综合多组学鉴定乳羊在早期过渡期的脂质代谢失调。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Shuai Jiao, Fei Li, Tianxi Zhang, Guojie Yang, Ronghui Lu, Fadi Li, Long Guo, Zhiyuan Ma, Pengshan Zhao, Baocang Liu
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引用次数: 0

摘要

在早期过渡时期的轻瘫是一种普遍的代谢紊乱在多产的奶羊,其特点是一个复杂的和知之甚少的发病机制。本研究从产前21天至产后1天对一组奶羊进行了纵向监测。在此期间,采集血液、粪便和初乳样本。通过血浆代谢组学和粪便16S测序揭示了轻瘫的途径,并确定了潜在的早期生物标志物。健康奶羊(HDS)和轻瘫奶羊(PDS)在产前(未轻瘫)和产后(轻瘫)期间的生理参数存在差异。元素分析显示,与HDS相比,PDS初乳中的铜、钾和镁含量更高。产前HDS和PDS的代谢组学分析鉴定出37种差异代谢物,酰基肉碱(3-羟基十六烯二烯基肉碱和3-羟基辛烷二酰基肉碱)成为有希望的早期诊断生物标志物。16S rRNA测序显示了不同的微生物特征,在PDS中富含梭杆菌属和丹毒杆菌属,而在HDS中更丰富的是Faecalibacterium和Bacillus。整合产后多组学数据,发现PDS和HDS在甘油磷脂代谢、苯丙氨酸、酪氨酸和色氨酸的生物合成、甘氨酸、丝氨酸和苏氨酸的代谢以及原发性胆酸的生物合成方面存在差异。我们的研究结果表明,乳羊的围产期轻瘫与异常的脂质和氨基酸代谢有关,并发现了早期潜在的生物标志物,如酰基肉碱。本研究为通过有针对性的营养干预和疾病控制来预防和管理围产期轻瘫提供了重要的见解。重要意义本研究调查了乳羊早期过渡期的轻瘫,确定了早期诊断的代谢和生理指标。纵向监测揭示了健康羊和腹泻羊在糖脂谱、肝酶和氧化应激标志物方面的差异。代谢组学鉴定出37种产前差异代谢物,包括酰基肉碱,作为潜在的生物标志物。肠道菌群分析显示,腹泻羊的肠道菌群中富含梭杆菌属和红毒杆菌属,健康羊的肠道菌群中含有粪杆菌属和芽孢杆菌属。多组学数据的产后整合显示,乳羊的轻瘫与脂质代谢和氨基酸代谢密切相关。这些发现支持有针对性的营养策略,以减轻围产期代谢紊乱,提高奶羊的健康和生产力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated multi-omics identifies dysregulated lipid metabolism of paresis in dairy sheep during the early transition period.

Paresis during the early transition period is a prevalent metabolic disorder in prolific dairy sheep, characterized by a complex and poorly understood pathogenesis. This study longitudinally monitored a cohort of dairy sheep from 21 days antepartum to 1 day postpartum. During this period, blood, fecal, and colostrum samples were collected. The pathway of paresis was revealed by plasma metabolome and fecal 16S sequencing, and potential early biomarkers were identified. The physiological parameters of healthy dairy sheep (HDS) and paretic dairy sheep (PDS) differed in both the antepartum (not yet paresis) and postpartum (paresis) periods. Elemental analysis revealed higher levels of copper, potassium, and magnesium in PDS colostrum compared to HDS. Metabolomic analysis of HDS and PDS in antepartum identified 37 differential metabolites, with acylcarnitines (3-hydroxyhexadecadienoylcarnitine and 3-hydroxyoctanedioylcarnitine) emerging as promising early diagnostic biomarkers. 16S rRNA sequencing revealed distinct microbial signatures, with genera such as Fusobacterium and Erysipelatoclostridium enriched in PDS, whereas Faecalibacterium and Bacillus were more abundant in HDS. Integration of multi-omics data in postpartum revealed differences in glycerophospholipid metabolism, phenylalanine, tyrosine and tryptophan biosynthesis, glycine, serine and threonine metabolism, and primary bile acid biosynthesis between PDS and HDS. Our findings suggest that periparturient paresis in dairy sheep is linked to abnormal lipid and amino acid metabolism, with early potential biomarkers such as acylcarnitines identified. This study provides critical insights for developing strategies to prevent and manage periparturient paresis through targeted nutritional interventions and disease control.IMPORTANCEThis study investigates paresis in dairy sheep during the early transition period, identifying metabolic and physiological markers for early diagnosis. Longitudinal monitoring revealed prepartum differences in glucolipid profiles, liver enzymes, and oxidative stress markers between healthy and paretic sheep. Metabolomics identified 37 antepartum differential metabolites, including acylcarnitines, as potential biomarkers. Gut microbiota analysis revealed genera such as Fusobacterium and Erysipelatoclostridium enriched in paretic sheep, and Faecalibacterium and Bacillus in healthy individuals. Postnatal integration of multi-omics data revealed that paresis is closely associated with lipid metabolism and amino acid metabolism in dairy sheep. These findings support targeted nutritional strategies to mitigate periparturient metabolic disorders, enhancing dairy sheep health and productivity.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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