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Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains

Yersinia pestis is the causative agent of at least three major plague pandemics (Justinianic, Medieval and Modern). Previous studies on ancient Y. pestis genomes revealed that several genomic alterations had occurred approximately 5000–3000 years ago and contributed to the remarkable virulence of th...

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Autores principales: Bonczarowska, Joanna H., Susat, Julian, Krause-Kyora, Ben, Dangvard Pedersen, Dorthe, Boldsen, Jesper, Larsen, Lars Agersnap, Seeberg, Lone, Nebel, Almut, Unterweger, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354491/
https://www.ncbi.nlm.nih.gov/pubmed/37464758
http://dx.doi.org/10.1098/rspb.2023.0622
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author Bonczarowska, Joanna H.
Susat, Julian
Krause-Kyora, Ben
Dangvard Pedersen, Dorthe
Boldsen, Jesper
Larsen, Lars Agersnap
Seeberg, Lone
Nebel, Almut
Unterweger, Daniel
author_facet Bonczarowska, Joanna H.
Susat, Julian
Krause-Kyora, Ben
Dangvard Pedersen, Dorthe
Boldsen, Jesper
Larsen, Lars Agersnap
Seeberg, Lone
Nebel, Almut
Unterweger, Daniel
author_sort Bonczarowska, Joanna H.
collection PubMed
description Yersinia pestis is the causative agent of at least three major plague pandemics (Justinianic, Medieval and Modern). Previous studies on ancient Y. pestis genomes revealed that several genomic alterations had occurred approximately 5000–3000 years ago and contributed to the remarkable virulence of this pathogen. How a subset of strains evolved to cause the Modern pandemic is less well-understood. Here, we examined the virulence-associated prophage (YpfΦ), which had been postulated to be exclusively present in the genomes of strains associated with the Modern pandemic. The analysis of two new Y. pestis genomes from medieval/early modern Denmark confirmed that the phage is absent from the genome of strains dating to this time period. An extended comparative genome analysis of over 300 strains spanning more than 5000 years showed that the prophage is found in the genomes of modern strains only and suggests an integration into the genome during recent Y. pestis evolution. The phage-encoded Zot protein showed structural homology to a virulence factor of Vibrio cholerae. Similar to modern Y. pestis, we observed phages with a common origin to YpfΦ in individual strains of other bacterial species. Our findings present an updated view on the prevalence of YpfΦ, which might contribute to our understanding of the host spectrum, geographical spread and virulence of Y. pestis responsible for the Modern pandemic.
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spelling pubmed-103544912023-07-20 Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains Bonczarowska, Joanna H. Susat, Julian Krause-Kyora, Ben Dangvard Pedersen, Dorthe Boldsen, Jesper Larsen, Lars Agersnap Seeberg, Lone Nebel, Almut Unterweger, Daniel Proc Biol Sci Genetics and Genomics Yersinia pestis is the causative agent of at least three major plague pandemics (Justinianic, Medieval and Modern). Previous studies on ancient Y. pestis genomes revealed that several genomic alterations had occurred approximately 5000–3000 years ago and contributed to the remarkable virulence of this pathogen. How a subset of strains evolved to cause the Modern pandemic is less well-understood. Here, we examined the virulence-associated prophage (YpfΦ), which had been postulated to be exclusively present in the genomes of strains associated with the Modern pandemic. The analysis of two new Y. pestis genomes from medieval/early modern Denmark confirmed that the phage is absent from the genome of strains dating to this time period. An extended comparative genome analysis of over 300 strains spanning more than 5000 years showed that the prophage is found in the genomes of modern strains only and suggests an integration into the genome during recent Y. pestis evolution. The phage-encoded Zot protein showed structural homology to a virulence factor of Vibrio cholerae. Similar to modern Y. pestis, we observed phages with a common origin to YpfΦ in individual strains of other bacterial species. Our findings present an updated view on the prevalence of YpfΦ, which might contribute to our understanding of the host spectrum, geographical spread and virulence of Y. pestis responsible for the Modern pandemic. The Royal Society 2023-07-26 2023-07-19 /pmc/articles/PMC10354491/ /pubmed/37464758 http://dx.doi.org/10.1098/rspb.2023.0622 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Genetics and Genomics
Bonczarowska, Joanna H.
Susat, Julian
Krause-Kyora, Ben
Dangvard Pedersen, Dorthe
Boldsen, Jesper
Larsen, Lars Agersnap
Seeberg, Lone
Nebel, Almut
Unterweger, Daniel
Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains
title Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains
title_full Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains
title_fullStr Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains
title_full_unstemmed Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains
title_short Ancient Yersinia pestis genomes lack the virulence-associated YpfΦ prophage present in modern pandemic strains
title_sort ancient yersinia pestis genomes lack the virulence-associated ypfφ prophage present in modern pandemic strains
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354491/
https://www.ncbi.nlm.nih.gov/pubmed/37464758
http://dx.doi.org/10.1098/rspb.2023.0622
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