4.6 Article

Clostridium scindens ATCC 35704: Integration of Nutritional Requirements, the Complete Genome Sequence, and Global Transcriptional Responses to Bile Acids

Journal

APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 85, Issue 7, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.00052-19

Keywords

Clostridium scindens; RNA-Seq; bile acid; defined medium; deoxycholic acid; growth factor requirements

Funding

  1. Department of Animal Sciences at the University of Illinois at Urbana-Champaign [Hatch ILLU-538-916]
  2. Illinois Campus Research Board [RB18068]
  3. Young Investigators Grant for Probiotic Research (Danone, Yakult)
  4. National Science Foundation
  5. UIC Cancer Education and Career Development Training Program award by the Institute for Health Research and Policy at the University of Illinois at Chicago
  6. National Cancer Institute [T32CA057699]
  7. Department of Biological Sciences at Eastern Illinois University
  8. College of Sciences at Eastern Illinois University
  9. Graduate School at Eastern Illinois University
  10. Sandra & Jack Pines Honors College at Eastern Illinois University
  11. [1RO1 CA204808-01]
  12. [NIH R01CA179243]

Ask authors/readers for more resources

In the human gut, Clostridium scindens ATCC 35704 is a predominant bacterium and one of the major bile acid 7 alpha-dehydroxylating anaerobes. While this organism is well-studied relative to bile acid metabolism, little is known about the basic nutrition and physiology of C. scindens ATCC 35704. To determine the amino acid and vitamin requirements of C. scindens, the leave-one-out (one amino acid group or vitamin) technique was used to eliminate the nonessential amino acids and vitamins. With this approach, the amino acid tryptophan and three vitamins (riboflavin, pantothenate, and pyridoxal) were found to be required for the growth of C. scindens. In the newly developed defined medium, C. scindens fermented glucose mainly to ethanol, acetate, formate, and H-2. The genome of C. scindens ATCC 35704 was completed through PacBio sequencing. Pathway analysis of the genome sequence coupled with transcriptome sequencing (RNA-Seq) under defined culture conditions revealed consistency with the growth requirements and end products of glucose metabolism. Induction with bile acids revealed complex and differential responses to cholic acid and deoxycholic acid, including the expression of potentially novel bile acid-inducible genes involved in cholic acid metabolism. Responses to toxic deoxycholic acid included expression of genes predicted to be involved in DNA repair, oxidative stress, cell wall maintenance/metabolism, chaperone synthesis, and downregulation of one-third of the genome. These analyses provide valuable insight into the overall biology of C. scindens which may be important in treatment of disease associated with increased colonic secondary bile acids. IMPORTANCE C. scindens is one of a few identified gut bacterial species capable of converting host cholic acid into disease associated secondary bile acids such as deoxycholic acid. The current work represents an important advance in understanding the nutritional requirements and response to bile acids of the medically important human gut bacterium, C. scindens ATCC 35704. A defined medium has been developed which will further the understanding of bile acid metabolism in the context of growth substrates, cofactors, and other metabolites in the vertebrate gut. Analysis of the complete genome supports the nutritional requirements reported here. Genome-wide transcriptomic analysis of gene expression in the presence of cholic acid and de oxycholic acid provides a unique insight into the complex response of C. scindens ATCC 35704 to primary and secondary bile acids. Also revealed are genes with the potential to function in bile acid transport and metabolism.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available