Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA.
School of Resources and Environmental Engineering, East China University of Science and Technology, Shanghai, China.
mBio. 2021 Mar 9;12(2):e03405-20. doi: 10.1128/mBio.03405-20.
The apicomplexan parasite contains an expanded family of 22 insulinase-like proteases (INS), a feature that contrasts with their otherwise streamlined genome. Here, we examined the function of INS1, which is most similar to the human insulinase protease that cleaves a variety of small peptide substrates. INS1 is an M16A clan member and contains a signal peptide, an N-terminal domain with the HXXEH active site, followed by three inactive domains. Unlike previously studied INS proteins that are expressed in sporozoites and during merogony, INS1 was expressed exclusively in macrogamonts, where it was localized in small cytoplasmic vesicles. Although INS1 did not colocalize with the oocyst wall protein recognized by the antibody OW50, immune-electron microscopy indicated that INS1 resides in small vesicles in the secretory system. Notably, these small INS1-positive vesicles were often in close proximity to large OW50-positive vacuoles resembling wall-forming bodies, which contain precursors for oocyst wall formation. Genetic deletion of INS1, or replacement with an active-site mutant, resulted in lower formation of macrogamonts and reduced oocyst shedding Our findings reveal that INS1 functions in the formation or maturation of macrogamonts and that its loss results in attenuated virulence in immunocompromised mice. Cryptosporidiosis is a debilitating diarrheal disease in young children in developing countries. The absence of effective treatments or vaccines makes this infection very difficult to manage in susceptible populations. Although the oral dose of oocysts needed to cause infection is low, infected individuals shed very high numbers of oocysts, readily contaminating the environment. Our studies demonstrate that the protease INS1 is important for formation of female sexual stages and that in its absence, parasites produce fewer oocysts and are attenuated in immunocompromised mice. These findings suggest that mutants lacking INS1, or related proteases, are useful for further characterizing the pathway that leads to macrogamont maturation and oocyst wall formation.
疟原虫含有一个扩展的 22 个胰岛素酶样蛋白酶家族(INS),这一特征与它们其他简化的基因组形成对比。在这里,我们研究了 INS1 的功能,它与人类胰岛素酶蛋白酶最相似,可切割多种小肽底物。INS1 是 M16A 族成员,含有信号肽、带有 HXXEH 活性位点的 N 端结构域,其后是三个无活性结构域。与先前研究的在孢子和裂殖体中表达的 INS 蛋白不同,INS1 仅在大配子体中表达,定位于小细胞质小泡中。尽管 INS1 与被抗体 OW50 识别的卵囊壁蛋白不共定位,但免疫电子显微镜表明 INS1 位于分泌系统中的小泡中。值得注意的是,这些小的 INS1 阳性小泡通常与大的 OW50 阳性空泡非常接近,类似于壁形成体,其中包含卵囊壁形成的前体。INS1 的基因缺失或活性位点突变的替换导致大配子体形成减少和卵囊脱落减少。我们的研究结果表明 INS1 参与大配子体的形成或成熟,其缺失导致免疫功能低下的小鼠毒力减弱。隐孢子虫病是发展中国家幼儿中一种使人虚弱的腹泻病。缺乏有效治疗方法或疫苗使这种感染在易感人群中非常难以控制。尽管引起感染所需的卵囊口服剂量很低,但受感染的个体排出的卵囊数量非常高,容易污染环境。我们的研究表明,蛋白酶 INS1 对雌性性阶段的形成很重要,在其缺失的情况下,寄生虫产生的卵囊较少,在免疫功能低下的小鼠中毒力减弱。这些发现表明,缺乏 INS1 或相关蛋白酶的突变体可用于进一步表征导致大配子体成熟和卵囊壁形成的途径。