TY - JOUR
T1 - Glycan cross-feeding supports mutualism between Fusobacterium and the vaginal microbiota
AU - Agarwal, Kavita
AU - Robinson, Lloyd S.
AU - Aggarwal, Somya
AU - Foster, Lynne R.
AU - Hernandez-Leyva, Ariel
AU - Lin, Hueylie
AU - Tortelli, Brett A.
AU - O’Brien, Valerie P.
AU - Miller, Liza
AU - Kau, Andrew L.
AU - Reno, Hilary
AU - Gilbert, Nicole M.
AU - Lewis, Warren G.
AU - Lewis, Amanda L.
N1 - Funding Information:
Funding: This work was funded by the National Institute of Allergy and Infectious Diseases (R01 AI114635 to ALL and WGL, R01 AI127554 to WGL, and K08 AI113184 to ALK), the National Institute of Diabetes and Digestive and Kidney Diseases (K01 DK110225 to NMG), the Eunice Kennedy Shriver National Institute of Child Health and Human Development (F30HD094435 to BAT), the Burroughs Wellcome Fund Preterm Birth Initiative (to ALL), a pilot grant from March of Dimes Prematurity Research Center at Washington University (to AL), and a Morse Postdoctoral Fellowship (to KA). The funders had no role in the study design; collection, analysis, and interpretation of data; writing of the paper; and/or decision to submit for publication. We thank Nadum Member-Meneh and Courtney Amegashie for technical contributions to clinical sample collection and processing, Justin Fay for advice on microbiome profiling, Justin Merritt for providing some of the Fusobacterium strains, Justin Perry for technical contributions to analysis of sialic acid consumption among Fusobacteria, Deborah Frank for editorial assistance and advice, and Marcy Hartstein for assistance with illustrations. We also thank Denise Spear, WHNP-BC, and Valerie Higginbotham, WHNP-BC, for their participation in collecting vaginal swabs from participants and the St. Louis County Department of Public Health for facilitating this study. Finally, we thank the women who have generously provided their informed consent and vaginal samples for use in these studies.
Funding Information:
Funding:ThisworkwasfundedbytheNational InstituteofAllergyandInfectiousDiseases(R01 AI114635toALLandWGL,R01AI127554to WGL,andK08AI113184toALK),theNational InstituteofDiabetesandDigestiveandKidney Diseases(K01DK110225toNMG),theEunice KennedyShriverNationalInstituteofChildHealth andHumanDevelopment(F30HD094435toBAT), theBurroughsWellcomeFundPretermBirth Initiative(toALL),apilotgrantfromMarchof DimesPrematurityResearchCenteratWashington University(toAL),andaMorsePostdoctoral Fellowship(toKA).Thefundershadnoroleinthe studydesign;collection,analysis,and interpretationofdata;writingofthepaper;and/or decisiontosubmitforpublication.
Publisher Copyright:
Copyright: © 2020 Agarwal et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2020/8
Y1 - 2020/8
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85089930023&partnerID=8YFLogxK
U2 - 10.1371/journal.pbio.3000788
DO - 10.1371/journal.pbio.3000788
M3 - Article
C2 - 32841232
AN - SCOPUS:85089930023
SN - 1544-9173
VL - 18
JO - PLoS Biology
JF - PLoS Biology
IS - 8
M1 - e3000788
ER -