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ABSTRACT: Background
The objective of our study was the development of a semi-quantitative real-time PCR to detect uropathogens. Two multiplex PCR reactions were designed to detect Escherichia coli, Klebsiella spp., Enterobacter spp., Citrobacter spp., Proteus mirabilis, Enterococcus faecalis, and Pseudomonas aeruginosa. 16S based PCR was performed in parallel to detect Gram-positive and Gram-negative bacteria. Firstly to identify non-targeted agents of infection in the same urine specimen, and secondly to quantify background flora. The method was evaluated in comparison with standard bacterial culture, and a commercial PCR kit for detection of uropathogens.Findings
Analysis with a known panel of 116 clinical isolates yielded a PCR specificity of 100%. Analysis of urine specimens fro
SUBMITTER: van der Zee A
PROVIDER: S-EPMC4783162 | biostudies-literature | 2016
REPOSITORIES: biostudies-literature