Development and validation of a foot-and-mouth disease virus SAT serotype-specific 3ABC assay to differentiate infected from vaccinated animals

被引:8
|
作者
Chitray, M. [1 ,2 ]
Grazioli, S. [3 ]
Willems, T. [4 ]
Tshabalala, T. [1 ]
De Vleeschauwer, A. [4 ]
Esterhuysen, J. J. [1 ]
Brocchi, E. [3 ]
De Clercq, K. [4 ]
Maree, F. F. [1 ,2 ]
机构
[1] Agr Res Council, Transboundary Anim Dis, Onderstepoort Vet Inst, Private Bag X05, ZA-0110 Onderstepoort, South Africa
[2] Univ Pretoria, Fac Agr & Nat Sci, Dept Microbiol & Plant Pathol, ZA-0002 Pretoria, South Africa
[3] IZSLER, Via Bianchi 7-9, I-25124 Brescia, Italy
[4] CODA CERVA VAR, Unit Vesicular & Exot Dis, Dept Virol, Groeselenberg 99, B-1180 Uccle, Belgium
关键词
FMD; ELISA; NSP; SAT; 3ABC; BUFFALO SYNCERUS CAFFER; NONSTRUCTURAL PROTEINS; CATTLE; ANTIBODIES; ELISA; RECOMBINANT; CONFIDENCE; AREA;
D O I
10.1016/j.jviromet.2018.02.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The effective control of foot-and-mouth disease (FMD) requires sensitive, specific and rapid diagnostic tools. However, the control and eradication of FMD in Africa is complicated by, among other factors, the existence of five of the seven FMD virus (FMDV) serotypes, including the SAT-serotypes 1, 2 and 3 that are genetically and antigenically the most variable FMDV serotypes. A key diagnostic assay to enable a country to re-gain its FMD-free status and for FMD surveillance, is the 3ABC or the non-structural protein (NSP) enzyme-linked immunosorbent assay (ELISA). Although many kits are available to detect 3ABC antibodies, none has been developed specifically for the variable SAT serotypes. This study designed a SAT-specific NSP ELISA and determined whether this assay could better detect NSP-specific antibodies from FMDV SAT-infected livestock. The assay's performance was compared to validated NSP assays (PrioCheck (R)-NSP and IZSLER-NSP), using panels of field and experimental sera, vaccinated and/or infected with FMDV SAT1, SAT2 or SAT3. The sensitivity () of the SAT-NSP was estimated as 76% (70%, 81%) whereas the specificity was 96% (95%, 98%) at a 95% confidence interval. The sensitivity and specificity were comparable to the commercial NSP assays, PrioCheck (R)-NSP (82% and 99%, respectively) and IZSLER-NSP (78% and 98%, respectively). Good correlations were observed for all three assays.
引用
收藏
页码:44 / 51
页数:8
相关论文
共 48 条
  • [41] Use of the recombinant nonstructural 3A, 3B, and 3AB proteins of foot-and-mouth disease virus in indirect ELISA for differentiation of vaccinated and infected cattle
    Yakovleva A.S.
    Shcherbakov A.V.
    Kan'shina A.V.
    Mudrak N.S.
    Fomina T.A.
    Molecular Biology, 2006, 40 (1) : 146 - 151
  • [42] Development of Foot-and-Mouth Disease Virus-Neutralizing Monoclonal Antibodies Derived From Plasmablasts of Infected Cattle and Their Germline Gene Usage
    Li, Kun
    Wang, Sheng
    Cao, Yimei
    Bao, Huifang
    Li, Pinghua
    Sun, Pu
    Bai, Xingwen
    Fu, Yuanfang
    Ma, Xueqing
    Zhang, Jing
    Li, Dong
    Chen, Yingli
    Liu, Xuerong
    An, Fanglan
    Wu, Faju
    Lu, Zengjun
    Liu, Zaixin
    FRONTIERS IN IMMUNOLOGY, 2019, 10
  • [43] Development of a Competitive Enzyme-Linked Immunosorbent Assay for Detection of Antibodies against the 3B Protein of Foot-and-Mouth Disease Virus
    Yang, Ming
    Parida, Satya
    Salo, Tim
    Hole, Kate
    Velazquez-Salinas, Lauro
    Clavijo, Alfonso
    CLINICAL AND VACCINE IMMUNOLOGY, 2015, 22 (04) : 389 - 397
  • [44] Implication of Broadly Neutralizing Bovine Monoclonal Antibodies in the Development of an Enzyme-Linked Immunosorbent Assay for Detecting Neutralizing Antibodies against Foot-and-Mouth Disease Virus Serotype O
    Cao, Yimei
    Li, Kun
    Wang, Sheng
    Fu, Yuanfang
    Sun, Pu
    Li, Pinghua
    Bai, Xingwen
    Zhang, Jing
    Ma, Xueqing
    Xing, Xiangchuan
    Zhou, Shasha
    Bao, Huifang
    Li, Dong
    Chen, Yingli
    Li, Zhiyong
    Lu, Zengjun
    Liu, Zaixin
    JOURNAL OF CLINICAL MICROBIOLOGY, 2019, 57 (12)
  • [45] Recombinant non-structural 3A, 3B and 3AB proteins of foot-and-mouth disease virus: Use in indirect ELISA for differentiation of vaccinated and infected cattle
    Yakovleva, AS
    Shcherbakov, AV
    Kanshina, AV
    Mudrak, NS
    Fomina, TA
    MOLECULAR BIOLOGY, 2006, 40 (01) : 165 - 171
  • [46] Development of Foot-and-Mouth Disease Virus-Neutralizing Monoclonal Antibodies Derived From Plasmablasts of Infected Cattle and Their Germline Gene Usage (vol 10, 2870, 2019)
    Li, Kun
    Wang, Sheng
    Cao, Yimei
    Bao, Huifang
    Li, Pinghua
    Sun, Pu
    Bai, Xingwen
    Fu, Yuanfang
    Ma, Xueqing
    Zhang, Jing
    Li, Dong
    Chen, Yingli
    Liu, Xuerong
    An, Fanglan
    Wu, Faju
    Lu, Zengjun
    Liu, Zaixin
    FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [47] Availability of a fetal goat tongue cell line ZZ-R 127 for isolation of Foot-and-mouth disease virus (FMDV) from clinical samples collected from animals experimentally infected with FMDV
    Fukai, Katsuhiko
    Onozato, Hiroyuki
    Kitano, Rie
    Yamazoe, Reiko
    Morioka, Kazuki
    Yamada, Manabu
    Ohashi, Seiichi
    Yoshida, Kazuo
    Kanno, Toru
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2013, 25 (06) : 770 - 774
  • [48] Further development of a reverse-transcription loop-mediated isothermal amplification (RT-LAMP) assay for the detection of foot-and-mouth disease virus and validation in the field with use of an internal positive control
    Bath, Carolyn
    Scott, Megan
    Sharma, Puspa Maya
    Gurung, Ratna B.
    Phuentshok, Yoenten
    Pefanis, Stephen
    Colling, Axel
    Singanallur Balasubramanian, Nagendrakumar
    Firestone, Simon M.
    Ungvanijban, Sahawatchara
    Ratthanophart, Jadsada
    Allen, John
    Rawlin, Grant
    Fegan, Mark
    Rodoni, Brendan
    TRANSBOUNDARY AND EMERGING DISEASES, 2020, 67 (06) : 2494 - 2506