Toxins, Butyric Acid, and Other Short-Chain Fatty Acids Are Coordinately Expressed and Down-Regulated by Cysteine in Clostridium difficile

Author:

Karlsson Sture12,Lindberg Anette3,Norin Elisabeth4,Burman Lars G.1,Åkerlund Thomas1

Affiliation:

1. Department of Bacteriology, Swedish Institute for Infectious Disease Control, S-171 82, Solna,1

2. Microbiology and Tumor Biology Center2 and

3. Department of Medical Biochemistry and Microbiology, Uppsala University, S-751 23, Uppsala,3 Sweden

4. Laboratory of Medical Microbial Ecology,4 Karolinska Institute, S-171 77, Stockholm, and

Abstract

ABSTRACT It was recently found that a mixture of nine amino acids down-regulate Clostridium difficile toxin production when added to peptone yeast extract (PY) cultures of strain VPI 10463 (S. Karlsson, L. G. Burman, and T. Åkerlund, Microbiology 145:1683–1693, 1999). In the present study, seven of these amino acids were found to exhibit a moderate suppression of toxin production, whereas proline and particularly cysteine had the greatest impact, on both reference strains ( n = 6) and clinical isolates ( n = 28) of C. difficile (>99% suppression by cysteine in the highest toxin-producing strain). Also, cysteine derivatives such as acetylcysteine, glutathione, and cystine effectively down-regulated toxin expression. An impact of both cysteine and cystine but not of thioglycolate on toxin yield indicated that toxin expression was not regulated by the oxidation-reduction potential. Several metabolic pathways, including butyric acid and butanol production, were coinduced with the toxins in PY and down-regulated by cysteine. The enzyme 3-hydroxybutyryl coenzyme A dehydrogenase, a key enzyme in solventogenesis in Clostridium acetobutylicum , was among the most up-regulated proteins during high toxin production. The addition of butyric acid to various growth media induced toxin production, whereas the addition of butanol had the opposite effect. The results indicate a coupling between specific metabolic processes and toxin expression in C. difficile and that certain amino acids can alter these pathways coordinately. We speculate that down-regulation of toxin production by the administration of such amino acids to the colon may become a novel approach to prophylaxis and therapy for C. difficile -associated diarrhea.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference27 articles.

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4. Regulated transcription of Clostridium difficile toxin genes;Dupuy B.;Mol. Microbiol.,1998

5. Solventogenic enzymes of Clostridium acetobutylicum: catalytic properties, genetic organization and transcriptional regulation;Dürre P.;FEMS Microbiol. Rev.,1995

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