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The evolutionary diversification of the Salmonella artAB toxin locus
Salmonella enterica is a diverse species of bacterial pathogens comprised of >2,500 serovars with variable host ranges and virulence properties. Accumulating evidence indicates that two AB(5)-type toxins, typhoid toxin and ArtAB toxin, contribute to the more severe virulence properties of the Sal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732031/ https://www.ncbi.nlm.nih.gov/pubmed/36504768 http://dx.doi.org/10.3389/fmicb.2022.1016438 |
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author | Ojiakor, Adaobi Gibbs, Rachel N. Chen, Zhe Gao, Xiang Fowler, Casey C. |
author_facet | Ojiakor, Adaobi Gibbs, Rachel N. Chen, Zhe Gao, Xiang Fowler, Casey C. |
author_sort | Ojiakor, Adaobi |
collection | PubMed |
description | Salmonella enterica is a diverse species of bacterial pathogens comprised of >2,500 serovars with variable host ranges and virulence properties. Accumulating evidence indicates that two AB(5)-type toxins, typhoid toxin and ArtAB toxin, contribute to the more severe virulence properties of the Salmonella strains that encode them. It was recently discovered that there are two distinct types of artAB-like genetic elements in Salmonella: those that encode ArtAB toxins (artAB elements) and those in which the artA gene is degraded and the ArtB homolog, dubbed PltC, serves as an alternative delivery subunit for typhoid toxin (pltC elements). Here, we take a multifaceted approach to explore the evolutionary diversification of artAB-like genetic elements in Salmonella. We identify 7 subtypes of ArtAB toxins and 4 different PltC sequence groups that are distributed throughout the Salmonella genus. Both artAB and pltC are encoded within numerous diverse prophages, indicating a central role for phages in their evolutionary diversification. Genetic and structural analyses revealed features that distinguish pltC elements from artAB and identified evolutionary adaptations that enable PltC to efficiently engage typhoid toxin A subunits. For both pltC and artAB, we find that the sequences of the B subunits are especially variable, particularly amongst amino acid residues that fine tune the chemical environment of their glycan binding pockets. This study provides a framework to delineate the remarkably complex collection of Salmonella artAB/pltC-like genetic elements and provides a window into the mechanisms of evolution for AB(5)-type toxins. |
format | Online Article Text |
id | pubmed-9732031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97320312022-12-10 The evolutionary diversification of the Salmonella artAB toxin locus Ojiakor, Adaobi Gibbs, Rachel N. Chen, Zhe Gao, Xiang Fowler, Casey C. Front Microbiol Microbiology Salmonella enterica is a diverse species of bacterial pathogens comprised of >2,500 serovars with variable host ranges and virulence properties. Accumulating evidence indicates that two AB(5)-type toxins, typhoid toxin and ArtAB toxin, contribute to the more severe virulence properties of the Salmonella strains that encode them. It was recently discovered that there are two distinct types of artAB-like genetic elements in Salmonella: those that encode ArtAB toxins (artAB elements) and those in which the artA gene is degraded and the ArtB homolog, dubbed PltC, serves as an alternative delivery subunit for typhoid toxin (pltC elements). Here, we take a multifaceted approach to explore the evolutionary diversification of artAB-like genetic elements in Salmonella. We identify 7 subtypes of ArtAB toxins and 4 different PltC sequence groups that are distributed throughout the Salmonella genus. Both artAB and pltC are encoded within numerous diverse prophages, indicating a central role for phages in their evolutionary diversification. Genetic and structural analyses revealed features that distinguish pltC elements from artAB and identified evolutionary adaptations that enable PltC to efficiently engage typhoid toxin A subunits. For both pltC and artAB, we find that the sequences of the B subunits are especially variable, particularly amongst amino acid residues that fine tune the chemical environment of their glycan binding pockets. This study provides a framework to delineate the remarkably complex collection of Salmonella artAB/pltC-like genetic elements and provides a window into the mechanisms of evolution for AB(5)-type toxins. Frontiers Media S.A. 2022-11-25 /pmc/articles/PMC9732031/ /pubmed/36504768 http://dx.doi.org/10.3389/fmicb.2022.1016438 Text en Copyright © 2022 Ojiakor, Gibbs, Chen, Gao and Fowler. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Ojiakor, Adaobi Gibbs, Rachel N. Chen, Zhe Gao, Xiang Fowler, Casey C. The evolutionary diversification of the Salmonella artAB toxin locus |
title | The evolutionary diversification of the Salmonella artAB toxin locus |
title_full | The evolutionary diversification of the Salmonella artAB toxin locus |
title_fullStr | The evolutionary diversification of the Salmonella artAB toxin locus |
title_full_unstemmed | The evolutionary diversification of the Salmonella artAB toxin locus |
title_short | The evolutionary diversification of the Salmonella artAB toxin locus |
title_sort | evolutionary diversification of the salmonella artab toxin locus |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732031/ https://www.ncbi.nlm.nih.gov/pubmed/36504768 http://dx.doi.org/10.3389/fmicb.2022.1016438 |
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