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Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics

Clostridioides difficile is a gram-positive, spore-forming, obligate anaerobe that infects the colon. C. difficile is estimated to cause nearly half a million cases in the United States annually, with about 29,000 associated deaths. Unfortunately, the current antibiotic treatment is not ideal. While...

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Autor principal: Wang, Ruojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203151/
https://www.ncbi.nlm.nih.gov/pubmed/37228365
http://dx.doi.org/10.3389/fmicb.2023.1182612
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author Wang, Ruojun
author_facet Wang, Ruojun
author_sort Wang, Ruojun
collection PubMed
description Clostridioides difficile is a gram-positive, spore-forming, obligate anaerobe that infects the colon. C. difficile is estimated to cause nearly half a million cases in the United States annually, with about 29,000 associated deaths. Unfortunately, the current antibiotic treatment is not ideal. While antibiotics can treat the infections, they also disrupt the gut microbiota that mediates colonization resistance against enteric pathogens, including C. difficile; disrupted gut microbiota provides a window of opportunity for recurrent infections. Therefore, therapeutics that restore the gut microbiota and suppress C. difficile are being evaluated for safety and efficacy. This review will start with mechanisms by which gut bacteria affect C. difficile pathogenesis, followed by a discussion on biotherapeutics for recurrent C. difficile infections.
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spelling pubmed-102031512023-05-24 Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics Wang, Ruojun Front Microbiol Microbiology Clostridioides difficile is a gram-positive, spore-forming, obligate anaerobe that infects the colon. C. difficile is estimated to cause nearly half a million cases in the United States annually, with about 29,000 associated deaths. Unfortunately, the current antibiotic treatment is not ideal. While antibiotics can treat the infections, they also disrupt the gut microbiota that mediates colonization resistance against enteric pathogens, including C. difficile; disrupted gut microbiota provides a window of opportunity for recurrent infections. Therefore, therapeutics that restore the gut microbiota and suppress C. difficile are being evaluated for safety and efficacy. This review will start with mechanisms by which gut bacteria affect C. difficile pathogenesis, followed by a discussion on biotherapeutics for recurrent C. difficile infections. Frontiers Media S.A. 2023-05-09 /pmc/articles/PMC10203151/ /pubmed/37228365 http://dx.doi.org/10.3389/fmicb.2023.1182612 Text en Copyright © 2023 Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wang, Ruojun
Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics
title Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics
title_full Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics
title_fullStr Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics
title_full_unstemmed Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics
title_short Clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics
title_sort clostridioides difficile infection: microbe-microbe interactions and live biotherapeutics
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203151/
https://www.ncbi.nlm.nih.gov/pubmed/37228365
http://dx.doi.org/10.3389/fmicb.2023.1182612
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