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用于检测肠球菌中耐万古霉素vanA和vanB基因的CPT-酶免疫分析

CPT-EIA assays for the detection of vancomycin resistant vanA and vanB genes in enterococci.

作者信息

Modrusan Z, Marlowe C, Wheeler D, Pirseyedi M, Bryan R N

机构信息

Incyte Pharmaceuticals, Microarray systems, Fremont, CA 94555, USA.

出版信息

Diagn Microbiol Infect Dis. 2000 May;37(1):45-50. doi: 10.1016/s0732-8893(99)00149-2.

Abstract

Cycling Probe Technology (CPT) was combined with a colorimetric enzyme-immuno assay (EIA) to develop two assays for the detection of vanA and vanB genes in vancomycin resistant enterococci (VRE). The CPT-EIA assay employs a gene-specific fluorescein labeled DNA-RNA-DNA probe that gets cleaved within the probe : target duplex. The cleaved DNA probe fragments dissociate from the target, making it available for further cycling. Following the separation of cleaved probe fragments, anti-fluorescein-horseradish peroxidase antibodies are used for the detection of uncleaved probes. The two CPT-EIA assays were used to screen a collection of 440 clinical isolates (Modrusan et al., 1999). All of the 154 VanA and 131 VanB isolates were correctly identified in the vanA and vanB CPT-EIA, respectively. The VanA and VanB isolates were differentiated from vancomycin sensitive enterococci (VSE) and also from the VanC isolates. In addition, an accurate VRE detection in the CPT-EIA assay was shown with cultures grown on eight different media.

摘要

循环探针技术(CPT)与比色酶免疫分析(EIA)相结合,开发了两种用于检测耐万古霉素肠球菌(VRE)中vanA和vanB基因的分析方法。CPT-EIA分析采用基因特异性荧光素标记的DNA-RNA-DNA探针,该探针在探针:靶标双链体内被切割。切割后的DNA探针片段与靶标解离,使其可用于进一步循环。在切割后的探针片段分离后,抗荧光素-辣根过氧化物酶抗体用于检测未切割的探针。这两种CPT-EIA分析方法用于筛选440株临床分离株(Modrusan等人,1999年)。在vanA和vanB CPT-EIA中,分别正确鉴定出了所有154株VanA和131株VanB分离株。VanA和VanB分离株与万古霉素敏感肠球菌(VSE)以及VanC分离株区分开来。此外,在CPT-EIA分析中,用在八种不同培养基上生长的培养物显示出准确的VRE检测结果。

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