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J.D. Teska

Publications and source records attributed to J.D. Teska.

16 recordsLinked to original sources
USGS1996

Epizootiological study of bacterial cold-water disease in Pacific salmon and further characterization of the etiologic agent, Flexibacterin psychrophila

Isolates of Flexibacter psychrophila were obtained from chinook salmon Oncorhynchus tshawytscha and coho salmon O. kisutch that had previously sustained epizootics of coldwater disease. The pathogen was readily isolated from kidney and mucus of convalescent fish. The organisms were relatively inert in most standard microbiological media but were structurally and serologically homogenous by examination of whole cell protein lysates by sodium dodecyl sulfate polyacrylamide gel electrophoresis. In contrast to the homogeneity observed in phenotypic and serologic assays, the isolates studied elaborated varied ribotypes. All isolates produced a single rDNA spacer amplification product of about 240 base pairs.

Journal of Aquatic Animal Health↗
USGS1996

Control of external Aeromonas salmonicida: topical disinfection of salmonids with Chloramine-T

Brook trout Salvelinus fontinalis were treated with single 60-min static baths of 250 mg formalin/L, 3% NaCl, and 15 mg Chloramine-T/L to evaluate the efficacy of these compounds against external infections of Aeromonas salmonicida. Prevalence of A. salmonicida was significantly lower in brook trout treated with Chloramine-T than among those treated with formalin or salt. Further laboratory tests substantiated the therapeutic value of a single treatment of ChloramineT (15 mg/L) against A. salmonicida . In two experiments, viable counts of A. salmonicida in mucus did not vary among replicate groups of treated brook trout, but the counts for treated fish were significantly (P < 0.05) lower than those for untreated controls. In vitro tube dilution assays indicated that mean minimum inhibitory concentrations of Chloramine-T for 10 isolates of A. salmonicida were 9.0 mg/L for 1 h and 2.25 mg/L, for 24 h. In field trials at the White River National Fish Hatchery (Bethel, Vermont), the pathogen was detected principally as an external infection of juvenile Atlantic salmon Salmo solar maintained in two culture ponds. In one pond, the bacterium accounted for 100% of the total distribution of tnicroflora isolated from mucus. Seven days after treatment with Chloramine-T, A. sahnonicida accounted for 11% of the total bacterial counts identified from these fish. In the second pond, A. salmonicida composed 3% of the counts of bacteria isolated from the mucus of fish before treatment but was not isolated after treatment.

Journal of Aquatic Animal Health↗
USGS1996

Use of non-lethal procedures to detect and monitor Aeromonas salmonicida in potentially endangered or threatened populations of migrating and post-Spawning salmon

Non-lethal assay of mucus was assessed for detection of Aeromonas salmonicida among feral populations of salmon returning to the Salmon River (Altmar, NY, USA). A. salmonicida was isolated from returns of 2 year classes of coho Oncorhynchus kisutch and chinook O. tshawytscha salmon. Data suggested that non-lethal assay of mucus was comparable to standard lethal procedures used to detect and isolate A. salmonicida from kidney tissues. Non-lethal procedures were also used to detect A. salmonicida and monitor the effectiveness of antibiotic therapy for the control of furunculosis among valuable Atlantic salmon Salmo salar broodstock maintained at the Richard Cronin National Salmon Station (Sunderland, MA, USA).

Diseases of Aquatic Organisms↗
USGS1993

Assay to evaluate the reaction kinetics of Chondroitin AC lynase produced by Cytophaga columnaris

The development of an assay to quantitate chondroitin AC lyase activity of Cytophaga columnaris isolates is described. Assay conditions were defined by using C. columnaris originally isolated from channel catfish Ictalurus punctatus , coho salmon Oncorhynchus kisutch , goldfish Carassius auratus , and striped bass Morone saxatilis affected with clinical columnaris disease. Supernatant and cellular components of broth cultures exhibited strong activity, and rates of chondroitin sulfate degradation ranged from 20.0 to 81.4 μg/(mL.h) for the cell component and from 35.4 to 83.4 μg/(mL.h) for the supernatant. Degradation rates were calculated by simple linear regression analysis, and most correlations ranged from −0.90 to −1.00. The assay provided results within 2–3 h, and the enzyme is active under a wide range of pH (5–9) and temperature (10–50°C) conditions. The assay can be used as a simple diagnostic aid to differentiate C. columnaris from Cytophaga psychrophila , but more importantly, as a quantitative tool to explore any relationship between specific chondroitin lyase activity and columnaris disease.

Journal of Aquatic Animal Health↗
USGS1992

Detection of Aeromonas salmonicida the mucus of salmonid fishes

Mucus of salmonids was evaluated as a source for nonlethal detection of the pathogen Aeromonas salmonicida in fish. The bacterium was readily isolated from mucus on dilution plates when Coomassie Brilliant Blue agar was the primary plating medium. Kidney samples from the fish that served as sources of mucus were similarly processed. Infection was detected in 56% of mucus samples from lake trout Salvelinus namaycush that were undergoing an epizootic of furunculosis, but only 6% of the kidneys from these fish were positive for the pathogen. Only 1% of asymptomatic brown trout Salmo trutta sampled at another fish hatchery had A. salmonicida in their mucus, and none had a kidney infection. Combined results from the examination of two pools of Atlantic salmon Salmo salar reared at a third hatchery indicated that 37% of these fish had mucus infections caused by A. salmonicida , but only 4% of the kidneys were infected.

Journal of Aquatic Animal Health↗
USGS1992

Molecular and genetic characterization of cytochrome oxidase negative Aeromonas salmonicida isolated from coho salmon (Oncorhynchus kisutch)

Cytochrome oxidase variants of the bacterial fish pathogen, Aeromonas salmonicida , were characterized for genetic and molecular homology with cytochrome oxidase-positive isolates that typically induce furunculosis in salmonids. Protein and lipopolysaccharide moieties of the cytochrome oxidase-negative variants were similar to their typical counterparts, based on sodium-dodecyl-sulfate polyacrylamide gel electrophoresis. Pathogenicity of aberrant isolates to brook trout ( Salvelinus fontinalis ) was similar to typical cytochrome oxidase-positive isolates. Colorimetric deoxyribonucleic acid (DNA) hybridization in 96-well microplates yielded homology values greater than 82.5% for typical aberrant A. salmonicida isolates when photobiotinylated DNA for reference A. salmonicida 3.101 was used as a probe. The only variation of these isolates from typical A. salmonicida was a negative cytochrome oxidase reaction.

Journal of Wildlife Diseases↗
USGS1991

Isolation and phenotypic characterization of an oxidase-negative Aeromonas salmonicida causing furunculosis in coho salmon (Oncorhynchus kisutch)

An oxidase-negative Aeromonas salmonicida was isolated from coho salmon ( Oncorhynchus kisutch ) suffering from an epizootic of furunculosis at the state hatchery near Belfair, Washington. Typical, oxidase-positive A. salmonicida was isolated concurrently from the same population of fish. Mortality was controlled with medicated feed treatments. Evidence supporting the identification of the two types of A. salmonicida is presented. Methods for the proper identification of oxidase-negative A. salmonicida isolates are evaluated.

Journal of Wildlife Diseases↗