1,019 research outputs found

    Surviving Bacterial Predation: A Comparative Study Between Predation Persistence and Antibiotic Persistence

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    Department of Biological SciencesMany infectious diseases may one day become uncontrollable. Thus, antibiotic-resistant bacteria have become a serious issue. And as the failing of antibiotics becoming a big problem, the needs for finding new antimicrobial agents are increasing. For an alternative of antibiotics, predatory bacteria are a promising approach since Bdellovibrio bacteriovorus is an obligate predator of other Gram-negative bacteria. However, even after predation by B. bacteriovorus, a small sub-population of prey cells remains a characteristic that is similar to bacterial persisters. And in a long-term predation in the continuous system was conducted to characterize these remaining sub-population of prey. One interesting finding from long-term predation is phenotypic changes of prey. So-called small colony variants (SCVs). The bacterial persisters are a small sub-population of the entire culture that exists within a dormant state and, although they lack any genetic mutations or modifications, they survive longer during exposures to antibiotics due to this temporal state. As these persister cells survive in the presence of different antibiotics, their existence is considered important as they may cause chronic or recurrent infections. In this study, I characterized both persister cells induced by a pre-treatment with antibiotics, i.e., antibiotic persisters (AP), and the sub-population of prey cells which survive predation by B. bacteriovorus HD100, i.e., the predation persisters (PP) cells. I found AP cells were also resistant to B. bacteriovorus predation and, conversely, the PP cells were better at surviving antibiotic treatments. The characteristics of these cultures were studied further to find common features for the two persister populations, by comparing the expression level of persister related genes in SCVs using transcriptome analysis.clos

    The effect of ephedrine on intraoperative hypothermia

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    BACKGROUND: Prevention of intraoperative hypothermia has become a standard of operative care. Since ephedrine has a thermogenic effect and it is frequently used to treat hypotension during anesthesia, this study was designed to determine the effect of ephedrine on intraoperative hypothermia of patients who are undergoing spine surgery. METHODS: Twenty-four patients were randomly divided to receive an ephedrine (the ephedrine group, n = 12) or normal saline (the control group, n = 12) infusion for 2 h. The esophageal temperature (the core temperature), the index finger temperature (the peripheral temperature) and the hemodynamic variables such as the mean blood pressure and heart rate were measured every 15 minutes after the intubation. RESULTS: At the end of the study period, the esophageal temperature and hemodynamic variables were significantly decreased in the control group, whereas those in the ephedrine group were stably maintained. The index finger temperature was significantly lower in the ephedrine group compared to that in the control group, suggesting the prevention of core-to-peripheral redistribution of the heat as the cause of temperature maintenance. CONCLUSIONS: An intraoperative infusion of ephedrine minimized the decrease of the core temperature and it stably maintained the hemodynamic variables during spine surgery with the patient under general anesthesia.ope

    Utilizing Latent Multi-Redox Activity of p-Type Organic Cathode Materials toward High Energy Density Lithium-Organic Batteries

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    Organic electrode materials hold great potential due to their cost-efficiency, eco-friendliness, and possibly high theoretical capacity. Nevertheless, most organic cathode materials exhibit a trade-off relationship between the specific capacity and the voltage, failing to deliver high energy density. Herein, it is shown that the trade-off can be mitigated by utilizing the multi-redox capability of p-type electrodes, which can significantly increase the specific capacity within a high-voltage region. The molecular structure of 5,10-dihydro-5,10-dimethylphenazine is modified to yield a series of phenoxazine and phenothiazine derivatives with elevated redox potentials by substitutions. Subsequently, the feasibility of the multi-redox capability is scrutinized for these high-voltage p-type organic cathodes, achieving one of the highest energy densities. It is revealed that the seemingly impractical second redox reaction is indeed dependent on the choice of the electrolyte and can be reversibly realized by tailoring the donor number and the salt concentration of the electrolyte, which places the voltage of the multi-redox reaction within the electrochemical stability window. The results demonstrate that high-energy-density organic cathodes can be practically achieved by rational design of multi-redox p-type organic electrode materials and the compatibility consideration of the electrolyte, opening up a new avenue toward advanced organic rechargeable batteries.

    Resting-state EEG activity related to impulsivity in gambling disorder

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    Background and aims Impulsivity is a core feature of gambling disorder (GD) and is related to the treatment response. Thus, it is of interest to determine objective neurobiological markers associated with impulsivity in GD. We explored resting-state electroencephalographic (EEG) activity in patients with GD according to the degree of impulsivity. Methods In total, 109 GD subjects were divided into three groups according to Barratt impulsiveness scale-11 (BIS-11) scores: high (HI; 25th percentile of BIS-11 scores, n = 29), middle (MI; 26th–74th percentile, n = 57), and low-impulsivity (LI) groups (75th percentile, n = 23). We used generalized estimating equations to analyze differences in EEG absolute power considering group (HI, MI, and LI), brain region (frontal, central, and posterior), and hemisphere (left, midline, and right) for each frequency band (delta, theta, alpha, beta, and gamma). Results The results indicated that GD patients in the HI group showed decreased theta absolute power, and decreased alpha and beta absolute power in the left, right, particularly midline frontocentral regions. Discussion and conclusions This study is a novel attempt to reveal impulsive features in GD by neurophysiological methods. The results suggest different EEG patterns among GD patients according to the degree of impulsivity, raising the possibility of neurophysiological objective features in GD and helping clinicians in treating GD patients with impulsive features

    Hu.4-1BB-Fc fusion protein inhibits allergic inflammation and airway hyperresponsiveness in a murine model of asthma

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    Purpose4-1BB (CD 137) is a costimulatory molecule expressed on activated T-cells. Repression by 4-1BB is thought to attenuate Th2-mediated allergic reactions. The aim of this study was to investigate the effect of 4-1BB on allergic airway inflammation in a murine asthma model.MethodsBALB/c mice were sensitized to and challenged with ovalbumin (OVA). Hu.4-1BB-Fc was administered 1 day before the first OVA sensitization or 1 day after the second OVA sensitization. Following antigen challenge, airway responsiveness to methacholine was assessed and bronchoalveolar lavage (BAL) fluid was analyzed. Total immunoglobulin (Ig) E, OVA-specific IgE, IgG1, and IgG2a levels in sera were measured by enzyme-linked immunosorbent assay. Lung pathology was also evaluated.ResultsIn mice treated with Hu.4-1BB-Fc before the first OVA sensitization, there was a marked decrease in airway hyperresponsiveness, total cell count, and eosinophil count in the BAL fluid. In addition, Hu.4-1BB-Fc treatment decreased serum OVA-specific IgG1 levels and increased serum IgG2a level significantly compared with the corresponding levels in mice sensitized to and challenged with OVA. Hu.4-1BB-Fc-treated mice also showed suppressed peribronchial and perivascular inflammatory cell infiltration. In contrast, treatment with Hu.4-1BB-Fc 1 day after sensitization had no effect on airway hyperresponsiveness and showed less suppression of inflammation in lung tissue.ConclusionAdministration of Hu.4-1BB-Fc can attenuate airway inflammation and hyperreactivity in a mouse model of allergic airway inflammation. In addition, administration before sensitization may be more effective. These findings suggest that 4-1BB may be a useful therapeutic molecule against asthma
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