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Evaluation of Leptospiral Recombinant Antigens MPL17 and MPL21 for Serological Diagnosis of Leptospirosis by Enzyme-Linked Immunosorbent Assays ▿

机译:酶联免疫吸附法评估钩端螺旋体重组抗原MPL17和MPL21在血清学诊断钩端螺旋体中的应用▿

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摘要

Leptospirosis is a zoonosis of multisystem involvement caused by pathogenic strains of the genus Leptospira. In the last few years, intensive studies aimed at the development of a vaccine have provided important knowledge about the nature of the immunological mechanisms of the host. The purpose of this study was to analyze the immune responses to two recombinant proteins, MPL17 and MPL21 (encoded by the genes LIC10765 and LIC13131, respectively) of Leptospira interrogans serovar Copenhageni in individuals during infection. The recombinant proteins were expressed in Escherichia coli as six-His tag fusion proteins and were purified from the soluble bacterial fraction by affinity chromatography with Ni2+-charged resin. The recombinant proteins were used to evaluate their ability to bind to immunoglobulin G (IgG) (and IgG subclass) or IgM antibodies in serum samples from patients in the early and convalescent phases of leptospirosis (n = 52) by enzyme-linked immunosorbent assays. The prevalences of total IgG antibodies against MPL17 and MPL21 were 38.5% and 21.2%, respectively. The titers achieved with MPL17 were statistically significantly higher than those obtained by the reference microscopic agglutination test. The specificity of the assay was estimated to be 95.5% for MPL17 and 80.6% for MPL21 when serum samples from individuals with unrelated febrile diseases and control healthy donors were tested. The proteins are conserved among Leptospira strains that cause human and animal diseases. MPL17 and MPL21 are most likely new surface proteins of leptospires, as revealed by liquid-phase immunofluorescence assays with living organisms. Our results demonstrate that these recombinant proteins are highly immunogenic and, when they are used together, might be useful as a means of diagnosing leptospirosis.
机译:钩端螺旋体病是由钩端螺旋体属的致病菌引起的多系统侵染的人畜共患病。在最近几年中,针对疫苗开发的深入研究提供了有关宿主免疫机制本质的重要知识。这项研究的目的是分析在感染过程中个体对问号钩端螺旋体serovar Copenhageni的两种重组蛋白MPL17和MPL21(分别由LIC10765和LIC13131基因编码)的免疫应答。重组蛋白在大肠杆菌中以6-His标签融合蛋白的形式表达,并通过Ni2 +负载树脂的亲和层析从可溶性细菌级分中纯化。重组蛋白用于通过酶联免疫吸附试验评估钩端螺旋体病早期和恢复期(n = 52)患者血清样品中免疫球蛋白G(IgG)(和IgG亚类)或IgM抗体的结合能力。针对MPL17和MPL21的总IgG抗体患病率分别为38.5%和21.2%。用MPL17达到的效价在统计学上显着高于通过参考显微凝集试验获得的效价。当测试患有不相关发热疾病的个体和对照健康供体的血清样品时,该测定的特异性对MPL17为95.5%,对MPL21为80.6%。这些蛋白质在导致人类和动物疾病的钩端螺旋体菌株中是保守的。 MPL17和MPL21最有可能是钩端螺旋体的新表面蛋白,如对活生物体进行的液相免疫荧光分析所揭示。我们的结果表明,这些重组蛋白具有高度的免疫原性,当将它们一起使用时,可能可用作诊断钩端螺旋体病的手段。

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