Dar J S, Ganai B A, Shahardar R A, Zargar U R
Centre of Research for Development, University of Kashmir, Srinagar, 190 006 India.
Department of Veterinary Parasitology, SKUAST, Kashmir, 190 006 India.
Helminthologia. 2019 Jun 1;56(2):93-107. doi: 10.2478/helm-2019-0003. eCollection 2019 Jun.
The control of the digenetic trematode has been the major challenge in both cattle and small ruminants as there is a paucity of an effective and commercial vaccine. Thus, the accurate identification and prepatent diagnosis of is an essential prerequisite for its successful prevention and control. In the present study, the morphologically identified specimens isolated from the liver and bile ducts of sheep () were validated through molecular data. The sequence analysis of ITS2 of our isolates showed high degree of similarity with and using BLAST function of NCBI. The phylogenetic analysis of our isolates showed a close relationship with previously described and isolates from different countries. The antigenic profile of somatic and E/S antigens of were revealed by SDS-PAGE and immunoblotting using sera from sheep naturally infected with . By SDS-PAGE, 20 distinct bands were revealed from crude somatic fraction. Immunoblotting analysis of these proteins with positive sera exhibited 8 sero-reactive bands ranging from 14 to 97 kDa. Among these 38 and 44 kDa bands were quite specific with high diagnostic specificity and sensitivity. The E/S fraction comprised 7 distinct bands, as revealed by SDS-PAGE analysis. Immunoblotting analysis of these proteins with positive sera exhibited 6 antigenic bands ranging from 23 - 54 kDa. Among these 27 and 33 kDa were found to be quite specific with high diagnostic specificity and sensitivity. The present study concludes that the protein bands of 38 and 44 kDa in somatic fraction and 27 and 33 kDa in E/S fraction can be used for the immunodiagnostic purpose for this economically important parasite, which may also entice further studies regarding their vaccine potential.
由于缺乏有效的商业疫苗,双殖吸虫的防控一直是牛和小型反刍动物面临的主要挑战。因此,准确识别和进行虫体感染前期诊断是成功预防和控制该病的必要前提。在本研究中,通过分子数据对从绵羊肝脏和胆管中分离出的经形态学鉴定的标本进行了验证。利用NCBI的BLAST功能对我们分离株的ITS2序列分析表明,其与[具体物种1]和[具体物种2]具有高度相似性。我们分离株的系统发育分析显示,与先前描述的来自不同国家的[具体物种3]和[具体物种4]分离株关系密切。通过SDS-PAGE和使用自然感染[具体吸虫名称]的绵羊血清进行免疫印迹,揭示了[具体吸虫名称]的体抗原和排泄分泌(E/S)抗原的抗原谱。通过SDS-PAGE,从粗体组分中显示出20条不同的条带。用阳性血清对这些蛋白质进行免疫印迹分析,显示出8条血清反应性条带,范围从14到97 kDa。其中,38 kDa和44 kDa的条带具有很高的诊断特异性和敏感性,相当特异。SDS-PAGE分析显示,E/S组分包含7条不同的条带。用阳性血清对这些蛋白质进行免疫印迹分析,显示出6条抗原条带,范围从23 - 54 kDa。其中,27 kDa和33 kDa的条带具有很高的诊断特异性和敏感性,相当特异。本研究得出结论,体组分中的38 kDa和44 kDa蛋白条带以及E/S组分中的27 kDa和33 kDa蛋白条带可用于这种具有重要经济意义的寄生虫的免疫诊断,这也可能吸引对其疫苗潜力的进一步研究。