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Detection of ostreid herpesvirus 1 DNA by PCR in bivalve molluscs: A critical review
- Source :
- Journal of Virological Methods (0166-0934) (Elsevier), 2007, Vol. 139, N. 1, P. 1-11
- Publication Year :
- 2007
- Publisher :
- Elsevier BV, 2007.
-
Abstract
- Herpes-like viral infections have been reported in different bivalve mollusc species throughout the world. High mortalities among hatchery-reared larvae and juveniles of different bivalve species have been associated often with such infections. The diagnosis of herpes-like viruses in bivalve molluscs has been performed traditionally by light and transmission electron microscopy. The genome sequencing of one of these viruses, oyster herpesvirus 1 (OsHV-1), allowed the development of DNA-based diagnostic techniques. The polymerase chain reaction (PCR) has been used for the detection of OsHV-1 DNA in bivalve molluscs at different development stages. In addition, the PCR used for detection of OsHV-1 has also allowed the amplification of DNA from an OsHV-1 variant. The literature on DNA extraction methods, primers, PCR strategies, and confirmatory procedures used for the detection and identification of herpesviruses that infect bivalve molluscs are reviewed. (c) 2006 Elsevier B.V. All rights reserved.
- Subjects :
- Oyster
Molecular Sequence Data
Biology
medicine.disease_cause
Polymerase Chain Reaction
Sensitivity and Specificity
DNA sequencing
Herpesviridae
Virus
law.invention
Microbiology
03 medical and health sciences
chemistry.chemical_compound
law
Virology
biology.animal
medicine
Animals
Polymerase chain reaction
030304 developmental biology
0303 health sciences
Base Sequence
Herpesvirus
04 agricultural and veterinary sciences
Ostreid herpesvirus 1
Bivalve molluscs
Ostreidae
DNA extraction
Bivalvia
3. Good health
OsHV 1
Detection
PCR
chemistry
DNA, Viral
040102 fisheries
0401 agriculture, forestry, and fisheries
DNA
Subjects
Details
- ISSN :
- 01660934
- Volume :
- 139
- Database :
- OpenAIRE
- Journal :
- Journal of Virological Methods
- Accession number :
- edsair.doi.dedup.....9bc394c77b6866531cabad078c944b36