Indirect ELISA (iELISA) standardization for the diagnosis of bovine enzootic leucosis

被引:0
作者
Resende, Claudia F. [1 ]
Galinari, Grazielle C. F. [1 ]
Victor, Raphael M. [2 ]
Kassar, Telissa C. [1 ]
Arcebispo, Thiago L. M. [3 ]
Delarmelina, Emilia [1 ]
Leite, Romulo C. [1 ]
Reis, Jenner K. P. [1 ]
机构
[1] Univ Fed Minas Gerais UFMG, Dept Vet Prevent Med, Grad Program Anim Sci, Lab Retroviroses,Escola Vet, Campus Pampulha,Av Antonio Carlos 6627, BR-31270901 Belo Horizonte, MG, Brazil
[2] Minist Agr Pecuaria & Abastecimento MAPA, Manaus, AM, Brazil
[3] Minist Agr Pecuaria & Abastecimento MAPA, Brasilia, DF, Brazil
来源
PESQUISA VETERINARIA BRASILEIRA | 2020年 / 40卷 / 12期
关键词
iELISA; bovine; enzyme-linked immunosorbent assay; Enzootic bovine leukosis; diagnosis; control; cattle; LEUKEMIA-VIRUS DNA; ANTIBODIES; PROTEIN; INFECTION; MILK;
D O I
10.1590/1678-5150-PVB-6731
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Enzootic bovine leukosis (EBL) is an infectious disease caused by bovine leukemia virus (BLV) that affects cattle worldwide. Agar gel immunodiffusion (AGID) was the reference test for EBL diagnosis for many years, but enzyme-linked immunosorbent assay (ELISA) showed higher sensitivity, was faster to perform, and resulted in an objective reading. However, the importation of ELISA kits is lengthy and expensive, and currently, no AGID kits are available in Brazil. The aim of this work was to standardize an indirect ELISA (iELISA) for EBL diagnosis using BLV antigens produced in Tadarida brasiliensis lung (Tb1Lu) cells, which are Bovine viral diarrhea virus (BVDV) free, unlike fetal lamb kidney (FLK) cells, currently used for this purpose. Following standardization, iELISA results were compared with those obtained by AGID and the commercial Chekit Leucose-Serum ELISA. Compared to AGID, iELISA had 94,44% sensitivity, 75.68% specificity, 79.10% positive predictive value (PPV) and 93.30% negative predictive value (NPV), with 84% concordance and a Kappa index of 0.699. Compared to the Chekit Leucose-Serum ELISA, iELISA showed 92.60% sensitivity, 87.09% specificity, 90.27% PPV and 90,00% NPV, with 90.27% concordance and a Kappa index of 0.801. Taking into account the high agreement with the traditional tests and the absence of non-specific reactions with BVDV, the developed assay could be used as diagnostic method to control EBL in Brazil.
引用
收藏
页码:977 / 984
页数:8
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