Replication-competent influenza A viruses expressing a red fluorescent protein

被引:68
作者
Nogales, Aitor [1 ]
Baker, Steven F. [1 ]
Martinez-Sobrido, Luis [1 ]
机构
[1] Univ Rochester, Dept Microbiol & Immunol, Rochester, NY 14642 USA
关键词
Influenza A virus; NS1; mCherry; Replication-competent virus; 2A; Neutralizing antibodies; Microneutralization assay; Virus neutralization assay; Antivirals; Interferon; In vivo imaging system (IVIS); NS1; PROTEIN; IN-VIVO; PYRIMIDINE BIOSYNTHESIS; REPORTER VIRUS; RNA-SYNTHESIS; GENERATION; INFECTION; CELLS; MICE; GENE;
D O I
10.1016/j.virol.2014.12.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Like most animal viruses, studying influenza A in model systems requires secondary methodologies to identify infected cells. To circumvent this requirement, we describe the generation of replicationcompetent influenza A red fluorescent viruses. These influenza A viruses encode mCherry fused to the viral non-structural 1 (NS1) protein and display comparable growth kinetics to wild-type viruses in vitro. Infection of cells with influenza A mCheny viruses was neutralized with monoclonal antibodies and inhibited with antivirals to levels similar to wild-type virus. Influenza A mCherry viruses were also able to lethally infect mice, and strikingly, dose- and time-dependent kinetics of viral replication were monitored in whole excised mouse lungs using an in vivo imaging system (IVIS). By eliminating the need for secondary labeling of infected cells, influenza A mCherry viruses provide an ideal tool in the ongoing struggle to better characterize the virus and identify new therapeutics against influenza A viral infections. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:206 / 216
页数:11
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