Influence of Early Season Moxidectin Treatments on Acquisition of Immunity to Ostertagia ostertagi in Calves

Moxidectin, a newly developed endectocide, has previously been demonstrated to have a high efficacy against gastrointestinal nematodes in cattle (Ranjan et al. 1992, Scholl et al. 1992). In a field trial (Yang, Satrija and Nansen, unpublished data) matched groups of 8 first-season Black Pied Friesian heifer calves, 6-8 months of age, were turned out in early May 1992 on a permanent pasture contaminated with trichostrongyles. The groups were grazed separately on comparable plots until they were housed in mid October 1992. Group Β was treated with moxidectin at turnout, and group C was treated at turnout and again 8 weeks after turnout. A third group served as non-treated controls (group A). The results showed that the 2 early season prophylactic treatments (group C) reduced the late season herbage trichostrongyle larval infectivity with 80 to 90%, whereas the reduction accomplished by only 1 treatment at turnout (group B) was much less. Group C excreted significantly lower numbers of strongyle eggs than groups A and B. The non-treated controls showed clinical signs of trichostrongylosis in late September, which coincided with a steep rise in serum pepsinogen levels reaching an average peak level of 3.5 IU tyrosine litre-1. A few animals in group Β showed softening of faeces particularly in the very late season. In contrast, animals receiving 2 moxidectin treatments remained in a clinically good condition throughout the season.     

The importance of scale and spatial variables for the fungivorous beetle Bolitophagus reticulatus (Coleoptera, Tenebrionidae) in a fragmented forest landscape

Effects of isolation, habitat size and several microhabitat variables on presence/absence of the monophagous Bolitophagus reticulatus (L.) (Coleoptera. Tenebrionidae) were investigated in 58 forest fragments in an agricultural landscape (15 km²) in south-eastern Norway, All potential habitats of the beetle, dead Fomes fomentarius (L,) Kiekx basidiocarps (n = 587), were collected from trees (n = l85) within the study area. The basidiocarps were dissected and the number of B, reticulatus specimens (larvae, pupae and adults) counted. The material was analysed at four distinguishable spatial scales; basidiocarp-. tree-, tree-group- and forest island level. Different patterns of beetle presence emerged at the different scales, increasing habitat size and decreasing degree of isolation increased the probability of B, reticulatus presence at three (basidiocarp-, tree- and forest island level) and one (tree level) scales, respectively, whilst no such trends were found at the fourth level (tree-group level). Increasing insolation and thereby higher ambient temperatures, indicated by several microhabitat variables, improved the probability of beetle presence amongst the trees. The number of beetle specimens correlated positively with an increase in the habitat size at the tree level.     

Is dispersal density-dependent in carabid beetles? A field experiment with Harpalus rufipes (Degeer) and Pterostichus niger (Schaller) (Col., Carabidae)

In order to investigate whether density affects dispersal, carabid beetles of two species, Harpalus rufipes (Degeer) and Pterostichus niger (Schaller), were released separately in six and two field enclosures, respectively. The enclosures were 4 m² each and located in an oat field. The former species was released in seven densities, each with 12 replicates and the latter in five densities each with four replicates. Beetles leaving the centre of the enclosures were captured in pitfall traps along a 1 m wide strip of bare soil. Logistic models were fitted to the data. There were no significant effects of the density treatment variable on P. niger. For H. rufipes the best model was obtained by specifying the density treatment as a nominal variable. The deviance accounted for by this model was highly significant. There were, however, no consistent trends for either species with respect to the density treatment. The inclusion of climatic variables, the number of new beetles introduced at the onset of each trial, or the date of the trial did not improve the fit of any of the models. It is concluded that density did not significantly increase dispersal in the two species. It thus appears that a possible increase in behavioural interactions (i.e. interference competition) did not increase the dispersal in adults of the two species examined in this experiment.     

GUB06‐046, a novel secretin/glucagon‐like peptide 1 co‐agonist,decreases food intake,improves glycemic control,and preserves beta cell mass in diabetic mice

Bariatric surgery is currently the most effective treatment of obesity, which has spurred an interest in developing pharmaceutical mimetics. It is thought that the marked body weight‐lowering effects of bariatric surgery involve stimulated secretion of appetite‐regulating gut hormones, including glucagon‐like peptide 1. We here report that intestinal expression of secretin is markedly upregulated in a rat model of Roux‐en‐Y gastric bypass, suggesting an additional role of secretin in the beneficial metabolic effects of Roux‐en‐Y gastric bypass. We therefore developed novel secretin‐based peptide co‐agonists and identified a lead compound, GUB06‐046, that exhibited potent agonism of both the secretin receptor and glucagon‐like peptide 1 receptor. Semi‐acute administration of GUB06‐046 to lean mice significantly decreased cumulative food intake and improved glucose tolerance. Chronic administration of GUB06‐046 to diabetic db/db mice for 8 weeks improved glycemic control, as indicated by a 39% decrease in fasting blood glucose and 1.6% reduction of plasma HbA1c levels. Stereological analysis of db/db mice pancreata revealed a 78% increase in beta‐cell mass after GUB06‐046 treatment, with no impact on exocrine pancreas mass or pancreatic duct epithelial mass. The data demonstrate beneficial effects of GUB06‐046 on appetite regulation, glucose homeostasis, and beta‐cell mass in db/db mice, without proliferative effects on the exocrine pancreas and the pancreatic duct epithelium. Copyright © 2017 European Peptide Society and John Wiley & Sons, Ltd.     

Development of Immunity to Ostertagia ostertagi (Trichostrongylidae: Nematoda) in Pastured Young Cattle

This experiment comprised 3 groups of calves, (+P2), (−P2) and (−P1), which all started their first grazing season as parasite-free calves. The (+P2)- and (−P2)-group grazed 2 seasons. In the first season the (−P2)-group of calves was grazing a pasture with no detectable trichostrongyles and treated with anthelmintics every second week. The untreated (+P2)-group grazed an Ostertagia ostertagi contaminated pasture. During the second grazing season these 2 original groups grazed together with a new group of first-year grazing calves (−P1) on paddocks infected with O.ostertagi. Parasitological analyses showed that (+P2)-group had negligible egg excretions in the second year in comparison with (−P2) and (−P1). This indicated, that the egg output may be regulated through acquired immunity. The difference in egg excretions was not reflected in the serum pepsinogen levels, which were only slightly elevated for all groups in the second year. Post mortem examination at the end of the experiment showed that only the (−P1)-group harboured relatively high numbers of worms in the abomasa at that time. Antibodies of 3 immunoglobulin classes were investigated: IgA, IgG1 and IgG2. The IgA and IgGl responses correlated with the presence of developing and adult worms in the abomasa and they remained elevated in the (+P2)-group throughout the experiment, perhaps indicating an involvement of these antibodies in a protective immune response. In the (−P2)-group the IgA and IgG1 showed fast and sharp rises during the second season that most likely were age-related and as such a result of maturation of the immune system. The role of IgG2 is unclear as the IgG2 response was weak in all groups of calves and difficult to relate to the parasitological data.     

Small-Angle X-Ray Scattering of the Cholesterol Incorporation into Human ApoA1-POPC Discoidal Particles

Structural and functional aspects of high-density lipoproteins have been studied for over half a century. Due to the plasticity of this highly complex system, new aspects continue to be discovered. Here, we present a structural study of the human Apolipoprotein A1 (ApoA1) and investigate the role of its N-terminal domain, the so-called globular domain of ApoA1, in discoidal complexes with phospholipids and increasing amounts of cholesterol. Using a combination of solution-based small-angle x-ray scattering (SAXS) and molecular constrained data modeling, we show that the ApoA1-1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC)-based particles are disk shaped with an elliptical cross section and composed by a central lipid bilayer surrounded by two stabilizing ApoA1 proteins. This structure is very similar to the particles formed in the so-called nanodisc system, which is based on N-terminal truncated ApoA1 protein. Although it is commonly agreed that the nanodisc is plain disk shaped, several more advanced structures have been proposed for the full-length ApoA1 in combination with POPC and cholesterol. This prompted us to make a detailed comparative study of the ApoA1 and nanodisc systems upon cholesterol uptake. Based on the presented SAXS analysis it is found that the N-terminal domains of ApoA1-POPC-cholesterol particles are not globular but instead an integrated part of the protein belt stabilizing the particles. Upon incorporation of increasing amounts of cholesterol, the presence of the N-terminal domain allows the bilayer thickness to increase while maintaining an overall flat bilayer structure. This is contrasted by the energetically more strained and less favorable lens shape required to fit the SAXS data from the N-terminal truncated nanodisc system upon cholesterol incorporation. This suggests that the N-terminal domain of ApoA1 actively participates in the stabilization of the ApoA1-POPC-cholesterol discoidal particle and allows for a more optimal lipid packing upon cholesterol uptake.     

Diversity of coleoptera of the bracket fungus Fomitopsis pinicola in a Norwegian spruce forest

The beetle fauna of 299 sporocarps of the bracket fungus Fomitopsis pinicola in a 200 ha spruce forest in southeastern Norway was investigated in relation to sporocarp, tree and forest variables. The sporocarps contained 36 species of beetles, of which six species are on the Norwegian Red List. Of 12,373 individual beetles collected, 91% were Cis glabratus. Plots of species accumulation curves suggested that there may be more than 60 beetle species present in F. pinicola in the area, but that probably all the specialist Ciidae were found. The major factor influencing beetle diversity turned out to be the level of dead wood at and in the vicinity of the sampling site, with a higher number of species per unit volume of sporocarps in areas with high levels of dead wood. There were also significantly more red-listed species in those areas. Analysing the species occurrence with stepwise logistic regression, we show preferential habitat selection of the six most abundant species of Ciidae. Conservation of beetles associated with bracket fungi using amount of dead wood as a surrogate measurement is discussed.     

Crystal structure of the TLDc domain of oxidation resistance protein 2 from zebrafish

The oxidation resistance proteins (OXR) help to protect eukaryotes from reactive oxygen species. The sole C‐terminal domain of the OXR, named TLDc is sufficient to perform this function. However, the mechanism by which oxidation resistance occurs is poorly understood. We present here the crystal structure of the TLDc domain of the oxidation resistance protein 2 from zebrafish. The structure was determined by X‐ray crystallography to atomic resolution (0.97Å) and adopts an overall globular shape. Two antiparallel β‐sheets form a central β‐sandwich, surrounded by two helices and two one‐turn helices. The fold shares low structural similarity to known structures. Proteins 2012. © 2012 Wiley Periodicals, Inc.