Author
Mandrell, Robert | |
Tian, Peng | |
Lee, Bertram | |
Yang, David | |
Bates, Anne | |
Cooley, Michael | |
Carychao, Diana | |
VINJE, JAN - National Center For Infectious Diseases | |
Quinones, Beatriz |
Submitted to: Meeting Abstract
Publication Type: Abstract Only Publication Acceptance Date: 10/25/2012 Publication Date: N/A Citation: N/A Interpretive Summary: Technical Abstract: The presence of Norovirus (NV) in watersheds in the vicinity of raw produce production is a concern. This could occur due to leaking septic systems, improper RV waste removal, improperly treated recycled wastewater, or other unknown factors. We used a qRT-PCR method to test for NV in rinsates from Moore Swabs collected usually every 2 weeks from 26 sites between Oct-2011 to Jul-2012 (487 swabs tested); 122 (25%) were considered NV+. The NV+ samples ranged between 11-42% by site; 8, 69 and 45 samples were G1+ only, G2+ only and G1+/G2+. The highest incidence of NV was in samples collected in the absence of any precipitation 5 days preceding the day of collection. In addition, a low density DNA microarray has been constructed for rapid and cheap detection of NV. Preliminary studies of RNA reference samples of known NV genogroup revealed specific detection of NV. Future studies will focus on analysis of NoroCORE samples for validation of the low density DNA microarray and utility for identification of NV genogroups in watershed samples, collected in a major produce production region in California. |