Development of a reverse genetics system to generate a recombinant Ebola virus Makona expressing a green fluorescent protein
Description
Previous studies have demonstrated the potential application of reverse genetics technology in studying a broad range of aspects of viral biology, including gene regulation, protein function, cell entry, and pathogenesis. Here, we describe a highly efficient reverse genetics system used to generate recombinant Ebola virus (EBOV) based on a recent isolate from a human patient infected during the 2014–2015 outbreak in Western Africa. We also rescued a recombinant EBOV expressing a fluorescent reporter protein from a cleaved VP40 protein fusion. Using this virus and an inexpensive method to quantitate the expression of the foreign gene, we demonstrate its potential usefulness as a tool for screening antiviral compounds and measuring neutralizing antibodies. - Highlights: • Recombinant Ebola virus (EBOV) derived from Makona variant was rescued. • New protocol for viral rescue allows 100% efficiency. • Modified EBOV expresses a green fluorescent protein from a VP40-fused protein. • Modified EBOV was tested as tool to screen antiviral compounds and measure neutralizing antibodies
Availability note (English)
Available from http://dx.doi.org/10.1016/j.virol.2015.06.013Additional details
Identifiers
- DOI
- 10.1016/j.virol.2015.06.013;
- PII
- S0042-6822(15)00291-3;
Publishing Information
- Journal Title
- Virology
- Journal Volume
- 484
- Journal Page Range
- p. 259-264
- ISSN
- 0042-6822
- CODEN
- VIRLAX
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47039977
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- AFRICA; ANTIBODIES; EFFICIENCY; FLUORESCENCE; GENE REGULATION; GENETICS; HUMAN POPULATIONS; PATHOGENESIS; PATIENTS; PROTEINS; SCREENING; VIRUSES
- Descriptors DEC
- BIOLOGY; EMISSION; LUMINESCENCE; MICROORGANISMS; ORGANIC COMPOUNDS; PARASITES; PHOTON EMISSION; POPULATIONS
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.