bacteriocins. Studies have shown that bacteriocins can mediate microbial interactions, but the mechanisms underlying patterns of inhibition are less well understood. We assembled a spatially structured collection of isolates of Pseudomonas aeruginosa from bathroom and kitchen sink drains in nine households. Growth inhibition of these P. aeruginosa by bacteriocins, known as pyocins in this species, was measured using pairwise inhibition assays. Carbon source usage of these isolates was measured, and genetic distance was estimated using multilocus sequencing. We found that as the distance between sites of isolation increased, there was a significantly higher probability of inhibition, and that pyocin inhibition and susceptibility vary greatly among isolates collected from different houses. We also detected support for other mechanisms influencing diversity: inhibition outcomes were influenced by the type of drain from which isolates were collected, and while we found no indication that carbon source utilization influences inhibition, inhibition was favoured at an intermediate genetic distance. Overall, these results suggest that the combined effects of dispersal limitation among sites and competitive exclusion within them maintain diversity in pyocin inhibition and susceptibility phenotypes, and that additional processes such as local adaptation and effects of phylogenetic distance could further contribute to spatial variability. The Royal Society 2020-11-11 2020-11-04 /pmc/articles/PMC7735282/ /pubmed/33143580 http://dx.doi.org/10.1098/rspb.2020.1706 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolution Mojesky, Aubrey A. Remold, Susanna K. Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa |
title | Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa |
title_full | Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa |
title_fullStr | Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa |
title_full_unstemmed | Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa |
title_short | Spatial structure maintains diversity of pyocin inhibition in household Pseudomonas aeruginosa |
title_sort | spatial structure maintains diversity of pyocin inhibition in household pseudomonas aeruginosa |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735282/ https://www.ncbi.nlm.nih.gov/pubmed/33143580 http://dx.doi.org/10.1098/rspb.2020.1706 |
work_keys_str_mv | AT mojeskyaubreya spatialstructuremaintainsdiversityofpyocininhibitioninhouseholdpseudomonasaeruginosa AT remoldsusannak spatialstructuremaintainsdiversityofpyocininhibitioninhouseholdpseudomonasaeruginosa |