4.4 Article

A plasmid-based reporter system for live cell imaging of dengue virus infected cells

期刊

JOURNAL OF VIROLOGICAL METHODS
卷 211, 期 -, 页码 55-62

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jviromet.2014.10.010

关键词

Dengue virus; Viral reporter; Protease; Fluorescence microscopy

资金

  1. NIH [P01 AI034533, P20 GM103430-12, P20 COBRE GM 104317 U01 AI070484]
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [P01AI034533, U01AI070484] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [P20GM104317, P20GM103430] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Cell culture models are used widely to study the effects of dengue virus (DENV) on host cell function. Current methods of identification of cells infected with an unmodified DENV requires fixation and permeablization of cells to allow DEN V-specific antibody staining. This method does not permit imaging of viable cells over time. In this report, a plasmid-based reporter was developed to allow non-destructive identification of DENV-infected cells. The plasmid-based reporter was demonstrated to be broadly applicable to the four DENV serotypes, including low-passaged strains, and was specifically cleaved by the viral protease with minimal interference on viral production. This study reveals the potential for this novel reporter system to advance the studies of virus-host interactions during DENV infection. (C) 2014 Elsevier B.V. All rights reserved.

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