7 research outputs found

    Genetic analysis of a rabies virus host shift event reveals within-host viral dynamics in a new host

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    Host shift events play an important role in epizootics as adaptation to new hosts can profoundly affect the spread of the disease and the measures needed to control it. During the late 1990s, an epizootic in Turkey resulted in a sustained maintenance of rabies virus (RABV) within the fox population. We used Bayesian inferences to investigate whole genome sequences from fox and dog brain tissues from Turkey to demonstrate that the epizootic occurred in 1997 (±1 year). Furthermore, these data indicated that the epizootic was most likely due to a host shift from locally infected domestic dogs, rather than an incursion of a novel fox or dog RABV. No evidence was observed for genetic adaptation to foxes at consensus sequence level and dN/dS analysis suggested purifying selection. Therefore, the deep sequence data were analysed to investigate the sub-viral population during a host shift event. Viral heterogeneity was measured in all RABV samples; viruses from the early period after the host shift exhibited greater sequence variation in comparison to those from the later stage, and to those not involved in the host shift event, possibly indicating a role in establishing transmission within a new host. The transient increase in variation observed in the new host species may represent virus replication within a new environment, perhaps due to increased replication within the CNS, resulting in a larger population of viruses, or due to the lack of host constraints present in the new host reservoir

    Measuring the Proton Conductivity of Ion-Exchange Membranes Using Electrochemical Impedance Spectroscopy and Through-Plane Cell

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    The role of the incorporation of conducting polymer (CP), doped with different sulfonic acid organic molecules, in polystyrene (PS) and high-impact polystyrene (HIPS) with poly­(styrene-ethylene-butylene) (SEBS) triblock copolymer has been investigated. Two factors associated with this model membrane system are addressed: (i) the influence of the presence of a low concentration of doped conducting polymer and (ii) the influence of the membrane preparation method. Membrane characterization and bulk conductivity measurements allowed the conclusion that proton conductivity has been promoted by the addition of CP; the best results were achieved for PAni-CSA, in either PS/SEBS or HIPS/SEBS blends. Additionally, the water uptake only decreased with the addition of PAni-doped molecules compared to the pure copolymer, without loss of ion-exchange capacity (IEC). Electrodialysis efficiency for HIPS/SEBS (before annealing) is higher than that for HIPS/SEBS (after annealing), indicating that membrane preparation method is crucial. Finally, through-plane cell arrangement proved to be an effective, quick, and time-saving tool for studying the main resistance parameters of isolating polymers, which is useful for application in industry and research laboratories working with membranes for electrodialysis or fuel cells

    Self-Diffusion of Chain Molecules in the Metal–Organic Framework IRMOF-1: Simulation and Experiment

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    Metal–organic frameworks (MOFs) possess characteristics, such as tunable pore size and chemical functionality, that make them attractive candidates for separations, catalysis, gas storage, and sensing applications. The rate of diffusion of guest molecules in the pores is an important property for all of these potential applications. In this work, the self-diffusion of hydrocarbons in IRMOF-1 was studied as a function of chain length with a combination of molecular dynamics simulations and pulsed field gradient NMR experiments. Excellent agreement is seen between the experiments and simulations, and the self-diffusion coefficients in IRMOF-1 are on the same order as those in the bulk liquid. Additionally, the effect of concentration on diffusivity was found to be very small for low to moderate loadings. Molecular dynamics simulations also provided insights about the preferential diffusion pathways of these guests in IRMOF-1

    2,6-Bis(5-(2,2-dimethylpropyl)-1<i>H</i>-pyrazol-3-yl)pyridine as a Ligand for Efficient Actinide(III)/Lanthanide(III) Separation

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    The N-donor complexing ligand 2,6-bis­(5-(2,2-dimethylpropyl)-1<i>H</i>-pyrazol-3-yl)­pyridine (C5-BPP) was synthesized and screened as an extracting agent selective for trivalent actinide cations over lanthanides. C5-BPP extracts Am­(III) from up to 1 mol/L HNO<sub>3</sub> with a separation factor over Eu­(III) of approximately 100. Due to its good performance as an extracting agent, the complexation of trivalent actinides and lanthanides with C5-BPP was studied. The solid-state compounds [Ln­(C5-BPP)­(NO<sub>3</sub>)<sub>3</sub>(DMF)] (Ln = Sm­(III), Eu­(III)) were synthesized, fully characterized, and compared to the solution structure of the Am­(III) 1:1 complex [Am­(C5-BPP)­(NO<sub>3</sub>)<sub>3</sub>]. The high stability constant of log β<sub>3</sub> = 14.8 ± 0.4 determined for the Cm­(III) 1:3 complex is in line with C5-BPP’s high distribution ratios for Am­(III) observed in extraction experiments
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