Forney L J, Marrs C F, Bektesh S L, Gilsdorf J R
Synergen, Inc., Boulder, Colorado 80301.
Infect Immun. 1991 Jun;59(6):1991-6. doi: 10.1128/iai.59.6.1991-1996.1991.
Previous studies have demonstrated antigenic differences among the pili expressed by various strains of Haemophilus influenzae type b (Hib). In order to understand the molecular basis for these differences, the structural gene for pilin was cloned from Hib strain Eagan (p+) and the nucleotide sequence was compared to those of strains M43 (p+) and 770235 b0f+, which had been previously determined. The pilin gene of Hib strain Eagan (p+) had a 648-bp open reading frame that encoded a 20-amino-acid leader sequence followed by the 196 amino acids found in mature pilin. The translated sequence was three amino acids larger than pilins of strains M43 (p+) and 770235 b0f+ and was 78% identical and 95% homologous when conservative amino acid substitutions were considered. Differences between the amino acid sequences were not localized to any one region but rather were distributed throughout the proteins. Comparison of protein hydrophilicity profiles showed several hydrophilic regions with sequences that were conserved between strain Eagan (p+) and pilins of other Hib strains, and these regions represent potentially conserved antigenic domains. Southern blot analyses using an intragenic probe from the pilin gene of strain Eagan (p+) showed that the pilin gene was conserved among all type b and nontypeable strains of H. influenzae examined, and only a single copy was present in these strains. Homologous genes were not present in the phylogenetically related species Pasteurella multocida, Pasteurella haemolytica, and Actinobacillus pleuropneumoniae. These data indicate that the pilin gene was highly conserved among different strains of H. influenzae and that small differences in the pilin amino acid sequences account for the observed antigenic differences of assembled pili from these strains.
先前的研究已证明,b型流感嗜血杆菌(Hib)不同菌株表达的菌毛之间存在抗原差异。为了了解这些差异的分子基础,从Hib菌株伊根(p+)中克隆了菌毛蛋白的结构基因,并将其核苷酸序列与先前已确定的菌株M43(p+)和770235 b0f+的序列进行比较。Hib菌株伊根(p+)的菌毛蛋白基因有一个648个碱基对的开放阅读框,编码一个20个氨基酸的前导序列,随后是成熟菌毛蛋白中的196个氨基酸。翻译后的序列比菌株M43(p+)和770235 b0f+的菌毛蛋白多三个氨基酸,当考虑保守氨基酸替换时,其序列一致性为78%,同源性为95%。氨基酸序列的差异并非局限于任何一个区域,而是分布在整个蛋白质中。蛋白质亲水性图谱的比较显示,伊根菌株(p+)与其他Hib菌株的菌毛蛋白之间有几个亲水区的序列是保守的,这些区域代表潜在的保守抗原结构域。使用来自伊根菌株(p+)菌毛蛋白基因的基因内探针进行的Southern印迹分析表明,菌毛蛋白基因在所有检测的b型和不可分型流感嗜血杆菌菌株中是保守的,并且这些菌株中仅存在一个拷贝。在系统发育相关的物种多杀巴斯德菌、溶血巴斯德菌和胸膜肺炎放线杆菌中不存在同源基因。这些数据表明,菌毛蛋白基因在不同的流感嗜血杆菌菌株中高度保守,并且菌毛蛋白氨基酸序列的微小差异解释了这些菌株组装菌毛所观察到的抗原差异。