Yi K, Murphy T F
Department of Microbiology, State University of New York at Buffalo, USA.
Microb Pathog. 1994 Oct;17(4):277-82. doi: 10.1006/mpat.1994.1073.
The P2 protein is the major outer-membrane protein of non-typeable Haemophilus influenzae (NTHI) and shows extreme heterogeneity among strains. Based on the analysis of antigenic structure, the P2 protein consists of eight potentially surface-exposed loops. Previous studies of monoclonal antibodies (mABs) to a single strain of NTHI showed that P2 contains potentially immunodominant epitopes in loop 5 of the molecule. The goal of the current work is to test the hypothesis that strain-specific and potentially immunodominant epitopes are located in loop 5 of P2 in other strains of NTHI as well. Gene fragments which encode peptides of loop 5 of strains 2019 and 5657 were cloned into an expression vector and subjected to immunoassays with mABs which recognize surface-exposed, bactericidal, strain-specific epitopes. Each mAB recognized loop 5 of the P2 protein of the homologous strain. Analysis of mutant clones with minor amino acid changes showed a loss of reactivity with the mABs. These observations indicate that loop 5 of the P2 molecule contains strain-specific, abundantly expressed surface-exposed epitopes. This further supports the hypothesis that loop 5 is an immunodominant region of the P2 molecule.
P2蛋白是非分型流感嗜血杆菌(NTHI)的主要外膜蛋白,在不同菌株间表现出极大的异质性。基于对抗抗原结构的分析,P2蛋白由八个潜在的表面暴露环组成。先前针对单一NTHI菌株的单克隆抗体(mABs)研究表明,P2分子的环5中含有潜在的免疫显性表位。当前研究的目的是检验以下假设:在其他NTHI菌株中,菌株特异性且潜在的免疫显性表位也位于P2的环5中。将编码2019株和5657株环5肽段的基因片段克隆到表达载体中,并用识别表面暴露、具有杀菌作用的菌株特异性表位的单克隆抗体进行免疫测定。每种单克隆抗体都识别同源菌株P2蛋白的环5。对氨基酸有微小变化的突变克隆进行分析,结果显示其与单克隆抗体的反应性丧失。这些观察结果表明,P2分子的环5含有菌株特异性、大量表达的表面暴露表位。这进一步支持了环5是P2分子免疫显性区域的假设。