# The lichen secondary metabolite lichesterinic acid exhibits antibiofilm activity against fungal pathogens

**Authors:** Martin N. Odabas, Katharina Kainz, Ingo Weinberger, Kerstin Schloffer, Sabrina Riedl, Marylène Chollet-Krugler, Dagmar Zweytick, Joël Boustie, Frank Madeo, Didac Carmona-Gutierrez

PMC · DOI: 10.3389/fcimb.2025.1730365 · Frontiers in Cellular and Infection Microbiology · 2026-01-12

## TL;DR

A lichen compound called lichesterinic acid shows strong antifungal activity, especially against biofilms, and could be a new treatment for resistant fungal infections.

## Contribution

Lichesterinic acid is identified as a novel antifungal agent with strong antibiofilm activity and moderate human cell tolerability.

## Key findings

- Lichesterinic acid effectively disrupts and prevents biofilm formation in Candida albicans and Nakaseomyces glabratus.
- The compound showed moderate tolerability in human cells and antifungal efficacy in an in vivo model.
- Paraconic acids, including lichesterinic acid, are promising candidates for new antifungal therapies.

## Abstract

Lichens are well known for producing unique secondary metabolites, some of which have been shown to exhibit medically relevant bioactivities, including antimicrobial effects. With the increasing prevalence of fungal infections and the growing resistance to commonly used antimycotics, there is an urgent need for new antifungal agents, especially for aged and/or immunocompromised individuals. In this study, we screened a collection of lichen-derived metabolites for antifungal properties in two medically relevant fungal pathogens, Candida albicans and Nakaseomyces glabratus. Several compounds exhibited inhibitory effects against planktonic cells and/or biofilm formation in at least one of these species. Notably, two related paraconic acids demonstrated the strongest activity against biofilms, structures that contribute significantly to antifungal resistance. Among them, lichesterinic acid was the most effective in disrupting pre-formed biofilms and preventing biofilm formation, key challenges in clinical mycology. Importantly, lichesterinic acid showed moderate tolerability in human cells. Furthermore, lichesterinic acid displayed antifungal efficacy in an in vivo model of fungal infection, supporting its potential for therapeutic development. These findings highlight lichen-derived metabolites, particularly paraconic acids, as promising candidates for new antifungal therapies targeting resistant and biofilm-associated fungal infections.

## Linked entities

- **Chemicals:** lichesterinic acid (PubChem CID 89841)
- **Species:** Candida albicans (taxon 5476), Nakaseomyces glabratus (taxon 5478)

## Full-text entities

- **Diseases:** fungal (MESH:D009181)
- **Chemicals:** lichesterinic acid (-), paraconic acids (MESH:C571316)
- **Species:** Homo sapiens (human, species) [taxon 9606], Candida albicans (species) [taxon 5476]

## Full text

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## Figures

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## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832668/full.md

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Source: https://tomesphere.com/paper/PMC12832668