Rice L B, Carias L L, Marshall S H, Bonafede M E
Department of Veterans Affairs Medical Center, University School of Medicine, Cleveland, Ohio 44106.
Plasmid. 1996 Mar;35(2):81-90. doi: 10.1006/plas.1996.0010.
We have previously reported the presence of the staphylococcal beta-lactamase gene in chromosomes of Enterococcus faecalis strains CH19 and CH116. CH116 also harbors a 26-kb mobile element, designated Tn5384, which confers resistance to erythromycin and gentamicin. Sequence analysis of the rightmost 9 kb of Tn5384 indicates that this element lies immediately upstream of the beta-lactamase determinant in E. faecalis CH116. This 9-kb region consists of sequences highly homologous to those previously described in staphylococcal beta-lactamase plasmids, including a beta-lactamase transposon indistinguishable from Tn552, an open reading frame encoding a deduced amino acid sequence 94% identical to a previously described potential staphylococcal invertase, an intact copy of staphylococcal insertion-like element IS257, and the major portion of the staphylococcal organomercurial lyase (merB) gene. These data are consistent with the hypothesis that several of the resistance genes encoded within the large transferable region of the CH116 chromosome were originally components of a staphylococcal beta-lactamase plasmid.
我们之前报道过粪肠球菌CH19和CH116菌株的染色体中存在葡萄球菌β-内酰胺酶基因。CH116还含有一个26 kb的可移动元件,命名为Tn5384,它赋予对红霉素和庆大霉素的抗性。对Tn5384最右侧9 kb的序列分析表明,该元件位于粪肠球菌CH116中β-内酰胺酶决定簇的紧邻上游。这个9 kb的区域由与之前在葡萄球菌β-内酰胺酶质粒中描述的序列高度同源的序列组成,包括一个与Tn552无法区分的β-内酰胺酶转座子、一个开放阅读框,其推导的氨基酸序列与之前描述的潜在葡萄球菌转化酶有94%的同一性、葡萄球菌插入样元件IS257的一个完整拷贝,以及葡萄球菌有机汞裂解酶(merB)基因的主要部分。这些数据与以下假设一致,即CH116染色体大的可转移区域内编码的几个抗性基因最初是葡萄球菌β-内酰胺酶质粒的组成部分。