Sanz M G, Oliveira A F, Loynachan A, Page A, Svansson V, Giguère S, Horohov D W
Maxwell H. Gluck Equine Research Center, Lexington, Kentucky, USA.
Department of Veterinary Science, Veterinary Diagnostic Laboratory, Lexington, Kentucky, USA.
Equine Vet J. 2016 Jan;48(1):103-8. doi: 10.1111/evj.12363. Epub 2015 Jan 25.
Rhodococcus equi (Rhodococcus hoagii/Prescottella equi) is a common cause of foal pneumonia, but its diagnosis remains a challenge for equine veterinarians. While the VapA-specific (virulence-associated protein A) immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) has low sensitivity and specificity for detecting pneumonic foals, little is known about VapA-specific IgG subclasses.
To evaluate the performance of VapA-specific ELISA for IgG and its subclasses IgGa, IgGb and IgG(T) in the early diagnosis of pneumonia caused by R. equi.
Assay validation followed by assessment of diagnostic performance using archived samples from animals of known status.
Serum samples from exposed (n = 125) and nonexposed adult horses (n = 10) and from experimentally challenged and naturally infected foals were used for ELISA validation. Post mortem and tissue culture records of the last 24 years from the Institute for Experimental Pathology at the University of Iceland in Keldur, Iceland laboratory were evaluated to confirm the absence of R. equi cases in Iceland. The diagnostic performance of VapA-specific IgG and its subclasses was evaluated using banked serum samples from pneumonic (n = 21) and healthy foals (n = 80). To evaluate each IgG assay, a cut-off value was selected based on receiver operating characteristic curve analysis and used to calculate sensitivity and specificity. The intra- and interassay coefficients of variation were calculated for each ELISA.
Using sera from Iceland, where R. equi infection has not been reported, the VapA-specific IgG ELISA differentiated exposed from nonexposed horses. When used to identify infected foals, VapA-specific IgG, IgGa and IgGb had no diagnostic value. In contrast, IgG(T) had high sensitivity and specificity.
Horses from Iceland are not exposed to VapA(+) R. equi and can serve as negative controls. VapA-specific IgG subclasses, with the exception of IgG(T), are poor predictors of disease. Further investigation on the use of IgG(T) as a diagnostic tool in field conditions is needed.
马红球菌(霍氏红球菌/马普雷斯科特氏菌)是幼驹肺炎的常见病因,但对马兽医而言,其诊断仍是一项挑战。虽然VapA特异性(毒力相关蛋白A)免疫球蛋白G(IgG)酶联免疫吸附测定(ELISA)在检测患肺炎幼驹时敏感性和特异性较低,但关于VapA特异性IgG亚类的情况却知之甚少。
评估VapA特异性ELISA检测IgG及其亚类IgGa、IgGb和IgG(T)在早期诊断马红球菌所致肺炎中的性能。
先进行检测方法验证,然后使用来自已知状态动物的存档样本评估诊断性能。
来自暴露组(n = 125)和非暴露组成年马(n = 10)以及实验性攻毒和自然感染幼驹的血清样本用于ELISA验证。对冰岛凯尔德乌尔市冰岛大学实验病理学研究所过去24年的尸检和组织培养记录进行评估,以确认冰岛不存在马红球菌病例。使用来自患肺炎幼驹(n = 21)和健康幼驹(n = 80)的储存血清样本评估VapA特异性IgG及其亚类的诊断性能。为评估每种IgG检测方法,根据受试者工作特征曲线分析选择一个临界值,并用于计算敏感性和特异性。计算每种ELISA的批内和批间变异系数。
使用来自未报告马红球菌感染的冰岛的血清,VapA特异性IgG ELISA可区分暴露组和非暴露组马匹。当用于识别感染幼驹时,VapA特异性IgG、IgGa和IgGb没有诊断价值。相比之下,IgG(T)具有较高的敏感性和特异性。
来自冰岛的马匹未接触VapA(+)马红球菌,可作为阴性对照。除IgG(T)外,VapA特异性IgG亚类对疾病的预测能力较差。需要进一步研究IgG(T)在现场条件下作为诊断工具的应用。