Validation of new real-time polymerase chain reaction assays for detection of hepatitis A virus RNA and parvovirus B19 DNA

Transfusion ◽  
2015 ◽  
Vol 56 (2) ◽  
pp. 440-448 ◽  
Author(s):  
Marijke W.A. Molenaar-de Backer ◽  
Mirjam de Waal ◽  
Margret C. Sjerps ◽  
Marco H.G.M. Koppelman
Vox Sanguinis ◽  
1994 ◽  
Vol 67 (1) ◽  
pp. 47-50
Author(s):  
F. McOmish ◽  
P.L. Yap ◽  
H. Hart ◽  
K. Peerlinck ◽  
S.M. Burns ◽  
...  

Hepatology ◽  
1996 ◽  
Vol 24 (1) ◽  
pp. 10-13 ◽  
Author(s):  
H Yotsuyanagi ◽  
K Koike ◽  
K Yasuda ◽  
K Moriya ◽  
Y Shintani ◽  
...  

2003 ◽  
Vol 66 (2) ◽  
pp. 331-334 ◽  
Author(s):  
DAVID H. KINGSLEY ◽  
GARY P. RICHARDS

We investigated the ability of hepatitis A virus (HAV) to persist for up to 6 weeks in Eastern oysters (Crassostrea virginica). Viral RNA was detected by reverse transcription–polymerase chain reaction 6 weeks after 16 h of exposure to 90,000 PFU (180 PFU/ml of seawater) of HAV. Assaying for infectious virus in oysters that received a daily feeding of phytoplankton recovered 3,800, 650, and 500 PFU of HAV 1, 2, and 3 weeks after contamination with 90,000 PFU of HAV, respectively. However, no infectious HAV was isolated from oysters 4, 5, or 6 weeks after contamination. These results support the position that shellfish depuration is insufficient for the complete removal of infectious viruses. Extended relay times (in excess of 4 weeks) may be required to produce virologically safe shellfish.


Sign in / Sign up

Export Citation Format

Share Document