Growth-independent cross-feeding modifies boundaries for coexistence in a bacterial mutualism

Environ Microbiol. 2017 Sep;19(9):3538-3550. doi: 10.1111/1462-2920.13847. Epub 2017 Jul 24.

Abstract

Nutrient cross-feeding can stabilize microbial mutualisms, including those important for carbon cycling in nutrient-limited anaerobic environments. It remains poorly understood how nutrient limitation within natural environments impacts mutualist growth, cross-feeding levels and ultimately mutualism dynamics. We examined the effects of nutrient limitation within a mutualism using theoretical and experimental approaches with a synthetic anaerobic coculture pairing fermentative Escherichia coli and phototrophic Rhodopseudomonas palustris. In this coculture, E. coli and R. palustris resemble an anaerobic food web by cross-feeding essential carbon (organic acids) and nitrogen (ammonium) respectively. Organic acid cross-feeding stemming from E. coli fermentation can continue in a growth-independent manner during nitrogen limitation, while ammonium cross-feeding by R. palustris is growth-dependent. When ammonium cross-feeding was limited, coculture trends changed yet coexistence persisted under both homogenous and heterogenous conditions. Theoretical modelling indicated that growth-independent fermentation was crucial to sustain cooperative growth under conditions of low nutrient exchange. In contrast to stabilization at most cell densities, growth-independent fermentation inhibited mutualistic growth when the E. coli cell density was adequately high relative to that of R. palustris. Thus, growth-independent fermentation can conditionally stabilize or destabilize a mutualism, indicating the potential importance of growth-independent metabolism for nutrient-limited mutualistic communities.

MeSH terms

  • Carbon / metabolism*
  • Carbon Cycle / physiology
  • Escherichia coli / growth & development
  • Escherichia coli / metabolism*
  • Fermentation
  • Models, Theoretical
  • Nitrogen / metabolism*
  • Rhodopseudomonas / growth & development
  • Rhodopseudomonas / metabolism*
  • Symbiosis / physiology*

Substances

  • Carbon
  • Nitrogen