Metabolic Reprogramming of Clostridioides difficile During the Stationary Phase With the Induction of Toxin Production

Medientyp: E-Book; Sonderdruck

Titel: Metabolic Reprogramming of Clostridioides difficile During the Stationary Phase With the Induction of Toxin Production

Beteiligte: Hofmann, Julia D. [Verfasser:in]; Otto, Andreas [Verfasser:in]; Berges, Mareike [Verfasser:in]; Biedendieck, Rebekka Katrin Johanna [Verfasser:in]; Michel, Annika-Marisa [Verfasser:in]; Becher, Dörte [Verfasser:in]; Jahn, Dieter [Verfasser:in]; Neumann-Schaal, Meina [Verfasser:in]

Erschienen: Braunschweig, 2018

Umfang: 1 Online-Ressource

Sprache: Englisch

DOI: 10.3389/fmicb.2018.01970

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Anmerkungen: Original erschienen in: Frontiers in microbiology, 9:1970. doi: 10.3389/fmicb.2018.01970

Beschreibung: The obligate anaerobe, spore forming bacterium Clostridioides difficile (formerly Clostridium difficile) causes nosocomial and community acquired diarrhea often associated with antibiotic therapy. Major virulence factors of the bacterium are the two large clostridial toxins TcdA and TcdB. The production of both toxins was found strongly connected to the metabolism and the nutritional status of the growth environment. Here, we systematically investigated the changes of the gene regulatory, proteomic and metabolic networks of C. difficile 630Δerm underlying the adaptation to the non-growing state in the stationary phase. Integrated data from time-resolved transcriptome, proteome and metabolome investigations performed under defined growth conditions uncovered multiple adaptation strategies. Overall changes in the cellular processes included the downregulation of ribosome production, lipid metabolism, cold shock proteins, spermine biosynthesis, and glycolysis and in the later stages of riboflavin and coenzyme A (CoA) biosynthesis. In contrast, different chaperones, several fermentation pathways, and cysteine, serine, and pantothenate biosynthesis were found upregulated. Focusing on the Stickland amino acid fermentation and the central carbon metabolism, we discovered the ability of C. difficile to replenish its favored amino acid cysteine by a pathway starting from the glycolytic 3-phosphoglycerate via L-serine as intermediate. Following the growth course, the reductive equivalent pathways used were sequentially shifted from proline via leucine/phenylalanine to the central carbon metabolism first to butanoate fermentation and then further to lactate fermentation. The toxin production was found correlated mainly to fluxes of the central carbon metabolism. Toxin formation in the supernatant was detected when the flux changed from butanoate to lactate synthesis in the late stationary phase. The holistic view derived from the combination of transcriptome, proteome and metabolome data allowed us to uncover the major metabolic strategies that are used by the clostridial cells to maintain its cellular homeostasis and ensure survival under starvation conditions.

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