The Response of Heterotrophic Prokaryote and Viral Communities to Labile Organic Carbon Inputs Is Controlled by the Predator Food Chain Structure

Viruses. 2017 Aug 23;9(9):238. doi: 10.3390/v9090238.

Abstract

Factors controlling the community composition of marine heterotrophic prokaryotes include organic-C, mineral nutrients, predation, and viral lysis. Two mesocosm experiments, performed at an Arctic location and bottom-up manipulated with organic-C, had very different results in community composition for both prokaryotes and viruses. Previously, we showed how a simple mathematical model could reproduce food web level dynamics observed in these mesocosms, demonstrating strong top-down control through the predator chain from copepods via ciliates and heterotrophic nanoflagellates. Here, we use a steady-state analysis to connect ciliate biomass to bacterial carbon demand. This gives a coupling of top-down and bottom-up factors whereby low initial densities of ciliates are associated with mineral nutrient-limited heterotrophic prokaryotes that do not respond to external supply of labile organic-C. In contrast, high initial densities of ciliates give carbon-limited growth and high responsiveness to organic-C. The differences observed in ciliate abundance, and in prokaryote abundance and community composition in the two experiments were in accordance with these predictions. Responsiveness in the viral community followed a pattern similar to that of prokaryotes. Our study provides a unique link between the structure of the predator chain in the microbial food web and viral abundance and diversity.

Keywords: ciliates; copepods; high latitude microbes; marine viral diversity; minimum food web model; nutrient limitation; trophic cascade; viral–host interaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria / growth & development
  • Bacteria / metabolism
  • Bacteria / virology
  • Bacteriolysis
  • Bacteriophages / growth & development*
  • Biodiversity*
  • Biomass
  • Carbon / metabolism*
  • Food Chain*
  • Heterotrophic Processes*
  • Minerals / metabolism
  • Models, Theoretical
  • Multivariate Analysis
  • Prokaryotic Cells / metabolism*
  • Prokaryotic Cells / virology*
  • Seawater / microbiology*
  • Seawater / virology*
  • Water Microbiology

Substances

  • Minerals
  • Carbon