Improving promiscuous mammalian cell entry by the baculovirus Autographa californica multiple nuclear polyhedrosis virus

• Published in: Bioscience reports Vol. 33; no. 1; pp. 23 - e00003
• Main Authors: O'Flynn, Neil M J, Patel, Avnish, Kadlec, Jan, Jones, Ian M
• Format: Journal Article
• Language: English
• Published: England Portland Press Ltd 30.11.2012; Portland Press, Biochemical Society
• Subjects: Animals; Autographa californica; Baculovirus; Cell Membrane - metabolism; Cell Membrane - virology; CHO Cells; Cricetinae; Cricetulus; fusion; gene transduction; Genes, Reporter; Genetic Vectors - genetics; Genetic Vectors - metabolism; gp64; Green Fluorescent Proteins - genetics; Green Fluorescent Proteins - metabolism; HEK293 Cells; Humans; Hydrogen-Ion Concentration; mammalian cell; Mutagenesis; Nuclear polyhedrosis virus; Nucleopolyhedroviruses - genetics; Nucleopolyhedroviruses - metabolism; Original Paper; Promoter Regions, Genetic; Sf9 Cells; Transformation, Genetic; Viral Fusion Proteins - genetics; Viral Fusion Proteins - metabolism; Viral Plaque Assay; Virus Attachment; virus entry; Virus Internalization
• ISSN: 0144-8463; 1573-4935
• DOI: 10.1042/BSR20120093

The insect baculovirus AcMNPV (Autographa californica multiple nuclear polyhedrosis virus) enters many mammalian cell lines, prompting its application as a general eukaryotic gene delivery agent, but the basis of entry is poorly understood. For adherent mammalian cells, we show that entry is favoured by low pH and by increasing the available cell-surface area through a transient release from the substratum. Low pH also stimulated baculovirus entry into mammalian cells grown in suspension which, optimally, could reach 90% of the transduced population. The basic loop, residues 268-281, of the viral surface glycoprotein gp64 was required for entry and a tetra mutant with increasing basicity increased entry into a range of mammalian cells. The same mutant failed to plaque in Sf9 cells, instead showing individual cell entry and minimal cell-to-cell spread, consistent with an altered fusion phenotype. Viruses grown in different insect cells showed different mammalian cell entry efficiencies, suggesting that additional factors also govern entry.