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. 2023 Apr;16(4):827-837.
doi: 10.1111/1751-7915.14226. Epub 2023 Feb 1.

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

Affiliations

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

Jie Li et al. Microb Biotechnol. 2023 Apr.

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.

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Flowchart of patient enrolment.

References

    1. Altun, O. , Almuhayawi, M. , Ullberg, M. & Ozenci, V. (2013) Clinical evaluation of the FilmArray blood culture identification panel in identification of bacteria and yeasts from positive blood culture bottles. Journal of Clinical Microbiology, 51, 4130–4136. - PMC - PubMed
    1. Barberino, M.G. , Silva, M.O. , Arraes, A.C.P. , Correia, L.C. & Mendes, A.V. (2017) Direct identification from positive blood broth culture by matrix‐assisted laser desorption‐ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS). The Brazilian Journal of Infectious Diseases, 21, 339–342. - PMC - PubMed
    1. Beal, S.G. , Ciurca, J. , Smith, G. , John, J. , Lee, F. , Doern, C. et al. (2013) Evaluation of the nanosphere verigene gram‐positive blood culture assay with the VersaTREK blood culture system and assessment of possible impact on selected patients. Journal of Clinical Microbiology, 51, 3988–3992. - PMC - PubMed
    1. Bizzini, A. & Greub, G. (2010) Matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry, a revolution in clinical microbial identification. Clinical Microbiology and Infection, 16, 1614–1619. - PubMed
    1. Buchan, B.W. , Ginocchio, C.C. , Manii, R. , Cavagnolo, R. , Pancholi, P. , Swyers, L. et al. (2013) Multiplex identification of gram‐positive bacteria and resistance determinants directly from positive blood culture broths: evaluation of an automated microarray‐based nucleic acid test. PLoS Medicine, 10, e1001478. - PMC - PubMed

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