首页> 外文期刊>Indian Journal of Animal Research >Immunodiagnostic potency of homologous antigens for natural Haemonchus contortus infection in small ruminants in plate and paper enzyme linked immunosorbent assay
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Immunodiagnostic potency of homologous antigens for natural Haemonchus contortus infection in small ruminants in plate and paper enzyme linked immunosorbent assay

机译:单层抗原的免疫因抗原免疫抗原在板材和纸酶中小反刍动物中的感染促进免疫吸附测定

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The objective of this study was to characterize Haemonchus contortus antigens, and to standardize and evaluate indirect plate and dot-ELISA using homologous antigens in the small ruminants. Electrophoretic separation of somatic antigen in reducing condition on 15% polyacrylamide gel resolved into 16 proteins of molecular weight ranging from 14-100 kDa. Two step ethanolic extraction of the supernatant of in-vitro culture of H. contortus yielded excretory-secretory (E-S) antigen/cathepsin L cysteine proteinase of molecular weight 28 kDa. The animals (Goats=103; Sheep=91) were broadly kept into post-mortem (PM) and faecal examined groups and further sub-grouped based on mono or multiply helminths infection. At many occasion, the somatic antigen found to cross reacts with other helminths parasites thus minimizing the specificity of the selected tests and antigens. There was no any direct correlation between the parasites load and ELISA reactivity pattern. The prevalence rate of haemonchosis was 55.7 (34/61) in goats/ 47.6 (40/84) % in sheep as per PM examination while it was 45.63 (47/103) in goats/ 41.76% (38/91) in sheep and 36.89 (38/103) in goats/ 35.16% (32/91) in sheep using E-S antigen based plate and dot-ELISA, respectively. With E-S antigen, the overall % sensitivity, specificity, positive and negative predictive values of plate-ELISA was 89.74 (goats)/ 80.95 (sheep), 81.25 (goats)/ 91.84 (sheep), 74.47 (goats)/ 89.47 (sheep), 92.86 (goats)/ 84.91 (sheep), respectively while for dot-ELISA it was 66.67 (goats)/ 61.9 (sheep), 81.25 (goats)/ 87.76 (sheep), 68.42 (goats)/ 81.25 (sheep), 80 (goats)/ 72.88 (sheep), respectively, so the tests and E-S antigen can be recommended for the detection haemonchosis in the small ruminants.
机译:本研究的目的是表征Haemonchus intortus抗原,并在小反刍动物中使用同源抗原标准化和评估间接板和DOT-ELISA。在15%聚丙烯酰胺凝胶中降低条件下细胞抗原的电泳分离成16-100kDa分子量的16蛋白。两步乙醇萃取对体外培养物的上清液的上清液产生排泄 - 分泌(E-S)抗原/组织蛋白酶L分子量28kDa的半胱氨酸蛋白酶。将动物(山羊= 103;绵羊= 91)大致被广泛地预留在后验尸(PM)和粪便检测的基团中,并进一步基于单体或乘法蠕虫感染进行分组。在许多场合中,发现与其他Helminths寄生虫相交的体细胞抗原,从而最小化所选测试和抗原的特异性。寄生虫载荷与ELISA反应性模式之间没有任何直接相关性。每PM检查羊皮中羊皮病的患病率为55.7(34/61)羊肉/ 47.6(40/84)%,而羊皮的山羊/ 41.76%(38/91)是45.63(47/103) 36.89(38/103)分别使用ES抗原的板和DOT-ELISA在羊羊/ 35.16%(32/91)中。具有ES抗原的敏感性,特异性,特异性,模板,阳性和消极预测值的总体敏感性,特异性,正负预测值为89.74(山羊)/ 80.95(绵羊),81.25(山羊)/ 91.84(羊),74.47(山羊)/ 89.47(羊) ,92.86(山羊)/ 84.91(绵羊)分别为DOT-ELISA,它为66.67(山羊)/ 61.9(羊),81.25(山羊)/ 87.76(羊),68.42(山羊)/ 81.25(绵羊),80 (山羊)/ 72.88(绵羊)分别,因此可以推荐测试和ES抗原用于在小反刍动物中检测Haemonchosis。

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