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...
Published in: | Proceedings of the National Academy of Sciences |
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Format: | Article in Journal/Newspaper |
Language: | English |
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2023
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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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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 |
_version_ |
1814718586983284736 |