Date of Award

2020

Degree Type

Thesis

Degree Name

Master of Science in Biological and Environmental Sciences (MSBES)

Department

Biological Sciences

First Advisor

Chris Lane

Abstract

Apicomplexa is a diverse protistan phylum composed almost exclusively of metazoan-infecting parasites, including the causative agents of malaria, cryptosporidiosis, and toxoplasmosis. A single apicomplexan genus, Nephromyces, was described in 2010 as a mutualist inside its tunicate host. Here we present genomic and transcriptomic data from the parasitic sister species to this mutualist, Cardiosporidium cionae, and its associated bacterial endosymbiont. Cardiosporidium cionae and Nephromyces both infect tunicate hosts, localize to similar organs within these hosts, and maintain bacterial endosymbionts. Though many other protists are known to harbor bacterial endosymbionts, these associations are completely unknown in Apicomplexa outside of the Nephromycidae clade. Our data indicate that a vertically transmitted 𝝰-proteobacteria has been retained in each lineage since Nephromyces and Cardiosporidium diverged. This 𝝰-proteobacterial endosymbiont contributes the essential amino acid lysine, and essential cofactor lipoic acid to its apicomplexan hosts. However, the contribution of the single 𝝰-proteobacterial endosymbiont in C. cionae is minimal compared to the three taxa of endosymbionts present in the Nephromyces system, and potentially accounts for the apparent virulence disparity between these lineages. This study demonstrates the potential for virulence reduction and life strategy transitions within Apicomplexa via bacterial endosymbiosis.

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