Eubacterium siraeum suppresses fat deposition via decreasing the tyrosine-mediated PI3K/AKT signaling pathway in high-fat diet-induced obesity.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Xueshuang Lai, Shuang Liu, Jian Miao, Ran Shen, Zhen Wang, Zhe Zhang, Huanfa Gong, Meng Li, Yuchun Pan, Qishan Wang
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引用次数: 0

Abstract

Background: Obesity in humans can lead to chronic diseases such as diabetes and cardiovascular disease. Similarly, subcutaneous fat (SCF) in pigs affects feed utilization, and excessive SCF can reduce the feed efficiency of pigs. Therefore, identifying factors that suppress fat deposition is particularly important. Numerous studies have implicated the gut microbiome in pigs' fat deposition, but research into its suppression remains scarce. The Lulai black pig (LL) is a hybrid breed derived from the Laiwu pig (LW) and the Yorkshire pig, with lower levels of SCF compared to the LW. In this study, we focused on these breeds to identify microbiota that regulate fat deposition. The key questions were: Which microbial populations reduce fat in LL pigs compared to LW pigs, and what is the underlying regulatory mechanism?

Results: In this study, we identified four different microbial strains, Eubacterium siraeum, Treponema bryantii, Clostridium sp. CAG:413, and Jeotgalibaca dankookensis, prevalent in both LW and LL pigs. Blood metabolome analysis revealed 49 differential metabolites, including tanshinone IIA and royal jelly acid, known for their anti-adipogenic properties. E. siraeum was strongly correlated with these metabolites, and its genes and metabolites were enriched in pathways linked to fatty acid degradation, glycerophospholipid, and glycerolipid metabolism. In vivo mouse experiments confirmed that E. siraeum metabolites curb weight gain, reduce SCF adipocyte size, increase the number of brown adipocytes, and regulate leptin, IL-6, and insulin secretion. Finally, we found that one important pathway through which E. siraeum inhibits fat deposition is by suppressing the phosphorylation of key proteins in the PI3K/AKT signaling pathway through the reduction of tyrosine.

Conclusions: We compared LW and LL pigs using fecal metagenomics, metabolomics, and blood metabolomics, identifying E. siraeum as a strain linked to fat deposition. Oral administration experiments in mice demonstrated that E. siraeum effectively inhibits fat accumulation, primarily through the suppression of the PI3K/AKT signaling pathway, a critical regulator of lipid metabolism. These findings provide a valuable theoretical basis for improving pork quality and offer insights relevant to the study of human obesity and related chronic metabolic diseases. Video Abstract.

在高脂饮食诱导的肥胖症中,西来酵母菌通过减少酪氨酸介导的 PI3K/AKT 信号通路抑制脂肪沉积。
背景:人类肥胖会导致糖尿病和心血管疾病等慢性疾病。同样,猪的皮下脂肪(SCF)也会影响饲料利用率,过多的皮下脂肪会降低猪的饲料效率。因此,确定抑制脂肪沉积的因素尤为重要。大量研究表明,肠道微生物组与猪的脂肪沉积有关,但对其抑制作用的研究仍然很少。鲁莱黑猪(LL)是由莱芜猪(LW)和约克夏猪(Yorkshire pig)杂交而来的品种,与莱芜猪相比,鲁莱黑猪的SCF水平较低。在本研究中,我们以这些猪种为研究对象,以确定调节脂肪沉积的微生物群。关键问题是与低体重猪相比,哪些微生物种群会减少低体重猪的脂肪,其潜在的调节机制是什么?在这项研究中,我们发现了四种不同的微生物菌株,分别是iraeum 幼杆菌、Treponema bryantii、CAG:413 梭状芽孢杆菌和 Jeotgalibaca dankookensis,它们在低体重猪和低体重猪中都很普遍。血液代谢组分析发现了 49 种不同的代谢物,包括丹参酮 IIA 和蜂王浆酸,它们具有抗脂肪生成的特性。E.siraeum与这些代谢物密切相关,其基因和代谢物富集于脂肪酸降解、甘油磷脂和甘油酯代谢的相关途径中。小鼠体内实验证实,E. siraeum代谢物可抑制体重增加,缩小SCF脂肪细胞体积,增加棕色脂肪细胞数量,调节瘦素、IL-6和胰岛素分泌。最后,我们发现未来草抑制脂肪沉积的一个重要途径是通过减少酪氨酸来抑制 PI3K/AKT 信号通路中关键蛋白的磷酸化:我们利用粪便元基因组学、代谢组学和血液代谢组学对低体重猪和低体重猪进行了比较,发现E. siraeum是一种与脂肪沉积有关的菌株。小鼠口服实验表明,E. siraeum能有效抑制脂肪堆积,主要是通过抑制PI3K/AKT信号通路(脂质代谢的关键调节因子)。这些发现为提高猪肉质量提供了宝贵的理论依据,并为人类肥胖症和相关慢性代谢疾病的研究提供了启示。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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