Holland J, Parsons T R, Hasan A A, Cook S M, Stevenson P, Griffiths E, Williams P
Department of Pharmaceutical Sciences, University of Nottingham, UK.
Microbiology (Reading). 1996 Dec;142 ( Pt 12):3505-13. doi: 10.1099/13500872-142-12-3505.
Haemophilus influenzae acquires iron from the iron-transporting glycoprotein transferrin via a receptor-mediated process. This involves two outer-membrane transferrin-binding proteins (Tbps) termed Tbp1 and Tbp2 which show considerable preference for the human form of transferrin. Since the Tbps are attracting considerable attention as potential vaccine components, we used transferrin affinity chromatography to examine their conservation amongst 28 H. influenzae type b strains belonging to different outer-membrane-protein subtypes as well as six non-typable strains. Whole cells of all type b and non-typable strains examined bound human transferrin; whilst most strains possessed a Tbp1 of approximately 105 kDa, the molecular mass of Tbp2 varied from 79 to 94 kDa. Antisera raised against affinity-purified native H. influenzae Tbp1/Tbp2 receptor complex cross-reacted on Western blots with the respective Tbps of all the Haemophilus strains examined. When used to probe Neisseria meningitidis Tbps, sera from each of four mice immunized with the Haemophilus Tbp1/2 complex recognized the 68 kDa Tbp2 of N. meningitidis strain B16B6 but not the 78 kDa Tbp2 of N. meningitidis strain 70942. Serum from one mouse also reacted weakly with Tbp1 of strain B16B6. Apart from a weak reaction with the Tbp2 of a serotype 5 strain, this mouse antiserum failed to recognize the Tbps of the porcine pathogen A. pleuropneumoniae. However, a monospecific polyclonal antiserum raised against the denatured Tbp2 of Neisseria meningitidis B16B6 recognized the Tbps of all Haemophilus and Actinobacillus strains examined. Since H. influenzae forms part of the natural flora of the upper respiratory tract, human sera were screened for the presence of antibodies to the Tbps. Sera from healthy adults contained antibodies which recognized both Tbp1 and Tbp2 from H. influenzae but not N. meningitidis. Convalescent sera from meningococcal meningitis patients contained antibodies which, on Western blots, recognized the Tbps2s of both pathogens. These data demonstrate the existence of shared epitopes on the Tbps of H. influenzae, N. meningitidis and A. pleuropneumoniae despite their transferrin species specificity.
流感嗜血杆菌通过受体介导的过程从铁转运糖蛋白转铁蛋白中获取铁。这涉及两种外膜转铁蛋白结合蛋白(Tbps),称为Tbp1和Tbp2,它们对人源转铁蛋白表现出相当大的偏好。由于Tbps作为潜在的疫苗成分受到了相当大的关注,我们使用转铁蛋白亲和色谱法来研究它们在28株属于不同外膜蛋白亚型的b型流感嗜血杆菌菌株以及6株不可分型菌株中的保守性。所有检测的b型和不可分型菌株的全细胞都能结合人转铁蛋白;虽然大多数菌株拥有约105 kDa的Tbp1,但Tbp2的分子量在79至94 kDa之间变化。针对亲和纯化的天然流感嗜血杆菌Tbp1/Tbp2受体复合物产生的抗血清在Western印迹上与所有检测的嗜血杆菌菌株的相应Tbps发生交叉反应。当用于探测脑膜炎奈瑟菌的Tbps时,用流感嗜血杆菌Tbp1/2复合物免疫的四只小鼠中的每只小鼠的血清都识别出脑膜炎奈瑟菌菌株B16B6的68 kDa Tbp2,但不识别脑膜炎奈瑟菌菌株70942的78 kDa Tbp2。一只小鼠的血清也与菌株B16B6的Tbp1发生了微弱反应。除了与5型菌株的Tbp2有微弱反应外,这种小鼠抗血清未能识别猪病原体胸膜肺炎放线杆菌的Tbps。然而,针对脑膜炎奈瑟菌B16B6变性Tbp2产生的单特异性多克隆抗血清识别了所有检测的嗜血杆菌和放线杆菌菌株的Tbps。由于流感嗜血杆菌是上呼吸道自然菌群的一部分,因此对人血清进行了针对Tbps抗体的筛查。健康成年人的血清中含有能识别流感嗜血杆菌的Tbp1和Tbp2但不能识别脑膜炎奈瑟菌的抗体。脑膜炎球菌性脑膜炎患者的恢复期血清中含有在Western印迹上能识别两种病原体的Tbps2s的抗体。这些数据表明,尽管流感嗜血杆菌、脑膜炎奈瑟菌和胸膜肺炎放线杆菌的Tbps具有转铁蛋白物种特异性,但它们的Tbps上仍存在共同表位。