Cargando…

Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1

Enteroaggregative Escherichia coli (EAEC) causes diarrhea and intestinal inflammation worldwide. EAEC strains are characterized by the presence of aggregative adherence fimbriae (AAF), which play a key role in pathogenesis by mediating attachment to the intestinal mucosa and by triggering host infla...

Descripción completa

Detalles Bibliográficos
Autores principales: Boll, Erik J., Ayala-Lujan, Jorge, Szabady, Rose L., Louissaint, Christopher, Smith, Rachel Z., Krogfelt, Karen A., Nataro, James P., Ruiz-Perez, Fernando, McCormick, Beth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461410/
https://www.ncbi.nlm.nih.gov/pubmed/28588132
http://dx.doi.org/10.1128/mBio.00717-17
_version_ 1783242331806236672
author Boll, Erik J.
Ayala-Lujan, Jorge
Szabady, Rose L.
Louissaint, Christopher
Smith, Rachel Z.
Krogfelt, Karen A.
Nataro, James P.
Ruiz-Perez, Fernando
McCormick, Beth A.
author_facet Boll, Erik J.
Ayala-Lujan, Jorge
Szabady, Rose L.
Louissaint, Christopher
Smith, Rachel Z.
Krogfelt, Karen A.
Nataro, James P.
Ruiz-Perez, Fernando
McCormick, Beth A.
author_sort Boll, Erik J.
collection PubMed
description Enteroaggregative Escherichia coli (EAEC) causes diarrhea and intestinal inflammation worldwide. EAEC strains are characterized by the presence of aggregative adherence fimbriae (AAF), which play a key role in pathogenesis by mediating attachment to the intestinal mucosa and by triggering host inflammatory responses. Here, we identify the epithelial transmembrane mucin MUC1 as an intestinal host cell receptor for EAEC, demonstrating that AAF-mediated interactions between EAEC and MUC1 facilitate enhanced bacterial adhesion. We further demonstrate that EAEC infection also causes elevated expression of MUC1 in inflamed human intestinal tissues. Moreover, we find that MUC1 facilitates AAF-dependent migration of neutrophils across the epithelium in response to EAEC infection. Thus, we show for the first time a proinflammatory role for MUC1 in the host response to an intestinal pathogen.
format Online
Article
Text
id pubmed-5461410
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-54614102017-06-07 Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1 Boll, Erik J. Ayala-Lujan, Jorge Szabady, Rose L. Louissaint, Christopher Smith, Rachel Z. Krogfelt, Karen A. Nataro, James P. Ruiz-Perez, Fernando McCormick, Beth A. mBio Research Article Enteroaggregative Escherichia coli (EAEC) causes diarrhea and intestinal inflammation worldwide. EAEC strains are characterized by the presence of aggregative adherence fimbriae (AAF), which play a key role in pathogenesis by mediating attachment to the intestinal mucosa and by triggering host inflammatory responses. Here, we identify the epithelial transmembrane mucin MUC1 as an intestinal host cell receptor for EAEC, demonstrating that AAF-mediated interactions between EAEC and MUC1 facilitate enhanced bacterial adhesion. We further demonstrate that EAEC infection also causes elevated expression of MUC1 in inflamed human intestinal tissues. Moreover, we find that MUC1 facilitates AAF-dependent migration of neutrophils across the epithelium in response to EAEC infection. Thus, we show for the first time a proinflammatory role for MUC1 in the host response to an intestinal pathogen. American Society for Microbiology 2017-06-06 /pmc/articles/PMC5461410/ /pubmed/28588132 http://dx.doi.org/10.1128/mBio.00717-17 Text en Copyright © 2017 Boll et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Boll, Erik J.
Ayala-Lujan, Jorge
Szabady, Rose L.
Louissaint, Christopher
Smith, Rachel Z.
Krogfelt, Karen A.
Nataro, James P.
Ruiz-Perez, Fernando
McCormick, Beth A.
Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1
title Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1
title_full Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1
title_fullStr Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1
title_full_unstemmed Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1
title_short Enteroaggregative Escherichia coli Adherence Fimbriae Drive Inflammatory Cell Recruitment via Interactions with Epithelial MUC1
title_sort enteroaggregative escherichia coli adherence fimbriae drive inflammatory cell recruitment via interactions with epithelial muc1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461410/
https://www.ncbi.nlm.nih.gov/pubmed/28588132
http://dx.doi.org/10.1128/mBio.00717-17
work_keys_str_mv AT bollerikj enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT ayalalujanjorge enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT szabadyrosel enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT louissaintchristopher enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT smithrachelz enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT krogfeltkarena enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT natarojamesp enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT ruizperezfernando enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1
AT mccormickbetha enteroaggregativeescherichiacoliadherencefimbriaedriveinflammatorycellrecruitmentviainteractionswithepithelialmuc1