A rapid and sensitive assay for detection of replication-competent adenoviruses by a combination of microcarrier cell culture and quantitative PCR

2007 ◽  
Vol 145 (2) ◽  
pp. 89-95 ◽  
Author(s):  
Johanna A.C. Schalk ◽  
Claudette G.J.C.A. de Vries ◽  
Tom J.H. Orzechowski ◽  
Marianne G. Rots
1982 ◽  
Vol 124 (2) ◽  
pp. 353-358 ◽  
Author(s):  
Toshiko Imamura ◽  
Charles L. Crespi ◽  
William G. Thilly ◽  
Henri Brunengraber

1986 ◽  
Vol 9 (4) ◽  
pp. 205-210
Author(s):  
U. Lindskog ◽  
B. Lundgren ◽  
I. Wergeland ◽  
D. Billig

PLoS ONE ◽  
2013 ◽  
Vol 8 (2) ◽  
pp. e56791 ◽  
Author(s):  
Maria Mrakovcic ◽  
Markus Absenger ◽  
Regina Riedl ◽  
Claudia Smole ◽  
Eva Roblegg ◽  
...  

2015 ◽  
Vol 78 (11) ◽  
pp. 2064-2069 ◽  
Author(s):  
DORIS SOBRAL MARQUES SOUZA ◽  
TAKAYUKI MIURA ◽  
CÉCILE LE MENNEC ◽  
CÉLIA REGINA MONTE BARARDI ◽  
FRANÇOISE S. LE GUYADER

To evaluate the persistence of infectious virus after heating, mussels contaminated with a rotavirus strain were prepared following the French recipe moules marinières (mariner's mussels). Rotavirus was then quantified by real-time quantitative PCR (RT-qPCR) and a cell culture infectivity assay. Results showed the persistence of infectious virus after 3 min of cooking. After 5 min, when no infectious virus could be detected, the RT-qPCR approach showed a 1-log decrease compared with concentrations detected after 1 min of cooking.


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