Donya Nikaein, Haleh Malekmadani, Babak Beikzadeh, Reza Mardanpour, Alireza Khosravi, Seyed Mohammad Moghadami
{"title":"酵母益生菌布拉氏酵母菌细胞壁提取物对 A549 细胞中曲霉菌过敏性的影响","authors":"Donya Nikaein, Haleh Malekmadani, Babak Beikzadeh, Reza Mardanpour, Alireza Khosravi, Seyed Mohammad Moghadami","doi":"10.22034/cmm.2024.345134.1463","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and purpose: </strong>Interest in probiotic use for respiratory allergies has increased. In this regard, the present study aimed to evaluate the effect of cell wall extract of <i>Saccharomyces boulardii</i> on <i>Aspergillus fumigatus</i> as an allergenic fungus and its effectiveness in reducing inflammatory cytokines in A549 cells sensitized with <i>A. fumigatus</i> conidia.</p><p><strong>Materials and methods: </strong>Cell wall of <i>S. boulardii</i> was prepared and challenged by <i>A. fumigatus</i> conidia at various concentrations. Secretory protease activity was tested using the Casein method. The <i>A. fumigatus</i> allergen 1 (Asp f1) gene expression was calculated by quantitative real-time polymerase chain reaction (qRT-PCR). In another experiment, qRT-PCR was used to examine gene expression of interleukin 13 and interleukin 17 by A549 lung epithelial cells exposed to <i>A. fumigatus</i> conidia and treated with different concentrations of <i>S. boulardii</i> cell wall extract.</p><p><strong>Results: </strong><i>Saccharomyces boulardii</i> cell wall extract significantly reduced the protease activity of <i>A. fumigatus</i> at concentrations of 10 and 20 mg/ml (<i>P</i><0.05). The Asp f1 gene expression was significantly down-regulated in each concentration of <i>S. boulardii</i> cell wall extract (<i>P</i><0.05). <i>Aspergillus fumigatus</i> conidia upregulated the expression of IL-13 and IL-17 in A549 cells, and <i>S. boulardii</i> cell wall extract could downregulate the expression of the mentioned cytokines at concentrations of 10 and 20 mg/ml (<i>P</i><0.05).</p><p><strong>Conclusion: </strong>According to the results, it can be concluded that <i>S. boulardii</i> cell wall extract could be a candidate for IL-13- and IL-17-induced Aspergillus-mediated allergy and asthma therapies. Nevertheless, future studies need to be conducted on the safety of <i>S. boulardii</i> cell wall extract <i>in vivo</i> and its effects on other arms of allergic hypersensitivity.</p>","PeriodicalId":10863,"journal":{"name":"Current Medical Mycology","volume":"9 4","pages":"1-8"},"PeriodicalIF":0.0000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11230140/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effect of yeast probiotic <i>Saccharomyces boulardii</i> cell wall extract on <i>Aspergillus fumigatus</i> allergenicity in A549 cells.\",\"authors\":\"Donya Nikaein, Haleh Malekmadani, Babak Beikzadeh, Reza Mardanpour, Alireza Khosravi, Seyed Mohammad Moghadami\",\"doi\":\"10.22034/cmm.2024.345134.1463\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and purpose: </strong>Interest in probiotic use for respiratory allergies has increased. In this regard, the present study aimed to evaluate the effect of cell wall extract of <i>Saccharomyces boulardii</i> on <i>Aspergillus fumigatus</i> as an allergenic fungus and its effectiveness in reducing inflammatory cytokines in A549 cells sensitized with <i>A. fumigatus</i> conidia.</p><p><strong>Materials and methods: </strong>Cell wall of <i>S. boulardii</i> was prepared and challenged by <i>A. fumigatus</i> conidia at various concentrations. Secretory protease activity was tested using the Casein method. The <i>A. fumigatus</i> allergen 1 (Asp f1) gene expression was calculated by quantitative real-time polymerase chain reaction (qRT-PCR). In another experiment, qRT-PCR was used to examine gene expression of interleukin 13 and interleukin 17 by A549 lung epithelial cells exposed to <i>A. fumigatus</i> conidia and treated with different concentrations of <i>S. boulardii</i> cell wall extract.</p><p><strong>Results: </strong><i>Saccharomyces boulardii</i> cell wall extract significantly reduced the protease activity of <i>A. fumigatus</i> at concentrations of 10 and 20 mg/ml (<i>P</i><0.05). The Asp f1 gene expression was significantly down-regulated in each concentration of <i>S. boulardii</i> cell wall extract (<i>P</i><0.05). <i>Aspergillus fumigatus</i> conidia upregulated the expression of IL-13 and IL-17 in A549 cells, and <i>S. boulardii</i> cell wall extract could downregulate the expression of the mentioned cytokines at concentrations of 10 and 20 mg/ml (<i>P</i><0.05).</p><p><strong>Conclusion: </strong>According to the results, it can be concluded that <i>S. boulardii</i> cell wall extract could be a candidate for IL-13- and IL-17-induced Aspergillus-mediated allergy and asthma therapies. Nevertheless, future studies need to be conducted on the safety of <i>S. boulardii</i> cell wall extract <i>in vivo</i> and its effects on other arms of allergic hypersensitivity.</p>\",\"PeriodicalId\":10863,\"journal\":{\"name\":\"Current Medical Mycology\",\"volume\":\"9 4\",\"pages\":\"1-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11230140/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Medical Mycology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22034/cmm.2024.345134.1463\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Medical Mycology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22034/cmm.2024.345134.1463","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
Effect of yeast probiotic Saccharomyces boulardii cell wall extract on Aspergillus fumigatus allergenicity in A549 cells.
Background and purpose: Interest in probiotic use for respiratory allergies has increased. In this regard, the present study aimed to evaluate the effect of cell wall extract of Saccharomyces boulardii on Aspergillus fumigatus as an allergenic fungus and its effectiveness in reducing inflammatory cytokines in A549 cells sensitized with A. fumigatus conidia.
Materials and methods: Cell wall of S. boulardii was prepared and challenged by A. fumigatus conidia at various concentrations. Secretory protease activity was tested using the Casein method. The A. fumigatus allergen 1 (Asp f1) gene expression was calculated by quantitative real-time polymerase chain reaction (qRT-PCR). In another experiment, qRT-PCR was used to examine gene expression of interleukin 13 and interleukin 17 by A549 lung epithelial cells exposed to A. fumigatus conidia and treated with different concentrations of S. boulardii cell wall extract.
Results: Saccharomyces boulardii cell wall extract significantly reduced the protease activity of A. fumigatus at concentrations of 10 and 20 mg/ml (P<0.05). The Asp f1 gene expression was significantly down-regulated in each concentration of S. boulardii cell wall extract (P<0.05). Aspergillus fumigatus conidia upregulated the expression of IL-13 and IL-17 in A549 cells, and S. boulardii cell wall extract could downregulate the expression of the mentioned cytokines at concentrations of 10 and 20 mg/ml (P<0.05).
Conclusion: According to the results, it can be concluded that S. boulardii cell wall extract could be a candidate for IL-13- and IL-17-induced Aspergillus-mediated allergy and asthma therapies. Nevertheless, future studies need to be conducted on the safety of S. boulardii cell wall extract in vivo and its effects on other arms of allergic hypersensitivity.