TY - JOUR
T1 - Galleria mellonella immune melanization is fungicidal during infection
AU - Smith, Daniel F.Q.
AU - Dragotakes, Quigly
AU - Kulkarni, Madhura
AU - Hardwick, J. Marie
AU - Casadevall, Arturo
N1 - Funding Information:
We would like to thank the entire Casadevall Lab for their contributions during lab meetings and other discussions of this project. We would like to thank Maryann Smith, Thomas Hitzelberger, and Kathy Spinnato for placing the years of weekly G. mellonella orders. Illustrations were created using Biorender.com. D.F.Q.S., Q.D., and A.C. are funded by National Institute of Allergy and Infection Disease R01 AI052733, R01 AI152078, and the National Heart, Lung, and Blood Institute R01 HL059842. D.F.Q.S. is funded by National Institutes of Health 5T32GM008752-18 and 1T32AI138953-01A1. J.M.H. and M.K. are funded by National Institutes of Health R56 AI168539 and R21 AI144373. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
We would like to thank the entire Casadevall Lab for their contributions during lab meetings and other discussions of this project. We would like to thank Maryann Smith, Thomas Hitzelberger, and Kathy Spinnato for placing the years of weekly G. mellonella orders. Illustrations were created using Biorender.com. D.F.Q.S., Q.D., and A.C. are funded by National Institute of Allergy and Infection Disease R01 AI052733, R01 AI152078, and the National Heart, Lung, and Blood Institute R01 HL059842. D.F.Q.S. is funded by National Institutes of Health 5T32GM008752-18 and 1T32AI138953-01A1. J.M.H. and M.K. are funded by National Institutes of Health R56 AI168539 and R21 AI144373. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - 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.
AB - 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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UR - http://www.scopus.com/inward/citedby.url?scp=85143992916&partnerID=8YFLogxK
U2 - 10.1038/s42003-022-04340-6
DO - 10.1038/s42003-022-04340-6
M3 - Article
C2 - 36510005
AN - SCOPUS:85143992916
SN - 2399-3642
VL - 5
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 1364
ER -