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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Use of an isogenic Escherichia coli panel to design tests for discrimination of beta-lactamase functional groups of Enterobacteriaceae.
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Use of an isogenic Escherichia coli panel to design tests for discrimination of beta-lactamase functional groups of Enterobacteriaceae.

机译:使用等基因大肠埃希菌组设计用于区分肠杆菌科细菌的β-内酰胺酶官能团的测试。

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A study was designed to determine if an isogenic panel of Escherichia coli strains containing many different beta-lactamases could be used for the preliminary screening of a large number of beta-lactam agents to identify which might be most useful in the development of a definitive test for specific beta-lactamases found among the members of family Enterobacteriaceae. The susceptibilities of 46 strains, comprising the isogenic panel, to expanded-spectrum cephalosporins, cephamycins, and aztreonam were determined in the presence and absence of beta-lactamase inhibitors in broth microdilution tests. The results indicated that strains producing extended-spectrum beta-lactamases (ESBLs) could be distinguished from strains producing other Bush-Jacoby-Medeiros functional group 2 or group 1 beta-lactamases. For strains producing group 1 beta-lactamases, cefpodoxime and ceftazidime MICs were > or = 4 micrograms/ml and addition of clavulanate did not reduce the MICs more than fourfold. For strains producing group 2 enzymes other than ESBLs, cefpodoxime and ceftazidime MICs were < or = 2 micrograms/ml. With a single exception (ceftazidime for the strain producing SHV-3), among strains producing ESBLs, cefpodoxime and ceftazidime MICs were > or = 4 micrograms/ml and addition of clavulanate reduced the MICs by more than eightfold. Cephamycins could also be used to discriminate between strains producing group 1 beta-lactamases and ESBLs, since only the former required cefotetan concentrations as high as 8 micrograms/ml or cefoxitin concentrations of > 16 micrograms/ml for inhibition. Other cephalosporins provided some discrimination between the various beta-lactamase producers, although they were not as reliable as either cefpodoxime or ceftazidime. These results indicate the utility of an isogenic panel for identification of candidate drugs among many for further testing with clinical isolates of the family Enterobacteriaceae to determine the best agents for detection of specific beta-lactamases in this family.
机译:设计一项研究来确定包含许多不同β-内酰胺酶的大肠杆菌菌株的等基因组是否可以用于大量β-内酰胺类药物的初步筛选,以鉴定哪种可能在确定性试验的开发中最有用肠杆菌科成员中发现的特定β-内酰胺酶。在肉汤微稀释试验中,在存在和不存在β-内酰胺酶抑制剂的情况下,确定了包括等基因组在内的46种菌株对扩谱头孢菌素,头孢霉素和氨曲南的敏感性。结果表明,产生广谱β-内酰胺酶(ESBLs)的菌株可以与产生其他Bush-Jacoby-Medeiros官能团2或1组β-内酰胺酶的菌株区分开。对于产生第1组β-内酰胺酶的菌株,头孢泊肟和头孢他啶的MIC≥4微克/ ml,添加克拉维酸盐不会使MIC降低四倍以上。对于产生除ESBLs外的第2组酶的菌株,头孢泊肟和头孢他啶的MIC≤2微克/ ml。除了一个例外(用于产生SHV-3的菌株的头孢他啶),在产生ESBLs的菌株中,头孢泊肟肟和头孢他啶的MIC≥4微克/ ml,加入克拉维酸盐会使MIC降低八倍以上。头孢菌素也可用于区分产生第1组β-内酰胺酶和ESBLs的菌株,因为只有前者需要抑制作用才能使头孢替坦的浓度高达8微克/毫升或头孢西丁的浓度大于16微克/毫升。其他头孢菌素在各种β-内酰胺酶生产者之间提供了一些区别,尽管它们不如头孢泊肟或头孢他啶可靠。这些结果表明,同基因检测板可用于鉴定多种候选药物,以进一步检测肠杆菌科的临床分离物,以确定该家族中检测特定β-内酰胺酶的最佳药物。

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