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首页> 外文期刊>Future microbiology >First fungemia case due to environmental yeast Wickerhamomyces myanmarensis: detection by multiplex qPCR and antifungal susceptibility
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First fungemia case due to environmental yeast Wickerhamomyces myanmarensis: detection by multiplex qPCR and antifungal susceptibility

机译:第一个血统案例由于环境酵母柳瓜莫氏菌,Myanmarensis:通过多重QPCR检测和抗真菌敏感性

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Aim: Presenting the first clinical case of Wickerhamomyces myanmarensis. Patients & methods: Yeast cells were isolated from blood and central venous catheter of a 5.5-year-old male subject. API 20C AUX, MALDI-TOF MS, ITS and LSU rDNA sequencing, and our qPCR assay were used for identification and the MIC values were determined by CLSI M27-A3. Results: ITS and LSU rDNA sequencing identified both isolates as W. myanmarensis, while API 20C AUX and MALDI-TOF MS did not identify them correctly. Our qPCR specifically distinguished W. myanmarensis from W. anomalus. Isolate obtained from blood showed a higher MIC value for fluconazole, voriconazole and posaconazole. Conclusion: Utilization of reliable identification tools might reveal the genuine spectrum of opportunistic yeast species.
机译:目的:介绍柳条柳苗缅甸的第一个临床病例。 患者及方法:从5.5岁男性受试者的血液和中央静脉导管中分离酵母细胞。 API 20C AUX,MALDI-TOF MS,其和LSU RDNA测序,以及我们的QPCR测定用于鉴定,并且通过CLSI M27-A3测定MIC值。 结果:其和LSU RDNA测序识别为W. MyAnmarensis的分离株,而API 20C AUX和MALDI-TOF MS没有正确识别它们。 我们的QPCR明显从W. Anomalus的W.Myanmarensis脱颖而出。 从血液中获得的分离物显示出氟康唑,伏立康唑和唑康唑的较高的MIC值。 结论:可靠识别工具的利用可能揭示了机会酵母菌的真正谱。

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