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1.
J Fish Dis ; 47(6): e13938, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38462942

ABSTRACT

Channel catfish (Ictalurus punctatus) are a food fish extensively reared in aquaculture facilities throughout the world and are also among the most abundant wild catfish species in North America, making them a popular target of anglers. Furthermore, channel catfish are important members of aquatic ecosystems; for example, they serve as a glochidial host for the endangered winged mapleleaf mussel (Quadrula fragosa), making them critical for conserving this species through hatchery-based restoration efforts. During a routine health inspection, a novel aquareovirus was isolated from channel catfish used in mussel propagation efforts at a fish hatchery in Wisconsin. This virus was isolated on brown bullhead cells (ATCC CCL-59) and identified through metagenomic sequencing as a novel member of the family Spinareoviridae, genus Aquareovirus. The virus genome consists of 11 segments, as is typical of the aquareoviruses, with phylogenetic relationships based on RNA-dependent RNA polymerase and major outer capsid protein amino acid sequences showing it to be most closely related to golden shiner virus (aquareovirus C) and aquareovirus C/American grass carp reovirus (aquareovirus G) respectively. The potential of the new virus, which we name genictpun virus 1 (GNIPV-1), to cause disease in channel catfish or other species remains unknown.


Subject(s)
Fish Diseases , Genome, Viral , Ictaluridae , Phylogeny , Animals , Ictaluridae/virology , Wisconsin , Fish Diseases/virology , Reoviridae/isolation & purification , Reoviridae/genetics , Reoviridae/classification , Reoviridae/physiology , Bivalvia/virology , Aquaculture
2.
Virus Genes ; 35(1): 87-95, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17048110

ABSTRACT

Five spring viremia of carp viruses (SVCV), Rhabdovirus carpio, were isolated in the United States (US) between 2002 and 2004. Single tube reverse transcription-polymerase chain reaction (RT-PCR) was used to generate overlapping cDNA fragments from the US isolates of SVCV. Multiple pairs of specific primers were designed to amplify a portion of the phosphoprotein gene, the matrix gene, and the glycoprotein gene of SVCV genogroup Id (corresponding to nucleotides 2174-4942 of GenBank accession NC_002803). Sequences were proofread and aligned to generate a consensus sequence for each isolate. Phylogenetic analysis of the 2705 nucleotide consensus sequence revealed that all five US isolates belong to SVCV genogroup Ia, Asian origin isolates, and a PCR primer binding site unique to SVCV genogroup Ia was identified.


Subject(s)
Carps/virology , Fish Diseases/virology , Rhabdoviridae Infections/virology , Rhabdoviridae/genetics , Rhabdoviridae/isolation & purification , Seasons , Viremia/virology , Amino Acid Sequence , Animals , Base Sequence , Cells, Cultured , Genes, Viral , Molecular Sequence Data , Phylogeny , Sequence Homology , United States
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