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首页> 外文期刊>BioMed research international >Misidentification ofCandida guilliermondiiasC. famataamong Strains Isolated from Blood Cultures by the VITEK 2 System
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Misidentification ofCandida guilliermondiiasC. famataamong Strains Isolated from Blood Cultures by the VITEK 2 System

机译:假丝酵母C.通过VITEK 2系统从血液培养物中分离出的famataamong菌株

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Introduction. The aim of this study was to differentiate betweenCandida famataandCandida guilliermondiicorrectly by using matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) and gene sequencing.Methods. Twenty-eightCandidastrains from blood cultures that had been identified asC. famata(N=25),C. famata/C. guilliermondii(N=2), andC. guilliermondii(N=1) by the VITEK 2 system using the YST ID card were included. We identified these strains by MALDI-TOF MS and gene sequencing using the 28S rRNA andITSgenes and compared the results with those obtained by the VITEK 2 system.Results. All 28 isolates were finally identified asC. guilliermondii.Sequencing analysis of the 28S rRNA gene showed 99.80%–100% similarity withC. guilliermondiifor all 28 strains. TheITSgene sequencing of the strains showed 98.34%–100% homology withC. guilliermondii.By MALDI-TOF, we could correctly identify 21 (75%) of 28C. guilliermondiiisolates.Conclusion. We should suspect misidentification whenC. famatais reported by the VITEK 2 system, and we always should keep in mind the possibility of misidentification of any organism when an uncommon species is reported.
机译:介绍。本研究的目的是通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)和基因测序来正确地区分Candida famata和Guidaer guilliermondii。来自血液培养的28株念珠菌已被鉴定为C. famata(N = 25),C。 famata / C。瓜利蒙德氏菌(N = 2)和C.包括使用YST ID卡的VITEK 2系统提供的guilliermondii(N = 1)。我们通过MALDI-TOF MS鉴定了这些菌株,并使用28S rRNA和ITS基因进行了基因测序,并将结果与​​通过VITEK 2系统获得的结果进行了比较。最后将所有28个分离株鉴定为C。 guilliermondii。28SrRNA基因的测序分析显示与C有99.80%–100%的相似性。 Guilliermondii用于所有28个菌株。菌株的ITS基因测序表明与C的同源性为98.34%–100%。通过MALDI-TOF,我们可以正确地识别出21C(75%)的28C。 Guilliermondiiisolates。结论。当C时,我们应该怀疑误认。由VITEK 2系统报告的Famatais,我们应始终牢记在报告罕见物种时可能会误识别任何生物。

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