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美国24家医院肺炎克雷伯菌分离株中新型β-内酰胺酶的出现情况。

Occurrence of newer beta-lactamases in Klebsiella pneumoniae isolates from 24 U.S. hospitals.

作者信息

Moland Ellen Smith, Black Jennifer A, Ourada Jason, Reisbig Mark D, Hanson Nancy D, Thomson Kenneth S

机构信息

Center for Research in Antiinfectives and Biotechnology, Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, Nebraska 68178, USA.

出版信息

Antimicrob Agents Chemother. 2002 Dec;46(12):3837-42. doi: 10.1128/AAC.46.12.3837-3842.2002.

Abstract

Despite the discovery of novel beta-lactamases such as extended-spectrum beta-lactamases (ESBLs), imported AmpC, and carbapenem-hydrolyzing beta-lactamases at least a decade ago, there remains a low level of awareness of their importance and how to detect them. There is a need to increase the levels of awareness of clinical laboratories about the detection of newer beta-lactamases. Therefore, a study was conducted in 2000 to investigate the occurrence of these beta-lactamases in Klebsiella pneumoniae isolates at 24 U.S. medical centers. To enhance the likelihood of detecting imported AmpC and carbapenem-hydrolyzing beta-lactamases, participating laboratories were permitted to include archived strains (1996 to 2000) that were intermediate or resistant to either cefoxitin or imipenem. The beta-lactamase production of 408 isolates positive by screening of 1,123 isolates was investigated by ESBL phenotypic confirmation tests; and for AmpC and carbapenem-hydrolyzing beta-lactamases, three-dimensional tests, isoelectric focusing, beta-lactamase inhibitor studies, spectrophotometric assays, induction assays, and molecular tests were used. ESBL-producing isolates were detected at 18 of the 24 sites (75%), imported AmpC-producing isolates were detected at 10 sites (42%), inducible imported AmpC-producing isolates were detected at 3 sites (12.5%), and a molecular class A carbapenem-hydrolyzing enzyme was detected at 1 site (4%). No class B or D carbapenem-hydrolyzing enzymes were detected. ESBLs and imported AmpC beta-lactamases were detected at a significant number of sites, indicating widespread penetration of these enzymes into U.S. medical institutions. Because these enzymes may significantly affect therapeutic outcomes, it is vital that clinical laboratories be aware of them and be able to detect their occurrence.

摘要

尽管至少在十年前就发现了新型β-内酰胺酶,如超广谱β-内酰胺酶(ESBLs)、导入型AmpC酶和碳青霉烯水解β-内酰胺酶,但人们对其重要性以及如何检测它们的认识仍然较低。有必要提高临床实验室对新型β-内酰胺酶检测的认识水平。因此,在2000年进行了一项研究,以调查美国24家医疗中心肺炎克雷伯菌分离株中这些β-内酰胺酶的发生情况。为了提高检测导入型AmpC酶和碳青霉烯水解β-内酰胺酶的可能性,参与研究的实验室被允许纳入对头孢西丁或亚胺培南呈中介或耐药的存档菌株(1996年至2000年)。通过ESBL表型确认试验对1123株分离株筛选出的408株阳性分离株的β-内酰胺酶产生情况进行了研究;对于AmpC酶和碳青霉烯水解β-内酰胺酶,使用了三维试验、等电聚焦、β-内酰胺酶抑制剂研究、分光光度法测定、诱导试验和分子检测方法。在24个地点中的18个(75%)检测到产ESBLs的分离株,在10个地点(42%)检测到产导入型AmpC酶的分离株,在3个地点(12.5%)检测到可诱导产导入型AmpC酶的分离株,在1个地点(4%)检测到一种分子类A碳青霉烯水解酶。未检测到B类或D类碳青霉烯水解酶。在大量地点检测到ESBLs和导入型AmpCβ-内酰胺酶,表明这些酶已广泛渗透到美国医疗机构。由于这些酶可能会显著影响治疗效果,临床实验室了解它们并能够检测它们的存在至关重要。

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