Giuseppe Sberna, Francesca Colavita, Maria Beatrice Valli, Fabiano Brillo, Fabrizio Carletti, Silvia Meschi, Cosmina Mija, Claudia Minosse, Valentina Valeriani, Gabriella Rozera, Giulia Berno, Flavia Smoquina, Lavinia Fabeni, Fabrizio Maggi, Eleonora Lalle
Arboviral infections represent a growing challenge for global public health due to vector expansion, globalization, and climate change. Dengue (DENV), Zika (ZIKV), Chikungunya (CHIKV), and West Nile virus (WNV) often co-circulate and present overlapping clinical manifestations, making rapid and accurate etiological diagnosis difficult. In this context, multiplex real-time RT-PCR assays can support clinical management and epidemiological surveillance. In this study, analytical and preliminary retrospective comparisons of the NovaplexTM Tropical Fever Virus Assay, a multiplex RT-PCR system designed for the simultaneous detection of DENV, ZIKV, CHIKV, and WNV, were performed. Analytical sensitivity was assessed using serial viral-stock dilutions and Probit regression analysis to estimate the limit of detection (LOD) at a 95% probability. The LOD was 4.41 Log copies/mL for WNV2, 3.67 for DENV2, 2.57 for ZIKV, and 3.43 for CHIKV in PBS. In spiked plasma or urine, LODs ranged from 2.04 to 4.79 Log copies/mL. No cross-reactivity with Usutu virus was observed under the conditions tested. In a retrospective comparison of 34 clinical specimens with singleplex assays, agreement was the highest for WNV, substantial for CHIKV, and limited for DENV. These findings support Novaplex as a complementary tool for arboviral diagnosis and surveillance, although further clinical studies are warranted.