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Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens
Within-host adaptation is a hallmark of chronic bacterial infections, involving substantial genomic changes. Recent large-scale genomic data from prolonged infections allow the examination of adaptive strategies employed by different pathogens and open the door to investigate whether they converge t...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947768/ https://www.ncbi.nlm.nih.gov/pubmed/33118035 http://dx.doi.org/10.1093/molbev/msaa278 |
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author | Gatt, Yair E Margalit, Hanah |
author_facet | Gatt, Yair E Margalit, Hanah |
author_sort | Gatt, Yair E |
collection | PubMed |
description | Within-host adaptation is a hallmark of chronic bacterial infections, involving substantial genomic changes. Recent large-scale genomic data from prolonged infections allow the examination of adaptive strategies employed by different pathogens and open the door to investigate whether they converge toward similar strategies. Here, we compiled extensive data of whole-genome sequences of bacterial isolates belonging to miscellaneous species sampled at sequential time points during clinical infections. Analysis of these data revealed that different species share some common adaptive strategies, achieved by mutating various genes. Although the same genes were often mutated in several strains within a species, different genes related to the same pathway, structure, or function were changed in other species utilizing the same adaptive strategy (e.g., mutating flagellar genes). Strategies exploited by various bacterial species were often predicted to be driven by the host immune system, a powerful selective pressure that is not species specific. Remarkably, we find adaptive strategies identified previously within single species to be ubiquitous. Two striking examples are shifts from siderophore-based to heme-based iron scavenging (previously shown for Pseudomonas aeruginosa) and changes in glycerol-phosphate metabolism (previously shown to decrease sensitivity to antibiotics in Mycobacterium tuberculosis). Virulence factors were often adaptively affected in different species, indicating shifts from acute to chronic virulence and virulence attenuation during infection. Our study presents a global view on common within-host adaptive strategies employed by different bacterial species and provides a rich resource for further studying these processes. |
format | Online Article Text |
id | pubmed-7947768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79477682021-03-16 Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens Gatt, Yair E Margalit, Hanah Mol Biol Evol Discoveries Within-host adaptation is a hallmark of chronic bacterial infections, involving substantial genomic changes. Recent large-scale genomic data from prolonged infections allow the examination of adaptive strategies employed by different pathogens and open the door to investigate whether they converge toward similar strategies. Here, we compiled extensive data of whole-genome sequences of bacterial isolates belonging to miscellaneous species sampled at sequential time points during clinical infections. Analysis of these data revealed that different species share some common adaptive strategies, achieved by mutating various genes. Although the same genes were often mutated in several strains within a species, different genes related to the same pathway, structure, or function were changed in other species utilizing the same adaptive strategy (e.g., mutating flagellar genes). Strategies exploited by various bacterial species were often predicted to be driven by the host immune system, a powerful selective pressure that is not species specific. Remarkably, we find adaptive strategies identified previously within single species to be ubiquitous. Two striking examples are shifts from siderophore-based to heme-based iron scavenging (previously shown for Pseudomonas aeruginosa) and changes in glycerol-phosphate metabolism (previously shown to decrease sensitivity to antibiotics in Mycobacterium tuberculosis). Virulence factors were often adaptively affected in different species, indicating shifts from acute to chronic virulence and virulence attenuation during infection. Our study presents a global view on common within-host adaptive strategies employed by different bacterial species and provides a rich resource for further studying these processes. Oxford University Press 2020-10-28 /pmc/articles/PMC7947768/ /pubmed/33118035 http://dx.doi.org/10.1093/molbev/msaa278 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Gatt, Yair E Margalit, Hanah Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens |
title | Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens |
title_full | Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens |
title_fullStr | Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens |
title_full_unstemmed | Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens |
title_short | Common Adaptive Strategies Underlie Within-Host Evolution of Bacterial Pathogens |
title_sort | common adaptive strategies underlie within-host evolution of bacterial pathogens |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947768/ https://www.ncbi.nlm.nih.gov/pubmed/33118035 http://dx.doi.org/10.1093/molbev/msaa278 |
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