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Short-Term Dietary Intervention with Whole Oats Protects from Antibiotic-Induced Dysbiosis.

Microbiology spectrum
August 17, 2023
Stephen K Costa et al. (6 authors)
Journal ArticleResearch Support, U.S. Gov't, Non-P.H.S.Research Support, N.I.H., ExtramuralAnimal Study
Study Details

Study Goal

The researchers aimed to determine how oat supplementation during antibiotic exposure influences gut microbiome dysbiosis compared to other dietary timings and dextrose.

Results Summary

Oat administration during amoxicillin challenge provided greater protection against antibiotic-induced dysbiosis (AID) than other oat diet timings or dextrose. Oats reduced Firmicutes elimination and shifted gut microbial metabolism toward stress management.

Population

Not specified (likely animal or in vitro model based on context).

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
diet supplemented with oats
decrease
antibiotic-induced gut microbiome dysbiosis (AID)
-
-
provides greater protection from
#1
oat administration during amoxicillin challenge
decrease
AID
-
-
provides greater protection from
#2
oats provided at the time of antibiotic exposure
decrease
AID
-
-
induced the greatest protection against
#3
oat diets
decrease
amoxicillin-driven elimination of Firmicutes
-
-
reduced
#4
dextrose diet
increase
respiratory metabolism and consequent metabolic stress management
gut communities
-
were carbohydrate starved and favored
#5
oat-fed communities
increase
antibiotic stress management
-
-
shifted their transcriptomic profile and emphasized
#6
diets supplemented with oats
decrease
antibiotic-induced dysbiosis (AID)
-
-
are able to confer protection against
#7
Abstract

Antibiotic-induced gut microbiome dysbiosis (AID) is known to be influenced by host dietary composition. However, how and when diet modulates gut dysbiosis remains poorly characterized. Thus, here, we utilize a multi-omics approach to characterize how a diet supplemented with oats, a rich source of microbiota-accessible carbohydrates, or dextrose impacts amoxicillin-induced changes to gut microbiome structure and transcriptional activity. We demonstrate that oat administration during amoxicillin challenge provides greater protection from AID than the always oats or recovery oats diet groups. In particular, the group in which oats were provided at the time of antibiotic exposure induced the greatest protection against AID while the other oat diets saw greater effects after amoxicillin challenge. The oat diets likewise reduced amoxicillin-driven elimination of Firmicutes compared to the dextrose diet. Functionally, gut communities fed dextrose were carbohydrate starved and favored respiratory metabolism and consequent metabolic stress management while oat-fed communities shifted their transcriptomic profile and emphasized antibiotic stress management. The metabolic trends were exemplified when assessing transcriptional activity of the following two common gut commensal bacteria: Akkermansia muciniphila and Bacteroides thetaiotaomicron. These findings demonstrate that while host diet is important in shaping how antibiotics effect the gut microbiome composition and function, diet timing may play an even greater role in dietary intervention-based therapeutics. IMPORTANCE We utilize a multi-omics approach to demonstrate that diets supplemented with oats, a rich source of microbiota-accessible carbohydrates, are able to confer protection against antibiotic-induced dysbiosis (AID). Our findings affirm that not only is host diet important in shaping antibiotics effects on gut microbiome composition and function but also that the timing of these diets may play an even greater role in managing AID. This work provides a nuanced perspective on dietary intervention against AID and may be informative on preventing AID during routine antibiotic treatment.

Medical Subject Headings (MeSH)
Anti-Bacterial AgentsAvenaDysbiosisCarbohydratesAmoxicillinGlucose
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality90/10
Citation Metrics
Total Citations2
Citations/Year1.0
Relative Citation Ratio0.37
NIH Percentile19.5%
Research Impact Scores
APT Score0.05
Weight Score2.04
Normalized Score0.72
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