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一种与补体结合抗体发生反应的粗球孢子菌特异性表位的定位。

Mapping of a Coccidioides immitis-specific epitope that reacts with complement-fixing antibody.

作者信息

Yang M C, Magee D M, Cox R A

机构信息

Department of Clinical Investigation, Texas Center for Infectious Disease, San Antonio 78223, USA.

出版信息

Infect Immun. 1997 Oct;65(10):4068-74. doi: 10.1128/iai.65.10.4068-4074.1997.

Abstract

We have previously cloned the cDNA fragment that encodes the complement fixation antigen of Coccidioides immitis. The recombinant protein was highly sensitive in detecting CF antibody in sera from patients with coccidioidomycosis but was not specific to C. immitis, as evidenced by its reactivity with sera from patients with histoplasmosis and, to lesser extent, blastomycosis. We undertook this study to determine if the epitope(s) that reacts with CF antibody is the same or differs from the epitopes that are shared with Histoplasma capsulatum and Blastomyces dermatitidis. PCR-generated CF/chitinase cDNA fragments were cloned and examined for their reactivity in enzyme-linked immunosorbent assays using sera from patients with coccidioidomycosis, histoplasmosis, or blastomycosis. A peptide domain comprised of amino acid residues 20 through 310 was shown to express an epitope(s) that is specific to anti-Coccidioides CF antibody. The peptide detected serum antibody in 21 (95%) of 22 patients with active coccidioidomycosis and was without reactivity with sera from 20 patients with histoplasmosis, 15 patients with blastomycosis, and 14 healthy subjects. Antibody titers to the recombinant peptide directly correlated with CF antibody titers (P < 0.01), and preadsorption of reference CF antiserum with the peptide ablated the reactivity of the antiserum in the immunodiffusion assay for CF antibody. The delineation of a recombinant peptide that has both sensitivity and specificity will provide a valuable tool for detecting CF antibody and for evaluating the role of CF antibody in the host response to C. immitis.

摘要

我们之前克隆了编码粗球孢子菌补体结合抗原的cDNA片段。该重组蛋白在检测球孢子菌病患者血清中的补体结合(CF)抗体时高度敏感,但并非粗球孢子菌所特有,因为它与组织胞浆菌病患者的血清有反应,与芽生菌病患者的血清反应较弱。我们开展这项研究以确定与CF抗体反应的表位是否与荚膜组织胞浆菌和皮炎芽生菌共有的表位相同或不同。通过聚合酶链反应(PCR)生成的CF/几丁质酶cDNA片段被克隆,并使用球孢子菌病、组织胞浆菌病或芽生菌病患者的血清在酶联免疫吸附试验中检测其反应性。由氨基酸残基20至310组成的肽结构域显示表达了一种对球孢子菌CF抗体特异的表位。该肽在22例活动性球孢子菌病患者中的21例(95%)检测到血清抗体,与20例组织胞浆菌病患者、15例芽生菌病患者和14名健康受试者的血清无反应。针对重组肽的抗体滴度与CF抗体滴度直接相关(P < 0.01),并且用该肽预吸附参考CF抗血清消除了抗血清在CF抗体免疫扩散试验中的反应性。确定一种兼具敏感性和特异性的重组肽将为检测CF抗体以及评估CF抗体在宿主对粗球孢子菌反应中的作用提供一个有价值的工具。

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