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Examines whether the F-specific RNA (FRNA) bacteriophages can be used as viral indicators in commercially depurated oysters sold for consumption. Monitoring of FRNA bacteriophages and Escherichia coli for two years in marketed oysters harvested from commercial sites; Ability of FRNA bacteriophages to indicate potential risks of contamination of oysters.

Noroviruses (NOV), which are members of the family Caliciviridae, are the most important cause of outbreaks of acute gastroenteritis worldwide and are commonly found in shellfish grown in polluted waters. In the present study, we developed broadly reactive one-step TaqMan reverse transcription (RT)-PCR assays for the detection of genogroup I (GI) and GII NoV in fecal samples, as well as shellfish samples. The specificity and sensitivity of all steps of the assays were systematically evaluated, and in the final format, the monoplex assays were validated by using RNA extracted from a panel of 84 stool specimens, which included NoV strains representing 19 different genotypes (7 GI, 11 GII, and 1 GIV strains). The assays were further validated with 38 shellfish cDNA extracts previously tested by nested PCR. Comparison with a recently described real-time assay showed that our assay had significantly higher sensitivity and was at least as sensitive as the nested PCR. For stool specimens, a one-step duplex TaqMan RT-PCR assay performed as well as individual genogroup-specific monoplex assays. All other enteric viruses examined were negative, and no cross-reaction between genogroups was observed. These TaqMan RT-PCR assays provide rapid (less than 90 rain), sensitive, and reliable detection of NoV and should prove to be useful for routine monitoring of both clinical and shellfish samples. [ABSTRACT FROM AUTHOR]