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Evaluation of a single-tube real-time PCR for detection and identification of 11 dermatophyte species in clinical material

机译:评价用于检测和鉴定临床材料中11种皮肤癣菌菌种的单管实时PCR

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摘要

We developed a dermatophyte-specific single-tube real-time PCR assay based on internal transcribed sequences. This assay allows the rapid detection and identification of 11 clinically relevant species within the three dermatophyte genera Trichophyton, Microsporum and Epidermophyton in nail, skin and hair samples within a few hours. Analysis of 145 clinical samples (107 nail, 36 skin scale, and two hair) by both real-time PCR and a PCR-reverse line blot (PCR-RLB) assay described earlier revealed that 133 of the 145 samples had concordant real-time PCR and PCR-RLB detection results (83 positive, 49 negative, and one inhibited). Six samples were positive by real-time PCR and negative by PCR-RLB, and two were negative by real-time PCR and positive by PCR-RLB. Four samples demonstrated inhibition in one of the two PCR assays. Only one of 83 positive samples had discordant identification results between both assays (Trichophyton verrucosum and Trichophyton erinacei by real-time PCR and Trichophyton erinacei by PCR-RLB). Der-matophytes present in seven positive samples that were incompletely identified as Trichophyton sp. by PCR-RLB were identified to the species level by real-time PCR as Trichophyton interdigitale and Trichophyton rubrum in six cases and one case, respectively. One hundred and twenty of 145 samples were also analysed by conventional dermatophyte culture and by direct microscopy. Our single-tube real-time PCR assay proved to be suitable for direct detection and identification of dermatophytes in nail, skin and hair samples with minimal total assay time (4 h after overnight lysis) and hands-on time, without the need for post-PCR analysis, and with good sensitivity and specificity.
机译:我们开发了基于内部转录序列的皮肤癣菌特异性单管实时PCR分析方法。该测定法可在几个小时内快速检测和鉴定指甲,皮肤和头发样品中的三种皮肤癣菌属,毛癣菌,微孢子菌和表皮癣菌属中的11种临床相关物种。通过实时PCR和先前描述的PCR反向线印迹(PCR-RLB)分析对145个临床样品(107个指甲,36个皮肤鳞屑和两根头发)进行分析,发现145个样品中的133个具有实时一致的PCR和PCR-RLB检测结果(83阳性,49阴性,1被抑制)。实时荧光定量PCR阳性6例,PCR-RLB阴性,实时荧光定量2例,PCR-RLB阳性。四种样品在两种PCR分析之一中显示出抑制作用。在这两种测定之间的83个阳性样品中,只有一个样品的鉴定结果不一致(实时荧光定量PCR的疣状毛癣菌和蛇形毛癣菌,而PCR-RLB的阳性毛癣菌)。存在于七个未完全鉴定为毛癣菌属(Trichophyton sp。)的阳性样品中的麦癣菌。通过实时荧光定量PCR(PCR-RLB)鉴定到物种水平的指内毛癣菌和红毛癣菌分别为6例和1例。还通过常规皮肤真菌培养和直接显微镜分析了145个样品中的120个。经证实,我们的单管实时PCR测定法适用于指甲,皮肤和头发样品中的皮肤真菌的直接检测和鉴定,而总测定时间(过夜裂解后4小时)和动手时间最短,而无需后期操作-PCR分析,并具有良好的敏感性和特异性。

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