Department of Animal Biosciences, University of Guelph, Guelph, ON, N1G 2W1, Canada.
Department of Clinical Studies, Ontario Veterinary College, Guelph, ON, N1G 2W1, Canada.
J Dairy Sci. 2020 Jun;103(6):5501-5508. doi: 10.3168/jds.2019-17718. Epub 2020 Apr 16.
Breeding stress-resilient livestock is a potential strategy to help mitigate the negative effect of environmental and pathogenic stressors. The hypothalamic-pituitary-adrenal axis and immune system are activated during stress events and release mediators into the circulation that help restore physiological homeostasis. The purpose of this study was to assess a comprehensive set of circulatory mediators released in response to an acute immune stress challenge to identify candidate biomarkers that can be used for the selection of stress-resilient animals. Fifteen female lambs were stress challenged with an intravenous bolus of lipopolysaccharide (LPS; 400 ng/kg), and blood was collected from the jugular vein at 0, 2, 4, and 6 h after LPS challenge to identify and monitor candidate stress biomarkers; temperature was also recorded over time. Biomarker responses were evaluated with a repeated-measures model to compare time points with baseline values. As expected, all sheep had a monophasic febrile response to LPS challenge, and cortisol increased and returned to baseline by 6 h. The cytokines tumor necrosis factor-α, IL-6, IFN-γ (proinflammatory), and IL-10 (anti-inflammatory) increased, but only tumor necrosis factor-α returned to baseline during the monitoring period. The cytokines IL-1α, IL-1β, IL-17α (proinflammatory), and IL-4 (anti-inflammatory) did not respond to LPS challenge. All chemokines (CCL2, CCL3, CCL4, CXCL10, and IL-8) responded to LPS challenge; however, only CCL2, CCL3, CCL4, and CXCL10 increased over time, and only CCL3, CCL4, and CXCL10 returned to baseline during the monitoring period. MicroRNA (miR-145, miR-233, and miR-1246) also increased and remained elevated during the study. In summary, the LPS challenge induced a strong stress response in Rideau-Dorset sheep that could be monitored with a distinct profile of circulatory biomarkers.
培育具有应激抗性的牲畜是一种潜在的策略,可以帮助减轻环境和致病应激源的负面影响。在应激事件中,下丘脑-垂体-肾上腺轴和免疫系统被激活,并将介质释放到循环中,以帮助恢复生理稳态。本研究的目的是评估一组应对急性免疫应激挑战时释放的循环介质,以确定可用于选择具有应激抗性的动物的候选生物标志物。15 只雌性羔羊接受静脉内脂多糖(LPS;400ng/kg)冲击,在 LPS 冲击后 0、2、4 和 6 小时从颈静脉采集血液,以鉴定和监测候选应激生物标志物;同时也记录了体温随时间的变化。采用重复测量模型评估生物标志物反应,以比较时间点与基线值。正如预期的那样,所有绵羊对 LPS 冲击均呈单相发热反应,皮质醇在 6 小时内升高并恢复到基线。细胞因子肿瘤坏死因子-α、IL-6、IFN-γ(促炎)和 IL-10(抗炎)增加,但在监测期间仅肿瘤坏死因子-α恢复到基线。细胞因子 IL-1α、IL-1β、IL-17α(促炎)和 IL-4(抗炎)对 LPS 冲击无反应。所有趋化因子(CCL2、CCL3、CCL4、CXCL10 和 IL-8)对 LPS 冲击均有反应;然而,只有 CCL2、CCL3、CCL4 和 CXCL10 随时间增加,并且仅 CCL3、CCL4 和 CXCL10 在监测期间恢复到基线。微小 RNA(miR-145、miR-233 和 miR-1246)也增加,并在研究期间保持升高。总之,LPS 冲击在 Rideau-Dorset 绵羊中诱导了强烈的应激反应,可以通过循环生物标志物的独特特征进行监测。