12 research outputs found
Towards understanding transfluthrin efficacy in a pyrethroid-resistant strain of the malaria vector Anopheles funestus with special reference to cytochrome P450-mediated detoxification
Malaria vector control interventions rely heavily on the application of insecticides against anopheline mosquitoes, in particular the fast-acting pyrethroids that target insect voltage-gated sodium channels (VGSC). Frequent applications of pyrethroids have resulted in resistance development in the major malaria vectors including Anopheles funestus, where resistance is primarily metabolic and driven by the overexpression of microsomal cytochrome P450 monooxygenases (P450s). Here we examined the pattern of cross-resistance of the pyrethroid-resistant An. funestus strain FUMOZ-R towards transfluthrin and multi-halogenated benzyl derivatives, permethrin, cypermethrin and deltamethrin in comparison to the susceptible reference strain FANG. Transfluthrin and two multi-fluorinated derivatives exhibited micromolar potency - comparable to permethrin - to functionally expressed dipteran VGSC in a cell-based cation influx assay. The activity of transfluthrin and its derivatives on VGSC was strongly correlated with their contact efficacy against strain FUMOZ-R, although no such correlation was obtained for the other pyrethroids due to their rapid detoxification by the resistant strain. The low resistance levels for transfluthrin and derivatives in strain FUMOZ-R were only weakly synergized by known P450 inhibitors such as piperonyl butoxide (PBO), triflumizole and 1-aminobenzotriazole (1-ABT). In contrast, deltamethrin toxicity in FUMOZ-R was synergized > 100-fold by all three P450 inhibitors. The biochemical profiling of a range of fluorescent resorufin and coumarin compounds against FANG and FUMOZ-R microsomes identified 7-benzyloxymethoxy-4-trifluoromethylcoumarin (BOMFC) as a highly sensitive probe substrate for P450 activity. BOMFC was used to develop a fluorescence-based high-throughput screening assay to measure the P450 inhibitory action of potential synergists. Azole fungicides prochloraz and triflumizole were identified as extremely potent nanomolar inhibitors of microsomal P450s, strongly synergizing deltamethrin toxicity in An. funestus. Overall, the present study contributed to the understanding of transfluthrin efficacy at the molecular and organismal level and identified azole compounds with potential to synergize pyrethroid efficacy in malaria vectors
Cryo-EM structural studies of the agonist complexed human TRPV4 ion-channel reveals novel structural rearrangements resulting in an open-conformation
The human transient receptor potential vanilloid 4 (hTRPV4) ion channel plays a critical role in a variety of biological processes. Whilst the activation of hTRPV4 gating properties has been reported for a broad spectrum of stimuli, including synthetic 4α-phorbols, the molecular basis of the activation is poorly understood. Here we report the novel cryo-EM structure of the hTRPV4 determined in the presence of the archetypical phorbol acid agonist, 4α-PDD. Complementary mutagenesis experiments support the EM-identified binding site as well as allowing rationalization of disruptive mutants located outside of the 4α-PDD binding site. This work represents the first structural information of hTRPV4 in a ligand-induced open conformation. Together, our data reveal the underlying molecular mechanisms resulting in the opening of the central pore and ion-channel activation and provide a structural template for designing inhibitors targeting the open-state conformation of hTRPV4
The synergistic action of imidacloprid and flumethrin and their release kinetics from collars applied for ectoparasite control in dogs and cats
<p>Abstract</p> <p>Background</p> <p>The control of tick and flea burdens in dogs and cats has become essential to the control of important and emerging vector borne diseases, some of which are zoonoses. Flea worry and flea bite hypersensitivity are additionally a significant disease entity in dogs and cats. Owner compliance in maintaining the pressure of control measures has been shown to be poor. For these reasons efforts are continuously being made to develop ectoparasiticides and application methods that are safe, effective and easy to apply for pet owners. A new polymer matrix collar has recently been developed which is registered for 8 months use in cats and dogs. The basic properties of this collar have been investigated in several <it>in vitro </it>and <it>in vivo </it>studies.</p> <p>Methods</p> <p>The effects of imidacloprid, flumethrin and the combination were evaluated in vitro by means of whole cell voltage clamp measurement experiments conducted on isolated neuron cells from <it>Spodoptera frugiperda</it>. The in vitro efficacy of the two compounds and the combination against three species of ticks and their life stages and fleas were evaluated in a dry surface glass vial assay. The kinetics of the compounds over time in the collar were evaluated by the change in mass of the collar and measurement of the surface concentrations and concentrations of the actives in the collar matrix by HPLC. Hair clipped from collar treated dogs and cats, collected at various time points, was used to assess the acaricidal efficacy of the actives ex vivo.</p> <p>Results</p> <p>An <it>in vitro </it>isolated insect nerve model demonstrated the synergistic neurotoxic effects of the pyrethroid flumethrin and the neonicotinoid imidacloprid. An <it>in vitro </it>glass vial efficacy and mortality study against various life stages of the ticks <it>Ixodes ricinus, Rhipicephalus sanguineus </it>and <it>Dermacentor reticulatus </it>and against the flea (<it>Ctenocephalides felis</it>) demonstrated that the combination of these products was highly effective against these parasites. The release kinetics of these actives from a neck collar (compounded with 10% imidacloprid and 4.5% flumethrin) was extensively studied in dogs and cats under laboratory and field conditions. Acaricidal concentrations of the actives were found to be consistently released from the collar matrix for 8 months. None of the collar studies in dogs or cats were associated with any significant collar related adverse event.</p> <p>Conclusion</p> <p>Here we demonstrated the synergism between the pyrethroid flumethrin and the neonicotinoid imidacloprid, both provided in therapeutically relevant doses by a slow release collar matrix system over 8 months. This collar is therefore a convenient and safe tool for a long-term protection against ectoparasites.</p
Ce SLO-1 and hum KCNMA1 currents are blocked by the BK channel antagonist penitrem A.
<p><b>A</b>. Representative whole cell currents recorded from HEK293 cells expressing either Ce SLO-1 or hum KCNMA1 before and after penitrem A (1μM) application. Membrane potential was held at -60mV and stepped to between -100 and +90mV in 10mV increments for 50ms. <b>B</b>. A time-course of steady state Ce SLO-1 and hum KCNMA1 currents at +70mV (stepped every 10s for 40ms from -60mV holding potential) before and during application of DMSO (0.01%) or penitrem A (1μM). The current response is shown as a percentage change from the mean of pre-drug current amplitude during the 0 to 2 min time period. An arrow indicates the time point at which the drug solution reached the chamber with the cells. Free intracellular [Ca<sup>2+</sup>] was 100μM for Ce SLO-1 and 300nM for hum KCNMA1. Data points are the mean ± s.e.mean. p<0.0001 for penitrem A inhibited current compared to DMSO treatment, two-way ANOVA with Bonferroni post-hoc tests.</p
The biphasic effect of emodepside on hum KCNMA1 currents.
<p>Time-course analysis of steady state hum KCNMA1 currents expressed in HEK293 cells at +70mV (stepped every 10s for 40ms from -60mV holding potential) before and during application of 0.01% DMSO or emodepside. The current response is shown as a percentage change from the mean of pre-drug current amplitude during the 0 to 2 min time period. Arrow indicates the time of emodepside application at <b>A</b>. 1nM <b>B</b>. 10nM and <b>C</b>. 100nM. Data points are the mean ± s.e.mean. 100nM emodepside had a biphasic effect on hum KCNMA1 currents eliciting a significant increase between 4 and 8 min application (p<0.05) and a significant decrease after 20 min application (p<0.001); two-way ANOVA with Bonferroni post-hoc tests.</p
Dm Slo currents are blocked by the BK channel antagonists verruculogen and penitrem A.
<p>Top panel shows representative traces of Dm Slo whole cell currents stable expressed in CHO cells before and after verruculogen (3μM) application. Membrane potential was held at -70mV and stepped to between -120 and +60mV in 10mV increments for 100ms. Bottom panel shows dose-response curves for verrucologen (circles) and penitrem A (squares) on Dm Slo. Membrane potential was held at -70mV. Test pulses to + 60mV for 100ms. Each data points represent the mean ± s.e. of n = 3 cells.</p
The effect of emodepside on voltage-activation of Ce SLO-1 and hum KCNMA1.
<p>Analysis of the current-voltage relationship of the data sets shown in <a href="http://www.plosntds.org/article/info:doi/10.1371/journal.pntd.0004062#pntd.0004062.g006" target="_blank">Fig 6</a> and Fig 7 for Ce SLO-1 and hum KCNMA1 whole cell currents expressed in HEK293 cells before and after treatment with emodepside (100nM). Ce SLO-1 currents were recorded before and 12 min after emodepside application. Hum KCNMA1 currents were recorded before and 5 min after emodepside application. Membrane potential was held at -60mV and stepped to between -100 and +90mV in 10mV increments for 50ms. Data points are the mean ± s.e.mean of n = 9 for Ce SLO-1 and n = 8 for hum KCNMA1. The amplitude of Ce SLO-1 currents in the presence of 100nM emodepside was significantly greater than currents recorded in the absence of emodepside between +20 and +90mV and for hum KCNMA1 was significantly greater than currents recorded in the absence of emodepside between +70 and +90mV; p<0.05; two-way ANOVA with Bonferroni post-hoc tests.</p
Intracellular Ca<sup>2+</sup> ions are required for emodepside activation of Dm Slo.
<p><b>A</b>. Representative traces of Dm Slo whole cell currents stable expressed in CHO cells before (left hand traces) and after (right hand traces) emodepside (10 μM) application at different free intracellular [Ca<sup>2+</sup>] (“0 nM”, 52 nM and 290 nM as indicated). Emodepside was applied for 10 min for experiments with low free intracellular [Ca<sup>2+</sup>] (“0 nM” and 52 nM). Membrane potential was held at -70 mV and stepped to between -120 and +60 mV in 10 mV increments for 100 ms. <b>B</b>. Current-voltage relationship of Dm Slo whole cell currents after emodepside application at two different free intracellular Ca<sup>2+</sup> concentrations, as indicated. Membrane potential was held at -70 mV and stepped to between -120 and +60 mV in 10 mV increments for 100 ms. Data points are the mean ± s.e.mean of n cell recordings.</p
A comparison of the voltage and Ca<sup>2+</sup> -dependent activation of human KCNMA1 and <i>C</i>. <i>elegans</i> SLO-1a.
<p><b>A</b>. Representative traces of currents recorded from HEK293 cells expressing eGFP alone (control), Ce SLO-1 or hum KCNMA1. Membrane potential was held at -60mV and stepped to between -100 and +90mV in 10mV increments for 50ms. Free [Ca<sup>2+</sup>] in the internal solution was 300nM or 100μM as indicated. <b>B</b>. Current-voltage relationship for whole cell currents recorded from cells expressing eGFP alone (control), Ce SLO-1 or hum KCNMA1 at 300nM or 100μM free intracellular [Ca<sup>2+</sup>]. Membrane potential was held at -60mV and stepped to between -100 and +90mV in 10mV increments for 50ms. Data points are the mean ± s.e.mean of ‘n’ cell recordings (shown in brackets). Currents recorded from Ce SLO-1 in the presence of 300nM Ca<sup>2+</sup>, Ce SLO-1 in the presence of 100μM Ca<sup>2+</sup> and hum KCNMA1 in the presence of 300nM Ca<sup>2+</sup> were significantly different from eGFP recorded in 300nM and 100μM Ca<sup>2+</sup>; p<0.001, two-way ANOVA with Bonferroni post-hoc test.</p