Ben-Mahrez K, Sioud M
Biochemistry and Biotechnology Laboratory, Faculty of Sciences of Tunis, 2092 El- Manar II, Tunisia.
Arch Inst Pasteur Tunis. 2010;87(1-2):77-81.
The streptomycin resistance of Escherichia coli 2418 strain has been shown to be associated with a 1.2-kb DNA fragment found in the naturally occurring plasmid R2418S. Here, nucleotide sequence analysis of the 1.2-kb DNA fragment revealed the presence of the strB gene which is located immediately downstream of the strA gene. Both sequences are identical to those of strA and strB genes in plasmid RSF1010. Thus, the observed resistance in the clinical isolate is due to the presence of strA-strB genes encoding streptomycin-modifying enzymes. The sequence downstream of strB gene showed a perfect homology with that of RSF1010. In addition, it contained the right inverted repeat of the transposon Tn5393 that has been suggested to be a relic of this transposon found in DNA plasmids isolated from human- and animal-associated bacteria.
已证明大肠杆菌2418菌株的链霉素抗性与天然存在的质粒R2418S中发现的一个1.2 kb DNA片段有关。在此,对该1.2 kb DNA片段的核苷酸序列分析揭示了strB基因的存在,其位于strA基因的紧邻下游。这两个序列与质粒RSF1010中的strA和strB基因序列相同。因此,在临床分离株中观察到的抗性是由于存在编码链霉素修饰酶的strA-strB基因。strB基因下游的序列与RSF1010的序列显示出完全同源性。此外,它包含转座子Tn5393的右反向重复序列,该转座子被认为是在从人类和动物相关细菌中分离的DNA质粒中发现的该转座子的遗迹。