A novel double recognition enzyme-linked immunosorbent assay based on the nucleocapsid protein for early detection of European porcine reproductive and respiratory syndrome virus infection

被引:22
|
作者
Venteo, A. [1 ]
Rebollo, B. [1 ]
Sarraseca, J. [1 ]
Rodriguez, M. J. [1 ]
Sanz, A. [1 ]
机构
[1] Inmunol & Genet Aplicada SA INGENASA, Madrid 28037, Spain
关键词
Double recognition enzyme-linked immunosorbent assay; PRRSV; Nucleocapsid protein; Early detection; IgM; SYNDROME PRRS VIRUS; ANTIBODY-RESPONSE; IMMUNE-RESPONSES; UNITED-STATES; DIFFERENTIATION; ELISA; VALIDATION; POLYMERASE; ANTIGEN; PIGS;
D O I
10.1016/j.jviromet.2012.01.024
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Precise and rapid detection of porcine reproductive respiratory syndrome virus (PRRSV) infection in swine farms is critical. Improvement of control procedures, such as testing incoming gilt and surveillance of seronegative herds requires more rapid and sensitive methods. However, standard serological techniques detect mainly IgG antibodies. A double recognition enzyme-linked immunosorbent assay (DR-ELISA) was developed for detection of antibodies specific to European PRRSV. This new assay can recognize both IgM and IgG antibodies to PRSSV which might be useful for detecting in routine surveillance assays pigs that are in the very early stages of infection and missed by conventional assays detecting only IgG antibodies. DR-ELISA is based on the double recognition of antigen by antibody. In this study, the recombinant nucleocapsid protein (N) of PRRSV was used both as the coating and the enzyme-conjugated antigen. To evaluate the sensitivity of the assay at early stages of the infection, sera from 69 pigs infected with PRRSV were collected during successive days post infection (pi) and tested. While standard methods showed low sensitivity rates before day 14 pi, DR-ELISA detected 88.4% seropositive samples at day 7 showing greater sensitivity at early stages of the infection. Further studies were carried out to assess the efficiency of the new assay, and the results showed DR-ELISA to be a sensitive and accurate method for early diagnosis of EU-PRRSV infection. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 113
页数:5
相关论文
共 50 条
  • [1] Development of recombinant nucleocapsid protein-based indirect enzyme-linked immunosorbent assay for sero-survey of porcine reproductive and respiratory syndrome
    Kashyap, S. Phani
    Hiremath, Jagadish
    Vinutha, S.
    Patil, Sharanagouda S.
    Suresh, Kuralayanapalya P.
    Roy, Parimal
    Hemadri, Divakar
    VETERINARY WORLD, 2020, 13 (12) : 2587 - 2595
  • [2] Multivalent nanobody-based sandwich enzyme-linked immunosorbent assay for sensitive detection of porcine reproductive and respiratory syndrome virus
    Sun, Mingxia
    Sun, Yue
    Yang, Yongbo
    Zhao, Man
    Cao, Dan
    Zhang, Minmin
    Xia, Dasong
    Wang, Tao
    Gao, Yanfei
    Wang, Shanghui
    Wang, Haiwei
    Cai, Xuehui
    An, Tongqing
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2024, 258
  • [3] Development of CD163 receptor-based enzyme-linked immunosorbent assay for diagnosis of porcine reproductive and respiratory syndrome virus
    Deb, Rajib
    Yadav, Ajay Kumar
    Sengar, Gyanendra Singh
    Sonowal, Joyshikh
    Lalita, D.
    Pegu, Seema Rani
    Singh, Indra
    Linda, Ningthoukhongjam
    Das, Pranab Jyoti
    Kumar, Satish
    Pal, Prasanna
    Paul, Souvik
    Rajkhowa, Swaraj
    Gupta, Vivek Kumar
    3 BIOTECH, 2022, 12 (11)
  • [4] Detection of antibodies against porcine reproductive and respiratory syndrome (PRRS) virus in swine sera by enzyme-linked immunosorbent assay
    Takikawa, N
    Kobayashi, S
    Ide, S
    Yamane, Y
    Tanaka, Y
    Yamagishi, H
    JOURNAL OF VETERINARY MEDICAL SCIENCE, 1996, 58 (04) : 355 - 357
  • [5] Development and application of a blocking enzyme-linked immunosorbent assay (ELISA) to differentiate antibodies against live and inactivated porcine reproductive and respiratory syndrome virus
    Cong, Yanlong
    Huang, Zhiqiang
    Sun, Yixue
    Ran, Wei
    Zhu, Lisai
    Yang, Guilian
    Ding, Xuemei
    Yang, Zhanqing
    Huang, Xiao
    Wang, Chunfeng
    Ding, Zhuang
    VIROLOGY, 2013, 444 (1-2) : 310 - 316
  • [6] Development of CD163 receptor-based enzyme-linked immunosorbent assay for diagnosis of porcine reproductive and respiratory syndrome virus
    Rajib Deb
    Ajay Kumar Yadav
    Gyanendra Singh Sengar
    Joyshikh Sonowal
    D. Lalita
    Seema Rani Pegu
    Indra Singh
    Ningthoukhongjam Linda
    Pranab Jyoti Das
    Satish Kumar
    Prasanna Pal
    Souvik Paul
    Swaraj Rajkhowa
    Vivek Kumar Gupta
    3 Biotech, 2022, 12
  • [7] Comparison of commercial enzyme-linked immunosorbent assays and fluorescent microbead immunoassays for detection of antibodies against porcine reproductive and respiratory syndrome virus in boars
    Gerber, Priscilla F.
    Gimenez-Lirola, Luis G.
    Halbur, Patrick G.
    Zhou, Lei
    Meng, Xiang-Jin
    Opriessnig, Tanja
    JOURNAL OF VIROLOGICAL METHODS, 2014, 197 : 63 - 66
  • [8] Comparison of two commercial enzyme-linked immunosorbent assays for the diagnosis of Porcine reproductive and respiratory syndrome virus infection
    Diaz, Ivan
    Venteo, Angel
    Rebollo, Belen
    Martin-Valls, Gerard E.
    Simon-Grife, Meritxell
    Sanz, Antonio
    Mateu, Enric
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2012, 24 (02) : 344 - 348
  • [9] AN ENZYME-LINKED-IMMUNOSORBENT-ASSAY (ELISA) FOR THE DETECTION OF ANTIBODIES TO THE PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME (PRRS) VIRUS
    ALBINA, E
    LEFORBAN, Y
    BARON, T
    DURAN, JP
    VANNIER, P
    ANNALES DE RECHERCHES VETERINAIRES, 1992, 23 (02): : 167 - 176
  • [10] A recombinant nucleocapsid protein-based indirect enzyme-linked immunosorbent assay to detect antibodies against porcine deltacoronavirus
    Su, Mingjun
    Li, Chunqiu
    Guo, Donghua
    Wei, Shan
    Wang, Xinyu
    Geng, Yufei
    Yao, Shuang
    Gao, Jing
    Wang, Enyu
    Zhao, Xiwen
    Wang, Zhihui
    Wang, Jianfa
    Wu, Rui
    Feng, Li
    Sun, Dongbo
    JOURNAL OF VETERINARY MEDICAL SCIENCE, 2016, 78 (04) : 601 - 606