TY - JOUR
T1 - Biomechanical modeling of spatiotemporal bacteria-phage competition
AU - Valdez, Andrés
AU - Sun, Hui
AU - Weiss, Howard Howie
AU - Aranson, Igor
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - 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. (Figure presented.)
AB - 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. (Figure presented.)
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U2 - 10.1038/s42005-025-02078-1
DO - 10.1038/s42005-025-02078-1
M3 - Article
AN - SCOPUS:105002787902
SN - 2399-3650
VL - 8
JO - Communications Physics
JF - Communications Physics
IS - 1
M1 - 139
ER -