952 research outputs found

    A Shift in Central Metabolism Accompanies Virulence Activation in Pseudomonas aeruginosa.

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    The availability of energy has significant impact on cell physiology. However, the role of cellular metabolism in bacterial pathogenesis is not understood. We investigated the dynamics of central metabolism during virulence induction by surface sensing and quorum sensing in early-stage biofilms of the multidrug-resistant bacterium Pseudomonas aeruginosa We established a metabolic profile for P. aeruginosa using fluorescence lifetime imaging microscopy (FLIM), which reports the activity of NADH in live cells. We identified a critical growth transition period during which virulence is activated. We performed FLIM measurements and direct measurements of NADH and NAD+ concentrations during this period. Here, planktonic (low-virulence) and surface-attached (virulence-activated) populations diverged into distinct metabolic states, with the surface-attached population exhibiting FLIM lifetimes that were associated with lower levels of enzyme-bound NADH and decreasing total NAD(H) production. We inhibited virulence by perturbing central metabolism using citrate and pyruvate, which further decreased the enzyme-bound NADH fraction and total NAD(H) production and suggested the involvement of the glyoxylate pathway in virulence activation in surface-attached populations. In addition, we induced virulence at an earlier time using the electron transport chain oxidase inhibitor antimycin A. Our results demonstrate the use of FLIM to noninvasively measure NADH dynamics in biofilms and suggest a model in which a metabolic rearrangement accompanies the virulence activation period.IMPORTANCE The rise of antibiotic resistance requires the development of new strategies to combat bacterial infection and pathogenesis. A major direction has been the development of drugs that broadly target virulence. However, few targets have been identified due to the species-specific nature of many virulence regulators. The lack of a virulence regulator that is conserved across species has presented a further challenge to the development of therapeutics. Here, we identify that NADH activity has an important role in the induction of virulence in the pathogen P. aeruginosa This finding, coupled with the ubiquity of NADH in bacterial pathogens, opens up the possibility of targeting enzymes that process NADH as a potential broad antivirulence approach

    Composing Information Literacy: A Pedagogical Partnership Between Rhet/Comp and Library Faculty

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    For more than a decade, the Program for Writing and Rhetoric (PWR) at the University of Colorado Boulder has partnered with teaching and learning librarians to design and deliver Information Literacy learning opportunities in first-year and upper-division composition classes. In recent years, this partnership has grown more robust as we have come to recognize that our two fields have much in common and are making similar pedagogical, theoretical, and practical moves. The guiding documents produced in both our fields (the ACRL’s “Framework for Information Literacy for Higher Education” and the WPA’s “Framework for Success in Post-Secondary Writing”) highlight the shared concerns and complementary values and educational goals of librarians and rhetoric and composition instructors. Additionally, the dynamic information and media environment in which we and our students live and work requires new kinds of information and digital literacies and thus new literacy curricula. As we began to re-think the PWR’s Information Literacy initiatives, we asked ourselves this question: If we could design a curriculum that no longer treats Information Literacy and Rhetoric and Composition as separate, and that acknowledges the complex information landscapes in which we reside and the multiple modes in which our students compose, what would it look like? For the past year, we have been developing this curriculum. In our presentation, we will provide an overview of this collaborative process, as well as the outcomes and materials developed. We will invite attendees to explore the characteristics of successful pedagogical partnerships dedicated to improving student learning through information literacy initiatives

    Kathryns Wheel: A spectacular galaxy collision discovered in the Galactic neighbourhood

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    We report the discovery of the closest collisional ring galaxy to the Milky Way. Such rare systems occur due to "bulls-eye" encounters between two reasonably matched galaxies. The recessional velocity of about 840 km/s is low enough that it was detected in the AAO/UKST Survey for Galactic Hα\alpha emission. The distance is only 10.0 Mpc and the main galaxy shows a full ring of star forming knots, 6.1 kpc in diameter surrounding a quiescent disk. The smaller assumed "bullet" galaxy also shows vigorous star formation. The spectacular nature of the object had been overlooked because of its location in the Galactic plane and proximity to a bright star and even though it is the 60th^{\rm th} brightest galaxy in the HI Parkes All Sky Survey (HIPASS) HI survey. The overall system has a physical size of ∌\sim15 kpc, a total mass of M∗=6.6×109M_\ast = 6.6\times 10^9 M⊙_\odot (stars + HI), a metallicity of [O/H]∌−0.4\sim-0.4, and a star formation rate of 0.2-0.5 M⊙_\odot\,yr−1^{-1}, making it a Magellanic-type system. Collisional ring galaxies therefore extend to much lower galaxy masses than commonly assumed. We derive a space density for such systems of 7×10−5 Mpc−37 \times 10^{-5}\,\rm Mpc^{-3}, an order of magnitude higher than previously estimated. This suggests Kathryn's Wheel is the nearest such system. We present discovery images, CTIO 4-m telescope narrow-band follow-up images and spectroscopy for selected emission components. Given its proximity and modest extinction along the line of sight, this spectacular system provides an ideal target for future high spatial resolution studies of such systems and for direct detection of its stellar populations.Comment: 18 pages, 12 figures, accepted for publication in MNRA

    Socioeconomic status, blood pressure progression, and incident hypertension in a prospective cohort of female health professionals

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    Aims The aim of this study was to examine the association between socioeconomic status, blood pressure (BP) progression, and incident hypertension. Methods and results We included 27 207 female health professionals free of hypertension and cardiovascular disease at baseline. Participants were classified into five education and six income categories. The main outcome variables were BP progression at 48 months of follow-up and incident hypertension during the entire study period. At 48 months, 48.1% of women had BP progression. The multivariable adjusted relative risks [95% confidence intervals (CIs)] for BP progression were 1.0 (referent), 0.96 (0.92-1.00), 0.92 (0.88-0.96), 0.90 (0.85-0.94), and 0.84 (0.78-0.91) (P for trend <0.0001) across increasing education categories and 1.0 (referent), 1.01 (0.94-1.08), 0.99 (0.93-1.06), 0.97 (0.91-1.04), 0.96 (0.90-1.03), and 0.89 (0.83-0.96) across increasing income categories (P for trend = 0.0001). During a median follow-up of 9.8 years, 8248 cases of incident hypertension occurred. Multivariable adjusted hazard ratios (95% CI) were 1.0 (referent), 0.92 (0.86-0.99), 0.85 (0.79-0.92), 0.87 (0.80-0.94), and 0.74 (0.65-0.84) (P for trend <0.0001) across increasing education categories and 1.0 (referent), 1.07 (0.95-1.21), 1.07 (0.95-1.20), 1.06 (0.94-1.18), 1.04 (0.93-1.16), and 0.93 (0.82-1.06) (P for trend 0.08) across increasing income categories. In joint analyses, education but not income remained associated with BP progression and incident hypertension. Conclusion Socioeconomic status, as determined by education but not by income, is a strong independent predictor of BP progression and incident hypertension in wome

    Cytokine-driven cell cycling is mediated through Cdc25A

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    Lymphocytes are the central mediators of the immune response, requiring cytokines for survival and proliferation. Survival signaling targets the Bcl-2 family of apoptotic mediators, however, the pathway for the cytokine-driven proliferation of lymphocytes is poorly understood. Here we show that cytokine-induced cell cycle progression is not solely dependent on the synthesis of cyclin-dependent kinases (Cdks) or cyclins. Rather, we observe that in lymphocyte cell lines dependent on interleukin-3 or interleukin-7, or primary lymphocytes dependent on interleukin 7, the phosphatase Cdc25A is the critical mediator of proliferation. Withdrawal of IL-7 or IL-3 from dependent lymphocytes activates the stress kinase, p38 MAPK, which phosphorylates Cdc25A, inducing its degradation. As a result, Cdk/cyclin complexes remain phosphorylated and inactive and cells arrest before the induction of apoptosis. Inhibiting p38 MAPK or expressing a mutant Cdc25A, in which the two p38 MAPK target sites, S75 and S123, are altered, renders cells resistant to cytokine withdrawal, restoring the activity of Cdk/cyclin complexes and driving the cell cycle independent of a growth stimulus
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