Literature DB >> 21392020

Performance and suitability of polymerase chain reaction for early detection of bacteria in platelet concentrates.

Ineke G H Rood1, Annika Pettersson, Paul H M Savelkoul, Dirk de Korte.   

Abstract

BACKGROUND: In this study the applicability of a 16S rRNA real-time reverse transcriptase polymerase chain reaction (RT-PCR) and a Staphylococcus genus-specific PCR for screening of bacterial contamination in platelet concentrates (PCs) was determined. STUDY DESIGN AND METHODS: A total of 336 sample bags, from PCs that were routinely tested in the BacT/ALERT (bioMérieux), were collected and frozen until testing by the PCR assays. Based on the BacT/ALERT results, 107 PCs were positive and 229 were negative for bacterial growth.
RESULTS: The analytical sensitivity of the 16S rRNA real-time RT-PCR ranged from 5 to 40 colony-forming units (CFUs)/mL. The PCR detected five positive samples, four of which were also positive in the BacT/ALERT. The sensitivity of the test was 3.8%, and the specificity was 99.5%. The analytical sensitivity of the Staphylococcus genus-specific PCR ranged from 5 to 15 CFUs/mL. Thirty-nine units that were BacT/ALERT positive for staphylococci were tested with this PCR. Six samples were positive with the PCR, five of which were also BacT/ALERT positive. The sensitivity of the Staphylococcus genus-specific PCR was 12.8%, and the specificity was 98.8%.
CONCLUSION: Despite the rapid availability of results compared to the BacT/ALERT, the analytical sensitivity of a generic or specific PCR assay is not high enough to be an alternative for the BacT/ALERT when PCs are screened on the day of production.
© 2011 American Association of Blood Banks.

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Year:  2011        PMID: 21392020     DOI: 10.1111/j.1537-2995.2011.03090.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  7 in total

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4.  Molecular detection of bacterial contamination in plasma using magnetic-based enrichment.

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5.  Characteristics of False-Positive Alarms in the BacT/Alert 3D System.

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6.  An Internal Reference Control Duplex Real-Time Polymerase Chain Reaction Assay for Detecting Bacterial Contamination in Blood Products.

Authors:  Jin-Ju Zhang; Jing-Jing Tian; Shuang-Shi Wei; Sheng-Bao Duan; Hong-Mei Wang; Ye-Zhou Chen; Shao-Hua Ding; Chun Zhang; Qing-Lin Meng; Yong Li
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7.  Evaluation of an ethidium monoazide-enhanced 16S rDNA real-time polymerase chain reaction assay for bacterial screening of platelet concentrates and comparison with automated culture.

Authors:  Jeremy A Garson; Poorvi Patel; Carl McDonald; Joanne Ball; Gillian Rosenberg; Kate I Tettmar; Susan R Brailsford; Tyrone Pitt; Richard S Tedder
Journal:  Transfusion       Date:  2013-05-23       Impact factor: 3.157

  7 in total

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