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Mefenoxam and pyraclostrobin: toxicity and in vitro inhibitory activity against Pythium insidiosum
P C Stibbe1, L B Ianiski1, C Weiblen2
1Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brazil.
Abstract:
The objective of this study is to verify in vitro susceptibility of Pythium insidiosum against the agricultural fungicides mefenoxam and pyraclostrobin and evaluate the toxicity of both compounds. Twenty-one P. insidiosum isolates were tested against mefenoxam and pyraclostrobin using the broth microdilution method. Minimum inhibitory and oomicidal concentrations for both compounds were established. Additionally, scanning electron microscopy was performed on P. insidiosum hyphae treated with the sublethal concentration of each fungicide. The toxicity of the compounds was evaluated in vivo Caenorhabditis elegans model. The concentration to inhibit 100% of P. insidiosum growth ranged from 0·625 to 10 μg ml-1 for mefenoxam and from 0·019 to 5 μg ml-1 for pyraclostrobin. The SEM analysis revealed changes on the surface of the hyphae treated with the fungicides, suggesting possible damage caused by these compounds. There was no evidence of toxicity in vivo models. Mefenoxam and pyraclostrobin did not show toxicity at the doses evaluated and have inhibitory effects on the pathogenic oomycete P. insidiosum. However, further evaluations of their pharmacokinetics and toxicity in different animal species and possible pharmacological interactions are necessary to infer a possible use in the clinical management of pythiosis.
Insights
Agricultural fungicides mefenoxam and pyraclostrobin show in vitro efficacy against the pathogen Pythium insidiosum. These compounds demonstrated no toxicity in vivo, suggesting potential for pythiosis treatment with further research.
Area of Science:
- Agricultural Science
- Mycology
- Veterinary Medicine
Background:
- Pythium insidiosum is an oomycete pathogen causing pythiosis, a serious disease in animals.
- Limited treatment options exist for pythiosis, necessitating the exploration of novel therapeutic agents.
Purpose of the Study:
- To determine the in vitro susceptibility of Pythium insidiosum to agricultural fungicides mefenoxam and pyraclostrobin.
- To evaluate the in vivo toxicity of mefenoxam and pyraclostrobin using a Caenorhabditis elegans model.
Main Methods:
- Broth microdilution method to determine minimum inhibitory and oomicidal concentrations.
- Scanning electron microscopy (SEM) to visualize fungicide effects on P. insidiosum hyphae.
- In vivo toxicity assessment using the Caenorhabditis elegans model.
Main Results:
- Mefenoxam and pyraclostrobin exhibited significant in vitro inhibitory effects against 21 P. insidiosum isolates.
- SEM revealed morphological changes on P. insidiosum hyphae treated with sublethal fungicide concentrations.
- No significant toxicity was observed in the Caenorhabditis elegans model at the evaluated doses.
Conclusions:
- Mefenoxam and pyraclostrobin possess inhibitory activity against Pythium insidiosum and are not toxic at tested doses.
- Further research into pharmacokinetics, toxicity in different species, and potential drug interactions is required for clinical application in pythiosis.
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