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一种用于中枢神经系统感染相关多种病因高通量分子诊断的重测序病原体微阵列方法。

A resequencing pathogen microarray method for high-throughput molecular diagnosis of multiple etiologies associated with central nervous system infection.

作者信息

Wang Ji, Yu Panhui, Xie Zhengde, Yan Tengfei, Chen Chen, Shen Xinxin, Chen Xiangpeng, Li Lixin, Wang Xiuxia, Sun Suzhen, Ma Xuejun

机构信息

National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.

Neurology Department, Children's Hospital of Hebei Province, Shijiazhuang, China.

出版信息

Arch Virol. 2017 Dec;162(12):3769-3778. doi: 10.1007/s00705-017-3550-7. Epub 2017 Sep 14.

Abstract

Central nervous system infection (CNSI) results in significant health and economic burdens worldwide, but the diversity of causative pathogens makes differential diagnosis very difficult. Although PCR and real-time fluorescent quantitative PCR (q-PCR) assays are widely applied for pathogen detection, they are generally optimized for the detection of a single or limited number of targets and are not suitable for the diagnosis of numerous CNSI agents. In this study, we describe the development of a resequencing pathogen microarray (RPM-IVDC4) method for the simultaneous detection of viruses, bacteria, fungi and parasites that cause CNSI. The test panel of this assay included more than 100 microorganism species across 45 genera and 30 families. The analytical specificity and sensitivity were examined using a panel of positive reference strains, and the clinical performance was evaluated using 432 clinical samples by comparing the results with q-PCR assays. Our results demonstrated good performance of the RPM-IVDC4 assay in terms of sensitivity, specificity and detection range, suggesting that the platform can be further developed for high-throughput CNSI diagnosis.

摘要

中枢神经系统感染(CNSI)在全球范围内造成了巨大的健康和经济负担,但致病病原体的多样性使得鉴别诊断非常困难。尽管聚合酶链反应(PCR)和实时荧光定量PCR(q-PCR)检测方法被广泛应用于病原体检测,但它们通常是针对单一或有限数量的靶标进行优化的,并不适用于众多中枢神经系统感染病原体的诊断。在本研究中,我们描述了一种重测序病原体微阵列(RPM-IVDC4)方法的开发,该方法可同时检测引起中枢神经系统感染的病毒、细菌、真菌和寄生虫。该检测方法的检测面板包括来自45个属和30个科的100多种微生物。使用一组阳性参考菌株检测分析特异性和敏感性,并通过与q-PCR检测结果进行比较,使用432份临床样本评估临床性能。我们的结果表明,RPM-IVDC4检测方法在敏感性、特异性和检测范围方面表现良好,表明该平台可进一步开发用于高通量中枢神经系统感染诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eac/7087039/4a185ec3e8cf/705_2017_3550_Fig1_HTML.jpg

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