Gerlach G F, Clegg S, Ness N J, Swenson D L, Allen B L, Nichols W A
Department of Microbiology, University of Iowa, Iowa City 52242.
Infect Immun. 1989 Mar;57(3):764-70. doi: 10.1128/iai.57.3.764-770.1989.
Deletions within the cloned genes (fimA) encoding the type 1 major fimbrial subunits of two isolates of Klebsiella pneumoniae resulted in a nonfimbriate but hemagglutinating phenotype after transformation of Escherichia coli HB101 or ORN103. Phenotypic expression of type 1 fimbriae could be restored by transformation with plasmids containing the fimA genes of the fimbrial gene clusters from different strains. The surface fimbriae expressed were serologically identical to those of the polymerized product of the introduced fimA gene. The fimA gene products of Salmonella typhimurium and Serratia marcescens could utilize the accessory fimbrial genes of K. pneumoniae to produce surface-associated, hemagglutinating fimbriae. The relatedness of the type 1 fimbrial gene clusters from multiple isolates of members of the family Enterobacteriaceae was examined by DNA hybridization techniques. These analyses demonstrated little nucleotide sequence agreement among distinct genera of the enteric bacteria.
编码肺炎克雷伯菌两个分离株1型主要菌毛亚基的克隆基因(fimA)内的缺失,导致在大肠杆菌HB101或ORN103转化后出现无菌毛但有血凝活性的表型。用含有来自不同菌株菌毛基因簇的fimA基因的质粒转化,可以恢复1型菌毛的表型表达。表达的表面菌毛在血清学上与导入的fimA基因聚合产物的菌毛相同。鼠伤寒沙门氏菌和粘质沙雷氏菌的fimA基因产物可以利用肺炎克雷伯菌的辅助菌毛基因来产生与表面相关的血凝菌毛。通过DNA杂交技术检测了肠杆菌科多个分离株1型菌毛基因簇的相关性。这些分析表明,肠道细菌不同属之间核苷酸序列一致性很低。