TY - JOUR
T1 - Changes in the Gut Microbiota following Bariatric Surgery Are Associated with Increased Alcohol Intake in a Female Rat Model
AU - Martin, Olivia A.
AU - Grant-Beurmann, Silvia
AU - Orellana, Elise R.
AU - Hajnal, Andras
AU - Fraser, Claire M.
N1 - Funding Information:
The authors have no financial disclosures to report. This work was supported by [1TL1TR003100-01], [1UL1TR003098-01], and the University of Maryland Baltimore Institute for Clinical and Translational Research granted to O.M. as a TL1 Post-Doctoral Fellow. This work was supported, in part, by the Dean's Endowed Professorship at the University of Maryland, School of Medicine given to C.M.F. This project was supported, in part, under a grant with the Pennsylvania Department of Health using Tobacco CURE Funds [SAP # 4100077246] to A.H. The Department specifically disclaims responsibility for any analyses, interpretations or conclusions. The content of this article does not necessarily represent the official views of the funders.
Publisher Copyright:
© 2021 The Author(s). Medical Council on Alcohol and Oxford University Press. All rights reserved.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - Aims: We aimed to investigate if differences in gut microbiota diversity and composition are associated with post-operative alcohol intake following bariatric surgery in a rat model. Methods: Twenty-four female rats were randomized to three treatment groups: sham surgery, vertical sleeve gastrectomy (VSG) or Roux-en-Y gastric bypass (RYGB). Stool was collected pre- and post-operatively and 16S rRNA gene amplification and sequencing was performed. Analysis focused on correlating microbial diversity, type of surgery and alcohol (EtOH) intake. Results: Pre-operative stools samples on regular diet showed similar taxonomic composition and Shannon diversity among the three treatment groups. There was a significant decrease in Shannon diversity and a change in taxonomic composition of the gut microbiota after rats was fed high fat diet. Post-operatively, the RYGB group showed significantly lower taxonomic diversity than the VSG and sham groups, while the VSG and sham groups diversity were not significantly different. Taxonomic composition and function prediction based on PICRUSt analysis showed the RYGB group to be distinct from the VSG and sham groups. Shannon diversity was found to be negatively associated with EtOH intake. Conclusions: Changes in the taxonomic profile of the gut microbiota following bariatric surgery, particularly RYGB, are associated with increased EtOH intake and may contribute to increased alcohol use disorder risk through the gut-brain-microbiome axis.
AB - Aims: We aimed to investigate if differences in gut microbiota diversity and composition are associated with post-operative alcohol intake following bariatric surgery in a rat model. Methods: Twenty-four female rats were randomized to three treatment groups: sham surgery, vertical sleeve gastrectomy (VSG) or Roux-en-Y gastric bypass (RYGB). Stool was collected pre- and post-operatively and 16S rRNA gene amplification and sequencing was performed. Analysis focused on correlating microbial diversity, type of surgery and alcohol (EtOH) intake. Results: Pre-operative stools samples on regular diet showed similar taxonomic composition and Shannon diversity among the three treatment groups. There was a significant decrease in Shannon diversity and a change in taxonomic composition of the gut microbiota after rats was fed high fat diet. Post-operatively, the RYGB group showed significantly lower taxonomic diversity than the VSG and sham groups, while the VSG and sham groups diversity were not significantly different. Taxonomic composition and function prediction based on PICRUSt analysis showed the RYGB group to be distinct from the VSG and sham groups. Shannon diversity was found to be negatively associated with EtOH intake. Conclusions: Changes in the taxonomic profile of the gut microbiota following bariatric surgery, particularly RYGB, are associated with increased EtOH intake and may contribute to increased alcohol use disorder risk through the gut-brain-microbiome axis.
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U2 - 10.1093/alcalc/agab041
DO - 10.1093/alcalc/agab041
M3 - Article
C2 - 34155502
AN - SCOPUS:85114984439
SN - 0735-0414
VL - 56
SP - 605
EP - 613
JO - Alcohol and Alcoholism
JF - Alcohol and Alcoholism
IS - 5
ER -