Marcello Lucio, Barry J David
Wellcome Centre for Molecular Parasitology, University of Glasgow, Glasgow Biomedical Research Centre, 120 University Place, Glasgow G12 8TA, UK.
J Eukaryot Microbiol. 2007 Jan-Feb;54(1):14-7. doi: 10.1111/j.1550-7408.2006.00227.x.
African trypanosomes evade humoral immunity through antigenic variation whereby, they switch expression of the variant surface glycoprotein (VSG) gene encoding their glycoprotein surface coat. Switching proceeds by duplication from an archive of silent VSG genes into a transcriptionally active locus, and precedent suggests silent genes can contribute, combinatorially to formation of expressed, functional genes through segmental gene conversion. The genome project has revealed that most of the silent archive consists of hundreds of VSG genes in subtelomeric tandem arrays, and that most of these are not functional genes. The aim of this review is to explore links between the uncovered trypanosome genotype and the phenotype of antigenic variation, stretching from the broad phenotype-transmission in the field and the overcoming of herd immunity-to events within single infections. Highlighting in particular the possible impact of phenotype selection on the evolution of the VSG archive and the mechanisms for its expression leads to a theoretical framework to further our understanding of this complex immune evasion strategy.
非洲锥虫通过抗原变异逃避体液免疫,在此过程中,它们会切换编码其糖蛋白表面 coat 的可变表面糖蛋白(VSG)基因的表达。切换过程是通过将沉默 VSG 基因库中的基因复制到转录活性位点来进行的,并且先前的研究表明,沉默基因可以通过片段基因转换组合地对表达的功能性基因的形成做出贡献。基因组计划已经揭示,大多数沉默基因库由数百个位于亚端粒串联阵列中的 VSG 基因组成,并且其中大多数不是功能性基因。本综述的目的是探索已揭示的锥虫基因型与抗原变异表型之间的联系,从广泛的表型——在野外的传播以及对群体免疫的克服——到单次感染中的事件。特别强调表型选择对 VSG 基因库进化的可能影响及其表达机制,从而形成一个理论框架,以加深我们对这种复杂免疫逃避策略的理解。