LowLoad-qPCR as a novel clinical strategy for detecting low-load bacteremia
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.
Authors
- G. Martín-Gutiérrez
- José Miguel Cisneros (ORCID: https://orcid.org/0000-0001-5001-672X)
- José Manuel Ortiz de la Rosa
- Paula Gómez Estévez
- José Antonio Lepe
Institutions
- Universidad Loyola Andalucía (ES)
- Centro de Investigación Biomédica en Red (ES)
- Instituto de Biomedicina de Sevilla (ES)
- Hospital Universitario Virgen del Rocío (ES)
- Universidad de Sevilla (ES)
Publication Details
- Journal
- Scientific Reports
- Published
- 2026-01-03
- DOI
- https://doi.org/10.1038/s41598-025-34230-w
- Primary Topic
- Bacterial Identification and Susceptibility Testing
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministerio de Ciencia, Innovación y Universidades
- European Commission
- Instituto de Salud Carlos III