Abstract
A method for the detection of Norwalk virus and hepatitis A virus from shellfish tissues by PCR was developed. Virus was added to the stomach and hepatopancreatic tissues of oysters or hard-shell clams, and viral nucleic acids were purified by a modification of a previously described method (R.L. Atmar, T.G. Metcalf, F.H. Neill, and M.K. Estes, Appl. Environ. Microbiol. 59:631-635, 1993). The new method had the following advantages compared with the previously described method: (i) more rapid sample processing; (ii) increased test sensitivity; (iii) decreased sample-associated interference with reverse transcription-PCR; and (iv) use of chloroform-butanol in place of the chlorofluorocarbon trichlorotrifluoroethane. In addition, internal standards for both Norwalk virus and hepatitis A virus were made which demonstrated when inhibitors to reverse transcription-PCR were present and allowed quantitation of the viral nucleic acids present in samples. This assay can be used to investigate shellfish-associated gastroenteritis outbreaks and to study factors involved in virus persistence in shellfish.
MeSH Terms
Animals
Base Sequence
Bivalvia/virology
Caliciviridae Infections/epidemiology,virology
DNA Primers/genetics
DNA, Viral/genetics
Disease Outbreaks
Gastroenteritis/epidemiology,virology
Hepatovirus/genetics,isolation & purification
Humans
Molecular Sequence Data
Norwalk virus/genetics,isolation & purification
Ostreidae/virology
Polymerase Chain Reaction/methods,standards,statistics & numerical data
RNA/standards
Reference Standards
Sensitivity and Specificity
Shellfish/virology
Chemicals
DNA Primers
DNA, Viral
RNA
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Atmar R L
Department of Medicine, Baylor College of Medicine, Houston, Texas 77030, USA.
Neill F H
Romalde J L
Le Guyader F
Woodley C M
Metcalf T G
Estes M K
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