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Columnaris disease generates substantial losses of many freshwater fish species; one is the hybrid striped bass. The ubiquitous aquatic bacterium Flavobacterium columnare can be highly effective in biofilm formation on fish skin and gills. Previous research showed a difference between columnaris disease susceptibility of hybrid striped bass (Morone saxatilis × M. chrysops) and white bass (M. chrysops). To understand these differential susceptibilities and possible mucosal relationship, we assessed total bacterial growth and biofilm formation with mucus derived from each moronid parental species: white bass and striped bass (M. saxatilis). Differential susceptibility was confirmed of the other parent species, the striped bass (M. saxatilis). In addition to intraspecies investigations, individual hybrid striped bass mucosal affects were also studied for deferential responses to bacterial growth and biofilm formation. Species- and concentration-dependent differences were detected in the total growth of the bacteria to host mucus. Our data suggest that bass mucus can significantly affect biofilm formation with the F. columnare isolate tested. There appears to be a correlation between the bacteria's response of growth and biofilms and bass species susceptibility. This study provides insight into our understanding of the host-pathogen interaction between F. columnare and moronids.

The antimicrobial activity and mode of action of chitosan were evaluated against Streptococcus iniae, a pathogenic Gram-positive bacterium of fish worldwide. Cell proliferation kinetics were examined following exposure to varying concentrations of chitosan. The action of chitosan on S. iniae was also investigated by measuring agglutination activity, conductivity, and extracellular and intracellular bacterial adenosine triphosphate (ATP) levels. Chitosan exhibited antibacterial activity against S. iniae at concentrations of 0.1% and above and was lethal at a concentration of 0.4% and higher. The mechanism of antibacterial activity of chitosan at the inhibitory level of bacterial growth appears to hinge upon the interaction between chitosan and the oppositely charged bacterial surface. This interplay causes agglutination, which was readily observed grossly and microscopically. After interacting with the cell surface via adsorption, an efflux of intracellular ATP was documented, which suggests that chitosan disrupts the bacterial cell causing leakage of cytosolic contents and ultimately cell death. Results suggest chitosan may be worth evaluating as a natural alternative to antibiotic against S. iniae infection of fish.

Columnaris disease generates substantial losses of many freshwater fish species; one is the hybrid striped bass. The ubiquitous aquatic bacterium Flavobacterium columnare can be highly effective in biofilm formation on fish skin and gills. Previous research showed a difference between columnaris disease susceptibility of hybrid striped bass (Morone saxatilis × M. chrysops) and white bass (M. chrysops). To understand these differential susceptibilities and possible mucosal relationship, we assessed total bacterial growth and biofilm formation with mucus derived from each moronid parental species: white bass and striped bass (M. saxatilis). Differential susceptibility was confirmed of the other parent species, the striped bass (M. saxatilis). In addition to intraspecies investigations, individual hybrid striped bass mucosal affects were also studied for deferential responses to bacterial growth and biofilm formation. Species- and concentration-dependent differences were detected in the total growth of the bacteria to host mucus. Our data suggest that bass mucus can significantly affect biofilm formation with the F. columnare isolate tested. There appears to be a correlation between the bacteria's response of growth and biofilms and bass species susceptibility. This study provides insight into our understanding of the host-pathogen interaction between F. columnare and moronids.

Our recent results in hybrid striped bass (HSB) concluded that ideal protein theory accurately predicts first-limiting amino acids in commercial diet formulations if accurate amino acid availability data are used and that appropriate levels of supplemental lysine are needed to improve fish performance from fishmeal-free diets. Our goal in this study was to elucidate how dietary lysine supplementation of a commercial fishmeal-free diet influences the expression of two genes, myostatin and myogenin, controlling myogenesis in differentially growing groups of HSB. Real-time RT-PCR results in HSB suggest that the levels of lysine added to the diet (17.8, 35.1, 51.0 g kg−1 of diet) has an impact on myogenin relative to the basal unsupplemented diet, but no effect on myostatin. Moreover, our data further suggest that the amount of dietary lysine supplementation influenced the ratio of myostatin/myogenin expression in HSB and that this pattern mimicked that of most of the growth, composition of growth and nutrient retention data from our previous study and may therefore be a useful marker for selecting fish for improved growth performance.

The development and testing of a visible implant elastomer pedigree-marking system was evaluated in sunshine bass, Morone chrysops Morone saxatilis ,a nd white bass, M. chrysops (Ra¢nesque). These tags were tested in sunshine bass ¢ngerlings at one of four subdermal body locations (posterior to the eye, dorsal ¢n musculature, caudal ¢n musculature or anal ¢n musculature). Tag visibility decreased with increased sunshine bass growth (63% after 56 days).Visibility diiered among body locations, with the caudal and anal tagging locations having lower visibility. White bass ¢ngerlings representing eight genetic groups were then tagged at one of two body locations (left or right subdermal along the dorsal musculature) using one of four £uorescent colours and reared for 42 days in a common garden growth trial. Tag visibility in white bass was 99.5% at 14 days, 98.2% at 28 days and 94.9% at 42 days after tagging. There was a signi¢cant change in weight among the eight genetic groups of white bass ¢ngerlings after 42 days (P 5 0.03). Testing of this pedigree tagging system successfully identi¢ed phenotypically diierent groups of white bass ¢ngerlings.