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Clinical evaluation of polymerase chain reaction coupled with quantum dot fluorescence analysis in the identification of bacteria and yeasts in patients with suspected bloodstream infections.
Li, Jie; Fan, Wenjia; Zou, Xuehan; Dai, Xuan; Zhao, Yueyue; Pan, Hongying; Wu, Shijin; Li, Xi; Huang, Haijun.
Affiliation
  • Li J; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, China.
  • Fan W; Department of Infectious Disease, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • Zou X; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, China.
  • Dai X; Department of Infectious Disease, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • Zhao Y; Department of Infectious Disease, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • Pan H; Department of Infectious Disease, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • Wu S; Department of Infectious Disease, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • Li X; Department of Infectious Disease, Zhejiang Provincial People's Hospital, Hangzhou, China.
  • Huang H; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, China.
Microb Biotechnol ; 16(4): 827-837, 2023 04.
Article in En | MEDLINE | ID: mdl-36722318
ABSTRACT
Bloodstream infections are serious and complex infectious diseases that often require a rapid diagnosis. Polymerase chain reaction coupled with quantum dot fluorescence analysis (PCR-QDFA) is a novel diagnostic technique. This study aimed to evaluate the diagnostic performance of PCR-QDFA for pathogen detection in patients with suspected bloodstream infections (BSIs). It evaluates 29 kinds of common pathogens (24 bacteria and 5 yeasts) from blood culture bottles. The results of PCR-QDFA identification and traditional microbial laboratory identification were compared, and the latter was used as the 'gold standard' to analyse the diagnostic performance of the PCR-QDFA. In total, 517 blood culture bottles were included in this study. The PCR-QDFA identified microorganisms in 368/422 (87.2%) samples with monomicrobial growth. For the pathogens on the PCR-QDFA list, the assay showed a higher sensitivity of 97.4% (368/378). When polymicrobial growth was analysed, the PCR-QDFA successfully detected 19/25 (76%) microorganisms on the PCR-QDFA list. In addition, 82/82 negative blood culture bottles also showed no pathogens by PCR-QDFA with a specificity of 100%. In conclusion, the PCR-QDFA assay could identify a majority of the common pathogens encountered in clinical practice, showing excellent diagnostic performance for pathogen detection in patients with suspected BSIs.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sepsis / Quantum Dots Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Microb Biotechnol Year: 2023 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sepsis / Quantum Dots Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Microb Biotechnol Year: 2023 Document type: Article Affiliation country: China