Effects of experimental warming on wild and transgenic oriental fruit fly,Bactrocera dorsalis

Climate change may influence the application efficiency of transgenic marking, such as in mark–release–recapture (MRR) experiments or sterile insect technique (SIT). Wild and transgenic fruit flies of Bactrocera dorsalis were subjected to oscillating regimes that represent current temperature conditions (mean: 28.6°C) and various future possible scenarios (means: 30.0, 32.5 and 35.0°C). As the temperature was increased to 30.0°C, the negative effects on adult fecundity and demographic parameters (net reproductive rate and intrinsic rate of increase) of only the transgenic cohorts increased. With a moderate warming (32.5°C), negative effects were observed on the net reproductive rate for both fly strains, and these effects on the life‐history traits (adult fecundity and longevity) and intrinsic rate of increase were stronger in the transgenic than in the wild cohorts, with reference to the trait values at 30.0°C. A severe warming (35.0°C) resulted in the failure of all individuals of both fly strains to reach adulthood. We suggest parametrical adjustments or decreased differences in fitness with refined transgenesis under current and future climate conditions, which can reduce the marking limitations of pest management and eradication programmes.     

Effects of gel concentration, human fibronectin, and cation supplement on the tissue-engineered cartilage

Cultivation of bovine knee chondrocytes (BKCs) in various cationic additives was studied using chitosan-gelatin scaffolds, whose surfaces were modified by human fibronectin (HFN). Here, the genipin-crosslinked scaffolds were fabricated by the freezing/lyophilization method with various concentrations of the precursory gels. The experimental results indicated that a lower freezing temperature led to higher moisture content, porosity, and specific surface area of a scaffold. The higher the precursor concentration, the larger the moisture content of a scaffold. A fast biodegradation of scaffold matrix was generated by a high porosity with BKCs. A higher concentration of HFN coated on scaffold surfaces yielded a faster rate of BKC attachment from the culture medium. The amounts of BKCs, glycosaminoglycans, and collagen over 28-day cultivation increased with the scaffold porosity, the coating concentration of HFN, the seeding density of BKCs, and the calcium concentration in medium.     

Developing a wetland IBI with statewide application after multiple testing iterations

An index of biotic integrity (IBI) is a frequently used approach for assessing the ecological integrity of streams with fish and macroinvertebrates the faunal assemblages most commonly used as indicator taxa. The IBI approach has been much less commonly applied to wetlands, despite the legal, policy and scientific need to assess wetland condition and develop ecological performance goals for wetland creation, restoration and enhancement. While some IBIs are sophisticated systems with statewide application that have undergone one or more testing iterations, many published IBIs are derived from single data sets of a single class of aquatic resource with limited geographic application. The State of Ohio initiated development of a wetland IBI using vascular plants in 1996. Sampling methods were investigated and ultimately a plot-based method was adopted. Potential attributes and different human disturbance gradients were evaluated in several studies. Ultimately, IBIs for emergent, forest and shrub dominated wetlands were developed. Data from the Vegetation IBI-emergent (VIBI-E) is presented to illustrate this process. Subsequent testing and refinement is a critical step in the development of a robust IBI with more than local application. Throughout its initial development (R² = 0.863, p < 0.001), first major testing iteration (R² = 82.2%, p < 0.001), second test iteration (R² = 75.0%, p < 0.001) and third test iteration (R² = 82.1%, p < 0.001), the VIBI-E has remained significantly correlated with the disturbance gradient. Eight of the original 10 metrics proposed continued to have significant and interpretable relationships with the disturbance gradient, with 4 metrics remaining completely unchanged, and 4 undergoing relatively minor modifications, and 2 being replaced. The VIBI-E and its component metrics were also evaluated against a new disturbance gradient (Landscape Development Index or LDI), derived from land use percentages within a 1 km radius of the wetlands, that was not used during VIBI-E development. The VIBI-E score and 9 of 10 metrics were significantly correlated with the LDI disturbance gradient providing separate confirmation of the VIBI. The Vegetation IBI-E consistently and reliably assessed wetland condition across the whole range of wetland types throughout Ohio's ecological regions.     

Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice

A homozygous mutation in the DST (dystonin) gene causes a newly identified lethal form of hereditary sensory and autonomic neuropathy in humans (HSAN-VI). DST loss of function similarly leads to sensory neuron degeneration and severe ataxia in dystonia musculorum (Dst^dt) mice. DST is involved in maintaining cytoskeletal integrity and intracellular transport. As autophagy is highly reliant upon stable microtubules and motor proteins, we assessed the influence of DST loss of function on autophagy using the Dst^dt-Tg4 mouse model. Electron microscopy (EM) revealed an accumulation of autophagosomes in sensory neurons from these mice. Furthermore, we demonstrated that the autophagic flux was impaired. Levels of LC3-II, a marker of autophagosomes, were elevated. Consequently, Dst^dt-Tg4 sensory neurons displayed impaired protein turnover of autophagosome substrate SQTSM1/p62 and of polyubiquitinated proteins. Interestingly, in a previously described Dst^dt-Tg4 mouse model that is partially rescued by neuronal specific expression of the DST-A2 isoform, autophagosomes, autolysosomes, and damaged organelles were reduced when compared to Dst^dt-Tg4 mutant mice. LC3-II, SQTSM1, polyubiquitinated proteins and autophagic flux were also restored to wild-type levels in the rescued mice. Finally, a significant decrease in DNAIC1 (dynein, axonemal, intermediate chain 1; the mouse ortholog of human DNAI1), a member of the DMC (dynein/dynactin motor complex), was noted in Dst^dt-Tg4 dorsal root ganglia and sensory neurons. Thus, DST-A2 loss of function perturbs late stages of autophagy, and dysfunctional autophagy at least partially underlies Dst^dt pathogenesis. We therefore conclude that the DST-A2 isoform normally facilitates autophagy within sensory neurons to maintain cellular homeostasis.     

Stable carbon isotope analysis reveals widespread drought stress in boreal black spruce forests

Unprecedented rates of climate warming over the past century have resulted in increased forest stress and mortality worldwide. Decreased tree growth in association with increasing temperatures is generally accepted as a signal of temperature‐induced drought stress. However, variations in tree growth alone do not reveal the physiological mechanisms behind recent changes in tree growth. Examining stable carbon isotope composition of tree rings in addition to tree growth can provide a secondary line of evidence for physiological drought stress. In this study, we examined patterns of black spruce growth and carbon isotopic composition in tree rings in response to climate warming and drying in the boreal forest of interior Alaska. We examined trees at three nested scales: landscape, toposequence, and a subsample of trees within the toposequence. At each scale, we studied the potential effects of differences in microclimate and moisture availability by sampling on northern and southern aspects. We found that black spruce radial growth responded negatively to monthly metrics of temperature at all examined scales, and we examined ?¹³C responses on a subsample of trees as representative of the wider region. The negative ?¹³C responses to temperature reveal that black spruce trees are experiencing moisture stress on both northern and southern aspects. Contrary to our expectations, ?¹³C from trees on the northern aspect exhibited the strongest drought signal. Our results highlight the prominence of drought stress in the boreal forest of interior Alaska. We conclude that if temperatures continue to warm, we can expect drought‐induced productivity declines across large regions of the boreal forest, even for trees located in cool and moist landscape positions.     

Crystal Structure of Calmodulin Binding Domain of Orai1 in Complex with Ca2+?Calmodulin Displays a Unique Binding Mode

Orai1 is a plasma membrane protein that in its tetrameric form is responsible for calcium influx from the extracellular environment into the cytosol in response to interaction with the Ca²⁺-depletion sensor STIM1. This is followed by a fast Ca²⁺·calmodulin (CaM)-dependent inhibition, resulting from CaM binding to an Orai1 region called the calmodulin binding domain (CMBD). The interaction between Orai1 and CaM at the atomic level remains unknown. Here, we report the crystal structure of a CaM·Orai1-CMBD complex showing one CMBD bound to the C-terminal lobe of CaM, differing from other CaM-target protein complexes, in which both N- and C-terminal lobes of CaM (CaM-N and CaM-C) are involved in target binding. Orai1-CMBD binds CaM-C mainly through hydrophobic interactions, primarily involving residue Trp⁷⁶ of Orai1-CMBD, which interacts with the hydrophobic pocket of CaM-C. However, NMR data, isothermal titration calorimetry data, and pulldown assays indicated that CaM-N and CaM-C both can bind Orai1-CMBD, with CaM-N having ∼4 times weaker affinity than CaM-C. Pulldown assays of a Orai1-CMBD(W76E) mutant, gel filtration chromatography data, and NOE signals indicated that CaM-N and CaM-C can each bind one Orai1-CMBD. Thus our studies support an unusual, extended 1:2 binding mode of CaM to Orai1-CMBDs, and quantify the affinity of Orai1 for CaM. We propose a two-step mechanism for CaM-dependent Orai1 inactivation initiated by binding of the C-lobe of CaM to the CMBD of one Orai1 followed by the binding of the N-lobe of CaM to the CMBD of a neighboring Orai1.