Yassien Mahmoud A, Ewis Hosam E, Lu Chung-Dar, Abdelal Ahmed T
Department of Microbiology and Immunology, Faculty of Pharmacy, Ain-Shams University, Cairo, Egypt.
Antimicrob Agents Chemother. 2002 Feb;46(2):360-6. doi: 10.1128/AAC.46.2.360-366.2002.
A genomic library from a strain of Salmonella enterica serovar Paratyphi B that exhibits multiple drug resistance (MDR) was constructed in Escherichia coli. Two of the recombinant plasmids, pNOR5 and pNOR5, conferred resistance only to fluoroquinolones in E. coli, whereas the third, pNCTR4, conferred the MDR phenotype. Sequence and subcloning analysis showed that it is the presence of RecA on the first two plasmids which confers resistance to fluoroquinolones in E. coli. A similar analysis established that the MDR phenotype conferred by pNCTR4 is due to a gene, rma (resistance to multiple antibiotics), which encodes a 13.5-kDa polypeptide. The derived sequence for Rma exhibits a high degree of similarity to those of a group of MarA-like activators that confer MDR in E. coli. A MalE-Rma fusion protein was purified to near homogeneity and was shown to interact with a DNA fragment carrying a MarA operator sequence. Furthermore, overexpression of rma in E. coli caused changes in the outer membrane protein profile that were similar to those reported for MarA. These results suggest that Rma might act as a transcriptional activator of the marA regulon.
构建了一株多重耐药的甲型副伤寒沙门氏菌的基因组文库,该文库存在于大肠杆菌中。其中两个重组质粒,pNOR5和pNOR5,仅使大肠杆菌对氟喹诺酮类药物产生耐药性,而第三个质粒pNCTR4则赋予了多重耐药表型。序列和亚克隆分析表明,前两个质粒上存在RecA,这使得大肠杆菌对氟喹诺酮类药物产生耐药性。类似的分析确定,pNCTR4赋予的多重耐药表型是由于一个名为rma(对多种抗生素耐药)的基因,该基因编码一种13.5 kDa的多肽。Rma的推导序列与一组在大肠杆菌中赋予多重耐药性的MarA样激活剂的序列高度相似。纯化了一种近乎纯质的MalE-Rma融合蛋白,并证明它与携带MarA操纵序列的DNA片段相互作用。此外,rma在大肠杆菌中的过表达导致外膜蛋白谱发生变化,这与报道的MarA情况相似。这些结果表明,Rma可能作为marA调控子的转录激活剂发挥作用。