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利用 MILLIPLEX 牛细胞因子/趋化因子多重分析检测试剂盒鉴定非洲水牛(Syncerus caffer)中的牛分枝杆菌感染生物标志物。

Use of the MILLIPLEX bovine cytokine/chemokine multiplex assay to identify Mycobacterium bovis-infection biomarkers in African buffaloes (Syncerus caffer).

机构信息

DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

Ezemvelo KwaZulu-Natal Wildlife, PO Box 25, Mtubatuba 3935, South Africa.

出版信息

Vet Immunol Immunopathol. 2021 Jan;231:110152. doi: 10.1016/j.vetimm.2020.110152. Epub 2020 Nov 11.

DOI:10.1016/j.vetimm.2020.110152
PMID:33227620
Abstract

As a recognized Mycobacterium bovis maintenance host, the African buffalo (Syncerus caffer) poses transmission risks to livestock, humans and other wildlife. Early detection of M. bovis infection is critical for limiting its spread. Currently, tests detecting cell-mediated immune responses are used for diagnosis in buffaloes. However, these may have suboptimal sensitivity or specificity, depending on the blood stimulation method. Recent evidence suggests that assays using combinations of host cytokine biomarkers may increase diagnostic performance. Therefore, this study aimed to investigate the application of a MILLIPLEX bovine cytokine/chemokine multiplex assay to identify candidate biomarkers of M. bovis infection in buffaloes. Whole blood from twelve culture-confirmed M. bovis-infected buffaloes, stimulated with the QuantiFERON TB Gold Plus in-tube system, was tested using the MILLIPLEX platform. Results indicated binding of bovine antibodies to fifteen buffalo cytokine/chemokine targets. Moreover, there was a significant difference in concentrations between unstimulated and TB antigen-stimulated buffalo samples for seven cytokines/chemokines included in the kit. Although these preliminary results require further investigation in larger sample sets and a comparison between M. bovis-infected and uninfected cohorts, the utility of the MILLIPLEX platform in a novel species was demonstrated, in addition to identifying potential African buffalo cytokines for future research.

摘要

作为公认的牛分枝杆菌维持宿主,非洲野牛(Syncerus caffer)对牲畜、人类和其他野生动物构成了传播风险。早期检测牛分枝杆菌感染对于限制其传播至关重要。目前,用于诊断野牛的检测方法是检测细胞介导的免疫反应。然而,根据血液刺激方法的不同,这些检测方法的敏感性或特异性可能不理想。最近的证据表明,使用宿主细胞因子生物标志物组合的检测方法可能会提高诊断性能。因此,本研究旨在探讨使用 MILLIPLEX 牛细胞因子/趋化因子多重分析检测方法来鉴定牛分枝杆菌感染的候选生物标志物。使用 MILLIPLEX 平台对经培养确认感染牛分枝杆菌的 12 头野牛进行全血检测,这些野牛用 QuantiFERON TB Gold Plus 管内系统进行刺激。结果表明,牛抗体与 15 个野牛细胞因子/趋化因子靶标结合。此外,试剂盒中包含的七种细胞因子/趋化因子在未刺激和 TB 抗原刺激的野牛样本之间的浓度存在显著差异。尽管这些初步结果需要在更大的样本集中进一步研究,并在感染和未感染的牛群之间进行比较,但本研究证明了 MILLIPLEX 平台在新型物种中的实用性,同时还确定了未来研究中潜在的非洲野牛细胞因子。

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