AFM combined to ATR-FTIR reveals Candida cell wall changes under caspofungin treatmentElectronic supplementary information (ESI) available. See 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 g...
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Format | Journal Article |
Language | English |
Published |
21.09.2017
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Abstract | 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.
AFM was combined to vibrational spectroscopy to decipher morphological, mechanical and biochemical changes induced by caspofungin treatment on
Candida
. |
---|---|
AbstractList | 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.
AFM was combined to vibrational spectroscopy to decipher morphological, mechanical and biochemical changes induced by caspofungin treatment on
Candida
. |
Author | Accoceberry, Isabelle Noël, Thierry Quilès, Fabienne Francius, Grégory Couzigou, Célia El-Kirat-Chatel, Sofiane |
AuthorAffiliation | Université de Lorraine Microbiologie Fondamentale et Pathogénicité CNRS Laboratoire de Chimie Physique et Microbiologie pour l'Environnement Université de Bordeaux UMR 5234 LCPME UMR 7564 |
AuthorAffiliation_xml | – name: Microbiologie Fondamentale et Pathogénicité – name: CNRS – name: UMR 5234 – name: Laboratoire de Chimie Physique et Microbiologie pour l'Environnement – name: Université de Lorraine – name: LCPME – name: UMR 7564 – name: Université de Bordeaux |
Author_xml | – sequence: 1 givenname: Fabienne surname: Quilès fullname: Quilès, Fabienne – sequence: 2 givenname: Isabelle surname: Accoceberry fullname: Accoceberry, Isabelle – sequence: 3 givenname: Célia surname: Couzigou fullname: Couzigou, Célia – sequence: 4 givenname: Grégory surname: Francius fullname: Francius, Grégory – sequence: 5 givenname: Thierry surname: Noël fullname: Noël, Thierry – sequence: 6 givenname: Sofiane surname: El-Kirat-Chatel fullname: El-Kirat-Chatel, Sofiane |
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Candida
genus are responsible for severe life-threatening infections and the antifungal arsenal is still limited. Caspofungin, an... |
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Title | AFM combined to ATR-FTIR reveals Candida cell wall changes under caspofungin treatmentElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nr02170d |
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