532 research outputs found

    Reptile Adenoviruses in cattle?

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    This paper describes a hypothesis on the origin of the members of the recently established adenovirus genus, Atadenovirus, invading cattle, sheep, deer, duck and poultry. Comparison of the phylogenetic trees of adenoviruses and their hosts suggests a very ancient but common origin for the atadenoviruses. The surprisingly large difference between these virus types and other adenoviruses infecting the same host can be easily understood by assuming their separate evolution in different hosts (e.g., in reptiles versus a coevolution with mammals and birds, respectively) followed by a later host switch

    The mutualistic fungus Piriformospora indica protects barley roots from a loss of antioxidant capacity caused by the necrotrophic pathogen Fusarium culmorum

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    Fusarium culmorum causes root rot in barley (Hordeum vulgare), resulting in severely reduced plant growth and yield. Pretreatment of roots with chlamydospores of the mutualistic root-colonizing basidiomycete Piriformospora indica (Agaricomycotina) prevented necrotization of root tissues and plant growth retardation commonly associated with Fusarium root rot. Quantification of Fusarium infections with a real-time PCR assay revealed a correlation between root rot symptoms and the relative amount of fungal DNA. Fusarium-infected roots showed reduced levels of ascorbate and glutathione (GSH), along with reduced activities of antioxidant enzymes such as superoxide dismutase (SOD), ascorbate peroxidase (APX), glutathione reductase (GR), dehydroascorbate reductase (DHAR), and monodehydroascorbate reductase (MDHAR). Consistent with this, Fusarium-infected roots showed elevated levels of lipid hydroperoxides and decreased ratios of reduced to oxidized forms of ascorbate and glutathione. In clear contrast, roots treated with P. indica prior to inoculation with F. culmorum showed levels of ascorbate and GSH that were similar to controls. Likewise, lipid peroxidation and the overall reduction in antioxidant enzyme activities were largely attenuated by P. indica in roots challenged by F. culmorum. These results suggest that P. indica protects roots from necrotrophic pathogens at least partly, through activating the plant’s antioxidant capacity

    3D Reconstruction for Partial Data Electrical Impedance Tomography Using a Sparsity Prior

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    In electrical impedance tomography the electrical conductivity inside a physical body is computed from electro-static boundary measurements. The focus of this paper is to extend recent result for the 2D problem to 3D. Prior information about the sparsity and spatial distribution of the conductivity is used to improve reconstructions for the partial data problem with Cauchy data measured only on a subset of the boundary. A sparsity prior is enforced using the 1\ell_1 norm in the penalty term of a Tikhonov functional, and spatial prior information is incorporated by applying a spatially distributed regularization parameter. The optimization problem is solved numerically using a generalized conditional gradient method with soft thresholding. Numerical examples show the effectiveness of the suggested method even for the partial data problem with measurements affected by noise.Comment: 10 pages, 3 figures. arXiv admin note: substantial text overlap with arXiv:1405.655

    Realtime calibration of the A4 electromagnetic lead fluoride calorimeter

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    Sufficient energy resolution is the key issue for the calorimetry in particle and nuclear physics. The calorimeter of the A4 parity violation experiment at MAMI is a segmented calorimeter where the energy of an event is determined by summing the signals of neighbouring channels. In this case the precise matching of the individual modules is crucial to obtain a good energy resolution. We have developped a calibration procedure for our total absorbing electromagnetic calorimeter which consists of 1022 lead fluoride (PbF_2) crystals. This procedure reconstructs the the single-module contributions to the events by solving a linear system of equations, involving the inversion of a 1022 x 1022-matrix. The system has shown its functionality at beam energies between 300 and 1500 MeV and represents a new and fast method to keep the calorimeter permanently in a well-calibrated state

    DNA sequence of a small, unidentified plasmid isolated from a Haemophilus somnus strain: Short communication

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    One of the plasmids present in a Haemophilus somnus strain isolated from nasal discharge of a cattle with respiratory disease was purified and cloned for DNA sequencing. The plasmid was found to be 1065 base pairs long with 39.2% G+C content, and showed no homology to any DNA sequenced so far. It has no capacity to code any protein longer than 43 residues. It is not clear yet if this plasmid codes Haemophilus somnus specific factors

    Characterisation of the fiber gene and partial sequence of the early region 4 of bovine adenovirus 2: Short communication

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    The full sequence of the fiber gene and partial sequence of the putative 17 kD protein gene of bovine adenovirus-2 (BAdV-2) were determined. The size of the fiber gene of BAdV-2 proved to be 561 amino acids, of which the amino acids 37 to 385 form a typical shaft domain of 22 repetitive motifs. On the complementary strand, a gene homologous to the 17 kD protein coded in the E4 region of several human adenoviruses was found. The sequence analysis seems to confirm the presence of an intron in the sequenced part of the E4 region

    Evidence for Strange Quark Contributions to the Nucleon's Form Factors at Q2Q^2 = 0.108 (GeV/c)2^2

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    We report on a measurement of the parity violating asymmetry in the elastic scattering of polarized electrons off unpolarized protons with the A4 apparatus at MAMI in Mainz at a four momentum transfer value of Q2Q^2 = \Qsquare (GeV/c)2^2 and at a forward electron scattering angle of 30<θe<40^\circ < \theta_e < 40^\circ. The measured asymmetry is ALR(ep)A_{LR}(\vec{e}p) = (\Aphys ±\pm \Deltastatstat_{stat} ±\pm \Deltasystsyst_{syst}) ×\times 106^{-6}. The expectation from the Standard Model assuming no strangeness contribution to the vector current is A0_0 = (\Azero ±\pm \DeltaAzero) ×\times 106^{-6}. We have improved the statistical accuracy by a factor of 3 as compared to our previous measurements at a higher Q2Q^2. We have extracted the strangeness contribution to the electromagnetic form factors from our data to be GEsG_E^s + \FakGMs GMsG_M^s = \GEsGMs ±\pm \DeltaGEsGMs at Q2Q^2 = \Qsquare (GeV/c)2^2. As in our previous measurement at higher momentum transfer for GEsG_E^s + 0.230 GMsG_M^s, we again find the value for GEsG_E^s + \FakGMs GMsG_M^s to be positive, this time at an improved significance level of 2 σ\sigma.Comment: 4 pages, 3 figure

    Measurement of the Transverse Beam Spin Asymmetry in Elastic Electron Proton Scattering and the Inelastic Contribution to the Imaginary Part of the Two-Photon Exchange Amplitude

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    We report on a measurement of the asymmetry in the scattering of transversely polarized electrons off unpolarized protons, A_\perp, at two Q2^2 values of \qsquaredaveragedlow (GeV/c)2^2 and \qsquaredaveragedhighII (GeV/c)2^2 and a scattering angle of 30<θe<4030^\circ < \theta_e < 40^\circ. The measured transverse asymmetries are A_{\perp}(Q2^2 = \qsquaredaveragedlow (GeV/c)2^2) = (\experimentalasymmetry alulowcorr ±\pm \statisticalerrorlowstat_{\rm stat} ±\pm \combinedsyspolerrorlowalucorsys_{\rm sys}) ×\times 106^{-6} and A_{\perp}(Q2^2 = \qsquaredaveragedhighII (GeV/c)2^2) = (\experimentalasymme tryaluhighcorr ±\pm \statisticalerrorhighstat_{\rm stat} ±\pm \combinedsyspolerrorhighalucorsys_{\rm sys}) ×\times 106^{-6}. The first errors denotes the statistical error and the second the systematic uncertainties. A_\perp arises from the imaginary part of the two-photon exchange amplitude and is zero in the one-photon exchange approximation. From comparison with theoretical estimates of A_\perp we conclude that π\piN-intermediate states give a substantial contribution to the imaginary part of the two-photon amplitude. The contribution from the ground state proton to the imaginary part of the two-photon exchange can be neglected. There is no obvious reason why this should be different for the real part of the two-photon amplitude, which enters into the radiative corrections for the Rosenbluth separation measurements of the electric form factor of the proton.Comment: 4 figures, submitted to PRL on Oct.

    Measurement of Strange Quark Contributions to the Nucleon's Form Factors at Q^2=0.230 (GeV/c)^2

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    We report on a measurement of the parity-violating asymmetry in the scattering of longitudinally polarized electrons on unpolarized protons at a Q2Q^2 of 0.230 (GeV/c)^2 and a scattering angle of \theta_e = 30^o - 40^o. Using a large acceptance fast PbF_2 calorimeter with a solid angle of \Delta\Omega = 0.62 sr the A4 experiment is the first parity violation experiment to count individual scattering events. The measured asymmetry is A_{phys} =(-5.44 +- 0.54_{stat} +- 0.27_{\rm sys}) 10^{-6}. The Standard Model expectation assuming no strangeness contributions to the vector form factors is A0=(6.30+0.43)106A_0=(-6.30 +- 0.43) 10^{-6}. The difference is a direct measurement of the strangeness contribution to the vector form factors of the proton. The extracted value is G^s_E + 0.225 G^s_M = 0.039 +- 0.034 or F^s_1 + 0.130 F^s_2 = 0.032 +- 0.028.Comment: 5 pages, 3 figures, submitted to Phys. Rev. Letters on Dec 11, 200

    Cold hardening protects cereals from oxidative stress and necrotrophic fungal pathogenesis

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    The effects of cold hardening of cereals on their cross-tolerance to treatments leading to oxidative stress were investigated. Long-term exposure to low non-freezing temperatures provided partial protection to wheat and barley plants from the damage caused by paraquat and hydrogen peroxide treatments. It also conferred resistance in two barley cultivars to the necrotic symptoms and growth of the fungal phytopathogen Pyrenophora teres f. teres . Pathogen-induced oxidative burst was also reduced in cold hardened plants. The possible roles of host-derived redox factors and other signaling components in the observed forms of cereal cross-tolerance are discussed
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