A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization

Vibrio cholerae, the causative agent of the disease cholera, is responsible for multiple pandemics. V. cholerae binds to and colonizes the gastrointestinal tract within the human host, as well as various surfaces in the marine environment (e.g., zooplankton) during interepidemic periods. A large adh...

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Published in:Proceedings of the National Academy of Sciences
Main Authors: Lloyd, Cameron J., Guo, Shuaiqi, Kinrade, Brett, Zahiri, Hossein, Eves, Robert, Ali, Syed Khalid, Yildiz, Fitnat, Voets, Ilja K., Davies, Peter L., Klose, Karl E.
Format: Article in Journal/Newspaper
Language:English
Published: 2023
Subjects:
Online Access:https://research.tue.nl/en/publications/449d9f03-ef19-4177-9ebd-35565e18f1b6
https://doi.org/10.1073/pnas.2308238120
https://pure.tue.nl/ws/files/312666588/lloyd-et-al-2023-a-peptide-binding-domain-shared-with-an-antarctic-bacterium-facilitates-vibrio-cholerae-human-cell.pdf
http://www.scopus.com/inward/record.url?scp=85171811782&partnerID=8YFLogxK
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spelling ftuniveindcris:oai:pure.tue.nl:publications/449d9f03-ef19-4177-9ebd-35565e18f1b6 2024-11-03T14:50:23+00:00 A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization Lloyd, Cameron J. Guo, Shuaiqi Kinrade, Brett Zahiri, Hossein Eves, Robert Ali, Syed Khalid Yildiz, Fitnat Voets, Ilja K. Davies, Peter L. Klose, Karl E. 2023-09-26 application/pdf https://research.tue.nl/en/publications/449d9f03-ef19-4177-9ebd-35565e18f1b6 https://doi.org/10.1073/pnas.2308238120 https://pure.tue.nl/ws/files/312666588/lloyd-et-al-2023-a-peptide-binding-domain-shared-with-an-antarctic-bacterium-facilitates-vibrio-cholerae-human-cell.pdf http://www.scopus.com/inward/record.url?scp=85171811782&partnerID=8YFLogxK eng eng info:eu-repo/semantics/openAccess Lloyd , C J , Guo , S , Kinrade , B , Zahiri , H , Eves , R , Ali , S K , Yildiz , F , Voets , I K , Davies , P L & Klose , K E 2023 , ' A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization ' , Proceedings of the National Academy of Sciences of the United States of America , vol. 120 , no. 39 , e2308238120 . https://doi.org/10.1073/pnas.2308238120 adhesin cholera peptide-binding Intestines Gastrointestinal Tract Humans Vibrio cholerae/genetics Infant Animals Cell Aggregation Bacteria Mice Diatoms /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being name=SDG 3 - Good Health and Well-being /dk/atira/pure/sustainabledevelopmentgoals/life_below_water name=SDG 14 - Life Below Water article 2023 ftuniveindcris https://doi.org/10.1073/pnas.2308238120 2024-10-24T00:06:19Z Vibrio cholerae, the causative agent of the disease cholera, is responsible for multiple pandemics. V. cholerae binds to and colonizes the gastrointestinal tract within the human host, as well as various surfaces in the marine environment (e.g., zooplankton) during interepidemic periods. A large adhesin, the Flagellar Regulated Hemagglutinin A (FrhA), enhances binding to erythrocytes and epithelial cells and enhances intestinal colonization. We identified a peptide-binding domain (PBD) within FrhA that mediates hemagglutination, binding to epithelial cells, intestinal colonization, and facilitates biofilm formation. Intriguingly, this domain is also found in the ice-binding protein of the Antarctic bacterium Marinomonas primoryensis, where it mediates binding to diatoms. Peptide inhibitors of the M. primoryensis PBD inhibit V. cholerae binding to human cells as well as to diatoms and inhibit biofilm formation. Moreover, the M. primoryensis PBD inserted into FrhA allows V. cholerae to bind human cells and colonize the intestine and also enhances biofilm formation, demonstrating the interchangeability of the PBD from these bacteria. Importantly, peptide inhibitors of PBD reduce V. cholerae intestinal colonization in infant mice. These studies demonstrate how V. cholerae uses a PBD shared with a diatom-binding Antarctic bacterium to facilitate intestinal colonization in humans and biofilm formation in the environment. Article in Journal/Newspaper Antarc* Antarctic Eindhoven University of Technology research portal Antarctic The Antarctic Proceedings of the National Academy of Sciences 120 39
institution Open Polar
collection Eindhoven University of Technology research portal
op_collection_id ftuniveindcris
language English
topic adhesin
cholera
peptide-binding
Intestines
Gastrointestinal Tract
Humans
Vibrio cholerae/genetics
Infant
Animals
Cell Aggregation
Bacteria
Mice
Diatoms
/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being
name=SDG 3 - Good Health and Well-being
/dk/atira/pure/sustainabledevelopmentgoals/life_below_water
name=SDG 14 - Life Below Water
spellingShingle adhesin
cholera
peptide-binding
Intestines
Gastrointestinal Tract
Humans
Vibrio cholerae/genetics
Infant
Animals
Cell Aggregation
Bacteria
Mice
Diatoms
/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being
name=SDG 3 - Good Health and Well-being
/dk/atira/pure/sustainabledevelopmentgoals/life_below_water
name=SDG 14 - Life Below Water
Lloyd, Cameron J.
Guo, Shuaiqi
Kinrade, Brett
Zahiri, Hossein
Eves, Robert
Ali, Syed Khalid
Yildiz, Fitnat
Voets, Ilja K.
Davies, Peter L.
Klose, Karl E.
A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization
topic_facet adhesin
cholera
peptide-binding
Intestines
Gastrointestinal Tract
Humans
Vibrio cholerae/genetics
Infant
Animals
Cell Aggregation
Bacteria
Mice
Diatoms
/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being
name=SDG 3 - Good Health and Well-being
/dk/atira/pure/sustainabledevelopmentgoals/life_below_water
name=SDG 14 - Life Below Water
description Vibrio cholerae, the causative agent of the disease cholera, is responsible for multiple pandemics. V. cholerae binds to and colonizes the gastrointestinal tract within the human host, as well as various surfaces in the marine environment (e.g., zooplankton) during interepidemic periods. A large adhesin, the Flagellar Regulated Hemagglutinin A (FrhA), enhances binding to erythrocytes and epithelial cells and enhances intestinal colonization. We identified a peptide-binding domain (PBD) within FrhA that mediates hemagglutination, binding to epithelial cells, intestinal colonization, and facilitates biofilm formation. Intriguingly, this domain is also found in the ice-binding protein of the Antarctic bacterium Marinomonas primoryensis, where it mediates binding to diatoms. Peptide inhibitors of the M. primoryensis PBD inhibit V. cholerae binding to human cells as well as to diatoms and inhibit biofilm formation. Moreover, the M. primoryensis PBD inserted into FrhA allows V. cholerae to bind human cells and colonize the intestine and also enhances biofilm formation, demonstrating the interchangeability of the PBD from these bacteria. Importantly, peptide inhibitors of PBD reduce V. cholerae intestinal colonization in infant mice. These studies demonstrate how V. cholerae uses a PBD shared with a diatom-binding Antarctic bacterium to facilitate intestinal colonization in humans and biofilm formation in the environment.
format Article in Journal/Newspaper
author Lloyd, Cameron J.
Guo, Shuaiqi
Kinrade, Brett
Zahiri, Hossein
Eves, Robert
Ali, Syed Khalid
Yildiz, Fitnat
Voets, Ilja K.
Davies, Peter L.
Klose, Karl E.
author_facet Lloyd, Cameron J.
Guo, Shuaiqi
Kinrade, Brett
Zahiri, Hossein
Eves, Robert
Ali, Syed Khalid
Yildiz, Fitnat
Voets, Ilja K.
Davies, Peter L.
Klose, Karl E.
author_sort Lloyd, Cameron J.
title A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization
title_short A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization
title_full A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization
title_fullStr A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization
title_full_unstemmed A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization
title_sort peptide-binding domain shared with an antarctic bacterium facilitates vibrio cholerae human cell binding and intestinal colonization
publishDate 2023
url https://research.tue.nl/en/publications/449d9f03-ef19-4177-9ebd-35565e18f1b6
https://doi.org/10.1073/pnas.2308238120
https://pure.tue.nl/ws/files/312666588/lloyd-et-al-2023-a-peptide-binding-domain-shared-with-an-antarctic-bacterium-facilitates-vibrio-cholerae-human-cell.pdf
http://www.scopus.com/inward/record.url?scp=85171811782&partnerID=8YFLogxK
geographic Antarctic
The Antarctic
geographic_facet Antarctic
The Antarctic
genre Antarc*
Antarctic
genre_facet Antarc*
Antarctic
op_source Lloyd , C J , Guo , S , Kinrade , B , Zahiri , H , Eves , R , Ali , S K , Yildiz , F , Voets , I K , Davies , P L & Klose , K E 2023 , ' A peptide-binding domain shared with an Antarctic bacterium facilitates Vibrio cholerae human cell binding and intestinal colonization ' , Proceedings of the National Academy of Sciences of the United States of America , vol. 120 , no. 39 , e2308238120 . https://doi.org/10.1073/pnas.2308238120
op_rights info:eu-repo/semantics/openAccess
op_doi https://doi.org/10.1073/pnas.2308238120
container_title Proceedings of the National Academy of Sciences
container_volume 120
container_issue 39
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