LowLoad-qPCR as a novel clinical strategy for detecting low-load bacteremia
Abstract
The primary obstacle in detecting bloodstream infections is their often extremely low bacterial concentration. To accurately detect such infections, we developed a quantitative PCR assay, named LowLoad-qPCR, based on the combination of increased input DNA by random priming amplification method and the use of multiple probes sharing a single fluorophore. Here, we detail the key improvements over conventional qPCR and evaluate its performance using blood samples.
Fields of Study & Subjects
Bacterial Identification and Susceptibility Testing
Biosensors and Analytical Detection
Molecular Biology Techniques and Applications
Publication details
- Journal / source
- Scientific Reports
- Volume
- 16
- Issue
- 1
- Pages
- 4163–4163
- Publication date
- 3 January 2026
- Language
- EN