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Galleria mellonella immune melanization is fungicidal during infection

A key component of the insect immune response is melanin production, including within nodules, or aggregations of immune cells surrounding microbes. Melanization produces oxidative and toxic intermediates that limit microbial infections. However, a direct fungicidal role of melanin during infection...

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Autores principales: Smith, Daniel F. Q., Dragotakes, Quigly, Kulkarni, Madhura, Hardwick, J. Marie, Casadevall, Arturo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744840/
https://www.ncbi.nlm.nih.gov/pubmed/36510005
http://dx.doi.org/10.1038/s42003-022-04340-6
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author Smith, Daniel F. Q.
Dragotakes, Quigly
Kulkarni, Madhura
Hardwick, J. Marie
Casadevall, Arturo
author_facet Smith, Daniel F. Q.
Dragotakes, Quigly
Kulkarni, Madhura
Hardwick, J. Marie
Casadevall, Arturo
author_sort Smith, Daniel F. Q.
collection PubMed
description A key component of the insect immune response is melanin production, including within nodules, or aggregations of immune cells surrounding microbes. Melanization produces oxidative and toxic intermediates that limit microbial infections. However, a direct fungicidal role of melanin during infection has not been demonstrated. We previously reported that the fungus Cryptococcus neoformans is encapsulated with melanin within nodules of Galleria mellonella hosts. Here we developed techniques to study melanin’s role during C. neoformans infection in G. mellonella. We provided evidence that in vivo melanin-encapsulation was fungicidal. To further study immune melanization, we applied tissue-clearing techniques to visualize melanized nodules in situ throughout the larvae. Further, we developed a time-lapse microscopy protocol to visualize the melanization kinetics in extracted hemolymph following fungal exposure. Using this technique, we found that cryptococcal melanin and laccase enhance immune melanization. We extended this approach to study the fungal pathogens Candida albicans and Candida auris. We find that the yeast morphologies of these fungi elicited robust melanization responses, while hyphal and pseudohyphal morphologies were melanin-evasive. Approximately 23% of melanin-encapsulated C. albicans yeast can survive and breakthrough the encapsulation. Overall, our results provide direct evidence that immune melanization functions as a direct antifungal mechanism in G. mellonella.
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spelling pubmed-97448402022-12-14 Galleria mellonella immune melanization is fungicidal during infection Smith, Daniel F. Q. Dragotakes, Quigly Kulkarni, Madhura Hardwick, J. Marie Casadevall, Arturo Commun Biol Article A key component of the insect immune response is melanin production, including within nodules, or aggregations of immune cells surrounding microbes. Melanization produces oxidative and toxic intermediates that limit microbial infections. However, a direct fungicidal role of melanin during infection has not been demonstrated. We previously reported that the fungus Cryptococcus neoformans is encapsulated with melanin within nodules of Galleria mellonella hosts. Here we developed techniques to study melanin’s role during C. neoformans infection in G. mellonella. We provided evidence that in vivo melanin-encapsulation was fungicidal. To further study immune melanization, we applied tissue-clearing techniques to visualize melanized nodules in situ throughout the larvae. Further, we developed a time-lapse microscopy protocol to visualize the melanization kinetics in extracted hemolymph following fungal exposure. Using this technique, we found that cryptococcal melanin and laccase enhance immune melanization. We extended this approach to study the fungal pathogens Candida albicans and Candida auris. We find that the yeast morphologies of these fungi elicited robust melanization responses, while hyphal and pseudohyphal morphologies were melanin-evasive. Approximately 23% of melanin-encapsulated C. albicans yeast can survive and breakthrough the encapsulation. Overall, our results provide direct evidence that immune melanization functions as a direct antifungal mechanism in G. mellonella. Nature Publishing Group UK 2022-12-12 /pmc/articles/PMC9744840/ /pubmed/36510005 http://dx.doi.org/10.1038/s42003-022-04340-6 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Smith, Daniel F. Q.
Dragotakes, Quigly
Kulkarni, Madhura
Hardwick, J. Marie
Casadevall, Arturo
Galleria mellonella immune melanization is fungicidal during infection
title Galleria mellonella immune melanization is fungicidal during infection
title_full Galleria mellonella immune melanization is fungicidal during infection
title_fullStr Galleria mellonella immune melanization is fungicidal during infection
title_full_unstemmed Galleria mellonella immune melanization is fungicidal during infection
title_short Galleria mellonella immune melanization is fungicidal during infection
title_sort galleria mellonella immune melanization is fungicidal during infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744840/
https://www.ncbi.nlm.nih.gov/pubmed/36510005
http://dx.doi.org/10.1038/s42003-022-04340-6
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