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New Skin Test for Detection of Bovine Tuberculosis on the Basis of Antigen-Displaying Polyester Inclusions Produced by Recombinant Escherichia coli

机译:基于重组大肠杆菌产生的展示抗原的聚酯包涵体检测牛结核的新皮肤试验

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The tuberculin skin test for diagnosing tuberculosis (TB) in cattle lacks specificity if animals are sensitized to environmental mycobacteria, as some antigens in purified protein derivative (PPD) prepared from Mycobacterium bovis are present in nonpathogenic mycobacteria. Three immunodominant TB antigens, ESAT6, CFP10, and Rv3615c, are present in members of the pathogenic Mycobacterium tuberculosis complex but absent from the majority of environmental mycobacteria. These TB antigens have the potential to enhance skin test specificity. To increase their immunogenicity, these antigens were displayed on polyester beads by translationally fusing them to a polyhydroxyalkanoate (PHA) synthase which mediated formation of antigen-displaying inclusions in recombinant Escherichia coli . The most common form of these inclusions is poly(3-hydroxybutyric acid) (PHB). The respective fusion proteins displayed on these PHB inclusions (beads) were identified using tryptic peptide fingerprinting analysis in combination with matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS). The surface exposure and accessibility of antigens were assessed by enzyme-linked immunosorbent assay (ELISA). Polyester beads displaying all three TB antigens showed greater reactivity with TB antigen-specific antibody than did beads displaying only one TB antigen. This was neither due to cross-reactivity of antibodies with the other two antigens nor due to differences in protein expression levels between beads displaying single or three TB antigens. The triple-antigen-displaying polyester beads were used for skin testing of cattle and detected all cattle experimentally infected with M. bovis with no false-positive reactions observed in those sensitized to environmental mycobacteria. The results suggested applicability of TB antigen-displaying polyester inclusions as diagnostic reagents for distinguishing TB-infected from noninfected animals.
机译:如果动物对环境分枝杆菌敏感,则用于诊断牛结核病(TB)的结核菌素皮肤试验缺乏特异性,因为从牛分枝杆菌制备的纯化蛋白衍生物(PPD)中的某些抗原存在于非致病性分枝杆菌中。致病性结核分枝杆菌复合体的成员中存在三种免疫优势的TB抗原ESAT6,CFP10和Rv3615c,但大多数环境分枝杆菌中却不存在。这些TB抗原具有增强皮肤测试特异性的潜力。为了提高其免疫原性,这些抗原通过翻译融合到聚羟基链烷酸酯(PHA)合酶上而在聚酯珠粒上展示,该酶介导重组大肠杆菌中抗原展示夹杂物的形成。这些夹杂物的最常见形式是聚(3-羟基丁酸)(PHB)。使用胰蛋白酶肽指纹分析与基质辅助激光解吸电离-飞行时间质谱(MALDI-TOF MS)结合,可以鉴定出这些PHB内含物(珠子)上显示的各个融合蛋白。通过酶联免疫吸附测定(ELISA)评估抗原的表面暴露和可及性。与仅显示一种TB抗原的珠子相比,显示所有三种TB抗原的聚酯珠子对TB抗原特异性抗体的反应性更高。这既不是由于抗体与其他两种抗原的交叉反应性,也不是由于展示单个或三个TB抗原的磁珠之间蛋白质表达水平的差异。展示三重抗原的聚酯珠用于牛的皮肤测试,并检测了所有实验感染牛分枝杆菌的牛,在对环境分枝杆菌敏感的动物中未观察到假阳性反应。结果表明,展示TB抗原的聚酯内含物可作为区分未感染TB和未感染TB的诊断试剂。

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