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Seizing control: How dense granule effector proteins enable Toxoplasma to take charge.夺取控制权:致密颗粒效应蛋白如何使弓形虫掌控全局。
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2
Identification of a novel protein complex essential for effector translocation across the parasitophorous vacuole membrane of Toxoplasma gondii.鉴定一种新型蛋白复合物对于刚地弓形虫效应子穿过寄生泡膜的易位是必需的。
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3
Coimmunoprecipitation with MYR1 Identifies Three Additional Proteins within the Toxoplasma gondii Parasitophorous Vacuole Required for Translocation of Dense Granule Effectors into Host Cells.与 MYR1 共免疫沉淀鉴定出刚地弓形虫噬菌体内共定位于宿主细胞的致密颗粒效应子的转运所必需的另外三种蛋白。
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Translocation of Dense Granule Effectors across the Parasitophorous Vacuole Membrane in Infected Cells Requires the Activity of ROP17, a Rhoptry Protein Kinase.感染细胞中致密颗粒效应器穿过寄生泡膜的易位需要 ROP17(一种rhoptry 蛋白激酶)的活性。
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Secretion of Rhoptry and Dense Granule Effector Proteins by Nonreplicating Toxoplasma gondii Uracil Auxotrophs Controls the Development of Antitumor Immunity.非复制型弓形虫尿嘧啶营养缺陷型分泌棒状体和致密颗粒效应蛋白可控制抗肿瘤免疫的发展。
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Controls Host Cyclin E Expression through the Use of a Novel MYR1-Dependent Effector Protein, HCE1.通过使用新型 MYR1 依赖性效应蛋白 HCE1 来控制宿主细胞周期蛋白 E 的表达。
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Does Not Secrete the GRA16 and GRA24 Effectors Beyond the Parasitophorous Vacuole Membrane of Tissue Cysts.该蛋白不会将 GRA16 和 GRA24 效应子分泌到组织囊肿的滋养体空泡膜之外。
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MYR1-Dependent Effectors Are the Major Drivers of a Host Cell's Early Response to , Including Counteracting MYR1-Independent Effects.MYR1 依赖性效应物是宿主细胞对 的早期反应的主要驱动因素,包括抵消 MYR1 非依赖性效应。
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Aspartyl Protease 5 Matures Dense Granule Proteins That Reside at the Host-Parasite Interface in Toxoplasma gondii.天冬氨酸蛋白酶 5 成熟位于刚地弓形虫宿主-寄生虫界面的致密颗粒蛋白。
mBio. 2018 Oct 30;9(5):e01796-18. doi: 10.1128/mBio.01796-18.

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Host MOSPD2 enrichment at the parasitophorous vacuole membrane varies between strains and involves complex interactions.宿主 MOSPD2 在寄生泡膜上的富集程度因菌株而异,涉及复杂的相互作用。
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ROP16-mediated activation of STAT6 enhances cyst development of type III Toxoplasma gondii in neurons.ROP16 介导的 STAT6 激活增强了 III 型弓形虫在神经元中的囊泡发育。
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Development and validation of a machine learning algorithm prediction for dense granule proteins in Apicomplexa.机器学习算法预测顶复门原虫中致密颗粒蛋白的开发和验证。
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本文引用的文献

1
Toxoplasma gondii Is Required for Placenta-Specific Induction of the Regulatory Chemokine CCL22 in Human and Mouse.弓形虫(Toxoplasma gondii)对于人源和鼠源胎盘特异性调控趋化因子 CCL22 的诱导是必需的。
mBio. 2021 Dec 21;12(6):e0159121. doi: 10.1128/mBio.01591-21. Epub 2021 Nov 16.
2
Toxoplasma gondii secreted effectors co-opt host repressor complexes to inhibit necroptosis.刚地弓形虫分泌效应物劫持宿主抑制物复合物抑制细胞坏死性凋亡。
Cell Host Microbe. 2021 Jul 14;29(7):1186-1198.e8. doi: 10.1016/j.chom.2021.04.016. Epub 2021 May 26.
3
Influence of the Host and Parasite Strain on the Immune Response During Infection.宿主和寄生虫株对感染期间免疫反应的影响。
Front Cell Infect Microbiol. 2020 Oct 15;10:580425. doi: 10.3389/fcimb.2020.580425. eCollection 2020.
4
Genome-wide screens identify Toxoplasma gondii determinants of parasite fitness in IFNγ-activated murine macrophages.全基因组筛选鉴定出在 IFNγ 激活的鼠巨噬细胞中影响弓形虫寄生虫适应性的决定因素。
Nat Commun. 2020 Oct 16;11(1):5258. doi: 10.1038/s41467-020-18991-8.
5
Toxoplasma gondii GRA60 is an effector protein that modulates host cell autonomous immunity and contributes to virulence.刚地弓形虫 GRA60 是一种效应蛋白,可调节宿主细胞自主免疫并有助于毒力。
Cell Microbiol. 2021 Feb;23(2):e13278. doi: 10.1111/cmi.13278. Epub 2020 Oct 23.
6
Uses GRA16 To Upregulate Host c-Myc.利用 GRA16 上调宿主 c-Myc。
mSphere. 2020 Jun 24;5(3):e00402-20. doi: 10.1128/mSphere.00402-20.
7
Head-to-head comparisons of Toxoplasma gondii and its near relative Hammondia hammondi reveal dramatic differences in the host response and effectors with species-specific functions.弓形虫与其近缘种哈氏弓形体的直接比较揭示了宿主反应和效应物的显著差异,具有物种特异性的功能。
PLoS Pathog. 2020 Jun 23;16(6):e1008528. doi: 10.1371/journal.ppat.1008528. eCollection 2020 Jun.
8
Differential Impacts on Host Transcription by ROP and GRA Effectors from the Intracellular Parasite Toxoplasma gondii.弓形虫细胞内寄生虫的 ROP 和 GRA 效应子对宿主转录的差异影响。
mBio. 2020 Jun 9;11(3):e00182-20. doi: 10.1128/mBio.00182-20.
9
The Secreted Acid Phosphatase Domain-Containing GRA44 from Toxoplasma gondii Is Required for c-Myc Induction in Infected Cells.弓形虫分泌的含酸性磷酸酶结构域的 GRA44 蛋白对于感染细胞中 c-Myc 的诱导是必需的。
mSphere. 2020 Feb 19;5(1):e00877-19. doi: 10.1128/mSphere.00877-19.
10
Coimmunoprecipitation with MYR1 Identifies Three Additional Proteins within the Toxoplasma gondii Parasitophorous Vacuole Required for Translocation of Dense Granule Effectors into Host Cells.与 MYR1 共免疫沉淀鉴定出刚地弓形虫噬菌体内共定位于宿主细胞的致密颗粒效应子的转运所必需的另外三种蛋白。
mSphere. 2020 Feb 19;5(1):e00858-19. doi: 10.1128/mSphere.00858-19.

夺取控制权:致密颗粒效应蛋白如何使弓形虫掌控全局。

Seizing control: How dense granule effector proteins enable Toxoplasma to take charge.

机构信息

Department Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Mol Microbiol. 2021 Mar;115(3):466-477. doi: 10.1111/mmi.14679. Epub 2021 Feb 6.

DOI:10.1111/mmi.14679
PMID:33400323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8344355/
Abstract

Control of the host cell is crucial to the Apicomplexan parasite, Toxoplasma gondii, while it grows intracellularly. To achieve this goal, these single-celled eukaryotes export a series of effector proteins from organelles known as "dense granules" that interfere with normal cellular processes and responses to invasion. While some effectors are found attached to the outer surface of the parasitophorous vacuole (PV) in which Toxoplasma tachyzoites reside, others are found in the host cell's cytoplasm and yet others make their way into the host nucleus, where they alter host transcription. Among the processes that are severely altered are innate immune responses, host cell cycle, and association with host organelles. The ways in which these crucial processes are altered through the coordinated action of a large collection of effectors is as elegant as it is complex, and is the central focus of the following review; we also discuss the recent advances in our understanding of how dense granule effector proteins are trafficked out of the PV.

摘要

宿主细胞的控制对于在细胞内生长的顶复门寄生虫刚地弓形虫至关重要。为了实现这一目标,这些单细胞真核生物从称为“致密颗粒”的细胞器中输出一系列效应蛋白,这些蛋白干扰正常的细胞过程和对入侵的反应。虽然一些效应物附着在刚地弓形虫速殖子所在的吞噬小泡 (PV) 的外表面,但其他效应物存在于宿主细胞质中,还有一些则进入宿主细胞核,在那里它们改变宿主转录。严重改变的过程包括先天免疫反应、宿主细胞周期和与宿主细胞器的关联。通过大量效应物的协调作用改变这些关键过程的方式既优雅又复杂,是以下综述的重点;我们还讨论了我们对致密颗粒效应蛋白如何从 PV 中运输出来的理解的最新进展。