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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Activity of NXL104 in combination with beta-lactams against genetically characterized Escherichia coli and Klebsiella pneumoniae isolates producing class A extended-spectrum beta-lactamases and class C beta-lactamases.
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Activity of NXL104 in combination with beta-lactams against genetically characterized Escherichia coli and Klebsiella pneumoniae isolates producing class A extended-spectrum beta-lactamases and class C beta-lactamases.

机译:NXL104与β-内酰胺类组合物对具有遗传特征的大肠埃希菌和肺炎克雷伯菌的分离物的活性,可产生A类广谱β-内酰胺酶和C类β-内酰胺酶。

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摘要

The novel non-beta-lactam beta-lactamase inhibitor NXL104, in combination with cefepime, ceftazidime, ceftriaxone, amdinocillin, and meropenem, was tested against 190 extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae isolates, 94 AmpC-hyperproducing E. coli isolates, and 8 AmpC/ESBL-coexpressing E. coli isolates. NXL104 restored 100% susceptibility to the partner cephalosporins for all isolates tested. Amdinocillin and meropenem MICs were modestly improved (2 to 32 times lower) by NXL104. These results suggest that NXL104 may be useful in combination with beta-lactams for the treatment of infections caused by ESBL- and AmpC-producing Enterobacteriaceae.
机译:测试了新型的非β-内酰胺β-内酰胺酶抑制剂NXL104与头孢吡肟,头孢他啶,头孢曲松,氨苄西林和美罗培南的组合,针对产生190倍广谱β-内酰胺酶(ESBL)的大肠杆菌和肺炎克雷伯菌分离株,94高产AmpC的大肠杆菌分离株和共表达8个AmpC / ESBL的大肠杆菌分离株。对于所有测试的分离物,NXL104恢复了对伙伴头孢菌素的100%敏感性。 NXL104对Amdinocillin和美罗培南的MIC有所改善(降低了2至32倍)。这些结果表明,NXL104与β-内酰胺类药物联合使用可用于治疗由产生ESBL和AmpC的肠杆菌科细菌引起的感染。

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