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Jay F. Levine

Publications and source records attributed to Jay F. Levine.

4 recordsLinked to original sources

A comparison of the chemical sensitivities between in vitro and in vivo propagated juvenile freshwater mussels: Implications for standard toxicity testing

Unionid mussels are ecologically important and are globally imperiled. Toxicants contribute to mussel declines, and toxicity tests using juvenile mussels—a sensitive life stage—are valuable in determining thresholds used to set water quality criteria. In vitro culture methods provide an efficient way to propagate juveniles for toxicity testing, but their relative chemical sensitivity compared with in vivo propagated juveniles is unknown. Current testing guidelines caution against using in vitro cultured juveniles until this sensitivity is described. Our objective was to evaluate the relative sensitivity of juvenile mussels produced from both in vitro and in vivo propagation methods to selected chemicals. We conducted 96-h acute toxicity tests according to ASTM International guidelines with 3 mussel species and 6 toxicants: chloride, nickel, ammonia, and 3 copper-based compounds. Statistically significant differences between in vitro and in vivo juvenile 96-h median effect concentrations were observed in 8 of 17 tests, and in vitro juveniles were more sensitive in 6 of the 8 significant differences. At 96 h, 4 of the 8 statistically different tests for a given chemical were within a factor of 2, which is the intralaboratory variation demonstrated in a recent evaluation of mussel toxicity tests. We found that although differences in chemical sensitivity exist between in vitro and in vivo propagated juvenile mussels, they are within normal toxicity test variation. Therefore, in vitro propagated juvenile mussels may be appropriate for use in ASTM International-based toxicity testing.

Environmental Toxicology and Chemistry↗

Exposure of unionid mussels to electric current: Assessing risks associated with electrofishing

Electric current is routinely applied in freshwater for scientific sampling of fish populations (i.e., electrofishing). Freshwater mussels (families Margaritiferidae and Unionidae) are distributed worldwide, but their recent declines in diversity and abundance constitute an imperilment of global significance. Freshwater mussels are not targeted for capture by electrofishing, and any exposure to electric current is unintentional. The effects of electric shock are not fully understood for mussels but could disrupt vital physiological processes and represent an additional threat to their survival. In a controlled laboratory environment, we examined the consequences of exposure to two typical electrofishing currents, 60-Hz pulsed DC and 60-Hz AC, for the survival of adult and early life stages of three unionid species; we included fish as a quality control measure. The outcomes suggest that electrical exposure associated with typical electrofishing poses little direct risk to freshwater mussels. That is, adult mussel survival and righting behaviors (indicators of sublethal stress) were not adversely affected by electrical exposure. Glochidia (larvae that attach to and become parasites on fish gills or fins) showed minimal immediate reduction in viability after exposure. Metamorphosis from glochidia to free-living juvenile mussels was not impaired after electric current simulated capture-prone behaviors (stunning) in infested host fish. In addition, the short-term survival of juvenile mussels was not adversely influenced by exposure to electric current. Any minimal risk to imperiled mussels must be weighed at the population level against the benefits gained by using the gear for scientific sampling of fish in the same waters. However, scientists sampling fish by electrofishing should be aware of mussel reproductive periods and processes in order to minimize the harmful effects to host fish, especially in areas where mussel conservation is a concern. ?? Copyright by the American Fisheries Society 2007.

Transactions of the American Fisheries Society↗

Magnetic resonance imaging of live freshwater mussels (Unionidae)

We examined the soft tissues of live freshwater mussels, Eastern elliptio Elliptio complanata , via magnetic resonance imaging (MRI), acquiring data with a widely available human whole-body MRI system. Anatomical features depicted in the profile images included the foot, stomach, intestine, anterior and posterior adductor muscles, and pericardial cavity. Noteworthy observations on soft tissue morphology included a concentration of lipids at the most posterior aspect of the foot, the presence of hemolymph-filled fissures in the posterior adductor muscle, the presence of a relatively large hemolymph-filled sinus adjacent to the posterior adductor muscle (at the ventral-anterior aspect), and segmentation of the intestine (a diagnostic description not reported previously in Unionidae). Relatively little is known about the basic biology and ecological physiology of freshwater mussels. Traditional approaches for studying anatomy and tissue processes, and for measuring sub-lethal physiological stress, are destructive or invasive. Our study, the first to evaluate freshwater mussel soft tissues by MRI, clarifies the body plan of unionid mussels and demonstrates the efficacy of this technology for in vivo evaluation of the structure, function, and integrity of mussel soft tissues.

Invertebrate Biology↗

Detection of spring viraemia of carp virus (SVCV) by loop-mediated isothermal amplification (LAMP) in koi carp, Cyprinus carpio L

Spring viraemia of carp virus (SVCV) is a rhabdovirus associated with systemic illness and mortality in cyprinids. Several diagnostic tests are available for detection of SVCV. However, most of these tests are time consuming and are not well adapted for field-based diagnostics. In this study, a diagnostic tool for SVCV detection based on reverse transcription loop-mediated isothermal amplification (RT-LAMP) has been developed. Based on the nucleotide sequence of the glycoprotein (G) gene of SVCV North Carolina (NC) isolate, four sets (each set containing two outer and two inner) of primers were designed. Temperature and time conditions were optimized to 65 ??C and 60 min, respectively, for LAMP and RT-LAMP using one primer set. In vitro specificity was evaluated using four different strains of fish rhabdoviruses and RT-LAMP was found to be specific to SVCV. Serial dilutions of SVCV NC isolate was used to evaluate the in vitro sensitivity of RT-LAMP. Sensitivity of the assays was similar to RT-PCR and detected SVCV even at the lowest dilution of 10 1 TCID50 mL-1. The ability of RT-LAMP to detect SVCV from infected carp was also tested and the assay detected SVCV from all infected fish. The isothermal temperature requirements, high specificity and sensitivity, and short incubation time of the RT-LAMP assay make it an excellent choice as a field diagnostic test for SVCV. ?? 2008 The Authors.

Journal of Fish Diseases↗