Detection of hepatitis A virus in Mercenaria mercenaria by coupled reverse transcription and polymerase chain reaction
Author(s) -
Biswendu B. Goswami,
Walter Koch,
Thomas A. Cebula
Publication year - 1993
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.59.9.2765-2770.1993
Subject(s) - reverse transcriptase , biology , virology , rna , rna extraction , reverse transcription polymerase chain reaction , virus , mercenaria , shellfish , rna directed dna polymerase , polymerase chain reaction , hepatitis a virus , polymerase , complementary dna , microbiology and biotechnology , messenger rna , gene , genetics , fishery , aquatic animal , fish <actinopterygii>
Hepatitis A virus (HAV) is a major cause of infectious hepatitis in humans. In this respect, bivalve mollusks pose a major health concern because they are filter feeders and can concentrate the virus up to 900-fold from contaminated water. Detection of HAV has been hampered because wild-type HAV grows poorly if at all in cell culture. Here we describe a technique for the detection of HAV in shellfish based on reverse transcription coupled with the polymerase chain reaction. RNA is isolated from hard-shell clam tissue and reverse transcribed with avian myeloblastosis virus reverse transcriptase. A portion of the cDNA pool is then amplified with primers specific for HAV. In experiments with an in vitro-synthesized HAV transcript, we were able to detect HAV sequence in the presence of a 200-million-fold excess of shellfish RNA. When intact virus was added to shellfish tissue before the isolation of RNA, the method was capable of detecting 10 viral RNA molecules in a reaction mixture.
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