Arora Ritu, Singh N K, Juyal P D, Ghosh S
J Parasit Dis. 2010 Apr;34(1):57-61. doi: 10.1007/s12639-010-0011-6. Epub 2010 Oct 8.
Polypeptide profile of somatic antigen of Paramphistomum epiclitum (PSAg) and Gastrothylax crumenifer (GSAg) was studied by SDS-PAGE. PSAg and GSAg showed 14 and 19 polypeptides in the range of 14.9-95.5 and 13.7-129.6 kDa with six common polypeptides of mol wt 16.8, 21.8, 23.7, 35.5, 43.4 and 70.8 kDa. P. epiclitum experimentally infected sheep sera were used for identification of specific immuno-dominant peptide in the range of 37-40 kDa against P. epiclitum by western blotting. Hyperimmune sera (HIS) was raised in rabbit against the identified polypeptide, IgG was separated from HIS and an immunoaffinity column was constructed with a binding percentage of 83.74 of IgG with CNBr activated Sepharose 4B. Purification of somatic antigen (PSAg) was done with immunoaffinity chromatography and 37-40 kDa protein antigen was isolated in pure form with recovery percentage of 2.97%. This purified fraction of somatic antigen can be used as a candidate antigen for development of serological assay for early diagnosis of paramphistomosis among livestock.
采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)对前后盘吸虫(PSAg)和皱襞腹袋吸虫(GSAg)的体抗原多肽图谱进行了研究。PSAg和GSAg分别显示出14条和19条多肽,分子量范围为14.9 - 95.5 kDa和13.7 - 129.6 kDa,其中有6条共同多肽,分子量分别为16.8、21.8、23.7、35.5、43.4和70.8 kDa。利用实验感染前后盘吸虫的绵羊血清,通过蛋白质印迹法鉴定出针对前后盘吸虫的37 - 40 kDa范围内的特异性免疫显性肽。用该鉴定出的多肽对家兔进行免疫,制备了超免疫血清(HIS),从HIS中分离出IgG,并构建了免疫亲和柱,IgG与溴化氰活化的琼脂糖4B的结合率为83.74%。采用免疫亲和层析法对体抗原(PSAg)进行纯化,以2.97%的回收率分离出了纯的37 - 40 kDa蛋白抗原。这种纯化的体抗原组分可作为候选抗原,用于开发家畜前后盘吸虫病早期诊断的血清学检测方法。