疾病诊断标记:猪血清PRRS的SELDI-TOF分析。

S Genini, M Cantu, S Botti, R Malinverni, A Costa, D Marras, E Giuffra
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引用次数: 2

摘要

猪繁殖与呼吸综合征(PRRS)是一种高度传染性的病毒性疾病,对养猪业造成严重损失。大多数断奶仔猪可能暴露于感染,并表现出与生产性能密切相关的至少无症状的PRRS病毒血症。本研究的目的是建立猪血清蛋白质组学分析的实验条件,并确定区分无症状断奶仔猪PRRS病毒血症阳性与阴性对照(PCR检测)的生物标志物,对随后临床PRRS的发生具有潜在的预测价值。采用Bio-Rad芯片WCX、IMAC30和H50进行SELDI-TOF质谱分析。发现阶段表明,WCX和IMAC30表面可以检测到一致数量的高度显著的蛋白峰;然而,这些峰值都没有在随后的验证阶段得到统计证实,这表明污染物和最丰富蛋白质的血清浓度是SELDI-TOF质谱研究的关键参数。目前的方案正在进一步优化和适应猪血清,以减少最丰富的蛋白质的不利影响,并增加潜在可检测的生物标志物的数量。此外,蛋白质组学指纹图谱已被证明是一种很有前途的诊断工具,在未来,它可能有助于深入了解体内早期病毒感染的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic markers for diseases: SELDI-TOF profiling of pig sera for PRRS.
Porcine reproductive and respiratory syndrome (PRRS) is a highly infectious viral disease causing severe losses to the pig industry. Most weaning piglets are likely to be exposed to the infection and show at least asymptomatic PRRS viremia strongly related to productive performance. The aims of this study were to set up experimental conditions for pig sera proteomic profiling and to identify biomarkers that differentiate weaning asymptomatic piglets positive to PRRS viremia from negative controls (PCR tested) with potential predictive value for the subsequent occurrence of clinical PRRS. Protein profiles were generated by SELDI-TOF MS using the Bio-Rad Chips WCX, IMAC30 and H50. The discovery phase revealed that a consistent number of highly significant protein peaks can be detected by the WCX and IMAC30 surfaces; however none of these peaks were statistically confirmed by the subsequent validation phase, highlighting that serum concentration of the contaminant and most abundant proteins is a crucial parameterfor SELDI-TOF MS studies. Current protocols are being furtheroptimized and adapted to pig sera to reduce the unfavourable effects of the most abundant proteins and to increase the number of potential detectable biomarkers. Furthermore, proteomic fingerprint profiling has been shown to be a promising diagnostic tool that, in the future, may be useful to provide also insights into the mechanisms of early viral infection in vivo.
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