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In vitro models to study Clostridioides difficile infection: current systems and future advances
Clostridioides difficile infection (CDI) is the most common cause of healthcare-associated diarrhoea in western countries, being categorized as an urgent healthcare threat. Historically, researchers have relied on the use of in vivo animal models to study CDI pathogenesis; however, differences in ph...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799034/ https://www.ncbi.nlm.nih.gov/pubmed/36504033 http://dx.doi.org/10.1097/MOG.0000000000000893 |
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author | Ewin, Duncan Birch, William Davis Moura, Ines B. |
author_facet | Ewin, Duncan Birch, William Davis Moura, Ines B. |
author_sort | Ewin, Duncan |
collection | PubMed |
description | Clostridioides difficile infection (CDI) is the most common cause of healthcare-associated diarrhoea in western countries, being categorized as an urgent healthcare threat. Historically, researchers have relied on the use of in vivo animal models to study CDI pathogenesis; however, differences in physiology and disease prognosis compared with humans limit their suitability to model CDI. In vitro models are increasingly being used as an alternative as they offer excellent process control, and some are able to use human ex-vivo prokaryotic and/or eukaryotic cells. RECENT FINDINGS: Simulating the colonic environment in vitro is particularly challenging. Bacterial fermentation models have been used to evaluate novel therapeutics, explore the re-modelling of the gut microbiota, and simulate disease progression. However, they lack the scalability to become more widespread. Models that co-culture human and bacterial cells are of particular interest, but the different conditions required by each cell type make these models challenging to run. Recent advancements in model design have allowed for longer culture times with more representative bacterial populations. SUMMARY: As in vitro models continue to evolve, they become more physiologically relevant, offering improved simulations of CDI, and extending their applicability. |
format | Online Article Text |
id | pubmed-9799034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-97990342023-01-04 In vitro models to study Clostridioides difficile infection: current systems and future advances Ewin, Duncan Birch, William Davis Moura, Ines B. Curr Opin Gastroenterol GASTROINTESTINAL INFECTIONS: Edited by Anthony Buckley Clostridioides difficile infection (CDI) is the most common cause of healthcare-associated diarrhoea in western countries, being categorized as an urgent healthcare threat. Historically, researchers have relied on the use of in vivo animal models to study CDI pathogenesis; however, differences in physiology and disease prognosis compared with humans limit their suitability to model CDI. In vitro models are increasingly being used as an alternative as they offer excellent process control, and some are able to use human ex-vivo prokaryotic and/or eukaryotic cells. RECENT FINDINGS: Simulating the colonic environment in vitro is particularly challenging. Bacterial fermentation models have been used to evaluate novel therapeutics, explore the re-modelling of the gut microbiota, and simulate disease progression. However, they lack the scalability to become more widespread. Models that co-culture human and bacterial cells are of particular interest, but the different conditions required by each cell type make these models challenging to run. Recent advancements in model design have allowed for longer culture times with more representative bacterial populations. SUMMARY: As in vitro models continue to evolve, they become more physiologically relevant, offering improved simulations of CDI, and extending their applicability. Lippincott Williams & Wilkins 2023-01 2022-11-03 /pmc/articles/PMC9799034/ /pubmed/36504033 http://dx.doi.org/10.1097/MOG.0000000000000893 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an-open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | GASTROINTESTINAL INFECTIONS: Edited by Anthony Buckley Ewin, Duncan Birch, William Davis Moura, Ines B. In vitro models to study Clostridioides difficile infection: current systems and future advances |
title | In vitro models to study Clostridioides difficile infection: current systems and future advances |
title_full | In vitro models to study Clostridioides difficile infection: current systems and future advances |
title_fullStr | In vitro models to study Clostridioides difficile infection: current systems and future advances |
title_full_unstemmed | In vitro models to study Clostridioides difficile infection: current systems and future advances |
title_short | In vitro models to study Clostridioides difficile infection: current systems and future advances |
title_sort | in vitro models to study clostridioides difficile infection: current systems and future advances |
topic | GASTROINTESTINAL INFECTIONS: Edited by Anthony Buckley |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799034/ https://www.ncbi.nlm.nih.gov/pubmed/36504033 http://dx.doi.org/10.1097/MOG.0000000000000893 |
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