Close

Microbial Feast or Famine: dietary carbohydrate composition and gut microbiota metabolic function

Blake Dirks, Alex E. Mohr, Karen D. Corbin, Elvis A. Carnero, Steven R. Smith, Corrie M. Whisner, Bruce E. Rittmann, Rosa Krajmalnik-Brown

Posted on: 11 December 2025

Preprint posted on 28 October 2025

Fibre for the win: Dietary influences on the gut microbiota

Selected by Jasmine Talevi

Categories: clinical trials, genomics

Background

There are many facets that contribute to overall human health. A physically small yet important one, is the diverse community of microorganisms living inside our gut, known as the microbiome. Our gut microbial community plays a role not only in digestion but has been linked to health concerns including diabetes, inflammatory diseases, and obesity.

The food that we consume influences our gut microbiome: high fibre diets are more beneficial compared to low fibre diets. Low fibre diets, typically associated with Western countries, are often absorbed almost entirely in the upper gastrointestinal tract (GI), leaving the microorganisms in the lower GI tract without any fuel. When this occurs, the microorganisms begin to consume mucin, which is the mucus lining that protects our GI tract, leading to inflammation and other health issues.

In this preprinted study, Dirks and collaborators conducted clinical trials to compare the functional activities of microbial gut communities when eating a low fibre, Western Diets (WD), compared to a high fibre, Microbiome Enhancer Diet (MBD). Participants were assigned to either the WD or MBD for 22 days straight, then given 14 days to resume their normal diet, followed by another 22 days of eating the opposite diet to the one they were first assigned. Throughout the study, participants were closely monitored and fecal samples were collected to measure differences in microbial composition and function for 11 days during each diet. Metatranscriptomic techniques were used to quantify the active gene expression of the microbial communities.

 

Key Findings

1) The overall diversity and composition of enzymes expressed by the microbial communities were similar between the WD and MBD.

This suggests functional redundancy of the gut microbiota, meaning many microbes can perform the same tasks. As a result, the gut community stays stable even when the available nutrients change, since its members can adjust their gene expression to keep key metabolic functions going.

2) The MBD microbiota expressed transcripts used for growth and digesting a variety of nutrients, whereas the WD expressed transcripts mostly for amino acid degradation.

This suggests that the microbes in the WD diet lack carbohydrates since amino acids are generally consumed once carbohydrates have been exhausted.

3) Transcripts indicated that MBD microbiota express CAZymes used to break down complex carbohydrates, whereas the WD CAZymes are used to degrade host-derived carbohydrates.

Out of a large group of enzymes important for breaking down and modifying carbohydrates (CAZymes) the difference in expression suggests that MBD delivered a rich source of polysaccharides to the microbiota to consume, while those polysaccharides were much lower in the WD. It can be speculated that, as a result, the WD microbiota turn to alternative, non-dietary carbohydrate sources, such as host tissue.

4) MBD microbiota expressed protein-degrading transcripts with a diversity of functions compared to the WD where enzymes were more focused on protein degradation (Fig. 1).

MBD transcripts are used for building cell walls, synthesizing new proteins, disposing of misfolded proteins. While these activities were still occurring under the WD, microbiota were more focused on protein degradation.

5) MBD microbiota protein degradation produces products important for maintaining the gut barrier, while WD microbiota produce toxin.

MDB produce polyamines (e.g., cadaverine, putrescine, and spermidine) important for the gut barrier while WD microbiota protein degradation produce uremic toxins, biogenic monoamine, and tryamine, which have been linked to gastrointestinal disorder (e.g. irritable bowel syndrome, Crohn’s disease).

 

Figure 1. Conceptual overview of the microbial functional response to the Microbiome Enhancer Dier (MBD) and Western Diet (WD). The gut microbiota were “resource-replete” with the MBD and “resource-limited” with the WD. The gut microbiota responded to this difference in resource availability with increased transcription for carbohydrate active enzymes (CAZymes) degrading polysaccharide and increased transcription for proteins contributing to biosynthesis pathways in the MBD. In contrast, the gut microbiota with the WD responded to limited resource availability by increasing transcription for amino acid degradation and CAZymes degrading host-glycans such as mucin.

 

Why I highlight this preprint

Although my primary field of study is marine biology, I have a personal interest in human health and wanted to highlight this study because it offers findings that may contribute to improving human well-being. Additionally, dietary modifications represent a relatively accessible intervention that many individuals can adopt to support gut health.

 

Questions for the authors

1) What were some of the high fibre foods the MBD participants were eating, and would you recommend these foods to support gut microbial health?

2) How quickly can the function and composition of our gut microbiota change after introducing a fibre rich diet similar to the MBD?

 

Tags: gastrointestinal tract, human health, metatranscriptomics, microbiome

Read preprint (No Ratings Yet)

Have your say

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Sign up to customise the site to your preferences and to receive alerts

Register here

Also in the clinical trials category:

Identifiability-Guided Assessment of Digital Twins in Alzheimer’s Disease Clinical Research and Care

Juliet Jiang, Jeffrey R. Petrella, Wenrui Hao, et al.

Selected by 08 November 2025

My Nguyen

Neuroscience

MCL1 may not mediate chemoresistance

Kylin A. Emhoff, Kunho Chung, Dongmei Zhang, et al.

Selected by 10 September 2025

Kanishka Parashar

Cell Biology

Modular control of time and space during vertebrate axis segmentation

Ali Seleit, Ian Brettell, Tomas Fitzgerald, et al.

AND

Natural genetic variation quantitatively regulates heart rate and dimension

Jakob Gierten, Bettina Welz, Tomas Fitzgerald, et al.

Selected by 24 June 2024

Girish Kale, Jennifer Ann Black

Developmental Biology

Also in the genomics category:

Microbial Feast or Famine: dietary carbohydrate composition and gut microbiota metabolic function

Blake Dirks, Alex E. Mohr, Karen D. Corbin, et al.

Selected by 11 December 2025

Jasmine Talevi

Clinical Trials

A high-coverage genome from a 200,000-year-old Denisovan

Stéphane Peyrégne, Diyendo Massilani, Yaniv Swiel, et al.

AND

A global map for introgressed structural variation and selection in humans

PingHsun Hsieh, Natthapon Soisangwan, David S. Gordon, et al.

Selected by 02 December 2025

Siddharth Singh

Evolutionary Biology

Human single-cell atlas analysis reveals heterogeneous endothelial signaling

Zimo Zhu, Rongbin Zheng, Yang Yu, et al.

Selected by 11 November 2025

Charis Qi

Bioinformatics

Also in the genomics category:

November in preprints – DevBio & Stem cell biology

preLighters with expertise across developmental and stem cell biology have nominated a few developmental and stem cell biology (and related) preprints posted in November they’re excited about and explain in a single paragraph why. Concise preprint highlights, prepared by the preLighter community – a quick way to spot upcoming trends, new methods and fresh ideas.

 



List by Aline Grata et al.

May in preprints – the CellBio edition

A group of preLighters, with expertise in different areas of cell biology, have worked together to create this preprint reading lists for researchers with an interest in cell biology. This month, categories include: 1) Biochemistry/metabolism 2) Cancer cell Biology 3) Cell adhesion, migration and cytoskeleton 4) Cell organelles and organisation 5) Cell signalling and 6) Genetics

 



List by Barbora Knotkova et al.

March in preprints – the CellBio edition

A group of preLighters, with expertise in different areas of cell biology, have worked together to create this preprint reading lists for researchers with an interest in cell biology. This month, categories include: 1) cancer biology 2) cell migration 3) cell organelles and organisation 4) cell signalling and mechanosensing 5) genetics and genomics 6) other

 



List by Girish Kale et al.

Biologists @ 100 conference preList

This preList aims to capture all preprints being discussed at the Biologists @100 conference in Liverpool, UK, either as part of the poster sessions or the (flash/short/full-length) talks.

 



List by Reinier Prosee, Jonathan Townson

Early 2025 preprints – the genetics & genomics edition

In this community-driven preList, a group of preLighters, with expertise in different areas of genetics and genomics have worked together to create this preprint reading list. Categories include: 1) bioinformatics 2) epigenetics 3) gene regulation 4) genomics 5) transcriptomics

 



List by Chee Kiang Ewe et al.

End-of-year preprints – the genetics & genomics edition

In this community-driven preList, a group of preLighters, with expertise in different areas of genetics and genomics have worked together to create this preprint reading list. Categories include: 1) genomics 2) bioinformatics 3) gene regulation 4) epigenetics

 



List by Chee Kiang Ewe et al.

BSCB-Biochemical Society 2024 Cell Migration meeting

This preList features preprints that were discussed and presented during the BSCB-Biochemical Society 2024 Cell Migration meeting in Birmingham, UK in April 2024. Kindly put together by Sara Morais da Silva, Reviews Editor at Journal of Cell Science.

 



List by Reinier Prosee

9th International Symposium on the Biology of Vertebrate Sex Determination

This preList contains preprints discussed during the 9th International Symposium on the Biology of Vertebrate Sex Determination. This conference was held in Kona, Hawaii from April 17th to 21st 2023.

 



List by Martin Estermann

Semmelweis Symposium 2022: 40th anniversary of international medical education at Semmelweis University

This preList contains preprints discussed during the 'Semmelweis Symposium 2022' (7-9 November), organised around the 40th anniversary of international medical education at Semmelweis University covering a wide range of topics.

 



List by Nándor Lipták

20th “Genetics Workshops in Hungary”, Szeged (25th, September)

In this annual conference, Hungarian geneticists, biochemists and biotechnologists presented their works. Link: http://group.szbk.u-szeged.hu/minikonf/archive/prg2021.pdf

 



List by Nándor Lipták

EMBL Conference: From functional genomics to systems biology

Preprints presented at the virtual EMBL conference "from functional genomics and systems biology", 16-19 November 2020

 



List by Jesus Victorino

TAGC 2020

Preprints recently presented at the virtual Allied Genetics Conference, April 22-26, 2020. #TAGC20

 



List by Maiko Kitaoka et al.

Zebrafish immunology

A compilation of cutting-edge research that uses the zebrafish as a model system to elucidate novel immunological mechanisms in health and disease.

 



List by Shikha Nayar