Experimental pathogenicity of reovirus 13p2 for juvenile American oysters Crassostrea virginica (Gmelin) and bluegill fingerlings Lepomis macrochirus (Rafinesque)

Abstract. A viral agent (13p₂), isolated from clinically normal juvenile American oysters ( Crassostrea virginica ) and characterized as a new serotype of reovirus, was tested to determine if it could replicate and produce disease in experimental juvenile oysters. Because the virus replicated well in the bluegill fry (BF-2) fish cell line, fingerling bluegills Lepomis macrochirus were included in the pathogenicity experiments. Exposure of oysters to the 13p₂ virus in ambient seawater resulted in no significant mortality and no increased virus titres or histological lesions. Virus particles were not observed in tissues of exposed oysters when examined with transmission electron microscopy (TEM). Intraperitoneal inoculation of the 13p₂ virus into bluegills resulted in 44% mortality associated with a focal necrotic hepatitis. Evidence of virus replication, when evaluated histological or by virus titration, was observed in 94% of 32 inoculated fish. Samples of infected livers examined with TEM revealed typical cytoplasmic arrays of 13p₂ virus particles in affected hepatocytes. Rising virus titres and hepatic lesions also occurred in bluegills exposed to water containing the 13p₂ virus. These results indicated the natural host of the 13p₂ virus was not the American oyster, but that it was a significant pathogen for at least one fish species.     

Toxicity and efficacy of Furanace on channel catfish Ictalurus punctatm (Rafinesque) infected experimentally with Aeromonas hydrophila

Abstract. The 96-h medium tolerance limit of Furanace (nifurpirinol: P-7138) for channel catfish Ictalurus punctatus at 21°C was 0-94 mg/1. The most effective treatment level for channel catfish, experimentally infected with Aeromonas hydrophila , was 2mg/1 for 6.5 h. Furanace at 0.5 and 1.0 mg/1 in brain heart infusion agar reduced in vitro growth of A. hydrophila and at 2.0 mg/1 growth was completely     

A bibliography of shrimp and prawn nutrition

This paper contains a bibliography of papers published on dietary and nutritional work with shrimps and prawns. In addition, selected papers on related topics, such as the nutrition of other crustacea, the natural food of shrimps and prawns, and physiology, are included. The bibliography is intended to be an aid to existing workers in the field of shrimp and prawn nutrition, to be a launch pad for scientists entering this field for the first time, and to assist those wishing to review specific aspects of this subject.     

Gas-liquid chromatographic determination of monosodium glutamate in soups and soup bases.

A method is given for determining monosodium glutamate (MSG) in soups and soup bases by gas-liquid chromatography (GLC) of the trimethylsilyl ether derivative of glutamic acid. This method compared favorably with existing methods including GLC of the trifluoroacetate (TFA)/butyl ester derivative, and analysis on an amino acid analyzer. In addition, some samples were analyzed by GLC/mass spectrometry. The MSG content of various products ranged from approximately 0.2% in some condensed soups to 13.1% on bouillon cubes. The method, which can detect as little as 0.05%, requires only a 10 min single step derivatization at room temperature and is preferred to the TFA/butyl ester technique.     

Degradation of ioxynil by a soil fungus, Fusarium solani

A fungus, Fusarium solani, isolated from the soil, degraded ioxynil (3,5-diiodo-4-hydroxyben-zonitrile) in pure culture into at least eight products. Five products were detected in the organic fractions extracted from a culture grown in [¹⁴C]cyano-labeled ioxynil. Three additional products were separated by ion-exchange chromatography of the acidified aqueous phase. Cultures grown in the presence of [¹⁴C]ring-labeled ioxynil produced the same products in the organic extract and four to five products in the aqueous phase. The cyano-carbon of ioxynil was released as CO₂ at a faster rate than that of ring-carbons and was released after the initial ring cleavage. Two of the metabolites were identified as 3,5-diiodo-4-hydroxybenzamide and 3,5-diiodo-4-hydroxybenzoic acid.     

A method for measuring adenosine triphosphate in soil

A method was devised for the extraction and measurement of adenosine 5'-triphosphate (ATP) in soil that minimizes sorption of ATP on the soil colloids. Soil was ultrasonified for 1 min with a solution containing trichloracetic acid (0.5 m). disodium hydrogen orthophosphate (0.25 m) and paraquat dichloride (0.1 m). The ATP content of the filtered extract was determined without further treatment in a scintillation spectrometer by the firefly luciferin-luciferase system. Recovery of added ATP was greater using the extratant containing trichloracetic acid, orthophosphate and paraquat than with trichloracetic acid alone or with a sulphuric acid extradant. Recoveries of added ATP ranged from 45% to 84% in thirteen different soils; ATP contents from 0.64 to 9.03 μg g^?1 soil.     

Biodegradation of litter in Eucalyptus pauciflora communities—II. Fungal succession in fungicide- and insecticide-treated leaves

Fungal succession on untreated and fungicide- and insecticide-treated leaves of Eucalyptus pauciflora was compared. Natural succession on untreated leaves fits the general scheme for succession on deciduous tree leaves. Initial colonizers are species of Coelomycetes and Moniliales. When the numbers of Coelomycetes decrease in the late stages of decomposition, the frequency of Penicillium species and species of Zygomycetes increases. The succession is affected only marginally by DDT and dieldrin treatment while benomyl severely restricts the occurrence of most fungal species. The effect of benomyl persists even after exposure for 48 weeks in the field.     

Some problems in assessing the fluorescein diacetate-active fungal biomass in the soil

A technique for assessing the metabolically-active fungal biomass by means of fluorescein diacetate (FDA) staining was recently described (Söderström, 1977). In this note some practical details in the application of this technique to studies of FDA-active fungal biomass in the soil are discussed.     

Interactions between bacteria and ectomycorrhizal fungi

Interactions between eight ectomycorrhizal fungi and eight bacteria were tested on five laboratory media and in the rhizoplane of Pinus radiata. Depression of growth of the fungi by the bacteria in laboratory media was dependent on the medium and bore little relation to effects in the rhizoplane. In the rhizoplane, different bacteria could depress, have no effect or even stimulate growth of mycorrhizal fungi. Competition and antagonism are suggested as mechanisms for depression of the fungi. Some bacteria gave protection against the depressive effects of other bacteria. Considerable differences occurred between ectomycorrhizal fungi in their colonization of the rhizoplane in the absence of bacteria and also in their presence. The common mycorrhizal fungi Rhizopogon luteolus and Thelephora terrestris generally colonized roots well but the strain of Pisolithus tinctorius studied colonized poorly. Direct microscopy showed the percentage cover of the root by microorganisms was usually only 10–20%.It is proposed that interactions of ectomycorrhizal fungi with soil organisms are important in determining the successful introduction and persistence of inoculated ectomycorrhizal fungi. Fungi should be selected for compatibility with a wide range of soil microflora as well as efficiency in plant stimulation.