Casey T A, Moseley S L, Moon H W
Physiopathology Research Unit, National Animal Disease Center, USDA-Agricultural Research Service, Ames, IA 50010.
Microb Pathog. 1990 Jun;8(6):383-92. doi: 10.1016/0882-4010(90)90025-l.
Certain DNA probes derived from accessory genes of cloned K88 and F41 determinants hybridize with Escherichia coli strains that express K88 or F41 and with certain other E. coli strains that do not express these antigens. We found that these probes hybridized with human enteroinvasive E. coli, and with bovine E. coli isolates which produced a fatal septicemia in experimentally infected piglets. These strains did not hybridize with probes derived from the structural subunit genes encoding the K88 and F41 antigens. E. coli strains isolated from turkeys with septicemia, Shigella and Salmonella strains did not hybridize to the K88 and F41 accessory gene probes. The K88 and F41 accessory genes probes hybridized with a 200 kb plasmid which is required for invasion by human enteroinvasive E. coli. The K88 and F41 accessory gene homology in the bovine isolates was located on a 150 kb transmissible plasmid but was unrelated to plasmids encoding aerobactin, Vir, or colicin V, which are suspected virulence factors in septicemic E. coli. A common plasmid-encoded antigen was associated with bovine isolates that hybridized with the K88 and F41 accessory gene probes. This included strains which express CS31A, a surface antigen associated with bovine septicemic E. coli, which also hybridized with the K88 and F4 accessory gene probes. The results suggest that the K88 and F41 accessory gene probes hybridized with sequences that may be associated with a common mechanism of pilus expression in distinct groups of E. coli pathogens.
某些源自克隆的K88和F41决定簇辅助基因的DNA探针,能与表达K88或F41的大肠杆菌菌株以及某些不表达这些抗原的其他大肠杆菌菌株杂交。我们发现这些探针能与人肠道侵袭性大肠杆菌以及在实验感染仔猪中引发致命败血症的牛大肠杆菌分离株杂交。这些菌株与源自编码K88和F41抗原的结构亚基基因的探针不杂交。从患有败血症的火鸡中分离出的大肠杆菌菌株、志贺氏菌和沙门氏菌菌株与K88和F41辅助基因探针不杂交。K88和F41辅助基因探针与一种200 kb的质粒杂交,该质粒是人类肠道侵袭性大肠杆菌入侵所必需的。牛分离株中的K88和F41辅助基因同源性位于一个150 kb的可传递质粒上,但与编码气杆菌素、Vir或大肠杆菌素V的质粒无关,这些质粒被怀疑是败血症性大肠杆菌的毒力因子。一种常见的质粒编码抗原与与K88和F41辅助基因探针杂交的牛分离株相关。这包括表达CS31A的菌株,CS31A是一种与牛败血症性大肠杆菌相关的表面抗原,它也与K88和F4辅助基因探针杂交。结果表明,K88和F41辅助基因探针与可能与不同组大肠杆菌病原体中菌毛表达的共同机制相关的序列杂交。