Evolution of Antigenic Variation in African Trypanosomes: Variant Surface Glycoprotein Expression, Structure, and Function

被引:30
|
作者
Bangs, James D. [1 ]
机构
[1] SUNY Buffalo, Jacobs Sch Med & Biomed Sci, Dept Microbiol & Immunol, 955 Main St, Buffalo, NY 14260 USA
关键词
African trypanosome; antigenic variation; gene conversion; protein folding; secretion; variant surface glycoprotein; GPI-ANCHORED PROTEINS; BLOOD-STREAM; GENE-EXPRESSION; INTRACELLULAR-TRANSPORT; BRUCEI; FORM; VSG; TRANSFERRIN; SPECIFICITY; PROCYCLIN;
D O I
10.1002/bies.201800181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The process of antigenic variation in parasitic African trypanosomes is a remarkable mechanism for outwitting the immune system of the mammalian host, but it requires a delicate balancing act for the monoallelic expression, folding and transport of a single variant surface glycoprotein (VSG). Only one of hundreds of VSG genes is expressed at time, and this from just one of approximate to 15 dedicated expression sites. By switching expression of VSGs the parasite presents a continuously shifting antigenic facade leading to prolonged chronic infections lasting months to years. The basics of VSG structure and switching have been known for several decades, but recent studies have brought higher resolution to many aspects this process. New VSG structures, in silico modeling of infections, studies of VSG codon usage, and experimental ablation of VSG expression provide insights that inform how this remarkable system may have evolved.
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页数:8
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