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Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication

Vibrio cholerae produces cholera toxin (CT), an AB(5) protein toxin that is primarily responsible for the profuse watery diarrhea of cholera. CT is secreted into the extracellular milieu, but the toxin attacks its Gsα target within the cytosol of a host cell. Thus, CT must cross a cellular membrane...

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Autores principales: Reddy, Srikar, Taylor, Michael, Zhao, Mojun, Cherubin, Patrick, Geden, Sandra, Ray, Supriyo, Francis, David, Teter, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764128/
https://www.ncbi.nlm.nih.gov/pubmed/24039929
http://dx.doi.org/10.1371/journal.pone.0073390
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author Reddy, Srikar
Taylor, Michael
Zhao, Mojun
Cherubin, Patrick
Geden, Sandra
Ray, Supriyo
Francis, David
Teter, Ken
author_facet Reddy, Srikar
Taylor, Michael
Zhao, Mojun
Cherubin, Patrick
Geden, Sandra
Ray, Supriyo
Francis, David
Teter, Ken
author_sort Reddy, Srikar
collection PubMed
description Vibrio cholerae produces cholera toxin (CT), an AB(5) protein toxin that is primarily responsible for the profuse watery diarrhea of cholera. CT is secreted into the extracellular milieu, but the toxin attacks its Gsα target within the cytosol of a host cell. Thus, CT must cross a cellular membrane barrier in order to function. This event only occurs after the toxin travels by retrograde vesicular transport from the cell surface to the endoplasmic reticulum (ER). The catalytic A1 polypeptide then dissociates from the rest of the toxin and assumes an unfolded conformation that facilitates its transfer to the cytosol by a process involving the quality control system of ER-associated degradation. Productive intoxication is blocked by alterations to the vesicular transport of CT and/or the ER-to-cytosol translocation of CTA1. Various plant compounds have been reported to inhibit the cytopathic activity of CT, so in this work we evaluated the potential anti-CT properties of grape extract. Two grape extracts currently sold as nutritional supplements inhibited CT and Escherichia coli heat-labile toxin activity against cultured cells and intestinal loops. CT intoxication was blocked even when the extracts were added an hour after the initial toxin exposure. A specific subset of host-toxin interactions involving both the catalytic CTA1 subunit and the cell-binding CTB pentamer were affected. The extracts blocked toxin binding to the cell surface, prevented unfolding of the isolated CTA1 subunit, inhibited CTA1 translocation to the cytosol, and disrupted the catalytic activity of CTA1. Grape extract could thus potentially serve as a novel therapeutic to prevent or possibly treat cholera.
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spelling pubmed-37641282013-09-13 Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication Reddy, Srikar Taylor, Michael Zhao, Mojun Cherubin, Patrick Geden, Sandra Ray, Supriyo Francis, David Teter, Ken PLoS One Research Article Vibrio cholerae produces cholera toxin (CT), an AB(5) protein toxin that is primarily responsible for the profuse watery diarrhea of cholera. CT is secreted into the extracellular milieu, but the toxin attacks its Gsα target within the cytosol of a host cell. Thus, CT must cross a cellular membrane barrier in order to function. This event only occurs after the toxin travels by retrograde vesicular transport from the cell surface to the endoplasmic reticulum (ER). The catalytic A1 polypeptide then dissociates from the rest of the toxin and assumes an unfolded conformation that facilitates its transfer to the cytosol by a process involving the quality control system of ER-associated degradation. Productive intoxication is blocked by alterations to the vesicular transport of CT and/or the ER-to-cytosol translocation of CTA1. Various plant compounds have been reported to inhibit the cytopathic activity of CT, so in this work we evaluated the potential anti-CT properties of grape extract. Two grape extracts currently sold as nutritional supplements inhibited CT and Escherichia coli heat-labile toxin activity against cultured cells and intestinal loops. CT intoxication was blocked even when the extracts were added an hour after the initial toxin exposure. A specific subset of host-toxin interactions involving both the catalytic CTA1 subunit and the cell-binding CTB pentamer were affected. The extracts blocked toxin binding to the cell surface, prevented unfolding of the isolated CTA1 subunit, inhibited CTA1 translocation to the cytosol, and disrupted the catalytic activity of CTA1. Grape extract could thus potentially serve as a novel therapeutic to prevent or possibly treat cholera. Public Library of Science 2013-09-05 /pmc/articles/PMC3764128/ /pubmed/24039929 http://dx.doi.org/10.1371/journal.pone.0073390 Text en © 2013 Reddy et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Reddy, Srikar
Taylor, Michael
Zhao, Mojun
Cherubin, Patrick
Geden, Sandra
Ray, Supriyo
Francis, David
Teter, Ken
Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication
title Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication
title_full Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication
title_fullStr Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication
title_full_unstemmed Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication
title_short Grape Extracts Inhibit Multiple Events in the Cell Biology of Cholera Intoxication
title_sort grape extracts inhibit multiple events in the cell biology of cholera intoxication
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764128/
https://www.ncbi.nlm.nih.gov/pubmed/24039929
http://dx.doi.org/10.1371/journal.pone.0073390
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