Warnick L D, Nielsen L R, Nielsen J, Greiner M
Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Prev Vet Med. 2006 Dec 18;77(3-4):284-303. doi: 10.1016/j.prevetmed.2006.08.001. Epub 2006 Sep 18.
The Danish government and cattle industry instituted a Salmonella surveillance program in October 2002 to help reduce Salmonella enterica subsp. enterica serotype Dublin (S. Dublin) infections. All dairy herds are tested by measuring antibodies in bulk tank milk at 3-month intervals. The program is based on a well-established ELISA, but the overall test program accuracy and misclassification was not previously investigated. We developed a model to simulate repeated bulk tank milk antibody measurements for dairy herds conditional on true infection status. The distributions of bulk tank milk antibody measurements for infected and noninfected herds were determined from field study data. Herd infection was defined as having either >or=1 Salmonella culture-positive fecal sample or >or=5% within-herd prevalence based on antibody measurements in serum or milk from individual animals. No distinction was made between Dublin and other Salmonella serotypes which cross-react in the ELISA. The simulation model was used to estimate the accuracy of herd classification for true herd-level prevalence values ranging from 0.02 to 0.5. Test program sensitivity was 0.95 across the range of prevalence values evaluated. Specificity was inversely related to prevalence and ranged from 0.83 to 0.98. For a true herd-level infection prevalence of 15%, the estimate for specificity (Sp) was 0.96. Also at the 15% herd-level prevalence, approximately 99% of herds classified as negative in the program would be truly noninfected and 80% of herds classified as positive would be infected. The predictive values were consistent with the primary goal of the surveillance program which was to have confidence that herds classified negative would be free of Salmonella infection.
2002年10月,丹麦政府和养牛业启动了一项沙门氏菌监测计划,以帮助减少肠炎沙门氏菌肠炎亚种都柏林血清型(S. 都柏林)感染。所有奶牛场每隔3个月通过检测混合奶罐中的抗体进行检测。该计划基于一种成熟的酶联免疫吸附测定(ELISA),但此前未对整个检测计划的准确性和错误分类情况进行调查。我们开发了一个模型,用于根据真实感染状况模拟对奶牛场混合奶罐牛奶抗体的重复检测。根据实地研究数据确定了感染和未感染牛群混合奶罐牛奶抗体检测结果的分布情况。牛群感染定义为有≥1份沙门氏菌培养阳性粪便样本,或根据个体动物血清或牛奶中的抗体检测结果,牛群内患病率≥5%。在ELISA中发生交叉反应的都柏林血清型和其他沙门氏菌血清型之间未作区分。该模拟模型用于估计真实牛群患病率在0.02至0.5范围内时牛群分类的准确性。在所评估的患病率范围内,检测计划的灵敏度为0.95。特异性与患病率呈负相关,范围从0.83至0.98。对于真实牛群感染患病率为15%的情况,特异性(Sp)估计值为0.96。同样在15%的牛群患病率水平下,该计划中分类为阴性的牛群中约99%实际未感染,分类为阳性的牛群中80%实际感染。预测值与监测计划的主要目标一致,即确信分类为阴性的牛群没有沙门氏菌感染。