# Repurposing antiviral agents against mucormycosis

## TL;DR

This study explores repurposing antiviral drugs to treat mucormycosis, a deadly fungal infection, by identifying compounds that either directly inhibit the fungus or enhance the effectiveness of existing antifungal drugs.

## Contribution

The study introduces antiviral repurposing as a novel approach to expand mucormycosis treatment options by identifying synergistic combinations with amphotericin B.

## Key findings

- Four antiviral compounds showed potent in vitro antifungal activity against Rhizopus delemar.
- Daclatasvir and velpatasvir synergized with amphotericin B, reducing its MIC by up to 32-fold.
- The tested compounds and their combinations with amphotericin B exhibited favorable safety margins in Vero cell viability assays.

## Abstract

Mucormycosis is a life-threatening fungal infection with limited treatment options and high mortality rates among immunocompromised individuals. To identify new therapeutic strategies, we screened a library of 618 antiviral compounds against Rhizopus delemar both alone and in combination with amphotericin B (AmB) to search for agents with intrinsic antifungal activity or the ability to enhance AmB’s efficacy. Four candidates, IMB-301, U18666A, BLT-1, and obefazimod, showed potent in vitro effects, with three sustaining growth suppression comparable to AmB for up to 48 h in time-kill assays. The hepatitis C antivirals daclatasvir (DAC) and velpatasvir (VEL) demonstrated strong synergy with AmB across Mucorales isolates, lowering AmB MICs by 4- to 32-fold (ΣFICI < 0.5) and achieving fungistatic suppression of R. delemar at subinhibitory AmB concentrations (0.25 µg/mL). Importantly, neither the standalone antivirals nor their combinations with AmB reduced Vero cell viability at concentrations exceeding 4–16 × their MICs, while selectivity indices ranging from 8 to >32 indicated favorable safety margins. These findings highlight antiviral repurposing as a promising strategy to expand treatment options for mucormycosis and support further translational development.