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革兰氏阴性菌中的新型β-内酰胺酶:多样性及其对抗菌治疗选择的影响

New beta-lactamases in gram-negative bacteria: diversity and impact on the selection of antimicrobial therapy.

作者信息

Bush K

机构信息

The R. W. Johnson Pharmaceutical Research Institute, Raritan, NJ, 08869, USA.

出版信息

Clin Infect Dis. 2001 Apr 1;32(7):1085-9. doi: 10.1086/319610. Epub 2001 Mar 21.

Abstract

Of the 340 discrete beta-lactamases that have been identified, the most important groups of enzymes that are continuing to proliferate include the plasmid-encoded cephalosporinases, the metallo-beta-lactamases, and the extended-spectrum beta-lactamases. Resistance to specific beta-lactam-containing antimicrobial agents frequently can be traced to a single beta-lactamase, but this task is becoming more difficult for the clinical microbiology laboratory. Other factors, such as multiple beta-lactamase production, transferable multidrug-resistance genes, alterations in outer-membrane porins, and possible antibiotic efflux, all may contribute to a resistance phenotype. Appreciation of these factors may help the physician make a more informed decision when choosing therapy to try to avoid selection of even more pathogenic strains.

摘要

在已鉴定出的340种离散β-内酰胺酶中,仍在不断增多的最重要的酶类包括质粒编码的头孢菌素酶、金属β-内酰胺酶和超广谱β-内酰胺酶。对特定含β-内酰胺抗菌药物的耐药性通常可追溯到单一的β-内酰胺酶,但对于临床微生物实验室而言,这项任务正变得越来越困难。其他因素,如多种β-内酰胺酶的产生、可转移的多药耐药基因、外膜孔蛋白的改变以及可能的抗生素外排,都可能导致耐药表型。了解这些因素可能有助于医生在选择治疗方法时做出更明智的决定,以尽量避免选择更具致病性的菌株。

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