• 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

时间进程全血转录组分析为对……的天然抗性机制提供了新见解。 (原文中“to”后面缺少具体内容)

Time-course whole blood transcriptome profiling provides new insights into natural resistance mechanism to .

作者信息

Dibo Nouhoum, Zhou Zhijun, Liu Xianshu, Li Zhuolin, Zhong Shukun, Liu Yan, Duan Juan, Xia Meng, Ma Zhenrong, Wu Xiang, Huang Shuaiqin

机构信息

Department of Medical Parasitology, Xiangya School of Basic Medicine, Central South University, Changsha, 410013, Hunan Province, China.

Department of Laboratory Animals, Hunan Key Laboratory of Animal Models for Human Diseases, Central South University, Changsha, 410013, Hunan, China.

出版信息

Heliyon. 2024 Sep 26;10(19):e38067. doi: 10.1016/j.heliyon.2024.e38067. eCollection 2024 Oct 15.

DOI:10.1016/j.heliyon.2024.e38067
PMID:39398025
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11471165/
Abstract

is known as a non-susceptible animal host of . A better understanding of this animal immune defense mechanism during the early stage of infection may offer an alternative route for vaccine development or therapy. Here, we analyzed the whole blood transcriptome of using next-generation sequencing (NGS) to identify immune genes of biological relevance that might be involved in the mechanism of its resistance. The blood samples were collected from uninfected animals (control group) and infected animals at different time points (3, 7, 10 and 14 days post-infection). We identified 5310 sequences as unigenes and successfully annotated 4636 of them. The immune response was more intense at 10 dpi. The upregulated genes at this time point were mainly activated in the TNF and NF-kappa B signaling pathways, Th1, Th2and Th17 cell differentiation as well as cytokine-cytokine receptor interaction. Based on the differentially expressed genes analysis, we report that the , , , , , , , , , , and could play important roles in the mechanism of resistance.

摘要

被认为是……的非易感动物宿主。在感染早期更好地了解这种动物的免疫防御机制可能为疫苗开发或治疗提供另一条途径。在此,我们使用下一代测序(NGS)分析了……的全血转录组,以鉴定可能参与其抗性机制的具有生物学相关性的免疫基因。血液样本从未感染动物(对照组)和感染后不同时间点(感染后3、7、10和14天)的感染动物中采集。我们将5310个序列鉴定为单基因,并成功注释了其中4636个。在感染后10天免疫反应更强。此时上调的基因主要在TNF和NF-κB信号通路、Th1、Th2和Th17细胞分化以及细胞因子-细胞因子受体相互作用中被激活。基于差异表达基因分析,我们报告……在……抗性机制中可能发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/c47c6197b2dc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/b91766162711/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/b791f006078d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/12d60981ca53/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/bab82b7740af/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/c47c6197b2dc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/b91766162711/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/b791f006078d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/12d60981ca53/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/bab82b7740af/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db71/11471165/c47c6197b2dc/gr5.jpg

相似文献

1
Time-course whole blood transcriptome profiling provides new insights into natural resistance mechanism to .时间进程全血转录组分析为对……的天然抗性机制提供了新见解。 (原文中“to”后面缺少具体内容)
Heliyon. 2024 Sep 26;10(19):e38067. doi: 10.1016/j.heliyon.2024.e38067. eCollection 2024 Oct 15.
2
De novo assembly and transcriptome characterization: novel insights into the natural resistance mechanisms of Microtus fortis against Schistosoma japonicum.从头组装与转录组特征分析:对东方田鼠抗日本血吸虫天然抗性机制的新见解
BMC Genomics. 2014 Jun 2;15(1):417. doi: 10.1186/1471-2164-15-417.
3
High throughput data analyses of the immune characteristics of Microtus fortis infected with Schistosoma japonicum.高通量数据分析感染日本血吸虫的东方田鼠的免疫特征。
Sci Rep. 2017 Sep 12;7(1):11311. doi: 10.1038/s41598-017-11532-2.
4
miR-181a regulates the host immune response against Schistosoma japonicum infection through the TLR4 receptor pathway.miR-181a 通过 TLR4 受体途径调节宿主对日本血吸虫感染的免疫反应。
Parasit Vectors. 2021 Oct 24;14(1):548. doi: 10.1186/s13071-021-05063-z.
5
Genome assembly and transcriptome analysis provide insights into the antischistosome mechanism of Microtus fortis.基因组组装和转录组分析为理解东方田鼠抗血吸虫机制提供了线索。
J Genet Genomics. 2020 Dec 20;47(12):743-755. doi: 10.1016/j.jgg.2020.11.009. Epub 2021 Feb 9.
6
Immunoproteomic analysis of Schistosoma japonicum schistosomulum proteins recognized by immunoglobulin G in the sera of susceptible and non-susceptible hosts.日本血吸虫童虫蛋白在易感和非易感宿主血清中被免疫球蛋白G识别的免疫蛋白质组学分析
J Proteomics. 2015 Jun 21;124:25-38. doi: 10.1016/j.jprot.2015.04.010. Epub 2015 Apr 17.
7
Study on differences in the pathology, T cell subsets and gene expression in susceptible and non-susceptible hosts infected with Schistosoma japonicum.日本血吸虫易感性和非易感性宿主感染的病理学、T 细胞亚群和基因表达差异研究。
PLoS One. 2010 Oct 18;5(10):e13494. doi: 10.1371/journal.pone.0013494.
8
Transcriptional profiling of Microtus fortis responses to S. japonicum: New sight into Mf-Hsp90α resistance mechanism.转录组分析东方田鼠对日本血吸虫的反应:揭示 Mf-Hsp90α 抗性机制的新视角。
Parasite Immunol. 2021 Aug;43(8):e12842. doi: 10.1111/pim.12842. Epub 2021 Jun 9.
9
A longitudinal study reveals the alterations of the Microtus fortis colonic microbiota during the natural resistance to Schistosoma japonicum infection.一项纵向研究揭示了东方田鼠在自然抵抗日本血吸虫感染过程中结肠微生物群的变化。
Exp Parasitol. 2020 Dec;219:108030. doi: 10.1016/j.exppara.2020.108030. Epub 2020 Oct 17.
10
Mechanisms of Resistance to Infection in , the Natural Non-permissive Host.天然非易感宿主对感染的抵抗机制。
Front Microbiol. 2020 Sep 3;11:2092. doi: 10.3389/fmicb.2020.02092. eCollection 2020.

本文引用的文献

1
Roles of S100A8, S100A9 and S100A12 in infection, inflammation and immunity.S100A8、S100A9和S100A12在感染、炎症和免疫中的作用。
Immunology. 2024 Mar;171(3):365-376. doi: 10.1111/imm.13722. Epub 2023 Nov 27.
2
Macrophage-mediated trogocytosis contributes to destroying human schistosomes in a non-susceptible rodent host, Microtus fortis.巨噬细胞介导的异体吞噬有助于在不敏感的啮齿动物宿主东方田鼠体内破坏人类血吸虫。
Cell Discov. 2023 Oct 5;9(1):101. doi: 10.1038/s41421-023-00603-6.
3
Vinblastine resets tumor-associated macrophages toward M1 phenotype and promotes antitumor immune response.
长春碱将肿瘤相关巨噬细胞重置为 M1 表型,并促进抗肿瘤免疫反应。
J Immunother Cancer. 2023 Aug;11(8). doi: 10.1136/jitc-2023-007253.
4
Pattern recognition receptor signaling and innate immune responses to schistosome infection.模式识别受体信号转导与血吸虫感染的固有免疫应答。
Front Cell Infect Microbiol. 2022 Oct 21;12:1040270. doi: 10.3389/fcimb.2022.1040270. eCollection 2022.
5
Development of the Sm14/GLA-SE Schistosomiasis Vaccine Candidate: An Open, Non-Placebo-Controlled, Standardized-Dose Immunization Phase Ib Clinical Trial Targeting Healthy Young Women.Sm14/GLA-SE血吸虫病候选疫苗的研发:一项针对健康年轻女性的开放、非安慰剂对照、标准化剂量免疫的Ib期临床试验
Vaccines (Basel). 2022 Oct 15;10(10):1724. doi: 10.3390/vaccines10101724.
6
Review of 2022 WHO guidelines on the control and elimination of schistosomiasis.《2022 年世界卫生组织控制和消除血吸虫病指南回顾》。
Lancet Infect Dis. 2022 Nov;22(11):e327-e335. doi: 10.1016/S1473-3099(22)00221-3. Epub 2022 May 17.
7
The Road to Elimination: Current State of Schistosomiasis Research and Progress Towards the End Game.消除之路:血吸虫病研究现状及迈向终局的进展。
Front Immunol. 2022 May 3;13:846108. doi: 10.3389/fimmu.2022.846108. eCollection 2022.
8
TNF plays a crucial role in inflammation by signaling via T cell TNFR2.TNF 通过 T 细胞 TNFR2 信号转导在炎症中发挥关键作用。
Proc Natl Acad Sci U S A. 2021 Dec 14;118(50). doi: 10.1073/pnas.2109972118.
9
Rhesus macaques self-curing from a schistosome infection can display complete immunity to challenge.恒河猴自身从血吸虫感染中痊愈后,可以对再次感染产生完全免疫力。
Nat Commun. 2021 Oct 26;12(1):6181. doi: 10.1038/s41467-021-26497-0.
10
The S100 Protein Family as Players and Therapeutic Targets in Pulmonary Diseases.S100 蛋白家族在肺部疾病中的作用及作为治疗靶点
Pulm Med. 2021 Jun 18;2021:5488591. doi: 10.1155/2021/5488591. eCollection 2021.