Evaluation of Aspirin Effect on Candida Glabrata Isolates with Resistance to Azole Compounds by Real-Time PCR

F. Nojoomi, M. Vafaei, F. Bagheri, Zohreh Zamanian
{"title":"Evaluation of Aspirin Effect on Candida Glabrata Isolates with Resistance to Azole Compounds by Real-Time PCR","authors":"F. Nojoomi, M. Vafaei, F. Bagheri, Zohreh Zamanian","doi":"10.15406/MOJI.2017.05.00173","DOIUrl":null,"url":null,"abstract":"Materials and methods: Five C. glabrata isolates were collected from patients with candidal vulvovaginitis referred to clinic. The antibiotic susceptibility test of isolates for fluconazole was performed according to the CLSI M38-A2 standard protocol. A 64μg/ml aspirin and 500ug/ml and likewise 64μg/ml fluconazole were used for the MIC detection test. The RNA of isolates was prepared according to the manufacturer’s instruction. Synthesis of cDNA was conducted with the 1621K kit (Fermentase).. The RT-PCR reaction was set up for ERG3, ERG6 and ERG11 genes and the housekeeping gene Beta-actin (β-actin) was amplified as internal control.","PeriodicalId":90928,"journal":{"name":"MOJ immunology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MOJ immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/MOJI.2017.05.00173","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Materials and methods: Five C. glabrata isolates were collected from patients with candidal vulvovaginitis referred to clinic. The antibiotic susceptibility test of isolates for fluconazole was performed according to the CLSI M38-A2 standard protocol. A 64μg/ml aspirin and 500ug/ml and likewise 64μg/ml fluconazole were used for the MIC detection test. The RNA of isolates was prepared according to the manufacturer’s instruction. Synthesis of cDNA was conducted with the 1621K kit (Fermentase).. The RT-PCR reaction was set up for ERG3, ERG6 and ERG11 genes and the housekeeping gene Beta-actin (β-actin) was amplified as internal control.
实时聚合酶链反应评价阿司匹林对含氮化合物耐药念珠菌的作用
材料与方法:从临床转诊的念珠菌性外阴阴道炎患者中分离得到5株光滑念珠菌。分离株对氟康唑的抗生素敏感性试验按照CLSI M38-A2标准方案进行。MIC检测试验使用64μg/ml阿司匹林和500μg/ml氟康唑,同样使用64μg/ml氟康唑。根据制造商的说明制备分离物的RNA。cDNA的合成是用1621K试剂盒(发酵酶)进行的。。建立ERG3、ERR6和ERG11基因的RT-PCR反应,扩增管家基因β-肌动蛋白(β-actin)作为内部对照。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信