Hughes Valerie, McNair Jim, Strain Samuel, Barry Claire, McLuckie Joyce, Nath Mintu, Caldow George, Stevenson Karen
Moredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik EH26 0PZ, United Kingdom.
Veterinary Sciences Division, Agri-Food and Biosciences Institute, Stoney Road, Stormont Belfast BT4 3SD, United Kingdom.
Res Vet Sci. 2017 Oct;114:244-253. doi: 10.1016/j.rvsc.2017.04.018. Epub 2017 Apr 29.
Johne's disease (JD), is a fatal enteritis of animals caused by infection with Mycobacterium avium subspecies paratuberculosis (Map). Diagnosis of subclinical JD is problematic as test sensitivity is limited. Th1 responses to Map are activated early, thus detection of a cell-mediated response, indicated by measuring interferon gamma (IFN-γ) stimulated by mycobacterial antigens, may give the first indication of sub-clinical infection. Crude extracts of Map (PPDJ) have been used to detect the cell-mediated response in infected cattle. More specific, quantifiable antigens may improve test specificity and reproducibility. Map-specific proteins, MAP_3651c and MAP_0268c, raised a cell-mediated immune response in sub-clinically infected sheep. Results presented in this manuscript demonstrate these proteins elicit a cell-mediated response in experimental and natural infections of cattle. Individual ranked IFN-γ responses of experimentally infected calves to PPDJ showed a high, statistically significant association with ranked responses of recombinant Map antigens. Responses of infected animals were higher than the control group. Threshold values determined using data from an experimental infection were applied to naturally infected animals. Some animals exhibited responses above these threshold values. Responses to MAP_3651c on a farm categorised as high-risk for JD showed strong evidence (P<0.001) that responses were significantly different to lower-risk farms. The IGRA test may prove to be an additional tool for the diagnosis of JD, and inclusion of specific antigens a refinement however, understanding and interpretation of IGRA results remain challenging and further investigation will be required to determine whether the IGRA test can detect exposure and hence predict clinical JD.
副结核(JD)是由副结核分枝杆菌亚种(Map)感染引起的一种致命性动物肠炎。亚临床JD的诊断存在问题,因为检测灵敏度有限。对Map的Th1反应早期就被激活,因此通过测量由分枝杆菌抗原刺激产生的干扰素γ(IFN-γ)来检测细胞介导的反应,可能会给出亚临床感染的首个迹象。Map的粗提物(PPDJ)已被用于检测感染牛的细胞介导反应。更具特异性、可量化的抗原可能会提高检测的特异性和可重复性。Map特异性蛋白MAP_3651c和MAP_0268c在亚临床感染的绵羊中引发了细胞介导的免疫反应。本手稿中呈现的结果表明,这些蛋白在牛的实验性感染和自然感染中引发了细胞介导的反应。实验感染的犊牛对PPDJ的个体IFN-γ反应排名与重组Map抗原的反应排名显示出高度的、具有统计学意义的相关性。感染动物的反应高于对照组。将根据实验性感染数据确定的阈值应用于自然感染的动物。一些动物的反应高于这些阈值。在一个被归类为JD高风险的农场中,对MAP_3651c的反应显示出有力证据(P<0.001),表明与低风险农场的反应存在显著差异。IGRA检测可能被证明是诊断JD的另一种工具,纳入特定抗原是一种改进,然而,对IGRA结果的理解和解释仍然具有挑战性,需要进一步研究以确定IGRA检测是否能够检测暴露并因此预测临床JD。