Department of Internal Medicine, Faculty of Medical Sciences, University of Campinas, Campinas, Sao Paulo, Brazil.
Medical Mycology Research Center, Chiba University, Chiba, Japan.
J Clin Microbiol. 2018 Apr 25;56(5). doi: 10.1128/JCM.01908-17. Print 2018 May.
A DNA microarray platform, based on the nucleotide sequences of the internal transcribed spacer regions (ITS1 and ITS2) of the rRNA gene, was developed to identify 32 fungal pathogens at the species level. The probe sequences were spotted onto polycarbonate slides with a mini-microarray printer, and after the hybridization, the results were visible with the naked eye. The performance of the microarray platform was evaluated against the commercial automated systems (Vitek 2 and BD Phoenix systems) and DNA sequencing (gold standard). A total of 461 blood culture bottles were tested: 127 positive for fungi, 302 positive for bacteria, and 32 that were negative. Once the microorganisms were identified by automated systems, fungal DNA was extracted directly from the blood culture bottles. The DNA products were tested using the microarray platform, and DNA sequencing was performed. The results of the microarray and DNA sequencing were concordant in 96.7% of cases, and the results from the automated systems and DNA sequencing were concordant in 98.4%. Of all the nucleotide sequences contained in the microarray platform, the microarray failed to identify four fungal isolates (one , two , and one ). Of note, the microarray detected DNA in two blood cultures from the same patient, whereas the automated system was only positive for Our microarray system provided reliable and fast fungal identification compared to that from DNA sequencing and the automated systems. The simplicity of reading the results by the naked eye made this DNA platform a suitable method for fungal molecular diagnosis.
一种基于 rRNA 基因内转录间隔区(ITS1 和 ITS2)核苷酸序列的 DNA 微阵列平台被开发出来,用于鉴定 32 种真菌病原体的种水平。探针序列通过微型微阵列打印机点样到聚碳酸酯载玻片上,杂交后,结果可以用肉眼观察到。该微阵列平台的性能通过与商业自动化系统(Vitek 2 和 BD Phoenix 系统)和 DNA 测序(金标准)进行评估。总共测试了 461 个血培养瓶:127 个阳性为真菌,302 个阳性为细菌,32 个为阴性。一旦通过自动化系统鉴定出微生物,就直接从血培养瓶中提取真菌 DNA。将 DNA 产物用微阵列平台进行检测,并进行 DNA 测序。微阵列和 DNA 测序的结果在 96.7%的情况下是一致的,而自动化系统和 DNA 测序的结果在 98.4%的情况下是一致的。在微阵列平台中包含的所有核苷酸序列中,微阵列未能鉴定出四种真菌分离物(一种 ,两种 ,一种 )。值得注意的是,微阵列在来自同一患者的两个血培养物中检测到 DNA,而自动化系统仅对 阳性。与 DNA 测序和自动化系统相比,我们的微阵列系统为真菌鉴定提供了可靠和快速的方法。通过肉眼读取结果的简单性使该 DNA 平台成为一种适合真菌分子诊断的方法。