Lintermans P F, Pohl P, Bertels A, Charlier G, Vandekerckhove J, Van Damme J, Schoup J, Schlicker C, Korhonen T, De Greve H
Department of Bacteriology, National Institute of Veterinary Research, Brussels, Belgium.
Am J Vet Res. 1988 Nov;49(11):1794-9.
The F17 antigen from bovine enterotoxigenic Escherichia coli strain (E coli 25KHO9), which adhered to calf intestinal villi, was isolated. An enterotoxin-negative derivative (25KHO9st) was used for further studies. Using an immunogold-labeling technique, the F17 antigen was characterized as a fimbrial protein. Pure fimbriae with a subunit molecular weight of 20,000 were obtained by homogenization and use of a sucrose gradient. The adhesion of E coli 25KHO9st was mediated by the F17 fimbriae, as both F17 antibodies and F17 protein blocked the adhesion of the strain 25KHO9st. The F17 fimbriae were serologically distinct from K88, K99, F41, and 987P fimbriae and did not agglutinate bovine, ovine, guinea pig, human, or chicken erythrocytes. Peptide fingerprint analysis revealed F17 and F(Y) adhesins to be homologous, if not identical.
从附着于牛小肠绒毛的产肠毒素大肠杆菌菌株(大肠杆菌25KHO9)中分离出F17抗原。使用一种肠毒素阴性衍生物(25KHO9st)进行进一步研究。采用免疫金标记技术,F17抗原被鉴定为一种菌毛蛋白。通过匀浆和使用蔗糖梯度获得了亚基分子量为20,000的纯菌毛。大肠杆菌25KHO9st的黏附由F17菌毛介导,因为F17抗体和F17蛋白均能阻断25KHO9st菌株的黏附。F17菌毛在血清学上与K88、K99、F41和987P菌毛不同,并且不凝集牛、羊、豚鼠、人或鸡的红细胞。肽指纹分析显示F17和F(Y)黏附素即使不完全相同也是同源的。