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1.
Dis Aquat Organ ; 126(1): 43-50, 2017 09 20.
Article in English | MEDLINE | ID: mdl-28930084

ABSTRACT

Wild goldsinny wrasse Ctenolabrus rupestris, corkwing wrasse Symphodus melops and ballan wrasse Labrus bergylta were collected at 8 sampling sites in Sweden and Norway during summer 2014. Brain tissue from 466 wrasses were analyzed for nervous necrosis virus (NNV) infections by real-time RT-PCR, and positive samples were subjected to sequencing and phylogenetic analysis of partial segments of the RNA2 and RNA1 genes. This study shows that NNV is present in wild ballan, corkwing and goldsinny wrasse along the coastline of Sweden and Norway. The overall prevalence in the sampled labrids was 6.7%. Prevalence was 6.4% in goldsinny, 6.3% in corkwing and 18% in ballan wrasse. The wrasse RNA2 NNV sequences revealed high genetic variability and were divided into 3 clusters within the cold water barfin flounder NNV (BFNNV) and warm water cluster red-spotted grouper NNV (RGNNV) genogroups. Within the BFNNV genogroup, wrasse NNVs clustered in 2 sub-genogroups, with grey mullet NNV (GMNNV) and with Atlantic halibut NNV (AHNNV). These groups were previously dominated by virus originating from Atlantic cod Gadus morhua and Atlantic halibut Hippoglossus hippoglossus from the northeast Atlantic. The presence of NNV in wild wrasse and the surprising high genetic variability observed in this study should be considered before moving wild-caught wrasse between geographically distant sites. The results show that use of wild-caught wrasse as brood fish in wrasse farming represents a risk of introducing NNV into aquaculture.


Subject(s)
Fish Diseases/virology , Genetic Variation , Nodaviridae/genetics , RNA Virus Infections/virology , Animals , Fish Diseases/epidemiology , Fishes , Norway/epidemiology , Phylogeny , RNA Virus Infections/epidemiology , Sweden/epidemiology
2.
Dis Aquat Organ ; 117(3): 171-6, 2016 Jan 13.
Article in English | MEDLINE | ID: mdl-26758650

ABSTRACT

The Pacific oyster Crassostrea gigas has recently expanded its range in Scandinavia. The expansion is presumably a result of northwards larval drift. Massive settlements were recorded in many areas along the Swedish west coast and southern Norway in 2013 and 2014. After the spawning season in 2014, the temperature of the surface water peaked at 24-26°C. After this period, high and sudden mortalities occurred in a Swedish hatchery and in wild populations along the Swedish west coast and south coast of Norway. Surveys and collected data showed that mortalities mainly occurred during 3 wk in September. All size classes were affected, and affected populations displayed a patchy distribution with heavily affected and unaffected populations in close proximity. Flat oysters Ostrea edulis and blue mussels Mytilus edulis were unaffected. Ostreid herpesvirus (OsHV) was detected in moribund Pacific oyster spat as well as in surviving adults. The virus was identified as OsHV-1 µvar. This is the first detection of this variant in Scandinavia, showing that OsHV-1 µvar is present in areas with recent establishments of Pacific oysters, and where there is no aquaculture of this species.


Subject(s)
Crassostrea/virology , Herpesviridae/physiology , Seasons , Animals , Base Sequence , DNA, Viral/isolation & purification , Genetic Variation , Herpesviridae/genetics , Host-Pathogen Interactions , Molecular Sequence Data , Norway , Polymerase Chain Reaction , Sweden
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