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Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile
Clostridioides difficile is the main cause of health-care-associated infectious diarrhoea. Toxins, TcdA and TcdB, secreted by this bacterium damage colonic epithelial cells and in severe cases this culminates in pseudomembranous colitis, toxic megacolon and death. Vaccines in human trials have focus...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913071/ https://www.ncbi.nlm.nih.gov/pubmed/33540694 http://dx.doi.org/10.3390/microorganisms9020306 |
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author | Karyal, Cansu Hughes, Jaime Kelly, Michelle L. Luckett, Jeni C. Kaye, Philip V. Cockayne, Alan Minton, Nigel P. Griffin, Ruth |
author_facet | Karyal, Cansu Hughes, Jaime Kelly, Michelle L. Luckett, Jeni C. Kaye, Philip V. Cockayne, Alan Minton, Nigel P. Griffin, Ruth |
author_sort | Karyal, Cansu |
collection | PubMed |
description | Clostridioides difficile is the main cause of health-care-associated infectious diarrhoea. Toxins, TcdA and TcdB, secreted by this bacterium damage colonic epithelial cells and in severe cases this culminates in pseudomembranous colitis, toxic megacolon and death. Vaccines in human trials have focused exclusively on the parenteral administration of toxin-based formulations. These vaccines promote toxin-neutralising serum antibodies but fail to confer protection from infection in the gut. An effective route to immunise against gut pathogens and stimulate a protective mucosal antibody response (secretory immunoglobulin A, IgA) at the infection site is the oral route. Additionally, oral immunisation generates systemic antibodies (IgG). Using this route, two different antigens were tested in the hamster model: The colonisation factor CD0873 and a TcdB fragment. Animals immunised with CD0873 generated a significantly higher titre of sIgA in intestinal fluid and IgG in serum compared to naive animals, which significantly inhibited the adherence of C. difficile to Caco-2 cells. Following challenge with a hypervirulent isolate, the CD0873-immunised group showed a mean increase of 80% in time to experimental endpoint compared to naïve animals. Survival and body condition correlated with bacterial clearance and reduced pathology in the cecum. Our findings advocate CD0873 as a promising oral vaccine candidate against C. difficile. |
format | Online Article Text |
id | pubmed-7913071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79130712021-02-28 Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile Karyal, Cansu Hughes, Jaime Kelly, Michelle L. Luckett, Jeni C. Kaye, Philip V. Cockayne, Alan Minton, Nigel P. Griffin, Ruth Microorganisms Communication Clostridioides difficile is the main cause of health-care-associated infectious diarrhoea. Toxins, TcdA and TcdB, secreted by this bacterium damage colonic epithelial cells and in severe cases this culminates in pseudomembranous colitis, toxic megacolon and death. Vaccines in human trials have focused exclusively on the parenteral administration of toxin-based formulations. These vaccines promote toxin-neutralising serum antibodies but fail to confer protection from infection in the gut. An effective route to immunise against gut pathogens and stimulate a protective mucosal antibody response (secretory immunoglobulin A, IgA) at the infection site is the oral route. Additionally, oral immunisation generates systemic antibodies (IgG). Using this route, two different antigens were tested in the hamster model: The colonisation factor CD0873 and a TcdB fragment. Animals immunised with CD0873 generated a significantly higher titre of sIgA in intestinal fluid and IgG in serum compared to naive animals, which significantly inhibited the adherence of C. difficile to Caco-2 cells. Following challenge with a hypervirulent isolate, the CD0873-immunised group showed a mean increase of 80% in time to experimental endpoint compared to naïve animals. Survival and body condition correlated with bacterial clearance and reduced pathology in the cecum. Our findings advocate CD0873 as a promising oral vaccine candidate against C. difficile. MDPI 2021-02-02 /pmc/articles/PMC7913071/ /pubmed/33540694 http://dx.doi.org/10.3390/microorganisms9020306 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Karyal, Cansu Hughes, Jaime Kelly, Michelle L. Luckett, Jeni C. Kaye, Philip V. Cockayne, Alan Minton, Nigel P. Griffin, Ruth Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile |
title | Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile |
title_full | Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile |
title_fullStr | Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile |
title_full_unstemmed | Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile |
title_short | Colonisation Factor CD0873, an Attractive Oral Vaccine Candidate against Clostridioides difficile |
title_sort | colonisation factor cd0873, an attractive oral vaccine candidate against clostridioides difficile |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913071/ https://www.ncbi.nlm.nih.gov/pubmed/33540694 http://dx.doi.org/10.3390/microorganisms9020306 |
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