Rezende Andrea de Fátima Silva, Brum Alexandre Antunes, Reis Carlos Guilherme, Angelo Henrique Ramos, Leal Karen Silva, Silva Mara Thais de Oliveira, Simionatto Simone, Azevedo Vasco, Santos Anderson, Portela Ricardo Wagner, Dellagostin Odir, Borsuk Sibele
Laboratório de Pesquisa em Doenças Infecciosas, Centro de Desenvolvimento Tecnológico, Biotecnologia, UFPel, Pelotas, RS 96010-900, Brazil.
Laboratório de Biologia Molecular, Faculdade de Ciências Ambientais, UFGD, Dourados, MS 79825-070, Brazil.
J Med Microbiol. 2016 Jun;65(6):521-529. doi: 10.1099/jmm.0.000263. Epub 2016 Apr 12.
Caseous lymphadenitis (CLA) is a disease caused by Corynebacterium pseudotuberculosis. It affects mainly small ruminants and causes significant economic losses worldwide. Because symptoms are not immediately noticeable, CLA clinical diagnosis is not effective. Numerous serological tests are being developed to detect the disease in asymptomatic animals, but currently available immunoassays have problems with sensitivity. Current ELISA formats use native bacterial antigens, and recombinant proteins could be useful for improving the immunoassay parameters. The C. pseudotuberculosis proteins CP0126a, CP0369 and CP1957 were identified from 2097 candidate proteins by mature epitope density (MED) analysis, expressed in Escherichia coli and evaluated in an indirect immunoenzymic system. The CP0126a, CP0369 and CP1957 ELISAs showed 77.5 %, 92.5 % and 92.5 % specificity and 95 %, 90 % and 85 % sensitivity, respectively. Receiver operating characteristic (ROC) curve analysis showed an area under the curve of 0.874, 0.951 and 0.881, respectively. The proteins identified in silico were recognized by antibodies in the sera from infected animals without being recognized in negative samples. The ELISA assay using the rCP0369 protein as antigen had the greatest specificity and sensitivity values, followed by rCP1957. This is an interesting strategy for seroepidemiological investigations in sheep flocks due to its significant specificity and sensitivity.
干酪性淋巴结炎(CLA)是一种由伪结核棒状杆菌引起的疾病。它主要影响小型反刍动物,并在全球范围内造成重大经济损失。由于症状不会立即显现,CLA的临床诊断并不有效。目前正在开发多种血清学检测方法来检测无症状动物中的该疾病,但现有的免疫测定法存在灵敏度问题。当前的ELISA检测形式使用天然细菌抗原,而重组蛋白可能有助于改善免疫测定参数。通过成熟表位密度(MED)分析从2097种候选蛋白中鉴定出伪结核棒状杆菌蛋白CP0126a、CP0369和CP1957,在大肠杆菌中表达并在间接免疫酶系统中进行评估。CP0126a、CP0369和CP1957 ELISA的特异性分别为77.5%、92.5%和92.5%,灵敏度分别为95%、90%和85%。受试者工作特征(ROC)曲线分析显示曲线下面积分别为0.874、0.951和0.881。通过计算机模拟鉴定出的蛋白能被感染动物血清中的抗体识别,而在阴性样本中未被识别。以rCP0369蛋白作为抗原的ELISA检测具有最高的特异性和灵敏度值,其次是rCP1957。由于其显著的特异性和灵敏度,这是一种用于羊群血清流行病学调查的有趣策略。