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Updated: Jan 4, 2026

Author Spotlight: Investigating Bacteriophage-Induced Immune Responses in Gnotobiotic Mice
Published on: January 26, 2024
Impact of bacteria motility in the encounter rates with bacteriophage in mucus
Kevin L Joiner1,2, Arlette Baljon3,4, Jeremy Barr5
1Computational Science Research Center, San Diego State University, San Diego, CA, 92182, USA. kevin.l.joiner1@navy.mil.
Abstract:
Bacteriophages-or phages-are viruses that infect bacteria and are present in large concentrations in the mucosa that cover the internal organs of animals. Immunoglobulin (Ig) domains on the phage surface interact with mucin molecules, and this has been attributed to an increase in the encounter rates of phage with bacteria in mucus. However, the physical mechanism behind this phenomenon remains unclear. A continuous time random walk (CTRW) model simulating the diffusion due to mucin-T4 phage interactions was developed and calibrated to empirical data. A Langevin stochastic method for Escherichia coli (E. coli) run-and-tumble motility was combined with the phage CTRW model to describe phage-bacteria encounter rates in mucus for different mucus concentrations. Contrary to previous theoretical analyses, the emergent subdiffusion of T4 in mucus did not enhance the encounter rate of T4 against bacteria. Instead, for static E. coli, the diffusive T4 mutant lacking Ig domains outperformed the subdiffusive T4 wild type. E. coli's motility dominated the encounter rates with both phage types in mucus. It is proposed, that the local fluid-flow generated by E. coli's motility combined with T4 interacting with mucins may be the mechanism for increasing the encounter rates between the T4 phage and E. coli bacteria.
Insights
Bacteriophages (phages) interacting with mucins do not enhance encounters with bacteria in mucus. Instead, bacterial motility drives phage-bacteria interactions, suggesting a new mechanism for increased encounter rates.
Area of Science:
- Microbiology
- Biophysics
- Computational Biology
Background:
- Bacteriophages (phages) are viruses that infect bacteria.
- Phages utilize surface immunoglobulin (Ig) domains to interact with mucins in animal mucosa.
- This interaction is hypothesized to increase phage-bacteria encounter rates in mucus, but the mechanism is unclear.
Purpose of the Study:
- To investigate the physical mechanism by which phage-mucin interactions affect phage-bacteria encounter rates in mucus.
- To model phage diffusion and bacterial motility in mucus environments.
Main Methods:
- Developed a continuous time random walk (CTRW) model for mucin-T4 phage interactions.
- Integrated a Langevin stochastic method for Escherichia coli (E. coli) run-and-tumble motility.
- Simulated phage-bacteria encounter rates across varying mucus concentrations.
Main Results:
- Subdiffusion of T4 phages in mucus, contrary to prior theories, did not enhance encounter rates with static E. coli.
- A diffusive T4 mutant lacking Ig domains showed higher encounter rates than wild-type T4 against static E. coli.
- E. coli motility was the dominant factor influencing encounter rates for both phage types.
Conclusions:
- Phage-mucin interactions do not inherently increase phage-bacteria encounter rates in mucus.
- Bacterial motility, through local fluid flow, is proposed as the primary mechanism enhancing encounters between T4 phages and E. coli in mucus.
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