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首页> 外文期刊>Frontiers in Microbiology >A Mechanism of Synergistic Effect of Streptomycin and Cefotaxime on CTX-M-15 Type β-lactamase Producing Strain of E. cloacae: A First Report
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A Mechanism of Synergistic Effect of Streptomycin and Cefotaxime on CTX-M-15 Type β-lactamase Producing Strain of E. cloacae: A First Report

机译:链霉素和头孢噻肟对<斜斜度CTX-M-15型β-内酰胺酶产生菌株的协同作用机制。 Cloacae:第一报告

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A bla _(CTX-M-15)gene is one of the most prevalent resistant marker found in member of enterobacteriaceae. It encodes cefotaxime hydrolysing β-lactamase-15 (CTX-M-15) causing resistance against beta lactam antibiotics. Since single antibiotic therapy fails to control infection caused by multidrug resistance strain, therefore combination therapy was came into practice as an effective treatment. We have first time explained the mechanism where two antibiotics of different classes work against resistant strains. Binding parameters obtained by spectroscopic approach showed significant interaction and complex formation between drugs and CTX-M-15 enzyme with decreased k_(sv)and k_(q)values. CD analysis showed altered conformation and significant changes in alpha helical content of CTX-M-15 enzyme on interaction with streptomycin in combination with cephalosporin. Steady state kinetics revealed decrease in hydrolytic efficiency of enzyme to about 27% by cooperative binding behavior upon sequential treatment of enzyme with streptomycin and cefotaxime. Therefore, the study concludes that combination therapy against CTX-M-15 producing strain with Cefotaxime/Streptomycin in 1:10 molar ratio, decreases CTX-M-15 efficiency significantly because of the fact that streptomycin induced structural changes in CTX-M-15 hence cefotaxime was not properly bound on its active site for hydrolysis rather available for the target to inhibit bacterial cells.
机译:BLA _(CTX-M-15)基因是在肠杆菌的成员中发现的最普遍的抗性标记之一。它编码Cefotaxime水解β-乳酰胺酶-15(CTX-M-15),导致对β内酰胺抗生素的抗性。由于单一抗生素治疗未能控制由多药耐药菌株引起的感染,因此联合治疗被实践为有效的治疗方法。我们第一次解释了不同类别的两种抗生素对抗抗性菌株的机制。通过光谱方法获得的结合参数在药物和CTX-M-15酶之间具有显着的相互作用和复杂的形成,其具有降低的K_(SV)和K_(Q)值。 CD分析显示CTX-M-15酶α螺旋含量的改变和显着变化与链孢菌素组合与链霉素的相互作用。稳态动力学通过合作结合行为在用链霉素和头孢噻肟酶顺序治疗时揭示了酶的水解效率降低至约27%。因此,该研究得出结论,在1:10摩尔比中对CTX-M-15产生菌株的联合治疗,并在1:10摩尔比下降低CTX-M-15效率,因为霉菌霉素诱导CTX-M-15的结构变化因此,Cefotaxime未在其活性位点上恰当地绑定,用于抑制靶点以抑制细菌细胞。

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