Arias P, Cutillas C, Oliveros R, Guevara D C
Department of Microbiology and Parasitology, Faculty of Pharmacy, University of Sevilla, Spain.
Parasitol Res. 1999 Nov;85(11):884-6. doi: 10.1007/s004360050652.
The glucose-6-phosphate dehydrogenase (G6PD, EC.1.1.1.49), glucose phosphate isomerase (GPI, EC.5.3.1.9), and malate dehydrogenase (MDH, EC.1.1.1.37) isoenzymatic patterns of Chabertia ovina were determined by starch-gel electrophoresis. The G6PD and GPI isoenzymatic patterns were characterized by the existence of three phenotypes: (1) a single and slow anodic band, (2) a single and fast anodic band, and (3) a large spot matching its migration with bands 1 and 2. These three phenotypes may be explained as the existence of only one gene locus for the G6PD and GPI in C. ovina. Allelic frequencies and the Hardy-Weinberg test were determined. This test indicated that the population was not in Hardy-Weinberg equilibrium. The MDH isoenzymatic pattern of C. ovina was characterized by the presence of two bands with anodic and cathodic migration. Furthermore, comparative isoenzyme studies were carried out between Oesophagostomum venulosum and C. ovina. The different G6PD, GPI, and MDH isoenzymatic patterns observed for the two species allowed us to distinguish them and, therefore, to use isoenzymatic patterns as a diagnostic tool to discriminate these species.
通过淀粉凝胶电泳测定了绵羊夏伯特线虫的葡萄糖-6-磷酸脱氢酶(G6PD,EC.1.1.1.49)、磷酸葡萄糖异构酶(GPI,EC.5.3.1.9)和苹果酸脱氢酶(MDH,EC.1.1.1.37)同工酶模式。G6PD和GPI同工酶模式的特征是存在三种表型:(1)一条单一且缓慢的阳极带,(2)一条单一且快速的阳极带,(3)一个大斑点,其迁移与带1和带2匹配。这三种表型可以解释为绵羊夏伯特线虫中G6PD和GPI仅存在一个基因位点。测定了等位基因频率并进行了哈迪-温伯格检验。该检验表明该群体不处于哈迪-温伯格平衡状态。绵羊夏伯特线虫的MDH同工酶模式的特征是存在两条具有阳极和阴极迁移的带。此外,还对微小食道口线虫和绵羊夏伯特线虫进行了同工酶比较研究。观察到的这两个物种不同的G6PD、GPI和MDH同工酶模式使我们能够区分它们,因此可以将同工酶模式用作鉴别这些物种的诊断工具。