Deposition of tungsten oxide and silver decorated tungsten oxide for use in oxygen gas sensing

Tungsten oxide and silver-decorated tungsten oxide were investigated for the detection of oxygen in a humid environment. The sensor materials were deposited onto alumina sensor substrates via aerosol-assisted chemical vapour deposition. Results indicated that our sensors showed good sensitivity to oxygen, following an almost a linear relationship over a 0 to 20% concentration range. In comparison to WO3, the Ag-decorated sensors showed a much higher sensitivity and better response (sensitivity of 0.22 per %O2 vs 0.80 per %O2 for Ag decorated), making Ag-WO3 based sensors an interseting alternative to existing Pb-based sensors for quantitative oxygen sensing

Aerosol-assisted CVD synthesis, characterisation and gas-sensing application of gold-functionalised tungsten oxide

Tungsten oxide nanoneedles (NNs) functionalised with gold nanoparticles (NPs) have been integrated with alumina gas-sensor platforms using a simple and effective co-deposition method via aerosol-assisted chemical vapour deposition (AACVD) utilising a novel gold precursor, (NH4)AuCl4. The gas-sensing results show that gold NP functionalisation of tungsten oxide NNs improves the sensitivity of response to ethanol, with sensitivity increasing and response time decreasing with increasing amount of gold

Development and Application of a Simple Plaque Assay for the Human Malaria Parasite Plasmodium falciparum.

Malaria is caused by an obligate intracellular protozoan parasite that replicates within and destroys erythrocytes. Asexual blood stages of the causative agent of the most virulent form of human malaria, Plasmodium falciparum, can be cultivated indefinitely in vitro in human erythrocytes, facilitating experimental analysis of parasite cell biology, biochemistry and genetics. However, efforts to improve understanding of the basic biology of this important pathogen and to develop urgently required new antimalarial drugs and vaccines, suffer from a paucity of basic research tools. This includes a simple means of quantifying the effects of drugs, antibodies and gene modifications on parasite fitness and replication rates. Here we describe the development and validation of an extremely simple, robust plaque assay that can be used to visualise parasite replication and resulting host erythrocyte destruction at the level of clonal parasite populations. We demonstrate applications of the plaque assay by using it for the phenotypic characterisation of two P. falciparum conditional mutants displaying reduced fitness in vitro

Highly sensitive contact pressure measurements using FBG patch in endotracheal tube cuff

A method for measuring the contact pressure between an endotracheal tube cuff and the trachea was designed and developed by using a fibre Bragg grating (FBG) based optical fibre sensor. The FBG sensor is encased in an epoxy based UV-cured cuboid patch and transduces the transversely loaded pressure into an axial strain that induces wavelength shift of the Bragg reflection. The polymer patch was created by using a PTFE based mould and increases tensile strength and sensitivity of the bare fibre FBG to pressure to 2.10×10-2 nm/kPa. The characteristics of the FBG patch allow for continuous measurement of contact pressure. The measurement of contact pressure was demonstrated by the use of a 3D printed model of a human trachea. The influence of temperature on the measurements is reduced significantly by the use of a second FBG sensor patch that is not in contact with the trachea. Intracuff pressure measurements performed using a commercial manometer agreed well with the FBG contact pressure measurements. © (2016) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only

Seismological imaging of ridge–arc interaction beneath the Eastern Lau Spreading Center from OBS ambient noise tomography

The Lau Basin displays large along-strike variations in ridge characters with the changing proximity of the adjacent subduction zone. The mechanism governing these changes is not well understood but one hypotheses relates them to interaction between the arc and back-arc magmatic systems. We present a 3D seismic velocity model of the shallow mantle beneath the Eastern Lau back-arc Spreading Center (ELSC) and the adjacent Tofua volcanic arc obtained from ambient noise tomography of ocean bottom seismograph data. Our seismic images reveal an asymmetric upper mantle low velocity zone (LVZ) beneath the ELSC. Two major trends are present as the ridge-to-arc distance increases: (1) the LVZ becomes increasingly offset from the ridge to the north, where crust is thinner and the ridge less magmatically active; (2) the LVZ becomes increasingly connected to a sub-arc low velocity zone to the south. The separation of the ridge and arc low velocity zones is spatially coincident with the abrupt transition in crustal composition and ridge morphology. Our results present the first mantle imaging confirmation of a direct connection between crustal properties and uppermost mantle processes at ELSC, and support the prediction that as ELSC migrates away from the arc, a changing mantle wedge flow pattern leads to the separation of the arc and ridge melting regions. Slab-derived water is cutoff from the ridge, resulting in abrupt changes in crustal lava composition and crustal porosity. The larger offset between mantle melt supply and the ridge along the northern ELSC may reduce melt extraction efficiency along the ridge, further decreasing the melt budget and leading to the observed flat and faulted ridge morphology, thinner crust and the lack of an axial melt lens

Control of Gammaherpesvirus Latency by Latent Antigen-Specific Cd8+ T Cells

The contribution of the latent antigen-specific CD8+ T cell response to the control of gammaherpesvirus latency is currently obscure. Some latent antigens induce potent T cell responses, but little is known about their induction or the role they play during the establishment of latency. Here we used the murine gammaherpesvirus system to examine the expression of the latency-associated M2 gene during latency and the induction of the CD8+ T cell response to this protein. M2, in contrast to the M3 latency-associated antigen, was expressed at day 14 after infection but was undetectable during long-term latency. The induction of the M291–99/Kd CD8+ T cell response was B cell dependent, transient, and apparently induced by the rapid increase in latently infected cells around day 14 after intranasal infection. These kinetics were consistent with a role in controlling the initial “burst” of latently infected cells. In support of this hypothesis, adoptive transfer of an M2-specific CD8+ T cell line reduced the initial load of latently infected cells, although not the long-term load. These data represent the first description of a latent antigen-specific immune response in this model, and suggest that vaccination with latent antigens such as M2 may be capable of modulating latent gammaherpesvirus infection

Direct in situ spectroscopic evidence of the crucial role played by surface oxygen vacancies in the O2-sensing mechanism of SnO2

NAP-XPS characterisation of SnO2 under operando conditions shows that resistance change, band bending and surface O-vacancy concentration are correlated with ambient O2 concentration, challenging current preconceptions of gas sensor function

Covalent Plasmodium falciparum-selective proteasome inhibitors exhibit a low propensity for generating resistance in vitro and synergize with multiple antimalarial agents

Therapeutics with novel modes of action and a low risk of generating resistance are urgently needed to combat drug-resistant Plasmodium falciparum malaria. Here, we report that the peptide vinyl sulfones WLL-vs (WLL) and WLW-vs (WLW), highly selective covalent inhibitors of the P. falciparum proteasome, potently eliminate genetically diverse parasites, including K13-mutant, artemisinin-resistant lines, and are particularly active against ring-stage parasites. Selection studies reveal that parasites do not readily acquire resistance to WLL or WLW and that mutations in the β2, β5 or β6 subunits of the 20S proteasome core particle or in components of the 19S proteasome regulatory particle yield only <five-fold decreases in parasite susceptibility. This result compares favorably against previously published non-covalent inhibitors of the Plasmodium proteasome that can select for resistant parasites with >hundred-fold decreases in susceptibility. We observed no cross-resistance between WLL and WLW. Moreover, most mutations that conferred a modest loss of parasite susceptibility to one inhibitor significantly increased sensitivity to the other. These inhibitors potently synergized multiple chemically diverse classes of antimalarial agents, implicating a shared disruption of proteostasis in their modes of action. These results underscore the potential of targeting the Plasmodium proteasome with covalent small molecule inhibitors as a means of combating multidrug-resistant malaria

Parasitophorous vacuole poration precedes its rupture and rapid host erythrocyte cytoskeleton collapse in Plasmodium falciparum egress.

In the asexual blood stages of malarial infection, merozoites invade erythrocytes and replicate within a parasitophorous vacuole to form daughter cells that eventually exit (egress) by sequential rupture of the vacuole and erythrocyte membranes. The current model is that PKG, a malarial cGMP-dependent protein kinase, triggers egress, activating malarial proteases and other effectors. Using selective inhibitors of either PKG or cysteine proteases to separately inhibit the sequential steps in membrane perforation, combined with video microscopy, electron tomography, electron energy loss spectroscopy, and soft X-ray tomography of mature intracellular Plasmodium falciparum parasites, we resolve intermediate steps in egress. We show that the parasitophorous vacuole membrane (PVM) is permeabilized 10-30 min before its PKG-triggered breakdown into multilayered vesicles. Just before PVM breakdown, the host red cell undergoes an abrupt, dramatic shape change due to the sudden breakdown of the erythrocyte cytoskeleton, before permeabilization and eventual rupture of the erythrocyte membrane to release the parasites. In contrast to the previous view of PKG-triggered initiation of egress and a gradual dismantling of the host erythrocyte cytoskeleton over the course of schizont development, our findings identify an initial step in egress and show that host cell cytoskeleton breakdown is restricted to a narrow time window within the final stages of egress