Borel Nicole, Kempf Evelyne, Hotzel Helmut, Schubert Evelyn, Torgerson Paul, Slickers Peter, Ehricht Ralf, Tasara Taurai, Pospischil Andreas, Sachse Konrad
Institute of Veterinary Pathology, University of Zurich, Switzerland.
Mol Cell Probes. 2008 Feb;22(1):55-64. doi: 10.1016/j.mcp.2007.06.003. Epub 2007 Jun 28.
While DNA microarrays have become a widely accepted tool for mRNA expression monitoring, their use in rapid diagnosis of bacterial and viral pathogens is only emerging. So far, insufficient sensitivity and high costs have been the major limiting factors preventing more widespread use of microarray platforms in direct testing of clinical samples. In the present study, a total of 339 samples, among them 293 clinical specimens from animals and humans, were examined by the ArrayTube (AT) DNA microarray assay to detect chlamydial DNA and identify the species of Chlamydia and Chlamydophila involved. Samples included nasal and conjunctival swabs, formalin-fixed, paraffin-embedded and fresh organ tissue, milk, feces and cell culture. Notably, the AT test was shown to detect mixed infections in clinical samples. The calculated median sensitivity of 0.81 over the entire panel of clinical samples was comparable to conventional 16S PCR, but slightly lower than real-time PCR and other PCR assays. However, when a panel of long-time stored swab samples was excluded from the calculation, the sensitivity was clearly higher (0.87) and equivalent to that of real-time PCR. Altogether, the data demonstrate the suitability of this DNA microarray assay for routine diagnosis.
虽然DNA微阵列已成为监测mRNA表达的一种广泛接受的工具,但它们在细菌和病毒病原体快速诊断中的应用才刚刚兴起。到目前为止,灵敏度不足和成本高昂一直是限制微阵列平台在临床样本直接检测中更广泛应用的主要因素。在本研究中,共339个样本,其中包括293份来自动物和人类的临床标本,通过ArrayTube(AT)DNA微阵列分析来检测衣原体DNA并鉴定所涉及的衣原体和嗜衣原体种类。样本包括鼻拭子和结膜拭子、福尔马林固定石蜡包埋及新鲜器官组织、牛奶、粪便和细胞培养物。值得注意的是,AT检测显示可检测临床样本中的混合感染。在整个临床样本组中计算出的中位数灵敏度为0.81,与传统的16S PCR相当,但略低于实时PCR和其他PCR检测。然而,当将一组长期保存的拭子样本排除在计算之外时,灵敏度明显更高(0.87),且与实时PCR相当。总体而言,数据表明这种DNA微阵列分析适用于常规诊断。