Purpose: The objective was to determine the numbers of F-RNA coliphages, BEC and RV on commercial vacuum packaged beef in Canada during the summer and winter months and perform molecular characterization of the isolates.
Methods: The entire surface of each sub-primal, purchased from retail stores, was swabbed with a sponge and viruses were dislodged from the sponges with a stomacher. Infectious F-RNA coliphages were detected by plaque assay. RNA was extracted from clarified and concentrated (ultrafiltration) supernatant and F-RNA coliphage, BEC and RV RNA were detected by real time RT-qPCR.
Results: Infectious F-RNA coliphages were recovered from 46/140 cuts at levels ranging from 0.26-80 plaque forming units/100 cm2where 24 samples were positive for F-RNA coliphages of human origin(1 GII and 23 GIII) and 24 were positive for F-RNA coliphages of animal origin (24 GI and 1GIV) while 4 samples contained genotypes of both human and animal origin. RV was detected in 6 samples by molecular detection while BEC was not detected. F-RNA GI was detected in only 1 sample by qRT-PCR
Significance: The low levels of infectious F-RNA coliphages are below the limit of detection by qRT-PCR in most instances. About 4% of samples were positive for RV. In addition, contamination by food handlers may be a concern as 50% of the positive samples were associated with F-RNA coliphages of human origin.