# Deciphering antifungal and antibiofilm mechanisms of isobavachalcone against Cryptococcus neoformans through RNA-seq and functional analyses

## TL;DR

This study explores how isobavachalcone fights the fungus Cryptococcus neoformans by disrupting cell walls, biofilms, and virulence through multiple pathways.

## Contribution

The study reveals the multifaceted antifungal and antibiofilm mechanisms of isobavachalcone against Cryptococcus neoformans using RNA-seq and functional analyses.

## Key findings

- Isobavachalcone disrupts cell wall/membrane integrity and inhibits biofilm formation in Cryptococcus neoformans.
- The compound modulates pathways related to drug resistance, apoptosis, and mitochondrial homeostasis.
- Isobavachalcone extends the lifespan of Cryptococcus neoformans-infected Caenorhabditis elegans.

## Abstract

Cryptococcus neoformans has been designated as critical fungal pathogens by the World Health Organization, mainly due to limited treatment options and the prevalence of antifungal resistance. Consequently, the utilization of novel antifungal agents is crucial for the effective treatment of C. neoformans infections. This study exposed that the minimum inhibitory concentration (MIC) of isobavachalcone (IBC) against C. neoformans H99 was 8 µg/mL, and IBC dispersed 48-h mature biofilms by affecting cell viability at 16 µg/mL. The antifungal efficacy of IBC was further validated through microscopic observations using specific dyes and in vitro assays, which confirmed the disruption of cell wall/membrane integrity. RNA-Seq analysis was employed to decipher the effect of IBC on the C. neoformans H99 transcriptomic profiles. Real-time quantitative reverse transcription PCR (RT-qPCR) analysis was performed to validate the transcriptomic data and identify the differentially expressed genes. The results showed that IBC exhibited various mechanisms to impede the growth, biofilm formation, and virulence of C. neoformans H99 by modulating multiple dysregulated pathways related to cell wall/membrane, drug resistance, apoptosis, and mitochondrial homeostasis. The transcriptomic findings were corroborated by the antioxidant analyses, antifungal drug sensitivity, molecular docking, capsule, and melanin assays. In vivo antifungal activity analysis demonstrated that IBC extended the lifespan of C. neoformans-infected Caenorhabditis elegans. Overall, the current study unveiled that IBC targeted multiple pathways simultaneously to inhibit growth significantly, biofilm formation, and virulence, as well as to disperse mature biofilms of C. neoformans H99 and induce cell death.

The online version contains supplementary material available at 10.1186/s12934-024-02369-2.