Severe acute respiratory syndrome diagnostics using a coronavirus protein microarray

被引:90
作者
Zhu, H
Hu, SH
Jona, G
Zhu, XW
Kreiswirth, N
Willey, BM
Mazzulli, T
Liu, GZ
Song, QF
Chen, P
Cameron, M
Tyler, A
Wang, J
Wen, J
Chen, WJ
Compton, S
Snyder, M [1 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Dept Comparat Med, New Haven, CT 06520 USA
[3] Yale Univ, Program Computat Biol & Bioinformat, New Haven, CT 06520 USA
[4] Chinese Acad Sci, Beijing Genom Inst, Biochip Platform Div, Beijing 101300, Peoples R China
[5] Mt Sinai Hosp, Dept Microbiol, Toronto, ON M5G 1X5, Canada
[6] Agr Univ Hebei, Coll Life Sci, Hebei 071001, Baoding, Peoples R China
关键词
infectious disease; protein chip; virus diagnostics;
D O I
10.1073/pnas.0510921103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To monitor severe acute respiratory syndrome (SARS) infection, a coronavirus protein microarray that harbors proteins from SARS coronavirus (SARS-CoV) and five additional coronaviruses was constructed. These microarrays were used to screen approximate to 400 Canadian sera from the SARS outbreak, including samples from confirmed SARS-CoV cases, respiratory illness patients, and healthcare professionals. A computer algorithm that uses multiple classifiers to predict samples from SARS patients was developed and used to predict 206 sera from Chinese fever patients. The test assigned patients into two distinct groups: those with antibodies to SARS-CoV and those without. The microarray also identified patients with sera reactive against other coronavirus proteins. Our results correlated well with an indirect immunofluorescence test and demonstrated that viral infection can be monitored for many months after infection. We show that protein microarrays can serve as a rapid, sensitive, and simple tool for large-scale identification of viral-specific antibodies in sera.
引用
收藏
页码:4011 / 4016
页数:6
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