Species history masks the effects of human-induced range loss--unexpected genetic diversity in the endangered giant mayfly Palingenia longicauda

Freshwater biodiversity has declined dramatically in Europe in recent decades. Because of massive habitat pollution and morphological degradation of water bodies, many once widespread species persist in small fractions of their original range. These range contractions are generally believed to be accompanied by loss of intraspecific genetic diversity, due to the reduction of effective population sizes and the extinction of regional genetic lineages. We aimed to assess the loss of genetic diversity and its significance for future potential reintroduction of the long-tailed mayfly Palingenia longicauda (Olivier), which experienced approximately 98% range loss during the past century. Analysis of 936 bp of mitochondrial DNA of 245 extant specimens across the current range revealed a surprisingly large number of haplotypes (87), and a high level of haplotype diversity (Hd = 0.875). In contrast, historic specimens (6) from the lost range (Rhine catchment) were not differentiated from the extant Rába population (F(ST) = 0.02, p = 0.61), despite considerable geographic distance separating the two rivers. These observations can be explained by an overlap of the current with the historic (Pleistocene) refugia of the species. Most likely, the massive recent range loss mainly affected the range which was occupied by rapid post-glacial dispersal. We conclude that massive range losses do not necessarily coincide with genetic impoverishment and that a species' history must be considered when estimating loss of genetic diversity. The assessment of spatial genetic structures and prior phylogeographic information seems essential to conserve once widespread species.     

Your unconscious knows your name

One''s own name constitutes a unique part of conscious awareness – but does this also hold true for unconscious processing? The present study shows that the own name has the power to bias a person''s actions unconsciously even in conditions that render any other name ineffective. Participants judged whether a letter string on the screen was a name or a non-word while this target stimulus was preceded by a masked prime stimulus. Crucially, the participant''s own name was among these prime stimuli and facilitated reactions to following name targets whereas the name of another, yoked participant did not. Signal detection results confirmed that participants were not aware of any of the prime stimuli, including their own name. These results extend traditional findings on “breakthrough” phenomena of personally relevant stimuli to the domain of unconscious processing. Thus, the brain seems to possess adroit mechanisms to identify and process such stimuli even in the absence of conscious awareness.     

Identification of a novel signaling pathway and its relevance for GluA1 recycling

We previously showed that the serum- and glucocorticoid-inducible kinase 3 (SGK3) increases the AMPA-type glutamate receptor GluA1 protein in the plasma membrane. The activation of AMPA receptors by NMDA-type glutamate receptors eventually leads to postsynaptic neuronal plasticity. Here, we show that SGK3 mRNA is upregulated in the hippocampus of new-born wild type Wistar rats after NMDA receptor activation. We further demonstrate in the Xenopus oocyte expression system that delivery of GluA1 protein to the plasma membrane depends on the small GTPase RAB11. This RAB-dependent GluA1 trafficking requires phosphorylation and activation of phosphoinositol-3-phosphate-5-kinase (PIKfyve) and the generation of PI(3,5)P(2). In line with this mechanism we could show PIKfyve mRNA expression in the hippocampus of wild type C57/BL6 mice and phosphorylation of PIKfyve by SGK3. Incubation of hippocampal slices with the PIKfyve inhibitor YM201636 revealed reduced CA1 basal synaptic activity. Furthermore, treatment of primary hippocampal neurons with YM201636 altered the GluA1 expression pattern towards reduced synaptic expression of GluA1. Our findings demonstrate for the first time an involvement of PIKfyve and PI(3,5)P(2) in NMDA receptor-triggered synaptic GluA1 trafficking. This new regulatory pathway of GluA1 may contribute to synaptic plasticity and memory.     

A stochastic description of Dictyostelium chemotaxis

Chemotaxis, the directed motion of a cell toward a chemical source, plays a key role in many essential biological processes. Here, we derive a statistical model that quantitatively describes the chemotactic motion of eukaryotic cells in a chemical gradient. Our model is based on observations of the chemotactic motion of the social ameba Dictyostelium discoideum, a model organism for eukaryotic chemotaxis. A large number of cell trajectories in stationary, linear chemoattractant gradients is measured, using microfluidic tools in combination with automated cell tracking. We describe the directional motion as the interplay between deterministic and stochastic contributions based on a Langevin equation. The functional form of this equation is directly extracted from experimental data by angle-resolved conditional averages. It contains quadratic deterministic damping and multiplicative noise. In the presence of an external gradient, the deterministic part shows a clear angular dependence that takes the form of a force pointing in gradient direction. With increasing gradient steepness, this force passes through a maximum that coincides with maxima in both speed and directionality of the cells. The stochastic part, on the other hand, does not depend on the orientation of the directional cue and remains independent of the gradient magnitude. Numerical simulations of our probabilistic model yield quantitative agreement with the experimental distribution functions. Thus our model captures well the dynamics of chemotactic cells and can serve to quantify differences and similarities of different chemotactic eukaryotes. Finally, on the basis of our model, we can characterize the heterogeneity within a population of chemotactic cells.     

Changes in community composition, carbon and nitrogen stable isotope signatures and feeding strategy in epilithic aquatic nematodes along a depth gradient

Periphyton is an important component within the littoral zones of lakes, but it is known to vary dramatically on small (cm–m) and large (km) spatial scales, showing differences in composition and abundance. Until relatively recently, changes in periphyton composition along depth gradients have not been studied sufficiently and the response of small meiobenthic invertebrates inhabiting the periphyton to vertically changing environmental conditions such as light are poorly understood. To investigate the changing community composition of epilithic (on stones) nematodes along a depth gradient, we conducted a field study at Lake Erken, Sweden, with the specific objective to investigate whether changes in periphyton composition (algae, bacteria) are reflected in changing nematode feeding types and what the consequences are for nematodes and their resource consumption. We analysed the abundance, species composition and feeding type distribution of epilithic nematodes along 11 depth levels, from 5 to 300?cm water depth. Our study resulted in the first measurements of carbon (¹³C) and nitrogen (¹⁵N) stable isotopes in free living nematodes in lakes. Nematode community composition and feeding type distribution exhibited dramatic changes along the depth gradient. Nematode feeding types changed from a dominance of algae-feeding species in the shallow littoral zone to one of bacteria-feeding species in the deep littoral zone. The ¹³C stable isotope signatures of nematodes and the small (<20?μm) periphyton fraction changed with increasing depth, with nematodes shown to feed on this small periphytic component. Nematodes were identified as primary consumers by means of trophic level calculations based on ¹⁵N stable isotopes.     

Constructed wetlands support bats in agricultural landscapes

Bats are known to use aquatic habitats as foraging habitats. Agricultural intensification is perceived to be a main reason for the loss of wetlands. However, artificial wetland creation (i.e. the construction of retention-ponds) in the agricultural landscape aiming at water or nutrient retention has recently gained importance. We evaluated to what extent bats use these artificial wetlands as foraging habitats in an agricultural landscape.Bat activity and prey density were compared in matched pairs at retention-ponds and neighbouring vineyard sites using stationary bat-detectors and sticky-traps, respectively. To examine if bat activity is related to the number of bat individuals, a thermal infrared imaging camera was used. Pipistrellus pipistrellus, the dominant species, served as an example to assess habitat selection between retention-ponds and vineyards. This was performed by relating foraging activity to the available area available within the potential home-range.Total bat activity and nocturnal prey density were significantly higher above the retention-ponds than above vineyards. High differences of activity levels between the ponds and the respective vineyard sites were found for Pipistrellus spp. (P. pipistrellus and P. nathusii) and Myotis spp. (M. daubentonii and M. mystacinus), being about 180 times and 50 times higher above the retention-ponds, respectively. A significant correlation was found between recorded bat activity and the maximum number of bat individuals observed with a thermal infrared imaging camera. When relating foraging activity to habitat availability within the assumed home-range of P. pipistrellus, retention-ponds had on average a higher importance as a foraging habitat than the complete vineyard area although they covered less than 0.1% of its area.This study indicates that artificial wetlands such as retention-ponds provide foraging habitats for bats. Therefore, creation of wetlands in intensively used agricultural landscapes benefits bats.     

FK506-binding protein 51 interacts with Clostridium botulinum C2 toxin and FK506 inhibits membrane translocation of the toxin in mammalian cells

The binary Clostridium botulinum C2 toxin consists of the binding/translocation component C2IIa and the separate enzyme component C2I. C2IIa delivers C2I into the cytosol of eukaryotic target cells where C2I ADP-ribosylates actin. After receptor-mediated endocytosis of the C2IIa/C2I complex, C2IIa forms pores in membranes of acidified early endosomes and unfolded C2I translocates through the pores into the cytosol. Membrane translocation of C2I is facilitated by the activities of host cell chaperone Hsp90 and the peptidyl-prolyl cis/trans isomerase (PPIase) cyclophilin A. Here, we demonstrated that Hsp90 co-precipitates with C2I from lysates of C2 toxin-treated cells and identified the FK506-binding protein (FKBP) 51 as a novel interaction partner of C2I in vitro and in intact mammalian cells. Prompted by this finding, we used the specific pharmacological inhibitor FK506 to investigate whether the PPIase activity of FKBPs plays a role during membrane translocation of C2 toxin. Treatment of cells with FK506 protected cultured cells from intoxication with C2 toxin. Moreover, FK506 inhibited the pH-dependent translocation of C2I across membranes into the cytosol but did not interfere with the enzyme activity of C2I or binding of C2 toxin to cells. Furthermore, FK506 treatment delayed intoxication with the related binary actin ADP-ribosylating toxins from Clostridium perfringens (iota toxin) and Clostridium difficile (CDT) but not with the Rho-glucosylating Clostridium difficile toxin A (TcdA). In conclusion, our results support the hypothesis that clostridial binary actin-ADP-ribosylating toxins share a specific FKBP-dependent translocation mechanism during their uptake into mammalian cells.