Faculty of Veterinary Science, University of Sydney, 425 Werombi Road, Camden, NSW 2570, Australia.
Prev Vet Med. 2013 Nov 1;112(3-4):203-12. doi: 10.1016/j.prevetmed.2013.08.006. Epub 2013 Aug 24.
Diagnostic tests used for Johne's disease in sheep either have poor sensitivity and specificity or only detect disease in later stages of infection. Predicting which of the infected sheep are likely to become infectious later in life is currently not feasible and continues to be a major hindrance in disease control. We conducted this longitudinal study to investigate if a suite of diagnostic tests conducted in Mycobacterium avium subspecies paratuberculosis (MAP) exposed lambs at 4 months post infection can accurately predict their clinical status at 12 months post infection. We tracked cellular and humoral responses and quantity of MAP shedding for up to 12 months post challenge in 20 controls and 37 exposed sheep. Infection was defined at necropsy by tissue culture and disease spectrum by lesion type. Data were analysed using univariable and multivariable logistic regression models and a subset of variables from the earliest period post inoculation (4 months) was selected for predicting disease outcomes later on (12 months). Sensitivity and specificity of tests and their combinations in series and parallel were determined. Early elevation in faecal MAP DNA quantity and a lower interferon gamma (IFNγ) response were significantly associated with sheep becoming infectious as well as progressing to severe disease. Conversely, early low faecal MAP DNA and higher interleukin-10 responses were significantly associated with an exposed animal developing protective immunity. Combination of early elevated faecal MAP DNA or lower IFNγ response had the highest sensitivity (75%) and specificity (81%) for identifying sheep that would become infectious. Collectively, these results highlight the potential for combined test interpretation to aid in the early prediction of sheep susceptibility to MAP infection.
用于绵羊约翰氏病的诊断检测要么敏感性和特异性差,要么只能在感染后期检测到疾病。预测哪些受感染的绵羊在以后的生活中可能具有传染性目前还不可行,这仍然是疾病控制的主要障碍。我们进行了这项纵向研究,以调查在感染后 4 个月对感染了牛分枝杆菌亚种副结核病(MAP)的羔羊进行的一系列诊断检测是否可以准确预测它们在感染后 12 个月的临床状况。我们跟踪了细胞和体液反应以及 MAP 脱落量,最多可达 12 个月。通过组织培养在剖检时定义感染,通过病变类型定义疾病谱。使用单变量和多变量逻辑回归模型对 20 只对照和 37 只暴露的绵羊进行数据分析,并从接种后最早的时期(4 个月)选择一组变量来预测以后的疾病结果(12 个月)。确定了测试及其组合的串联和并联的敏感性和特异性。粪便中 MAP DNA 数量的早期升高和较低的干扰素γ(IFNγ)反应与绵羊成为感染源以及发展为严重疾病显著相关。相反,早期粪便中 MAP DNA 较低和白细胞介素-10 反应较高与暴露动物产生保护性免疫显著相关。早期粪便中 MAP DNA 升高或 IFNγ 反应降低的组合对识别可能具有传染性的绵羊具有最高的敏感性(75%)和特异性(81%)。总的来说,这些结果强调了联合测试解释的潜力,可以帮助早期预测绵羊对 MAP 感染的易感性。