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首页> 外文期刊>Journal of Clinical Microbiology >Simultaneous Detection of Four Human Pathogenic Microsporidian Species from Clinical Samples by Oligonucleotide Microarray
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Simultaneous Detection of Four Human Pathogenic Microsporidian Species from Clinical Samples by Oligonucleotide Microarray

机译:利用寡核苷酸芯片同时检测临床样本中四种人类致病性微孢子虫种类

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Microsporidian species have been rapidly emerging as human enteric pathogens in immunocompromised and immunocompetent individuals in recent years. Routine diagnostic techniques for microsporidia in clinical laboratories are laborious and insensitive and tend to underestimate their presence. In most instances, they are unable to differentiate species of spores due to their small sizes and similar morphologies. In this study, we report the development of another protozoan oligonucleotide microarray assay for the simultaneous detection and identification to the species level of four major microsporidian species: Enterocytozoon bieneusi, Encephalitozoon cuniculi, Encephalitozoon hellem, and Encephalitozoon intestinalis. The 18S small-subunit rRNA gene was chosen as the amplification target, labeled with fluorescence dye, and hybridized to a series of species-specific oligonucleotide probes immobilized on a microchip. The specificity and sensitivity of the microarray were clearly demonstrated by the unique hybridization profiles exhibited by each species of microsporidian tested and its ability to detect as few as 10 spores. In order to assess the applicability of this microarray in a clinical setting, we conducted microarray assays of 20 fecal samples from AIDS patients. Twelve of these samples were positive for the presence of microsporidia and could be confidently identified; 11 of them were positive for more than one species. Our results suggested that this microarray-based approach represents an attractive diagnostic tool for high-throughput detection and identification of microsporidian species in clinical and epidemiological investigations.
机译:近年来,微孢子虫物种已在免疫功能低下和具有免疫能力的个体中迅速出现,成为人类肠道病原体。临床实验室中用于微孢子虫的常规诊断技术费力且不灵敏,并且往往低估了它们的存在。在大多数情况下,由于它们的小尺寸和相似的形态,它们无法区分孢子的种类。在这项研究中,我们报告了另一种原生动物寡核苷酸微阵列检测技术的发展,用于同时检测和鉴定四种主要微孢子虫物种的物种水平: Enterocytozoon bieneusi Encephalitozoon cuniculi Encephalitozoon hellem Encephalitozoon intestinalis 。选择18S小亚基rRNA基因作为扩增目标,用荧光染料标记,并与固定在微芯片上的一系列物种特异性寡核苷酸探针杂交。微阵列的特异性和灵敏性通过所测试的微孢子虫的每种物种表现出的独特杂交图谱以及其检测至少至10个孢子的能力得以清楚地证明。为了评估该微阵列在临床上的适用性,我们对来自艾滋病患者的20份粪便样本进行了微阵列分析。这些样品中有十二个为小孢子虫病阳性,可以自信地鉴定出来。其中有11种对一种以上物种呈阳性。我们的结果表明,这种基于微阵列的方法代表了一种有吸引力的诊断工具,可用于在临床和流行病学调查中对微孢子虫种类进行高通量检测和鉴定。

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