Tracing Baculovirus AcMNPV Infection Using a Real-Time Method Based on ANCHORTM DNA Labeling Technology

• Published in: Viruses Vol. 12; no. 1; p. 50
• Main Authors: Hinsberger, Aurélie, Graillot, Benoît, Blachère Lopez, Christine, Juliant, Sylvie, Cerutti, Martine, King, Linda A., Possee, Robert D., Gallardo, Franck, Lopez Ferber, Miguel
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 02.01.2020; MDPI
• Subjects: baculovirus infection; Cell culture; Cloning; Deoxyribonucleic acid; DNA; DNA-binding protein; Environmental impact; fluorescence labelling; Gene expression; Gene loci; Genomes; Infections; Labeling; Life cycles; Nucleotide sequence; Occlusion bodies; Plasmids; Proteins; real-time imaging; Viruses; France; United States > US
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v12010050

Many steps in the baculovirus life cycle, from initial ingestion to the subsequent infection of all larval cells, remain largely unknown; primarily because it has hitherto not been possible to follow individual genomes and their lineages. Use of ANCHORTM technology allows a high intensity fluorescent labelling of DNA. When applied to a virus genome, it is possible to follow individual particles, and the overall course of infection. This technology has been adapted to enable labelling of the baculovirus Autographa californica Multiple NucleoPolyhedroVirus genome, as a first step to its application to other baculoviruses. AcMNPV was modified by inserting the two components of ANCHORTM: a specific DNA-binding protein fused to a fluorescent reporter, and the corresponding DNA recognition sequence. The resulting modified virus was stable, infectious, and replicated correctly in Spodoptera frugiperda 9 (Sf9) cells and in vivo. Both budded viruses and occlusion bodies were clearly distinguishable, and infecting cells or larvae allowed the infection process to be monitored in living cells or tissues. The level of fluorescence in the culture medium of infected cells in vitro showed a good correlation with the number of infectious budded viruses. A cassette that can be used in other baculoviruses has been designed. Altogether our results introduce for the first time the generation of autofluorescent baculovirus and their application to follow infection dynamics directly in living cells or tissues.