Journal
INTERNATIONAL JOURNAL FOR PARASITOLOGY
Volume 53, Issue 4, Pages 233-245Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.ijpara.2023.01.002
Keywords
Membrane trafficking; Trichomonas vaginalis; Evolutionary cell biology; Clathrin; COPI; Metamonada
Categories
Ask authors/readers for more resources
The study investigates the evolution of protein machinery in the eukaryotic phylum Parabasalia, focusing on the veterinary parasite Tritrichomonas foetus and the human parasite Trichomonas vaginalis. It reveals the unique cellular biology of T. vaginalis as a counter-example to the reduction in cell biology usually associated with a parasitic lifestyle. The research provides insights into the evolutionary dynamics of protein expansion in parasitic systems, shedding light on the complement and evolution of proteins involved in vesicle trafficking in parabasalids.
The eukaryotic phylum Parabasalia is composed primarily of anaerobic, endobiotic organisms such as the veterinary parasite Tritrichomonas foetus and the human parasite Trichomonas vaginalis, the latter causing the most prevalent, non-viral, sexually transmitted disease world-wide. Although a parasitic lifestyle is generally associated with a reduction in cell biology, T. vaginalis provides a striking counter-example. The 2007 T. vaginalis genome paper reported a massive and selective expansion of encoded proteins involved in vesicle trafficking, particularly those implicated in the late secretory and endocytic systems. Chief amongst these were the hetero-tetrameric adaptor proteins or 'adaptins', with T. vaginalis encoding -3.5 times more such proteins than do humans. The provenance of such a complement, and how it relates to the transition from a free-living or endobiotic state to parasitism, remains unclear. In this study, we performed a comprehensive bioinformatic and molecular evolutionary investigation of the heterotetrameric cargo adaptor-derived coats, comparing the molecular complement and evolution of these proteins between T. vaginalis, T. foetus and the available diversity of endobiotic parabasalids. Notably, with the recent discovery of Anaeramoeba spp. as the free-living sister lineage to all parabasalids, we were able to delve back to time points earlier in the lineage's history than ever before. We found that, although T. vaginalis still encodes the most HTAC subunits amongst parabasalids, the duplications giving rise to the complement took place more deeply and at various stages across the lineage. While some duplications appear to have convergently shaped the parasitic lineages, the largest jump is in the transition from free-living to endobiotic lifestyle with both gains and losses shaping the encoded complement. This work details the evolution of a cellular system across an important lineage of parasites and provides insight into the evolutionary dynamics of an example of expansion of protein machinery, counter to the more common trends observed in many parasitic systems.(c) 2023 Australian Society for Parasitology. Published by Elsevier Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available