Matúš Štefánek, Lucia Černáková, Jaroslava Dekkerová, Helena Bujdáková
{"title":"光动力失活可干扰耳念珠菌CDR1和MDR1外排基因的上调,但可有效根除耳念珠菌生物膜。","authors":"Matúš Štefánek, Lucia Černáková, Jaroslava Dekkerová, Helena Bujdáková","doi":"10.3390/jof8111137","DOIUrl":null,"url":null,"abstract":"<p><p><i>Candida auris</i>, in recent years, has emerged as a dangerous nosocomial pathogen. It represents a challenge for effective treatment because of its multiresistance. Photodynamic inactivation (PDI) is a promising way to solve problems with a wide range of resistant microorganisms. This study aimed to use PDI for the eradication of <i>C. auris</i> biofilms. Moreover, the regulation of the <i>CDR1</i>, <i>CDR2</i>, and <i>MDR1</i> resistance genes was studied. Experiments were performed on 24 h biofilms formed by three clinical isolates of <i>C. auris in vitro</i>. PDI was performed in the presence of the photosensitizer methylene blue (0.25 mM) and samples were irradiated with a red laser (λ = 660 nm, 190 mW/cm<sup>2</sup>) for 79, 120, and 300 s. To confirm the PDI effect, confocal laser scanning microscopy was performed after treatment. Effective PDI was achieved in all strains. The highest inhibition was observed after 300 s irradiation, with over 90% inhibition compared with the non-irradiated control sample. PDI was observed to upregulate the expression of the <i>CDR1</i> gene, but mainly the <i>MDR1</i> gene. Despite this observation, PDI significantly decreased the survival of <i>C. auris</i> biofilm cells and proved to have great potential for the eradication of problematic resistant yeasts.</p>","PeriodicalId":520671,"journal":{"name":"Journal of fungi (Basel, Switzerland)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697027/pdf/","citationCount":"3","resultStr":"{\"title\":\"Photodynamic Inactivation Effectively Eradicates <i>Candida auris</i> Biofilm despite Its Interference with the Upregulation of <i>CDR1</i> and <i>MDR1</i> Efflux Genes.\",\"authors\":\"Matúš Štefánek, Lucia Černáková, Jaroslava Dekkerová, Helena Bujdáková\",\"doi\":\"10.3390/jof8111137\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Candida auris</i>, in recent years, has emerged as a dangerous nosocomial pathogen. It represents a challenge for effective treatment because of its multiresistance. Photodynamic inactivation (PDI) is a promising way to solve problems with a wide range of resistant microorganisms. This study aimed to use PDI for the eradication of <i>C. auris</i> biofilms. Moreover, the regulation of the <i>CDR1</i>, <i>CDR2</i>, and <i>MDR1</i> resistance genes was studied. Experiments were performed on 24 h biofilms formed by three clinical isolates of <i>C. auris in vitro</i>. PDI was performed in the presence of the photosensitizer methylene blue (0.25 mM) and samples were irradiated with a red laser (λ = 660 nm, 190 mW/cm<sup>2</sup>) for 79, 120, and 300 s. To confirm the PDI effect, confocal laser scanning microscopy was performed after treatment. Effective PDI was achieved in all strains. The highest inhibition was observed after 300 s irradiation, with over 90% inhibition compared with the non-irradiated control sample. PDI was observed to upregulate the expression of the <i>CDR1</i> gene, but mainly the <i>MDR1</i> gene. Despite this observation, PDI significantly decreased the survival of <i>C. auris</i> biofilm cells and proved to have great potential for the eradication of problematic resistant yeasts.</p>\",\"PeriodicalId\":520671,\"journal\":{\"name\":\"Journal of fungi (Basel, Switzerland)\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-10-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697027/pdf/\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of fungi (Basel, Switzerland)\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3390/jof8111137\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of fungi (Basel, Switzerland)","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/jof8111137","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Photodynamic Inactivation Effectively Eradicates Candida auris Biofilm despite Its Interference with the Upregulation of CDR1 and MDR1 Efflux Genes.
Candida auris, in recent years, has emerged as a dangerous nosocomial pathogen. It represents a challenge for effective treatment because of its multiresistance. Photodynamic inactivation (PDI) is a promising way to solve problems with a wide range of resistant microorganisms. This study aimed to use PDI for the eradication of C. auris biofilms. Moreover, the regulation of the CDR1, CDR2, and MDR1 resistance genes was studied. Experiments were performed on 24 h biofilms formed by three clinical isolates of C. auris in vitro. PDI was performed in the presence of the photosensitizer methylene blue (0.25 mM) and samples were irradiated with a red laser (λ = 660 nm, 190 mW/cm2) for 79, 120, and 300 s. To confirm the PDI effect, confocal laser scanning microscopy was performed after treatment. Effective PDI was achieved in all strains. The highest inhibition was observed after 300 s irradiation, with over 90% inhibition compared with the non-irradiated control sample. PDI was observed to upregulate the expression of the CDR1 gene, but mainly the MDR1 gene. Despite this observation, PDI significantly decreased the survival of C. auris biofilm cells and proved to have great potential for the eradication of problematic resistant yeasts.