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Novel protein microarray for the detection of avian influenza virus antibodies and simultaneous distinction of antibodies against H5 and H7 subtypes

机译:用于检测禽流感病毒抗体的新型蛋白质微阵列以及对H5和H7亚型的同时区分抗体

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摘要

Avian influenza virus (AIV) can cause serious zoonotic disease, thereby threatening the poultry industry and human health. An efficient and rapid detection approach is crucial to prevent and control the spread of avian influenza. In this study, a novel protein microarray was developed. Haemagglutinin proteins of H5 and H7 subtypes and nucleoprotein (NP) were purified and spotted onto the initiator-integrated poly-(dimethylsiloxane) as antigens. Monoclonal antibodies with inhibition effect were screened and utilized for the synchronous detection of three avian influenza antibodies in different species. In the protein microarray, the cut-off values were 40%, 50% and 30% inhibition for H5 antibody detection; 50%, 50% and 20% for NP antibody detection; 40%, 50% and 40% for H7 antibody detection in chicken, peacock and duck sera, respectively. The 95 serum samples were detected by microarray, and results were compared with the findings of AIV antibody test enzyme-linked immunosorbent assay (ELISA) or haemagglutination inhibition (HI) test. NP antibody detection in the microarray showed 100% (55/55) agreement ratio in chicken using ELISA. Compared with HI, H5 antibody detection in the microarray showed 100% (95/95) agreement ratio in chicken, peacock and duck, whilst those of H7 displayed 98.18% (54/55) agreement in chicken, 100% (20/20) in peacock and 90% (18/20) in duck. In conclusion, this novel protein microarray is a high-throughput and specific method for the detection of AIV antibodies and simultaneous distinction of antibodies against H5 and H7 subtypes. It can be applied to the serological diagnosis and epidemiological investigation of AIV.
机译:禽流感病毒(AIV)可引起严重的动物疾病,从而威胁禽类工业和人类健康。一种有效和快速的检测方法对于预防和控制禽流感的传播至关重要。在该研究中,开发了一种新的蛋白质微阵列。纯化H5和H7亚型和核蛋白(NP)的Haemagglutinin蛋白并从抗原作为抗原的引发剂 - 整合的聚 - (二甲基硅氧烷)上。筛选抑制效果的单克隆抗体,并用于不同物种中的三个禽流感抗体的同步检测。在蛋白质微阵列中,对H5抗体检测的截止值为40%,50%和30%的抑制; NP抗体检测50%,50%和20%;分别为鸡,孔雀和鸭血清中H7抗体检测40%,50%和40%。通过微阵列检测到95个血清样品,并将结果与​​AIV抗体试验酶联免疫吸附测定(ELISA)或血凝凝集抑制(HI)试验进行比较。微阵列中的NP抗体检测显示使用ELISA的鸡肉中100%(55/55)的协议比。与HI,H5抗体检测在微阵列中显示出100%(95/95)的鸡,孔雀和鸭子协定比,而H7的H7展示98.18%(54/55)协议,100%(20/20)在孔雀和90%(18/20)的鸭子。总之,这种新的蛋白质微阵列是检测AIV抗体的高通量和特定方法,以及针对H5和H7亚型的抗体的同时区别。它可以应用于AIV的血清学诊断和流行病学调查。

著录项

  • 来源
    《Avian Pathology》 |2019年第6期|共9页
  • 作者单位

    Nanjing Agr Univ MOE Joint Int Res Lab Anim Hlth &

    Food Safety Jiangsu Engn Lab Anim Immunol Jiangsu Detect Ctr Terr Wildlife Dis Inst Immunol Nanjing Jiangsu Peoples R China;

    Nanjing Agr Univ MOE Joint Int Res Lab Anim Hlth &

    Food Safety Jiangsu Engn Lab Anim Immunol Jiangsu Detect Ctr Terr Wildlife Dis Inst Immunol Nanjing Jiangsu Peoples R China;

    Nanjing Agr Univ MOE Joint Int Res Lab Anim Hlth &

    Food Safety Jiangsu Engn Lab Anim Immunol Jiangsu Detect Ctr Terr Wildlife Dis Inst Immunol Nanjing Jiangsu Peoples R China;

    Nanjing Agr Univ MOE Joint Int Res Lab Anim Hlth &

    Food Safety Jiangsu Engn Lab Anim Immunol Jiangsu Detect Ctr Terr Wildlife Dis Inst Immunol Nanjing Jiangsu Peoples R China;

    Zhejiang Univ Key Lab Anim Virol Hangzhou Zhejiang Peoples R China;

    Zhejiang Univ Key Lab Anim Virol Hangzhou Zhejiang Peoples R China;

    Nanjing Agr Univ MOE Joint Int Res Lab Anim Hlth &

    Food Safety Jiangsu Engn Lab Anim Immunol Jiangsu Detect Ctr Terr Wildlife Dis Inst Immunol Nanjing Jiangsu Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学;
  • 关键词

    Protein microarray; antibody detection; AIV; H5; H7; NP;

    机译:蛋白质微阵列;抗体检测;AIV;H5;H7;NP;

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