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Comparison of clinical methods for detecting carbapenem-resistant Enterobacteriaceae

机译:耐碳青霉烯类肠杆菌科的临床检测方法比较

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We evaluated detection of carbapenem-resistant Enterobacteriaceae (CRE) by routine minimal inhibitory concentration (MIC) testing, polymerase chain reaction (PCR) using Xpert? Carba-R assay, hydrolysis of ertapenem and imipenem detected by matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS), and hydrolysis by colorimetry using the EPI-CRE assay. Ninety-six Enterobacteriaceae isolates possessing carbapenemase genes and 29 carbapenem-susceptible Enterobacteriaceae were available for testing. The sensitivity and specificity of each assay was determined. For sensitivity, discrepant results from each assay compared to reference genotype were arbitrated with MIC and/ or PCR testing to assess loss of plasmid-mediated resistance. Xpert Carba-R was evaluated for resistance genes in their FDA claim (i.e., the genes encoding KPC; NDM; VIM; IMP; and OXA-48). The sensitivity for the assays was: MIC (N=96), 96.8%, (discrepant analysis to 98.9% [2 cured plasmids]); Xpert Carba-R (N=85), 97.6% (discrepant analysis to 100% % [2 cured plasmids]); EPI-CRE (N=96), 91.7% (discrepant analysis to 91.7%); MALDI-TOF MS (N=96) ertapenem hydrolysis using Compass software for interpretation (2 h incubation), 92.7% (discrepant analysis to 94.7% % [2 cured plasmids]); MALDI-TOF MS (N=96) imipenem hydrolysis (1 h incubation), 97.9% (discrepant analysis to 98.9% % [1 cured plasmid]). The specificity for each assay was: MIC (N=29), 100%; EPI-CRE (N=29), 96.6%; MALDI-TOF MS ertapenem hydrolysis (N=29), 100%; MALDI-TOF MS imipenem hydrolysis (N=29), 96.6%. All isolates tested to ensure specificity demonstrated susceptible MIC results for carbapenems and did not qualify for testing with Xpert Carba-R. No single assay detected all of the known genetic markers of carbapenem hydrolysis. Highlights ? Matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS), Cepheid Xpert Carba-R PCR, minimum inhibitory concentration testing (MIC), and EPI-CRE (colorimetric) detected 90% of all carbapenem-resistant Enterobacteriaceae (CRE) tested. ? Sensitivities were: 1. MIC (N=96), 96.8%; 2. Xpert Carba-R (N=85), 97.6%; 3. EPI-CRE (N=96), 91.7%; 4. MALDI-TOF MS (N=96) ertapenem hydrolysis, 92.7; 5. MALDI-TOF MS (N=96) imipenem hydrolysis, 97.9%. ? Testing was confounded by the loss of the resistance plasmid during testing. ? No single assay detected all CRE.
机译:我们通过常规最小抑菌浓度(MIC)测试,使用Xpert?的聚合酶链反应(PCR)评估了对碳青霉烯类耐药肠杆菌科(CRE)的检测。 Carba-R分析,通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)检测的厄他培南和亚胺培南水解,以及使用EPI-CRE分析的比色法水解。拥有碳青霉烯酶基因的九十六种肠杆菌科细菌分离株和29种对碳青霉烯敏感的肠杆菌科细菌可供测试。确定每种测定的敏感性和特异性。为了提高灵敏度,将每个测定与参考基因型相比的差异结果通过MIC和/或PCR测试进行仲裁,以评估质粒介导的抗性的丧失。 Xpert Carba-R在其FDA声明中评估了抗药性基因(即编码KPC,NDM,VIM,IMP和OXA-48的基因)。该测定的灵敏度为:MIC(N = 96),96.8%,(对98.9%的差异分析[2个固化质粒]); Xpert Carba-R(N = 85),97.6%(对100%%的分散剂分析[2个固化质粒]); EPI-CRE(N = 96),占91.7%(差异分析为91.7%); MALDI-TOF MS(N = 96)厄他培南水解,使用Compass软件进行解释(2 h孵育),占92.7%(对94.7%%的分散体分析[2个固化质粒]); MALDI-TOF MS(N = 96)亚胺培南水解(1 h孵育​​),97.9%(对98.9%%的分散体分析[1个固化质粒])。每种测定的特异性为:MIC(N = 29),100%; EPI-CRE(N = 29),占96.6%; MALDI-TOF MS厄他培南水解(N = 29),100%; MALDI-TOF MS亚胺培南水解(N = 29),96.6%。经测试以确保特异性的所有分离物均对碳青霉烯类药物表现出敏感的MIC结果,并且不符合使用Xpert Carba-R进行测试的资格。没有任何一项检测能够检测到碳青霉烯水解的所有已知遗传标记。强调 ?基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS),造父变星Xpert Carba-R PCR,最小抑菌浓度测试(MIC)和EPI-CRE(比色法)检测到> 90%的耐碳青霉烯肠杆菌科细菌(CRE)测试。 ?敏感性为:1. MIC(N = 96),96.8%; 2. Xpert Carba-R(N = 85),97.6%; 3. EPI-CRE(N = 96),占91.7%; 4. MALDI-TOF MS(N = 96)厄他培南水解,92.7; 5.MALDI-TOF MS(N = 96)亚胺培南水解,97.9%。 ?由于在测试期间抗性质粒的丢失而使测试感到困惑。 ?没有任何一项检测能够检测到所有CRE。

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