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A 2.9 kDa Fasciola hepatica-recombinant protein based ELISA test for the detection of current-ovine fasciolosis trickle infected

机译:基于2.9 kDa的Fasciola肝重组蛋白的ELISA试验,用于检测当前绵羊的fasciolosis trick流感染

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The suitability of an enzyme linked immunosorbent assay (ELISA) test with a 2.9 kDa Fasciola hepatica-recombinant protein (FhrAPS) for diagnosing early and current-ovine fasciolosis was analyzed, and compared to that obtained by using a direct ELISA for detecting F. hepatica-circulating FhES antigens and to the coprological sedimentation for fluke egg quantitation. Fourteen Gallega autochthonous breed sheep were experimentally infected with metacercariae by a trickle system (small repetitive infections) and divided into two groups: G-I represented a primary infection for 34 weeks; G-R, animals with primary infection and reinfected 18 w.a.p.i. Seven sheep were left uninfected as the control group (G-C). Serum IgG antibody values against the FhrAPS rose rapidly by 1st w.a.p.i. in all infected sheep. Antibody levels in those with primary infection (G-I, G-C) peaked at 10 weeks, diminishing slightly and levelling from 16 to 34 weeks. Those with primary infection reinfected at 18 weeks had a rebound effect with the highest values observed. Circulating F. hepatica-ES antigens were detected by the 1st w.a.p.i. in all infected groups peaking at 6 weeks, decreasing rapidly to uninfected control values by 10 weeks of infection. Faecal egg-output started 11 weeks after primary infection. An increase in the IgG antibody as well as antigen responses to the FhrAPS and to anti-FhES from the 18 w.a.p.i. was recorded in G-T and G-R after the challenge infection. Antibody levels remained high whereas antigenemia values diminished after 6 weeks. A positive significant correlation between the IgG response against the FhrAPS and the F. hepatica circulating antigens (r2 = 0.428, p = 0.001) was obtained. In conclusion, our standardized diagnostic ELISA for fasciolosis based on the detection of IgG responses to the FhrAPS would be a valuable tool to diagnosis early and current F. hepatica-infections in sheep.
机译:分析了使用2.9 kDa肝片Fasciola重组蛋白(FhrAPS)进行的酶联免疫吸附测定(ELISA)试验对早期和当前绵羊筋膜炎的诊断的适用性,并将其与使用直接ELISA法检测肝炎性肝炎的结果进行了比较。循环FhES抗原,并通过菌落沉淀进行for卵定量。用trick流系统实验性地将14只Gallega本地种羊用meta虫感染(小重复性感染),分为两组:G-I代表原发感染持续34周。 G-R,原发感染动物,经18 w.a.p.i再感染。留下七只未感染的绵羊作为对照组(G-C)。第一次w.a.p.i时,针对FhrAPS的血清IgG抗体值迅速上升。在所有被感染的绵羊中初次感染者(G-1,G-C)的抗体水平在第10周达到峰值,略有下降,从16周降至34周。那些在18周被再次感染的原发感染者具有反弹作用,观察到的数值最高。第1次w.a.p.i检测到了循环中的F.hepatica-ES抗原。在所有感染组中,所有感染组在6周时达到峰值,感染10周后迅速降至未感染对照值。初次感染后11周开始排卵。从18 w.a.p.i开始,IgG抗体的增加以及对FhrAPS和抗FhES的抗原反应。感染后在G-T和G-R中记录了T.抗体水平仍然很高,而6周后抗原血症值却降低了。获得的针对FhrAPS的IgG应答与肝炎链球菌循环抗原之间存在正相关(r2 = 0.428,p = 0.001)。总之,基于对FhrAPS的IgG反应的检测,我们针对筋膜病的标准化诊断ELISA将成为诊断绵羊早期和当前感染肝炎性肝炎的有价值的工具。

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