Whiley S J, Lanser J A, Manning P A, Murray C, Steele T W
Division of Clinical Microbiology, Institute of Medical and Veterinary Science, Adelaide, Australia.
Appl Environ Microbiol. 1988 Jun;54(6):1591-4. doi: 10.1128/aem.54.6.1591-1594.1988.
After an outbreak of salmonellosis in humans caused by Salmonella typhimurium bacteriophage type 135, 62 isolates from human, animal, and water sources were retained for further analysis. Most of the isolates (92%) could be placed in one of five plasmid pattern groups, with a majority containing a common 60-kilobase plasmid and a smaller 3.8-kilobase-pair plasmid. This small plasmid, pIMVS1, was labeled with [32P]phosphate and used as a probe in subsequent colony and Southern hybridization studies. We concluded that pIMVS1 from isolates obtained from humans was genetically different from plasmids of a similar size found in isolates from chickens. Studies to characterize pIMVS1 were undertaken to determine if it codes for known virulence factors. It did not appear to be associated with the formation of attachment pili or major outer membrane proteins. By using transposon mutagenesis techniques, Tn3(Apr) was inserted into pIMVS1, and the existence of a restriction and modification system was deduced.
在由135型鼠伤寒沙门氏菌噬菌体引起的人类沙门氏菌病爆发后,保留了62株来自人类、动物和水源的分离株用于进一步分析。大多数分离株(92%)可归入五个质粒图谱组之一,大多数含有一个常见的60千碱基质粒和一个较小的3.8千碱基对质粒。这个小质粒pIMVS1用[32P]磷酸盐标记,并在随后的菌落和Southern杂交研究中用作探针。我们得出结论,从人类分离株中获得的pIMVS1在基因上与从鸡分离株中发现的类似大小的质粒不同。对pIMVS1进行了表征研究,以确定它是否编码已知的毒力因子。它似乎与附着菌毛或主要外膜蛋白的形成无关。通过使用转座子诱变技术,将Tn3(Apr)插入pIMVS1,并推断出存在限制和修饰系统。