Generic detection of coronaviruses and differentiation at the prototype strain level by reverse transcription-PCR and nonfluorescent low-density microarray

被引:104
作者
de Souza Luna, Luciano Kleber
Heiser, Volker
Regamey, Nicolas
Panning, Marcus
Drexler, Jan Felix
Mulangu, Sabue
Poon, Leo
Baumgarte, Sigrid
Haijema, Bert Jan
Kaiser, Laurent
Drosten, Christian [1 ]
机构
[1] Bernhard Nocht Inst Trop Med, Clin Virol Sect, Bernhard Nocht Str 74, D-20359 Hamburg, Germany
[2] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, London, England
[3] Chipron GmbH, Berlin, Germany
[4] Inst Natl Rech Biomed, Kinshasa, DEM REP CONGO
[5] Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
[6] Inst Hyg & Environm Hlth, Hamburg, Germany
[7] Univ Utrecht, Fac Vet Med, Inst Virol, Utrecht, Netherlands
[8] Univ Hosp Geneva, Cent Lab Virol, Geneva, Switzerland
关键词
D O I
10.1128/JCM.02426-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A nonfluorescent low-cost, low-density oligonucleotide array was designed for detecting the whole coronavirus genus after reverse transcription (RT)-PCR. The limit of detection was 15.7 copies/reaction. The clinical detection limit in patients with severe acute respiratory syndrome was 100 copies/sample. In 39 children suffering from coronavirus 229E, NL63, OC43, or HKU1, the sensitivity was equal to that of individual real-time RT-PCRs.
引用
收藏
页码:1049 / 1052
页数:4
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