Differential Effects of Sulfur Amino Acid-Restricted and Low-Calorie Diets on Gut Microbiome Profile and Bile Acid Composition in Male C57BL6/J Mice

Author:

Nichenametla Sailendra N1ORCID,Mattocks Dwight A L1,Midya Vishal2,Shneyder Jelena1

Affiliation:

1. Animal Science Laboratory, Orentreich Foundation for the Advancement of Science, Cold Spring-on-Hudson, New York

2. Division of Biostatistics and Bioinformatics, Penn State College of Medicine, Penn State University, Hershey, Pennsylvania

Abstract

Abstract Diet can affect health and longevity by altering the gut microbiome profile. Sulfur amino acid restriction (SAAR), like caloric restriction, extends lifespan. But, its effect on the gut microbiome profile and functional significance of such effects are understudied. We investigated whether SAAR alters the gut microbiome profile and bile acid composition, an index of microbial metabolism. We also compared these changes with those induced by a 12% low-calorie diet (LCD). Male 21-week-old C57BL6/J mice were fed control (CD; 0.86% methionine), SAAR (0.12% methionine), and LCD diets (0.86% methionine). After 10 weeks on the diet, plasma markers and fecal microbial profiles were determined. SAAR mice had lower body weights and IGF-1, and higher food intake and FGF-21 than CD mice. Compared to SAAR mice, LCD mice had higher body weights, and lower FGF-21 and food intake, but similar IGF-1. β-Diversity indices were different between SAAR and LCD, and LCD and CD, but not between CD and SAAR. In groupwise comparisons of individual taxa, differences were more discernable between SAAR and LCD than between other groups. Abundances of Firmicutes, Clostridiaceae, and Turicibacteraceae were higher, but Verrucomicrobia was lower in SAAR than in LCD. Secondary bile acids and the ratio of secondary to primary bile acids were lower in SAAR than in LCD. SAAR favored bile acid conjugation with glycine at the expense of taurine. Overall, SAAR and LCD diets induced distinct changes in the gut microbiome and bile acid profiles. Additional studies on the role of these changes in improving health and lifespan are warranted.

Funder

Orentreich Foundation for the Advancement of Science

National Institutes of Health

National Cancer Institute

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Ageing

Reference49 articles.

1. Starch utilization by the human large intestinal microflora;Macfarlane;J Appl Bacteriol,1986

2. Protein degradation by human intestinal bacteria;Macfarlane;J Gen Microbiol,1986

3. Low methionine ingestion by rats extends life span;Orentreich;J Nutr,1993

4. The Journal of Nutrition. Volume 18 July–December, 1939. Pages 1–13. Retarded growth, life span, ultimate body size and age changes in the Albino rat after feeding diets restricted in calories;McCay;Nutr Rev,1975

5. Metabonomic investigations of aging and caloric restriction in a life-long dog study;Wang;J Proteome Res,2007

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