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The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation

Clostridioides difficile is a nosocomial pathogen which causes severe diarrhea and colonic inflammation. C. difficile causes disease in susceptible patients when endospores germinate into the toxin-producing vegetative form. The action of these toxins results in diarrhea and the spread of spores int...

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Autores principales: Nerber, Hailee N., Sorg, Joseph A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452069/
https://www.ncbi.nlm.nih.gov/pubmed/34496003
http://dx.doi.org/10.1371/journal.ppat.1009516
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author Nerber, Hailee N.
Sorg, Joseph A.
author_facet Nerber, Hailee N.
Sorg, Joseph A.
author_sort Nerber, Hailee N.
collection PubMed
description Clostridioides difficile is a nosocomial pathogen which causes severe diarrhea and colonic inflammation. C. difficile causes disease in susceptible patients when endospores germinate into the toxin-producing vegetative form. The action of these toxins results in diarrhea and the spread of spores into the hospital and healthcare environments. Thus, the destruction of spores is imperative to prevent disease transmission between patients. However, spores are resilient and survive extreme temperatures, chemical exposure, and UV treatment. This makes their elimination from the environment difficult and perpetuates their spread between patients. In the model spore-forming organism, Bacillus subtilis, the small acid-soluble proteins (SASPs) contribute to these resistances. The SASPs are a family of small proteins found in all endospore-forming organisms, C. difficile included. Although these proteins have high sequence similarity between organisms, the role(s) of the proteins differ. Here, we investigated the role of the main α/β SASPs, SspA and SspB, and two annotated putative SASPs, CDR20291_1130 and CDR20291_3080, in protecting C. difficile spores from environmental insults. We found that SspA is necessary for conferring spore UV resistance, SspB minorly contributes, and the annotated putative SASPs do not contribute to UV resistance. In addition, the SASPs minorly contribute to the resistance of nitrous acid. Surprisingly, the combined deletion of sspA and sspB prevented spore formation. Overall, our data indicate that UV resistance of C. difficile spores is dependent on SspA and that SspA and SspB regulate/serve as a checkpoint for spore formation, a previously unreported function of SASPs.
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spelling pubmed-84520692021-09-21 The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation Nerber, Hailee N. Sorg, Joseph A. PLoS Pathog Research Article Clostridioides difficile is a nosocomial pathogen which causes severe diarrhea and colonic inflammation. C. difficile causes disease in susceptible patients when endospores germinate into the toxin-producing vegetative form. The action of these toxins results in diarrhea and the spread of spores into the hospital and healthcare environments. Thus, the destruction of spores is imperative to prevent disease transmission between patients. However, spores are resilient and survive extreme temperatures, chemical exposure, and UV treatment. This makes their elimination from the environment difficult and perpetuates their spread between patients. In the model spore-forming organism, Bacillus subtilis, the small acid-soluble proteins (SASPs) contribute to these resistances. The SASPs are a family of small proteins found in all endospore-forming organisms, C. difficile included. Although these proteins have high sequence similarity between organisms, the role(s) of the proteins differ. Here, we investigated the role of the main α/β SASPs, SspA and SspB, and two annotated putative SASPs, CDR20291_1130 and CDR20291_3080, in protecting C. difficile spores from environmental insults. We found that SspA is necessary for conferring spore UV resistance, SspB minorly contributes, and the annotated putative SASPs do not contribute to UV resistance. In addition, the SASPs minorly contribute to the resistance of nitrous acid. Surprisingly, the combined deletion of sspA and sspB prevented spore formation. Overall, our data indicate that UV resistance of C. difficile spores is dependent on SspA and that SspA and SspB regulate/serve as a checkpoint for spore formation, a previously unreported function of SASPs. Public Library of Science 2021-09-08 /pmc/articles/PMC8452069/ /pubmed/34496003 http://dx.doi.org/10.1371/journal.ppat.1009516 Text en © 2021 Nerber, Sorg https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nerber, Hailee N.
Sorg, Joseph A.
The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation
title The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation
title_full The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation
title_fullStr The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation
title_full_unstemmed The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation
title_short The small acid-soluble proteins of Clostridioides difficile are important for UV resistance and serve as a check point for sporulation
title_sort small acid-soluble proteins of clostridioides difficile are important for uv resistance and serve as a check point for sporulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452069/
https://www.ncbi.nlm.nih.gov/pubmed/34496003
http://dx.doi.org/10.1371/journal.ppat.1009516
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