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Specific antibody responses to West Nile virus infections in horses preimmunized with inactivated Japanese encephalitis vaccine: evaluation of blocking enzyme-linked immunosorbent assay and complement-dependent cytotoxicity assay.

机译:用灭活的日本脑炎疫苗预免疫的马对西尼罗河病毒感染的特异性抗体反应:评估封闭酶联免疫吸附测定和补体依赖性细胞毒性测定。

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West Nile virus (WNV) and Japanese encephalitis (JE) virus are distributed separately in the world with some exceptions. There is a concern that WNV may invade into Asia where JE virus exists. On and after such invasion, any differential diagnosis could be complicated by serological crossreactivities. We previously demonstrated experimentally using horses infected with WNV that preimmunization with inactivated JE vaccine considerably affected the ability of neutralization tests and immunoglobulin M (IgM) antibody-capture enzyme-linked immunosorbent assay (ELISA) to diagnose WNV infection. Here, we investigated WNV-specific antibody responses in vaccinated horses using a blocking ELISA and complement-dependent cytotoxicity (CDC) assay to evaluate these two newly developed serodiagnostic methods for WNV infection. Sera previously collected from six experimentally infected horses were used: Three were vaccinated before the infection, whereas the other three remained unvaccinated. WNV-specific antibody responses were successfully detected in the vaccinated and unvaccinated horses using both new methods, except for one vaccinated horse in which responses were not induced, probably as a result of crossprotection induced by JE vaccination. Specific antibody responses were at earliest detected from days 9 to 10 postinfection in the blocking ELISA, whereas the CDC assay provided earlier detection (at days 7-8) in all horses. The time courses of antibody levels were similar between vaccinated and unvaccinated horses in either method, indicating no notable effect of vaccination on detection of specific antibody responses, as far as antibodies were induced. These results indicated that blocking ELISA, but preferably the CDC assay, can be useful for detecting WNV infection in JE-vaccinated horses.
机译:西尼罗河病毒(WNV)和日本脑炎(JE)病毒在世界各地分别分发,但有一些例外。人们担心WNV可能会侵入存在JE病毒的亚洲。在这种侵袭中和侵袭之后,任何血清学交叉反应都可能使鉴别诊断变得复杂。我们之前通过实验证明,使用感染WNV的马匹,用灭活的JE疫苗进行预免疫会大大影响中和测试和免疫球蛋白M(IgM)抗体捕获酶联免疫吸附测定(ELISA)诊断WNV感染的能力。在这里,我们使用阻断ELISA和补体依赖性细胞毒性(CDC)分析方法调查了接种马匹中WNV特异性抗体的反应,以评估这两种新开发的WNV感染的血清学诊断方法。使用先前从六只经实验感染的马中收集的血清:三只在感染前进行了疫苗接种,而其他三只仍未进行疫苗接种。使用两种新方法都可以在接种和未接种的马匹中成功检测到WNV特异性抗体应答,除了其中一匹未诱导应答的接种马匹,这可能是由于JE疫苗接种引起的交叉保护。最早在封闭ELISA中从感染后第9天到第10天检测到特异性抗体反应,而CDC分析在所有马匹中提供了更早的检测(在7-8天)。在这两种方法中,接种和未接种的马之间抗体水平的时程相似,表明就诱导抗体而言,接种对特异性抗体应答的检测没有显着影响。这些结果表明,阻断ELISA(但最好是CDC分析)可用于检测接种JE的马匹中的WNV感染。

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