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首页> 外文期刊>BMC Veterinary Research >Development and evaluation of a diagnostic cytokine-release assay for Mycobacterium suricattae infection in meerkats ( Suricata suricatta )
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Development and evaluation of a diagnostic cytokine-release assay for Mycobacterium suricattae infection in meerkats ( Suricata suricatta )

机译:猫鼬(Suricata suricatta)苏里分枝杆菌感染的诊断性细胞因子释放测定法的开发和评估。

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Background Sensitive diagnostic tools are necessary for the detection of Mycobacterium suricattae infection in meerkats ( Suricata suricatta ) in order to more clearly understand the epidemiology of tuberculosis and the ecological consequences of the disease in this species. We therefore aimed to develop a cytokine release assay to measure antigen-specific cell-mediated immune responses of meerkats. Results Enzyme-linked immunosorbent assays (ELISAs) were evaluated for the detection of interferon-gamma (IFN-γ) and IFN-γ inducible protein 10 (IP-10) in meerkat plasma. An IP-10 ELISA was selected to measure the release of this cytokine in whole blood in response to Bovigam? PC-HP Stimulating Antigen, a commercial peptide pool of M. bovis antigens. Using this protocol, captive meerkats with no known M. suricattae exposure ( n =?10) were tested and results were used to define a diagnostic cut off value (mean plus 2 standard deviations). This IP-10 release assay (IPRA) was then evaluated in free-living meerkats with known M. suricattae exposure, categorized as having either a low, moderate or high risk of infection with this pathogen. In each category, respectively, 24.7%, 27.3% and 82.4% of animals tested IPRA-positive. The odds of an animal testing positive was 14.0 times greater for animals with a high risk of M. suricattae infection compared to animals with a low risk. Conclusion These results support the use of this assay as a measure of M. suricattae exposure in meerkat populations. Ongoing longitudinal studies aim to evaluate the value of the IPRA as a diagnostic test of M. suricattae infection in individual animals.
机译:背景技术灵敏的诊断工具对于检测猫鼬(Suricata suricatta)中的分枝杆菌分枝杆菌感染是必不可少的,以便更清楚地了解结核病的流行病学和该病在该物种中的生态后果。因此,我们旨在开发一种细胞因子释放测定法,以测量猫鼬的抗原特异性细胞介导的免疫反应。结果评估了酶联免疫吸附测定(ELISA)在猫鼬血浆中检测干扰素-γ(IFN-γ)和IFN-γ诱导型蛋白10(IP-10)的能力。选择IP-10 ELISA来测量响应Bovigam?的全血中该细胞因子的释放。 PC-HP刺激性抗原,牛分枝杆菌抗原的商业肽库。使用该方案,测试了没有已知的suricattae暴露(n =?10)的圈养猫鼬,并将结果用于定义诊断临界值(平均值加2标准差)。然后在已知有suricattae暴露的自由生活猫鼬中评估该IP-10释放测定法(IPRA),将其分类为具有这种病原体感染风险的低,中或高风险。在每个类别中,分别有24.7%,27.3%和82.4%的动物测试IPRA阳性。 Suricattae感染高风险动物的测试结果为阳性的几率比低风险动物高14.0倍。结论这些结果支持该方法作为猫鼬种群中M. suricattae暴露量的一种方法。正在进行的纵向研究旨在评估IPRA作为个别动物对suricatta感染的诊断测试的价值。

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