• 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

肠道微生物群变化对小鼠免疫功能的影响。

Influence of changes in the intestinal microflora on the immune function in mice.

作者信息

Kishida Shigefumi, Kato-Mori Yuko, Hagiwara Katsuro

机构信息

School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Hokkaido 069-8501 Japan.

Graduate School of Science, Technology and Innovation, Kobe University, Hyogo 657-8501, Japan.

出版信息

J Vet Med Sci. 2018 Mar 24;80(3):440-446. doi: 10.1292/jvms.17-0485. Epub 2018 Feb 8.

DOI:10.1292/jvms.17-0485
PMID:29415902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5880823/
Abstract

The composition of the intestinal microbiota is related to the health and immune function of the host. Administration of antibiotics affects the composition of the intestinal microbiota. However, the effects of immune function on the composition of the intestinal microbiota are still unclear. In this study, we investigated the lymphocyte composition and determined the relationships between lymphocyte function and the intestinal microbiota following antibiotic treatment in mice. To change the composition of the intestinal microbiota, mice were treated with or without antibiotics. Analysis of intestinal microbiota was performed by metagenomic analysis targeting 16S rRNA. Lymphocyte subsets of splenocytes were measured by flow cytometry. For functional analysis of T cells, splenocytes were stimulated with concanavalin (Con A), and cytokine gene expression was measured by real-time polymerase chain reaction. Firmicutes were predominant in the control group, whereas Bacteroidetes predominated in the antibiotic-treated group, as determined by metagenomic analysis. The diversity of the microbiota decreased in the antibiotic-treated group. Analysis of lymphocyte subsets showed that CD3 cells decreased, whereas CD19 cells increased in the antibiotic-treated group. All cytokine genes in splenocytes treated with Con A were downregulated in the antibiotic-treated group; in particular, genes encoding interferon-γ, interleukin (IL)-6, and IL-13 significantly decreased. Taken together, these results revealed that changes in the composition of the intestinal microbiota by antibiotic treatment influenced the population of lymphocytes in splenocytes and affected the immune response.

摘要

肠道微生物群的组成与宿主的健康和免疫功能相关。抗生素的使用会影响肠道微生物群的组成。然而,免疫功能对肠道微生物群组成的影响仍不清楚。在本研究中,我们调查了淋巴细胞组成,并确定了小鼠抗生素治疗后淋巴细胞功能与肠道微生物群之间的关系。为了改变肠道微生物群的组成,对小鼠进行了有无抗生素治疗。通过针对16S rRNA的宏基因组分析进行肠道微生物群分析。通过流式细胞术测量脾细胞的淋巴细胞亚群。为了对T细胞进行功能分析,用伴刀豆球蛋白(Con A)刺激脾细胞,并通过实时聚合酶链反应测量细胞因子基因表达。宏基因组分析确定,对照组中厚壁菌门占主导,而抗生素治疗组中拟杆菌门占主导。抗生素治疗组中微生物群的多样性降低。淋巴细胞亚群分析表明,抗生素治疗组中CD3细胞减少,而CD19细胞增加。用Con A处理的脾细胞中的所有细胞因子基因在抗生素治疗组中均下调;特别是,编码干扰素-γ、白细胞介素(IL)-6和IL-13的基因显著减少。综上所述,这些结果表明抗生素治疗引起的肠道微生物群组成变化影响了脾细胞中淋巴细胞的数量,并影响了免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/8982c5ebbdf2/jvms-80-440-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/2bebbcf5be07/jvms-80-440-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/21c78b381740/jvms-80-440-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/3416d3fc9059/jvms-80-440-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/d69fb56d0af7/jvms-80-440-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/8982c5ebbdf2/jvms-80-440-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/2bebbcf5be07/jvms-80-440-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/21c78b381740/jvms-80-440-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/3416d3fc9059/jvms-80-440-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/d69fb56d0af7/jvms-80-440-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aed/5880823/8982c5ebbdf2/jvms-80-440-g005.jpg

相似文献

1
Influence of changes in the intestinal microflora on the immune function in mice.肠道微生物群变化对小鼠免疫功能的影响。
J Vet Med Sci. 2018 Mar 24;80(3):440-446. doi: 10.1292/jvms.17-0485. Epub 2018 Feb 8.
2
The Probiotic Compound VSL#3 Modulates Mucosal, Peripheral, and Systemic Immunity Following Murine Broad-Spectrum Antibiotic Treatment.益生菌组合VSL#3对小鼠进行广谱抗生素治疗后的黏膜、外周和全身免疫具有调节作用。
Front Cell Infect Microbiol. 2017 May 5;7:167. doi: 10.3389/fcimb.2017.00167. eCollection 2017.
3
Effect of administration of a probiotic preparation on gut microbiota and immune response in healthy women in India: an open-label, single-arm pilot study.益生菌制剂对印度健康女性肠道微生物群和免疫反应的影响:一项开放标签、单臂试点研究。
BMC Gastroenterol. 2018 Jun 15;18(1):85. doi: 10.1186/s12876-018-0819-6.
4
[Effects of ovalbumin atomization on the T lymphocyte subsets of BALB/c mice with intestinal microflora disruption].
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2010 May;26(5):473-6.
5
Long-term effects of early life microbiota disturbance on adaptive immunity in laying hens.早期生命微生物群紊乱对蛋鸡适应性免疫的长期影响。
Poult Sci. 2016 Jul 1;95(7):1543-1554. doi: 10.3382/ps/pew088. Epub 2016 Mar 14.
6
Perturbation of microbiota in one-day old broiler chickens with antibiotic for 24 hours negatively affects intestinal immune development.用抗生素处理一日龄肉鸡24小时会扰乱其微生物群,对肠道免疫发育产生负面影响。
BMC Genomics. 2017 Mar 20;18(1):241. doi: 10.1186/s12864-017-3625-6.
7
Streptomycin treatment alters the intestinal microbiome, pulmonary T cell profile and airway hyperresponsiveness in a cystic fibrosis mouse model.链霉素治疗可改变囊性纤维化小鼠模型的肠道微生物群、肺部T细胞谱和气道高反应性。
Sci Rep. 2016 Jan 12;6:19189. doi: 10.1038/srep19189.
8
Antibiotics in 16-day-old broilers temporarily affect microbial and immune parameters in the gut.16 日龄肉鸡中使用抗生素会暂时影响肠道中的微生物和免疫参数。
Poult Sci. 2017 Sep 1;96(9):3068-3078. doi: 10.3382/ps/pex133.
9
Commensal microbiota affects ischemic stroke outcome by regulating intestinal γδ T cells.共生微生物群通过调节肠道γδ T细胞影响缺血性中风的预后。
Nat Med. 2016 May;22(5):516-23. doi: 10.1038/nm.4068. Epub 2016 Mar 28.
10
Changes in intestinal immunity, gut microbiota, and expression of energy metabolism-related genes explain adenoma growth in bilberry and cloudberry-fed Apc mice.肠道免疫、肠道微生物群的变化以及能量代谢相关基因的表达解释了食用越橘和云莓的Apc小鼠腺瘤生长的原因。
Nutr Res. 2016 Nov;36(11):1285-1297. doi: 10.1016/j.nutres.2016.10.003. Epub 2016 Oct 15.

引用本文的文献

1
Could Adverse Effects of Antibiotics Due to Their Use/Misuse Be Linked to Some Mechanisms Related to Nonalcoholic Fatty Liver Disease?抗生素的使用/滥用所产生的不良反应是否与非酒精性脂肪性肝病的某些机制有关?
Int J Mol Sci. 2024 Feb 6;25(4):1993. doi: 10.3390/ijms25041993.
2
Compound small peptide of Chinese medicine alleviates cyclophosphamide induced immunosuppression in mice by Th17/Treg and jejunum intestinal flora.中药复方小肽通过Th17/Treg和空肠肠道菌群减轻环磷酰胺诱导的小鼠免疫抑制。
Front Microbiol. 2023 Mar 28;14:1039287. doi: 10.3389/fmicb.2023.1039287. eCollection 2023.
3
Autoclaved Diet with Inactivated Spores of spp. Decreased Reproductive Performance of and Mice.

本文引用的文献

1
Influence of antibiotic use in early childhood on asthma and allergic diseases at age 5.幼儿期使用抗生素对5岁时哮喘和过敏性疾病的影响。
Ann Allergy Asthma Immunol. 2017 Jul;119(1):54-58. doi: 10.1016/j.anai.2017.05.013.
2
Gut microbial diversity in health and disease: experience of healthy Indian subjects, and colon carcinoma and inflammatory bowel disease patients.健康与疾病中的肠道微生物多样性:健康印度受试者、结肠癌患者及炎症性肠病患者的情况
Microb Ecol Health Dis. 2017 May 19;28(1):1322447. doi: 10.1080/16512235.2017.1322447. eCollection 2017.
3
Immune Responses to Broad-Spectrum Antibiotic Treatment and Fecal Microbiota Transplantation in Mice.
含有特定种灭活孢子的高压灭菌饮食降低了特定品系小鼠的繁殖性能。
Animals (Basel). 2022 Sep 13;12(18):2399. doi: 10.3390/ani12182399.
4
Effects of compound small peptides of Chinese medicine on intestinal immunity and cecal intestinal flora in CTX immunosuppressed mice.中药复方小肽对环磷酰胺免疫抑制小鼠肠道免疫及盲肠肠道菌群的影响
Front Microbiol. 2022 Jul 25;13:959726. doi: 10.3389/fmicb.2022.959726. eCollection 2022.
5
Effects of Natural Products on Bacterial Communication and Network-Quorum Sensing.天然产物对细菌通讯和网络群体感应的影响。
Biomed Res Int. 2020 May 24;2020:8638103. doi: 10.1155/2020/8638103. eCollection 2020.
6
Immunodeficiency Promotes Adaptive Alterations of Host Gut Microbiome: An Observational Metagenomic Study in Mice.免疫缺陷促进宿主肠道微生物群的适应性改变:一项小鼠宏基因组观察研究
Front Microbiol. 2019 Nov 1;10:2415. doi: 10.3389/fmicb.2019.02415. eCollection 2019.
7
Cathelicidin- derived PR39 protects enterohemorrhagic Escherichia coli O157:H7 challenged mice by improving epithelial function and balancing the microbiota in the intestine.抗菌肽 PR39 可改善肠上皮功能和平衡肠道微生物群,从而保护感染肠出血性大肠杆菌 O157:H7 的小鼠。
Sci Rep. 2019 Jul 1;9(1):9456. doi: 10.1038/s41598-019-45913-6.
小鼠对广谱抗生素治疗和粪便微生物群移植的免疫反应。
Front Immunol. 2017 Apr 19;8:397. doi: 10.3389/fimmu.2017.00397. eCollection 2017.
4
Low-dose penicillin in early life induces long-term changes in murine gut microbiota, brain cytokines and behavior.生命早期低剂量青霉素诱导小鼠肠道微生物群、大脑细胞因子和行为的长期变化。
Nat Commun. 2017 Apr 4;8:15062. doi: 10.1038/ncomms15062.
5
A distinct microbiota composition is associated with protection from food allergy in an oral mouse immunization model.在口腔小鼠免疫模型中,独特的微生物群组成与预防食物过敏相关。
Clin Immunol. 2016 Dec;173:10-18. doi: 10.1016/j.clim.2016.10.009. Epub 2016 Oct 24.
6
Early-life gut microbiome composition and milk allergy resolution.早期肠道微生物群组成与牛奶过敏的缓解
J Allergy Clin Immunol. 2016 Oct;138(4):1122-1130. doi: 10.1016/j.jaci.2016.03.041. Epub 2016 May 10.
7
The gut microbiome of healthy Japanese and its microbial and functional uniqueness.健康日本人的肠道微生物群及其微生物和功能独特性。
DNA Res. 2016 Apr;23(2):125-33. doi: 10.1093/dnares/dsw002. Epub 2016 Mar 6.
8
Allergy associations with the adult fecal microbiota: Analysis of the American Gut Project.过敏与成人粪便微生物群的关联:美国肠道计划分析。
EBioMedicine. 2015 Nov 27;3:172-179. doi: 10.1016/j.ebiom.2015.11.038. eCollection 2016 Jan.
9
Evidence that asthma is a developmental origin disease influenced by maternal diet and bacterial metabolites.证据表明,哮喘是一种发育起源疾病,受母体饮食和细菌代谢物的影响。
Nat Commun. 2015 Jun 23;6:7320. doi: 10.1038/ncomms8320.
10
Manipulation of the quorum sensing signal AI-2 affects the antibiotic-treated gut microbiota.群体感应信号AI-2的调控会影响经抗生素处理的肠道微生物群。
Cell Rep. 2015 Mar 24;10(11):1861-71. doi: 10.1016/j.celrep.2015.02.049.