Pinon G, Quentin R, Dubray G
Laboratoire de Bactériologie, CHU Bretonneau, Tours, France.
Ann Inst Pasteur Microbiol. 1986 Sep-Oct;137B(2):195-205.
The techniques of capsular serotype, biotype determination and sodium dodecylsulphate polyacrylamide gel electrophoresis of sarcosinate-insoluble outer membrane protein (OMP) and of proteinase K lipopolysaccharide (LPS) preparations were applied to 41 genital and neonatal Haemophilus influenzae isolates. Twelve percent were capsulated (4b, 1a). Distribution of strains between biotypes was similar to that of isolates of other non-systemic pathogenic origin; only one isolate was biotype IV. The OMP profiles showed great variability with 4 group of proteins: a 16-Kd major peptide which was observed in all strains; 27-30-Kd major OMP including one constant 30-Kd peptide present in all strains except one; 32- to 50-Kd major OMP; and 49- to 54-Kd minor OMP. The rough LPS profiles also revealed heterogeneity. In view of the variability observed among H. influenzae strains, it is not possible to establish a relationship between pathogenicity and a macromolecular marker.
采用荚膜血清型、生物型测定技术以及肌氨酸不溶性外膜蛋白(OMP)和蛋白酶K脂多糖(LPS)制剂的十二烷基硫酸钠聚丙烯酰胺凝胶电泳技术,对41株生殖道和新生儿流感嗜血杆菌分离株进行检测。12%的菌株有荚膜(4b、1a)。生物型之间菌株的分布与其他非系统性致病源分离株的分布相似;只有一株分离株为生物型IV。OMP图谱显示出很大的变异性,有4组蛋白质:在所有菌株中均观察到的16-Kd主要肽段;27 - 30-Kd主要OMP,包括除一株菌株外所有菌株中均存在的一个恒定的30-Kd肽段;32至50-Kd主要OMP;以及49至54-Kd次要OMP。粗糙LPS图谱也显示出异质性。鉴于在流感嗜血杆菌菌株中观察到的变异性,不可能在致病性和大分子标志物之间建立联系。