Cargando…

Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota

Women with bacterial vaginosis (BV), an imbalance of the vaginal microbiome, are more likely to be colonized by potential pathogens such as Fusobacterium nucleatum, a bacterium linked with intrauterine infection and preterm birth. However, the conditions and mechanisms supporting pathogen colonizati...

Descripción completa

Detalles Bibliográficos
Autores principales: Agarwal, Kavita, Robinson, Lloyd S., Aggarwal, Somya, Foster, Lynne R., Hernandez-Leyva, Ariel, Lin, Hueylie, Tortelli, Brett A., O’Brien, Valerie P., Miller, Liza, Kau, Andrew L., Reno, Hilary, Gilbert, Nicole M., Lewis, Warren G., Lewis, Amanda L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447053/
https://www.ncbi.nlm.nih.gov/pubmed/32841232
http://dx.doi.org/10.1371/journal.pbio.3000788
_version_ 1783574235458830336
author Agarwal, Kavita
Robinson, Lloyd S.
Aggarwal, Somya
Foster, Lynne R.
Hernandez-Leyva, Ariel
Lin, Hueylie
Tortelli, Brett A.
O’Brien, Valerie P.
Miller, Liza
Kau, Andrew L.
Reno, Hilary
Gilbert, Nicole M.
Lewis, Warren G.
Lewis, Amanda L.
author_facet Agarwal, Kavita
Robinson, Lloyd S.
Aggarwal, Somya
Foster, Lynne R.
Hernandez-Leyva, Ariel
Lin, Hueylie
Tortelli, Brett A.
O’Brien, Valerie P.
Miller, Liza
Kau, Andrew L.
Reno, Hilary
Gilbert, Nicole M.
Lewis, Warren G.
Lewis, Amanda L.
author_sort Agarwal, Kavita
collection PubMed
description Women with bacterial vaginosis (BV), an imbalance of the vaginal microbiome, are more likely to be colonized by potential pathogens such as Fusobacterium nucleatum, a bacterium linked with intrauterine infection and preterm birth. However, the conditions and mechanisms supporting pathogen colonization during vaginal dysbiosis remain obscure. We demonstrate that sialidase activity, a diagnostic feature of BV, promoted F. nucleatum foraging and growth on mammalian sialoglycans, a nutrient resource that was otherwise inaccessible because of the lack of endogenous F. nucleatum sialidase. In mice with sialidase-producing vaginal microbiotas, mutant F. nucleatum unable to consume sialic acids was impaired in vaginal colonization. These experiments in mice also led to the discovery that F. nucleatum may also “give back” to the community by reinforcing sialidase activity, a biochemical feature of human dysbiosis. Using human vaginal bacterial communities, we show that F. nucleatum supported robust outgrowth of Gardnerella vaginalis, a major sialidase producer and one of the most abundant organisms in BV. These results illustrate that mutually beneficial relationships between vaginal bacteria support pathogen colonization and may help maintain features of dysbiosis. These findings challenge the simplistic dogma that the mere absence of “healthy” lactobacilli is the sole mechanism that creates a permissive environment for pathogens during vaginal dysbiosis. Given the ubiquity of F. nucleatum in the human mouth, these studies also suggest a possible mechanism underlying links between vaginal dysbiosis and oral sex.
format Online
Article
Text
id pubmed-7447053
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-74470532020-08-31 Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota Agarwal, Kavita Robinson, Lloyd S. Aggarwal, Somya Foster, Lynne R. Hernandez-Leyva, Ariel Lin, Hueylie Tortelli, Brett A. O’Brien, Valerie P. Miller, Liza Kau, Andrew L. Reno, Hilary Gilbert, Nicole M. Lewis, Warren G. Lewis, Amanda L. PLoS Biol Research Article Women with bacterial vaginosis (BV), an imbalance of the vaginal microbiome, are more likely to be colonized by potential pathogens such as Fusobacterium nucleatum, a bacterium linked with intrauterine infection and preterm birth. However, the conditions and mechanisms supporting pathogen colonization during vaginal dysbiosis remain obscure. We demonstrate that sialidase activity, a diagnostic feature of BV, promoted F. nucleatum foraging and growth on mammalian sialoglycans, a nutrient resource that was otherwise inaccessible because of the lack of endogenous F. nucleatum sialidase. In mice with sialidase-producing vaginal microbiotas, mutant F. nucleatum unable to consume sialic acids was impaired in vaginal colonization. These experiments in mice also led to the discovery that F. nucleatum may also “give back” to the community by reinforcing sialidase activity, a biochemical feature of human dysbiosis. Using human vaginal bacterial communities, we show that F. nucleatum supported robust outgrowth of Gardnerella vaginalis, a major sialidase producer and one of the most abundant organisms in BV. These results illustrate that mutually beneficial relationships between vaginal bacteria support pathogen colonization and may help maintain features of dysbiosis. These findings challenge the simplistic dogma that the mere absence of “healthy” lactobacilli is the sole mechanism that creates a permissive environment for pathogens during vaginal dysbiosis. Given the ubiquity of F. nucleatum in the human mouth, these studies also suggest a possible mechanism underlying links between vaginal dysbiosis and oral sex. Public Library of Science 2020-08-25 /pmc/articles/PMC7447053/ /pubmed/32841232 http://dx.doi.org/10.1371/journal.pbio.3000788 Text en © 2020 Agarwal et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Agarwal, Kavita
Robinson, Lloyd S.
Aggarwal, Somya
Foster, Lynne R.
Hernandez-Leyva, Ariel
Lin, Hueylie
Tortelli, Brett A.
O’Brien, Valerie P.
Miller, Liza
Kau, Andrew L.
Reno, Hilary
Gilbert, Nicole M.
Lewis, Warren G.
Lewis, Amanda L.
Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota
title Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota
title_full Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota
title_fullStr Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota
title_full_unstemmed Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota
title_short Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota
title_sort glycan cross-feeding supports mutualism between fusobacterium and the vaginal microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447053/
https://www.ncbi.nlm.nih.gov/pubmed/32841232
http://dx.doi.org/10.1371/journal.pbio.3000788
work_keys_str_mv AT agarwalkavita glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT robinsonlloyds glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT aggarwalsomya glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT fosterlynner glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT hernandezleyvaariel glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT linhueylie glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT tortellibretta glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT obrienvaleriep glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT millerliza glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT kauandrewl glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT renohilary glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT gilbertnicolem glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT lewiswarreng glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota
AT lewisamandal glycancrossfeedingsupportsmutualismbetweenfusobacteriumandthevaginalmicrobiota