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Quantifying the strength of quorum sensing crosstalk within microbial communities
In multispecies microbial communities, the exchange of signals such as acyl-homoserine lactones (AHL) enables communication within and between species of Gram-negative bacteria. This process, commonly known as quorum sensing, aids in the regulation of genes crucial for the survival of species within...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663516/ https://www.ncbi.nlm.nih.gov/pubmed/29049387 http://dx.doi.org/10.1371/journal.pcbi.1005809 |
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author | Silva, Kalinga Pavan T. Chellamuthu, Prithiviraj Boedicker, James Q. |
author_facet | Silva, Kalinga Pavan T. Chellamuthu, Prithiviraj Boedicker, James Q. |
author_sort | Silva, Kalinga Pavan T. |
collection | PubMed |
description | In multispecies microbial communities, the exchange of signals such as acyl-homoserine lactones (AHL) enables communication within and between species of Gram-negative bacteria. This process, commonly known as quorum sensing, aids in the regulation of genes crucial for the survival of species within heterogeneous populations of microbes. Although signal exchange was studied extensively in well-mixed environments, less is known about the consequences of crosstalk in spatially distributed mixtures of species. Here, signaling dynamics were measured in a spatially distributed system containing multiple strains utilizing homologous signaling systems. Crosstalk between strains containing the lux, las and rhl AHL-receptor circuits was quantified. In a distributed population of microbes, the impact of community composition on spatio-temporal dynamics was characterized and compared to simulation results using a modified reaction-diffusion model. After introducing a single term to account for crosstalk between each pair of signals, the model was able to reproduce the activation patterns observed in experiments. We quantified the robustness of signal propagation in the presence of interacting signals, finding that signaling dynamics are largely robust to interference. The ability of several wild isolates to participate in AHL-mediated signaling was investigated, revealing distinct signatures of crosstalk for each species. Our results present a route to characterize crosstalk between species and predict systems-level signaling dynamics in multispecies communities. |
format | Online Article Text |
id | pubmed-5663516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56635162017-11-08 Quantifying the strength of quorum sensing crosstalk within microbial communities Silva, Kalinga Pavan T. Chellamuthu, Prithiviraj Boedicker, James Q. PLoS Comput Biol Research Article In multispecies microbial communities, the exchange of signals such as acyl-homoserine lactones (AHL) enables communication within and between species of Gram-negative bacteria. This process, commonly known as quorum sensing, aids in the regulation of genes crucial for the survival of species within heterogeneous populations of microbes. Although signal exchange was studied extensively in well-mixed environments, less is known about the consequences of crosstalk in spatially distributed mixtures of species. Here, signaling dynamics were measured in a spatially distributed system containing multiple strains utilizing homologous signaling systems. Crosstalk between strains containing the lux, las and rhl AHL-receptor circuits was quantified. In a distributed population of microbes, the impact of community composition on spatio-temporal dynamics was characterized and compared to simulation results using a modified reaction-diffusion model. After introducing a single term to account for crosstalk between each pair of signals, the model was able to reproduce the activation patterns observed in experiments. We quantified the robustness of signal propagation in the presence of interacting signals, finding that signaling dynamics are largely robust to interference. The ability of several wild isolates to participate in AHL-mediated signaling was investigated, revealing distinct signatures of crosstalk for each species. Our results present a route to characterize crosstalk between species and predict systems-level signaling dynamics in multispecies communities. Public Library of Science 2017-10-19 /pmc/articles/PMC5663516/ /pubmed/29049387 http://dx.doi.org/10.1371/journal.pcbi.1005809 Text en © 2017 Silva et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Silva, Kalinga Pavan T. Chellamuthu, Prithiviraj Boedicker, James Q. Quantifying the strength of quorum sensing crosstalk within microbial communities |
title | Quantifying the strength of quorum sensing crosstalk within microbial communities |
title_full | Quantifying the strength of quorum sensing crosstalk within microbial communities |
title_fullStr | Quantifying the strength of quorum sensing crosstalk within microbial communities |
title_full_unstemmed | Quantifying the strength of quorum sensing crosstalk within microbial communities |
title_short | Quantifying the strength of quorum sensing crosstalk within microbial communities |
title_sort | quantifying the strength of quorum sensing crosstalk within microbial communities |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663516/ https://www.ncbi.nlm.nih.gov/pubmed/29049387 http://dx.doi.org/10.1371/journal.pcbi.1005809 |
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