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Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile
The virulence of Clostridioides difficile (formerly Clostridium difficile) is mainly caused by its two toxins A and B. Their formation is significantly regulated by metabolic processes. Here we investigated the influence of various sugars (glucose, fructose, mannose, trehalose), sugar derivatives (m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7790285/ https://www.ncbi.nlm.nih.gov/pubmed/33411772 http://dx.doi.org/10.1371/journal.pone.0244988 |
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author | Hofmann, Julia Danielle Biedendieck, Rebekka Michel, Annika-Marisa Schomburg, Dietmar Jahn, Dieter Neumann-Schaal, Meina |
author_facet | Hofmann, Julia Danielle Biedendieck, Rebekka Michel, Annika-Marisa Schomburg, Dietmar Jahn, Dieter Neumann-Schaal, Meina |
author_sort | Hofmann, Julia Danielle |
collection | PubMed |
description | The virulence of Clostridioides difficile (formerly Clostridium difficile) is mainly caused by its two toxins A and B. Their formation is significantly regulated by metabolic processes. Here we investigated the influence of various sugars (glucose, fructose, mannose, trehalose), sugar derivatives (mannitol and xylitol) and L-lactate on toxin synthesis. Fructose, mannose, trehalose, mannitol and xylitol in the growth medium resulted in an up to 2.2-fold increase of secreted toxin. Low glucose concentration of 2 g/L increased the toxin concentration 1.4-fold compared to growth without glucose, while high glucose concentrations in the growth medium (5 and 10 g/L) led to up to 6.6-fold decrease in toxin formation. Transcriptomic and metabolic investigation of the low glucose effect pointed towards an inactive CcpA and Rex regulatory system. L-lactate (500 mg/L) significantly reduced extracellular toxin formation. Transcriptome analyses of the later process revealed the induction of the lactose utilization operon encoding lactate racemase (larA), electron confurcating lactate dehydrogenase (CDIF630erm_01321) and the corresponding electron transfer flavoprotein (etfAB). Metabolome analyses revealed L-lactate consumption and the formation of pyruvate. The involved electron confurcation process might be responsible for the also observed reduction of the NAD(+)/NADH ratio which in turn is apparently linked to reduced toxin release from the cell. |
format | Online Article Text |
id | pubmed-7790285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77902852021-01-27 Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile Hofmann, Julia Danielle Biedendieck, Rebekka Michel, Annika-Marisa Schomburg, Dietmar Jahn, Dieter Neumann-Schaal, Meina PLoS One Research Article The virulence of Clostridioides difficile (formerly Clostridium difficile) is mainly caused by its two toxins A and B. Their formation is significantly regulated by metabolic processes. Here we investigated the influence of various sugars (glucose, fructose, mannose, trehalose), sugar derivatives (mannitol and xylitol) and L-lactate on toxin synthesis. Fructose, mannose, trehalose, mannitol and xylitol in the growth medium resulted in an up to 2.2-fold increase of secreted toxin. Low glucose concentration of 2 g/L increased the toxin concentration 1.4-fold compared to growth without glucose, while high glucose concentrations in the growth medium (5 and 10 g/L) led to up to 6.6-fold decrease in toxin formation. Transcriptomic and metabolic investigation of the low glucose effect pointed towards an inactive CcpA and Rex regulatory system. L-lactate (500 mg/L) significantly reduced extracellular toxin formation. Transcriptome analyses of the later process revealed the induction of the lactose utilization operon encoding lactate racemase (larA), electron confurcating lactate dehydrogenase (CDIF630erm_01321) and the corresponding electron transfer flavoprotein (etfAB). Metabolome analyses revealed L-lactate consumption and the formation of pyruvate. The involved electron confurcation process might be responsible for the also observed reduction of the NAD(+)/NADH ratio which in turn is apparently linked to reduced toxin release from the cell. Public Library of Science 2021-01-07 /pmc/articles/PMC7790285/ /pubmed/33411772 http://dx.doi.org/10.1371/journal.pone.0244988 Text en © 2021 Hofmann et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Hofmann, Julia Danielle Biedendieck, Rebekka Michel, Annika-Marisa Schomburg, Dietmar Jahn, Dieter Neumann-Schaal, Meina Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile |
title | Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile |
title_full | Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile |
title_fullStr | Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile |
title_full_unstemmed | Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile |
title_short | Influence of L-lactate and low glucose concentrations on the metabolism and the toxin formation of Clostridioides difficile |
title_sort | influence of l-lactate and low glucose concentrations on the metabolism and the toxin formation of clostridioides difficile |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7790285/ https://www.ncbi.nlm.nih.gov/pubmed/33411772 http://dx.doi.org/10.1371/journal.pone.0244988 |
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