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首页> 外文期刊>Journal of Clinical Microbiology >Development of Novel Real-Time PCR Assays for Detection and Differentiation of Eleven Medically Important Aspergillus and Candida Species in Clinical Specimens
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Development of Novel Real-Time PCR Assays for Detection and Differentiation of Eleven Medically Important Aspergillus and Candida Species in Clinical Specimens

机译:用于检测和区分临床标本中的11种医学上重要的曲霉和念珠菌的新型实时PCR检测方法的开发

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In the present study, novel real-time PCR assays targeting the fungal ITS2 region were developed for the detection and differentiation of medically important Aspergillus species (Aspergillus fumigatus, Aspergillus flavus, Aspergillus nidulans, Aspergillus niger, and Aspergillus terreus) and Candida species (Candida albicans, Candida dubliniensis, Candida glabrata, Candida krusei, Candida parapsilosis, and Candida tropicalis) using a LightCycler instrument. The combination of a group-specific and a universal primer with five Aspergillus or six Candida species-specific biprobes in one reaction mixture facilitated rapid screening and species differentiation by the characteristic peak melting temperatures of the biprobes. Both assays can be performed either as single assays or simultaneously in the same LightCycler run. The analytical sensitivity using pure cultures and EDTA-anticoagulated blood, cerebrospinal fluid (CSF), and tissue samples spiked with A. fumigatus and C. albicans cell suspensions was shown to be at least 1 CFU per PCR, corresponding to 5 to 10 CFU/ml blood and 10 CFU/200 μl CSF or 0.02 g tissue. To assess the clinical applicability, 26 respiratory samples, 4 tissue samples from the maxillary sinus, and 1 blood sample were retrospectively tested and real-time PCR results were compared with results from culture, histology, or a galactomannan enzyme-linked immunosorbent assay (ELISA). Twenty samples (64.5%) were both culture positive and positive by real-time PCR. Six samples (19.4%) showed no growth of fungi but were positive by real-time PCR. However, all of the tissue samples were positive by both PCR and histology. The blood sample showed no growth of Aspergillus, but aspergillosis was confirmed by positive galactomannan ELISA, histology, and PCR results. The remaining samples (16.1%) were culture and PCR negative; also, no other signs indicating fungal infection were observed. Our data suggest that the Aspergillus and Candida assays may be appropriate for use in clinical laboratories as simple and rapid screening tests for the most frequently encountered Aspergillus and Candida species and might become an important tool in the early diagnosis of fungal infections in the future.
机译:在本研究中,开发了针对真菌ITS2区域的新型实时PCR检测试剂盒,用于检测和区分医学上重要的曲霉 Aspergillus fumigatus Aspergillus黄曲霉黑曲霉黑曲霉土曲霉)和 Candida 种(白色念珠菌杜比里尼念珠菌 glabrata念珠菌克鲁斯念珠菌副寄生念珠菌和< em>热带念珠菌)。在一种反应混合物中,将一组特定引物和一个通用引物与五个曲霉或六个 Candida 物种特异性双探针组合在一起,可通过特征峰解链促进快速筛选和物种分化双探针的温度。两种测定均可作为单个测定进行,也可在同一LightCycler运行中同时进行。使用纯培养物和EDTA抗凝血液,脑脊液(CSF)和掺有 A的组织样品的分析灵敏度。烟熏 C。每次PCR显示,白色念珠菌细胞悬浮液至少为1 CFU,相当于5至10 CFU / ml血液和10 CFU / 200μlCSF或0.02 g组织。为了评估临床适用性,对26份呼吸道样本,4份上颌窦组织样本和1份血液样本进行了回顾性测试,并将实时PCR结果与培养,组织学或半乳甘露聚糖酶联免疫吸附试验(ELISA)的结果进行了比较)。实时PCR检测到20个样品(64.5%)均为培养阳性和阳性。六个样品(19.4%)显示无真菌生长,但通过实时PCR呈阳性。然而,通过PCR和组织学,所有组织样品均为阳性。血样中没有曲霉的生长,但通过半乳甘露聚糖ELISA,组织学和PCR结果阳性证实了曲霉病。其余样品(16.1%)为培养物,PCR阴性。另外,未观察到其他指示真菌感染的迹象。我们的数据表明,曲霉 Candida 检测方法可能适合临床实验室,因为它是对最常见的曲霉进行简单,快速的筛选测试和 Candida 物种,可能会成为将来真菌感染早期诊断的重要工具。

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