In vitro interactions between Neoparamoeba sp. and Atlantic salmon epithelial cells

Neoparamoeba sp., including the putative aetiological agent of amoebic gill disease in cultured fish (N. pemaquidensis), were incubated in vitro with an Atlantic salmon gill epithelium (RGE-2) cell line. Proliferation by the amoeba population was dependent upon culture osmolarity; no growth occurred at 330 mm x kg(-1) but a sixfold increase was observed at 1000 mm x kg(-1). At 780 mm x kg(-1) there was a fourfold increase in the amoeba population but a concurrent decrease in RGE-2 cell density that was significantly greater than that caused by the high culture osmolarity alone. This apparent cytopathic effect (CPE) developed rapidly and resulted in complete cytolysis of the monolayer in 5 days. CPE occurred in multiple foci and presented as cell vacuolation, rounding and clumping, and the rapid clearance of large areas of the cell monolayer. The possibility that CPE is because of the presence of Neoparamoeba sp. derived cytolytic products is discussed in the context of the pathology of the disease in vivo and the occurrence of secreted cytopathogenic compounds in other amoeba species.     

Genestic differences between successive year classes of two strains of reared rainbow trout, Oncorhynchus mykiss (Walbaum)

The genetic composition of consecutive year classes of two farmed rainbow trout, Oncorhynchus mykiss (Walbaum), strains was assessed, using starch gel electrophoresis of 11 enzymes encoded by a minimum of 23 loci, many of which have been shown to be polymorphic in previous studies. Angle frequencies at the majority of polymorphic loci varied significantly between year classes of each strain. Several alleles which were present at low frequency in the 1900 year classes, were absent in the samples from the 1991 cohorts. However, mean heterozygosity per locus (H) did not differ significantly between year classes of either strain, illustrating that allelic diversity is a more sensitive indicator of loss of genetic variability than mean heterozygosity. This heterogeneity between cohorts is probably due either to broodstock maintenance practices such as the use of insufficient numbers of spawners, or, in the case of one strain, to bottlenecking caused by selection for late maturation and increased growth rate. Genetic monitoring of all year classes of reared strains is suggested, if insufficient breeding and distribution records are available from egg producers. Such records are often unavailable in commercial situations.     

Changes in the concentrations of serum IgG, IgA and IgM of sows throughout the reproductive cycle

The concentrations of IgG, IgM and IgA in sera collected from 3855 sows (3208 pregnant and 647 lactating) at a single time point were determined. This experimental design allowed changes in serum immunoglobulin over the reproductive cycle to be studied without bias from seasonal influence. The concentrations of the three immunoglobulins changed independently during the reproductive cycle. Serum levels of IgM and IgG began a progressive postpartal decline during the 14th–17th week of gestation. At the onset of lactation serum IgG levels progressively increased while IgM levels continued to decline, the latter reaching their lowest level during the third week of lactation. In contrast to IgM and IgG, serum IgA levels increased 35% during weeks 14–17 of gestation and continued to increase throughout lactation, reaching their highest serum levels in the third week of lactation; the serum IgA concentration at this time was twice that observed during the first 13 weeks of gestation. Results of these studies allowed the reproductive cycle to be classified into four phases on the basis of serum immunoglobulin concentrations: (1) weeks 1–4 of gestation; (2) weeks 5–13 of gestation; (3) weeks 14–17 of gestation and (4) lactation.     

Reduced chromosome association between the short arms of 5H homologues in Hordeum vulgare L. at metaphase I

Rod or ring bivalents at metaphase I (MI) reflect whether crossing-over has occurred on one or both pairs of chromosome arms, respectively, during meiotic prophase (pachytene). In cultivated barley ( Hordeum vulgare ) the highest frequencies of rod bivalents were found for satellite chromosomes (either 5H or 6H). To distinguish between chromosome 5H and 6H associations, a recombinant line derived from an H. vulgare × H. bulbosum hybrid with a hemizygous introgression from H. bulbosum on the short arm of chromosome 6H was probed with 45S rDNA and pSc119.2 using fluorescent in situ hybridization and compared with non-recombinant H. vulgare. The frequencies of rod bivalents, caused by failure of the short arms of 5H chromosomes (5HS) to associate during meiosis in the recombinant line, were similar to the frequencies of rod bivalents involving the satellite chromosomes in H. vulgare. Hence, rod bivalent formation in H. vulgare satellite chromosomes is probably based on reduced association of 5HS, corresponding to a low frequency of genetic recombination. 5HS is, therefore, more likely to show linkage disequilibrium than the other chromosome arms.     

Soil nitrogen mineralization not affected by grass species traits

Species N use traits was evaluated as a mechanism whereby Bromus inermis (Bromus), an established invasive, might alter soil N supply in a Northern mixed-grass prairie. We compared soils under stands of Bromus with those from three representative native grasses of different litter C/N: Andropogon gerardii (Andropogon), Nassella viridula (Nassella) and Pascopyrum smithii (Pascopyrum); in ascending order of litter quality. Net mineralization (per g soil N) measured in year-long laboratory incubations showed no differences in comparisons of Bromus with two of the three native grasses: Andropogon and Nassella. Higher mineralization in Pascopyrum stands relative to Bromus was consistent with its higher litter quality. However, an unusually high occurrence of an N-fixing legume in Pascopyrum stands, potentially favoring high mineralization rates, confounded any conclusions regarding the effects of plant N use on N mineralization. Instead of an initial flush of net mineralization, as would be expected in laboratory incubation, we observed an initial lag phase. This lag in net N mineralization coincided with high microbial activity (respiration) that suggests strong N limitation of the microbial biomass. Further support for the importance of immobilization initially came from modeling mineralization dynamics, which was explained better when we accounted for microbial growth in our model. The absence of strong differences in net mineralization beneath these grasses suggests that differences in plant N use alone were unlikely to influence soil N mineralization through substrate quality, particularly under strong N control of the microbial biomass.