Adaptin evolution in kinetoplastids and emergence of the variant surface glycoprotein coat in African trypanosomatids

作者：Manna Paul T; Kelly Steven; Field Mark C^*

来源：Molecular Phylogenetics and Evolution, 2013, 67(1): 123-128.

DOI：10.1016/j.ympev.2013.01.002

• Endocytosis
• Variant surface glycoprotein
• Adaptin
• Trypanosoma grayi

The kinetoplastids are an important group of protozoa from the Excavata supergroup, and cause numerous diseases with wide environmental, economic and ecological impact. Trypanosome brucei, the causative agent of human African trypanosomiasis, expresses a dense variant surface glycoprotein (VSG) coat, facilitating immune evasion via rapid switching and antigenic variation. Coupled to VSG switching is efficient clathrin-mediated endocytosis (CME), which removes anti-VSG antibody from the parasite surface. While the precise molecular basis for an extreme CME flux is unknown, genes encoding the AP2 complex, central to CME in most organisms, are absent from T. brucei, suggesting a mechanistic divergence in trypanosome CME. Here we identify the AP complex gene cohorts of all available kinetoplastid genomes and a new Trypanosome grayi genome. We find multiple secondary losses of AP complexes, but that loss of AP2 is restricted to T. brucei and closest relatives. Further, loss of AP2 correlates precisely with the presence of VSG genes, supporting a model whereby these two adaptations may function synergistically in immune evasion.

• 出版日期2013-4