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致病卵菌寄生腐霉的74千道尔顿免疫显性抗原是一种假定的外切1,3-β-葡聚糖酶。

The 74-kilodalton immunodominant antigen of the pathogenic oomycete Pythium insidiosum is a putative exo-1,3-beta-glucanase.

作者信息

Krajaejun Theerapong, Keeratijarut Angsana, Sriwanichrak Kanchana, Lowhnoo Tassanee, Rujirawat Thidarat, Petchthong Thanom, Yingyong Wanta, Kalambaheti Thareerat, Smittipat Nat, Juthayothin Tada, Sullivan Thomas D

机构信息

Department of Pathology, Faculty of Medicine-Ramathibodi Hospital, Mahidol University, Rama 6 Road, Bangkok, Thailand.

出版信息

Clin Vaccine Immunol. 2010 Aug;17(8):1203-10. doi: 10.1128/CVI.00515-09. Epub 2010 Mar 17.

Abstract

The oomycetous, fungus-like, aquatic organism Pythium insidiosum is the causative agent of pythiosis, a life-threatening infectious disease of humans and animals living in tropical and subtropical areas of the world. Common sites of infection are the arteries, eyes, cutaneous/subcutaneous tissues, and gastrointestinal tract. Diagnosis of pythiosis is time-consuming and difficult. Radical excision of the infected organs is the main treatment for pythiosis because conventional antifungal drugs are ineffective. An immunotherapeutic vaccine prepared from P. insidiosum crude extract showed limited efficacy in the treatment of pythiosis patients. Many pythiosis patients suffer lifelong disabilities or die from an advanced infection. Recently, we identified a 74-kDa major immunodominant antigen of P. insidiosum which could be a target for development of a more effective serodiagnostic test and vaccines. Mass spectrometric analysis identified two peptides of the 74-kDa antigen (s74-1 and s74-2) which perfectly matched a putative exo-1,3-ss-glucanase (EXO1) of Phytophthora infestans. Using degenerate primers derived from these peptides, a 1.1-kb product was produced by PCR, and its sequence was found to be homologous to that of the P. infestans exo-1,3-ss-glucanase gene, EXO1. Enzyme-linked immunosorbent assays targeting the s74-1 and s74-2 synthetic peptides demonstrated that the 74-kDa antigen was highly immunoreactive with pythiosis sera but not with control sera. Phylogenetic analysis using part of the 74-kDa protein-coding sequence divided 22 Thai isolates of P. insidiosum into two clades. Further characterization of the putative P. insidiosum glucanase could lead to new diagnostic tests and to antimicrobial agents and vaccines for the prevention and management of the serious and life-threatening disease of pythiosis.

摘要

卵菌纲、真菌样、水生生物隐孢子虫是腐霉病的病原体,腐霉病是一种威胁生活在世界热带和亚热带地区的人类和动物生命的传染病。常见的感染部位是动脉、眼睛、皮肤/皮下组织和胃肠道。腐霉病的诊断既耗时又困难。由于传统抗真菌药物无效,对感染器官进行根治性切除是腐霉病的主要治疗方法。由隐孢子虫粗提物制备的免疫治疗疫苗在治疗腐霉病患者方面显示出有限的疗效。许多腐霉病患者终身残疾或死于晚期感染。最近,我们鉴定出一种74 kDa的隐孢子虫主要免疫显性抗原,它可能成为开发更有效的血清诊断测试和疫苗的靶点。质谱分析鉴定出74 kDa抗原的两种肽段(s74-1和s74-2),它们与致病疫霉的一种假定的外切-1,3-β-葡聚糖酶(EXO1)完全匹配。使用从这些肽段衍生的简并引物,通过PCR产生了一个1.1 kb的产物,其序列与致病疫霉外切-1,3-β-葡聚糖酶基因EXO1的序列同源。针对s74-1和s74-2合成肽的酶联免疫吸附测定表明,74 kDa抗原与腐霉病血清具有高度免疫反应性,但与对照血清无反应。使用74 kDa蛋白质编码序列的一部分进行的系统发育分析将22株泰国隐孢子虫分离株分为两个进化枝。对假定的隐孢子虫葡聚糖酶的进一步表征可能会带来新的诊断测试以及用于预防和管理严重且危及生命的腐霉病的抗菌剂和疫苗。

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