Moreover, the universality of the ASM-mDON model was further confirmed by simulating mDON production in a full-scale wastewater treatment plant. A reasonable prediction of mDON formation was shown in a full-scale test (1.98 ± 0.71 mg/L in June and 1.51 ± 0.54 mg/L in July) and is indirectly supported by an algal bioassay (p less then 0.05, t-test). This study provides a useful approach to the efficient and accurate evaluation of mDON formation, which will improve current strategies designed to minimize the effluent mDON in wastewater bioprocesses. Using persulfate (PS) oxidation to remove the persistent perfluorooctanoic acid (PFOA) in water typically requires an elevated temperature or an extended reaction time. Under relatively ambient temperatures (15-45 °C), feasibility of employing PS with iron-modified activated carbon (AC) for PFOA oxidation was evaluated. With presence of Fe/AC in PS oxidation, 61.7% of PFOA was decomposed to fluoride ions and intermediates of short-chain perfluorinated carboxylic acids (PFCAs) with a 41.9% defluorination efficiency at 25 °C after 10 h. Adsorption of PFOA onto Fe/AC can be regarded as a pre-concentration step prior to subsequent oxidation of PFOA. Fe/AC not only removes PFOA through adsorption, but also activates PS to form sulfate radicals that accelerate the decomposition and mineralization of PFOA. With Fe/AC in the PS system, activation energies (Ea) of PFOA removal and defluorination were significantly reduced from 66.8 to 13.2 and 97.3 to 14.5 kJ/mol, respectively. It implies that PFOA degradation and defluorination could proceed at a lower reaction temperature within a shorter reaction time. Besides, the surface characteristics of AC and Fe/AC before and after PS oxidation were evaluated by XPS and SEM. A quenching test used MeOH as an inhibitor and EPR spectra of free radicals were conducted to develop the proposed reaction mechanisms for PFOA oxidation. The sources of microplastics and other anthropogenic particles in freshwater are not well understood. The Greater Toronto Area, Canada's most populous urban area, offers a great study area for understanding the sources and pathways for microplastics to enter freshwater ecosystems. Here, we quantified and characterized microplastics and other anthropogenic particles from Lake Ontario surface waters and source waters (including stormwater runoff, agricultural runoff, and treated wastewater effluent) to better understand sources to the Great Lakes. Anthropogenic particle concentrations in lake samples were 0.8 particles L-1. In source waters, average concentrations were relatively higher in stormwater and wastewater, with 15.4 particles L-1 and 13.3 particles L-1, respectively, compared to 0.9 particles L-1 on average in agricultural runoff. Source waters revealed distinct signatures related to the morphologies of anthropogenic particles, e.g., fibers in wastewater. In addition, many upstream watershed characteristics were found to be significant predictors of anthropogenic particle concentration. Proximity to urban areas were positively correlated to anthropogenic particle concentrations. Future studies should focus on local source-apportionment to inform management and prevent further contamination of microplastics to freshwater ecosystems. A hierarchically assembled superomniphobic membrane with three levels of reentrant structure was designed and fabricated to enable effective treatment of low surface tension, hypersaline oily wastewaters using direct contact membrane distillation (DCMD). The overall structure is a combination of macro corrugations obtained by surface imprinting, with the micro spherulites morphology achieved through the applied phase inversion method and nano patterns obtained by fluorinated Silica nanoparticles (SiNPs) coating. This resulted in a superomniphobic membrane surface with remarkable anti-wetting properties repelling both high surface tension water and low surface tension oils. Measurements of contact angle (CA) with DI water, an anionic surfactant, oil, and ethanol demonstrated a robust wetting resistance against low surface tension liquids showing both superhydrophobicity and superoleophobicity. CA values of 160.8 ± 2.3° and 154.3 ± 1.9° for water and oil were obtained, respectively. Calculations revealed a high liquid-vapor interface for the fabricated membrane with more than 89% of the water droplet contact area being with air pockets entrapped between adjacent SiNPs and only 11% come into contact with the solid membrane surface. Moreover, the high liquid-vapor interface imparts the membrane with high liquid repellency, self-cleaning and slippery effects, characterized by a minimum droplet-membrane interaction and complete water droplet bouncing on the surface within only 18 ms. When tested in DCMD with synthetic hypersaline oily wastewaters, the fabricated superomniphobic membrane demonstrated stable, non-wetting MD operation over 24 h, even at high concentrations of low surface tension 1.0 mM Sodium dodecyl sulfate and 400 ppm oil, potentially offering a sustainable option for treatment of low surface tension oily industrial wastewater. OBJECTIVES Resistance to polymyxins has been increasing in many regions and appropriate determination of polymyxin susceptibility is now a major challenge worldwide. Many clinical laboratories rely on gradient diffusion methods to assess polymyxin susceptibility, although broth microdilution (BMD) is the only method currently recommended by CLSI and EUCAST. The aim of this work was to assess the performance of polymyxin B (PMB) Etest® in a setting with high prevalence of KPC-producing K. pneumoniae. METHODS The commercial Etest® susceptibility testing method was evaluated and compared to the reference BMD, considering isolates with a minimal inhibitory concentration (MIC) ≤ 2 mg/L for PMB as susceptible to this drug. A total of 310 clinical isolates of KPC-producing K. https://www.selleckchem.com/products/smoothened-agonist-sag-hcl.html pneumoniae were evaluated. RESULTS Susceptibility was significantly higher by Etest® compared with BMD (82.6% versus 75.8%, respectively). The MIC50, MIC90 and modal MICs for PMB were 0.25, 32 and 0.25 mg/L (27.1%) by BMD and 0.5, 16 and 0.5 mg/L (49.7%) by Etest® method, respectively. Although categorical agreement was 90%, there was a poor essential agreement (53.9%) between them. A high rate (34.7%) of very major error (VME) and a relatively low rate (2.1%) of major errors were found. CONCLUSIONS The considerable number of resistant isolates in this study allowed an accurate estimation of VME rates and, consequently, a more comprehensive assessment in susceptibility testing for polymyxins. Etest® did not meet fully acceptance criteria for the FDA requirements. Our data do not support the use of this commercial method for determining PMB MICs in carbapenem-resistant Enterobacterales populations. While ectoparasitic Varroa mites cause minimal damage to their co-evolved ancestral host, the eastern honey bee (Apis cerana), they devastate their novel host, the western honey bee (Apis mellifera). Over several decades, the host switch caused worldwide population collapses, threatening global food security. Varroa management strategies have focused on breeding bees for tolerance. But, can Varroa overcome these counter-adaptations in a classic coevolutionary arms race? Despite increasing evidence for Varroa genetic diversity and evolvability, this eventuality has largely been neglected. We therefore suggest a more holistic paradigm for studying this host-parasite interaction, one in which 'Varroa-tolerant' bee traits should be viewed as a shared phenotype resulting from Varroa and honey bee interaction. L-DOPA-induced dyskinesia (LID) is a major complication of long-term dopamine replacement therapy in Parkinson's disease. Characteristic neural oscillation and abnormal activity of striatal projection neurons (SPNs) are typical pathological events of LID, which would be reliable biomarkers for assessment of novel anti-dyskinetic approach if fully profiled. Glutamate dysregulation plays a critical role in the development of LID, and the group II metabotropic glutamate receptors (mGluR2/3) is believed to regulate the release of glutamate on the presynaptic terminals and inhibits postsynaptic excitation. However, the anti-dyskinetic effect of modulating mGluR2/3 is still unclear. In this study, rats with unilateral dopaminergic lesion were injected with L-DOPA (12 mg/kg, i.p.) for seven days, while motor behavior was correlated with in vivo electrophysiology analyzing LFP and single-cell activity in both primary motor cortex and dorsolateral striatum. Our study showed that as LID established, high γ oscillation (hγ) predominated during LID, the number of unstable responses of SPN to dopamine increased, and the coherence between these patterns of oscillation and spiking activity also increased. We found that pretreatment of NMDA receptor antagonist, amantadine 60 mg/kg, i.p. (AMAN) significantly reduced abnormal involuntary movements (AIMs), in parallel with the reduction of hγ oscillation, and more markedly with a decrease in unstable responses of SPNs. In contrast, a mGluR2/3 agonist, LY354740 12 mg/kg, i.p. (LY) significantly shortened the duration of LID but merely exhibited a weak effect in diminishing the intensity of LID or reversing SPN responses. Together results indicate that AIMs in the rat model of PD are associated with abnormal corticostriatal signaling, which could be reversed by NMDAR antagonism more efficiently than mGluR2/3 agonism. The cytoplasmic dynein motor complex transports essential signals and organelles from the cell periphery to perinuclear region, hence is critical for the survival and function of highly polarized cells such as neurons. Dynein Light Chain Roadblock-Type 1 (DYNLRB1) is thought to be an accessory subunit required for specific cargos, but here we show that it is essential for general dynein-mediated transport and sensory neuron survival. Homozygous Dynlrb1 null mice are not viable and die during early embryonic development. Furthermore, heterozygous or adult knockdown animals display reduced neuronal growth, and selective depletion of Dynlrb1 in proprioceptive neurons compromises their survival. Conditional depletion of Dynlrb1 in sensory neurons causes deficits in several signaling pathways, including β-catenin subcellular localization, and a severe impairment in the axonal transport of both lysosomes and retrograde signaling endosomes. Hence, DYNLRB1 is an essential component of the dynein complex, and given dynein's critical functions in neuronal physiology, DYNLRB1 could have a prominent role in the etiology of human neurodegenerative diseases. BACKGROUND AND AIM Patients with Parkinson's disease (PD) are often characterized by functional gastrointestinal disorders. Such disturbances can occur at all stages of PD and precede the typical motor symptoms of the disease by many years. However, the morphological alterations associated with intestinal disturbances in PD are undetermined. This study examined the remodelling of colonic wall in 6-hydroxydopamine (6-OHDA)-induced PD rats. METHODS 8 weeks after 6-OHDA injection animals were sacrificed. Inflammatory infiltrates, collagen deposition and remodelling of intestinal epithelial barrier and tunica muscularis in the colonic wall were assessed by histochemistry, immunohistochemistry, immunofluorescence and western blot analysis. RESULTS 6-OHDA rats displayed significant alterations of colonic tissues as compared with controls. Signs of mild inflammation (eosinophil infiltration) and a transmural deposition of collagen fibres were observed. Superficial colonic layers were characterized by severe morphological alterations.