| Literature DB >> 34528911 |
Juyoun Shin1, Sun Shina2, Seung-Hyun Jung3, Chulmin Park4, Sung-Yeon Cho4,5, Dong-Gun Lee4,5, Yeun-Jun Chung1,2.
Abstract
Early and accurate detection of pathogens is important to improve clinical outcomes of bloodstream infections (BSI), especially in the case of drug-resistant pathogens. In this study, we aimed to develop a culture-independent digital PCR (dPCR) system for multiplex detection of major sepsiscausing gram-negative pathogens and antimicrobial resistance genes using plasma DNA from BSI patients. Our duplex dPCR system successfully detected nine targets (five bacteria-specific targets and four antimicrobial resistance genes) through five reactions within 3 hours. The minimum detection limit was 50 ag of bacterial DNA, suggesting that 1 CFU/ml of bacteria in the blood can be detected. To validate the clinical applicability, cell-free DNA samples from febrile patients were tested with our system and confirmed high consistency with conventional blood culture. This system can support early identification of some drug-resistant gram-negative pathogens, which can help improving treatment outcomes of BSI.Entities:
Keywords: Digital PCR; Gram-negative; antimicrobial resistance; blood-stream infection; bloodstream infection
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Year: 2021 PMID: 34528911 DOI: 10.4014/jmb.2103.03044
Source DB: PubMed Journal: J Microbiol Biotechnol ISSN: 1017-7825 Impact factor: 2.351