Cargando…

Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans

The human fungal pathogen, Cryptococcus neoformans, is responsible for deadly infections among immunocompromised individuals with the evolution of antifungal resistance driving the solution to discover new compounds that inhibit fungal virulence factors rather than kill the pathogen. Recently, explo...

Descripción completa

Detalles Bibliográficos
Autores principales: Gutierrez-Gongora, Davier, Raouf-Alkadhimi, Fouad, Prosser, Ryan S., Geddes-McAlister, Jennifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040410/
https://www.ncbi.nlm.nih.gov/pubmed/36967422
http://dx.doi.org/10.1038/s41598-023-32140-3
_version_ 1784912476544958464
author Gutierrez-Gongora, Davier
Raouf-Alkadhimi, Fouad
Prosser, Ryan S.
Geddes-McAlister, Jennifer
author_facet Gutierrez-Gongora, Davier
Raouf-Alkadhimi, Fouad
Prosser, Ryan S.
Geddes-McAlister, Jennifer
author_sort Gutierrez-Gongora, Davier
collection PubMed
description The human fungal pathogen, Cryptococcus neoformans, is responsible for deadly infections among immunocompromised individuals with the evolution of antifungal resistance driving the solution to discover new compounds that inhibit fungal virulence factors rather than kill the pathogen. Recently, exploration into natural sources (e.g., plants, invertebrates, microbes) of antifungal agents has garnered attention by integrating a One Health approach for new compound discovery. Here, we explore extracts from three mollusk species (freshwater and terrestrial) and evaluate effects against the growth and virulence factor production (i.e., thermotolerance, melanin, capsule, and biofilm) in C. neoformans. We demonstrate that clarified extracts of Planorbella pilsbryi have a fungicidal effect on cryptococcal cells comparable to fluconazole. Similarly, all extracts of Cipangopaludina chinensis affect cryptococcal thermotolerance and impair biofilm and capsule production, with clarified extracts of Cepaea nemoralis also conveying the latter effect. Next, inhibitory activity of extracts against peptidases related to specific virulence factors, combined with stress assays and quantitative proteomics, defined distinct proteome signatures and proposed proteins driving the observed anti-virulence properties. Overall, this work highlights the potential of compounds derived from natural sources to inhibit virulence factor production in a clinically important fungal pathogen.
format Online
Article
Text
id pubmed-10040410
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-100404102023-03-28 Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans Gutierrez-Gongora, Davier Raouf-Alkadhimi, Fouad Prosser, Ryan S. Geddes-McAlister, Jennifer Sci Rep Article The human fungal pathogen, Cryptococcus neoformans, is responsible for deadly infections among immunocompromised individuals with the evolution of antifungal resistance driving the solution to discover new compounds that inhibit fungal virulence factors rather than kill the pathogen. Recently, exploration into natural sources (e.g., plants, invertebrates, microbes) of antifungal agents has garnered attention by integrating a One Health approach for new compound discovery. Here, we explore extracts from three mollusk species (freshwater and terrestrial) and evaluate effects against the growth and virulence factor production (i.e., thermotolerance, melanin, capsule, and biofilm) in C. neoformans. We demonstrate that clarified extracts of Planorbella pilsbryi have a fungicidal effect on cryptococcal cells comparable to fluconazole. Similarly, all extracts of Cipangopaludina chinensis affect cryptococcal thermotolerance and impair biofilm and capsule production, with clarified extracts of Cepaea nemoralis also conveying the latter effect. Next, inhibitory activity of extracts against peptidases related to specific virulence factors, combined with stress assays and quantitative proteomics, defined distinct proteome signatures and proposed proteins driving the observed anti-virulence properties. Overall, this work highlights the potential of compounds derived from natural sources to inhibit virulence factor production in a clinically important fungal pathogen. Nature Publishing Group UK 2023-03-26 /pmc/articles/PMC10040410/ /pubmed/36967422 http://dx.doi.org/10.1038/s41598-023-32140-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gutierrez-Gongora, Davier
Raouf-Alkadhimi, Fouad
Prosser, Ryan S.
Geddes-McAlister, Jennifer
Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans
title Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans
title_full Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans
title_fullStr Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans
title_full_unstemmed Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans
title_short Differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in Cryptococcus neoformans
title_sort differentiated extracts from freshwater and terrestrial mollusks inhibit virulence factor production in cryptococcus neoformans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040410/
https://www.ncbi.nlm.nih.gov/pubmed/36967422
http://dx.doi.org/10.1038/s41598-023-32140-3
work_keys_str_mv AT gutierrezgongoradavier differentiatedextractsfromfreshwaterandterrestrialmollusksinhibitvirulencefactorproductionincryptococcusneoformans
AT raoufalkadhimifouad differentiatedextractsfromfreshwaterandterrestrialmollusksinhibitvirulencefactorproductionincryptococcusneoformans
AT prosserryans differentiatedextractsfromfreshwaterandterrestrialmollusksinhibitvirulencefactorproductionincryptococcusneoformans
AT geddesmcalisterjennifer differentiatedextractsfromfreshwaterandterrestrialmollusksinhibitvirulencefactorproductionincryptococcusneoformans