Rapid detection of heat stress biomarkers in Atlantic salmon (Salmo salar) liver using targeted proteomics

IF 1.1 Q3 FISHERIES
Omar Mendoza-Porras, Anca G. Rusu, Christopher Stratford, Nicholas M. Wade
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Abstract

Most fish are ectothermic; therefore, their physiology is significantly affected by temperature. Aquaculture fish have limited ability to avoid elevated water temperatures, with impacts increasing as a result of climate change. To date, quantifying gene expression has been proposed to monitor heat stress in salmon liver. This study aimed to establish a faster multiplexed proteomics method to measure the abundance of thermal stress biomarkers in liver of salmon reared at 15°C or 20°C. Moreover, this study aimed to determine the effects that sample pooling, and data normalisation using housekeeping (HK) protein peptides would exert over the statistical significance of these thermal stress markers. A multiple reaction monitoring (MRM) mass spectrometry method, comprised 45 peptides derived from thermal stress markers and 10 peptides from HK proteins, was applied to measure these markers in liver of salmon reared at 15°C or 20°C. When samples were processed individually, 34 peptides were significant between salmon livers at 15°C or 20°C. In pooled samples, this decreased to five significant peptides. Peptides hprt1_HYADDLDR (hypoxanthine phosphoribosyl transferase) and gapdh_VPTPNVSVVDLTVR (glyceraldehyde-3-phosphate dehydrogenase) were the most stable and unstable HK protein peptides, respectively. When data was normalised with hprt1_HYADDLDR, 16 peptides were significant in individual samples and 13 in pooled samples. Significant peptides serpinh1a_ADLSNISGK, SerpinH1_TNSILFIGR, ela2_VVGGEDVR and gapdh_VPTPNVSVVDLTVR were common regardless of data strategy. A fast and reliable MRM method was established to validate thermal stress markers in salmon liver, where individual samples yielded better results than pooled samples. Sample pooling was only better when combined with normalisation as it validated twice the number of markers than sample pooling alone. This method could be applied to monitoring stress response in experiments involving feeding additives designed to mitigate thermal stress or in selective breeding programs to help understanding family variance in thermal tolerance.

Abstract Image

利用靶向蛋白质组学快速检测大西洋鲑(Salmo salar)肝脏中的热应激生物标记物
大多数鱼类都是外温动物;因此,它们的生理机能受温度影响很大。水产养殖鱼类躲避水温升高的能力有限,而气候变化对它们的影响会越来越大。迄今为止,已有人提出通过量化基因表达来监测鲑鱼肝脏的热应力。本研究旨在建立一种更快的多重蛋白质组学方法,以测量在15°C或20°C条件下饲养的鲑鱼肝脏中热应激生物标志物的丰度。此外,本研究还旨在确定样本池和使用看家(HK)蛋白肽进行数据归一化对这些热应力标记物的统计意义的影响。该研究采用了一种多反应监测(MRM)质谱方法,其中包括 45 个来自热应力标记物的肽段和 10 个来自 HK 蛋白的肽段,用于测量在 15°C 或 20°C 温度条件下饲养的鲑鱼肝脏中的这些标记物。在单独处理样本时,有 34 种肽在 15°C 或 20°C 的三文鱼肝脏中具有显著性差异。在集合样本中,这一指标下降到 5 个重要肽段。肽段 hprt1_HYADDLDR(次黄嘌呤磷酸核糖转移酶)和 gapdh_VPTPNVSVVDLTVR(甘油醛-3-磷酸脱氢酶)分别是最稳定和最不稳定的香港蛋白质肽段。用 hprt1_HYADDLDR 对数据进行归一化处理后,16 个肽段在单个样本中具有显著性,13 个肽段在集合样本中具有显著性。无论采用哪种数据策略,都有一些重要肽段serpinh1a_ADLSNISGK、SerpinH1_TNSILFIGR、ela2_VVGGEDVR和gapdh_VPTPNVSVVDLTVR。建立了一种快速可靠的 MRM 方法来验证鲑鱼肝脏中的热应力标记物,单个样品的结果优于集合样品。只有当样品池与归一化相结合时才会更好,因为它验证的标记物数量是单独样品池的两倍。这种方法可用于监测旨在减轻热应力的喂养添加剂实验中的应激反应,或用于选择性育种计划,以帮助了解热耐受性的家族变异。
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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