Identification of candidate blood biomarkers through metabolomics analysis in bovine superovulation.

IF 2.6 2区 农林科学 Q1 VETERINARY SCIENCES
Frontiers in Veterinary Science Pub Date : 2025-04-30 eCollection Date: 2025-01-01 DOI:10.3389/fvets.2025.1552045
Xiaohu Su, Guangqi Gao, Liqiang Chen, Liguo Zhang, Guangnan Liu, Chao Bian, Guanghua Su, Lei Yang
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Abstract

Superovulation and embryo transfer technologies provide strong support for improving the productivity of cattle population. A non-invasive diagnostic method for superovulation prediction is necessary to improve its efficiency. Compared to macromolecular substances, there has been an increasing number of studies on small molecular metabolites as biomarkers. This study aimed to identify key biomarkers associated with superovulation outcomes in cows through serum metabolomics analysis. In this study, 36 induced estrus cows were selected, and the blood samples were collected at three time points: before FSH injection, before artificial insemination, and before embryo collection. Then, the cows were classified into high embryonic yield (HEY) and low embryonic yield (LEY) groups based on the total number of embryos. Furthermore, a serum untargeted metabolomics analysis of the two groups was conducted using liquid chromatography with tandem mass spectrometry (LC-MS/MS). A total of 372 embryos were collected. The metabolomics analysis revealed that 1,158 metabolites were detected, and 617 were annotated. In the before FSH injection samples, 121 differential metabolites were identified between the two groups. In the before artificial insemination samples, 129 differential metabolites were identified. In the before embryo collection samples, 201 differential metabolites were identified. A total of 11 differential metabolites were shared between the before FSH injection and before artificial insemination samples, while five differential metabolites were shared across all three samples. The majority of the differential metabolites were significantly enriched in pathways related to amino acid and fatty acid metabolism, digestive system secretion, and ovarian steroidogenesis. This study showed that phosphatidylcholine [PC; 14:0/22:1(13Z)], phosphatidylethanolamine [PE; DiMe (11, 3)], triacylglycerol [TG; 15:0/16:0/22:4 (7Z, 10Z, 13Z, 16Z)], phosphatidylinositol [PI; 16:0/22:2 (13Z, 16Z)], and phosphatidylserine [PS; 18:0/20:4(8Z, 11Z, 14Z, 17Z)] were differentially expressed in the serum during the superovulation period. These could serve as potential biomarkers for embryonic yield prediction in bovine superovulation. The lipid and amino acid metabolic pathways may have an impact on the ovarian response. The results of this study could provide novel screening indexes of donors for bovine superovulation, although the accuracy of the relevant factors requires further investigation.

通过代谢组学分析鉴定牛超排卵候选血液生物标志物。
超排卵和胚胎移植技术为提高牛群体的生产能力提供了强有力的支持。为提高超排卵预测的效率,需要一种无创的诊断方法。与大分子物质相比,小分子代谢物作为生物标志物的研究越来越多。本研究旨在通过血清代谢组学分析确定与奶牛超排卵结果相关的关键生物标志物。本研究选取36头诱导发情奶牛,分别在FSH注射前、人工授精前和胚胎采集前三个时间点采集血液样本。然后,根据胚胎总数将奶牛分为高胚胎产量组(HEY)和低胚胎产量组(LEY)。此外,采用液相色谱串联质谱(LC-MS/MS)对两组患者进行血清非靶向代谢组学分析。共收集胚胎372个。代谢组学分析显示,检测到1158种代谢物,其中617种被注释。在FSH注射前的样品中,两组之间鉴定出121种差异代谢物。在人工授精前的样本中,鉴定出129种差异代谢物。在胚胎采集前的样品中,鉴定出201种差异代谢物。在FSH注射前和人工授精前的样本中共有11种差异代谢物,而在所有三个样本中共有5种差异代谢物。大多数差异代谢物在氨基酸和脂肪酸代谢、消化系统分泌和卵巢类固醇生成相关的途径中显著富集。本研究表明磷脂酰胆碱[PC;14:0/22:1(13Z)],磷脂酰乙醇胺[PE;DiMe(11,3)],三酰基甘油[TG;15:0/16:0/22:4 (7Z, 10Z, 13Z, 16Z)],磷脂酰肌醇[PI;16:0/22:2 (13Z, 16Z)]和磷脂酰丝氨酸[PS;[18:0 . 20:4] (8Z, 11Z, 14Z, 17Z)在超排卵期血清中有差异表达。这些可以作为预测牛超排卵胚胎产量的潜在生物标志物。脂质和氨基酸代谢途径可能对卵巢反应有影响。本研究结果为牛超排卵供体筛选提供了新的指标,但相关因素的准确性有待进一步研究。
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
Frontiers in Veterinary Science
Frontiers in Veterinary Science Veterinary-General Veterinary
CiteScore
4.80
自引率
9.40%
发文量
1870
审稿时长
14 weeks
期刊介绍: Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy. Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field. Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.
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