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PMID: 8382024 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Detection of enteric viruses in oysters by using the polymerase chain reaction.

Applied and environmental microbiology ·Vol. 59 ·No. 2 ·1993-02-00 ·Pages 631-5

Atmar RL, Metcalf TG, Neill FH, Estes MK

Abstract

A procedure for the detection of enteric viral nucleic acid in oysters by the polymerase chain reaction was developed. Known quantities of poliovirus type 1 were seeded into oysters. Virus was extracted and concentrated by using organic flocculation and polyethylene glycol precipitation. Inhibitors of reverse transcription-polymerase chain reaction were present in the oyster extracts, preventing amplification of target viral nucleic acid. The use of cetyltrimethylammonium bromide precipitation sufficiently removed inhibitors to allow detection of as few as 10 PFU of poliovirus. Norwalk virus also could be detected after being seeded into oysters. This methodology may be useful for the detection of these and other shellfish-borne viral pathogens.

MeSH Terms
Animals Base Sequence Food Microbiology Hepatovirus/isolation & purification Molecular Sequence Data Norwalk virus/isolation & purification Ostreidae/microbiology Polymerase Chain Reaction
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Atmar R L
Department of Medicine, Baylor College of Medicine, Houston, Texas 77030.
Metcalf T G
Neill F H
Estes M K
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Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
1993-02-00
Pages
631-5
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC202159
Subset
IM
Grants
NCRR NIH HHS · RR-00350 · United States
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