Search results for: CPER

Authors: Sun fang, Zhang Wenxin

Abstract:

This paper establishes an evaluation index system for spatio-temporal patterns of urbanization, with the county as research unit. We use the Entropy Weight method, coefficient variance, the Theil index and ESDA-GIS to analyze spatial patterns and evolutionary characteristics of New-Type Urbanization in the Central Plains Economic Region (CPER) between 2000 and 2011. Results show that economic benefit, non-agricultural employment level and level of market development are the most important factors influencing the level of New-Type Urbanization in the CPER; overall regional differences in New-Type Urbanization have declined while spatial correlations have increased from 2000 to 2011. The overall spatial pattern has changed little, however; differences between the western and eastern areas of the CPER are clear, and the pattern of a strong west and weak east did not change significantly over the study period. Areas with high levels of New-Type Urbanization were mostly distributed along the Beijing-Guangzhou and LongHai Railways on both sides, a new influx of urbanization was tightly clustered around ZhengZhou in the Central Henan Urban Agglomeration, but this trend was found to be weakening slightly. The level of New-Type Urbanization in municipal districts was found to be much higher than it was in the county generally. Provincial borders experienced a lower rate of growth and a lower level of New-Type Urbanization than did any other areas, consistently forming clusters of cold spots and sub-cold spots. The analysis confirms that historical development, location, and diffusion effects of urban agglomeration are the main drivers of changes in New-Type Urbanization patterns in CPER.

Keywords: new-type urbanization, spatial pattern, central plains economic region, spatial evolution

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Authors: Xiang Jinhua, Mclinden James, Chang Qing, Fosdick Micaela, Ploss Alexander, Bhattarai Nirjal, Houtman Jon, Stapleton Jack

Abstract:

Background: Clinical outcomes differ among dengue virus (DENV) serotypes though few serotype-specific differences are identified. We previously found that ZIKV and DENV-2 envelope proteins do not inhibit T cell receptor (TCR) signaling. Here, we investigated the effect of DENV-1-4 infection and env expression on T cell functions. Methods: DENV-1 though 4 were added to PBMCs or Jurkat T cells prior to TCR stimulation. Signaling was measured by IL-2 release. The effect of DENV env (1-4) expression in primary and Jurkat T cells on TCR was measured. DENV env regions required for TCR inhibition were mapped by chimera, deletions, and point mutagenesis. Results were confirmed by reverse genetics using replication competent DENV generated by CPER. Results: DENV-1-4 caused abortive infection in T cells, yet DENV-1 and -4 inhibited TCR signaling measured by IL-2 release in primary and transformed T cells while DENV-2 and -3 did not. This was not due to differences in binding, entry or RNA production. DENV-1 and -4 env expression in Jurkat or exposure in primary T cells recapitulated TCR inhibition. The Env sequences in volved were mapped and mutation of Env a.a V55 to the T present in DENV-2 and -3 abolished TCR inhibition in replicating viruses. Substituting the DENV-1 55V into DENV 2, 3 led to partial TCR inhibition; however, addition T66S into the V55T DENV-2 and -3 rescued the TCR inhibition found in DENV-1 and -4. Preliminary data suggest that the envelope substitutions may reduce replication kinetics in different mammalian or insect cells, and this is under further study. Conclusions: Epidemiological data suggest that DENV 2 and 3 are more often associated with severe dengue including hemorrhagic fever and shock. Since DENV-1 and -4 interfere with TCR, it is possible that this TCR effect blunts host immunologic responses during infection, mitigating immune-mediated pathogenic effects of DENV. Recombinant viruses demonstrate that DENV1 V55T substitution is sufficient to remove the TCR inhibitory phenotype, and that changing DENV-2, -3 aa 55 and 66 to that seen in DENV-1 mimics TCR inhibition observed in DENV-1 and -4. These findings may provide an approach to safer live-attenuated DENV vaccines.

Keywords: dengue Viruses, TCR signaling, CPER, dengue viral envelope protein

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