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用于检测针对某基因中Y132F突变的氟康唑耐药性的聚合酶链反应标准化。 (你提供的原文中部分信息不完整,比如“in ”后面缺少具体内容,我按照完整可理解的部分进行了翻译)

Standardization of polymerase chain reaction for detection of fluconazole resistance targeting Y132F mutation in gene in .

作者信息

Karthika Kanagasabapathi, Premamalini Thayanidhi, Vijayakishore Thanneru, Kindo Anupama Jyoti

机构信息

Department of Microbiology, Sri Ramachandra Medical College & Research Institute, SRIHER, Porur, Chennai 600116, India.

出版信息

Curr Med Mycol. 2024 May 7;10. doi: 10.22034/cmm.2024.345209.1517. eCollection 2024.

Abstract

BACKGROUND AND PURPOSE

is the third most commonly isolated species from candidemia patients admitted to Indian intensive care units. Outbreak of infection and emergence of fluconazole resistance associated with this particular species has been increasingly documented since 2018. Worldwide data has documented that Y132F substitution in the gene is the predominant fluconazole resistance mechanism among . Hence, this study aimed to detect fluconazole resistance by targeting Y132F mutation in the gene in , by conventional polymerase chain reaction (PCR) assay with in-house designed primers.

MATERIALS AND METHODS

A total of 75 isolates were collected from candidemia patients (Jan-Dec 2023). All the isolates were subjected to phenotypic and genotypic characterization. PCR-restriction fragment length polymorphism was performed for identification and confirmation of isolates. The antifungal susceptibility testing by broth microdilution method was performed according to the Clinical and Laboratory Standards Institute guidelines (M27-A3) for all against fluconazole, itraconazole, voriconazole, and posaconazole to determine their minimum inhibitory concentration (MIC) values. -specific PCR assay was developed with in-house designed primers to detect Y132F mutation in the gene.

RESULTS

In this study, among 75 candidemia patients (Jan-Dec 2023), about 24% of the candidemia was caused by . Fluconazole resistance among was found to be 16.7% with a MIC range of 32-64 µg/ml. The PCR assay successfully identified all three fluconazole-resistant with Y132F mutation, thereby confirming the PCR results. Furthermore, validation of the presence and absence of Y132F mutation in resistant and susceptible isolates by DNA sequencing showed that the results were in concordance with our PCR assay.

CONCLUSION

The developed PCR assay successfully detected the Y132F mutation within 3 h. This assay can be useful for early detection of fluconazole-resistant isolates in candidemia patients, which helps the provision of early antifungal treatment for better patient management.

摘要

背景与目的

是印度重症监护病房收治的念珠菌血症患者中第三常见的分离菌种。自2018年以来,与该特定菌种相关的感染暴发及氟康唑耐药性的出现已有越来越多的文献记载。全球数据表明,该基因中的Y132F替换是该菌种中主要的氟康唑耐药机制。因此,本研究旨在通过使用自行设计的引物进行常规聚合酶链反应(PCR)检测,针对该菌种基因中的Y132F突变来检测氟康唑耐药性。

材料与方法

从念珠菌血症患者(2023年1月至12月)中总共收集了75株该菌种的分离株。所有该菌种的分离株均进行了表型和基因型鉴定。采用PCR-限制性片段长度多态性方法对该菌种的分离株进行鉴定和确认。根据临床和实验室标准协会指南(M27-A3),采用肉汤微量稀释法对所有该菌种分离株针对氟康唑、伊曲康唑、伏立康唑和泊沙康唑进行抗真菌药敏试验,以确定其最低抑菌浓度(MIC)值。使用自行设计的引物开发了该菌种特异性PCR检测方法,以检测该基因中的Y132F突变。

结果

在本研究中,75例念珠菌血症患者(2023年1月至12月)中,约24%的念珠菌血症由该菌种引起。该菌种的氟康唑耐药率为16.7%,MIC范围为32 - 64μg/ml。PCR检测成功鉴定出所有三株具有Y132F突变的氟康唑耐药该菌种,从而证实了PCR结果。此外,通过DNA测序对耐药和敏感分离株中Y132F突变的有无进行验证,结果与我们的PCR检测一致。

结论

所开发的PCR检测方法在3小时内成功检测到Y132F突变。该检测方法可用于早期检测念珠菌血症患者中氟康唑耐药的该菌种分离株,有助于为更好地管理患者提供早期抗真菌治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9783/11686929/77b0c4f02630/CMM-10-e2024.345209.1517-g001.jpg

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