Diesel exhaust and house dust mite allergen lead to common changes in the airway methylome and hydroxymethylome.

Exposures to diesel exhaust particles (DEP) from traffic and house dust mite (HDM) allergens significantly increase risks of airway diseases, including asthma. This negative impact of DEP and HDM may in part be mediated by epigenetic mechanisms. Beyond functioning as a mechanical barrier, airway epithelial cells provide the first line of immune defense towards DEP and HDM exposures. To understand the epigenetic responses of airway epithelial cells to these exposures, we exposed human bronchial epithelial cells to DEP and HDM and studied genome-wide 5-methyl-cytosine (5mC) and 5-hydroxy-methylcytosine (5hmC) at base resolution. We found that exposures to DEP and HDM result in elevated TET1 and DNMT1 expression, associated with 5mC and 5hmC changes. Interestingly, over 20% of CpG sites are responsive to both exposures and changes in 5mC at these sites negatively correlated with gene expression differences. These 5mC and 5hmC changes are located in genes and pathways related to oxidative stress responses, epithelial function and immune cell responses and are enriched for binding sites of transcription factors (TFs) involved in these pathways. Histone marks associated with promoters, enhancers and actively transcribed gene bodies were associated with exposure-induced DNA methylation changes. Collectively, our data suggest that exposures to DEP and HDM alter 5mC and 5hmC levels at regulatory regions bound by TFs, which coordinate with histone marks to regulate gene networks of oxidative stress responses, epithelial function and immune cell responses. These observations provide novel insights into the epigenetic mechanisms that mediate the epithelial responses to DEP and HDM in airways

Data Fusion of Electronic Nose and Electronic Tongue for Detection of Mixed Edible-Oil

For the problem of the waste of the edible-oil in the food processing, on the premise of food security, they often need to add new edible-oil to the old frying oil which had been used in food processing to control the cost of the production. Due to the fact that the different additive proportion of the oil has different material and different volatile gases, we use fusion technology based on the electronic nose and electronic tongue to detect the blending ratio of the old frying oil and the new edible-oil in this paper. Principal component analysis (PCA) is used to distinguish the different proportion of the old frying oil and new edible-oil; on the other hand we use partial least squares (PLS) to predict the blending ratio of the old frying oil and new edible-oil. Two conclusions were proposed: data fusion of electronic nose and electronic tongue can be used to detect the blending ratio of the old frying oil and new edible-oil; in contrast to single used electronic nose or single used electronic tongue, the detection effect has increased by using data fusion of electronic nose and electronic tongue

Influence of various experimental parameters on the capacitive removal of phosphate from aqueous solutions using LDHs/AC composite electrodes

The efficient uptake of phosphate from aqueous solutions was achieved on layered double hydroxides (LDHs)-based electrodes via capacitive desalination in our previous study. The current follow-up work was mainly carried out to study the influence of various experimental parameters on the capacitive removal of phosphate using LDHs/activated carbon (LDHs/AC) composite electrodes. A series of batch experiments were implemented to investigate the experimental factors, including Mg2+/Al3+ ratios (2, 3, and 4), trivalent metal cations (Al3+, Fe3+, Cr3+), initial solution pH (from 3 to 10), coexisting anions (NO3-, Cl-, SO42-), and ion strengths, in capacitive deionization. The electrode materials before and after capacitive deionization were characterized to reinforce the analysis of the adsorption mechanisms by X-ray powder diffraction, scanning electron microscopy, energy dispersive X-ray, cyclic voltammetry, and electrochemical impedance spectroscopy. Results indicated that the Mg-Al LDHs/AC electrodes exhibited higher phosphate adsorption capacity (80.43 mg PO43-/g), more regular morphology, and higher degree of crystallinity than that of Mg-Fe LDHs/AC and Mg-Cr LDHs/AC. Increasing Mg2+/Al3+ ratios enhanced the adsorption capacity of phosphate. The uptake of phosphate by Mg-Al LDHs/AC under circumneutral pH and low ion strength reached the maximum level. Furthermore, the presence of coexisting anions lowered the adsorption capacity of phosphate mainly due to the occurrence of a compressed electrical double layer. Therefore, the influence of different experimental parameters on phosphate removal via capacitive deionization by Mg-Al LDHs/AC necessitates a systematic investigation to optimize the preparation conditions of LDHs-based electrodes and several important operating parameters

Enhanced phosphate removal under an electric field via multiple mechanisms on MgAl-LDHs/AC composite electrode

Phosphorus removal is essential to avoid eutrophication in water bodies. Layered double hydroxides (LDHs) are widely used to scavenge phosphate through intercalated ion exchange or surface complexation. Moreover, LDHs have attracted increasing attention as electrode modifiers for supercapacitors. Researchers have begun to re-delve the electrosorption technology according to the fundamental principle of electrical double layers. Herein, we propose a new phosphate removal method inspired by the adsorption characteristic and electrical double-layer capacitive properties of LDHs through electrosorption via capacitive deionization. We present a series of experiments to study the enhanced phosphate removal under an electric field via multiple mechanisms on the MgAl-LDHs/AC electrode. The uptake of phosphate by MgAl-LDHs/AC was investigated as a function of phosphate concentration, applied voltage, electrode materials, and temperature. The MgAl-LDHs/AC electrode possessed a salt removal capacity of 67.92 mg PO43−·g−1 (1.2 V, 250 mg·L−1 KH2PO4, 30 °C). The electrosorption kinetics of phosphate ions onto the capacitive deionization electrode followed the pseudo-second-order kinetics model rather than the pseudo-first-order kinetics model. Furthermore, the adsorption isotherms of phosphate on the MgAl-LDHs/AC electrode fitted the Freundlich model better than the Langmuir model. The proposed method could be used for phosphate removal

Hydrothermal synthesis of reduced graphene oxide-LiNi0.5Mn1.5O4 composites as 5V cathode materials for Li-ion batteries

Composite materials consisting of reduced graphene oxide and LiNi0.5Mn1.5O4 were in situ prepared by a simple one-step hydrothermal treating method. The physical property and electrochemical performance of the composite materials were characterized by X-ray diffraction, Raman spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, cyclic voltammetry, charge/discharge testing, and electrochemical impedance spectroscopy. The results demonstrate that the graphene oxide is partially reduced and uniformly in situ anchored on the surface of LiNi0.5Mn1.5O4. As a result, the specific surface area of the composite material dramatically increases from 0.2488 to 8.71 m2 g−1, and the initial specific discharge capacity improves from 125.8 to 140.2 mAh g−1, respectively. Furthermore, the capacity retention maintains 95.8% after 100 cycles, and the electrode polarization has significantly been lessened. At rates of 1, 2, and 5 C, the composite material with 5% reduced graphene oxide can deliver much higher capacities than the pristine LiNi0.5Mn1.5O4. Moreover, AC impedance test results show that the interfacial charge transfer impedance obviously reduced. It is confirmed that the introduction of reduced graphene oxide through hydrothermal treating is effective to enhance the electrochemical performance of the composite material

Magnetically attracted iron scrap anode based electrocoagulation for phosphate removal

This study shows the effectiveness of a novel electrocoagulation process using magnetically attracted iron scrap anodes for phosphate removal from aqueous solution. The effect of contact time, reaction temperature, dose of iron scrap, initial phosphate concentration, applied voltage, pH, magnetic force, and the species of competing anions on the efficiency of phosphate removal and the reaction products has been investigated. The techniques of XRD, XPS, and VSM were used to characterize the elemental composition and the types of the reaction products in order to clarify the interaction between novel anode and phosphate ions. The removal of phosphate was fitted by a pseudo first-order reaction kinetic model. The results showed that magnetically attracted iron scrap anodes were electrodissoluted under an applied potential and reacted with phosphate into Fe-hydroxo-phosphate complexes. The work suggested that electrocoagulation using magnetically attracted iron scrap anodes had the potential to become a promising technique for phosphate precipitation

Enhanced hydrophilicity and antibacterial activity of PVDF ultrafiltration membrane using Ag3PO4/TiO2 nanocomposite against E. coli

Ag3PO4/TiO2, nanocomposite was fabricated by an in situ precipitation method and then blended into poly(vinylidene fluoride) (PVDF) casting solution to prepare the ultrafiltration membrane via wet phase inversion technique. The water flux and bovine serum albumin (BSA) rejection rate of membrane were investigated; meanwhile, the ultrafiltration membrane morphologies and structural properties were analyzed using scanning electron microscope (SEM) and X-ray diffraction. Compared with the control membrane, the permeate performance of blended membranes was improved while possessing a steady BSA retention due to enhanced hydrophilicity. Mechanical tests revealed that the modified membranes exhibited a larger tensile strength and breakage elongation. SEM images and the halo zone testing were employed to assess the antibacterial performances of the nanocomposite membranes against Escherichia coli. The antibacterial tests confirmed that the modified membranes showed an effective antibacterial property against E. coli

Private specificities of CD8 T cell responses control patterns of heterologous immunity

CD8 T cell cross-reactivity between viruses can play roles in protective heterologous immunity and damaging immunopathology. This cross-reactivity is sometimes predictable, such as between lymphocytic choriomeningitis virus (LCMV) and Pichinde virus, where cross-reactive epitopes share six out of eight amino acids. Here, however, we demonstrate more subtle and less predictable cross-reactivity between LCMV and the unrelated vaccinia virus (VV). Epitope-specific T cell receptor usage differed between individual LCMV-infected C57BL/6 mice, even though the mice had similar epitope-specific T cell hierarchies. LCMV-immune mice challenged with VV showed variations, albeit in a distinct hierarchy, in proliferative expansions of and down-regulation of IL-7Rα by T cells specific to different LCMV epitopes. T cell responses to a VV-encoded epitope that is cross-reactive with LCMV fluctuated greatly in VV-infected LCMV-immune mice. Adoptive transfers of splenocytes from individual LCMV-immune donors resulted in nearly identical VV-induced responses in each of several recipients, but responses differed depending on the donor. This indicates that the specificities of T cell responses that are not shared between individuals may influence cross-reactivity with other antigens and play roles in heterologous immunity upon encounter with another pathogen. This variability in cross-reactive T cell expansion that is unique to the individual may underlie variation in the pathogenesis of infectious diseases