Bagut Elena Tatiana, Cambier Ludivine, Heinen Marie-Pierre, Cozma Vasile, Monod Michel, Mignon Bernard
Department of Parasitology and Parasitic Diseases, Faculty of Veterinary Medicine, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Cluj-Napoca, Romania.
Clin Vaccine Immunol. 2013 Aug;20(8):1150-4. doi: 10.1128/CVI.00243-13. Epub 2013 Jun 5.
The aim of this study was to develop an in-house enzyme-linked immunosorbent assay (ELISA) for the serological diagnosis of ringworm infection in cattle. We used available recombinant forms of Trichophyton rubrum dipeptidyl peptidase V (TruDppV) and T. rubrum leucin aminopeptidase 2 (TruLap2), which are 98% identical to Trichophyton verrucosum orthologues. Field serum samples from 135 cattle with ringworm infection, as confirmed by direct microscopy, fluorescence microscopy, and PCR, and from 55 cattle without any apparent skin lesions or history of ringworm infection that served as negative controls were used. Sensitivities, specificities, and positive and negative predictive values were determined to evaluate the diagnostic value of our ELISA. Overall, the ELISAs based on recombinant TruDppV and TruLap2 discriminated well between infected animals and healthy controls. Highly significant differences (P < 0.0001, Mann-Whitney U test) were noted between optical density values obtained when sera from infected versus control cattle were tested. The ELISA developed for the detection of specific antibodies against DppV gave 89.6% sensitivity, 92.7% specificity, a 96.8% positive predictive value, and a 78.4% negative predictive value. The recombinant TruLap2-based ELISA displayed 88.1% sensitivity, 90.9% specificity, a 95.9% positive predictive value, and a 75.7% negative predictive value. To the best of our knowledge, this is the first ELISA based on recombinant antigens for assessing immune responses to ringworm infection in cattle; it is particularly suitable for epidemiological studies and also for the evaluation of vaccines and/or vaccination procedures.
本研究的目的是开发一种用于牛皮肤癣菌感染血清学诊断的内部酶联免疫吸附测定(ELISA)。我们使用了红色毛癣菌二肽基肽酶V(TruDppV)和红色毛癣菌亮氨酸氨肽酶2(TruLap2)的可用重组形式,它们与疣状毛癣菌直系同源物的相似度为98%。使用了135头经直接显微镜检查、荧光显微镜检查和PCR确诊为皮肤癣菌感染的牛的现场血清样本,以及55头无任何明显皮肤病变或皮肤癣菌感染病史的牛作为阴性对照。通过确定敏感性、特异性以及阳性和阴性预测值来评估我们ELISA的诊断价值。总体而言,基于重组TruDppV和TruLap2的ELISA能够很好地区分感染动物和健康对照。在检测感染牛与对照牛的血清时获得的光密度值之间存在高度显著差异(P < 0.0001,曼-惠特尼U检验)。用于检测针对DppV的特异性抗体的ELISA的敏感性为89.6%,特异性为92.7%,阳性预测值为96.8%,阴性预测值为78.4%。基于重组TruLap2的ELISA的敏感性为88.1%,特异性为90.9%,阳性预测值为95.9%,阴性预测值为75.7%。据我们所知,这是第一种基于重组抗原的ELISA,用于评估牛对皮肤癣菌感染的免疫反应;它特别适用于流行病学研究,也适用于疫苗和/或疫苗接种程序的评估。