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Volume 10, Number 7, July 2004

SARS Coronavirus Detection

Andreas Nitsche,* Brunhilde Schweiger,* Heinz Ellerbrok,* Matthias Niedrig,* and Georg Pauli*
*Robert Koch-Institut, Berlin, Germany

 
 
Figure.
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Figure. LightCycler amplification curves of the three single SARS-coronavirus (CoV)-specific assays and the combined assay. Five hundred genome equivalents (GE) of SARS-CoV were amplified with the three single assays-NS pp1a, NS pp1ab, and SS GP-as well as with the combination of the three assays. No fluorescence signal was observed for control pathogens. In the inset, the respective agarose gel analysis of the amplification products in a 3% gel is shown. Lane 1: 50-bp marker, lane 2: 500 GE SARS-CoV amplified with the assay combination (products of assays NS pp1ab and SS GP are not clearly distinguishable because of sizes of 88 bp and 79 bp, respectively), lane 3: human CoV 229E, lane 4: respiratory syncytial virus, lane 5: rhinovirus, lane 6: human metapneumovirus, lane 7: Mycoplasma pneumoniae, or lane 8: Chlamydia pneumoniae.

 

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Emerging Infectious Diseases Journal
National Center for Infectious Diseases
Centers for Disease Control and Prevention