80 research outputs found

    Radio Sources from a 31 GHz Sky Survey with the Sunyaev-Zel'dovich Array

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    We present the first sample of 31-GHz selected sources to flux levels of 1 mJy. From late 2005 to mid 2007, the Sunyaev-Zel'dovich Array (SZA) observed 7.7 square degrees of the sky at 31 GHz to a median rms of 0.18 mJy/beam. We identify 209 sources at greater than 5 sigma significance in the 31 GHz maps, ranging in flux from 0.7 mJy to ~200 mJy. Archival NVSS data at 1.4 GHz and observations at 5 GHz with the Very Large Array are used to characterize the sources. We determine the maximum-likelihood integrated source count to be N(>S) = (27.2 +- 2.5) deg^-2 x (S_mJy)^(-1.18 +- 0.12) over the flux range 0.7 - 15 mJy. This result is significantly higher than predictions based on 1.4-GHz selected samples, a discrepancy which can be explained by a small shift in the spectral index distribution for faint 1.4-GHz sources. From comparison with previous measurements of sources within the central arcminute of massive clusters, we derive an overdensity of 6.8 +- 4.4, relative to field sources.Comment: 13 pages, 5 figure

    Adaptive immunity restricts replication of novel murine astroviruses

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    The mechanisms of astrovirus pathogenesis are largely unknown, in part due to a lack of a small-animal model of disease. Using shotgun sequencing and a custom analysis pipeline, we identified two novel astroviruses capable of infecting research mice, murine astrovirus (MuAstV) STL1 and STL2. Subsequent analysis revealed the presence of at least two additional viruses (MuAstV STL3 and STL4), suggestive of a diverse population of murine astroviruses in research mice. Complete genomic characterization and subsequent phylogenetic analysis showed that MuAstV STL1 to STL4 are members of the mamastrovirus genus and are likely members of a new mamastrovirus genogroup. Using Rag1(−/−) mice deficient in B and T cells, we demonstrate that adaptive immunity is required to control MuAstV infection. Furthermore, using Stat1(−/−) mice deficient in innate signaling, we demonstrate a role for the innate immune response in the control of MuAstV replication. Our results demonstrate that MuAstV STL permits the study of the mechanisms of astrovirus infection and host-pathogen interactions in a genetically manipulable small-animal model. Finally, we detected MuAstV in commercially available mice, suggesting that these viruses may be present in academic and commercial research mouse facilities, with possible implications for interpretation of data generated in current mouse models of disease

    Application of a Self-Similar Pressure Profile to Sunyaev-Zel'dovich Effect Data from Galaxy Clusters

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    We investigate the utility of a new, self-similar pressure profile for fitting Sunyaev-Zel'dovich (SZ) effect observations of galaxy clusters. Current SZ imaging instruments - such as the Sunyaev-Zel'dovich Array (SZA) - are capable of probing clusters over a large range in physical scale. A model is therefore required that can accurately describe a cluster's pressure profile over a broad range of radii, from the core of the cluster out to a significant fraction of the virial radius. In the analysis presented here, we fit a radial pressure profile derived from simulations and detailed X-ray analysis of relaxed clusters to SZA observations of three clusters with exceptionally high quality X-ray data: A1835, A1914, and CL J1226.9+3332. From the joint analysis of the SZ and X-ray data, we derive physical properties such as gas mass, total mass, gas fraction and the intrinsic, integrated Compton y-parameter. We find that parameters derived from the joint fit to the SZ and X-ray data agree well with a detailed, independent X-ray-only analysis of the same clusters. In particular, we find that, when combined with X-ray imaging data, this new pressure profile yields an independent electron radial temperature profile that is in good agreement with spectroscopic X-ray measurements.Comment: 28 pages, 6 figures, accepted by ApJ for publication (probably April 2009

    A surface groove essential for viral Bcl-2 function during chronic infection in vivo

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    Antiapoptotic Bcl-2 family proteins inhibit apoptosis in cultured cells by binding BH3 domains of proapoptotic Bcl-2 family members via a hydrophobic BH3 binding groove on the protein surface. We investigated the physiological importance of the BH3 binding groove of an antiapoptotic Bcl-2 protein in mammals in vivo by analyzing a viral Bcl-2 family protein. We show that the gamma-herpesvirus 68 (gammaHV68) Bcl-2 family protein (gammaHV68 v-Bcl-2), which is known to inhibit apoptosis in cultured cells, inhibits both apoptosis in primary lymphocytes and Bax toxicity in yeast. Nuclear magnetic resonance determination of the gammaHV68 v-Bcl-2 structure revealed a BH3 binding groove that binds BH3 domain peptides from proapoptotic Bcl-2 family members Bax and Bak via a molecular mechanism shared with host Bcl-2 family proteins, involving a conserved arginine in the BH3 peptide binding groove. Mutations of this conserved arginine and two adjacent amino acids to alanine (SGR to AAA) within the BH3 binding groove resulted in a properly folded protein that lacked the capacity of the wild-type gammaHV68 v-Bcl-2 to bind Bax BH3 peptide and to block Bax toxicity in yeast. We tested the physiological importance of this v-Bcl-2 domain during viral infection by engineering viral mutants encoding a v-Bcl-2 containing the SGR to AAA mutation. This mutation resulted in a virus defective for both efficient reactivation of gammaHV68 from latency and efficient persistent gammaHV68 replication. These studies demonstrate an essential functional role for amino acids in the BH3 peptide binding groove of a viral Bcl-2 family member during chronic infection

    Cosmological Constraints from a 31 GHz Sky Survey with the Sunyaev-Zel'dovich Array

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    We present the results of a 6.1 square degree survey for clusters of galaxies via their Sunyaev- Zel'dovich (SZ) effect at 31 GHz. From late 2005 to mid 2007 the Sunyaev-Zel'dovich Array (SZA) observed four fields of roughly 1.5 square degrees each. One of the fields shows evidence for significant diffuse Galactic emission, and we therefore restrict our analysis to the remaining 4.4 square degrees. We estimate the cluster detectability for the survey using mock observations of simulations of clusters of galaxies; and determine that, at intermediate redshifts (z ~ 0.8), the survey is 50% complete to a limiting mass (M200 rho mean) of ~ 6.0 x 10^14M_{solar}, with the mass limit decreasing at higher redshifts. We detect no clusters at a significance greater than 5 times the RMS noise level in the maps, and place an upper limit on \sigma_8, the amplitude of mass density fluctuations on a scale of 8h^-1 Mpc, of 0.84 + 0.07 at 95% confidence, where the uncertainty reflects calibration and systematic effects. This result is consistent with estimates from other cluster surveys and CMB anisotropy experiments.Comment: 10 pages, 7 figures, 3 table

    LoCuSS: A Comparison of Sunyaev-Zel'dovich Effect and Gravitational Lensing Measurements of Galaxy Clusters

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    We present the first measurement of the relationship between the Sunyaev-Zel'dovich effect signal and the mass of galaxy clusters that uses gravitational lensing to measure cluster mass, based on 14 X-ray luminous clusters at z~0.2 from the Local Cluster Substructure Survey. We measure the integrated Compton y-parameter, Y, and total projected mass of the clusters (M_GL) within a projected clustercentric radius of 350 kpc, corresponding to mean overdensities of 4000-8000 relative to the critical density. We find self-similar scaling between M_GL and Y, with a scatter in mass at fixed Y of 32%. This scatter exceeds that predicted from numerical cluster simulations, however, it is smaller than comparable measurements of the scatter in mass at fixed T_X. We also find no evidence of segregation in Y between disturbed and undisturbed clusters, as had been seen with T_X on the same physical scales. We compare our scaling relation to the Bonamente et al. relation based on mass measurements that assume hydrostatic equilibrium, finding no evidence for a hydrostatic mass bias in cluster cores (M_GL = 0.98+/-0.13 M_HSE), consistent with both predictions from numerical simulations and lensing/X-ray-based measurements of mass-observable scaling relations at larger radii. Overall our results suggest that the Sunyaev-Zel'dovich effect may be less sensitive than X-ray observations to the details of cluster physics in cluster cores.Comment: Minor changes to match published version: 2009 ApJL 701:114-11

    Observations of High-Redshift X-Ray Selected Clusters with the Sunyaev-Zel'dovich Array

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    We report measurements of the Sunyaev-Zel'dovich (SZ) effect in three high-redshift (0.89 ≤ z ≤ 1.03), X-ray selected galaxy clusters. The observations were obtained at 30 GHz during the commissioning period of a new, eight-element interferometer—the Sunyaev-Zel'dovich Array (SZA)—built for dedicated SZ effect observations. The SZA observations are sensitive to angular scales larger than those subtended by the virial radii of the clusters. Assuming isothermality and hydrostatic equilibrium for the intracluster medium and gas-mass fractions consistent with those for clusters at moderate redshift, we calculate electron temperatures, gas masses, and total cluster masses from the SZ data. The SZ-derived masses, integrated approximately to the virial radii, are 1.9^(+0.5)_(-0.4) × 10^(14) M_☉ for Cl J1415.1+3612, 3.4^(+0.6)_(-0.5) × 10^(14) M_☉ for Cl J1429.0+4241, and 7.2^(+1.3)_(-0.9) × 10^(14) M_☉ for Cl J1226.9+3332. The SZ-derived quantities are in good agreement with the cluster properties derived from X-ray measurements

    A Measurement of Arcminute Anisotropy in the Cosmic Microwave Background with the Sunyaev-Zel'dovich Array

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    We present 30 GHz measurements of the angular power spectrum of the cosmic microwave background (CMB) obtained with the Sunyaev-Zel'dovich Array. The measurements are sensitive to arcminute angular scales, where secondary anisotropy from the Sunyaev-Zel'dovich effect (SZE) is expected to dominate. For a broad bin centered at multipole 4066 we find 67+77-50 uK^2, of which 26+/-5 uK^2 is the expected contribution from primary CMB anisotropy and 80+/-54 uK^2 is the expected contribution from undetected radio sources. These results imply an upper limit of 155 uK^2 (95% CL) on the secondary contribution to the anisotropy in our maps. This level of SZE anisotropy power is consistent with expectations based on recent determinations of the normalization of the matter power spectrum, i.e., sigma_8~0.8.Comment: ApJ, 713, 82-89, (2010

    Research priorities in the field of posttraumatic pain and disability: Results of a transdisciplinary consensus-generating workshop

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    © Copyright 2016 David M.Walton et al. Background. Chronic or persistent pain and disability following noncatastrophic \u27musculoskeletal\u27 (MSK) trauma is a pervasive public health problem. Recent intervention trials have provided little evidence of benefit from several specific treatments for preventing chronic problems. Such findings may appear to argue against formal targeted intervention for MSK traumas. However, these negative findings may reflect a lack of understanding of the causal mechanisms underlying the transition from acute to chronic pain, rendering informed and objective treatment decisions difficult. The Canadian Institutes of Health Research (CIHR) Institute ofMusculoskeletalHealth and Arthritis (IMHA) has recently identified better understanding of causalmechanisms as one of three priority foci of their most recent strategic plan. Objectives. A 2-day invitation-only active participation workshop was held inMarch 2015 that included 30 academics, clinicians, and consumers with the purpose of identifying consensus research priorities in the field of trauma-relatedMSK pain and disability, prediction, and prevention. Methods. Conversations were recorded, explored thematically, and member-checked for accuracy. Results. From the discussions, 13 themes were generated that ranged from a focus on identifying causal mechanisms and models to challenges with funding and patient engagement. Discussion. Novel priorities included the inclusion of consumer groups in research from the early conceptualization and design stages and interdisciplinary longitudinal studies that include evaluation of integrated phenotypes and mechanisms
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