Patrick C C, Kimura A, Jackson M A, Hermanstorfer L, Hood A, McCracken G H, Hansen E J
Department of Pediatrics, Southwestern Medical School, Dallas, Texas.
Infect Immun. 1987 Dec;55(12):2902-11. doi: 10.1128/iai.55.12.2902-2911.1987.
Monoclonal antibodies (MAbs) directed against epitopes in the oligosaccharide portion of the lipooligosaccharide (LOS) of nontypable Haemophilus influenzae (NTHI) were used to characterize the LOS of this pathogen. Western blot (immunoblot) analysis with four LOS-specific MAbs and proteinase K-derived LOS preparations from 69 NTHI strains allowed the classification of these strains into nine LOS antigenic groups. The use of these MAbs in a more sensitive colony blot radioimmunoassay system together with these same NTHI strains identified 14 LOS antigenic groups. Extensive cross-reactivity was detected between the LOS epitopes of these NTHI strains and the LOS of H. influenzae type b. The epitopes recognized by these MAbs were not accessible to antibody on the surface of every strain. These LOS epitopes were also not stably expressed by NTHI growing in vitro; the observed frequency of LOS antigen variation ranged from 1 to 24% when large numbers of colonies of NTHI strains were screened for reactivity with the LOS-directed MAbs in the colony blot radioimmunoassay. This LOS antigenic variation was sometimes associated with alterations in the profile of the LOS molecule as resolved by dodecyl sulfate-polyacrylamide gradient gel electrophoresis followed by staining with silver. These data indicate that considerable antigenic diversity exists among NTHI strains with regard to the oligosaccharide epitopes in their LOS molecules.
针对不可分型流感嗜血杆菌(NTHI)脂寡糖(LOS)寡糖部分表位的单克隆抗体(MAb)被用于鉴定该病原体的LOS。用四种LOS特异性单克隆抗体和来自69株NTHI菌株的蛋白酶K衍生的LOS制剂进行蛋白质印迹(免疫印迹)分析,可将这些菌株分为九个LOS抗原组。在更灵敏的菌落印迹放射免疫分析系统中使用这些单克隆抗体,结合相同的NTHI菌株,鉴定出14个LOS抗原组。在这些NTHI菌株的LOS表位与b型流感嗜血杆菌的LOS之间检测到广泛的交叉反应性。这些单克隆抗体识别的表位并非在每个菌株表面都能被抗体识别。这些LOS表位在体外生长的NTHI中也不稳定表达;当在菌落印迹放射免疫分析中筛选大量NTHI菌株菌落与LOS导向单克隆抗体的反应性时,观察到的LOS抗原变异频率为1%至24%。这种LOS抗原变异有时与LOS分子谱的改变有关,这种改变通过十二烷基硫酸钠-聚丙烯酰胺梯度凝胶电泳分离,然后用银染色来确定。这些数据表明,NTHI菌株在其LOS分子中的寡糖表位方面存在相当大的抗原多样性。