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Inferring evolutionary pathways and directed genotype networks of foodborne pathogens
Modelling the emergence of foodborne pathogens is a crucial step in the prediction and prevention of disease outbreaks. Unfortunately, the mechanisms that drive the evolution of such continuously adapting pathogens remain poorly understood. Here, we combine molecular genotyping with network science...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7657559/ https://www.ncbi.nlm.nih.gov/pubmed/33125373 http://dx.doi.org/10.1371/journal.pcbi.1008401 |
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author | Cliff, Oliver M. McLean, Natalia Sintchenko, Vitali Fair, Kristopher M. Sorrell, Tania C. Kauffman, Stuart Prokopenko, Mikhail |
author_facet | Cliff, Oliver M. McLean, Natalia Sintchenko, Vitali Fair, Kristopher M. Sorrell, Tania C. Kauffman, Stuart Prokopenko, Mikhail |
author_sort | Cliff, Oliver M. |
collection | PubMed |
description | Modelling the emergence of foodborne pathogens is a crucial step in the prediction and prevention of disease outbreaks. Unfortunately, the mechanisms that drive the evolution of such continuously adapting pathogens remain poorly understood. Here, we combine molecular genotyping with network science and Bayesian inference to infer directed genotype networks—and trace the emergence and evolutionary paths—of Salmonella Typhimurium (STM) from nine years of Australian disease surveillance data. We construct networks where nodes represent STM strains and directed edges represent evolutionary steps, presenting evidence that the structural (i.e., network-based) features are relevant to understanding the functional (i.e., fitness-based) progression of co-evolving STM strains. This is argued by showing that outbreak severity, i.e., prevalence, correlates to: (i) the network path length to the most prevalent node (r = −0.613, N = 690); and (ii) the network connected-component size (r = 0.739). Moreover, we uncover distinct exploration-exploitation pathways in the genetic space of STM, including a strong evolutionary drive through a transition region. This is examined via the 6,897 distinct evolutionary paths in the directed network, where we observe a dominant 66% of these paths decrease in network centrality, whilst increasing in prevalence. Furthermore, 72.4% of all paths originate in the transition region, with 64% of those following the dominant direction. Further, we find that the length of an evolutionary path strongly correlates to its increase in prevalence (r = 0.497). Combined, these findings indicate that longer evolutionary paths result in genetically rare and virulent strains, which mostly evolve from a single transition point. Our results not only validate our widely-applicable approach for inferring directed genotype networks from data, but also provide a unique insight into the elusive functional and structural drivers of STM bacteria. |
format | Online Article Text |
id | pubmed-7657559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76575592020-11-18 Inferring evolutionary pathways and directed genotype networks of foodborne pathogens Cliff, Oliver M. McLean, Natalia Sintchenko, Vitali Fair, Kristopher M. Sorrell, Tania C. Kauffman, Stuart Prokopenko, Mikhail PLoS Comput Biol Research Article Modelling the emergence of foodborne pathogens is a crucial step in the prediction and prevention of disease outbreaks. Unfortunately, the mechanisms that drive the evolution of such continuously adapting pathogens remain poorly understood. Here, we combine molecular genotyping with network science and Bayesian inference to infer directed genotype networks—and trace the emergence and evolutionary paths—of Salmonella Typhimurium (STM) from nine years of Australian disease surveillance data. We construct networks where nodes represent STM strains and directed edges represent evolutionary steps, presenting evidence that the structural (i.e., network-based) features are relevant to understanding the functional (i.e., fitness-based) progression of co-evolving STM strains. This is argued by showing that outbreak severity, i.e., prevalence, correlates to: (i) the network path length to the most prevalent node (r = −0.613, N = 690); and (ii) the network connected-component size (r = 0.739). Moreover, we uncover distinct exploration-exploitation pathways in the genetic space of STM, including a strong evolutionary drive through a transition region. This is examined via the 6,897 distinct evolutionary paths in the directed network, where we observe a dominant 66% of these paths decrease in network centrality, whilst increasing in prevalence. Furthermore, 72.4% of all paths originate in the transition region, with 64% of those following the dominant direction. Further, we find that the length of an evolutionary path strongly correlates to its increase in prevalence (r = 0.497). Combined, these findings indicate that longer evolutionary paths result in genetically rare and virulent strains, which mostly evolve from a single transition point. Our results not only validate our widely-applicable approach for inferring directed genotype networks from data, but also provide a unique insight into the elusive functional and structural drivers of STM bacteria. Public Library of Science 2020-10-30 /pmc/articles/PMC7657559/ /pubmed/33125373 http://dx.doi.org/10.1371/journal.pcbi.1008401 Text en © 2020 Cliff 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 Cliff, Oliver M. McLean, Natalia Sintchenko, Vitali Fair, Kristopher M. Sorrell, Tania C. Kauffman, Stuart Prokopenko, Mikhail Inferring evolutionary pathways and directed genotype networks of foodborne pathogens |
title | Inferring evolutionary pathways and directed genotype networks of foodborne pathogens |
title_full | Inferring evolutionary pathways and directed genotype networks of foodborne pathogens |
title_fullStr | Inferring evolutionary pathways and directed genotype networks of foodborne pathogens |
title_full_unstemmed | Inferring evolutionary pathways and directed genotype networks of foodborne pathogens |
title_short | Inferring evolutionary pathways and directed genotype networks of foodborne pathogens |
title_sort | inferring evolutionary pathways and directed genotype networks of foodborne pathogens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7657559/ https://www.ncbi.nlm.nih.gov/pubmed/33125373 http://dx.doi.org/10.1371/journal.pcbi.1008401 |
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