Integrated omics profiling of individual variations in intestinal damage to the soybean allergen in piglets.

IF 2.9 2区 农林科学 Q1 VETERINARY SCIENCES Frontiers in Veterinary Science Pub Date : 2025-01-15 eCollection Date: 2024-01-01 DOI:10.3389/fvets.2024.1521544
Mengmeng Mi, Yaqing Zheng, Xin Fu, Nan Bao, Li Pan, Guixin Qin, Yuan Zhao
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Abstract

Introduction: A small number of soybean allergens [including Glycinin (11S) and β-Conglycinin (7S)] in the commercially available corn-soybean meal diet can still cause allergy in some weaned piglets, which may be the result of the interaction of genetic, and nutrition, but the specific mechanism is still unclear.

Methods: In this study, 20 allergic piglets and 20 non-allergic piglets were selected from 92 weaned piglets by skin sensitization tests, which were used to examine the whole sequence genome. The indicators related to humoral and cellular immunity, transcriptomics, and metabolomics analysis were determined by randomly selecting 5 boars in the allergic group and non-allergic group and then performing a validation in vitro.

Results: The sensitization rate of soybean antigen in the corn-soybean meal diet was 21.74% and there was a gender difference with the sensitization rate of female pigs (31.34%) being higher than that of male pigs (13.23%). Moreover, the levels of inflammatory factors (IL-1β, IL-4, TNF-α) and antibodies (IgG, IgE, and specific IgG) in allergic piglets were significantly higher than those in non-allergic piglets (P < 0.05). Whole genome re-sequencing analysis revealed specific mutations in the exons and URT5 of TRAPPC2, PIR, CFP, and SOWAHD genes and showed significantly higher expression levels of related genes in the spleen of allergic piglets (P < 0.05). Transcriptome analysis identified IL17REL, CCL19, CD1E, CD1.1, etc. immune differential genes, metabolomics results showed that soybean antigen affected the utilization and metabolism of intestinal nutrients in piglets, mainly the digestion and absorption of protein and the synthesis and metabolism of amino acids. Transfection of CFP/TRAPPC2/CCL19 siRNA could partially alleviate the injury of RAW264.7 cells or IPEC-J2 cells induced by β-Conglycinin.

Conclusion: Therefore, the individual differences in intestinal damage induced by soybean antigen protein in the corn-soybean meal diet are closely related to PIR, CFP, TRAPPC2, SOWAHD, and CCL19 genes. Soybean antigens affect the intestinal nutrient utilization and metabolism of piglets, which provides a scientific reference for the study of soybean antigen sensitization mechanisms, precision nutrition, disease prevention, and control of piglets, and also lays a foundation for human foodborne diseases.

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大豆过敏原对仔猪肠道损伤个体差异的综合组学分析。
导语:市售玉米-豆粕日粮中少量大豆过敏原[包括甘氨酸(11S)和β-甘氨酸(7S)]仍可引起部分断奶仔猪过敏,可能是遗传和营养相互作用的结果,但具体机制尚不清楚。方法:本研究从92头断奶仔猪中选取20头过敏仔猪和20头非过敏仔猪进行皮肤致敏试验,采用全序列基因组检测。随机选择过敏组和非过敏组5头公猪,进行体液免疫和细胞免疫相关指标、转录组学和代谢组学分析,并进行体外验证。结果:玉米-豆粕型饲粮中大豆抗原的致敏率为21.74%,且存在性别差异,母猪的致敏率(31.34%)高于公猪(13.23%)。过敏仔猪的炎症因子(IL-1β、IL-4、TNF-α)和抗体(IgG、IgE和特异性IgG)水平显著高于非过敏仔猪(P < 0.05)。全基因组重测序分析发现,TRAPPC2、PIR、CFP和SOWAHD基因外显子和URT5发生特异性突变,相关基因在过敏仔猪脾脏中的表达水平显著升高(P < 0.05)。转录组分析鉴定出IL17REL、CCL19、CD1E、CD1.1等免疫差异基因,代谢组学结果显示大豆抗原影响仔猪肠道营养物质的利用和代谢,主要影响蛋白质的消化吸收和氨基酸的合成代谢。转染CFP/TRAPPC2/CCL19 siRNA可部分减轻β- conglycin对RAW264.7细胞或IPEC-J2细胞的损伤。结论:因此,玉米-豆粕日粮中大豆抗原蛋白诱导肠道损伤的个体差异与PIR、CFP、TRAPPC2、SOWAHD和CCL19基因密切相关。大豆抗原影响仔猪肠道营养物质利用和代谢,为研究大豆抗原致敏机制、仔猪精准营养、疾病防治等提供科学参考,也为人类食源性疾病研究奠定基础。
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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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