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Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant

Clostridioides difficile, a Gram-positive, spore-forming bacterium, is the primary cause of infectious nosocomial diarrhea. Antibiotics are a major risk factor for C. difficile infection (CDI), as they disrupt the gut microbial community, enabling increased germination of spores and growth of vegeta...

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Autores principales: Leslie, Jhansi L., Jenior, Matthew L., Vendrov, Kimberly C., Standke, Alexandra K., Barron, Madeline R., O’Brien, Tricia J., Unverdorben, Lavinia, Thaprawat, Pariyamon, Bergin, Ingrid L., Schloss, Patrick D., Young, Vincent B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092246/
https://www.ncbi.nlm.nih.gov/pubmed/33785619
http://dx.doi.org/10.1128/mBio.00522-21
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author Leslie, Jhansi L.
Jenior, Matthew L.
Vendrov, Kimberly C.
Standke, Alexandra K.
Barron, Madeline R.
O’Brien, Tricia J.
Unverdorben, Lavinia
Thaprawat, Pariyamon
Bergin, Ingrid L.
Schloss, Patrick D.
Young, Vincent B.
author_facet Leslie, Jhansi L.
Jenior, Matthew L.
Vendrov, Kimberly C.
Standke, Alexandra K.
Barron, Madeline R.
O’Brien, Tricia J.
Unverdorben, Lavinia
Thaprawat, Pariyamon
Bergin, Ingrid L.
Schloss, Patrick D.
Young, Vincent B.
author_sort Leslie, Jhansi L.
collection PubMed
description Clostridioides difficile, a Gram-positive, spore-forming bacterium, is the primary cause of infectious nosocomial diarrhea. Antibiotics are a major risk factor for C. difficile infection (CDI), as they disrupt the gut microbial community, enabling increased germination of spores and growth of vegetative C. difficile. To date, the only single-species bacterial preparation that has demonstrated efficacy in reducing recurrent CDI in humans is nontoxigenic C. difficile. Using multiple infection models, we determined that precolonization with a less virulent strain is sufficient to protect from challenge with a lethal strain of C. difficile, surprisingly even in the absence of adaptive immunity. Additionally, we showed that protection is dependent on high levels of colonization by the less virulent strain and that it is mediated by exclusion of the invading strain. Our results suggest that reduction of amino acids, specifically glycine following colonization by the first strain of C. difficile, is sufficient to decrease germination of the second strain, thereby limiting colonization by the lethal strain.
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spelling pubmed-80922462021-05-04 Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant Leslie, Jhansi L. Jenior, Matthew L. Vendrov, Kimberly C. Standke, Alexandra K. Barron, Madeline R. O’Brien, Tricia J. Unverdorben, Lavinia Thaprawat, Pariyamon Bergin, Ingrid L. Schloss, Patrick D. Young, Vincent B. mBio Research Article Clostridioides difficile, a Gram-positive, spore-forming bacterium, is the primary cause of infectious nosocomial diarrhea. Antibiotics are a major risk factor for C. difficile infection (CDI), as they disrupt the gut microbial community, enabling increased germination of spores and growth of vegetative C. difficile. To date, the only single-species bacterial preparation that has demonstrated efficacy in reducing recurrent CDI in humans is nontoxigenic C. difficile. Using multiple infection models, we determined that precolonization with a less virulent strain is sufficient to protect from challenge with a lethal strain of C. difficile, surprisingly even in the absence of adaptive immunity. Additionally, we showed that protection is dependent on high levels of colonization by the less virulent strain and that it is mediated by exclusion of the invading strain. Our results suggest that reduction of amino acids, specifically glycine following colonization by the first strain of C. difficile, is sufficient to decrease germination of the second strain, thereby limiting colonization by the lethal strain. American Society for Microbiology 2021-03-30 /pmc/articles/PMC8092246/ /pubmed/33785619 http://dx.doi.org/10.1128/mBio.00522-21 Text en Copyright © 2021 Leslie et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Leslie, Jhansi L.
Jenior, Matthew L.
Vendrov, Kimberly C.
Standke, Alexandra K.
Barron, Madeline R.
O’Brien, Tricia J.
Unverdorben, Lavinia
Thaprawat, Pariyamon
Bergin, Ingrid L.
Schloss, Patrick D.
Young, Vincent B.
Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant
title Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant
title_full Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant
title_fullStr Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant
title_full_unstemmed Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant
title_short Protection from Lethal Clostridioides difficile Infection via Intraspecies Competition for Cogerminant
title_sort protection from lethal clostridioides difficile infection via intraspecies competition for cogerminant
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092246/
https://www.ncbi.nlm.nih.gov/pubmed/33785619
http://dx.doi.org/10.1128/mBio.00522-21
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