Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/185838
Título: Identification and characterisation of vaginal bacteria-glycan interactions implicated in reproductive tract health and pregnancy outcomes
Autor: Tajadura-Ortega, Virginia
Chai, Wengang
Roberts, Lauren A.
Zhang, Yibing
Di Maio, Antonio
Decout, Alexiane C.
Pinheiro, Benedita A.
Palma, Angelina S.
De Nicola, Gian
Riaposova, Lucia
Gimeno-Molina, Belen
Lee, Yun S.
Cao, Hongzhi
Piskarev, Vladimir
Akune, Yukie
Costa, Tiago R. D.
Amin, Himani
Sykes, Lynne
Bennett, Phillip R.
Marchesi, Julian R.
Feizi, Ten
Liu, Yan
MacIntyre, David A.
Palavras-chave: Chemistry(all)
Biochemistry, Genetics and Molecular Biology(all)
Physics and Astronomy(all)
Data: 5-Jun-2025
Resumo: Lactobacillus displacement from the vaginal microbiome associates with adverse health outcomes and is linked to increased risk of preterm birth. Glycans mediate bacterial adhesion events involved in colonisation and infection. Using customised glycan microarrays, we establish glycan interaction profiles of vaginal bacteria implicated in reproductive health. Glycan binding signatures of the opportunistic pathogens Escherichia coli, Fusobacterium nucleatum and Streptococcus agalactiae to oligomannose N-glycans, galactose-terminating glycans and hyaluronic acid, respectively are highly distinct from Lactobacillus commensals. Binding to sulphated glycosaminoglycans by vaginal bacteria is pH dependent, as is binding to neutral and sialic acid-terminating glycans by F. nucleatum. Adhesion of Lactobacillus crispatus, Lactobacillus iners, Gardnerella vaginalis, S. agalactiae and F. nucleatum to vaginal epithelial cells is partially mediated by chondroitin sulphate. S. agalactiae binding to chondroitin sulphate C oligosaccharides is inhibited by L. crispatus. This study highlights glycans as mediators of vaginal bacterial binding events involved in reproductive health and disease.
Descrição: Funding Information: This work has been funded by the March of Dimes European Prematurity Research Centre grant 22-FY18-82 awarded to Imperial College London (ICL). The glycan microarray studies were performed in the ICL Carbohydrate Microarray Facility supported by the Wellcome Trust Biomedical Resource Grants (WT099197/Z/12/Z, 108430/Z/15/Z and 218304/Z/19/Z). The sequence-defined glycan microarrays contain oligosaccharides provided by collaborators including CFG Core D, Nicolai Bovin, Chunxia Li, Akihiro Imamura, Ulrika Westerlind, Kelly Moremen, and Apoorva Srivastava whom we thank. J.R.M. and the Division of Digestive Diseases at ICL receive financial and infrastructure support from the NIHR Imperial Biomedical Research Centre (BRC) based at ICL and ICL Healthcare NHS Trust. L.S. and B.G.M. are supported by Imperial Health Charity in partnership with the Parasol Foundation and the Rosetrees Trust. P.R.B. and L.S. receive infrastructure support from the NIHR Imperial Biomedical Research Centre (BRC) based at ICL and IC Healthcare NHS Trust. Y.L., A.S.P. and B.A.P., thank the GLYCOTwinning project HORIZON-WIDERA-2021-101079417 funded by European the Commission and a DL-57/2016 Program Contract to B.A.P. We would like to acknowledge the Centre for Biomolecular Spectroscopy at King’s College London that is funded by the Wellcome Trust and the British Heart Foundation (WT202767/Z/16/Z and IG/16/2/32273). V.P. receives financial support of the Ministry of Science and Higher Education of the Russian Federation (Contract No. 075-00277-24-00). The authors thank Prof Barbara Mulloy for her help in NMR data interpretation and Dr. Daniel Slade for the delta galkt and delta galkt fap2 F. nucleatum 23726 mutants. Publisher Copyright: © The Author(s) 2025.
Peer review: yes
URI: http://hdl.handle.net/10362/185838
DOI: https://doi.org/10.1038/s41467-025-60404-1
ISSN: 2041-1723
Aparece nas colecções:Home collection (FCT)

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