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ROP9、MIC3和SAG2是刚地弓形虫中的肝素结合蛋白,参与宿主细胞的附着和侵袭。

ROP9, MIC3, and SAG2 are heparin-binding proteins in Toxoplasma gondii and involved in host cell attachment and invasion.

作者信息

Zhang Dongchao, Jiang Ning, Chen Qijun

机构信息

Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonoses, College of Veterinary Medicine, Jilin University, Changchun, China.

Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonoses, College of Veterinary Medicine, Jilin University, Changchun, China; Key Laboratory of Zoonosis, Shenyang Agricultural University, Shenyang, China.

出版信息

Acta Trop. 2019 Apr;192:22-29. doi: 10.1016/j.actatropica.2019.01.001. Epub 2019 Jan 18.

Abstract

Toxoplasma gondii (T. gondii) is an obligatory intracellular parasite that can infect varieties of warm-blooded animals, including humans and birds. Heparan sulfate (HS) is widely distributed on the eukaryotic cell surface of vertebrates and can inhibit T. gondii invasion. In this study, we investigated the transcription and expression of the level of TgROP9, TgMIC3, and TgSAG2 in T. gondii RH strain, and found that the expression levels of these three proteins in invading parasites were higher compared to those free ranging parasites. The recombinant proteins showed specific binding activity to both heparin and host cell surface. Incubation of these proteins with the host cells could block T. gondiiinvasion. Furthermore, protein-specific antibodies also blocked parasite invasion. Antibodies in the sera of T. gondii infected individuals recognized the recombinant TgROP9, TgMIC3, and TgSAG2, which suggested the exposure of these proteins to human immune system. Mice immunized with the three proteins exhibited protective immunity against lethal challenge. The data collectively suggested that these parasitic proteins may be used as candidate antigens for development of anti-toxoplasmosis vaccine.

摘要

刚地弓形虫是一种专性细胞内寄生虫,可感染包括人类和鸟类在内的多种温血动物。硫酸乙酰肝素广泛分布于脊椎动物的真核细胞表面,能够抑制刚地弓形虫的入侵。在本研究中,我们调查了刚地弓形虫RH株中TgROP9、TgMIC3和TgSAG2的转录水平和表达情况,发现这三种蛋白在入侵寄生虫中的表达水平高于游离寄生虫。重组蛋白对肝素和宿主细胞表面均表现出特异性结合活性。将这些蛋白与宿主细胞共同孵育可阻断刚地弓形虫的入侵。此外,蛋白特异性抗体也可阻断寄生虫的入侵。刚地弓形虫感染个体血清中的抗体可识别重组TgROP9、TgMIC3和TgSAG2,这表明这些蛋白已暴露于人体免疫系统。用这三种蛋白免疫的小鼠对致死性攻击表现出保护性免疫。这些数据共同表明,这些寄生虫蛋白可作为开发抗弓形虫病疫苗的候选抗原。

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