Duim B, van Alphen L, Eijk P, Jansen H M, Dankert J
Department of Medical Microbiology, Academic Medical Centre, Amsterdam, The Netherlands.
Mol Microbiol. 1994 Mar;11(6):1181-9. doi: 10.1111/j.1365-2958.1994.tb00394.x.
The sequence of the gene encoding major outer membrane protein (MOMP) P2 of antigenic variants of non-encapsulated Haemophilus influenzae isolated from persistently infected chronic bronchitis patients was analysed. Antigenic drift was shown to result from single base changes in the P2 gene, all generating amino acid changes in the surface-exposed loops of MOMP P2, predominantly in loop 6. Similar single base changes were observed in H. influenzae persistently present in a subcutaneous cage implanted in rabbits, as well as in a spontaneous H. influenzae mutant that had survived MOMP P2 specific monoclonal-antibody-dependent bactericidal killing in vitro. We hypothesize that accumulation of point mutations under the selection pressure of immunity is a mechanism of antigenic drift of a surface-exposed protein during persistent H. influenzae infection.
对从持续感染的慢性支气管炎患者中分离出的非包膜流感嗜血杆菌抗原变异体的主要外膜蛋白(MOMP)P2编码基因序列进行了分析。结果表明,抗原漂移是由P2基因中的单碱基变化引起的,所有这些变化都导致MOMP P2表面暴露环中的氨基酸变化,主要发生在环6中。在植入兔子皮下笼中的持续存在的流感嗜血杆菌以及在体外经MOMP P2特异性单克隆抗体依赖性杀菌杀伤存活的自发流感嗜血杆菌突变体中也观察到了类似的单碱基变化。我们推测,在免疫选择压力下点突变的积累是持续性流感嗜血杆菌感染期间表面暴露蛋白抗原漂移的一种机制。