No 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.

HighlightsBMAA could be detected in seafood which have been imported to Sweden origin from four different continents.Quantification of both free and total concentrations BMAA in mussels and scallops.The highest concentration of total BMAA was found in imported cooked and canned mussels.

Ochroconis globalis, a novel species of the melanized genus Ochroconis (Sympoventuriaceae, Venturiales), is described and illustrated and distinguished phenotypically and molecularly from existing ochroconis-like species. Phylogenetic analyses using nuclear ribosomal DNA genes (nuSSU, ITS, nuLSU) and coding gene fragments (ACT1, BT2, TEF1) revealed clustering of all strains as a monophyletic clade which was well separated from known Ochroconis species. Most strains of the new species were obtained from human-made environments, while the natural habitat of the species remains enigmatic. The new combination Ochroconis musae is introduced for one of the most commonly encountered Ochroconis species, and a phenotypic key to all species is provided.

Marteilia refringens causes marteiliosis in oysters, mussels and other bivalve molluscs. This parasite previously comprised two species, M. refringens and Marteilia maurini, which were synonymized in 2007 and subsequently referred to as M. refringens ‘O-type’ and ‘M-type’. O-type has caused mass mortalities of the flat oyster Ostrea edulis. We used high throughput sequencing and histology to intensively screen flat oysters and mussels (Mytilus edulis) from the UK, Sweden and Norway for infection by both types and to generate multi-gene datasets to clarify their genetic distinctiveness. Mussels from the UK, Norway and Sweden were more frequently polymerase chain reaction (PCR)-positive for M-type (75/849) than oysters (11/542). We did not detect O-type in any northern European samples, and no histology-confirmed Marteilia-infected oysters were found in the UK, Norway and Sweden, even where co-habiting mussels were infected by the M-type. The two genetic lineages within ‘M. refringens’ are robustly distinguishable at species level. We therefore formally define them as separate species: M. refringens (previously O-type) and Marteilia pararefringens sp. nov. (M-type). We designed and tested new Marteilia-specific PCR primers amplifying from the 3’ end of the 18S rRNA gene through to the 5.8S gene, which specifically amplified the target region from both tissue and environmental samples.

The freshwater pearl mussel Margaritifera margaritifera is an endangered species in Sweden with more than 600 known populations distributed in 16 out of 21 counties. Only approximately one-third of these populations are considered viable and healthy with signs of recent juvenile recruitment. From 2011 to 2017, research documented an increased mortality in this species, of up to 100% in some populations, but no etiological cause of these mortalities has been identified. With this paper, we provide current knowledge of locations where mass mortality of freshwater pearl mussel has been found in Sweden and discuss possible causes. Postmortem sampling and histopathological findings from two counties in 2016-17 detected lesions in digestive glands indicating a reduced capacity for nutrient uptake. Results from these macroscopic and microscopic investigations also indicate a reduction in, or a lack of, reproductive output compared with reference populations.

Free spores of a Derrnocystidiurn-like organism were recovered from the epidermis and covering mucus of gills and fins of moribund farmed salmon Salmo salar. The parasite appeared in juvenile fish only and at low water temperatures (15°C). The most prominent external macroscopical clinical signs of disease were thickened fins that gave the tips a pronounced greyish opaque appearance often in combination with signs of fin rot/fin erosion. The gills were swollen and pale and could also be necrotic. Examination of fresh mounts and tissues prepared for light and electron microscopy showed vacuolated spherical spores typical for parasites of the genus Dermocystidium. Irregularly vacuolated spores with 1 or multiple nuclel were also observed. Histological examination of infected salmon indicated concurrent Flexibacter sp. infection that was venfied in Gram-negative stained imprints. The present findmg is the first observation of Dermocystidlum in Sweden. In addition, this is the first record of a Dermocystidiurn-hke agent that occurs freely in the mucus and epidermis of freshwater teleosts.

We report the first description of a new Rhabdoviridae tentatively named eelpout rhabdovirus (EpRV genus Perhabdovirus). This virus was associated with mass mortalities in eelpout (Zoarces viviparous, Linnaeus) along the Swedish Baltic Sea coast line in 2014. Diseased fish showed signs of central nervous system infection, and brain lesions were confirmed by histology. A cytopathogenic effect was observed in cell culture, but ELISAs for the epizootic piscine viral haemorrhagic septicaemia virus (VHSV), infectious pancreas necrosis virus (IPNV), infectious haematopoietic necrosis virus (IHNV) and spring viraemia of carp virus (SVCV) were negative. Further investigations by chloroform inactivation, indirect fluorescence antibody test and electron microscopy indicated the presence of a rhabdovirus. By deep sequencing of original tissue suspension and infected cell culture supernatant, the full viral genome was assembled and we confirmed the presence of a rhabdovirus with 59.5% nucleotide similarity to the closest relative Siniperca chuatsi rhabdovirus. The full-genome sequence of this new virus, eelpout rhabdovirus (EpRV), has been deposited in GenBank under accession number KR612230. An RT-PCR based on the L-gene sequence confirmed the presence of EpRV in sick/dead eelpout, but the virus was not found in control fish. Additional investigations to characterize the pathogenicity of EpRV are planned.