Quentin Nevers

This study shows that during rabies virus infection, protein synthesis occurs outside viral factories (Negri bodies) and newly synthesized viral proteins are later targeted to these compartments.

This study identifies a non-peptidic cyclophilin ligand, F83233, that inhibits replication of feline and porcine alpha-coronaviruses in multiple species.

The paper identifies artificial proteins (αReps) that inhibit influenza virus replication by targeting FluPol subunits, showing efficacy against multiple virus subtypes.

This study shows that anchoring a SARS-CoV-2 neutralizing nanobinder to mucin increases its residence time in the nasal cavity, enhancing antiviral efficacy in hamsters.

This paper identifies an intracellular nanobody that inhibits influenza A virus RNA-polymerase by blocking PA-PB1 dimer nuclear import, showing potential for antiviral development.

This study uses long-read sequencing to characterize equine influenza A H3N8 viruses, identifying antigenic drift and a virulence-enhancing PB1-F2 protein variant.