Increased human pathogenic potential of Escherichia coli from polymicrobial urinary tract infections in comparison to isolates from monomicrobial culture samples

The current diagnostic standard procedure outlined by the Health Protection Agency for urinary tract infections (UTIs) in clinical laboratories does not report bacteria isolated from samples containing three or more different bacterial species. As a result many UTIs go unreported and untreated, particularly in elderly patients, where polymicrobial UTI samples are especially prevalent. This study reports the presence of the major uropathogenic species in mixed culture urine samples from elderly patients, and of resistance to front-line antibiotics, with potentially increased levels of resistance to ciprofloxacin and trimethoprim. Most importantly, the study highlights that Escherichia coli present in polymicrobial UTI samples are statistically more invasive (P<0.001) in in vitro epithelial cell infection assays than those isolated from monomicrobial culture samples. In summary, the results of this study suggest that the current diagnostic standard procedure for polymicrobial UTI samples needs to be reassessed, and that E. coli present in polymicrobial UTI samples may pose an increased risk to human health

Near-IR imaging of T Cha: evidence for scattered-light disk structures at solar system scales

T Chamaeleontis is a young star surrounded by a transitional disk, and a plausible candidate for ongoing planet formation. Recently, a substellar companion candidate was reported within the disk gap of this star. However, its existence remains controversial, with the counter-hypothesis that light from a high inclination disk may also be consistent with the observed data. The aim of this work is to investigate the origin of the observed closure phase signal to determine if it is best explained by a compact companion. We observed T Cha in the L and K s filters with sparse aperture masking, with 7 datasets covering a period of 3 years. A consistent closure phase signal is recovered in all L and K s datasets. Data were fit with a companion model and an inclined circumstellar disk model based on known disk parameters: both were shown to provide an adequate fit. However, the absence of expected relative motion for an orbiting body over the 3-year time baseline spanned by the observations rules out the companion model. Applying image reconstruction techniques to each dataset reveals a stationary structure consistent with forward scattering from the near edge of an inclined disk.Comment: 6 pages, 3 figures, accepted for publication in MNRAS Letter

Test-retest reliability of segment kinetic energy measures in the golf swing

Analyses of segment kinetic energy (KE) can provide the most appropriate means of exploring sequential movements. As the reliability associated with its measurement has not been reported, the aim of this study was to examine the test-retest reliability of segment KE measures in the golf swing. On two occasions, seven male golfers hit five shots with three different clubs. Body segment inertia parameters were estimated for 17 rigid bodies and 3D kinematic data were collected during each swing. The magnitude and timing of peak total, linear and angular kinetic energies were then calculated for each rigid body and for four segment groups. Regardless of club type, KE was measured with high reliability for almost all rigid bodies and segment groups. However, significantly larger magnitudes of peak total (p = 0.039) and linear (p = 0.021) lower body KE were reported in test 2 than in test 1. The high reliability reported in this study provides support for the use of analyses of segment kinetic energy. However, practitioners should pay careful attention to the identification of anatomical landmarks which define the thigh, pelvis and thorax as this was the main cause of variability in repeated measures of segment kinetic energy

Induced Pluripotent Stem Cells for Inherited Optic Neuropathies—Disease Modeling and Therapeutic Development

Background: Inherited optic neuropathies (IONs) cause progressive irreversible visual loss in children and young adults. There are limited disease-modifying treatments, and most patients progress to become severely visually impaired, fulfilling the legal criteria for blind registration. The seminal discovery of the technique for reprogramming somatic nondividing cells into induced pluripotent stem cells (iPSCs) has opened several exciting opportunities in the field of ION research and treatment. / Evidence Acquisition: A systematic review of the literature was conducted with PubMed using the following search terms: autosomal dominant optic atrophy, ADOA, dominant optic atrophy, DOA, Leber hereditary optic neuropathy, LHON, optic atrophy, induced pluripotent stem cell, iPSC, iPSC derived, iPS, stem cell, retinal ganglion cell, and RGC. Clinical trials were identified on the ClinicalTrials.gov website. / Results: This review article is focused on disease modeling and the therapeutic strategies being explored with iPSC technologies for the 2 most common IONs, namely, dominant optic atrophy and Leber hereditary optic neuropathy. The rationale and translational advances for cell-based and gene-based therapies are explored, as well as opportunities for neuroprotection and drug screening. / Conclusions: iPSCs offer an elegant, patient-focused solution to the investigation of the genetic defects and disease mechanisms underpinning IONs. Furthermore, this group of disorders is uniquely amenable to both the disease modeling capability and the therapeutic potential that iPSCs offer. This fast-moving area will remain at the forefront of both basic and translational ION research in the coming years, with the potential to accelerate the development of effective therapies for patients affected with these blinding diseases

The role of the ER stress response protein PERK in rhodopsin retinitis pigmentosa

Mutations in rhodopsin, the light sensitive protein of rod cells, are the most common cause of dominant retinitis pigmentosa (RP), a type of inherited blindness caused by the dysfunction and death of photoreceptor cells. The P23H mutation, the most frequent single cause of RP in the USA, causes rhodopsin misfolding and induction of the unfolded protein response (UPR), an adaptive ER stress response and signalling network that aims to enhance the folding and degradation of misfolded proteins to restore proteostasis. Prolonged UPR activation, and in particular the PERK branch, can reduce protein synthesis and initiate cell death through induction of pro-apoptotic pathways. Here, we investigated the effect of pharmacological PERK inhibition on retinal disease process in the P23H-1 transgenic rat model of retinal degeneration. PERK inhibition with GSK2606414A led to an inhibition of eIF2α phosphorylation, which correlated with reduced ERG function and decreased photoreceptor survival at both high and low doses of PERK inhibitor. Additionally, PERK inhibition increased the incidence of inclusion formation in cultured cells overexpressing P23H rod opsin, and increased rhodopsin aggregation in the P23H-1 rat retina, suggesting enhanced P23H misfolding and aggregation. In contrast, treatment of P23H-1 rats with an inhibitor of eIF2α phosphatase, salubrinal, led to improved photoreceptor survival. Collectively, these data suggest the activation of PERK is part of a protective response to mutant rhodopsin that ultimately limits photoreceptor cell death

A new route for the synthesis of open-framework metal phosphates using organophosphates

Use of tributylphosphate, an organophosphate, as the phosphorus source in place of phosphoric acid, has enabled the synthesis of several new open-framework zinc(II) and cobalt(II) phosphates, under solvothermal conditions

Optimization of Brownian ratchets for the manipulation of charged components within supported lipid bilayers

In probability theory, there is a counter-intuitive result that it is possible to construct a winning strategy from two individually losing (or at most breaking-even) "games" by alternating between them. The work presented here demonstrates the application of this principle to supported lipid bilayers (SLBs) in order to create directed motion of charged lipid components in the membrane, which was achieved through the use of "Brownian ratchets" in patterned SLBs. Both a finite element analysis model and an experimental setup have been used to investigate the role of key parameters for the operation of these ratchets: (1) the asymmetry of the ratchet teeth and (2) the relation of the ratchet height to the period of the applied electric field. Importantly, we find that the efficiency of the ratchet for a given charged species is dependent on the diffusion coefficient. This opens the possibility for separation of membrane species according to their size or viscous drag coefficient within the membrane

Non-perturbative approach for the time-dependent symmetry breaking

We present a variational method which uses a quartic exponential function as a trial wave-function to describe time-dependent quantum mechanical systems. We introduce a new physical variable $y$ which is appropriate to describe the shape of wave-packet, and calculate the effective action as a function of both the dispersion $\sqrt{}$ and $y$. The effective potential successfully describes the transition of the system from the false vacuum to the true vacuum. The present method well describes the long time evolution of the wave-function of the system after the symmetry breaking, which is shown in comparison with the direct numerical computations of wave-function.Comment: 8 pages, 3 figure

Oxide phosphors for light upconversion; Yb3+ and Tm3+ co-doped Y2BaZnO5

Copyright 2011 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. This article appeared in Journal of Applied Physics 109, 063104 (2011) and may be found at