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首页> 外文期刊>OMICS: A journal of integrative biology >Biomarkers for Prediction of Bovine Respiratory Disease Outcome
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Biomarkers for Prediction of Bovine Respiratory Disease Outcome

机译:牛呼吸道的预测生物标志物疾病的结果

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Fatal bovine respiratory disease (BRD) is frequently the result of a primary viral and a secondary bacterial respiratory infection. In cattle, BRD causes more than half of feedlot deaths and has a major impact on financial losses in the cattle industry in North America. It is, therefore, very important to understand the mechanism of this complex disease process as well to predict and identify BRD susceptible cattle to enhance treatment efficacy. We recently established the value of using combinatorial omics approaches to identify candidate biomarkers associated with stress responses, a factor that can increase the severity of BRD. The objective of the present investigation was to experimentally recreate fatal BRD and to use a combinatorial analysis of proteomic, metabonomic, and elemental profiles in serum samples to determine if multimethod analysis of these biomarkers could predict disease outcome. The proteomic studies revealed that changes in the serum proteome were significant on day 4 postviral infection when compared to preinfection (day 0) serum samples. Proteomic studies identified a group of acute phase proteins (haptoglobin and apolipoprotein AI), which could be linked to a primary viral respiratory infection, but there was no significant association observed with fatal BRD. In contrast, metabonomic and elemental analyses identified candidate biomarkers for viral infection (glucose, LDL, valine, phosphorous, and iron) and disease outcome (lactate, glucose, iron). While multivariate analysis of proteomic and metabolite profiles did not discriminate between animals that survived or died postsynergic viral- bacterial infection by analyzing preinfection (day 0) serum samples, analysis of serum elemental profiles prior to infection was, however, predictive of BRD outcome. Furthermore, discriminant analyses of all three methodologies used to profile serum (collected on day 4 postviral but prior to bacterial infection) revealed differential trends between animal
机译:致命的牛呼吸道疾病(BRD)经常原发性病毒性和的结果继发性细菌性呼吸道感染。牛,BRD导致超过一半的饲养场死亡和经济损失有重大影响牛行业在北美。因此,非常重要的理解这种复杂的疾病过程的机制预测和识别BRD易感牛提高治疗效果。建立了使用组合的价值组学方法确定候选生物标志物与应激反应有关,一个因素可以增加BRD的严重程度。目前的调查实验重现致命BRD和使用metabonomic组合的蛋白质组学分析,和元素配置文件在血清样本确定多重方法的分析生物标志物可以预测疾病的结果。蛋白质组学研究显示的变化血清蛋白质组是重要的第四天感染病毒后preinfection相比(天0)血清样本。确定一组急性期蛋白质(结合珠蛋白和载脂蛋白AI)与原发性病毒性呼吸道感染,但没有意义协会与致命BRD观察。metabonomic和元素分析确认候选人生物标志物为病毒感染(葡萄糖、低密度脂蛋白、缬氨酸、磷和铁)疾病的结果(乳酸、葡萄糖、铁)。多变量分析蛋白质和代谢物配置文件没有区分动物生存或死亡postsynergic病毒-通过分析preinfection细菌感染(天0)血清样本,分析血清基本概要文件感染之前,然而,预测BRD结果。判别分析的三种方法用于配置文件血清(收集了4天病毒后但细菌感染之前)揭示了微分动物之间的趋势

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