源自脂肪组织的异常微生物会导致代谢紊乱,并加剧仔猪出生后的生长迟缓。

Life metabolism Pub Date : 2024-01-17 eCollection Date: 2024-04-01 DOI:10.1093/lifemeta/load052
Tongxing Song, Ming Qi, Yucheng Zhu, Nan Wang, Zhibo Liu, Na Li, Jiacheng Yang, Yanxu Han, Jing Wang, Shiyu Tao, Zhuqing Ren, Yulong Yin, Jinshui Zheng, Bie Tan
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引用次数: 0

摘要

出生后生长迟缓(PGR)在仔猪出生后早期发育过程中经常发生,并导致高死亡率。迄今为止,PGR的机制仍然知之甚少。脂肪组织衍生的微生物已被证明与几种代谢和身体生长紊乱有关。然而,脂肪组织的微生物干扰与猪PGR之间的关系尚不清楚。本研究对PGR仔猪进行了研究,发现PGR仔猪的脂肪组织具有代谢障碍、脂肪异常和变形杆菌可培养细菌特异性富集的特征。仔猪灌胃少动鞘氨单胞菌(一种来自α变形菌门的鞘氨单胞菌属)诱导PGR。此外,这种细菌还可能导致代谢紊乱和对急性应激的易感性,从而导致小鼠体重减轻。机制上,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反应。进一步的实验证明,其中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鞘脂单胞菌的数量。总之,这些结果强调微生物-宿主串扰可能调节脂肪组织对PGR的代谢功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abnormal adipose tissue-derived microbes drive metabolic disorder and exacerbate postnatal growth retardation in piglet.

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 Proteobacteria. Gavage of Sphingomonas paucimobilis, a species of Sphingomonas genus from the alphaproteobacteria, 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 Sphingomonas 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.

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