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一种广谱头孢菌素(Ro 48 - 8391)单独以及与两种新型β-内酰胺酶抑制剂(Ro 48 - 5545和Ro 48 - 8724)联合使用时的活性。

Activity of a broad-spectrum cephalosporin (Ro 48-8391) alone and in combination with two novel beta-lactamase inhibitors (Ro 48-5545 and Ro 48-8724).

作者信息

Jones R N, Marshall S A, Varnam D J

机构信息

Department of Pathology, University of Iowa College of Medicine, Iowa City 52242, USA.

出版信息

Diagn Microbiol Infect Dis. 1998 Oct;32(2):85-94. doi: 10.1016/s0732-8893(98)00045-5.

Abstract

The susceptibility of a group of beta-lactamase-producing and drug-resistant Gram-positive and Gram-negative organisms was tested against a novel cephalosporin (Ro 48-8391) alone and in combination with two bridged carbacephem beta-lactamase inhibitors (Ro 48-5545 or Ro 48-8724) and compared with that of ceftriaxone, ceftazidime, and cefepime (representative "third- and fourth-generation" cephalosporins), imipenem, and a combination of piperacillin and tazobactam. Five hundred and one selected clinical isolates were tested using the reference broth microdilution method (National Committee for Clinical Laboratory Standards). Ro 48-8391 has a spectrum of activity and potency most similar to ceftriaxone but with improved activity against Gram-positive species. The two beta-lactamase inhibitors, Ro 48-5545 and Ro 48-8724, have modest antimicrobial activity. When combined with Ro 48-8391, the beta-lactamase inhibitor Ro 48-8724 was superior to the combination of Ro 48-8391 and Ro 48-5545 in spectrum and enzyme inhibition against extended spectrum beta-lactamase enzyme-producing Escherichia coli and Klebsiella pneumoniae, and against Enterobacteriaceae with "stably derepressed" Bush-Jacoby-Medeiros gr 1 enzymes (ceftazidime-resistant Enterobacter and Citrobacter). Ro 48-5545 and Ro 48-8724 appear to be promising beta-lactamase inhibitors with potential application against chromosomal- and plasmid-mediated enzymes. Ro 48-8391, although superior to some currently available "third-generation" cephems, was not a well-matched active codrug because of limited activity against several commonly isolated species of clinically important bacteria. Further efforts are necessary to find a penicillin or cephem with activity more complementary to that of the tested beta-lactamase inhibitors and the Ro 48-8391 compound could be focused for therapeutic use in serious streptococcal infections.

摘要

对一组产β-内酰胺酶且耐药的革兰氏阳性和革兰氏阴性菌,单独用一种新型头孢菌素(Ro 48-8391)以及将其与两种桥连碳青霉烯β-内酰胺酶抑制剂(Ro 48-5545或Ro 48-8724)联合使用进行药敏试验,并与头孢曲松、头孢他啶和头孢吡肟(代表性的“第三代”和“第四代”头孢菌素)、亚胺培南以及哌拉西林和他唑巴坦的联合用药进行比较。采用参考肉汤微量稀释法(美国国家临床实验室标准委员会)对501株挑选出的临床分离菌株进行检测。Ro 48-8391的活性谱和效力与头孢曲松最为相似,但对革兰氏阳性菌的活性有所提高。两种β-内酰胺酶抑制剂Ro 48-5545和Ro 48-8724具有适度的抗菌活性。当与Ro 48-8391联合使用时,β-内酰胺酶抑制剂Ro 48-8724在对产超广谱β-内酰胺酶的大肠杆菌和肺炎克雷伯菌以及对具有“稳定去阻遏”的Bush-Jacoby-Medeiros 1组酶(对头孢他啶耐药的肠杆菌属和柠檬酸杆菌属)的肠杆菌科细菌的活性谱和酶抑制方面优于Ro 48-8391与Ro 48-5545的联合用药。Ro 48-5545和Ro 48-8724似乎是很有前景的β-内酰胺酶抑制剂,可能对染色体介导和质粒介导的酶都有应用价值。Ro 48-8391虽然优于一些现有的“第三代”头孢菌素,但由于对几种临床重要细菌的常见分离菌株活性有限,并不是一种匹配良好的活性联合用药。有必要进一步努力寻找一种青霉素或头孢菌素,其活性与受试的β-内酰胺酶抑制剂更具互补性,并且Ro 48-8391化合物可专注于在严重链球菌感染的治疗中使用。

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