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Updated: May 6, 2026

Author Spotlight: Investigating Bacteriophage-Induced Immune Responses in Gnotobiotic Mice
Published on: January 26, 2024
Innate and acquired bacteriophage-mediated immunity
Jeremy J Barr1, Merry Youle, Forest Rohwer
1Department of Biology; San Diego State University; San Diego, CA USA.
Abstract:
We recently described a novel, non-host-derived, phage-mediated immunity active at mucosal surfaces, the main site of pathogen entry in metazoans. In that work, we showed that phage T4 adheres to mucus glycoproteins via immunoglobulin-like domains displayed on its capsid. This adherence positions the phage in mucus surfaces where they are more likely to encounter and kill bacteria, thereby benefiting both the phage and its metazoan host. We presented this phage-metazoan symbiosis based on an exclusively lytic model of phage infection. Here we extend our bacteriophage adherence to mucus (BAM) model to consider the undoubtedly more complex dynamics in vivo. We hypothesize how mucus-adherent phages, both lytic and temperate, might impact the commensal microbiota as well as protect the metazoan epithelium from bacterial invasion. We suggest that BAM may provide both an innate and an acquired antimicrobial immunity.
Insights
Bacteriophage T4 adheres to mucus, providing phage-mediated immunity at mucosal surfaces. This bacteriophage adherence to mucus (BAM) model suggests a symbiotic relationship benefiting both phages and their hosts.
Area of Science:
- Microbiology
- Immunology
- Symbiotic relationships
Background:
- Mucosal surfaces are primary sites for pathogen entry in metazoans.
- Phage T4 was previously shown to adhere to mucus glycoproteins via its capsid.
- A lytic phage-metazoan symbiosis model was previously established.
Purpose of the Study:
- To extend the bacteriophage adherence to mucus (BAM) model to in vivo dynamics.
- To hypothesize the impact of mucus-adherent phages (lytic and temperate) on microbiota and host protection.
- To explore BAM's role in innate and acquired antimicrobial immunity.
Main Methods:
- Literature review and theoretical modeling.
- Extension of the existing BAM model.
- Hypothetical analysis of phage-host-microbiota interactions.
Main Results:
- The BAM model was extended to encompass in vivo conditions.
- Hypotheses were formulated regarding the influence of mucus-adherent phages on commensal microbiota.
- Potential roles of BAM in both innate and acquired immunity were proposed.
Conclusions:
- Bacteriophage adherence to mucus is a significant factor in host-microbe interactions.
- Mucus-adherent phages, both lytic and temperate, may modulate the microbiota and protect the host epithelium.
- The BAM model offers a framework for understanding phage-mediated mucosal immunity.
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