A universal microarray for detection of SARS coronavirus

作者：Long, WH; Xiao, HS; Gu, XM; Zhang, QH; Yang, HJ; Zhao, GP; Liu, JH^*

来源：Journal of Virological Methods, 2004, 121(1): 57-63.

DOI：10.1016/j.jviromet.2004.06.016

• SARS
• SARS-CoV
• universal microarray
• LDR
• Zip Code

Severe acute respiratory syndrome (SARS) is caused by the SARS coronavirus (SARS-CoV). There are many point mutations among SARS-CoV genome sequences. Previous studies suggested that the mutations are correlated closely with the SARS epidemic. It was found that the bases of six nucleotide positions (nt9404, nt9479, nt19838, nt21721, nt22222 and nt27827) with high-mutation rate have an important relationship with the SARS epidemic. For viral detection as well as genotyping, a universal microarray system was developed that combines RT-PCR and ligase detection reaction (LDR). The Zip Codes attached covalently to a slide remain constant and their complementary Zip Codes (cZip Codes) can be used for tagging target sequence, making the microarrays universal. The discriminating oligonucleotides contain on the 5' end "cZip Codes" that are used to direct LDR product to specific Zip Codes attached covalently to a slide. Since Zip Codes have no homology to either the target sequence or to other sequences in the genomes of both human host and SARS-CoV, there was no false signal due to mismatch hybridizations. 20 samples assayed with the universal microarray were confirmed by DNA sequencing, demonstrating that this microarray system is a promising diagnostic tool for detection and genotyping of the SARS-CoV.

• 出版日期2004-10
• 单位上海华冠生物芯片有限公司; 上海交通大学