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Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny
Shigella flexneri is a major health burden in low- and middle-income countries, where it is a leading cause of mortality associated with diarrhoea in children, and shows an increasing incidence among travellers and men having sex with men. Like all Shigella spp., S. flexneri has evolved from commens...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Microbiology Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455713/ https://www.ncbi.nlm.nih.gov/pubmed/35759406 http://dx.doi.org/10.1099/mgen.0.000846 |
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author | Pilla, Giulia Arcari, Gabriele Tang, Christoph M. Carattoli, Alessandra |
author_facet | Pilla, Giulia Arcari, Gabriele Tang, Christoph M. Carattoli, Alessandra |
author_sort | Pilla, Giulia |
collection | PubMed |
description | Shigella flexneri is a major health burden in low- and middle-income countries, where it is a leading cause of mortality associated with diarrhoea in children, and shows an increasing incidence among travellers and men having sex with men. Like all Shigella spp., S. flexneri has evolved from commensal Escherichia coli following the acquisition of a large plasmid pINV, which contains genes essential for virulence. Current sequence typing schemes of Shigella are based on combinations of chromosomal genetic loci, since pINV-encoded virulence genes are often lost during growth in the laboratory, making these elements inappropriate for sequence typing. By performing comparative analysis of pINVs from S. flexneri strains isolated from different geographical regions and belonging to different serotypes, we found that in contrast to plasmid-encoded virulence genes, plasmid maintenance genes are highly stable pINV-encoded elements. For the first time, to our knowledge, we have developed a S. flexneri plasmid multilocus sequence typing (pMLST) method based on different combinations of alleles of the vapBC and yacAB toxin–antitoxin (TA) systems, and the parAB partitioning system. This enables typing of S. flexneri pINV plasmids into distinct ‘virulence sequence types’ (vSTs). Furthermore, the phylogenies of vST alleles and bacterial host core genomes suggests an intimate co-evolution of pINV with the chromosome of its bacterial host, consistent with previous findings. This work demonstrates the potential of plasmid maintenance loci as genetic characteristics to study as well as to trace the molecular phylogenesis of S. flexneri pINV and the phylogenetic relationship of this plasmid with its bacterial host. |
format | Online Article Text |
id | pubmed-9455713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94557132022-09-09 Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny Pilla, Giulia Arcari, Gabriele Tang, Christoph M. Carattoli, Alessandra Microb Genom Research Articles Shigella flexneri is a major health burden in low- and middle-income countries, where it is a leading cause of mortality associated with diarrhoea in children, and shows an increasing incidence among travellers and men having sex with men. Like all Shigella spp., S. flexneri has evolved from commensal Escherichia coli following the acquisition of a large plasmid pINV, which contains genes essential for virulence. Current sequence typing schemes of Shigella are based on combinations of chromosomal genetic loci, since pINV-encoded virulence genes are often lost during growth in the laboratory, making these elements inappropriate for sequence typing. By performing comparative analysis of pINVs from S. flexneri strains isolated from different geographical regions and belonging to different serotypes, we found that in contrast to plasmid-encoded virulence genes, plasmid maintenance genes are highly stable pINV-encoded elements. For the first time, to our knowledge, we have developed a S. flexneri plasmid multilocus sequence typing (pMLST) method based on different combinations of alleles of the vapBC and yacAB toxin–antitoxin (TA) systems, and the parAB partitioning system. This enables typing of S. flexneri pINV plasmids into distinct ‘virulence sequence types’ (vSTs). Furthermore, the phylogenies of vST alleles and bacterial host core genomes suggests an intimate co-evolution of pINV with the chromosome of its bacterial host, consistent with previous findings. This work demonstrates the potential of plasmid maintenance loci as genetic characteristics to study as well as to trace the molecular phylogenesis of S. flexneri pINV and the phylogenetic relationship of this plasmid with its bacterial host. Microbiology Society 2022-06-27 /pmc/articles/PMC9455713/ /pubmed/35759406 http://dx.doi.org/10.1099/mgen.0.000846 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution. |
spellingShingle | Research Articles Pilla, Giulia Arcari, Gabriele Tang, Christoph M. Carattoli, Alessandra Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny |
title | Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny |
title_full | Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny |
title_fullStr | Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny |
title_full_unstemmed | Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny |
title_short | Virulence plasmid pINV as a genetic signature for Shigella flexneri phylogeny |
title_sort | virulence plasmid pinv as a genetic signature for shigella flexneri phylogeny |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455713/ https://www.ncbi.nlm.nih.gov/pubmed/35759406 http://dx.doi.org/10.1099/mgen.0.000846 |
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