From Triplex to Quadruplex: Enhancing CDC’s Respiratory qPCR Assay with RSV Detection on Panther Fusion® Open Access™
Andy Caballero Méndez, Mayeline N. Sosa Ortiz, Roberto A. Reynoso de la Rosa, Miguel E. Abreu Bencosme, Karla V. Montero Lebrón

TL;DR
This study improves a respiratory virus detection test by adding RSV to an automated system that already detects influenza and SARS-CoV-2.
Contribution
The novel contribution is the development of a fully automated quadruplex RT-qPCR assay for detecting four respiratory viruses with high accuracy.
Findings
The LDRA assay achieved amplification efficiencies of 97–105% and detected 32 RSV variants without cross-reactivity.
The assay demonstrated ≥98% agreement with other diagnostic tests and reliably detected mixed infections.
The system is suitable for middle-income healthcare settings, offering rapid and accurate detection of four respiratory viruses.
Abstract
The overlapping circulation of influenza (Flu), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2; SC2), and respiratory syncytial virus (RSV) continues to challenge clinical laboratories, particularly in settings with limited automation and fragmented healthcare coverage. This study expanded the CDC Flu-SC2 assay by incorporating a laboratory-developed test (LDT) for RSV A/B detection into a fully automated quadruplex RT-qPCR (LDRA) on the Panther Fusion® Open Access™ system. The design, based on more than 8000 RSV genomic sequences targeting the conserved M gene, achieved optimal amplification efficiencies (97–105%) and full multiplex compatibility. Analytical assessment established limits of detection between 9.6 and 37.8 copies per reaction, absence of cross-reactivity with 30 respiratory pathogens, and inclusivity for 32 viral variants. Commutability and diagnostic…
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Taxonomy
TopicsRespiratory viral infections research · SARS-CoV-2 detection and testing · Biosensors and Analytical Detection
