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脆弱拟杆菌群典型培养菌株以及水解头孢西丁、拉氧头孢和亚胺培南的菌株的β-内酰胺酶

Beta-lactamases of type culture strains of the Bacteroides fragilis group and of strains that hydrolyse cefoxitin, latamoxef and imipenem.

作者信息

Eley A, Greenwood D

出版信息

J Med Microbiol. 1986 Feb;21(1):49-57. doi: 10.1099/00222615-21-1-49.

DOI:10.1099/00222615-21-1-49
PMID:3485198
Abstract

Susceptibilities to beta-lactam antibiotics and beta-lactamase content of two groups of Bacteroides strains were compared. Type cultures produced low levels of beta-lactamase and were susceptible to cefoxitin, latamoxef, imipenem and the combination of benzylpenicillin and clavulanic acid. Other Bacteroides strains that produced higher levels of beta-lactamase were generally less susceptible to these antibiotics; this resistance was more closely related to enzyme type than to the amount of enzyme present. The beta-lactamases produced by the test strains fell into three broad groups on the basis of antibiotic degradation and inhibitor profiles: those that inactivated benzylpenicillin, but not cefoxitin, latamoxef or imipenem, and were susceptible to inhibition by beta-lactamase inhibitors; those that hydrolysed benzylpenicillin, cefoxitin and latamoxef, but not imipenem, and which were less susceptible to inhibition by beta-lactamase inhibitors; an enzyme that inactivated all the antibiotics and was not inhibited by beta-lactamase inhibitors.

摘要

比较了两组拟杆菌菌株对β-内酰胺抗生素的敏感性和β-内酰胺酶含量。标准菌株产生低水平的β-内酰胺酶,对头孢西丁、拉氧头孢、亚胺培南以及苄青霉素与克拉维酸的组合敏感。其他产生较高水平β-内酰胺酶的拟杆菌菌株通常对这些抗生素较不敏感;这种耐药性与酶的类型比与酶的含量更密切相关。根据抗生素降解和抑制剂谱,测试菌株产生的β-内酰胺酶可分为三大类:一类能使苄青霉素失活,但不能使头孢西丁、拉氧头孢或亚胺培南失活,且对β-内酰胺酶抑制剂敏感;一类能水解苄青霉素头孢西丁和拉氧头孢,但不能水解亚胺培南,且对β-内酰胺酶抑制剂不太敏感;还有一种酶能使所有抗生素失活,且不受β-内酰胺酶抑制剂抑制。

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Beta-lactamases of type culture strains of the Bacteroides fragilis group and of strains that hydrolyse cefoxitin, latamoxef and imipenem.脆弱拟杆菌群典型培养菌株以及水解头孢西丁、拉氧头孢和亚胺培南的菌株的β-内酰胺酶
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J Bacteriol. 1996 Apr;178(7):1914-8. doi: 10.1128/jb.178.7.1914-1918.1996.
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Genotypic identification of two groups within the species Bacteroides fragilis by ribotyping and by analysis of PCR-generated fragment patterns and insertion sequence content.
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J Bacteriol. 1995 Sep;177(18):5270-5. doi: 10.1128/jb.177.18.5270-5275.1995.
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Antimicrob Agents Chemother. 1988 Aug;32(8):1243-6. doi: 10.1128/AAC.32.8.1243.
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