• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

异常的脂肪组织衍生微生物会引发代谢紊乱,并加剧仔猪出生后的生长迟缓。

Abnormal adipose tissue-derived microbes drive metabolic disorder and exacerbate postnatal growth retardation in piglet.

作者信息

Song Tongxing, Qi Ming, Zhu Yucheng, Wang Nan, Liu Zhibo, Li Na, Yang Jiacheng, Han Yanxu, Wang Jing, Tao Shiyu, Ren Zhuqing, Yin Yulong, Zheng Jinshui, Tan Bie

机构信息

College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, China.

College of Animal Science and Technology, Hunan Agricultural University, Changsha, Hunan 410000, China.

出版信息

Life Metab. 2024 Jan 17;3(2):load052. doi: 10.1093/lifemeta/load052. eCollection 2024 Apr.

DOI:10.1093/lifemeta/load052
PMID:39872217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11749387/
Abstract

Postnatal growth retardation (PGR) frequently occurs during early postnatal development of piglets and induces high mortality. To date, the mechanism of PGR remains poorly understood. Adipose tissue-derived microbes have been documented to be associated with several disorders of metabolism and body growth. However, the connection between microbial disturbance of adipose tissue and pig PGR remains unclear. Here, we investigated piglets with PGR and found that the adipose tissue of PGR piglets was characterized by metabolism impairment, adipose abnormality, and specific enrichment of culturable bacteria from . Gavage of , a species of genus from the , induced PGR in piglets. Moreover, this bacterium could also lead to metabolic disorders and susceptibility to acute stress, resulting in weight loss in mice. Mechanistically, multi-omics analysis indicated the changes in lipid metabolism as a response of adipose tissue to abnormal microbial composition. Further experimental tests proved that one of the altered lipids phosphatidylethanolamines could rescue the metabolism disorder and growth retardation, thereby suppressing the amount of in the adipose tissue. Together, these results highlight that the microbe-host crosstalk may regulate the metabolic function of adipose tissue in response to PGR.

摘要

产后生长迟缓(PGR)在仔猪出生后的早期发育阶段频繁发生,并导致高死亡率。迄今为止,PGR的机制仍知之甚少。有文献记载,脂肪组织衍生的微生物与多种代谢紊乱和身体生长有关。然而,脂肪组织的微生物紊乱与仔猪PGR之间的联系仍不清楚。在此,我们对患有PGR的仔猪进行了研究,发现PGR仔猪的脂肪组织具有代谢受损、脂肪异常以及来自[具体来源未明确]的可培养细菌的特异性富集等特征。用来自[具体属]属的一种[具体菌种]对仔猪进行灌胃,可诱导仔猪出现PGR。此外,这种细菌还可导致代谢紊乱和对急性应激的易感性,致使小鼠体重减轻。从机制上讲,多组学分析表明脂质代谢的变化是脂肪组织对异常微生物组成的一种反应。进一步的实验测试证明,一种改变的脂质磷脂酰乙醇胺可以挽救代谢紊乱和生长迟缓,从而抑制脂肪组织中[具体物质未明确]的量。总之,这些结果突出表明,微生物与宿主之间的相互作用可能会调节脂肪组织的代谢功能以应对PGR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c9f/11749387/784e3b067bba/load052_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c9f/11749387/784e3b067bba/load052_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c9f/11749387/784e3b067bba/load052_fig9.jpg

相似文献

1
Abnormal adipose tissue-derived microbes drive metabolic disorder and exacerbate postnatal growth retardation in piglet.异常的脂肪组织衍生微生物会引发代谢紊乱,并加剧仔猪出生后的生长迟缓。
Life Metab. 2024 Jan 17;3(2):load052. doi: 10.1093/lifemeta/load052. eCollection 2024 Apr.
2
β-hydroxybutyrate administration improves liver injury and metabolic abnormality in postnatal growth retardation piglets.给予β-羟基丁酸可改善出生后生长迟缓仔猪的肝损伤和代谢异常。
Front Vet Sci. 2023 Nov 3;10:1294095. doi: 10.3389/fvets.2023.1294095. eCollection 2023.
3
Postnatal growth retardation is associated with deteriorated intestinal mucosal barrier function using a porcine model.利用猪模型研究发现,出生后生长迟缓与肠道黏膜屏障功能恶化有关。
J Cell Physiol. 2021 Apr;236(4):2631-2648. doi: 10.1002/jcp.30028. Epub 2020 Aug 27.
4
Small intestinal transcriptome analysis revealed changes of genes involved in nutrition metabolism and immune responses in growth retardation piglets1.小肠转录组分析揭示了生长迟缓仔猪中与营养代谢和免疫反应相关基因的变化1。
J Anim Sci. 2019 Sep 3;97(9):3795-3808. doi: 10.1093/jas/skz205.
5
Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets.新生儿生长迟缓与仔猪肠黏膜线粒体功能障碍和能量状态异常有关。
J Cell Mol Med. 2020 Sep;24(17):10100-10111. doi: 10.1111/jcmm.15621. Epub 2020 Jul 15.
6
Phosphatidylethanolamine Improves Postnatal Growth Retardation by Regulating Mucus Secretion of Intestinal Goblet Cells in Piglets.磷脂酰乙醇胺通过调节仔猪肠道杯状细胞黏液分泌改善出生后生长迟缓。
Animals (Basel). 2024 Apr 16;14(8):1193. doi: 10.3390/ani14081193.
7
Supplementation of palmitoleic acid improved piglet growth and reduced body temperature drop upon cold exposure.补充棕榈油酸可改善仔猪生长状况,降低仔猪受寒时体温下降幅度。
J Anim Sci. 2023 Jan 3;101. doi: 10.1093/jas/skad372.
8
The impact of wild-boar-derived microbiota transplantation on piglet microbiota, metabolite profile, and gut proinflammatory cytokine production differs from sow-derived microbiota.野猪源微生物群移植对仔猪微生物群、代谢物谱和肠道促炎细胞因子产生的影响不同于母猪源微生物群。
Appl Environ Microbiol. 2025 Mar 19;91(3):e0226524. doi: 10.1128/aem.02265-24. Epub 2025 Feb 4.
9
Translocation of gut microbes to epididymal white adipose tissue drives lipid metabolism disorder under heat stress.热应激下肠道微生物易位至附睾白色脂肪组织会导致脂质代谢紊乱。
Sci China Life Sci. 2023 Dec;66(12):2877-2895. doi: 10.1007/s11427-022-2320-y. Epub 2023 Jul 17.
10
Transcriptome Analysis Reveals the Early Development in Subcutaneous Adipose Tissue of Laiwu Piglets.转录组分析揭示莱芜仔猪皮下脂肪组织的早期发育
Animals (Basel). 2024 Oct 14;14(20):2955. doi: 10.3390/ani14202955.

本文引用的文献

1
Tumor-resident intracellular microbiota promotes metastatic colonization in breast cancer.肿瘤驻留细胞内微生物群促进乳腺癌的转移定植。
Cell. 2022 Apr 14;185(8):1356-1372.e26. doi: 10.1016/j.cell.2022.02.027. Epub 2022 Apr 7.
2
Importance of the pig as a human biomedical model.猪作为人类生物医学模型的重要性。
Sci Transl Med. 2021 Nov 24;13(621):eabd5758. doi: 10.1126/scitranslmed.abd5758.
3
Microbiota in mesenteric adipose tissue from Crohn's disease promote colitis in mice.肠黏膜脂肪组织中的微生物群促进克罗恩病小鼠的结肠炎
Microbiome. 2021 Nov 23;9(1):228. doi: 10.1186/s40168-021-01178-8.
4
Metabolic control of T cells and humoral immunity by phosphatidylethanolamine.磷脂酰乙醇胺对 T 细胞和体液免疫的代谢控制。
Nature. 2021 Jul;595(7869):724-729. doi: 10.1038/s41586-021-03692-z. Epub 2021 Jul 7.
5
Gut microbiome contributions to altered metabolism in a pig model of undernutrition.肠道微生物组对营养不良猪模型代谢改变的贡献。
Proc Natl Acad Sci U S A. 2021 May 25;118(21). doi: 10.1073/pnas.2024446118.
6
Lipid and glucose metabolism in white adipocytes: pathways, dysfunction and therapeutics.白色脂肪细胞中的脂类和糖代谢:途径、功能障碍与治疗学。
Nat Rev Endocrinol. 2021 May;17(5):276-295. doi: 10.1038/s41574-021-00471-8. Epub 2021 Feb 24.
7
The microbiota-gut-brain axis: A novel nutritional therapeutic target for growth retardation.肠道菌群-肠-脑轴:生长迟缓的新型营养治疗靶点。
Crit Rev Food Sci Nutr. 2022;62(18):4867-4892. doi: 10.1080/10408398.2021.1879004. Epub 2021 Feb 1.
8
Systemic Immunoregulatory Consequences of Gut Commensal Translocation.肠道共生菌易位的系统性免疫调节后果。
Trends Immunol. 2021 Feb;42(2):137-150. doi: 10.1016/j.it.2020.12.005.
9
Identification of new enterosynes using prebiotics: roles of bioactive lipids and mu-opioid receptor signalling in humans and mice.利用益生元鉴定新型肠促胰素:生物活性脂质和μ-阿片受体信号通路在人和小鼠中的作用。
Gut. 2021 Jun;70(6):1078-1087. doi: 10.1136/gutjnl-2019-320230. Epub 2020 Oct 5.
10
Translocation of Viable Gut Microbiota to Mesenteric Adipose Drives Formation of Creeping Fat in Humans.肠道共生菌易位至肠系膜脂肪促进人类“爬行脂肪”的形成。
Cell. 2020 Oct 29;183(3):666-683.e17. doi: 10.1016/j.cell.2020.09.009. Epub 2020 Sep 28.