Rice L B, Marshall S H
Division of Infectious Disease, Department of Veteran's Affairs Medical Center, Cleveland, Ohio.
Antimicrob Agents Chemother. 1992 Sep;36(9):1843-6. doi: 10.1128/AAC.36.9.1843.
We recently reported the chromosomal location of the staphylococcal beta-lactamase gene in four strains of Enterococcus faecalis. Transfer of this gene from strain CH19 to an enterococcal recipient was accompanied by transfer of numerous other antimicrobial resistance determinants in the absence of detectable plasmid DNA. A restriction map developed by comparing digestions of the regions surrounding the beta-lactamase gene in donor and recipient chromosomes resembles published maps of previously described staphylococcal beta-lactamase transposons, particularly in the area of the structural gene and its downstream region. In addition, DNA sequence analysis of the region immediately downstream of the beta-lactamase gene from both CH19 and its transcipient, CX19, revealed the presence of a 121-bp inverted repeat region found in Tn552 and Tn4002, two previously described staphylococcal beta-lactamase transposons. These results suggest that the chromosomal beta-lactamase gene of E. faecalis CH19 is incorporated into a transposonlike element derived from staphylococci.
我们最近报道了粪肠球菌四株菌株中葡萄球菌β-内酰胺酶基因的染色体定位。该基因从CH19菌株转移至肠球菌受体菌的过程中,在未检测到质粒DNA的情况下,还伴随着许多其他抗微生物耐药决定簇的转移。通过比较供体和受体染色体中β-内酰胺酶基因周围区域的消化产物所绘制的限制性图谱,类似于先前描述的葡萄球菌β-内酰胺酶转座子的已发表图谱,特别是在结构基因及其下游区域。此外,对CH19及其转导子CX19的β-内酰胺酶基因紧邻下游区域的DNA序列分析显示,存在一个在Tn552和Tn4002(两个先前描述的葡萄球菌β-内酰胺酶转座子)中发现的121 bp反向重复区域。这些结果表明,粪肠球菌CH19的染色体β-内酰胺酶基因被整合到一个源自葡萄球菌的类转座子元件中。