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肠球菌对β-内酰胺类抗生素的耐药机制。

Mechanisms of resistance of enterococci to beta-lactam antibiotics.

作者信息

Fontana R, Canepari P, Lleò M M, Satta G

机构信息

Istituto di Microbiologia, Università degli Studi di Verona, Italy.

出版信息

Eur J Clin Microbiol Infect Dis. 1990 Feb;9(2):103-5. doi: 10.1007/BF01963633.

Abstract

Two mechanisms are responsible for resistance of enterococci to beta-lactam antibiotics: alterations of penicillin-binding proteins and production of a beta-lactamase. The latter has been found in a few clinical isolates of Enterococcus faecalis, whereas the former appears to account for resistance in most strains. A correlation has been established between the amount of a particular penicillin-binding protein which has a low affinity for penicillin and the level of resistance. The higher activity of some penicillins, as compared to cephalosporins, has been related to the relatively higher affinity for these penicillins of the penicillin-binding protein involved in the mechanism of resistance. Alterations in the autolytic enzyme pattern have been associated with the paradoxical response to bactericidal activity of penicillin often exhibited by Enterococcus faecalis clinical isolates.

摘要

肠球菌对β-内酰胺类抗生素耐药的机制有两种:青霉素结合蛋白的改变和β-内酰胺酶的产生。后者在少数粪肠球菌临床分离株中被发现,而前者似乎是大多数菌株耐药的原因。已确定对青霉素亲和力低的特定青霉素结合蛋白的量与耐药水平之间存在相关性。与头孢菌素相比,一些青霉素的活性较高,这与参与耐药机制的青霉素结合蛋白对这些青霉素的相对较高亲和力有关。自溶酶模式的改变与粪肠球菌临床分离株常表现出的对青霉素杀菌活性的矛盾反应有关。

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