Emergent metabolic parasitism driven by organelle sequestration.

Abstract

Stable acquisitions of metabolism, such as the endosymbiotic incorporation of eukaryotic chloroplasts, are thought to proceed through mechanisms that increase the genetic repertoire of the host and allow for vertical integration of new metabolism. Here, we test these predictions using the chloroplast-stealing marine ciliate genus <i>Mesodinium</i> by comparing transcriptomes from species that represent a spectrum from full heterotrophy to nearly full phototrophy. We find a notable divestment in metabolic autonomy with increased reliance on acquired photosynthesis. The highly photosynthetic, red tide-forming <i>Mesodinium rubrum</i> appears to have lost the capacity to synthesize amino acids, metabolize fatty acids, and produce peroxisomes. Our results portray a metabolic parasite, masquerading as a free-living ciliate that is nonetheless incapable of satisfying most of its basic anabolic needs and which provides an alternate model for understanding evolutionary transitions from heterotrophy to phototrophy.