• 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

分化过程中毒力因子的调节

Modulation of Virulence Factors during Differentiation.

作者信息

Oliveira Camila, Holetz Fabíola Barbieri, Alves Lysangela Ronalte, Ávila Andréa Rodrigues

机构信息

Laboratório de Regulação da Expressão Gênica, Instituto Carlos Chagas, Fiocruz Paraná, Curitiba 81350-010, Brazil.

Centre de Recherche CERVO, Université Laval, Québec City, QC G1V 0A6, Canada.

出版信息

Pathogens. 2022 Dec 25;12(1):32. doi: 10.3390/pathogens12010032.

DOI:10.3390/pathogens12010032
PMID:36678380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9865030/
Abstract

Chagas disease is a neglected tropical disease caused by . This protozoan developed several mechanisms to infect, propagate, and survive in different hosts. The specific expression of proteins is responsible for morphological and metabolic changes in different parasite stages along the parasite life cycle. The virulence strategies at the cellular and molecular levels consist of molecules responsible for mediating resistance mechanisms to oxidative damage, cellular invasion, and immune evasion, performed mainly by surface proteins. Since parasite surface coat remodeling is crucial to invasion and infectivity, surface proteins are essential virulence elements. Understanding the factors involved in these processes improves the knowledge of parasite pathogenesis. Genome sequencing has opened the door to high-throughput technologies, allowing us to obtain a deeper understanding of gene reprogramming along the parasite life cycle and identify critical molecules for survival. This review therefore focuses on proteins regulated during differentiation into infective forms considered virulence factors and addresses the current known mechanisms acting in the modulation of gene expression, emphasizing mRNA signals, regulatory factors, and protein complexes.

摘要

恰加斯病是一种由……引起的被忽视的热带疾病。这种原生动物发展出了多种机制,以便在不同宿主中进行感染、繁殖和生存。蛋白质的特异性表达导致寄生虫在其生命周期的不同阶段出现形态和代谢变化。细胞和分子水平上的毒力策略由负责介导对氧化损伤、细胞侵袭和免疫逃避的抗性机制的分子组成,这些机制主要由表面蛋白执行。由于寄生虫表面被膜重塑对于侵袭和感染性至关重要,表面蛋白是必不可少的毒力元件。了解这些过程中涉及的因素有助于增进对寄生虫发病机制的认识。基因组测序为高通量技术打开了大门,使我们能够更深入地了解寄生虫生命周期中的基因重编程,并识别生存所需的关键分子。因此,本综述聚焦于分化为感染性形式过程中被调控的蛋白质,这些蛋白质被视为毒力因子,并探讨了目前已知的在基因表达调控中起作用的机制,重点关注mRNA信号、调控因子和蛋白质复合物。

相似文献

1
Modulation of Virulence Factors during Differentiation.分化过程中毒力因子的调节
Pathogens. 2022 Dec 25;12(1):32. doi: 10.3390/pathogens12010032.
2
Comparative Analysis of Virulence Mechanisms of Trypanosomatids Pathogenic to Humans.对人类致病的锥虫的毒力机制的比较分析
Front Cell Infect Microbiol. 2021 Apr 16;11:669079. doi: 10.3389/fcimb.2021.669079. eCollection 2021.
3
Role of Virulence Factors of Trypanosomatids in the Insect Vector and Putative Genetic Events Involved in Surface Protein Diversity.锥虫科的毒力因子在昆虫媒介中的作用及表面蛋白多样性涉及的假定遗传事件。
Front Cell Infect Microbiol. 2022 Apr 28;12:807172. doi: 10.3389/fcimb.2022.807172. eCollection 2022.
4
Further in vivo evidence implying DNA apurinic/apyrimidinic endonuclease activity in Trypanosoma cruzi oxidative stress survival.进一步表明 DNA 无嘌呤/无嘧啶内切核酸酶活性在克氏锥虫氧化应激存活中的体内证据。
J Cell Biochem. 2019 Oct;120(10):16733-16740. doi: 10.1002/jcb.28931. Epub 2019 May 17.
5
Reevaluating the Trypanosoma cruzi proteomic map: The shotgun description of bloodstream trypomastigotes.重新评估克氏锥虫蛋白质组图谱:血流型锥鞭毛体的鸟枪法描述。
J Proteomics. 2015 Feb 6;115:58-65. doi: 10.1016/j.jprot.2014.12.003. Epub 2014 Dec 20.
6
The RNA-binding protein TcUBP1 up-regulates an RNA regulon for a cell surface-associated glycoprotein and promotes parasite infectivity.RNA 结合蛋白 TcUBP1 上调一个与细胞表面相关的糖蛋白的 RNA 调节子,促进寄生虫感染力。
J Biol Chem. 2019 Jun 28;294(26):10349-10364. doi: 10.1074/jbc.RA118.007123. Epub 2019 May 21.
7
Extensive Translational Regulation through the Proliferative Transition of Trypanosoma cruzi Revealed by Multi-Omics.多组学揭示了克氏锥虫增殖转换过程中的广泛翻译调控
mSphere. 2021 Oct 27;6(5):e0036621. doi: 10.1128/mSphere.00366-21. Epub 2021 Sep 1.
8
Parasite-Mediated Remodeling of the Host Microfilament Cytoskeleton Enables Rapid Egress of Trypanosoma cruzi following Membrane Rupture.寄生虫介导的宿主微丝细胞骨架重排使克氏锥虫能够在膜破裂后迅速逸出。
mBio. 2021 Jun 29;12(3):e0098821. doi: 10.1128/mBio.00988-21. Epub 2021 Jun 22.
9
Comprehensive glycoprofiling of the epimastigote and trypomastigote stages of Trypanosoma cruzi.全面糖基谱分析克氏锥虫的前鞭毛体和无鞭毛体阶段。
J Proteomics. 2017 Jan 16;151:182-192. doi: 10.1016/j.jprot.2016.05.034. Epub 2016 Jun 16.
10
Trypanosoma cruzi surface mucins: host-dependent coat diversity.克氏锥虫表面黏蛋白:宿主依赖性包膜多样性
Nat Rev Microbiol. 2006 Mar;4(3):229-36. doi: 10.1038/nrmicro1351.

引用本文的文献

1
Animal Trypanosomiasis: Challenges and Prospects for New Vaccination Strategies.动物锥虫病:新疫苗接种策略的挑战与前景
Microorganisms. 2024 Dec 13;12(12):2575. doi: 10.3390/microorganisms12122575.
2
Transcriptomic analysis of N-terminal mutated Trypanosoma cruzi UBP1 knockdown underlines the importance of this RNA-binding protein in parasite development.转录组分析表明,N 端突变的克氏锥虫 UBP1 敲低后,这种 RNA 结合蛋白在寄生虫发育中具有重要作用。
PLoS Negl Trop Dis. 2024 May 17;18(5):e0012179. doi: 10.1371/journal.pntd.0012179. eCollection 2024 May.
3
A versatile 2A peptide-based strategy for ectopic expression and endogenous gene tagging in .一种基于2A肽的通用策略,用于在……中进行异位表达和内源基因标记。
Heliyon. 2024 Jan 17;10(2):e24595. doi: 10.1016/j.heliyon.2024.e24595. eCollection 2024 Jan 30.

本文引用的文献

1
pathogenicity involves virulence factor expression and upregulation of bioenergetic and biosynthetic pathways.致病性涉及毒力因子表达和生物能量及生物合成途径的上调。
Virulence. 2022 Dec;13(1):1827-1848. doi: 10.1080/21505594.2022.2132776.
2
Role of Virulence Factors of Trypanosomatids in the Insect Vector and Putative Genetic Events Involved in Surface Protein Diversity.锥虫科的毒力因子在昆虫媒介中的作用及表面蛋白多样性涉及的假定遗传事件。
Front Cell Infect Microbiol. 2022 Apr 28;12:807172. doi: 10.3389/fcimb.2022.807172. eCollection 2022.
3
A profile of research on the parasitic trypanosomatids and the diseases they cause.寄生的动基体目原生动物和它们引起的疾病的研究概述。
PLoS Negl Trop Dis. 2022 Jan 13;16(1):e0010040. doi: 10.1371/journal.pntd.0010040. eCollection 2022 Jan.
4
Extensive Translational Regulation through the Proliferative Transition of Trypanosoma cruzi Revealed by Multi-Omics.多组学揭示了克氏锥虫增殖转换过程中的广泛翻译调控
mSphere. 2021 Oct 27;6(5):e0036621. doi: 10.1128/mSphere.00366-21. Epub 2021 Sep 1.
5
Mechanisms Associated with Host Target Cell Adhesion, Recognition and Internalization.与宿主靶细胞黏附、识别和内化相关的机制
Life (Basel). 2021 Jun 9;11(6):534. doi: 10.3390/life11060534.
6
Comparative Analysis of Virulence Mechanisms of Trypanosomatids Pathogenic to Humans.对人类致病的锥虫的毒力机制的比较分析
Front Cell Infect Microbiol. 2021 Apr 16;11:669079. doi: 10.3389/fcimb.2021.669079. eCollection 2021.
7
An Alba-domain protein required for proteome remodelling during trypanosome differentiation and host transition.一种 Alba 结构域蛋白,在锥虫分化和宿主转换过程中用于蛋白质组重塑。
PLoS Pathog. 2021 Jan 25;17(1):e1009239. doi: 10.1371/journal.ppat.1009239. eCollection 2021 Jan.
8
A zinc finger protein that is implicated in the control of epimastigote-specific gene expression and metacyclogenesis.一种锌指蛋白,参与调控锥虫特异基因表达和循环体形成。
Parasitology. 2021 Sep;148(10):1171-1185. doi: 10.1017/S0031182020002176. Epub 2020 Nov 16.
9
Identification of Novel Interspersed DNA Repetitive Elements in the Genome Associated with the 3'UTRs of Surface Multigenic Families.鉴定与表面多基因家族 3'UTR 相关的基因组中新的分散 DNA 重复元件。
Genes (Basel). 2020 Oct 21;11(10):1235. doi: 10.3390/genes11101235.
10
Genome: Organization, Multi-Gene Families, Transcription, and Biological Implications.基因组:组织、多基因家族、转录及生物学意义。
Genes (Basel). 2020 Oct 14;11(10):1196. doi: 10.3390/genes11101196.