• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

揭示上呼吸道微生物群在新冠病毒易感性和严重程度中的作用。

Unveiling the role of the upper respiratory tract microbiome in susceptibility and severity to COVID-19.

作者信息

von Ameln Lovison Otávio, Zempulski Volpato Fabiana Caroline, Weber Lorenzo Gómez, Barth Afonso Luis, Simon Coitinho Adriana, Martins Andreza Francisco

机构信息

Laboratório de Pesquisa em Resistência Bacteriana (LABRESIS), Hospital de Clínicas de Porto Alegre (HCPA), Centro de Pesquisa Experimental, Porto Alegre, Brazil.

Laboratório de Microbiologia e Saúde Única do Instituto de Ciências Básicas da Saúde (ICBS) da Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

出版信息

Front Cell Infect Microbiol. 2025 May 13;15:1531084. doi: 10.3389/fcimb.2025.1531084. eCollection 2025.

DOI:10.3389/fcimb.2025.1531084
PMID:40433668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12106449/
Abstract

It is argued that commensal bacteria in the upper respiratory tract (URT) protect against pathogen colonization and infection, including respiratory viruses. Given that the microbiome can mediate immune modulation, a link between the URT microbiome (URTM) and COVID-19 susceptibility and severity is expected. This 16S metagenomics cross-sectional study assessed URTM composition, metabolic prediction, and association with laboratory biomarkers in non-COVID-19 pneumonia (NO-CoV), moderate (M-CoV), severe (S-CoV) COVID-19 patients, as well as COVID-19-negative, asymptomatic (NC) patients. The S-CoV group exhibited reduced URTM diversity, primarily due to a decreased abundance of eubiotic taxa. Some of these taxa (e.g., sp., sp.) were also associated with inflammatory biomarkers. Multiple metabolic pathways (e.g., short-chain fatty acids, vitamin B12) linked to immune response, antiviral activity, and host susceptibility showed decreased abundance in S-CoV. These pathways could suggest potential alternatives for the therapeutic arsenal against COVID-19, providing reassurance about the progress in understanding and treating this disease.

摘要

有人认为,上呼吸道(URT)中的共生细菌可预防病原体定植和感染,包括呼吸道病毒。鉴于微生物群可介导免疫调节,预计URT微生物群(URTM)与COVID-19易感性和严重程度之间存在联系。这项16S宏基因组学横断面研究评估了非COVID-19肺炎(NO-CoV)、中度(M-CoV)、重度(S-CoV)COVID-19患者以及COVID-19阴性无症状(NC)患者的URTM组成、代谢预测以及与实验室生物标志物的关联。S-CoV组的URTM多样性降低,主要是由于有益生物类群的丰度降低。其中一些类群(如 属、 属)也与炎症生物标志物有关。与免疫反应、抗病毒活性和宿主易感性相关的多种代谢途径(如短链脂肪酸、维生素B12)在S-CoV组中的丰度降低。这些途径可能为对抗COVID-19的治疗手段提供潜在的替代方案,为理解和治疗这种疾病的进展提供保障。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/8388bbfc9d01/fcimb-15-1531084-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/cda712585ec2/fcimb-15-1531084-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/8ce8af69be66/fcimb-15-1531084-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/3dcc60b794f8/fcimb-15-1531084-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/8388bbfc9d01/fcimb-15-1531084-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/cda712585ec2/fcimb-15-1531084-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/8ce8af69be66/fcimb-15-1531084-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/3dcc60b794f8/fcimb-15-1531084-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b5/12106449/8388bbfc9d01/fcimb-15-1531084-g004.jpg

相似文献

1
Unveiling the role of the upper respiratory tract microbiome in susceptibility and severity to COVID-19.揭示上呼吸道微生物群在新冠病毒易感性和严重程度中的作用。
Front Cell Infect Microbiol. 2025 May 13;15:1531084. doi: 10.3389/fcimb.2025.1531084. eCollection 2025.
2
SARS-CoV-2 infection and viral load are associated with the upper respiratory tract microbiome.SARS-CoV-2 感染和病毒载量与上呼吸道微生物组有关。
J Allergy Clin Immunol. 2021 Apr;147(4):1226-1233.e2. doi: 10.1016/j.jaci.2021.02.001. Epub 2021 Feb 9.
3
Signatures of COVID-19 Severity and Immune Response in the Respiratory Tract Microbiome.COVID-19 严重程度和呼吸道微生物组免疫反应特征。
mBio. 2021 Aug 31;12(4):e0177721. doi: 10.1128/mBio.01777-21. Epub 2021 Aug 17.
4
General dynamics of the URT microbiome and microbial signs of recovery in COVID-19 patients.COVID-19患者上呼吸道微生物群的一般动态及恢复的微生物迹象。
Benef Microbes. 2024 Feb 22;15(2):145-164. doi: 10.1163/18762891-bja00004.
5
Severe COVID-19 Is Associated With an Altered Upper Respiratory Tract Microbiome.严重 COVID-19 与上呼吸道微生物组改变有关。
Front Cell Infect Microbiol. 2022 Jan 24;11:781968. doi: 10.3389/fcimb.2021.781968. eCollection 2021.
6
Metagenomic Next-Generation Sequencing of Nasopharyngeal Specimens Collected from Confirmed and Suspect COVID-19 Patients.对确诊和疑似 COVID-19 患者的鼻咽拭子标本进行宏基因组下一代测序。
mBio. 2020 Nov 20;11(6):e01969-20. doi: 10.1128/mBio.01969-20.
7
The Upper Respiratory Tract Microbiome Network Impacted by SARS-CoV-2.上呼吸道微生物组网络受 SARS-CoV-2 影响。
Microb Ecol. 2023 Aug;86(2):1428-1437. doi: 10.1007/s00248-022-02148-9. Epub 2022 Dec 13.
8
High abundance of butyrate-producing bacteria in the naso-oropharynx of SARS-CoV-2-infected persons in an African population: implications for low disease severity.在非洲人群中,SARS-CoV-2 感染患者的鼻咽部存在大量产生丁酸的细菌:这可能与疾病严重程度较低有关。
BMC Infect Dis. 2024 Sep 20;24(1):1020. doi: 10.1186/s12879-024-09948-z.
9
The characteristics of microbiome in the upper respiratory tract of COVID-19 patients.新型冠状病毒肺炎患者上呼吸道微生物群的特征
BMC Microbiol. 2024 Apr 24;24(1):138. doi: 10.1186/s12866-024-03281-w.
10
Prolonged Impairment of Short-Chain Fatty Acid and L-Isoleucine Biosynthesis in Gut Microbiome in Patients With COVID-19.COVID-19 患者肠道微生物组中短链脂肪酸和 L-异亮氨酸生物合成的长期损伤。
Gastroenterology. 2022 Feb;162(2):548-561.e4. doi: 10.1053/j.gastro.2021.10.013. Epub 2021 Oct 21.

本文引用的文献

1
COVID-19 mRNA vaccine-mediated antibodies in human breast milk and their association with breast milk microbiota composition.新冠病毒mRNA疫苗介导的人母乳抗体及其与母乳微生物群组成的关联。
NPJ Vaccines. 2023 Oct 5;8(1):151. doi: 10.1038/s41541-023-00745-4.
2
ggpicrust2: an R package for PICRUSt2 predicted functional profile analysis and visualization.ggpicrust2:一个用于 PICRUSt2 预测功能谱分析和可视化的 R 包。
Bioinformatics. 2023 Aug 1;39(8). doi: 10.1093/bioinformatics/btad470.
3
Gut bacterial metabolism contributes to host global purine homeostasis.
肠道细菌代谢有助于宿主嘌呤整体稳态。
Cell Host Microbe. 2023 Jun 14;31(6):1038-1053.e10. doi: 10.1016/j.chom.2023.05.011. Epub 2023 Jun 5.
4
coda4microbiome: compositional data analysis for microbiome cross-sectional and longitudinal studies.coda4microbiome:微生物组横断面和纵向研究的组成数据分析。
BMC Bioinformatics. 2023 Mar 6;24(1):82. doi: 10.1186/s12859-023-05205-3.
5
tRNA abundance, modification and fragmentation in nasopharyngeal swabs as biomarkers for COVID-19 severity.鼻咽拭子中tRNA丰度、修饰和片段化作为新冠病毒疾病严重程度的生物标志物
Front Cell Dev Biol. 2022 Nov 1;10:999351. doi: 10.3389/fcell.2022.999351. eCollection 2022.
6
Short Chain Fatty Acids: Fundamental mediators of the gut-lung axis and their involvement in pulmonary diseases.短链脂肪酸:肠-肺轴的基本介质及其在肺部疾病中的作用。
Chem Biol Interact. 2022 Dec 1;368:110231. doi: 10.1016/j.cbi.2022.110231. Epub 2022 Oct 23.
7
Vulnerability to SARS-CoV-2 infection and disease: ripping the curl after the storm.易感染 SARS-CoV-2 病毒和患病的脆弱性:风暴过后的余波。
Rev Esp Quimioter. 2022 Oct;35 Suppl 3(Suppl 3):2-5. doi: 10.37201/req/s03.01.2022. Epub 2022 Oct 24.
8
Oropharyngeal microbiome profiled at admission is predictive of the need for respiratory support among COVID-19 patients.入院时检测的口咽微生物群可预测COVID-19患者对呼吸支持的需求。
Front Microbiol. 2022 Sep 30;13:1009440. doi: 10.3389/fmicb.2022.1009440. eCollection 2022.
9
Alterations in the respiratory tract microbiome in COVID-19: current observations and potential significance.COVID-19 患者呼吸道微生物组的改变:当前观察结果及潜在意义。
Microbiome. 2022 Oct 5;10(1):165. doi: 10.1186/s40168-022-01342-8.
10
Dissecting the role of the human microbiome in COVID-19 via metagenome-assembled genomes.通过宏基因组组装基因组解析人类微生物组在 COVID-19 中的作用。
Nat Commun. 2022 Sep 6;13(1):5235. doi: 10.1038/s41467-022-32991-w.