Abozar Nasiri-Jahrodi, M. Shams-Ghahfarokhi, Mehdi Razzaghi Abyaneh
{"title":"Effects of Eugenol-Loaded Chitosan Biopolymer Nanoparticles on CYP51A and CYP51B Expression in Aspergillus fumigatus","authors":"Abozar Nasiri-Jahrodi, M. Shams-Ghahfarokhi, Mehdi Razzaghi Abyaneh","doi":"10.52547/iem.8.1.17","DOIUrl":null,"url":null,"abstract":"Backgrounds: Aspergillus fumigatus is a pathogen responsible for invasive aspergillosis and the main leading cause of death in immunosuppressed individuals. The present study aimed to evaluate the impact of eugenol-loaded chitosan nanoparticles on the expression of CYP51a and CYP51b , two well-known genes responsible for triazole drug resistance in A. fumigatus . The minimum inhibitory concentration (MIC) of eugenol-loaded chitosan nanoparticles, chitosan, eugenol, and itraconazole was determined based on the Clinical and Laboratory Standards Institute M38-E3 method at concentrations of 4.6-2400, 11.7-12000, 2-2048, and 1-256 μ g/mL, respectively. The expression of CYP51A and CYP51B was evaluated in A. fumigatus exposed to 0.5, 1, and 2× of MIC concentration of NPs and itraconazole using the real-time polymerase chain reaction. Findings: The obtained results showed that eugenol-loaded chitosan nanoparticles sucessfully reduced eugenol, and itraconazole was measured to be 6000, 256, and 4 μg/mL, respectively. The results of real-time PCR also revealed that eugenol-loaded chitosan nanoparticles increased the expression of both CYP51A and CYP51B in a dose-dependent manner. The expression of fungal CYP51A and CYP51B at mRNA level was significantly increased 1.26, 1.93, and 3.1-fold as well as 1.2, 2.1, and 2.4-fold at concentrations of 150, 300, and 600 μg/mL , respectively ( p <.05). However, it seems that the prepared nanoparticles had a lower impact on the expression of these genes compared to itraconazole. findings the treatment of with eugenol-chitosan nanoparticles increase the of the CYP51 suggesting the antifungal property of these nanoparticles.","PeriodicalId":34545,"journal":{"name":"Infection Epidemiology and Microbiology","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection Epidemiology and Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52547/iem.8.1.17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Backgrounds: Aspergillus fumigatus is a pathogen responsible for invasive aspergillosis and the main leading cause of death in immunosuppressed individuals. The present study aimed to evaluate the impact of eugenol-loaded chitosan nanoparticles on the expression of CYP51a and CYP51b , two well-known genes responsible for triazole drug resistance in A. fumigatus . The minimum inhibitory concentration (MIC) of eugenol-loaded chitosan nanoparticles, chitosan, eugenol, and itraconazole was determined based on the Clinical and Laboratory Standards Institute M38-E3 method at concentrations of 4.6-2400, 11.7-12000, 2-2048, and 1-256 μ g/mL, respectively. The expression of CYP51A and CYP51B was evaluated in A. fumigatus exposed to 0.5, 1, and 2× of MIC concentration of NPs and itraconazole using the real-time polymerase chain reaction. Findings: The obtained results showed that eugenol-loaded chitosan nanoparticles sucessfully reduced eugenol, and itraconazole was measured to be 6000, 256, and 4 μg/mL, respectively. The results of real-time PCR also revealed that eugenol-loaded chitosan nanoparticles increased the expression of both CYP51A and CYP51B in a dose-dependent manner. The expression of fungal CYP51A and CYP51B at mRNA level was significantly increased 1.26, 1.93, and 3.1-fold as well as 1.2, 2.1, and 2.4-fold at concentrations of 150, 300, and 600 μg/mL , respectively ( p <.05). However, it seems that the prepared nanoparticles had a lower impact on the expression of these genes compared to itraconazole. findings the treatment of with eugenol-chitosan nanoparticles increase the of the CYP51 suggesting the antifungal property of these nanoparticles.