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Title: Gut microbial features can predict host phenotype response to protein deficiency

Journal Article · · Physiological Reports
 [1];  [2];  [3];  [4];  [2];  [5]
  1. Univ. of Illinois at Chicago, Chicago, IL (United States). Dept. of Medicine, Div. of Endocrinology, Diabetes, and Metabolism; University of Illinois at Chicago
  2. Univ. of Chicago, Chicago, IL (United States). Dept. of Surgery; Argonne National Laboratory (ANL), Argonne, IL (United States). Biosciences Div. (BIO)
  3. Loyola Univ., Chicago, IL (United States). Public Health Sciences; Stritch School of Medicine, Maywood, IL (United States)
  4. UWI SODECO (Solutions for Developing Countries), Univ. of the West Indies, Kingston, Jamaica
  5. Univ. of Illinois at Chicago, Chicago, IL (United States). Dept. of Medicine, Div. of Endocrinology, Diabetes, and Metabolism; Jesse Brown Veterans Affair Medical Center, Chicago, IL (United States)

Malnutrition remains a major health problem in low- and middle-income countries. During low protein intake, <0.67 g/kg/day, there is a loss of nitrogen (N2) balance, due to the unavailability of amino acid for metabolism and unbalanced protein catabolism results. However, there are individuals, who consume the same low protein intake, and preserve N2 balance for unknown reasons. A novel factor, the gut microbiota, may account for these N2 balance differences. To investigate this, we correlated gut microbial profiles with the growth of four murine strains (C57Bl6/J, CD-1, FVB, and NIH-Swiss) on protein deficient (PD) diet. Results show that a PD diet exerts a strain-dependent impact on growth and N2 balance as determined through analysis of urinary urea, ammonia and creatinine excretion. Bacterial alpha diversity was significantly (P < 0.05, FDR) lower across all strains on a PD diet compared to normal chow (NC). Multi-group analyses of the composition of microbiomes (ANCOM) revealed significantly differential microbial signatures between the four strains independent of diet. However, mice on a PD diet demonstrated differential enrichment of bacterial genera including, Allobaculum (C57Bl6/J), Parabacteroides (CD-1), Turicibacter (FVB), and Mucispirillum (NIH-Swiss) relative to NC. For instance, selective comparison of the CD-1 (gained weight) and C57Bl6/J (did not gain weight) strains on PD diet also demonstrated significant pathway enrichment of dihydroorodate dehydrogenase, rRNA methyltransferases, and RNA splicing ligase in the CD-1 strains compared to C57Bl6/ J strains; which might account in their ability to retain growth despite a protein deficient diet. Taken together, these results suggest a potential relationship between the specific gut microbiota, N2 balance and animal response to malnutrition.

Research Organization:
Argonne National Lab (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1629359
Journal Information:
Physiological Reports, Journal Name: Physiological Reports Journal Issue: 23 Vol. 6; ISSN 2051-817X
Publisher:
American Physiological Society and The Physiological SocietyCopyright Statement
Country of Publication:
United States
Language:
English

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