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Establishment of a stable transfection method in Babesia microti and identification of a novel bidirectional promoter of Babesia microti.建立微小巴贝斯虫稳定转染方法并鉴定微小巴贝斯虫新型双向启动子。
Sci Rep. 2020 Sep 24;10(1):15614. doi: 10.1038/s41598-020-72489-3.
2
PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum.PfMAP-2 对疟原虫恶性疟原虫的雄性配子体发生是必需的。
Sci Rep. 2020 Jul 17;10(1):11930. doi: 10.1038/s41598-020-68717-5.
3
Fussing About Fission: Defining Variety Among Mainstream and Exotic Apicomplexan Cell Division Modes.纠结于裂变:定义主流和外来顶复门细胞分裂模式的多样性。
Front Cell Infect Microbiol. 2020 Jun 5;10:269. doi: 10.3389/fcimb.2020.00269. eCollection 2020.
4
The Bradyzoite: A Key Developmental Stage for the Persistence and Pathogenesis of Toxoplasmosis.缓殖子:弓形虫病持续存在和发病机制的关键发育阶段。
Pathogens. 2020 Mar 21;9(3):234. doi: 10.3390/pathogens9030234.
5
Bumped Kinase Inhibitors as therapy for apicomplexan parasitic diseases: lessons learned. bumped 激酶抑制剂作为治疗顶复门寄生虫病的药物:经验教训。
Int J Parasitol. 2020 May;50(5):413-422. doi: 10.1016/j.ijpara.2020.01.006. Epub 2020 Mar 26.
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Loss of a conserved MAPK causes catastrophic failure in assembly of a specialized cilium-like structure in .丧失一个保守的 MAPK 会导致在 中专门的纤毛样结构的组装中灾难性的失败。
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Identification of essential exported Plasmodium falciparum protein kinases in malaria-infected red blood cells.鉴定疟原虫感染红细胞中必需的 exported Plasmodium falciparum protein kinases。
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Protein Kinase A Is Essential for Invasion of Plasmodium falciparum into Human Erythrocytes.蛋白激酶 A 对于恶性疟原虫侵入人类红细胞是必需的。
mBio. 2019 Oct 8;10(5):e01972-19. doi: 10.1128/mBio.01972-19.

疟原虫属物种生命周期中的信号传导框架。

A framework for signaling throughout the life cycle of Babesia species.

机构信息

Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

出版信息

Mol Microbiol. 2021 May;115(5):882-890. doi: 10.1111/mmi.14650. Epub 2020 Dec 15.

DOI:10.1111/mmi.14650
PMID:33274587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10209834/
Abstract

Babesia species are tick-borne intracellular parasites that infect the red blood cells of their mammalian host, leading to severe or fatal disease. Babesia spp. infect a wide range of mammalian species and cause a significant economic burden globally, predominantly through disease in cattle. Several Babesia spp. are increasingly being recognized as zoonotic pathogens of humans. Babesia spp. have complex life cycles involving multiple stages in the tick and the mammalian host. The parasite utilizes complex signaling pathways during replication, egress, and invasion in each of these stages. They must also rapidly respond to their environment when switching between the mammalian and tick stages. This review will focus on the signaling pathways and environmental stimuli that Babesia spp. utilize in the bloodstream and for transmission to the tick, with an emphasis on the role of phosphorylation- and calcium-based signaling during egress and invasion. The expanding availability of in vitro and in vivo culture systems, genomes, transcriptomes, and transgenic systems available for a range of Babesia spp. should encourage further biological and translational studies of these ubiquitous parasites.

摘要

巴贝西虫属是蜱传的细胞内寄生虫,感染哺乳动物宿主的红细胞,导致严重或致命疾病。巴贝西虫属感染范围广泛的哺乳动物物种,并在全球范围内造成重大经济负担,主要是通过牛的疾病。几种巴贝西虫属越来越被认为是人类的人畜共患病病原体。巴贝西虫属具有复杂的生命周期,涉及蜱和哺乳动物宿主中的多个阶段。寄生虫在每个阶段的复制、出芽和入侵过程中利用复杂的信号通路。当它们在哺乳动物和蜱阶段之间切换时,它们还必须快速响应环境。本综述将重点介绍巴贝西虫属在血液中和传播到蜱虫中利用的信号通路和环境刺激物,重点介绍磷酸化和基于钙的信号在出芽和入侵过程中的作用。越来越多的体外和体内培养系统、基因组、转录组以及各种巴贝西虫属的转基因系统的可用性,应该鼓励对这些无处不在的寄生虫进行进一步的生物学和转化研究。