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A new perspective on ancient Mitis group streptococcal genetics

Mitis group Streptococcus are human obligate bacteria residing in the nasopharynx and oral cavity. They comprise both commensal and pathogenic species with the most well-known being Streptococcus pneumoniae – a leading cause of meningitis and pneumonia. A primary difference between the commensal and...

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Autores principales: Belman, Sophie, Chaguza, Chrispin, Kumar, Narender, Lo, Stephanie, Bentley, Stephen D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8942026/
https://www.ncbi.nlm.nih.gov/pubmed/35225216
http://dx.doi.org/10.1099/mgen.0.000753
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author Belman, Sophie
Chaguza, Chrispin
Kumar, Narender
Lo, Stephanie
Bentley, Stephen D.
author_facet Belman, Sophie
Chaguza, Chrispin
Kumar, Narender
Lo, Stephanie
Bentley, Stephen D.
author_sort Belman, Sophie
collection PubMed
description Mitis group Streptococcus are human obligate bacteria residing in the nasopharynx and oral cavity. They comprise both commensal and pathogenic species with the most well-known being Streptococcus pneumoniae – a leading cause of meningitis and pneumonia. A primary difference between the commensal and pathogenic species is the presence of the polysaccharide capsule – a major virulence factor in S. pneumoniae , also present in other commensal species. Our current understanding of the evolutionary divergence of the pathogenic and commensal species has been inferred from extant strains. Ancient genomes can further elucidate streptococcal evolutionary history. We extracted streptococcal genome reads from a 5700-year-old ancient metagenome and worked towards characterizing them. Due to excessive within- and between-species recombination common among streptococci we were unable to parse individual species. Further, the composite reads of the ancient metagenome do not fit within the diversity of any specific extant species. Using a capsular gene database and AT-content analysis we determined that this ancient metagenome is missing polysaccharide synthesis genes integral to streptococcal capsule formation. The presence of multiple zinc metalloproteases suggests that adaptation to host IgA1 had begun and the presence of other virulence factors further implies development of close host–microbe interactions, though the absence of a capsule suggests an inability to cause invasive disease. The presence of specific virulence factors such as pneumolysin implies stable maintenance of such genes through streptococcal evolution that may strengthen their value as anti-pneumococcal vaccine antigens, while maintaining awareness of their potential presence in commensal species. Following from Jensen et al.’s initial analysis we provide historical context for this long time human nasopharyngeal resident, the Mitis group Streptococcus .
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spelling pubmed-89420262022-03-29 A new perspective on ancient Mitis group streptococcal genetics Belman, Sophie Chaguza, Chrispin Kumar, Narender Lo, Stephanie Bentley, Stephen D. Microb Genom Research Articles Mitis group Streptococcus are human obligate bacteria residing in the nasopharynx and oral cavity. They comprise both commensal and pathogenic species with the most well-known being Streptococcus pneumoniae – a leading cause of meningitis and pneumonia. A primary difference between the commensal and pathogenic species is the presence of the polysaccharide capsule – a major virulence factor in S. pneumoniae , also present in other commensal species. Our current understanding of the evolutionary divergence of the pathogenic and commensal species has been inferred from extant strains. Ancient genomes can further elucidate streptococcal evolutionary history. We extracted streptococcal genome reads from a 5700-year-old ancient metagenome and worked towards characterizing them. Due to excessive within- and between-species recombination common among streptococci we were unable to parse individual species. Further, the composite reads of the ancient metagenome do not fit within the diversity of any specific extant species. Using a capsular gene database and AT-content analysis we determined that this ancient metagenome is missing polysaccharide synthesis genes integral to streptococcal capsule formation. The presence of multiple zinc metalloproteases suggests that adaptation to host IgA1 had begun and the presence of other virulence factors further implies development of close host–microbe interactions, though the absence of a capsule suggests an inability to cause invasive disease. The presence of specific virulence factors such as pneumolysin implies stable maintenance of such genes through streptococcal evolution that may strengthen their value as anti-pneumococcal vaccine antigens, while maintaining awareness of their potential presence in commensal species. Following from Jensen et al.’s initial analysis we provide historical context for this long time human nasopharyngeal resident, the Mitis group Streptococcus . Microbiology Society 2022-02-28 /pmc/articles/PMC8942026/ /pubmed/35225216 http://dx.doi.org/10.1099/mgen.0.000753 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.
spellingShingle Research Articles
Belman, Sophie
Chaguza, Chrispin
Kumar, Narender
Lo, Stephanie
Bentley, Stephen D.
A new perspective on ancient Mitis group streptococcal genetics
title A new perspective on ancient Mitis group streptococcal genetics
title_full A new perspective on ancient Mitis group streptococcal genetics
title_fullStr A new perspective on ancient Mitis group streptococcal genetics
title_full_unstemmed A new perspective on ancient Mitis group streptococcal genetics
title_short A new perspective on ancient Mitis group streptococcal genetics
title_sort new perspective on ancient mitis group streptococcal genetics
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8942026/
https://www.ncbi.nlm.nih.gov/pubmed/35225216
http://dx.doi.org/10.1099/mgen.0.000753
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