Wound infections caused by inducible meticillin-resistant Staphylococcus aureus strains

被引:9
|
作者
Penn, Christopher [1 ]
Moddrell, Carol [1 ]
Tickler, Isabella A. [2 ]
Henthorne, Mary Ann [1 ]
Kehrli, Megan [1 ]
Goering, Richard V. [3 ]
Tenover, Fred C. [2 ]
机构
[1] Lawrence Mem Hosp, Lawrence, KS 66044 USA
[2] Cepheid, Sunnyvale, CA 94089 USA
[3] Creighton Univ, Omaha, NE 68178 USA
关键词
Staphylococcus aureus; Meticillin resistance; mecA; Oxacillin; Cefoxitin screen; PENICILLIN-BINDING PROTEIN; METHICILLIN-RESISTANT; MECA-GENE; TESTING METHODS; BLOOD CULTURES; REGION; MRSA;
D O I
10.1016/j.jgar.2013.03.009
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Detection of meticillin resistance in Staphylococcus aureus isolates continues to be a challenge. Clinical specimens obtained from abscesses from two epidemiologically unrelated outpatients were positive for meticillin-resistant Staphylococcus aureus (MRSA) by a commercial PCR assay, but colonies obtained by culture were susceptible to oxacillin by an automated testing method. The colonies were also negative using a penicillin-binding protein 2a (PBP2a) latex agglutination test. Because of the discrepancy between the genotypic and phenotypic results, both isolates were re-tested by PCR, disc diffusion, VITEK(R) 2 and MicroScan(R) and were plated on chromogenic agar. Both isolates also underwent cefoxitin induction for additional susceptibility testing studies. Following overnight induction with cefoxitin, both isolates demonstrated resistance to oxacillin and cefoxitin by the two automated methods and by disc diffusion, and were positive using PBP2a latex agglutination tests. Population analysis failed to identify heteroresistant subpopulations in uninduced isolates. Identifying the presence of MRSA by PCR directly in the specimens was critical for determining the appropriate course of antimicrobial therapy for the patients. Both infections resolved with non-beta-lactam therapy. (C) 2013 International Society for Chemotherapy of Infection and Cancer. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:79 / 83
页数:5
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