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Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth

The emerging fungal amphibian pathogen, Batrachochytrium salamandrivorans (Bsal), is currently spreading across Europe and given its estimated invasion potential, has the capacity to decimate salamander populations worldwide. Fungicides are a promising in situ management strategy for Bsal due to the...

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Autores principales: Tompros, Adrianna, Wilber, Mark Q., Fenton, Andy, Carter, Edward Davis, Gray, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605044/
https://www.ncbi.nlm.nih.gov/pubmed/36294589
http://dx.doi.org/10.3390/jof8101025
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author Tompros, Adrianna
Wilber, Mark Q.
Fenton, Andy
Carter, Edward Davis
Gray, Matthew J.
author_facet Tompros, Adrianna
Wilber, Mark Q.
Fenton, Andy
Carter, Edward Davis
Gray, Matthew J.
author_sort Tompros, Adrianna
collection PubMed
description The emerging fungal amphibian pathogen, Batrachochytrium salamandrivorans (Bsal), is currently spreading across Europe and given its estimated invasion potential, has the capacity to decimate salamander populations worldwide. Fungicides are a promising in situ management strategy for Bsal due to their ability to treat the environment and infected individuals. However, antifungal drugs or pesticides could adversely affect the environment and non-target hosts, thus identifying safe, effective candidate fungicides for in situ treatment is needed. Here, we estimated the inhibitory fungicidal efficacy of five plant-derived fungicides (thymol, curcumin, allicin, 6-gingerol, and Pond Pimafix(®)) and one chemical fungicide (Virkon(®) Aquatic) against Bsal zoospores in vitro. We used a broth microdilution method in 48-well plates to test the efficacy of six concentrations per fungicide on Bsal zoospore viability. Following plate incubation, we performed cell viability assays and agar plate growth trials to estimate the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of each fungicide. All six fungicides exhibited inhibitory and fungicidal effects against Bsal growth, with estimated MIC concentrations ranging from 60 to 0.156 μg/mL for the different compounds. Allicin showed the greatest efficacy (i.e., lowest MIC and MFC) against Bsal zoospores followed by curcumin, Pond Pimafix(®), thymol, 6-gingerol, and Virkon(®) Aquatic, respectively. Our results provide evidence that plant-derived fungicides are effective at inhibiting and killing Bsal zoospores in vitro and may be useful for in situ treatment. Additional studies are needed to estimate the efficacy of these fungicides at inactivating Bsal in the environment and treating Bsal-infected amphibians.
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spelling pubmed-96050442022-10-27 Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth Tompros, Adrianna Wilber, Mark Q. Fenton, Andy Carter, Edward Davis Gray, Matthew J. J Fungi (Basel) Article The emerging fungal amphibian pathogen, Batrachochytrium salamandrivorans (Bsal), is currently spreading across Europe and given its estimated invasion potential, has the capacity to decimate salamander populations worldwide. Fungicides are a promising in situ management strategy for Bsal due to their ability to treat the environment and infected individuals. However, antifungal drugs or pesticides could adversely affect the environment and non-target hosts, thus identifying safe, effective candidate fungicides for in situ treatment is needed. Here, we estimated the inhibitory fungicidal efficacy of five plant-derived fungicides (thymol, curcumin, allicin, 6-gingerol, and Pond Pimafix(®)) and one chemical fungicide (Virkon(®) Aquatic) against Bsal zoospores in vitro. We used a broth microdilution method in 48-well plates to test the efficacy of six concentrations per fungicide on Bsal zoospore viability. Following plate incubation, we performed cell viability assays and agar plate growth trials to estimate the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of each fungicide. All six fungicides exhibited inhibitory and fungicidal effects against Bsal growth, with estimated MIC concentrations ranging from 60 to 0.156 μg/mL for the different compounds. Allicin showed the greatest efficacy (i.e., lowest MIC and MFC) against Bsal zoospores followed by curcumin, Pond Pimafix(®), thymol, 6-gingerol, and Virkon(®) Aquatic, respectively. Our results provide evidence that plant-derived fungicides are effective at inhibiting and killing Bsal zoospores in vitro and may be useful for in situ treatment. Additional studies are needed to estimate the efficacy of these fungicides at inactivating Bsal in the environment and treating Bsal-infected amphibians. MDPI 2022-09-28 /pmc/articles/PMC9605044/ /pubmed/36294589 http://dx.doi.org/10.3390/jof8101025 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tompros, Adrianna
Wilber, Mark Q.
Fenton, Andy
Carter, Edward Davis
Gray, Matthew J.
Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth
title Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth
title_full Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth
title_fullStr Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth
title_full_unstemmed Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth
title_short Efficacy of Plant-Derived Fungicides at Inhibiting Batrachochytrium salamandrivorans Growth
title_sort efficacy of plant-derived fungicides at inhibiting batrachochytrium salamandrivorans growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605044/
https://www.ncbi.nlm.nih.gov/pubmed/36294589
http://dx.doi.org/10.3390/jof8101025
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