Chowdry N, Threlfall E J, Rowe B, Stanley J
NCTC Molecular Genetics Unit, Public Health Laboratory Service, London, UK.
Epidemiol Infect. 1993 Apr;110(2):217-25. doi: 10.1017/s0950268800068138.
An analysis of genotype was made for representative strains of Salmonella dublin. The collection consisted primarily of strains isolated from humans in England and Wales, and were of both intestinal and extra-intestinal origin. Three genetic elements were characterized by DNA hybridization. They were the spvBC genes, extrachromosomal virulence determinants, the salmonella-specific insertion sequence IS200, and the 16S ribosomal RNA genes, a phylogenetic marker. Two clones of S. dublin (SdRI and SdRII) which shared an identical IS200 profile, were identified on the basis of restriction fragment length polymorphism at the 16S rRNA locus. With one exception, all strains harboured a 52 MDa plasmid which contained a conserved 3.7 kbp Hind III fragment homologous to the spvBC mouse-virulence genes of S. typhimurium. However, a single plasmid-free strain of SdRI, isolated from a patient with septicaemia exhibited no spc homology. In SdRI there was no observable genotype distinction between strains causing gastroenteritis or bacteraemia. In contrast, none of the strains of SdRII were from cases of bacteraemia, and all human isolates of this clone were from cases of gastroenteritis.
对都柏林沙门氏菌的代表性菌株进行了基因型分析。该菌株收集主要包括从英格兰和威尔士的人类中分离出的菌株,有肠道和肠道外来源。通过DNA杂交鉴定了三种遗传元件。它们是spvBC基因、染色体外毒力决定簇、沙门氏菌特异性插入序列IS200以及16S核糖体RNA基因(一种系统发育标记)。根据16S rRNA基因座处的限制性片段长度多态性,鉴定出两个具有相同IS200图谱的都柏林沙门氏菌克隆(SdRI和SdRII)。除了一个例外,所有菌株都携带一个52 MDa的质粒,该质粒包含一个与鼠伤寒沙门氏菌的spvBC小鼠毒力基因同源的保守3.7 kbp Hind III片段。然而,从一名败血症患者分离出的一株无质粒的SdRI菌株没有spc同源性。在SdRI中,引起肠胃炎或菌血症的菌株之间没有可观察到的基因型差异。相比之下,SdRII的菌株均非来自菌血症病例,该克隆的所有人类分离株均来自肠胃炎病例。