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A novel comprehensive set of fungal Real time PCR assays (fuPCR) for the detection of fungi in immunocompromised haematological patients-A pilot study

机译:一套新颖的真菌实时荧光定量PCR检测试剂盒(fuPCR),用于检测免疫功能低下的血液病患者中的真菌-初步研究

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Fungal infections are recognized in an increasing number of patients with immunological deficits and are associated with high rates of mortality (Brown et al., 2012a). In this pilot-study, a rapid Real time PCR (fuPCR) was designed for the detection and differentiation of fungal pathogens in clinical specimens of haematological patients. The fuPCR, targeting the internal transcribed spacer region 2 (ITS2) of rDNA region, is comprised of seven multiplex reactions, which were shown to be specific and sensitive for a comprehensive spectrum of clinically relevant fungal species. This was validated by testing respective fungal DNAs in each fuPCR reaction and 28 respiratory samples of fungal pneumonia-proven patients. Clinical sample sets of throat swab, EDTA-blood and blood sera from 50 patients with severe haematological malignancies, including haematopoietic stem cell transfer (HSCT), and samples from 30 healthy individuals were then analysed. In a first step, 198 samples of immunosuppressed patients were solely examined by fuPCR; and 50.8% (33/65) respiratory swabs, 4.8% (3/63) EDTA blood samples and 1.4% (1/70) blood serum samples were tested positive. In a second step, 56 respiratory samples of immunosuppressed patients and 30 of healthy individuals were simultaneously analysed by fuPCR and standard cultivation techniques. By both methods 30.4% (17/56) swabs of the immunocompromised patients were tested positive, 37.5% (21/56) were tested negative and 32.1% (18/56) were tested fuPCR positive and culture negative. In analysing the blood samples of the immunocompromised patients 5.4% (3/56) EDTA blood samples and 16.1% (9/56) sera samples were tested fuPCR-positive, whereas all samples of 30 healthy individuals with no signs of immunological deficits were tested negative by fuPCR.
机译:越来越多的免疫缺陷患者认识到真菌感染,并与高死亡率相关(Brown等,2012a)。在该初步研究中,设计了一种快速实时荧光定量PCR(fuPCR),用于检测和区分血液病患者临床标本中的真菌病原体。靶向rDNA区域的内部转录间隔区2(ITS2)的fuPCR由七个多重反应组成,这些反应对临床相关真菌物种的全面光谱具有特异性和敏感性。通过测试每个fuPCR反应中相应的真菌DNA和经真菌性肺炎验证的患者的28个呼吸道样本来验证这一点。从50例包括造血干细胞移植(HSCT)在内的严重血液恶性肿瘤患者的咽拭子,EDTA血液和血液血清的临床样本集,然后对30例健康个体的样本进行分析。第一步,仅用fuPCR检查了198个免疫抑制患者的样本;检测到50.8%(33/65)的呼吸拭子,4.8%(3/63)的EDTA血液样本和1.4%(1/70)的血清样本呈阳性。第二步,通过fuPCR和标准培养技术同时分析了56个免疫抑制患者的呼吸道样本和30个健康个体。通过这两种方法,免疫受损患者的拭子中30.4%(17/56)呈阳性,37.5%(21/56)呈阴性,32.1%(18/56)fuPCR呈阳性,培养阴性。在分析免疫受损患者的血液样本中,fuPCR阳性检测了5.4%(3/56)EDTA血液样本和16.1%(9/56)血清,而30例健康个体的所有样本均未检测到免疫缺陷迹象fuPCR阴性。

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