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Quantitation of Acute Phase Proteins and Protein Electrophoresis in Monitoring the Acute Inflammatory Process in Experimentally and Naturally Infected Mice

机译:定量定量急性期蛋白和蛋白质电泳以监测实验和自然感染小鼠的急性炎症过程

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摘要

Serologic screening for infectious disease in sentinel mice from rodent colonies is expensive and labor-intensive, often involving multiple assays for several different infectious agents. Previously, we established normal reference ranges for the protein fractions of several laboratory strains of mice by using a commercially available agarose system of protein electrophoresis. In the current study, we address protein fractionation and quantitation of acute phase proteins (APP) in mice experimentally infected with Sendai virus or mouse parvovirus. We further investigate this methodology by using samples from sentinel mice from colonies with endemic infection. All study groups showed significant increases in γ globulins. Various other protein fractions showed mild variable changes; significant differences were not detected for individual APP. These results contrast the significant changes observed in APP and protein electrophoresis by using the standard methods of inducing inflammatory responses through injection of complete Freund adjuvant or LPS. These present data suggest that although quantitation of individual APP may not be helpful, γ globulin levels may reflect infection in laboratory mice and provide a possible adjunct to traditional screening methods.
机译:对来自啮齿动物菌落的前哨小鼠进行感染性疾病的血清学筛查是昂贵且费力的,通常涉及针对几种不同感染因子的多种测定。以前,我们通过使用市售的琼脂糖蛋白质电泳系统为几种实验室品系小鼠的蛋白质部分建立了正常参考范围。在当前的研究中,我们研究了用仙台病毒或小鼠细小病毒感染的小鼠的蛋白质分离和急性期蛋白质(APP)的定量。我们通过使用来自地方性感染菌落的前哨小鼠样本进一步研究这种方法。所有研究组均显示γ球蛋白显着增加。其他各种蛋白质组分显示出轻微的可变性变化;未检测到单个APP的显着差异。这些结果通过使用注射完整的弗氏佐剂或LPS诱导炎症反应的标准方法,对比了APP和蛋白质电泳中观察到的显着变化。这些现有数据表明,尽管定量单个APP可能无济于事,但γ球蛋白水平可能反映了实验室小鼠的感染,并为传统筛选方法提供了可能的辅助手段。

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