al-Khedery B, Barnwell J W, Galinski M R
Department of Medical and Molecular Parasitology, New York University School of Medicine, New York 10010, USA.
Mol Cell. 1999 Feb;3(2):131-41. doi: 10.1016/s1097-2765(00)80304-4.
Antigenic variation of malaria parasites was discovered in P. knowlesi, using a schizont-infected cell agglutination (SICA) assay to detect variant antigens expressed at the surface of infected erythrocytes. Later studies utilizing stable clones, Pk1(A+) and its direct derivative, Pk1(B+)1+, showed that SICA[+] clones express distinct parasite-encoded antigens of approximately 200 kDa. Here we identify a P. knowlesi variant antigen gene and cDNA and demonstrate that it encodes the 205 kDa variant antigen expressed by B+ parasites. This gene belongs to a multigene family, which we term SICAvar. Its ten-exon structure with seven cysteine-rich coding modules is unique compared to P. falciparum var genes. Further, we highlight a 3' genomic alteration that we predict is related to SICAvar gene switching.
利用裂殖体感染细胞凝集(SICA)试验检测感染红细胞表面表达的变异抗原,在诺氏疟原虫中发现了疟原虫的抗原变异。后来利用稳定克隆Pk1(A+)及其直接衍生物Pk1(B+)1+进行的研究表明,SICA[+]克隆表达约200 kDa的独特寄生虫编码抗原。在此,我们鉴定出一个诺氏疟原虫变异抗原基因及其cDNA,并证明它编码由B+寄生虫表达的205 kDa变异抗原。该基因属于一个多基因家族,我们将其命名为SICAvar。与恶性疟原虫var基因相比,其具有七个富含半胱氨酸编码模块的十外显子结构是独特的。此外,我们强调了一个3'基因组改变,我们预测它与SICAvar基因转换有关。