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Dietary modulation of the gut phageome: a cross-kingdom dialogue in Crohn’s disease
  1. Markus Tschurtschenthaler1,2
  1. 1Center for Translational Cancer Research (TranslaTUM), Klinikum rechts der Isar, School of Medicine and Health, Technical University of Munich, Munich, Germany
  2. 2Division of Translational Cancer Research, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg, Germany
  1. Correspondence to Dr Markus Tschurtschenthaler; markus.tschurtschenthaler{at}tum.de

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The importance of the gut microbiota in health and disease is a well-established paradigm, particularly in the context of inflammatory bowel diseases (IBD). Over the past decade, research increasingly focused on how environmental factors, most notably diet, modulate gut microbial composition and function, influencing disease risk. While most studies have focused on the bacterial component of the microbiome (the bacteriome), the gut virome, including bacteriophages (phages), remains comparatively underexplored. In Gut, Su et al present a pioneering study revealing how dietary whey protein confers protection against Crohn’s disease (CD) by orchestrating cross-kingdom interactions between phages and bacteria, with potential implications for microbiome-targeted dietary therapies in IBD.1

Combining a multiomics approach in a large CD cohort with mechanistic validation in preclinical models, the authors found that whey protein had a profound effect on the gut phageome, even more so than on the bacteriome, suggesting that dietary modulation of phage populations might be a previously underappreciated mechanism in host-microbe interactions. They identified a previously uncharacterised phage, AkkZT003P, enriched in whey protein-fed mice, which selectively lysed Akkermansia muciniphila. While A. muciniphila, a mucin-degrading bacterium typically associated with barrier-supportive and anti-inflammatory roles, it has also been reported to exacerbate inflammation …

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Footnotes

  • X @MarTschu

  • Contributors MT: conceived the idea and wrote the text.

  • Funding MT receives funding from the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under project ID 395357507 – SFB 1371 ‘Microbiome Signatures’.

  • Competing interests None declared.

  • Provenance and peer review Commissioned; internally peer reviewed.

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