Tan T Y, Ng S Y, Teo L, Koh Y, Teok C H
Division of Laboratory Medicine, Changi General Hospital, Singapore.
J Clin Pathol. 2008 May;61(5):642-4. doi: 10.1136/jcp.2007.053470. Epub 2007 Dec 5.
This study investigated the prevalence of plasmid-mediated AmpC production in selected clinical isolates of Escherichia coli, Klebsiella species and Proteus mirabilis, and compared the results of boronic acid disc screening with conventional susceptibility testing for the detection of AmpC-positive isolates.
E coli, Klebsiella species and P mirabilis with reduced susceptibility to amoxycillin-clavulanate, cefuroxime and cephalexin, but without phenotypic evidence of extended-spectrum beta-lactamases were screened for AmpC activity using enzyme-extraction methods. The presence of plasmid-mediated ampC was determined by multiplex PCR. Antibiotic susceptibilities were determined using both disc and dilution-based methods. A disc-based screening method for detection of AmpC-producing strains was evaluated using boronic acid as an inhibitor of AmpC, and cefoxitin as the antibiotic substrate.
Plasmid-mediated ampC was present in 26% of study isolates, with CMY-like enzymes detected predominantly in E coli and DHA-like enzymes predominantly in Klebsiella pneumoniae. Current susceptibility methods failed to detect a significant proportion of plasmid-mediated AmpC-producing isolates, with 33% of such strains interpreted as susceptible to third-generation cephalosporins using current Clinical Laboratory Standards Institute breakpoints. The boronic acid disc method showed sensitivity and specificity of 90% and 98% respectively in detecting AmpC-positive isolates.
The prevalence of plasmid-mediated ampC was high in the study population, and may be missed by conventional susceptibility testing methods. Inhibitor-based screening methods would improve detection of this emerging resistance phenotype.
本研究调查了大肠埃希菌、克雷伯菌属和奇异变形杆菌特定临床分离株中质粒介导的AmpC产生情况,并比较了硼酸纸片筛查与传统药敏试验检测AmpC阳性分离株的结果。
使用酶提取法筛选对阿莫西林-克拉维酸、头孢呋辛和头孢氨苄敏感性降低但无超广谱β-内酰胺酶表型证据的大肠埃希菌、克雷伯菌属和奇异变形杆菌的AmpC活性。通过多重聚合酶链反应确定质粒介导的ampC的存在。使用纸片法和稀释法测定抗生素敏感性。使用硼酸作为AmpC抑制剂和头孢西丁作为抗生素底物,评估一种基于纸片的检测产AmpC菌株的筛查方法。
26%的研究分离株存在质粒介导的ampC,CMY样酶主要在大肠埃希菌中检测到,DHA样酶主要在肺炎克雷伯菌中检测到。目前的药敏方法未能检测到相当比例的质粒介导的产AmpC分离株,根据当前临床实验室标准协会的断点,33%的此类菌株被判定对第三代头孢菌素敏感。硼酸纸片法检测AmpC阳性分离株的敏感性和特异性分别为90%和98%。
研究人群中质粒介导的ampC流行率较高,传统药敏试验方法可能会漏检。基于抑制剂的筛查方法将改善对这种新出现的耐药表型的检测。