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
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