Department of Molecular and Cell Biology, Boston University Goldman School of Dental Medicine, Boston, Massachusetts, United States of America.
Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts, United States of America.
PLoS Negl Trop Dis. 2019 May 16;13(5):e0007352. doi: 10.1371/journal.pntd.0007352. eCollection 2019 May.
Acanthamoeba castellanii, which causes keratitis and blindness in under-resourced countries, is an emerging pathogen worldwide, because of its association with contact lens use. The wall makes cysts resistant to sterilizing reagents in lens solutions and to antibiotics applied to the eye.
METHODOLOGY/PRINCIPAL FINDINGS: Transmission electron microscopy and structured illumination microscopy (SIM) showed purified cyst walls of A. castellanii retained an outer ectocyst layer, an inner endocyst layer, and conical ostioles that connect them. Mass spectrometry showed candidate cyst wall proteins were dominated by three families of lectins (named here Jonah, Luke, and Leo), which bound well to cellulose and less well to chitin. An abundant Jonah lectin, which has one choice-of-anchor A (CAA) domain, was made early during encystation and localized to the ectocyst layer of cyst walls. An abundant Luke lectin, which has two carbohydrate-binding modules (CBM49), outlined small, flat ostioles in a single-layered primordial wall and localized to the endocyst layer and ostioles of mature walls. An abundant Leo lectin, which has two unique domains with eight Cys residues each (8-Cys), localized to the endocyst layer and ostioles. The Jonah lectin and glycopolymers, to which it binds, were accessible in the ectocyst layer. In contrast, Luke and Leo lectins and the glycopolymers, to which they bind, were mostly inaccessible in the endocyst layer and ostioles.
CONCLUSIONS/SIGNIFICANCE: The most abundant A. castellanii cyst wall proteins are three sets of lectins, which have carbohydrate-binding modules that are conserved (CBM49s of Luke), newly characterized (CAA of Jonah), or unique to Acanthamoebae (8-Cys of Leo). Cyst wall formation is a tightly choreographed event, in which lectins and glycopolymers combine to form a mature wall with a protected endocyst layer. Because of its accessibility in the ectocyst layer, an abundant Jonah lectin is an excellent diagnostic target.
棘阿米巴原虫会导致资源匮乏国家的角膜炎和失明,是一种新兴的病原体,因为它与隐形眼镜的使用有关。其细胞壁使包囊能够抵抗隐形眼镜溶液中的杀菌试剂和应用于眼睛的抗生素。
方法/主要发现:透射电子显微镜和结构光照明显微镜(SIM)显示,经过纯化的棘阿米巴原虫包囊壁保留了一个外囊层、一个内囊层和连接它们的锥形口孔。质谱分析显示,囊壁蛋白候选物主要由三个家族的凝集素组成(这里称为约拿、路加和利奥),它们与纤维素结合良好,与几丁质结合较差。一种丰富的约拿凝集素,具有一个选择锚定 A(CAA)结构域,在包囊形成过程中早期形成,并定位于囊壁的外囊层。一种丰富的路加凝集素,具有两个碳水化合物结合模块(CBM49),在原始壁的单层中勾勒出小而平坦的口孔,并定位于成熟壁的内囊层和口孔。一种丰富的利奥凝集素,具有两个独特的含有 8 个半胱氨酸残基的结构域(8-Cys),定位于内囊层和口孔。约拿凝集素及其结合的糖聚合物在外囊层中是可及的。相比之下,路加和利奥凝集素及其结合的糖聚合物在内囊层和口孔中大多不可及。
结论/意义:棘阿米巴原虫最丰富的囊壁蛋白是三组凝集素,它们具有保守的碳水化合物结合模块(路加的 CBM49)、新描述的(约拿的 CAA)或仅存在于棘阿米巴属中的(利奥的 8-Cys)。囊壁形成是一个紧密协调的事件,其中凝集素和糖聚合物结合形成具有受保护的内囊层的成熟壁。由于其在外囊层中的可及性,丰富的约拿凝集素是一个极好的诊断靶标。