Skimming and storage factors affect the detection of heat shock protein 70 in raw bovine milk

IF 2.2
M.R.H. Rakib , V. Messina , J.I. Gargiulo , N.A. Lyons , I.N. Pathirana , P.C. Thomson , S.C. Garcia
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Abstract

Heat shock proteins (HSP) play a vital role in maintaining cellular function under elevated temperatures. Among these, heat shock protein 70 (HSP70) has recently been detected in bovine milk using competitive ELISA, highlighting its potential as a noninvasive marker of cellular stress and a tool for detecting heat stress (HS) in dairy cows. However, optimal management and storage conditions of milk samples for detection of HSP70 are yet to be determined. This study aimed to evaluate how different management and storage practices affect detection of HSP70 in milk samples. Samples were skimmed by centrifugation either before storage (SBS) or after storage (SAS), and then stored under different temperatures: (a) room temperature (T1, ∼22°C), (b) refrigerated (T2, 4°C), (c) frozen (T3, −20°C), and (d) refrigerated at 4°C with a preservative (bronopol; T4). Samples were analyzed every 2 d until d 15 (d 1, d 3, …, d 15) using a competitive ELISA system (sensitivity range 31.25–2,000 ng/mL) to detect HSP70 levels. Result showed that SBS samples had the smallest reduction in HSP70 levels on d 3 when stored at T2 or T3, with decreases of 4.4% and 7.9%, respectively. In contrast, SAS samples exhibited greater reductions (44.2% at T2 and 53.9% at T3). Samples stored at room temperature (T1) showed the greatest degradation, especially in SAS samples, whereas the use of a preservative (T4) did not consistently maintain HSP70 levels in either SBS or SAS samples. The HSP70 detection showed lower variability during early storage (d 1–3) across all treatments, with SBS samples demonstrating greater stability than SAS; however, variability significantly increased by d 9 in both sample types. An apparent increase in HSP70 levels was observed from d 11 to 15 in both SBS and SAS, suggesting the influence of protein stability and interactions affecting ELISA reactivity, where further research is required. Overall, samples stored as skim milk until d 3 at 4°C or −20°C preserved HSP70 levels more effectively than whole milk, with room temperature storage being the least favorable. This pioneering study explored how sample storage and management affect HSP70 detection, providing practical guidelines for farmers and processors to preserve milk sample integrity for assessment of HSP70 as indicator of cellular stress and, potentially, HS.
脱脂和贮存因素影响生牛乳中热休克蛋白70的检测
热休克蛋白在高温下维持细胞功能方面起着至关重要的作用。其中,热休克蛋白70 (HSP70)最近通过竞争性ELISA在牛奶中检测到,突出了它作为一种无创细胞应激标记物和检测奶牛热应激(HS)的工具的潜力。然而,检测HSP70的牛奶样品的最佳管理和储存条件尚未确定。本研究旨在评估不同的管理和储存方式对牛奶样品HSP70检测的影响。样品在储存前(SBS)或储存后(SAS)通过离心脱脂,然后在不同的温度下储存:(a)室温(T1, ~ 22°C), (b)冷藏(T2, 4°C), (C)冷冻(T3, - 20°C), (d)在4°C冷藏,并添加防腐剂(bronopol;T4)。使用竞争性ELISA系统(灵敏度范围31.25 ~ 2000 ng/mL)检测HSP70水平,每2天分析一次样品,直到第15天(第1、3、…、15天)。结果表明,SBS样品在T2和T3贮藏时,第3天HSP70水平下降幅度最小,分别为4.4%和7.9%。相反,SAS样品表现出更大的减少(在T2时为44.2%,在T3时为53.9%)。在室温(T1)下保存的样品表现出最大的降解,特别是在SAS样品中,而使用防腐剂(T4)并不能始终保持SBS或SAS样品中的HSP70水平。在所有处理中,HSP70检测在贮藏早期(1-3天)的变异性较低,SBS样品比SAS样品表现出更大的稳定性;然而,在两种样本类型中,变异性显著增加了9。从第11天到第15天,SBS和SAS的HSP70水平明显升高,这表明蛋白质稳定性和相互作用影响了ELISA反应性,这需要进一步的研究。总体而言,在4°C或- 20°C下以脱脂牛奶形式保存至3 d的样品比全脂牛奶更有效地保存了HSP70水平,而室温保存效果最差。这项开创性的研究探讨了样品储存和管理如何影响HSP70检测,为农民和加工商提供实用指南,以保持牛奶样品的完整性,以评估HSP70作为细胞应激和潜在HS的指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JDS communications
JDS communications Animal Science and Zoology
CiteScore
2.00
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