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

被引:2
|
作者
Li, Jie [1 ,2 ]
Fan, Wenjia [1 ,2 ]
Zou, Xuehan [2 ]
Dai, Xuan [2 ]
Zhao, Yueyue [2 ]
Pan, Hongying [2 ]
Wu, Shijin [1 ,6 ]
Li, Xi [3 ,5 ]
Huang, Haijun [2 ,4 ]
机构
[1] Zhejiang Univ Technol, Coll Biotechnol & Bioengn, Hangzhou, Peoples R China
[2] Zhejiang Prov Peoples Hosp, Dept Infect Dis, Hangzhou, Peoples R China
[3] Zhejiang Prov Peoples Hosp, Ctr Lab Med, Hangzhou, Peoples R China
[4] Zhejiang Prov Peoples Hosp, Dept Infect Dis, Hangzhou 310014, Peoples R China
[5] Zhejiang Prov Peoples Hosp, Ctr Lab Med, Hangzhou 310014, Peoples R China
[6] Zhejiang Univ Technol, Coll Biotechnol & Bioengn, Hangzhou 310014, Peoples R China
来源
MICROBIAL BIOTECHNOLOGY | 2023年 / 16卷 / 04期
基金
中国国家自然科学基金;
关键词
FLIGHT MASS-SPECTROMETRY; CULTURE-SYSTEM; SEPSIS; THERAPY; IMPACT; PROBE; PANEL;
D O I
10.1111/1751-7915.14226
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 PCRQDFA list. In addition, 82/82 negative blood culture bottles also showed no pathogens by PCR- QDFA with a specificity of 100%. In conclusion, the PCRQDFA 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.
引用
收藏
页码:827 / 837
页数:11
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