Gołebiewski M, Kern-Zdanowicz I, Zienkiewicz M, Adamczyk M, Zylinska J, Baraniak A, Gniadkowski M, Bardowski J, Cegłowski P
Department of Microbial Biochemistry, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawińskiego 5a, 02-106 Warsaw, Poland.
Antimicrob Agents Chemother. 2007 Nov;51(11):3789-95. doi: 10.1128/AAC.00457-07. Epub 2007 Aug 13.
Here we report the nucleotide sequence of pCTX-M3, a highly conjugative plasmid that is responsible for the extensive spread of the gene coding for the CTX-M-3 extended-spectrum beta-lactamase in clinical populations of the family Enterobacteriaceae in Poland. The plasmid belongs to the IncL/M incompatibility group, is 89,468 bp in size, and carries 103 putative genes. Besides bla(CTX-M-3), it also bears the bla(TEM-1), aacC2, and armA genes, as well as integronic aadA2, dfrA12, and sul1, which altogether confer resistance to the majority of beta-lactams and aminoglycosides and to trimethoprim-sulfamethoxazole. The conjugal transfer genes are organized in two blocks, tra and trb, separated by a spacer sequence where almost all antibiotic resistance genes and multiple mobile genetic elements are located. Only bla(CTX-M-3), accompanied by an ISEcp1 element, is placed separately, in a DNA fragment previously identified as a fragment of the Kluyvera ascorbata chromosome. On the basis of sequence analysis, we speculate that pCTX-M3 might have arisen from plasmid pEL60 from plant pathogen Erwinia amylovora by acquiring mobile elements with resistance genes. This suggests that plasmids of environmental bacterial strains could be the source of those plasmids now observed in bacteria pathogenic for humans.
在此,我们报告了pCTX-M3的核苷酸序列,它是一种高度可接合的质粒,负责编码CTX-M-3超广谱β-内酰胺酶的基因在波兰肠杆菌科临床菌株中的广泛传播。该质粒属于IncL/M不相容群,大小为89,468 bp,携带103个推定基因。除bla(CTX-M-3)外,它还携带bla(TEM-1)、aacC2和armA基因,以及整合子aadA2、dfrA12和sul1,这些基因共同赋予对大多数β-内酰胺类、氨基糖苷类以及甲氧苄啶-磺胺甲恶唑的抗性。接合转移基因分为两个区域,即tra和trb,由一个间隔序列隔开,几乎所有抗生素抗性基因和多个可移动遗传元件都位于该间隔序列中。只有bla(CTX-M-3),伴随着一个ISEcp1元件,单独位于先前鉴定为克吕沃氏菌染色体片段的一个DNA片段中。基于序列分析,我们推测pCTX-M3可能是通过获得带有抗性基因的可移动元件,从植物病原菌梨火疫欧文氏菌的质粒pEL60衍生而来。这表明环境细菌菌株的质粒可能是现在在人类病原菌中观察到的那些质粒的来源。