Neary J M, Yi K, Karalus R J, Murphy T F
Department of Microbiology, State University of New York at Buffalo, Buffalo, New York 14215, USA.
Infect Immun. 2001 Feb;69(2):773-8. doi: 10.1128/IAI.69.2.773-778.2001.
The P2 porin protein is the most abundant protein in the outer membrane of nontypeable Haemophilus influenzae (NTHI). Analysis of sequences of P2 from different strains reveals the presence of both heterogeneous and conserved surface-exposed loops of the P2 molecule among strains. The present study was undertaken to test the hypothesis that antibodies to a conserved surface-exposed loop are bactericidal for multiple strains of NTHI and could thus form the basis of vaccines to prevent infection due to NTHI. Polyclonal antiserum to a peptide corresponding to loop 6 was raised and was immunopurified over a loop 6 peptide column. Analysis of the antibodies to whole organisms and peptides corresponding to each of the eight loops of P2 by immunoassays revealed that the antibodies were highly specific for loop 6 of P2. The immunopurified antibodies bound to P2 of 14 of 15 strains in immunoblot assays. These antibodies to loop 6 demonstrated complement-mediated bactericidal killing of 8 of 15 strains. These results support the concept of using conserved regions of the P2 protein as a vaccine antigen.
P2孔蛋白是不可分型流感嗜血杆菌(NTHI)外膜中含量最丰富的蛋白质。对不同菌株的P2序列分析表明,各菌株中P2分子存在异质性和保守的表面暴露环。本研究旨在验证以下假设:针对保守表面暴露环的抗体对多种NTHI菌株具有杀菌作用,因此可作为预防NTHI感染疫苗的基础。制备了针对对应环6的肽段的多克隆抗血清,并在环6肽柱上进行免疫纯化。通过免疫分析对针对全菌以及对应P2八个环中每个环的肽段的抗体进行分析,结果显示这些抗体对P2的环6具有高度特异性。在免疫印迹分析中,免疫纯化的抗体与15株菌株中的14株的P2结合。这些针对环6的抗体在15株菌株中对8株表现出补体介导的杀菌作用。这些结果支持将P2蛋白的保守区域用作疫苗抗原的概念。