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N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status

Human cervicovaginal fluid (CVF) is a complex, functionally important and glycan rich biological fluid, fundamental in mediating physiological events associated with reproductive health. Using a comprehensive glycomic strategy we reveal an extremely rich and complex N-glycome in CVF of pregnant and...

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Autores principales: Wu, Gang, Grassi, Paola, MacIntyre, David A., Molina, Belen Gimeno, Sykes, Lynne, Kundu, Samit, Hsiao, Cheng-Te, Khoo, Kay-Hooi, Bennett, Phillip R., Dell, Anne, Haslam, Stuart M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551102/
https://www.ncbi.nlm.nih.gov/pubmed/36216861
http://dx.doi.org/10.1038/s41598-022-20608-7
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author Wu, Gang
Grassi, Paola
MacIntyre, David A.
Molina, Belen Gimeno
Sykes, Lynne
Kundu, Samit
Hsiao, Cheng-Te
Khoo, Kay-Hooi
Bennett, Phillip R.
Dell, Anne
Haslam, Stuart M.
author_facet Wu, Gang
Grassi, Paola
MacIntyre, David A.
Molina, Belen Gimeno
Sykes, Lynne
Kundu, Samit
Hsiao, Cheng-Te
Khoo, Kay-Hooi
Bennett, Phillip R.
Dell, Anne
Haslam, Stuart M.
author_sort Wu, Gang
collection PubMed
description Human cervicovaginal fluid (CVF) is a complex, functionally important and glycan rich biological fluid, fundamental in mediating physiological events associated with reproductive health. Using a comprehensive glycomic strategy we reveal an extremely rich and complex N-glycome in CVF of pregnant and non-pregnant women, abundant in paucimannose and high mannose glycans, complex glycans with 2–4 N-Acetyllactosamine (LacNAc) antennae, and Poly-LacNAc glycans decorated with fucosylation and sialylation. N-glycosylation profiles were observed to differ in relation to pregnancy status, microbial composition, immune activation, and pregnancy outcome. Compared to CVF from women experiencing term birth, CVF from women who subsequently experienced preterm birth showed lower sialylation, which correlated to the presence of a diverse microbiome, and higher fucosylation, which correlated positively to pro-inflammatory cytokine concentration. This study is the first step towards better understanding the role of cervicovaginal glycans in reproductive health, their contribution to the mechanism of microbial driven preterm birth, and their potential for preventative therapy.
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spelling pubmed-95511022022-10-12 N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status Wu, Gang Grassi, Paola MacIntyre, David A. Molina, Belen Gimeno Sykes, Lynne Kundu, Samit Hsiao, Cheng-Te Khoo, Kay-Hooi Bennett, Phillip R. Dell, Anne Haslam, Stuart M. Sci Rep Article Human cervicovaginal fluid (CVF) is a complex, functionally important and glycan rich biological fluid, fundamental in mediating physiological events associated with reproductive health. Using a comprehensive glycomic strategy we reveal an extremely rich and complex N-glycome in CVF of pregnant and non-pregnant women, abundant in paucimannose and high mannose glycans, complex glycans with 2–4 N-Acetyllactosamine (LacNAc) antennae, and Poly-LacNAc glycans decorated with fucosylation and sialylation. N-glycosylation profiles were observed to differ in relation to pregnancy status, microbial composition, immune activation, and pregnancy outcome. Compared to CVF from women experiencing term birth, CVF from women who subsequently experienced preterm birth showed lower sialylation, which correlated to the presence of a diverse microbiome, and higher fucosylation, which correlated positively to pro-inflammatory cytokine concentration. This study is the first step towards better understanding the role of cervicovaginal glycans in reproductive health, their contribution to the mechanism of microbial driven preterm birth, and their potential for preventative therapy. Nature Publishing Group UK 2022-10-10 /pmc/articles/PMC9551102/ /pubmed/36216861 http://dx.doi.org/10.1038/s41598-022-20608-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wu, Gang
Grassi, Paola
MacIntyre, David A.
Molina, Belen Gimeno
Sykes, Lynne
Kundu, Samit
Hsiao, Cheng-Te
Khoo, Kay-Hooi
Bennett, Phillip R.
Dell, Anne
Haslam, Stuart M.
N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status
title N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status
title_full N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status
title_fullStr N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status
title_full_unstemmed N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status
title_short N-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status
title_sort n-glycosylation of cervicovaginal fluid reflects microbial community, immune activity, and pregnancy status
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551102/
https://www.ncbi.nlm.nih.gov/pubmed/36216861
http://dx.doi.org/10.1038/s41598-022-20608-7
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