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由呼吸微生物 Aeromicrobium camelliae 介导的溶酶磷脂缓解了 H9N2 对小鼠的挑战。

LysoPE mediated by respiratory microorganism Aeromicrobium camelliae alleviates H9N2 challenge in mice.

机构信息

College of Veterinary Medicine, Jilin Provincial Engineering Research Center of Animal Probiotics, Jilin Provincial Key Laboratory of Animal Microecology and Healthy Breeding, Engineering Research Center of Microecological Vaccines (Drugs) for Major Animal Diseases, Ministry of Education, Jilin Agricultural University, Changchun, 130118, China.

出版信息

Vet Res. 2024 Oct 11;55(1):136. doi: 10.1186/s13567-024-01391-x.

DOI:10.1186/s13567-024-01391-x
PMID:39390593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11468851/
Abstract

Influenza remains a severe respiratory illness that poses significant global health threats. Recent studies have identified distinct microbial communities within the respiratory tract, from nostrils to alveoli. This research explores specific anti-influenza respiratory microbes using a mouse model supported by 16S rDNA sequencing and untargeted metabolomics. The study found that transferring respiratory microbes from mice that survived H9N2 influenza to antibiotic-treated mice enhanced infection resistance. Notably, the levels of Aeromicrobium were significantly higher in the surviving mice. Mice pre-treated with antibiotics and then inoculated with Aeromicrobium camelliae showed reduced infection severity, as evidenced by decreased weight loss, higher survival rates, and lower lung viral titres. Metabolomic analysis revealed elevated LysoPE (16:0) levels in mildly infected mice. In vivo and in vitro experiments indicated that LysoPE (16:0) suppresses inducible nitric oxide synthase (INOS) and cyclooxygenase-2 (COX2) expression, enhancing anti-influenza defences. Our findings suggest that Aeromicrobium camelliae could serve as a potential agent for influenza prevention and a prognostic marker for influenza outcomes.

摘要

流感仍然是一种严重的呼吸道疾病,对全球健康构成重大威胁。最近的研究已经确定了呼吸道内的不同微生物群落,从鼻孔到肺泡。本研究使用 16S rDNA 测序和非靶向代谢组学的小鼠模型来探索特定的抗流感呼吸道微生物。研究发现,将存活 H9N2 流感的小鼠的呼吸道微生物转移到抗生素处理的小鼠中,增强了感染的抵抗力。值得注意的是,存活的小鼠中 Aeromicrobium 的水平明显更高。用抗生素预处理然后接种 Aeromicrobium camelliae 的小鼠表现出感染严重程度降低,体重减轻减少、存活率更高和肺部病毒滴度更低。代谢组学分析显示轻度感染的小鼠中 LysoPE(16:0)水平升高。体内和体外实验表明 LysoPE(16:0)抑制诱导型一氧化氮合酶(INOS)和环氧化酶-2(COX2)的表达,增强抗流感防御。我们的研究结果表明,Aeromicrobium camelliae 可能成为流感预防的潜在手段和流感结局的预后标志物。

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本文引用的文献

1
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J Vet Sci. 2023 Jan;24(1):e5. doi: 10.4142/jvs.22216. Epub 2022 Dec 5.
2
Status and Challenges for Vaccination against Avian H9N2 Influenza Virus in China.中国H9N2亚型禽流感病毒疫苗接种的现状与挑战
Life (Basel). 2022 Aug 27;12(9):1326. doi: 10.3390/life12091326.
3
Role of dietary amino acids and microbial metabolites in the regulation of pig intestinal health.日粮氨基酸和微生物代谢产物在猪肠道健康调节中的作用。
肠道微生物群衍生的异戊酸通过肠-肺轴改善流感病毒感染。
NPJ Biofilms Microbiomes. 2025 Jul 1;11(1):116. doi: 10.1038/s41522-025-00753-3.
Anim Nutr. 2021 Oct 23;9:1-6. doi: 10.1016/j.aninu.2021.10.004. eCollection 2022 Jun.
4
0111 Protects Against Influenza Virus by Modulating Intestinal Microbial-Mediated Immune Responses.0111 通过调节肠道微生物介导的免疫反应预防流感病毒。
Front Microbiol. 2022 Jun 30;13:820484. doi: 10.3389/fmicb.2022.820484. eCollection 2022.
5
Natural Reassortment of Eurasian Avian-Like Swine H1N1 and Avian H9N2 Influenza Viruses in Pigs, China.中国猪中欧亚类禽 H1N1 和禽 H9N2 流感病毒的自然重配。
Emerg Infect Dis. 2022 Jul;28(7):1509-1512. doi: 10.3201/eid2807.220642.
6
Interactions between Influenza A Virus Nucleoprotein and Gene Segment Untranslated Regions Facilitate Selective Modulation of Viral Gene Expression.甲型流感病毒核蛋白与基因片段非翻译区的相互作用有助于病毒基因表达的选择性调节。
J Virol. 2022 May 25;96(10):e0020522. doi: 10.1128/jvi.00205-22. Epub 2022 Apr 25.
7
Probiotics as a biotherapeutics for the management and prevention of respiratory tract diseases.益生菌作为一种生物治疗剂,用于管理和预防呼吸道疾病。
Microbiol Immunol. 2022 Jun;66(6):277-291. doi: 10.1111/1348-0421.12980. Epub 2022 May 27.
8
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9
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Front Vet Sci. 2022 Feb 8;8:824179. doi: 10.3389/fvets.2021.824179. eCollection 2021.