Approximate Accuracy Approaches to Attribute Reduction for Information Systems

The key problem for attribute reduction to information systems is how to evaluate the importance of an attribute. The algorithms are challenged by the variety of data forms in information system. Based on rough sets theory we present a new approach to attribute reduction for incomplete information systems and fuzzy valued information systems. In order to evaluate the importance of an attribute effectively, a novel algorithm with rigorous theorem is proposed. Experiments show the effect of proposed algorithm

An outbreak of aseptic meningitis caused by coxsackievirus A9 in Gansu, the People's Republic of China

<p>Abstract</p> <p>Background</p> <p>An outbreak of aseptic meningitis occurred in Tianshui city of Gansu Province, the People's Republic of China, from March to June 2005. A total of 85 patients were clinical confirmed as aseptic meningitis in this outbreak.</p> <p>Results</p> <p>CVA9 was mainly responsible for this outbreak supported by the clinical manifestations of the patients, epidemiological data of the outbreak, the results of RT-PCR and complete VP1 sequence determination, conventional neutralization assays, IgM serological assays, viral isolation and phylogenetics analysis. Through phylogenetic analysis and homogeneity analysis for partial VP1 gene, the nucleotide and amino acid homologies between Gansu isolates and former Chinese CVA9 strains were 88.2%-96.1% and 97.2%-99.2%, respectively. Multiple transmission chains of CVA9 occurred in different provinces or years in China. Moreover, in order to clarify the genotype of CVA9, Gansu CVA9 strains isolated in this outbreak were compared with other CVA9 isolates based on VP1/2A junction regions (genotyping region) and they might belong to a new genotype of CVA9, which could be assigned for genotype XIII,</p> <p>Conclusions</p> <p>CVA9 was confirmed as the pathogen responsible for this outbreak. The phylogenetic analysis indicated that the CVA9 strains isolated in this outbreak might belong to a new genotype.</p

Refactorizing NRQCD short-distance coefficients in exclusive quarkonium production

In a typical exclusive quarkonium production process, when the center-of-mass energy, $\sqrt{s}$, is much greater than the heavy quark mass $m$, large kinematic logarithms of $s/m^2$ will unavoidably arise at each order of perturbative expansion in the short-distance coefficients of the nonrelativistic QCD (NRQCD) factorization formalism, which may potentially harm the perturbative expansion. This symptom reflects that the hard regime in NRQCD factorization is too coarse and should be further factorized. We suggest that this regime can be further separated into "hard" and "collinear" degrees of freedom, so that the familiar light-cone approach can be employed to reproduce the NRQCD matching coefficients at the zeroth order of $m^2/s$ and order by order in $\alpha_s$. Taking two simple processes, exclusive $\eta_b+\gamma$ production in $e^+ e^-$ annihilation and Higgs boson radiative decay into $\Upsilon$, as examples, we illustrate how the leading logarithms of $s/m^2$ in the NRQCD matching coefficients are identified and summed to all orders in $\alpha_s$ with the aid of Brodsky-Lepage evolution equation.Comment: v2, 17 pages, 2 figures; presentation improved, one important reference added, and Note adde

Recombinant Newcastle disease virus (NDV/Anh-IL-2) expressing human IL-2 as a potential candidate for suppresses growth of hepatoma therapy

AbstractNewcastle disease virus (NDV) have shown oncolytic therapeutic efficacy in preclinical study and are currently approved for clinical trials. NDV Anhinga strain which is a mesogenic strain should be classified as lytic strain and has a therapeutic efficacy in hepatocellular cancer. In this study, we evaluated the capacity of NDV Anhinga strain to elicit immune reaction in vivo and the possibility for using as a vaccine vector for expressing tumor therapeutic factors. Interleukin-2 (IL-2) could boost the immune response against the tumor cells. Therefore, we use NDV Anhinga strain as backbone to construct a recombinant virus (NDV/Anh-IL-2) expressing IL-2. The virus growth curve showed that the production of recombinant NDV/Anh-IL-2 was slightly delayed compared to the wild type. The NDV/Anh-IL-2 strain could express soluble IL-2 and effectively inhibit the growth of hepatocellular carcinoma in vivo. 60 days post-treatment, mice which were completely cured by previous treatment were well protected when rechallenged with the same tumor cell. From the H&E-stained sections, intense infiltration of lymphocyte was observed in the NDV Anhinga strain treated group, especially in NDV/Anh-IL-2 group. The NDV Anhinga strain could not only kill the tumor directly, but could also elicit immune reaction and a potent immunological memory when killing tumor in vivo. In conclusion, the Anhinga strain could be an effective vector for tumor therapy; the recombinant NDV/Anh-IL-2 strain expressing soluble IL-2 is a promising candidate for hepatoma therapy

Fibroblast growth factor (FGF21) protects mouse liver against D-galactose-induced oxidative stress and apoptosis via activating Nrf2 and PI3K/Akt pathways

FGF21 is recently discovered with pleiotropic effects on glucose and lipid metabolism. However, the potential protective effect of FGF21 against D-gal-induced injury in the liver has not been demonstrated. The aim of this study is to investigate the pathophysiological role of FGF21 on hepatic oxidative injury and apoptosis in mice induced by D-gal. The 3-month-old Kunming mice were subcutaneously injected with D-gal (180 mg kg(-1) d(1)) for 8 weeks and administered simultaneously with FGF21 (5 or 1 mg kg(-1) d(1)). Our results showed that the administration of FGF21 significantly alleviated histological lesion including structure damage, degeneration, and necrosis of hepatocytes induced by D-gal, and attenuated the elevation of liver injury markers, serum AST, and ALP in a dosedependent manner. FGF21 treatment also suppressed D-galinduced profound elevation of ROS production and oxidative stress, as evidenced by an increase of the MDA level and depletion of the intracellular GSH level in the liver, and restored the activities of antioxidant enzymes SOD, CAT, GSH-Px, and T-AOC. Moreover, FGF21 treatment increased the nuclear abundance of Nrf2 and subsequent up regulation of several antioxidant genes. Furthermore, a TUNEL assay showed that D-gal-induced apoptosis in the mouse liver was significantly inhibited by FGF21. The expression of caspase-3 was markedly inhibited by the treatment of FGF21 in the liver of D-gal-treated mice. The levels of PI3K and PBK/Akt were also largely enhanced, which in turn inactivated pro-apoptotic signaling events, restoring the balance between pro-and anti-apoptotic Bcl-2 and Bax proteins in the liver of D-gal-treated mice. In conclusion, these results suggest that FGF21 protects the mouse liver against D-gal-induced hepatocyte oxidative stress via enhancing Nrf2-mediated antioxidant capacity and apoptosis via activating PI3K/Akt pathway

Identification and isolation of Genotype-I Japanese Encephalitis virus from encephalitis patients

Historically, Japanese Encephalitis virus (JEV) genotype III (GIII) has been responsible for human diseases. In recent years, JEV genotype I (GI) has been isolated from mosquitoes collected in numerous countries, but has not been isolated from patients with encephalitis. In this study, we report recovery of JEV GI live virus and identification of JEV GI RNA from cerebrospinal fluid (CSF) of encephalitis patients in JE endemic areas of China. Whole-genome sequencing and molecular phylogenetic analysis of the JEV isolate from the CSF samples was performed. The isolate in this study is highly similar to other JEV GI strains which isolated from mosquitoes at both the nucleotide and deduced amino acid levels. Phylogenetic analysis based on the genomic sequence showed that the isolate belongs to JEV GI, which is consistent with the phylogenetic analysis based on the pre-membrane (PrM) and Glycoprotein genes. As a conclusion, this is the first time to isolate JEV GI strain from CSF samples of encephalitis patients, so continuous survey and evaluate the infectivity and pathogenecity of JEV GI strains are necessary, especially for the JEV GI strains from encephalitis patients. With respect to the latter, because all current JEV vaccines (live and inactivated are derived from JEV GIII strains, future studies should be aimed at investigating and monitoring cross-protection of the human JEV GI isolates against widely used JEV vaccines

Real-time Monitoring for the Next Core-Collapse Supernova in JUNO

Core-collapse supernova (CCSN) is one of the most energetic astrophysical events in the Universe. The early and prompt detection of neutrinos before (pre-SN) and during the SN burst is a unique opportunity to realize the multi-messenger observation of the CCSN events. In this work, we describe the monitoring concept and present the sensitivity of the system to the pre-SN and SN neutrinos at the Jiangmen Underground Neutrino Observatory (JUNO), which is a 20 kton liquid scintillator detector under construction in South China. The real-time monitoring system is designed with both the prompt monitors on the electronic board and online monitors at the data acquisition stage, in order to ensure both the alert speed and alert coverage of progenitor stars. By assuming a false alert rate of 1 per year, this monitoring system can be sensitive to the pre-SN neutrinos up to the distance of about 1.6 (0.9) kpc and SN neutrinos up to about 370 (360) kpc for a progenitor mass of 30$M_{\odot}$ for the case of normal (inverted) mass ordering. The pointing ability of the CCSN is evaluated by using the accumulated event anisotropy of the inverse beta decay interactions from pre-SN or SN neutrinos, which, along with the early alert, can play important roles for the followup multi-messenger observations of the next Galactic or nearby extragalactic CCSN.Comment: 24 pages, 9 figure

Effect of Prior Cyclic Loading on Triaxial Compression Strength of Sliding Zone Soil of the Huangtupo Landslide

Earthquakes or cyclic loadings cause significant changes in the strength characteristics of soil. These changes, especially for sliding zone soil, can lead to catastrophic landslides. Taking into account this characteristic, this paper investigates the effects of prior cyclic loading on the consolidated undrained triaxial compression strength of sliding zone soil with the KTL triaxial automated system. Our experimental results indicate that the prior cyclic loading has a significant effect on the strength behaviour of saturated sliding zone soil. Under different confining pressures, cycle periods, and number of cycles, the samples exhibit the characteristics of strain-hardening. Deviatoric stress under cyclic loading condition is smaller than that with monotonic loading condition under different confining pressures, cycle periods, and number of cycles. As the confining pressure and cycle period increase, the failure stress ratio decreases. The axial strain exhibits a steep rise first and then stays stable under a cycle period of 90 s, while the axial strain shows a linear increase with an increase in the number of cycles under a cycle period of 10 s under confining pressures of 100 kPa and 400 kPa, respectively. The logarithmic relation correlates well with the failure stress ratio in the cyclic loading tests, which preliminary validates the applicability of logarithmic relation for sliding zone soil influenced by prior cyclic loading, providing a theoretical basis and guidance for the further understanding of strength characteristics of sliding zone soil