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Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae

The influence that bacterial adaptation (or niche partitioning) within species has on gene spillover and transmission among bacterial populations occupying different niches is not well understood. Streptococcus agalactiae is an important bacterial pathogen that has a taxonomically diverse host range...

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Autores principales: Richards, Vincent P, Velsko, Irina M, Alam, Md Tauqeer, Zadoks, Ruth N, Manning, Shannon D, Pavinski Bitar, Paulina D, Hassler, Hayley B, Crestani, Chiara, Springer, Garrett H, Probert, Brett M, Town, Christopher D, Stanhope, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805230/
https://www.ncbi.nlm.nih.gov/pubmed/31350563
http://dx.doi.org/10.1093/molbev/msz169
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author Richards, Vincent P
Velsko, Irina M
Alam, Md Tauqeer
Zadoks, Ruth N
Manning, Shannon D
Pavinski Bitar, Paulina D
Hassler, Hayley B
Crestani, Chiara
Springer, Garrett H
Probert, Brett M
Town, Christopher D
Stanhope, Michael J
author_facet Richards, Vincent P
Velsko, Irina M
Alam, Md Tauqeer
Zadoks, Ruth N
Manning, Shannon D
Pavinski Bitar, Paulina D
Hassler, Hayley B
Crestani, Chiara
Springer, Garrett H
Probert, Brett M
Town, Christopher D
Stanhope, Michael J
author_sort Richards, Vincent P
collection PubMed
description The influence that bacterial adaptation (or niche partitioning) within species has on gene spillover and transmission among bacterial populations occupying different niches is not well understood. Streptococcus agalactiae is an important bacterial pathogen that has a taxonomically diverse host range making it an excellent model system to study these processes. Here, we analyze a global set of 901 genome sequences from nine diverse host species to advance our understanding of these processes. Bayesian clustering analysis delineated 12 major populations that closely aligned with niches. Comparative genomics revealed extensive gene gain/loss among populations and a large pan genome of 9,527 genes, which remained open and was strongly partitioned among niches. As a result, the biochemical characteristics of 11 populations were highly distinctive (significantly enriched). Positive selection was detected and biochemical characteristics of the dispensable genes under selection were enriched in ten populations. Despite the strong gene partitioning, phylogenomics detected gene spillover. In particular, tetracycline resistance (which likely evolved in the human-associated population) from humans to bovine, canines, seals, and fish, demonstrating how a gene selected in one host can ultimately be transmitted into another, and biased transmission from humans to bovines was confirmed with a Bayesian migration analysis. Our findings show high bacterial genome plasticity acting in balance with selection pressure from distinct functional requirements of niches that is associated with an extensive and highly partitioned dispensable genome, likely facilitating continued and expansive adaptation.
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spelling pubmed-68052302019-10-25 Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae Richards, Vincent P Velsko, Irina M Alam, Md Tauqeer Zadoks, Ruth N Manning, Shannon D Pavinski Bitar, Paulina D Hassler, Hayley B Crestani, Chiara Springer, Garrett H Probert, Brett M Town, Christopher D Stanhope, Michael J Mol Biol Evol Discoveries The influence that bacterial adaptation (or niche partitioning) within species has on gene spillover and transmission among bacterial populations occupying different niches is not well understood. Streptococcus agalactiae is an important bacterial pathogen that has a taxonomically diverse host range making it an excellent model system to study these processes. Here, we analyze a global set of 901 genome sequences from nine diverse host species to advance our understanding of these processes. Bayesian clustering analysis delineated 12 major populations that closely aligned with niches. Comparative genomics revealed extensive gene gain/loss among populations and a large pan genome of 9,527 genes, which remained open and was strongly partitioned among niches. As a result, the biochemical characteristics of 11 populations were highly distinctive (significantly enriched). Positive selection was detected and biochemical characteristics of the dispensable genes under selection were enriched in ten populations. Despite the strong gene partitioning, phylogenomics detected gene spillover. In particular, tetracycline resistance (which likely evolved in the human-associated population) from humans to bovine, canines, seals, and fish, demonstrating how a gene selected in one host can ultimately be transmitted into another, and biased transmission from humans to bovines was confirmed with a Bayesian migration analysis. Our findings show high bacterial genome plasticity acting in balance with selection pressure from distinct functional requirements of niches that is associated with an extensive and highly partitioned dispensable genome, likely facilitating continued and expansive adaptation. Oxford University Press 2019-11 2019-07-25 /pmc/articles/PMC6805230/ /pubmed/31350563 http://dx.doi.org/10.1093/molbev/msz169 Text en © The Author(s) 2019. 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
Richards, Vincent P
Velsko, Irina M
Alam, Md Tauqeer
Zadoks, Ruth N
Manning, Shannon D
Pavinski Bitar, Paulina D
Hassler, Hayley B
Crestani, Chiara
Springer, Garrett H
Probert, Brett M
Town, Christopher D
Stanhope, Michael J
Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae
title Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae
title_full Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae
title_fullStr Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae
title_full_unstemmed Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae
title_short Population Gene Introgression and High Genome Plasticity for the Zoonotic Pathogen Streptococcus agalactiae
title_sort population gene introgression and high genome plasticity for the zoonotic pathogen streptococcus agalactiae
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805230/
https://www.ncbi.nlm.nih.gov/pubmed/31350563
http://dx.doi.org/10.1093/molbev/msz169
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