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Novel Pneumocystis Antigen Discovery Using Fungal Surface Proteomics

机译:使用真菌表面蛋白质组学的新型肺孢子虫抗原发现。

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摘要

Pneumonia due to the fungus Pneumocystis jirovecii is a life-threatening infection that occurs in immunocompromised patients. The inability to culture the organism as well as the lack of an annotated genome has hindered antigen discovery that could be useful in developing novel vaccine- or antibody-based therapies as well as diagnostics for this infection. Here we report a novel method of surface proteomics analysis of Pneumocystis murina that reliably detected putative surface proteins that are conserved in Pneumocystis jirovecii. This technique identified novel CD4+ T-cell epitopes as well as a novel B-cell epitope, Meu10, which encodes a glycosylphosphatidylinositol (GPI)-anchored protein thought to be involved in ascospore assembly. The described technique should facilitate the discovery of novel target proteins for diagnostics and therapeutics for Pneumocystis infection.
机译:由于真菌肺炎支原体引起的肺炎是威胁生命的感染,发生在免疫功能低下的患者中。无法培养生物体以及缺少注释的基因组阻碍了抗原的发现,而抗原的发现可用于开发基于疫苗或抗体的新型疗法以及这种感染的诊断方法。在这里,我们报告尘肺孢子虫的表面蛋白质组学分析的一种新方法,该方法可以可靠地检测到在吉氏肺孢子虫中保守的推定表面蛋白。该技术鉴定了新的CD4 + T细胞表位以及新的B细胞表位Meu10,该表位编码糖基磷脂酰肌醇(GPI)锚定的蛋白质,被认为参与子囊孢子的组装。所描述的技术应有助于发现新的靶蛋白,用于诊断和治疗肺孢子虫感染。

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