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通过显微镜检查和流式细胞术对子孢子侵袭、迁移和发育进行定量分析。

Quantification of sporozoite invasion, migration, and development by microscopy and flow cytometry.

作者信息

Sinnis Photini, De La Vega Patricia, Coppi Alida, Krzych Urszula, Mota Maria M

机构信息

Department of Molecular Microbiology and Immunology, John Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

出版信息

Methods Mol Biol. 2013;923:385-400. doi: 10.1007/978-1-62703-026-7_27.

DOI:10.1007/978-1-62703-026-7_27
PMID:22990793
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3951895/
Abstract

There is an important role for in vitro assays to better understand the initial steps of malaria infection. In this section, we describe both microscopy-based and flow cytometry-based sporozoite invasion, migration and development assays with the rodent malaria parasites, Plasmodium berghei and Plasmodium yoelii, and the human malaria parasite, Plasmodium falciparum.

摘要

体外试验在更好地理解疟疾感染的初始步骤方面发挥着重要作用。在本节中,我们描述了基于显微镜和流式细胞术的子孢子入侵、迁移和发育试验,这些试验使用的是啮齿类疟原虫伯氏疟原虫和约氏疟原虫,以及人类疟原虫恶性疟原虫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e999/3951895/27f498657375/nihms556219f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e999/3951895/27f498657375/nihms556219f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e999/3951895/27f498657375/nihms556219f1.jpg

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Methods Mol Biol. 2013;923:385-400. doi: 10.1007/978-1-62703-026-7_27.
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本文引用的文献

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Inactivation of a Plasmodium apicoplast protein attenuates formation of liver merozoites.疟原虫质体蛋白失活可减弱肝脏裂殖子的形成。
Mol Microbiol. 2011 Sep;81(6):1511-25. doi: 10.1111/j.1365-2958.2011.07787.x. Epub 2011 Aug 17.
2
The malaria circumsporozoite protein has two functional domains, each with distinct roles as sporozoites journey from mosquito to mammalian host.疟原虫环子孢子蛋白有两个功能域,每个功能域在子孢子从蚊子到哺乳动物宿主的旅程中都有不同的作用。
J Exp Med. 2011 Feb 14;208(2):341-56. doi: 10.1084/jem.20101488. Epub 2011 Jan 24.
3
A Plasmodium falciparum strain expressing GFP throughout the parasite's life-cycle.一株表达 GFP 的恶性疟原虫株,在寄生虫的整个生命周期中都有表达。
PLoS One. 2010 Feb 10;5(2):e9156. doi: 10.1371/journal.pone.0009156.
4
Role of Plasmodium berghei cGMP-dependent protein kinase in late liver stage development.疟原虫 cGMP 依赖蛋白激酶在肝脏晚期发育阶段的作用。
J Biol Chem. 2010 Jan 29;285(5):3282-8. doi: 10.1074/jbc.M109.070367. Epub 2009 Nov 24.
5
Preerythrocytic, live-attenuated Plasmodium falciparum vaccine candidates by design.设计的恶性疟原虫前体红细胞期减毒活疫苗候选物。
Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):13004-9. doi: 10.1073/pnas.0906387106. Epub 2009 Jul 22.
6
Host cell transcriptional profiling during malaria liver stage infection reveals a coordinated and sequential set of biological events.疟疾肝脏期感染期间宿主细胞转录谱分析揭示了一系列协调且有序的生物学事件。
BMC Genomics. 2009 Jun 17;10:270. doi: 10.1186/1471-2164-10-270.
7
Clonal conditional mutagenesis in malaria parasites.疟原虫中的克隆条件性诱变
Cell Host Microbe. 2009 Apr 23;5(4):386-96. doi: 10.1016/j.chom.2009.03.008.
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A small molecule inhibitor of signal peptide peptidase inhibits Plasmodium development in the liver and decreases malaria severity.信号肽肽酶的小分子抑制剂可抑制疟原虫在肝脏中的发育并减轻疟疾严重程度。
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HIV protease inhibitors inhibit the development of preerythrocytic-stage plasmodium parasites.HIV蛋白酶抑制剂可抑制疟原虫前体红细胞期寄生虫的发育。
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