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The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms
Candida auris is a potential multidrug-resistant pathogen able to persist on indwelling devices as a biofilm, which serve as a source of catheter-associated infections. Neosartorya fischeri antifungal protein 2 (NFAP2) is a cysteine-rich, cationic protein with potent anti-Candida activity. We studie...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828714/ https://www.ncbi.nlm.nih.gov/pubmed/33466640 http://dx.doi.org/10.3390/ijms22020771 |
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author | Kovács, Renátó Nagy, Fruzsina Tóth, Zoltán Forgács, Lajos Tóth, Liliána Váradi, Györgyi Tóth, Gábor K. Vadászi, Karina Borman, Andrew M. Majoros, László Galgóczy, László |
author_facet | Kovács, Renátó Nagy, Fruzsina Tóth, Zoltán Forgács, Lajos Tóth, Liliána Váradi, Györgyi Tóth, Gábor K. Vadászi, Karina Borman, Andrew M. Majoros, László Galgóczy, László |
author_sort | Kovács, Renátó |
collection | PubMed |
description | Candida auris is a potential multidrug-resistant pathogen able to persist on indwelling devices as a biofilm, which serve as a source of catheter-associated infections. Neosartorya fischeri antifungal protein 2 (NFAP2) is a cysteine-rich, cationic protein with potent anti-Candida activity. We studied the in vitro activity of NFAP2 alone and in combination with fluconazole, amphotericin B, anidulafungin, caspofungin, and micafungin against C. auris biofilms. The nature of interactions was assessed utilizing the fractional inhibitory concentration index (FICI), a Bliss independence model, and LIVE/DEAD viability assay. NFAP2 exerted synergy with all tested antifungals with FICIs ranging between 0.312–0.5, 0.155–0.5, 0.037–0.375, 0.064–0.375, and 0.064–0.375 for fluconazole, amphotericin B, anidulafungin, caspofungin, and micafungin, respectively. These results were confirmed using a Bliss model, where NFAP2 produced 17.54 μM(2)%, 2.16 μM(2)%, 33.31 μM(2)%, 10.72 μM(2)%, and 111.19 μM(2)% cumulative synergy log volume in combination with fluconazole, amphotericin B, anidulafungin, caspofungin, and micafungin, respectively. In addition, biofilms exposed to echinocandins (32 mg/L) showed significant cell death in the presence of NFAP2 (128 mg/L). Our study shows that NFAP2 displays strong potential as a novel antifungal compound in alternative therapies to combat C. auris biofilms. |
format | Online Article Text |
id | pubmed-7828714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78287142021-01-25 The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms Kovács, Renátó Nagy, Fruzsina Tóth, Zoltán Forgács, Lajos Tóth, Liliána Váradi, Györgyi Tóth, Gábor K. Vadászi, Karina Borman, Andrew M. Majoros, László Galgóczy, László Int J Mol Sci Article Candida auris is a potential multidrug-resistant pathogen able to persist on indwelling devices as a biofilm, which serve as a source of catheter-associated infections. Neosartorya fischeri antifungal protein 2 (NFAP2) is a cysteine-rich, cationic protein with potent anti-Candida activity. We studied the in vitro activity of NFAP2 alone and in combination with fluconazole, amphotericin B, anidulafungin, caspofungin, and micafungin against C. auris biofilms. The nature of interactions was assessed utilizing the fractional inhibitory concentration index (FICI), a Bliss independence model, and LIVE/DEAD viability assay. NFAP2 exerted synergy with all tested antifungals with FICIs ranging between 0.312–0.5, 0.155–0.5, 0.037–0.375, 0.064–0.375, and 0.064–0.375 for fluconazole, amphotericin B, anidulafungin, caspofungin, and micafungin, respectively. These results were confirmed using a Bliss model, where NFAP2 produced 17.54 μM(2)%, 2.16 μM(2)%, 33.31 μM(2)%, 10.72 μM(2)%, and 111.19 μM(2)% cumulative synergy log volume in combination with fluconazole, amphotericin B, anidulafungin, caspofungin, and micafungin, respectively. In addition, biofilms exposed to echinocandins (32 mg/L) showed significant cell death in the presence of NFAP2 (128 mg/L). Our study shows that NFAP2 displays strong potential as a novel antifungal compound in alternative therapies to combat C. auris biofilms. MDPI 2021-01-14 /pmc/articles/PMC7828714/ /pubmed/33466640 http://dx.doi.org/10.3390/ijms22020771 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kovács, Renátó Nagy, Fruzsina Tóth, Zoltán Forgács, Lajos Tóth, Liliána Váradi, Györgyi Tóth, Gábor K. Vadászi, Karina Borman, Andrew M. Majoros, László Galgóczy, László The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms |
title | The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms |
title_full | The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms |
title_fullStr | The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms |
title_full_unstemmed | The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms |
title_short | The Neosartorya fischeri Antifungal Protein 2 (NFAP2): A New Potential Weapon against Multidrug-Resistant Candida auris Biofilms |
title_sort | neosartorya fischeri antifungal protein 2 (nfap2): a new potential weapon against multidrug-resistant candida auris biofilms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828714/ https://www.ncbi.nlm.nih.gov/pubmed/33466640 http://dx.doi.org/10.3390/ijms22020771 |
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