Bachofen Claudia, Bollinger Barbara, Peterhans Ernst, Stalder Hanspeter, Schweizer Matthias
1Claudia Bachofen, Institute of Veterinary Virology, University of Bern, Länggassstraße 122, PO Box 8466, CH-3001 Bern, Switzerland.
J Vet Diagn Invest. 2013 Sep;25(5):655-61. doi: 10.1177/1040638713501172.
Detection of antibodies against Bovine viral diarrhea virus (BVDV) in serum and milk by enzyme-linked immunosorbent assay (ELISA) is a crucial part of all ongoing national schemes to eradicate this important cattle pathogen. Serum and milk are regarded as equally suited for antibody measurement. However, when retesting a seropositive cow 1 day after calving, the serum was negative in 6 out of 9 different ELISAs. To further investigate this diagnostic gap around parturition, pre- and postcalving serum and milk samples of 5 cows were analyzed by BVDV antibody ELISA and serum neutralization test (SNT). By ELISA, 3 out of the 5 animals showed a diagnostic gap in the serum for up to 12 days around calving but all animals remained positive in SNT. In milk, the ELISA was strongly positive after birth but antibody levels decreased considerably within the next few days. Because of the immunoglobulin G (IgG)1-specific transport of serum antibodies into the mammary gland for colostrum production, the IgG subclass specificity of the total and the BVDV-specific antibodies were determined. Although all 5 animals showed a clear decrease in the total and BVDV-specific IgG1 antibody levels at parturition, the precalving IgG1-to-IgG2 ratios of the BVDV-specific antibodies were considerably lower in animals that showed the diagnostic gap. Results showed that BVDV seropositive cows may become "false" negative in several ELISAs in the periparturient period and suggest that the occurrence of this diagnostic gap is influenced by the BVDV-specific IgG subclass response of the individual animal.
通过酶联免疫吸附测定(ELISA)检测血清和牛奶中针对牛病毒性腹泻病毒(BVDV)的抗体,是所有正在进行的根除这种重要牛病原体的国家计划的关键部分。血清和牛奶被认为同样适合进行抗体检测。然而,在产犊后1天对血清学阳性奶牛进行重新检测时,9种不同的ELISA中有6种检测血清呈阴性。为了进一步研究分娩前后的这一诊断差距,对5头奶牛产犊前后的血清和牛奶样本进行了BVDV抗体ELISA和血清中和试验(SNT)分析。通过ELISA检测,5头动物中有3头在产犊前后长达12天的血清中出现诊断差距,但所有动物在SNT中仍呈阳性。在牛奶中,出生后ELISA检测呈强阳性,但在接下来的几天内抗体水平大幅下降。由于血清抗体通过免疫球蛋白G(IgG)1特异性转运进入乳腺以产生初乳,因此测定了总抗体和BVDV特异性抗体的IgG亚类特异性。尽管所有5头动物在分娩时总抗体和BVDV特异性IgG1抗体水平均明显下降,但出现诊断差距的动物在产犊前BVDV特异性抗体的IgG1与IgG2比值明显较低。结果表明,BVDV血清学阳性奶牛在围产期的几种ELISA中可能会出现“假”阴性,这表明这种诊断差距的出现受个体动物BVDV特异性IgG亚类反应的影响。