360 research outputs found

    ShenZhen transportation system (SZTS): a novel big data benchmark suite

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    Data analytics is at the core of the supply chain for both products and services in modern economies and societies. Big data workloads, however, are placing unprecedented demands on computing technologies, calling for a deep understanding and characterization of these emerging workloads. In this paper, we propose ShenZhen Transportation System (SZTS), a novel big data Hadoop benchmark suite comprised of real-life transportation analysis applications with real-life input data sets from Shenzhen in China. SZTS uniquely focuses on a specific and real-life application domain whereas other existing Hadoop benchmark suites, such as HiBench and CloudRank-D, consist of generic algorithms with synthetic inputs. We perform a cross-layer workload characterization at the microarchitecture level, the operating system (OS) level, and the job level, revealing unique characteristics of SZTS compared to existing Hadoop benchmarks as well as general-purpose multi-core PARSEC benchmarks. We also study the sensitivity of workload behavior with respect to input data size, and we propose a methodology for identifying representative input data sets

    Complementary Therapy with Traditional Chinese Medicine for Childhood Asthma

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    Asthma is a heterogeneous disease that is typically characterized by chronic airway inflammation and obstruction of airflow; it frequently presents in early childhood and is the leading chronic disease in children in the western world. This review presents a brief description of the pathophysiology of asthma and summarizes recent research results on the mechanisms of action of anti-asthma Chinese herbal medicine commonly used in clinical practice. Other interventions of traditional Chinese medicine (TCM), such as acupuncture, tai chi, and meditation are also briefly discussed. We believe that this contribution is theoretically and practically relevant because the prevalence of asthma is increasing and, in addition to standard treatment, the use of complementary therapy is increasing and there is increasing scientific evidence demonstrating that TCM has potential for the treatment of childhood asthma

    Prevalence and molecular typing of the antiseptic resistance genes qacA/B among Staphylococcus aureus strains isolated in a teaching hospital

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    The qacA/B genes are found in Staphylococcus aureus and confer resistance to various antiseptics and disinfectants. Herein, the prevalence of the qacA/B genes in methicillin-resistant S. aureus (MRSA) and methicillin-sensitive S. aureus (MSSA) was investigated. Molecular typing systems were used to analyse the relatedness of these qacA/B-positive strains. 176 six strains of clinically isolated S. aureus were collected between July, 2008 and June, 2010. The strains carrying the qacA/B genes were characterised by pulse-field gel electrophoresis (PFGE) typing, Staphylococcus protein A (spa) typing, Panton-Valentine leucocidin (pvl) polymerase chain reaction (PCR) detection, staphylococcal chromosomal cassette (SCC) mec typing, and antimicrobial resistance profiles. Strains carrying the qacA/B genes composed 9.1% of the strains isolated, but the incidence of qacA/B genes in MRSA strains was significantly higher than that in MSSA strains (14.6 versus 4.3%, p < 0.05). Additionally, two predominant PFGE (B and A) and spa types (t037 and t042) were identified along with two major antimicrobial resistance profiles. All of these qacA/B-positive strains strains were pvl-negative by PCR. The qacA/B-positive MRSA strains all contained the group III SCCmec element. These strains were obtained mainly from patients in surgical wards; therefore, the neurosurgical ward and ICU may be considered as a source of MRSA strains carrying the qacA/B genes. Finally, the strain identified as spa type t037 is likely to be an epidemiological clone. The presence of the antiseptic resistance genes qacA/B by MRSA could potentially lead to MRSA strain prevalence. Thus, the optimal usage of antiseptics and disinfectants is warranted. A policy of molecular typing needs to be implemented to track the possible dissemination of these resistance genes.Key words: Staphylococcus aureus, mecA, qacA/B and pvl genes, methicillin-resistant,  Staphylococcus aureus (MRSA), methicillin-sensitive Staphylococcus aureus (MSSA)

    Effect of Furin inhibitor on lung adenocarcinoma cell growth and metastasis

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    BACKGROUND: To investigate the mechanisms of lung adenocarcinoma cell metastasis and provide a theoretical basis for the in-depth study of lung adenocarcinoma. METHODS: A549 cells are incubated with different concentrations of Furin inhibitor for indicated times. The proliferation and migration were confirmed with MTT, colony formation, wound Healing and Transwell assayes. Hochest 33342 / PI double staining was used to detect apoptosis. Cell migration and apoptosis associated proteins were analysed by enzyme-linked immunosorbent assay (ELISA) and western blot. RESULTS: We have found that Furin inhibitor play a significant role in inhibition A549 cell growth. And we also found cell migration was inhibited significantly upon Furin inhibitor treatment. CONCLUSION: The proliferration and migration of A549 cell were inhibited by Furin inbitor through down-regulation the expression of migration and apoptosis related proteins

    Online quality control of panaxatriol saponins percolation extraction using near-infrared technology

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    Purpose: To establish a new prediction model for online quality control of the percolation extraction of panaxatriol saponins (PTS), viz, ginsenoside Rg1, ginsenoside Re and notoginsenoside R1, from notoginseng by near-infrared (NIR) technology coupled with partial least squares (PLS) analysis.Methods: Ten batches of PTS (420 samples) were collected and the  constituents were determined using HPLC. The NIR spectroscopy of samples was determined using a Fourier-Transform nearinfrared spectrometer with an optical fiber transmission PbS detector. Eight sample batches were the calibration set, and two batches were the forecast set. Calibration models were established based on min-max normalization (MMN).Results: The root mean square errors of cross-validation (RMSECV) of Rg1, Re, and R1 were 0.798, 0.095, and 0.259 mg/mL, respectively. The root mean square errors of prediction (RMSEP) were 1.110, 0.496, and 0.390 mg/mL, respectively. The correlation coefficients (R2) of cross-validation were 0.9682, 0.9681, and 0.9626, respectively, while the correlation coefficients (R2) of prediction were 0.9831, 0.9198, and 0.9661,  respectively.Conclusion: The results indicate that NIR is a quick and effective tool for online quality control of PTS (ginsenoside Rg1, ginsenoside Re, and notoginsenoside R1) in the percolation extraction process.Keywords: Online monitoring, Near infrared technology, Panaxatriol  saponins, Partial least square

    Auxin inhibits chlorophyll accumulation through ARF7-IAA14-mediated repression of chlorophyll biosynthesis genes in Arabidopsis

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    Auxin is a well-known important phytohormone in plant that plays vital roles in almost every development process throughout plant lifecycle. However, the effect of auxin on the metabolism of chlorophyll, one of the most important pigments involved in the photosynthesis, was intertwined and the underlying mechanism remained to be explored. Here, we found the auxin-defective yuc2 yuc6 double mutant displayed dark-green leaf color with higher chlorophyll content than wildtype, suggesting a negative regulatory role of auxin in chlorophyll biosynthesis. The chloroplast number and structure in mesophyll cells were altered and the photosynthetic efficiency was improved in yuc2 yuc6. In addition, the chlorophyll level was significantly improved during seedling de-etiolation in yuc2 yuc6 mutant, and decreased dramatically under IAA treatment, confirming the inhibitory role of auxin in chlorophyll biosynthesis. The analyses of gene expression in mature leaves and de-etiolation seedlings suggested that auxin suppressed the expression of many chlorophyll biosynthesis genes, especially PROTOCHLOROPHYLLIDE OXIDOREDUCTASE A (PORA) and GENOMES UNCOUPLED 5 (GUN5). Yeast-one-hybrid and luciferase assays demonstrated that the AUXIN RESPONSE FACTOR 2 (ARF2) and ARF7 bind to the promoter of PORA and GUN5 to suppress their expression with the help of INDOLE-3-ACETIC ACID14 (IAA14). Collectively, our research explicitly unraveled the direct inhibitory role of auxin in chlorophyll biosynthesis, and provided new insight into the interplay between auxin signaling and chlorophyll metabolism
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