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Recombinant Antigen Targets for Serodiagnosis of African Swine Fever

机译:重组抗原靶标对非洲猪瘟的血清学诊断

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摘要

African swine fever (ASF) is an infectious and economically important disease of domestic pigs. There is no vaccine, and so reliable diagnosis is essential for control strategies. The performance of four recombinant ASF virus (ASFV) protein (pK205R, pB602L, p104R, and p54)-based enzyme-linked immunosorbent assays (ELISAs) was evaluated with European porcine field sera that had been established by Office International des Epizooties (OIE)-approved tests to be ASFV negative (n = 119) and ASFV positive (n = 80). The κ values showed that there was almost perfect agreement between the results of the “gold standard” test (immunoblotting) and the results obtained by the p54-specific ELISA (κ = 0.95; 95% confidence interval [CI], 0.90 to 0.99) and the pK205R-specific ELISA or the pB602L-specific ELISA (κ = 0.92; 95% CI, 0.86 to 0.97). For the pA104R-specific ELISA, there was substantial to almost perfect agreement (κ = 0.81; 95% CI, 0.72 to 0.89). Similar results were observed by the OIE-approved ELISA (κ = 0.89; 95% CI, 0.82 to 0.95). Importantly, antibodies against these proteins were detectable early after infection of domestic pigs. Preliminary testing of 9 positive and 17 negative serum samples from pigs from West Africa showed identical results by the recombinant protein-based ELISA and the OIE-approved tests. In contrast, there was a high degree of specificity but a surprisingly a low level of sensitivity with 7 positive and 342 negative serum samples from pigs from East Africa. With poorly preserved sera, only the p104R-specific ELISA showed a significant reduction in sensitivity compared to that of the OIE-approved ELISA. Finally, these recombinant proteins also detected antibodies in the sera of the majority of infected warthogs. Thus, recombinant ASFV proteins p54, pB602L, and pK205R provide sensitive and specific targets for the detection of antibodies in European and West African domestic pigs and warthogs.
机译:非洲猪瘟(ASF)是家猪的一种传染性和经济上重要的疾病。没有疫苗,因此可靠的诊断对于控制策略至关重要。使用由Office International des Epizooties(OIE)建立的欧洲猪场血清评估了四种基于重组ASF病毒(ASFV)蛋白(pK205R,pB602L,p104R和p54)的酶联免疫吸附测定(ELISA)的性能批准的测试为ASFV阴性(n = 119)和ASFV阳性(n = 80)。 κ值表明“金标准”测试(免疫印迹)的结果与通过p54特异性ELISA获得的结果几乎完全吻合(κ= 0.95; 95%置信区间[CI],0.90至0.99)以及pK205R特异性ELISA或pB602L特异性ELISA(κ= 0.92; 95%CI,0.86至0.97)。对于pA104R特异性ELISA,基本一致或几乎完全一致(κ= 0.81; 95%CI,0.72至0.89)。通过OIE批准的ELISA观察到相似的结果(κ= 0.89; 95%CI,0.82至0.95)。重要的是,在家猪感染后早期就可以检测到针对这些蛋白质的抗体。通过基于蛋白质的重组ELISA和OIE批准的测试,对来自西非猪的9份阳性和17份阴性血清样品的初步测试显示了相同的结果。相反,来自东非猪的7份阳性和342份阴性血清样品具有很高的特异性,但出乎意料的低灵敏度。与保存较差的血清相比,只有p104R特异性ELISA与OIE批准的ELISA相比灵敏度显着降低。最后,这些重组蛋白还在大多数被感染的疣猪的血清中检测到抗体。因此,重组ASFV蛋白p54,pB602L和pK205R为检测欧洲和西非家养猪和疣猪中的抗体提供了灵敏而特异性的靶标。

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