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Recombinant protein-based ELISA for detection and differentiation of antibodies against avian reovirus in vaccinated and non-vaccinated chickens

机译:基于重组蛋白的ELISA检测和区分接种和未接种鸡的禽呼肠孤病毒抗体

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摘要

Two nonstructural genes, sigma NS and P17, of avian reovirus (ARV) were cloned into the expression plasmid vector PGEX4T-1. Expressed proteins for sigma NS and P17 of avian reovirus were purified and used as antigens. Three indirect sigma NS enzyme-linked immunosorbent assays (ELISAs), sigma NS-ELISA, P17-ELISA and sigma NS-P17-ELISA were optimized and used as specific tests. Serum samples from reovirus-infected and vaccinated SPF chickens were tested with the three ELISAs and an agar gel precipitin (AGP) method. ELISAs specific for sigma NS, P17 and sigma NS-P17 were able to detect specific antibodies for avian reovirus in 88.9%, 61.1%, and 88.9% in infected samples, respectively, whereas the AGP detected 55.6% of the infected samples. The detection rates of ELISA specific antibodies for sigma NS, P17 and sigma NS-P17 on sera of vaccinated chickens were 6.7%, 0% and 6.7%. However, in comparison the AGP method detected 60.6% of antibodies in serum samples from vaccinated chickens. The results showed that the use of ELISAs specific for the nonstructural proteins might be able to distinguish between reovirus vaccinated and infected chickens. Further studies are in progress to validate these recombinant protein-based ELISAs under field conditions.
机译:将禽呼肠孤病毒(ARV)的两个非结构基因sigma NS和P17克隆到表达质粒载体PGEX4T-1中。纯化了针对禽呼肠孤病毒的σNS和P17的表达蛋白,并将其用作抗原。优化了三种间接sigma NS酶联免疫吸附测定(ELISA),sigma NS-ELISA,P17-ELISA和sigma NS-P17-ELISA。用三种ELISA和琼脂凝胶沉淀(AGP)方法测试了呼肠孤病毒感染和接种SPF鸡的血清样品。特异性针对sigma NS,P17和sigma NS-P17的ELISA能够在感染样品中分别检测出88.9%,61.1%和88.9%的禽呼肠孤病毒特异性抗体,而AGP检测到55.6%的感染样品。接种鸡的血清中针对sigma NS,P17和sigma NS-P17的ELISA特异性抗体的检出率为6.7%,0%和6.7%。然而,相比之下,AGP方法在接种鸡的血清样品中检测到60.6%的抗体。结果表明,使用针对非结构蛋白的特异性ELISA可能能够区分呼肠孤病毒疫苗和感染鸡。进一步的研究正在进行中,以在野外条件下验证这些基于重组蛋白的ELISA。

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