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CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile
Bacteria that reside in the gastrointestinal tract of healthy humans are essential for our health, sustenance and well-being. About 50–60% of those bacteria have the ability to produce resilient spores that are important for the life cycle in the gut and for host-to-host transmission. A genomic sign...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041843/ https://www.ncbi.nlm.nih.gov/pubmed/33846410 http://dx.doi.org/10.1038/s41598-021-86878-9 |
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author | Martins, Diogo DiCandia, Michael A. Mendes, Aristides L. Wetzel, Daniela McBride, Shonna M. Henriques, Adriano O. Serrano, Mónica |
author_facet | Martins, Diogo DiCandia, Michael A. Mendes, Aristides L. Wetzel, Daniela McBride, Shonna M. Henriques, Adriano O. Serrano, Mónica |
author_sort | Martins, Diogo |
collection | PubMed |
description | Bacteria that reside in the gastrointestinal tract of healthy humans are essential for our health, sustenance and well-being. About 50–60% of those bacteria have the ability to produce resilient spores that are important for the life cycle in the gut and for host-to-host transmission. A genomic signature for sporulation in the human intestine was recently described, which spans both commensals and pathogens such as Clostridioides difficile and contains several genes of unknown function. We report on the characterization of a signature gene, CD25890, which, as we show is involved in the control of sporulation initiation in C. difficile under certain nutritional conditions. Spo0A is the main regulatory protein controlling entry into sporulation and we show that an in-frame deletion of CD25890 results in increased expression of spo0A per cell and increased sporulation. The effect of CD25890 on spo0A is likely indirect and mediated through repression of the sinRR´ operon. Deletion of the CD25890 gene, however, does not alter the expression of the genes coding for the cytotoxins or the genes involved in biofilm formation. Our results suggest that CD25890 acts to modulate sporulation in response to the nutrients present in the environment. |
format | Online Article Text |
id | pubmed-8041843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80418432021-04-13 CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile Martins, Diogo DiCandia, Michael A. Mendes, Aristides L. Wetzel, Daniela McBride, Shonna M. Henriques, Adriano O. Serrano, Mónica Sci Rep Article Bacteria that reside in the gastrointestinal tract of healthy humans are essential for our health, sustenance and well-being. About 50–60% of those bacteria have the ability to produce resilient spores that are important for the life cycle in the gut and for host-to-host transmission. A genomic signature for sporulation in the human intestine was recently described, which spans both commensals and pathogens such as Clostridioides difficile and contains several genes of unknown function. We report on the characterization of a signature gene, CD25890, which, as we show is involved in the control of sporulation initiation in C. difficile under certain nutritional conditions. Spo0A is the main regulatory protein controlling entry into sporulation and we show that an in-frame deletion of CD25890 results in increased expression of spo0A per cell and increased sporulation. The effect of CD25890 on spo0A is likely indirect and mediated through repression of the sinRR´ operon. Deletion of the CD25890 gene, however, does not alter the expression of the genes coding for the cytotoxins or the genes involved in biofilm formation. Our results suggest that CD25890 acts to modulate sporulation in response to the nutrients present in the environment. Nature Publishing Group UK 2021-04-12 /pmc/articles/PMC8041843/ /pubmed/33846410 http://dx.doi.org/10.1038/s41598-021-86878-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Martins, Diogo DiCandia, Michael A. Mendes, Aristides L. Wetzel, Daniela McBride, Shonna M. Henriques, Adriano O. Serrano, Mónica CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile |
title | CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile |
title_full | CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile |
title_fullStr | CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile |
title_full_unstemmed | CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile |
title_short | CD25890, a conserved protein that modulates sporulation initiation in Clostridioides difficile |
title_sort | cd25890, a conserved protein that modulates sporulation initiation in clostridioides difficile |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041843/ https://www.ncbi.nlm.nih.gov/pubmed/33846410 http://dx.doi.org/10.1038/s41598-021-86878-9 |
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