Biomechanical modeling of spatiotemporal bacteria-phage competition

Bacteriophages are viral predators of bacteria. Understanding the bacteria-phage competition is crucial for horizontal gene transfer and treatment of antibiotic-resistant bacterial infections. Here, we investigate the interaction dynamics between common rod-shaped bacteria such as Escherichia coli or Pseudomonas aeruginosa and lytic phages within 2D and 3D environments. Our computational study is based on established experimental observations of bacteria-phage interactions. A lytic phage effectively kills bacterial cells in a colony, leading to significant consequences for its morphology and expansion. Through computational modeling, we observe that phage interactions with bacteria produce phage-plaque regions characterized by cell death, reorganization, and altered colony growth dynamics. As phages predate, surviving cells tend to re-align toward the phage-affected region, forming a more ordered structure. This reordering effect not only reduces the radial spread of the colony but, in highly virulent scenarios, generates an inflow of cells toward the phage-plaque, effectively “devouring” portions of the colony. Our work highlights how phages control the self-organization of proliferating active matter and offers insights into targeted approaches for managing bacterial populations in biofilm-associated environments. Understanding the bacteria-phage competition is crucial for horizontal gene transfer and treatment of antibiotic-resistant bacterial infections. This work investigates the interaction between common rod-shaped bacteria such as Escherichia coli or Pseudomonas aeruginosa and lytic phages to provide insights into their proliferating active dynamics in 2D and 3D environments.

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Publication Details

Journal
Communications Physics
Published
2025-04-08
DOI
https://doi.org/10.1038/s42005-025-02078-1
Citations
4
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
6.87

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article

Biomechanical modeling of spatiotemporal bacteria-phage competition

Igor Aronson, Andrés Valdez, Hui Sun, Howard M. Weiss
4 citations
Communications Physics
Bacteriophages and microbial interactions
6.87
article

Biomechanical modeling of spatiotemporal bacteria-phage competition

Igor Aronson, Andrés Valdez, Hui Sun, Howard M. Weiss
article en
4 citations

Abstract

Bacteriophages are viral predators of bacteria. Understanding the bacteria-phage competition is crucial for horizontal gene transfer and treatment of antibiotic-resistant bacterial infections. Here, we investigate the interaction dynamics between common rod-shaped bacteria such as Escherichia coli or Pseudomonas aeruginosa and lytic phages within 2D and 3D environments. Our computational study is based on established experimental observations of bacteria-phage interactions. A lytic phage effectively kills bacterial cells in a colony, leading to significant consequences for its morphology and expansion. Through computational modeling, we observe that phage interactions with bacteria produce phage-plaque regions characterized by cell death, reorganization, and altered colony growth dynamics. As phages predate, surviving cells tend to re-align toward the phage-affected region, forming a more ordered structure. This reordering effect not only reduces the radial spread of the colony but, in highly virulent scenarios, generates an inflow of cells toward the phage-plaque, effectively “devouring” portions of the colony. Our work highlights how phages control the self-organization of proliferating active matter and offers insights into targeted approaches for managing bacterial populations in biofilm-associated environments. Understanding the bacteria-phage competition is crucial for horizontal gene transfer and treatment of antibiotic-resistant bacterial infections. This work investigates the interaction between common rod-shaped bacteria such as Escherichia coli or Pseudomonas aeruginosa and lytic phages to provide insights into their proliferating active dynamics in 2D and 3D environments.

Communications PhysicsVol. 8(1)
Pennsylvania State University (US), California State University, Long Beach (US)
National Science Foundation
Openalex Percentile: Top 4%
Bacteriophages and microbial interactions
6.87
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