Loli A, Tzouvelekis L S, Tzelepi E, Carattoli A, Vatopoulos A C, Tassios P T, Miriagou V
Laboratory of Bacteriology, Institute Pasteur Hellenique, Athens, Greece.
J Antimicrob Chemother. 2006 Sep;58(3):669-72. doi: 10.1093/jac/dkl302. Epub 2006 Jul 26.
To elucidate the mechanisms responsible for the diversity of beta-lactam resistance phenotypes among isolates of a VIM-1-producing Klebsiella pneumoniae (VPKP) strain that is endemic in Greek hospitals.
Five VPKP clinical isolates were studied. MICs of beta-lactams were determined by agar dilution. PFGE of XbaI-digested genomic DNA was used for typing. Profiles of outer membrane proteins (OMPs) were determined by SDS-PAGE. Selected isolates were transformed with a plasmid encoding the Omp36K porin. beta-Lactamase activities were analysed by IEF and imipenem hydrolysis was assessed by spectrophotometry. VIM-1-encoding, self-transmissible plasmids were characterized by replicon typing, RFLP and hybridization with bla(VIM)- and IS26-specific probes. Characterization of integrons was performed by PCR, cloning and sequencing.
Isolates exhibited highly similar PFGE patterns. Imipenem MICs were 2, 4, 16, 32 and 64 mg/L. The isolate with the highest imipenem MIC (Vipm-64) lacked a 36 kDa OMP. Expression of a cloned OmpK36 in this isolate reduced the imipenem MIC to susceptibility levels. Imipenem-hydrolysing activity was significantly higher in Vipm-16 as compared with the other isolates that expressed similar amounts of VIM-1. All isolates transferred beta-lactam resistance to Escherichia coli through conjugative, IncN plasmids that exhibited differences in the RFLP and hybridization patterns with bla(VIM)- and IS26-specific probes. The Vipm-16 plasmid, mediating the higher imipenem MICs among transconjugants, carried two copies of bla(VIM-1). Cloning and sequencing showed In-e541-like integrons truncated at the 5'CS by insertion of IS26 elements at two different positions.
A VIM-1-producing strain of K. pneumoniae has evolved through OMP alterations and rearrangements in the bla(VIM-1)-carrying plasmid probably mediated by IS26, generating isolates with imipenem MICs ranging from susceptibility to resistance.
阐明希腊医院中流行的产VIM-1型肺炎克雷伯菌(VPKP)菌株分离株中β-内酰胺耐药表型多样性的相关机制。
对5株VPKP临床分离株进行研究。采用琼脂稀释法测定β-内酰胺类抗生素的最低抑菌浓度(MIC)。用XbaI酶切基因组DNA进行脉冲场凝胶电泳(PFGE)分型。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)测定外膜蛋白(OMP)图谱。用编码Omp36K孔蛋白的质粒转化选定的分离株。通过等电聚焦(IEF)分析β-内酰胺酶活性,用分光光度法评估亚胺培南水解情况。通过复制子分型、限制性片段长度多态性(RFLP)以及与bla(VIM)和IS26特异性探针杂交对携带VIM-1的自我传递质粒进行特征分析。通过聚合酶链反应(PCR)、克隆和测序对整合子进行特征分析。
分离株呈现高度相似的PFGE图谱。亚胺培南的MIC分别为2、4、16、32和64mg/L。亚胺培南MIC最高的分离株(Vipm-64)缺乏一种36kDa的OMP。在该分离株中克隆的OmpK36表达使亚胺培南MIC降至敏感水平。与表达相似量VIM-1的其他分离株相比,Vipm-16中亚胺培南水解活性显著更高。所有分离株通过接合性IncN质粒将β-内酰胺耐药性转移至大肠杆菌,这些质粒在与bla(VIM)和IS26特异性探针的RFLP和杂交模式上存在差异。在转接合子中介导更高亚胺培南MIC的Vipm-16质粒携带两个bla(VIM-1)拷贝。克隆和测序显示In-e541样整合子在5'保守序列(5'CS)处因IS26元件在两个不同位置插入而截短。
一株产VIM-1的肺炎克雷伯菌通过OMP改变以及携带bla(VIM-1)的质粒重排(可能由IS26介导)进化而来,产生了亚胺培南MIC范围从敏感到耐药的分离株。