Inflammatory Bowel Disease (IBD) and Microbiome: Etiopathogenesis, Diagnosis, and Therapeutic Advances

A special issue of Microorganisms (ISSN 2076-2607). This special issue belongs to the section "Medical Microbiology".

Deadline for manuscript submissions: 30 April 2025 | Viewed by 619

Special Issue Editor


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Guest Editor
Division of Gastroenterology and Hepatology, Medical University Department, Kantonsspital Aarau, 5001 Aarau, Switzerland
Interests: Helicobacter pylori; IBD; gut dysbiosis; MASLD
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Special Issue Information

Dear Colleagues,

This Special Issue, “Inflammatory Bowel Disease (IBD) and Microbiome: Etiopathogenesis, Diagnosis, and Therapeutic Advances”, addresses the growing interest in understanding the microbiome's role in the onset, progression, and management of inflammatory bowel disease (IBD).

Emerging studies have shown that the gut microbiome plays a vital role in shaping immune responses, maintaining mucosal integrity, and modulating inflammation in IBD patients. Disruptions to this delicate microbial balance—commonly known as dysbiosis—are increasingly recognized as contributors to the development and exacerbation of IBD, including Crohn’s disease and ulcerative colitis. A deeper understanding of these microbiome-driven mechanisms has the potential to transform our diagnostic and therapeutic approaches for these chronic, often debilitating conditions.

This Special Issue invites submissions of original research, review articles, and clinical studies that examine the relationship between the microbiome and IBD. We welcome studies that explore how microbiome shifts impact immune pathways, intestinal barrier function, and systemic inflammation, as well as research into novel microbiome-targeted therapies. We encourage submissions on a range of topics, including the following:

  • Microbiome–Immune Interactions: Insights into how microbiome alterations influence immune modulation and inflammatory responses in IBD.
  • Therapeutic Potential of Microbiome Modulation: Studies on probiotics, prebiotics, fecal microbiota transplantation (FMT), and next-generation microbial therapies.
  • Gut–Brain and Gut–Liver Axes: Exploration of the systemic impact of gut dysbiosis in IBD, including the effects on mental health, liver function, and overall disease progression.
  • Diagnostic and Prognostic Biomarkers: Identification of microbial markers for early diagnosis, monitoring, and predicting therapeutic response in IBD patients.
  • Host–Microbiome Interactions and Epigenetics: Research on genetic and epigenetic factors that contribute to individual responses to microbiome changes in IBD.

By gathering cutting-edge research in this Special Issue, we aim to deepen understanding of the microbiome’s role in IBD and foster new avenues for personalized, microbiome-centered therapies.

Dr. Michael Doulberis
Guest Editor

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Keywords

  • inflammatory bowel disease
  • microbiome-immune interactions
  • microbiome modulation
  • gut–brain axes
  • gut–liver axes
 

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Published Papers (1 paper)

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Research

24 pages, 17338 KiB  
Article
Impact of Microbiota Diversity on Inflammatory Bowel Disease
by Ashwag J. Alzahrani, Basma M. Al-Hebshi, Zolfekar A. Yahia, Effat A. Al-Judaibi, Khloud H. Alsaadi and Awatif A. Al-Judaibi
Microorganisms 2025, 13(4), 710; https://doi.org/10.3390/microorganisms13040710 - 21 Mar 2025
Viewed by 425
Abstract
Inflammatory bowel disease (IBD) is a chronic condition that includes two main types, Crohn’s disease (CD) and ulcerative colitis (UC), involving inflammation of the gastrointestinal (GI) tract. The exact cause of IBD is unknown but could be a combination of genetic, environmental, and [...] Read more.
Inflammatory bowel disease (IBD) is a chronic condition that includes two main types, Crohn’s disease (CD) and ulcerative colitis (UC), involving inflammation of the gastrointestinal (GI) tract. The exact cause of IBD is unknown but could be a combination of genetic, environmental, and immune system factors. This study investigated the impact of IBD on microbiota diversity by evaluating the differences in microbial composition and the microbiota of a control group (A) of healthy individuals and a group (B) of IBD patients. Sixty biopsies were collected from participants recruited from hospitals in Makkah, Saudi Arabia. Biopsy specimens were taken during colonoscopy examination, and bacterial identification was performed by extracting ribosomal DNA from sigmoid colon biopsies using a DNeasy Blood & Tissue Kit. Metagenomics and bioinformatics analyses were then conducted to analyze and compare the microbiota in the two groups. The results showed that the varieties of core microbiome species were 3.81% greater in the IBD patients than in the members of the control group. Furthermore, the differences between the groups were significantly greater than the variations within each group. Differences between the two groups were detected in the relative abundance of Clostridium nexile, Ruminococcus gnavus, Ruminococcus faecis, and Escherichia coli. These results indicate that microbiota could play a role in the pathogenesis of IBD and suggest that microbial diversity can serve as a biomarker for diagnosing the disease and monitoring its progression. Full article
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