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Recombinant Truncated Flagellin of Burkholderia pseudomallei as a Molecular Probe for Diagnosis of Melioidosis

机译:重组截短的伯克霍尔德菌鞭毛蛋白作为诊断类胡萝卜素的分子探针

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摘要

Current serological tests for melioidosis, using impure or uncharacterized cell antigens from Burkholderia pseudomallei, have problems in detection sensitivity and specificity. Therefore, we designed and expressed the recombinant flagellin (truncated at both the N- and C-terminal ends), and used the antigen to develop an indirect enzyme-linked immunosorbent assay (ELISA) to diagnose melioidosis. Comparison of the immunoreactivities of the full-length and truncated flagellins reveals that the truncated flagellin performed much better in detection specificity and sensitivity. Only the full-length flagellin was recognized by other bacterial causing septicemia and gave a false-positive result in Western analysis, indicating that the cross-reactive epitopes were located on the more highly conserved N- and C-terminal regions of flagellin. The indirect ELISA using recombinant truncated flagellin as the antigen achieved 93.8% sensitivity and 96.3% specificity and offered a more efficient serodiagnosis of melioidosis.
机译:当前使用不纯或未鉴定的假疟原虫(Burkholderia pseudomallei)细胞抗原进行的类li虫病血清学检测在检测灵敏度和特异性方面存在问题。因此,我们设计并表达了重组鞭毛蛋白(在N端和C端均被截短),并使用该抗原开发了间接酶联免疫吸附测定(ELISA)来诊断类鼻疮。全长鞭毛蛋白和截短的鞭毛蛋白的免疫反应性的比较表明,截短的鞭毛蛋白在检测特异性和灵敏度方面表现更好。仅全长鞭毛蛋白可被引起败血症的其他细菌识别,并在Western分析中给出假阳性结果,表明交叉反应性抗原决定簇位于鞭毛蛋白N和C端保守性更高的区域。使用重组截短的鞭毛蛋白作为抗原的间接ELISA可获得93.8%的敏感性和96.3%的特异性,并提供了更有效的血清病诊断。

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