AFM combined to ATR-FTIR reveals Candida cell wall changes under caspofungin treatment

• Published in: Nanoscale Vol. 9; no. 36; pp. 13731 - 13738
• Main Authors: Quilès, Fabienne, Accoceberry, Isabelle, Couzigou, Célia, Francius, Grégory, Noël, Thierry, El-Kirat-Chatel, Sofiane
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 2017
• Subjects: Antifungal Agents - pharmacology; Candida - drug effects; Caspofungin - pharmacology; Cell Wall - drug effects; Echinocandins; Life Sciences; Lipopeptides; Microbial Sensitivity Tests; Microbiology and Parasitology; Microscopy, Atomic Force; Spectroscopy, Fourier Transform Infrared
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/c7nr02170d

Fungal pathogens from Candida genus are responsible for severe life-threatening infections and the antifungal arsenal is still limited. Caspofungin, an antifungal drug used for human therapy, acts as a blocking agent of the cell wall synthesis by inhibiting the β-1,3-glucan-synthase encoded by FKS genes. Despite its efficiency, the number of genetic mutants that are resistant to caspofungin is increasing. An important challenge to improve antifungal therapy is to understand cellular phenomenon that are associated with drug resistance. Here we used atomic force microscopy (AFM) combined to Fourier transform infrared spectroscopy in attenuated total reflection mode (ATR-FTIR) to decipher the effect of low and high drug concentration on the morphology, mechanics and cell wall composition of two Candida strains, one susceptible and one resistant to caspofungin. Our results confirm that caspofungin induces a dramatic cell wall remodelling via activation of stress responses, even at high drug concentration. Additionally, we highlighted unexpected changes related to drug resistance, suggesting that caspofungin resistance associated with FKS gene mutations comes from a combination of effects: (i) an overall remodelling of yeast cell wall composition; and (ii) cell wall stiffening through chitin synthesis. This work demonstrates that AFM combined to ATR-FTIR is a valuable approach to understand at the molecular scale the biological mechanisms associated with drug resistance.