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miRNA-146a 缺乏通过调节肠道微生物群来保护机体免受李斯特菌感染。

MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota.

机构信息

Key Laboratory of Zoonosis, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun 130062, China.

College of Animal Sciences, Jilin University, Changchun 130062, China.

出版信息

Int J Mol Sci. 2018 Mar 26;19(4):993. doi: 10.3390/ijms19040993.

Abstract

The gut microbiota and microRNAs play important roles in the defense against infection. However, the role of miR-146a in infection and gut microbiota remains unclear. We tried to determine whether miR-146a controlled infection by regulating the gut microbiota. Wild-type and miR-146a-deficient mice or macrophages were used to characterize the impact of miR-146a on animal survival, cell death, bacterial clearance, and gut microbiota following challenge. We found that infection induced miR-146a expression both in vitro and in vivo. When compared to wild-type mice, miR-146a-deficient mice were more resistant to infection. MiR-146a deficiency in macrophages resulted in reduced invasion and intracellular survival of . High-throughput sequencing of 16S rRNA revealed that the gut microbiota composition differed between miR-146a-deficient and wild-type mice. Relative to wild-type mice, miR-146a-deficient mice had decreased levels of the phylum, family, and genus, and significantly increased short-chain fatty acid producing bacteria, including the genera , , and . Wild-type mice co-housed with miR-146a-deficient mice had increased resistance to , indicating that miR-146a deficiency guides the gut microbiota to alleviate infection. Together, these results suggest that miR-146a deficiency protects against infection by regulating the gut microbiota.

摘要

肠道微生物群和 microRNAs 在抗感染中发挥重要作用。然而,miR-146a 在 感染和肠道微生物群中的作用尚不清楚。我们试图确定 miR-146a 是否通过调节肠道微生物群来控制 感染。使用野生型和 miR-146a 缺陷型小鼠或巨噬细胞来表征 miR-146a 对动物存活、细胞死亡、细菌清除和 感染后肠道微生物群的影响。我们发现, 感染在体外和体内均诱导 miR-146a 的表达。与野生型小鼠相比,miR-146a 缺陷型小鼠对 感染的抵抗力更强。巨噬细胞中 miR-146a 的缺失导致 的侵袭和细胞内存活减少。16S rRNA 的高通量测序显示,miR-146a 缺陷型和野生型小鼠的肠道微生物群组成存在差异。与野生型小鼠相比,miR-146a 缺陷型小鼠的 门、 科和 属水平降低,而短链脂肪酸产生菌,包括 属、 属、 属和 属,显著增加。与 miR-146a 缺陷型小鼠共饲养的野生型小鼠对 感染的抵抗力增加,表明 miR-146a 缺陷型指导肠道微生物群减轻感染。总之,这些结果表明,miR-146a 缺乏通过调节肠道微生物群来保护机体免受 感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4edf/5979314/fb53c1f62b5d/ijms-19-00993-g001.jpg

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