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一氧化氮合酶通过 ERK-NF-κB 通路调节虾肠道微生物组稳态。

Nitric Oxide Synthase Regulates Gut Microbiota Homeostasis by ERK-NF-κB Pathway in Shrimp.

机构信息

Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, China.

出版信息

Front Immunol. 2021 Dec 3;12:778098. doi: 10.3389/fimmu.2021.778098. eCollection 2021.

Abstract

The gut microbiota is a complex group of microorganisms that is not only closely related to intestinal immunity but also affects the whole immune system of the body. Antimicrobial peptides and reactive oxygen species participate in the regulation of gut microbiota homeostasis in invertebrates. However, it is unclear whether nitric oxide, as a key mediator of immunity that plays important roles in antipathogen activity and immune regulation, participates in the regulation of gut microbiota homeostasis. In this study, we identified a nitric oxide synthase responsible for NO production in the shrimp . The expression of and the NO concentration in the gastrointestinal tract were increased significantly in shrimp orally infected with . After RNA interference of or treatment with an inhibitor of NOS, L-NMMA, NO production decreased and the gut bacterial load increased significantly in shrimp. Treatment with the NO donor, sodium nitroprusside, increased the NO level and reduced the bacterial load significantly in the shrimp gastrointestinal tract. Mechanistically, infection increased NO level upregulation of NOS and induced phosphorylation of ERK. The activated ERK phosphorylated the NF-κB-like transcription factor, dorsal, and caused nuclear translocation of dorsal to increase expression of antimicrobial peptides (AMPs) responsible for bacterial clearance. In summary, as a signaling molecule, NOS-produced NO regulates intestinal microbiota homeostasis by promoting AMP expression against infected pathogens the ERK-dorsal pathway in shrimp.

摘要

肠道微生物群是一组复杂的微生物群,不仅与肠道免疫密切相关,而且还影响全身免疫系统。抗菌肽和活性氧参与无脊椎动物肠道微生物群稳态的调节。然而,尚不清楚作为在抗病原体活性和免疫调节中发挥重要作用的免疫关键介质的一氧化氮是否参与肠道微生物群稳态的调节。在这项研究中,我们鉴定了一种在虾中负责产生 NO 的一氧化氮合酶。在虾经口感染 后, 和肠道中的 NO 浓度显著增加。在虾中干扰 或用 NOS 抑制剂 L-NMMA 处理后,NO 产生减少,肠道细菌负荷显著增加。NO 供体硝普钠处理可显著增加虾胃肠道中的 NO 水平并降低细菌负荷。在机制上, 感染通过上调 NOS 增加 NO 水平并诱导 ERK 磷酸化。激活的 ERK 磷酸化 NF-κB 样转录因子 dorsal,导致 dorsal 核转位,增加负责清除细菌的抗菌肽 (AMP) 的表达。总之,作为一种信号分子,NOS 产生的 NO 通过促进 AMP 表达来调节肠道微生物群稳态,从而对抗感染病原体。在虾中,该途径涉及 ERK-dorsal 通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a78/8678275/71eac43c9844/fimmu-12-778098-g001.jpg

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