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磷酸葡萄糖变位酶 1 有助于弓形虫中囊泡的最佳发育。

Phosphoglucomutase 1 contributes to optimal cyst development in Toxoplasma gondii.

机构信息

Department of Biology, Laney College, Oakland, CA, USA.

School of Medicine, University of California San Francisco, San Francisco, CA, USA.

出版信息

BMC Res Notes. 2022 May 21;15(1):188. doi: 10.1186/s13104-022-06073-5.

DOI:10.1186/s13104-022-06073-5
PMID:35597992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9123713/
Abstract

OBJECTIVE

Toxoplasma gondii is a ubiquitous parasite of medical and veterinary importance; however, there exists no cure for chronic toxoplasmosis. Metabolic enzymes required for the production and maintenance of tissue cysts represent promising targets for novel therapies. Here, we use reverse genetics to investigate the role of Toxoplasma phosphoglucomutase 1, PGM1, in Toxoplasma growth and cystogenesis.

RESULTS

We found that disruption of pgm1 did not significantly affect Toxoplasma intracellular growth and the lytic cycle. pgm1-defective parasites could differentiate into bradyzoites and produced cysts containing amylopectin in vitro. However, cysts produced in the absence of pgm1 were significantly smaller than wildtype. Together, our findings suggest that PGM1 is dispensable for in vitro growth but contributes to optimal Toxoplasma cyst development in vitro, thereby necessitating further investigation into the function of this enzyme in Toxoplasma persistence in its host.

摘要

目的

刚地弓形虫是一种普遍存在的寄生虫,具有医学和兽医重要性;然而,目前尚无慢性弓形虫病的治愈方法。用于产生和维持组织包囊的代谢酶代表了新疗法的有希望的靶标。在这里,我们使用反向遗传学来研究弓形虫磷酸葡萄糖变位酶 1(PGM1)在弓形虫生长和囊形成中的作用。

结果

我们发现 pgm1 的破坏并没有显著影响弓形虫的细胞内生长和裂解周期。pgm1 缺陷型寄生虫可以分化为缓殖子,并在体外产生含有支链淀粉的包囊。然而,在没有 pgm1 的情况下产生的包囊明显小于野生型。总之,我们的研究结果表明,PGM1 对于体外生长不是必需的,但有助于体外弓形虫囊的最佳发育,因此需要进一步研究该酶在弓形虫在宿主中的持续存在中的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5601/9123713/a6b754360ec3/13104_2022_6073_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5601/9123713/9363a709bc64/13104_2022_6073_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5601/9123713/7f57ad71f06d/13104_2022_6073_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5601/9123713/a6b754360ec3/13104_2022_6073_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5601/9123713/9363a709bc64/13104_2022_6073_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5601/9123713/7f57ad71f06d/13104_2022_6073_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5601/9123713/a6b754360ec3/13104_2022_6073_Fig3_HTML.jpg

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本文引用的文献

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Transcriptional ups and downs: patterns of gene expression in the life cycle of Toxoplasma gondii.转录的起伏:刚地弓形虫生命周期中基因表达的模式。
Microbes Infect. 2020 Nov-Dec;22(10):525-533. doi: 10.1016/j.micinf.2020.09.001. Epub 2020 Sep 12.
2
Identification of a Master Regulator of Differentiation in Toxoplasma.鉴定弓形虫分化的主要调控因子。
Cell. 2020 Jan 23;180(2):359-372.e16. doi: 10.1016/j.cell.2019.12.013. Epub 2020 Jan 16.
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ToxoDB: Functional Genomics Resource for Toxoplasma and Related Organisms.ToxoDB:弓形虫和相关生物的功能基因组学资源。
Methods Mol Biol. 2020;2071:27-47. doi: 10.1007/978-1-4939-9857-9_2.
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The One Health Approach to Toxoplasmosis: Epidemiology, Control, and Prevention Strategies.《弓形虫病的综合健康方法:流行病学、控制和预防策略》。
Ecohealth. 2019 Jun;16(2):378-390. doi: 10.1007/s10393-019-01405-7. Epub 2019 Apr 3.
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Transcriptional Analysis Shows a Robust Host Response to during Early and Late Chronic Infection in Both Male and Female Mice.转录分析显示,在雌雄小鼠的早期和晚期慢性感染期间,宿主对 均有强烈反应。
Infect Immun. 2019 Apr 23;87(5). doi: 10.1128/IAI.00024-19. Print 2019 Mar.
6
Glycolysis is important for optimal asexual growth and formation of mature tissue cysts by Toxoplasma gondii.糖酵解对于刚地弓形虫的最佳无性生长和成熟组织囊形成很重要。
Int J Parasitol. 2018 Oct;48(12):955-968. doi: 10.1016/j.ijpara.2018.05.013. Epub 2018 Aug 31.
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A latent ability to persist: differentiation in Toxoplasma gondii.潜伏的持久能力:刚地弓形虫的分化。
Cell Mol Life Sci. 2018 Jul;75(13):2355-2373. doi: 10.1007/s00018-018-2808-x. Epub 2018 Mar 30.
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