Department of Parasitology, Faculty of Science, Charles University, BIOCEV, Vestec, Czech Republic.
Department of Cell Biology, Faculty of Science, Charles University, BIOCEV, Vestec, Czech Republic.
PLoS Pathog. 2021 Nov 15;17(11):e1010041. doi: 10.1371/journal.ppat.1010041. eCollection 2021 Nov.
Entamoeba histolytica is believed to be devoid of peroxisomes, like most anaerobic protists. In this work, we provided the first evidence that peroxisomes are present in E. histolytica, although only seven proteins responsible for peroxisome biogenesis (peroxins) were identified (Pex1, Pex6, Pex5, Pex11, Pex14, Pex16, and Pex19). Targeting matrix proteins to peroxisomes is reduced to the PTS1-dependent pathway mediated via the soluble Pex5 receptor, while the PTS2 receptor Pex7 is absent. Immunofluorescence microscopy showed that peroxisomal markers (Pex5, Pex14, Pex16, Pex19) are present in vesicles distinct from mitosomes, the endoplasmic reticulum, and the endosome/phagosome system, except Pex11, which has dual localization in peroxisomes and mitosomes. Immunoelectron microscopy revealed that Pex14 localized to vesicles of approximately 90-100 nm in diameter. Proteomic analyses of affinity-purified peroxisomes and in silico PTS1 predictions provided datasets of 655 and 56 peroxisomal candidates, respectively; however, only six proteins were shared by both datasets, including myo-inositol dehydrogenase (myo-IDH). Peroxisomal NAD-dependent myo-IDH appeared to be a dimeric enzyme with high affinity to myo-inositol (Km 0.044 mM) and can utilize also scyllo-inositol, D-glucose and D-xylose as substrates. Phylogenetic analyses revealed that orthologs of myo-IDH with PTS1 are present in E. dispar, E. nutalli and E. moshkovskii but not in E. invadens, and form a monophyletic clade of mostly peroxisomal orthologs with free-living Mastigamoeba balamuthi and Pelomyxa schiedti. The presence of peroxisomes in E. histolytica and other archamoebae breaks the paradigm of peroxisome absence in anaerobes and provides a new potential target for the development of antiparasitic drugs.
内阿米巴原虫被认为像大多数厌氧原生动物一样缺乏过氧化物酶体。在这项工作中,我们首次提供了过氧化物酶体存在于内阿米巴原虫中的证据,尽管只鉴定出了 7 种负责过氧化物酶体生物发生的蛋白质(过氧化物酶)(Pex1、Pex6、Pex5、Pex11、Pex14、Pex16 和 Pex19)。靶向过氧化物酶体的基质蛋白被减少到依赖 PTS1 的途径,该途径通过可溶性 Pex5 受体介导,而 PTS2 受体 Pex7 不存在。免疫荧光显微镜显示,过氧化物酶体标志物(Pex5、Pex14、Pex16、Pex19)存在于与线粒体、内质网和内体/吞噬体系统不同的小泡中,除了 Pex11,它在过氧化物酶体和线粒体中有双重定位。免疫电子显微镜显示 Pex14 定位于直径约 90-100nm 的小泡中。亲和纯化过氧化物酶体的蛋白质组学分析和计算机 PTS1 预测分别提供了 655 个和 56 个过氧化物酶候选物的数据集;然而,只有 6 种蛋白质同时存在于这两个数据集,包括肌醇脱氢酶(myo-IDH)。过氧化物酶体 NAD 依赖性肌醇脱氢酶似乎是一种具有高肌醇亲和力(Km 0.044mM)的二聚酶,也可以利用 scyllo-肌醇、D-葡萄糖和 D-木糖作为底物。系统发育分析表明,具有 PTS1 的肌醇脱氢酶的同源物存在于 E. dispar、E. nutalli 和 E. moshkovskii 中,但不存在于 E. invadens 中,并且与自由生活的 Mastigamoeba balamuthi 和 Pelomyxa schiedti 形成一个过氧化物酶体同源物的单系群。过氧化物酶体在内阿米巴原虫和其他原生动物中的存在打破了厌氧生物中过氧化物酶体缺失的范式,并为开发抗寄生虫药物提供了一个新的潜在靶点。