首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Comparison of the inoculum effects of members of the family Enterobacteriaceae on cefoxitin and other cephalosporins beta-lactamase inhibitor combinations and the penicillin-derived components of these combinations.
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Comparison of the inoculum effects of members of the family Enterobacteriaceae on cefoxitin and other cephalosporins beta-lactamase inhibitor combinations and the penicillin-derived components of these combinations.

机译:比较肠杆菌科成员对头孢西丁和其他头孢菌素β-内酰胺酶抑制剂组合以及这些组合中青霉素衍生的成分的接种效果。

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摘要

We compared the inoculum effects of 105 recent clinical isolates of the family Enterobacteriaceae on cefoxitin, other cephalosporins, aztreonam, and three beta-lactamase inhibitors (clavulanic acid, sulbactam, and tazobactam) and their penicillin-derived components. Piperacillin and aztreonam showed the largest inoculum effect, and cefoxitin showed the smallest. The other cephalosporins tested (cefotetan, ceftizoxime, and ceftriaxone) showed an intermediate inoculum effect. In general, the inoculum effect was of greater magnitude for the penicillin and beta-lactamase inhibitor combinations than for the cephalosporins tested. Bactericidal activity was assayed and morphologic changes were monitored for selected strains exhibiting a large inoculum effect. MICs correlated with bactericidal activity at an inoculum level of 10(5) CFU/ml, while activity at 10(8) CFU/ml was variable. Cefoxitin demonstrated the least filamentous transformation and the most rapid bactericidal activity. Aztreonam showed the most marked filamentous transformation and was no longer bactericidal at 10(8) CFU/ml. The beta-lactamase inhibitor combinations showed variable bactericidal activity, and regrowth occurred with a number of strains with all three agents tested.
机译:我们比较了肠杆菌科的105个近期临床分离株对头孢西丁,其他头孢菌素,氨曲南和三种β-内酰胺酶抑制剂(克拉维酸,舒巴坦和他唑巴坦)及其青霉素衍生成分的接种量影响。哌拉西林和氨曲南显示最大的接种效果,头孢西丁显示最小。测试的其他头孢菌素(头孢替坦,头孢唑肟和头孢曲松)显示出中等的接种效果。通常,青霉素和β-内酰胺酶抑制剂组合的接种效果要比所测试的头孢菌素更大。测定了杀菌活性并监测了表现出较大接种效果的选定菌株的形态变化。 MIC与接种量为10(5)CFU / ml的杀菌活性相关,而10(8)CFU / ml的杀菌活性却是可变的。头孢西丁显示出最少的丝状转化和最快的杀菌活性。 Aztreonam显示出最明显的丝状转化,并且不再以10(8)CFU / ml杀菌。 β-内酰胺酶抑制剂组合显示出不同的杀菌活性,并且在测试所有这三种药物的许多菌株中都发生了再生长。

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