Molecular Characterization of Novel Fish Viruses from Technical Assistance Cases
Viruses occur in many cultured and wild stocks of fish. William Batts collaborates with many government, state, tribal, and private research and diagnostic laboratories to aid in identification of these unknown replicating agents of uncertain pathogenicity. Typically, viruses can be replicated in a variety of fish cell lines and investigated at several temperatures to see if the cytopathic effect is different from existing fish viruses. When they are unknown to the diagnosticians, the viruses are sent to the Western Fisheries Research Center in Seattle for attempts at characterization.
Often unknown viruses are an existing strain of virus that was simply unfamiliar to the diagnostic lab, perhaps due to this virus never being isolated in the geographic region or in the fish species being investigated. However, the technical assistance service we provide has led to scientific publications on a wide variety of fish viruses including novel members of orthomyxoviruses, aquareoviruses, picornaviruses, nidoviruses, hepeviruses, paramyxoviruses, and rhabdoviruses.
We use amplification of the viral nucleic acids by the polymerase chain reaction (PCR) to obtain sufficient DNA for molecular sequencing. This authentic DNA sequence is used to search for existing viral sequences accessioned into DNA databases. If no virus match occurs, it is possible that the agent is quite unique, never observed before in any fish population.
Below are publications associated with this project.
Isolation and characterization of the fall Chinook aquareovirus
Molecular characterization of a novel orthomyxovirus from rainbow and steelhead trout (Oncorhynchus mykiss)
Isolation and molecular characterization of a novel picornavirus from baitfish in the USA
Genetic analysis of a novel nidovirus from fathead minnows
A novel member of the family Hepeviridae from cutthroat trout (Oncorhynchus clarkii)
Genetic analysis of paramyxovirus isolates from pacific salmon reveals two independently co-circulating lineages
Molecular characterisation of Atlantic salmon paramyxovirus (ASPV): A novel paramyxovirus associated with proliferative gill inflammation
Isolation of viral haemorrhagic septicaemia virus from muskellunge, Esox masquinongy (Mitchill), in Lake St Clair, Michigan, USA reveals a new sublineage of the North American genotype
Genetic typing of infectious hematopoietic necrosis virus
Isolation and characterization of a rhabdovirus from starry flounder (Platichthys stellatus) collected from the northern portion of Puget Sound, Washington, USA
Partners include: Alaska Department of Fish and Game, Alberta Environment and Parks, California Department of Fish and Wildlife, Clear Springs Foods, Colorado Parks and Wildlife, Northwest Indian Fisheries Commission, Oregon Department of Fish and Wildlife, U.S. Fish and Wildlife Service, Univiersity of California - Davis, University of Florida - Gainesville, Utah Division of Wildlife Resources, W
Viruses occur in many cultured and wild stocks of fish. William Batts collaborates with many government, state, tribal, and private research and diagnostic laboratories to aid in identification of these unknown replicating agents of uncertain pathogenicity. Typically, viruses can be replicated in a variety of fish cell lines and investigated at several temperatures to see if the cytopathic effect is different from existing fish viruses. When they are unknown to the diagnosticians, the viruses are sent to the Western Fisheries Research Center in Seattle for attempts at characterization.
Often unknown viruses are an existing strain of virus that was simply unfamiliar to the diagnostic lab, perhaps due to this virus never being isolated in the geographic region or in the fish species being investigated. However, the technical assistance service we provide has led to scientific publications on a wide variety of fish viruses including novel members of orthomyxoviruses, aquareoviruses, picornaviruses, nidoviruses, hepeviruses, paramyxoviruses, and rhabdoviruses.
We use amplification of the viral nucleic acids by the polymerase chain reaction (PCR) to obtain sufficient DNA for molecular sequencing. This authentic DNA sequence is used to search for existing viral sequences accessioned into DNA databases. If no virus match occurs, it is possible that the agent is quite unique, never observed before in any fish population.
Below are publications associated with this project.
Isolation and characterization of the fall Chinook aquareovirus
Molecular characterization of a novel orthomyxovirus from rainbow and steelhead trout (Oncorhynchus mykiss)
Isolation and molecular characterization of a novel picornavirus from baitfish in the USA
Genetic analysis of a novel nidovirus from fathead minnows
A novel member of the family Hepeviridae from cutthroat trout (Oncorhynchus clarkii)
Genetic analysis of paramyxovirus isolates from pacific salmon reveals two independently co-circulating lineages
Molecular characterisation of Atlantic salmon paramyxovirus (ASPV): A novel paramyxovirus associated with proliferative gill inflammation
Isolation of viral haemorrhagic septicaemia virus from muskellunge, Esox masquinongy (Mitchill), in Lake St Clair, Michigan, USA reveals a new sublineage of the North American genotype
Genetic typing of infectious hematopoietic necrosis virus
Isolation and characterization of a rhabdovirus from starry flounder (Platichthys stellatus) collected from the northern portion of Puget Sound, Washington, USA
Partners include: Alaska Department of Fish and Game, Alberta Environment and Parks, California Department of Fish and Wildlife, Clear Springs Foods, Colorado Parks and Wildlife, Northwest Indian Fisheries Commission, Oregon Department of Fish and Wildlife, U.S. Fish and Wildlife Service, Univiersity of California - Davis, University of Florida - Gainesville, Utah Division of Wildlife Resources, W