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

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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