Department of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, United States of America.
Department of Physiology and Biophysics, Weill Cornell Medical College, New York, New York, United States of America.
PLoS Biol. 2019 May 13;17(5):e3000271. doi: 10.1371/journal.pbio.3000271. eCollection 2019 May.
Malaria parasites possess the remarkable ability to maintain chronic infections that fail to elicit a protective immune response, characteristics that have stymied vaccine development and cause people living in endemic regions to remain at risk of malaria despite previous exposure to the disease. These traits stem from the tremendous antigenic diversity displayed by parasites circulating in the field. For Plasmodium falciparum, the most virulent of the human malaria parasites, this diversity is exemplified by the variant gene family called var, which encodes the major surface antigen displayed on infected red blood cells (RBCs). This gene family exhibits virtually limitless diversity when var gene repertoires from different parasite isolates are compared. Previous studies indicated that this remarkable genome plasticity results from extensive ectopic recombination between var genes during mitotic replication; however, the molecular mechanisms that direct this process to antigen-encoding loci while the rest of the genome remains relatively stable were not determined. Using targeted DNA double-strand breaks (DSBs) and long-read whole-genome sequencing, we show that a single break within an antigen-encoding region of the genome can result in a cascade of recombination events leading to the generation of multiple chimeric var genes, a process that can greatly accelerate the generation of diversity within this family. We also found that recombinations did not occur randomly, but rather high-probability, specific recombination products were observed repeatedly. These results provide a molecular basis for previously described structured rearrangements that drive diversification of this highly polymorphic gene family.
疟原虫具有维持慢性感染的非凡能力,而这种感染无法引发保护性免疫反应,这一特征阻碍了疫苗的开发,使生活在流行地区的人们尽管以前曾接触过这种疾病,但仍面临疟疾的风险。这些特征源于在野外循环的寄生虫表现出的巨大抗原多样性。对于恶性疟原虫,即最致命的人类疟疾寄生虫,这种多样性体现在一个名为 var 的变体基因家族中,该基因家族编码感染的红细胞(RBC)上主要的表面抗原。当比较不同寄生虫分离株的 var 基因库时,这个基因家族表现出几乎无限的多样性。以前的研究表明,这种显著的基因组可塑性是由于在有丝分裂复制过程中 var 基因之间广泛的异位重组所致;然而,指导这一过程到抗原编码基因座的分子机制,而基因组的其余部分保持相对稳定,尚未确定。通过靶向 DNA 双链断裂(DSBs)和长读长全基因组测序,我们表明基因组中一个抗原编码区域内的单个断裂可以导致一系列重组事件,从而产生多个嵌合 var 基因,这一过程可以极大地加速该家族内多样性的产生。我们还发现,重组不是随机发生的,而是观察到高概率的、特定的重组产物反复出现。这些结果为以前描述的结构重排提供了分子基础,这些重排驱动了这个高度多态性基因家族的多样化。