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Updated: Jun 22, 2026

Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
Published on: June 11, 2015
Bacteriophages drive strain diversification in a marine Flavobacterium: implications for phage resistance and
Mathias Middelboe1, Karin Holmfeldt, Lasse Riemann
1Marine Biological Laboratory, University of Copenhagen, DK-3000 Helsingør, Denmark. mmiddelboe@bio.ku.dk
Abstract:
Genetic, structural and physiological differences between strains of the marine bacterium Cellulophaga baltica MM#3 (Flavobacteriaceae) developing in response to the activity of two virulent bacteriophages, Phi S(M) and Phi S(T), was investigated during 3 weeks incubation in chemostat cultures. A distinct strain succession towards increased phage resistance and a diversification of the metabolic properties was observed. During the incubation the bacterial population diversified from a single strain, which was sensitive to 24 tested Cellulophaga phages, into a multistrain and multiresistant population, where the dominant strains had lost susceptibility to up to 22 of the tested phages. By the end of the experiment the cultures reached a quasi steady state dominated by Phi S(T)-resistant and Phi S(M) + Phi S(T)-resistant strains coexisting with small populations of phage-sensitive strains sustaining both phages at densities of > 10(6) plaque forming units (pfu) ml(-1). Loss of susceptibility to phage infection was associated with a reduction in the strains' ability to metabolize various carbon sources as demonstrated by BIOLOG assays. This suggested a cost of resistance in terms of reduced physiological capacity. However, there was no direct correlation between the degree of resistance and the loss of metabolic properties, suggesting either the occurrence of compensatory mutations in successful strains or that the cost of resistance in some strains was associated with properties not resolved by the BIOLOG assay. The study represents the first direct demonstration of phage-driven generation of functional diversity within a marine bacterial host population with significant implications for both phage susceptibility and physiological properties. We propose, therefore, that phage-mediated selection for resistant strains contributes significantly to the extensive microdiversity observed within specific bacterial species in marine environments.
Insights
Marine bacteria evolved phage resistance, leading to metabolic diversity. This phage-driven selection significantly contributes to the microdiversity seen in marine bacterial populations.
Area of Science:
- Microbiology
- Marine Biology
- Bacteriology
Background:
- Marine bacterial populations exhibit significant microdiversity.
- Bacteriophages are key drivers of microbial evolution in marine ecosystems.
- Understanding host-phage interactions is crucial for marine microbial ecology.
Purpose of the Study:
- To investigate genetic, structural, and physiological changes in *Cellulophaga baltica* strains under phage pressure.
- To determine the impact of bacteriophages Phi S(M) and Phi S(T) on bacterial strain succession and metabolic properties.
- To demonstrate phage-driven generation of functional diversity in a marine bacterial population.
Main Methods:
- Chemostat cultures of *Cellulophaga baltica* MM#3 were incubated for 3 weeks.
- Bacterial resistance to 24 different *Cellulophaga* phages was assessed.
- Metabolic profiling of bacterial strains was performed using BIOLOG assays.
Main Results:
- Bacterial population diversified from a single sensitive strain to a multi-strain, multi-resistant population.
- Dominant strains lost susceptibility to up to 22 tested phages.
- Loss of phage susceptibility correlated with reduced metabolic capacity, suggesting a cost of resistance.
Conclusions:
- Phage-mediated selection drives the evolution of phage resistance and functional diversity in marine bacteria.
- This process significantly contributes to the microdiversity observed in marine bacterial species.
- Compensatory mutations or unmeasured physiological costs may explain variations in resistance-metabolism trade-offs.
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