el-Bahi M M, Malone J B, Todd W J, Schnorr K L
Department of Veterinary Microbiology and Parasitology, School of Veterinary Medicine, Louisiana State University, Baton Rouge 70803.
Vet Parasitol. 1992 Dec;45(1-2):157-67. doi: 10.1016/0304-4017(92)90039-c.
Diagnostic antigens in bile and feces from Fasciola hepatica infected cattle were detected and characterized by enzyme-linked immunotransfer blot (EITB) techniques. As sources of antigen, samples of bile, intestinal contents and feces were collected from five uninfected calves and from 10 calves with known Fasciola hepatica burdens. A band detected by EITB using a densitometer in the area corresponding to 26 kDa reacted with rabbit anti-fresh fluke antigen and infected cattle sera but not with fluke-negative rabbit sera, rabbit anti-Fasciola hepatica egg sera, Fascioloides magna positive or negative cattle sera. This band was not detected by Coomassie blue in sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE) gels or by Ponceau-S stained nitrocellulose strips. Band groups located at 104-66, 66-42, 42-26 and 25-16 kDa reacted inconsistently with the above sera. Sera from mice hyperimmunized with Fasciola hepatica excretory-secretory (ES) products detected only the 26 kDa band by EITB, without cross-reactivity with bands in the other molecular weight (MW) ranges. The results suggest that the 26 kDa antigen may consist of a stable component of ES products and/or tegument-related worm antigen. Diagnosis of Fasciola hepatica through detection of specific, stable antigens in feces of infected animals offers potential advantages over serum-based tests of better sample accessibility, discrimination between previous and current infections, and possible semi-quantitation of fluke burdens.
采用酶联免疫转印印迹(EITB)技术检测并鉴定了感染肝片吸虫的牛胆汁和粪便中的诊断抗原。作为抗原来源,从5头未感染的小牛以及10头已知感染肝片吸虫的小牛中采集胆汁、肠内容物和粪便样本。通过EITB使用密度计在对应于26 kDa的区域检测到的一条带与兔抗新鲜吸虫抗原和感染牛血清发生反应,但与吸虫阴性兔血清、兔抗肝片吸虫卵血清、巨片形吸虫阳性或阴性牛血清不发生反应。在十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)凝胶中用考马斯亮蓝或用丽春红S染色的硝酸纤维素膜条均未检测到这条带。位于104 - 66、66 - 42、42 - 26和25 - 16 kDa的带组与上述血清反应不一致。用肝片吸虫排泄-分泌(ES)产物进行超免疫的小鼠血清通过EITB仅检测到26 kDa的带,与其他分子量(MW)范围内的带无交叉反应。结果表明,26 kDa抗原可能由ES产物的稳定成分和/或与体表相关的蠕虫抗原组成。通过检测感染动物粪便中的特异性、稳定抗原诊断肝片吸虫,与基于血清的检测相比具有潜在优势,如样本获取更容易、能区分既往感染和当前感染以及可能对吸虫负荷进行半定量。