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Published on: July 9, 2012
Rapid screening by real-time 16S rDNA PCR for bacterial contamination of blood products
Hendrik W Reesink1, Tamimount Mohammadi, Rubyn N I Pietersz
1Sanquin Blood Bank North-West Region and Sanquin Diagnostic Services, Amsterdam, The Netherlands. h.reesink@sanquin.nl
Abstract:
Although blood component transfusion is currently regarded as safe, adverse events may occur in recipients of these products. Among those, blood borne viral, bacterial and parasitic infections are best known. For detection of bacterial contamination in platelet concentrates various methods are available or under investigation. One of these methods, real-time polymerase chain reaction (PCR) with particular focus on real-time 16S rDNA detection, will be discussed in this review.
Insights
Bacterial contamination in platelet concentrates can cause adverse transfusion events. This review focuses on real-time polymerase chain reaction (PCR) for detecting bacterial 16S rDNA in these products.
Area of Science:
- Microbiology
- Transfusion Medicine
- Molecular Diagnostics
Background:
- Blood component transfusion, while generally safe, carries risks of adverse events, including infectious complications.
- Blood-borne infections from transfused products remain a significant concern for patient safety.
- Platelet concentrates are particularly susceptible to bacterial contamination.
Purpose of the Study:
- To review methods for detecting bacterial contamination in platelet concentrates.
- To specifically discuss real-time polymerase chain reaction (PCR) for bacterial detection.
- To highlight the application of real-time 16S rDNA detection in this context.
Main Methods:
- Review of existing literature on bacterial detection methods in platelet concentrates.
- Focus on molecular techniques, specifically real-time PCR.
- Detailed examination of real-time 16S rDNA detection assays.
Main Results:
- Various methods exist for bacterial detection in platelet concentrates.
- Real-time PCR offers a sensitive approach for identifying bacterial contaminants.
- 16S rDNA real-time PCR is a promising technique for rapid and accurate detection.
Conclusions:
- Bacterial contamination detection in platelet concentrates is crucial for transfusion safety.
- Real-time PCR, particularly 16S rDNA detection, represents an advanced method for this purpose.
- Further investigation and implementation of such methods can enhance the safety of blood products.
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