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首页> 外文期刊>Clinical and diagnostic laboratory immunology >Development of a Nucleoprotein-Based Enzyme-Linked Immunosorbent Assay Using a Synthetic Peptide Antigen for Detection of Avian Metapneumovirus Antibodies in Turkey Sera
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Development of a Nucleoprotein-Based Enzyme-Linked Immunosorbent Assay Using a Synthetic Peptide Antigen for Detection of Avian Metapneumovirus Antibodies in Turkey Sera

机译:发展基于核蛋白的酶联免疫吸附测定法,使用合成肽抗原检测土耳其血清中的禽偏肺病毒抗体。

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摘要

Avian metapneumoviruses (aMPV) cause an upper respiratory tract disease with low mortality but high morbidity, primarily in commercial turkeys, that can be exacerbated by secondary infections. There are three types of aMPV, of which type C is found only in the United States. The aMPV nucleoprotein (N) amino acid sequences of serotypes A, B, and C were aligned for comparative analysis. On the basis of the predicted antigenicity of consensus sequences, five aMPV-specific N peptides were synthesized for development of a peptide antigen enzyme-linked immunosorbent assay (aMPV N peptide-based ELISA) to detect aMPV-specific antibodies among turkeys. Sera from naturally and experimentally infected turkeys were used to demonstrate the presence of antibodies reactive to the chemically synthesized aMPV N peptides. Subsequently, aMPV N peptide 1, which had the sequence 10-DLSYKHAILKESQYTIKRDV-29, with variations at only three amino acids among aMPV serotypes, was evaluated as a universal aMPV ELISA antigen. Data obtained with the peptide-based ELISA correlated positively with total aMPV viral antigen-based ELISAs, and the peptide ELISA provided higher optical density readings. The results indicated that aMPV N peptide 1 can be used as a universal ELISA antigen to detect antibodies for all aMPV serotypes.
机译:禽亚肺炎病毒(aMPV)主要在商业火鸡中引起低死亡率但高发病率的上呼吸道疾病,继发感染可加剧该疾病。有三种类型的aMPV,其中C型仅在美国发现。对比血清型A,B和C的aMPV核蛋白(N)氨基酸序列进行比较分析。根据共有序列的预测抗原性,合成了五种aMPV特异性N肽,用于开发肽抗原酶联免疫吸附测定(基于aMPV N肽的ELISA),以检测火鸡中的aMPV特异性抗体。来自自然和实验感染的火鸡的血清用于证明存在与化学合成的aMPV N肽具有反应性的抗体。随后,将具有序列10-DLSYKHAILKESQYTIKRDV-29的aMPV N肽1,在aMPV血清型中仅三个氨基酸处变异,被评估为通用aMPV ELISA抗原。通过基于肽的ELISA获得的数据与基于总aMPV病毒抗原的ELISA呈正相关,并且基于肽ELISA的光密度读数更高。结果表明,aMPV N肽1可用作通用ELISA抗原来检测所有aMPV血清型的抗体。

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