Chen Shuxiong, Parlane Natalie A, Lee Jason, Wedlock D Neil, Buddle Bryce M, Rehm Bernd H A
Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
Appl Environ Microbiol. 2014 Apr;80(8):2526-35. doi: 10.1128/AEM.04168-13. Epub 2014 Feb 14.
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.
如果动物对环境分枝杆菌敏感,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)中的一些抗原也存在于非致病性分枝杆菌中。三种免疫显性结核抗原,ESAT6、CFP10和Rv3615c,存在于致病性结核分枝杆菌复合群成员中,但大多数环境分枝杆菌中不存在。这些结核抗原有可能提高皮肤试验的特异性。为了提高它们的免疫原性,通过将这些抗原与聚羟基链烷酸酯(PHA)合酶翻译融合,使其展示在聚酯珠上,该合酶介导重组大肠杆菌中抗原展示包涵体的形成。这些包涵体最常见的形式是聚(3-羟基丁酸)(PHB)。结合基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS),使用胰蛋白酶肽指纹图谱分析鉴定展示在这些PHB包涵体(珠子)上的各自融合蛋白。通过酶联免疫吸附测定(ELISA)评估抗原的表面暴露和可及性。展示所有三种结核抗原的聚酯珠与结核抗原特异性抗体的反应性比仅展示一种结核抗原的珠子更强。这既不是由于抗体与其他两种抗原的交叉反应,也不是由于展示单一或三种结核抗原的珠子之间蛋白质表达水平的差异。三抗原展示聚酯珠用于牛的皮肤试验,检测到所有实验感染牛分枝杆菌的牛,而对环境分枝杆菌敏感的牛未观察到假阳性反应。结果表明,展示结核抗原的聚酯包涵体作为区分感染结核和未感染动物的诊断试剂具有适用性。