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微小隐孢子虫蛋白酶INS6在寄生虫增殖和致病性中起重要作用。

Cryptosporidium parvum protease INS6 plays an important role in parasite proliferation and pathogenicity.

作者信息

He Wei, Yang Zuwei, Wang Jing, Yang Fuxian, Li Na, Xu Rui, Zeng Songrong, Xiao Lihua, Feng Yaoyu, Guo Yaqiong

机构信息

State Key Laboratory for Animal Disease Control and Prevention, Center for Emerging and Zoonotic Diseases, College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.

School of Biology and Agriculture, Shaoguan University, Shaoguan, China.

出版信息

PLoS Negl Trop Dis. 2025 Sep 12;19(9):e0013532. doi: 10.1371/journal.pntd.0013532. eCollection 2025 Sep.

Abstract

BACKGROUND

Cryptosporidium parvum is a common protozoan pathogen responsible for moderate to severe diarrhea in humans and animals. Parasite invasion and egress cause damage to intestinal epithelial cells, which is mediated by a variety of secretory proteins from several unique organelles, such as micronemes. Previous spatial proteomic analysis has identified insulinase-like protease 6 (INS6) as a putative microneme protein in C. parvum. However, the functional contribution of INS6 to Cryptosporidium pathogenicity remains poorly characterized. In this study, we used genetic manipulation techniques to investigate the expression and biological functions of INS6 in C. parvum.

METHODOLOGY/PRINCIPAL FINDINGS: The INS6 gene was tagged and deleted in C. parvum using CRISPR/Cas9 technology. The expression of INS6 was determined by immunofluorescence analysis, ultrastructure-expansion microscopy, and immunoelectron microscopy. Endogenous labelling showed low levels of INS6 expression, which is found in C. parvum micronemes and is absent during the male gamont stage. The effect of INS6 deletion on parasite growth and pathogenicity was assessed in vitro using HCT-8 cultures and in vivo by infection of interferon-γ knockout mice. Deletion of the INS6 gene impaired C. parvum proliferation in vitro and significantly reduced the parasite burden in infected mice. In addition, mice infected with the Δins6 strain showed a significant reduction in the intestinal villus-to-crypt ratio, attenuated body weight loss and increased survival rates, compared to those infected with the INS6-3HA strain.

CONCLUSIONS/SIGNIFICANCE: These results indicate that INS6 protein is involved in C. parvum proliferation and plays a critical role in modulating the pathogenicity of this zoonotic parasite. Deletion of this gene affects the invasion efficiency and pathogenicity of the parasite.

摘要

背景

微小隐孢子虫是一种常见的原生动物病原体,可导致人和动物出现中度至重度腹泻。寄生虫的入侵和逸出会对肠道上皮细胞造成损害,这是由来自几个独特细胞器(如微线体)的多种分泌蛋白介导的。先前的空间蛋白质组学分析已将胰岛素酶样蛋白酶6(INS6)鉴定为微小隐孢子虫中一种假定的微线体蛋白。然而,INS6对隐孢子虫致病性的功能贡献仍不清楚。在本研究中,我们使用基因操作技术来研究INS6在微小隐孢子虫中的表达和生物学功能。

方法/主要发现:使用CRISPR/Cas9技术在微小隐孢子虫中对INS6基因进行标记和缺失。通过免疫荧光分析、超微结构扩展显微镜和免疫电子显微镜确定INS6的表达。内源性标记显示INS6表达水平较低,在微小隐孢子虫的微线体中发现,在雄配子体阶段不存在。使用HCT-8培养物在体外评估INS6缺失对寄生虫生长和致病性的影响,并通过感染干扰素-γ基因敲除小鼠在体内进行评估。INS6基因的缺失损害了微小隐孢子虫在体外的增殖,并显著降低了感染小鼠体内的寄生虫负荷。此外,与感染INS6-3HA菌株的小鼠相比,感染Δins6菌株的小鼠肠绒毛与隐窝比值显著降低,体重减轻减轻,存活率提高。

结论/意义:这些结果表明,INS6蛋白参与微小隐孢子虫的增殖,并在调节这种人畜共患寄生虫的致病性中起关键作用。该基因的缺失影响寄生虫的入侵效率和致病性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c77b/12443312/48d746ddb80e/pntd.0013532.g001.jpg

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