Kampa Jaruwan, Ståhl Karl, Renström Lena H M, Alenius Stefan
Department of Clinical Sciences, Swedish University of Agricultural Science (SLU), SE-75007, Uppsala, Sweden.
Acta Vet Scand. 2007 Mar 13;49(1):7. doi: 10.1186/1751-0147-49-7.
Bovine viral diarrhoea virus (BVDV) is an important pathogen in cattle. The ability of the virus to cross the placenta during early pregnancy can result in the birth of persistently infected (PI) calves. These calves shed the virus during their entire lifespan and are the key transmitters of infection. Consequently, identification (and subsequent removal) of PI animals is necessary to rapidly clear infected herds from the virus. The objective of this study was to evaluate the suitability of a commercial Erns-capture ELISA, in comparison to the indirect immunoperoxidase test (IPX), for routine diagnostic detection of BVDV within a control programme. In addition, the effect of passive immunity and heat-inactivation of the samples on the performance of the ELISA was studied.
In the process of virus clearance within the Swedish BVDV control programme, all calves born in infected herds are tested for virus and antibodies. From such samples, sent in for routine diagnostics to SVA, we selected 220 sera collected from 32 beef herds and 29 dairy herds. All sera were tested for BVDV antigen using the Erns ELISA, and the results were compared to the results from the IPX used within the routine diagnostics.
All 130 samples categorized as virus negative by IPX were tested negative in the ELISA, and all 90 samples categorized as virus positive were tested positive, i.e. the relative sensitivity and specificity of the ELISA was 100% in relation to IPX, and the agreement between the tests was perfect.
We can conclude that the Erns ELISA is a valid alternative that has several advantages compared to IPX. Our results clearly demonstrate that it performs well under Swedish conditions, and that its performance is comparable with the IPX test. It is highly sensitive and specific, can be used for testing of heat-inactivated samples, precolostral testing, and probably to detect PI animals at an earlier age than the IPX.
牛病毒性腹泻病毒(BVDV)是牛群中的一种重要病原体。该病毒在妊娠早期穿过胎盘的能力可导致出生持续感染(PI)的犊牛。这些犊牛在其整个生命期内都排出病毒,是感染的主要传播者。因此,识别(并随后清除)PI动物对于从病毒中快速清除受感染牛群是必要的。本研究的目的是评估一种商业化的Erns捕获ELISA与间接免疫过氧化物酶试验(IPX)相比,在对照程序中对BVDV进行常规诊断检测的适用性。此外,还研究了样品的被动免疫和热灭活对ELISA性能的影响。
在瑞典BVDV对照程序的病毒清除过程中,对感染牛群中出生的所有犊牛进行病毒和抗体检测。从送往瑞典兽医研究所进行常规诊断的此类样品中,我们选择了从32个肉牛群和29个奶牛群中收集的220份血清。使用Erns ELISA对所有血清进行BVDV抗原检测,并将结果与常规诊断中使用的IPX结果进行比较。
IPX分类为病毒阴性的所有130份样品在ELISA中检测为阴性,IPX分类为病毒阳性的所有90份样品检测为阳性,即ELISA相对于IPX的相对敏感性和特异性为100%,且试验之间的一致性完美。
我们可以得出结论,Erns ELISA是一种有效的替代方法,与IPX相比有几个优点。我们的结果清楚地表明,它在瑞典条件下表现良好,其性能与IPX试验相当。它高度敏感和特异,可用于检测热灭活样品、初乳前检测,并且可能比IPX更早地检测到PI动物。