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疟原虫的生存之战:在获取营养的同时逃避清除。

Plasmodium's fight for survival: escaping elimination while acquiring nutrients.

机构信息

Department of Molecular Genetics and Microbiology, Duke University, Durham, NC, USA.

Department of Chemistry, Duke University, Durham, NC, USA.

出版信息

Trends Parasitol. 2022 Jul;38(7):544-557. doi: 10.1016/j.pt.2022.04.004. Epub 2022 May 6.

DOI:10.1016/j.pt.2022.04.004
PMID:35534377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9187605/
Abstract

Plasmodium parasites extensively alter their host hepatocyte to evade host detection and support an unprecedented replication rate. Host cell manipulation includes association with the host early and late endomembrane systems, where Plasmodium accesses nutrients while suppressing cellular immune processes. Early endomembrane organelles provide an opportunity to sequester an abundance of lipids and proteins, but the association with late endomembrane organelles also risks autophagy-mediated elimination. While not all parasites survive, those that do benefit from a plethora of nutrients provided through this pathway. In this review, we discuss recent advances in our understanding of how Plasmodium parasites balance the need for host nutrients while avoiding elimination during the liver stage.

摘要

疟原虫广泛改变其宿主肝细胞以逃避宿主检测并支持前所未有的复制率。宿主细胞操纵包括与宿主早期和晚期内体系统的关联,疟原虫在抑制细胞免疫过程的同时获取营养。早期内体细胞器提供了隔离大量脂质和蛋白质的机会,但与晚期内体细胞器的关联也有被自噬介导消除的风险。虽然并非所有寄生虫都能存活下来,但那些存活下来的寄生虫受益于通过这条途径提供的大量营养。在这篇综述中,我们讨论了我们对疟原虫寄生虫如何平衡对宿主营养的需求与在肝脏阶段避免消除之间的理解的最新进展。

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本文引用的文献

1
A genome-wide CRISPR-Cas9 screen identifies CENPJ as a host regulator of altered microtubule organization during Plasmodium liver infection.全基因组 CRISPR-Cas9 筛选鉴定出 CENPJ 是疟原虫肝脏感染期间改变微管组织的宿主调节剂。
Cell Chem Biol. 2022 Sep 15;29(9):1419-1433.e5. doi: 10.1016/j.chembiol.2022.06.001. Epub 2022 Jun 22.
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Hijacking of the host cell Golgi by Plasmodium berghei liver stage parasites.疟原虫肝期寄生虫对宿主细胞高尔基体的劫持。
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How Malaria Parasites Acquire Nutrients From Their Host.
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and associate with host Arfs during infection.并在感染过程中与宿主 Arfs 相关联。
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All Roads Lead to Cytosol: Multi-Strategic Approach to Invasion.条条大路通胞质溶胶:入侵的多策略方法
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Zonal human hepatocytes are differentially permissive to Plasmodium falciparum malaria parasites.区域性人肝细胞对疟原虫疟原虫的感染具有不同的易感性。
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Disrupting Plasmodium UIS3-host LC3 interaction with a small molecule causes parasite elimination from host cells.用小分子破坏疟原虫UIS3与宿主LC3的相互作用可导致寄生虫从宿主细胞中被清除。
Commun Biol. 2020 Nov 19;3(1):688. doi: 10.1038/s42003-020-01422-1.
7
CREBH: A Complex Array of Regulatory Mechanisms in Nutritional Signaling, Metabolic Inflammation, and Metabolic Disease.CREBH:营养信号、代谢炎症和代谢性疾病中复杂的调控机制。
Mol Nutr Food Res. 2021 Jan;65(1):e2000771. doi: 10.1002/mnfr.202000771. Epub 2020 Oct 20.
8
A Humanized Mouse Model for Plasmodium vivax to Test Interventions that Block Liver Stage to Blood Stage Transition and Blood Stage Infection.用于测试阻断间日疟原虫肝期向血期转变及血期感染干预措施的人源化小鼠模型。
iScience. 2020 Aug 21;23(8):101381. doi: 10.1016/j.isci.2020.101381. Epub 2020 Jul 18.
9
Targeting the Extrinsic Pathway of Hepatocyte Apoptosis Promotes Clearance of Plasmodium Liver Infection.靶向肝细胞凋亡的外在途径可促进疟原虫肝感染的清除。
Cell Rep. 2020 Mar 31;30(13):4343-4354.e4. doi: 10.1016/j.celrep.2020.03.032.
10
RNA-Seq Analysis Illuminates the Early Stages of Liver Infection.RNA-Seq 分析揭示了肝脏感染的早期阶段。
mBio. 2020 Feb 4;11(1):e03234-19. doi: 10.1128/mBio.03234-19.