The genus Tenacibaculum, a member of the family Flavobacteriaceae, is an abundant component of marine bacterial ecosystems that also hosts several fish pathogens, some of which are of serious concern for marine aquaculture. Here, we applied multilocus sequence analysis (MLSA) to 114 representatives of most known species in the genus and of the worldwide diversity of the major fish pathogen Tenacibaculum maritimum. Recombination hampers precise phylogenetic reconstruction, but the data indicate intertwined environmental and pathogenic lineages, which suggests that pathogenicity evolved independently in several species. At lower phylogenetic levels recombination is also important, and the species T. maritimum constitutes a cohesive group of isolates. Importantly, the data reveal no trace of long-distance dissemination that could be linked to international fish movements. Instead, the high number of distinct genotypes suggests an endemic distribution of strains. The MLSA scheme and the data described in this study will help in monitoring Tenacibaculum infections in marine aquaculture; we show, for instance, that isolates from tenacibaculosis outbreaks in Norwegian salmon farms are related to T. dicentrarchi, a recently described species.

No abstract

In fall 2013, anorexia, lethargy and mortalities up to 10-12,000 dead fish per week were observed in rainbow trout Oncorhynchus mykiss in three fresh water hatcheries (salinity 0-1 ‰) on the west coast of Norway. The fish (25-100 g) showed signs of circulatory failure with haemorrhages, ascites and anaemia. The histopathological findings comprised inflammation of the heart and red muscle and liver necrosis. The affected fish had a common origin. Disease and mortalities were also observed up to four months after sea water transfer. Microbiological examination did not reveal presence of any known pathogens. Based on histopathological similarities to heart and skeletal inflammation (HSMI) in Atlantic salmon, associated with piscine orthoreovirus (PRV), extended investigations to detect a virus within the family Reoviridae were conducted. By the use of primer sets targeting the PRV genome, a sequence with 85% identity to a part of segment S1 of PRV was obtained. Further analysis showed that the virus sequence could only be aligned with PRV and no other reoviruses both on amino acid and nucleotide level. Two PCR assays were developed for specific detection of the virus. High amounts of the virus were detected in diseased fish at all affected farms and low amounts were detected in low prevalence at the broodfish farms. Further investigations are needed to determine if the virus is associated with the new disease in rainbow trout and to further characterize the virus with respect to classification, relationship with PRV, virulence, pathology and epidemiology.

No abstract

A rickettsia-hke organism was isolated from diseased Atlantic salmon S a h o salar in Norway. Because of morphological and serological similarities to the type strain the suggested name of the organism is Plscinckettsia salmonis. The bacteilum is considered the most probable cause of a systemic disease diagnosed in 51 farms along the west coast of Norway. Most of the cases occurred in the autumn of 1988. The disease was only recorded in smolts after exposure to sea water and cumulative mortality has been low. In 63% of fish with gross lesions examined d u n n g outbreak of disease in 14 of the affected farms, the typical macroscopic finding was a normal coloured liver with white, circular, sometimes haemorrhagic foci. Of fish with gross lesions, 35 % showed pale gllls, a yellow, mottled liver, and haemorrhages scattered throughout the skeletal muscles, perivisceral fat, the stomach wall and the swimbladder Histomorphological changes were most often observed as necrosis and granulomatous inflammation in the 11ver. Intracellular, intravacuolar bacteria-like inclusions with a n affinity for phagocytic host cells were observed Transmission electron rnicroscopy revealed individual or paired organisms enclosed in membrane-bound vacuoles.