Construction and manipulation of a full-length infectious bacterial artificial chromosome clone of equine herpesvirus type 3 (EHV-3)

• Published in: Virus research Vol. 228; pp. 30 - 38
• Main Authors: Akhmedzhanov, Maksat, Scrochi, Mariela, Barrandeguy, Maria, Vissani, Aldana, Osterrieder, Nikolaus, Damiani, Armando Mario
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15-01-2017
• Subjects: BAC; Cells, Cultured; Chromosomes, Artificial, Bacterial; Cloning, Molecular; DNA, Recombinant; ECE; EHV-3; Escherichia coli; Gene Expression; Gene Order; Genetic Engineering; Genetic Vectors - genetics; Genome, Viral; Herpesviridae; Herpesvirus 3, Equid - genetics; Mutagenesis; Open Reading Frames; Transfection; Viral Plaque Assay; Virus Replication; BAC; ECE; gE; EHV-3
• ISSN: 0168-1702; 1872-7492
• DOI: 10.1016/j.virusres.2016.11.012

•EHV-3 is efficiently cloned as BAC.•EHV-3 BAC can be easily manipulated in E. coli and reintroduced in eukaryotic cells to produce infectious viruses.•EHV-3 gE is dispensable for growth in vitro.•An approximately 110-kDa gE is expressed in infected cells.•GE mutants are impaired to spread cell-to-cell in vitro.
Equine herpesvirus type 3 (EHV-3) is the causal agent of equine coital exanthema, a disease characterized by pox-like lesions on the penis of stallions and the vulva of mares. Although the complete genomic sequence of EHV-3 has been recently made available, its genomic content remains poorly characterized and the molecular mechanisms of disease development not yet elucidated. In an attempt to facilitate genetic manipulation of EHV-3, we describe here the construction of a full-length infectious bacterial artificial chromosome (BAC) clone of EHV-3. Mini-F vector sequences were inserted into the intergenic region between ORF19 and ORF20 (UL41 and UL40, respectively) of EHV-3 strain C175 by homologous recombination in equine dermal cells (NBL-6). DNA of the resulting recombinant virus was electroporated into E. coli and a full-length EHV-3 BAC clone was recovered. Virus reconstituted after transfection of the EHV-3 BAC into NBL-6 cells showed growth properties in vitro that were indistinguishable from those of the parental virus. To assess the feasibility of mutagenesis of the cloned EHV-3 genome, recombinant viruses targeting the glycoprotein E (gE) gene were generated using Red recombination in E. coli and in vitro growth properties of the recombinant viruses were evaluated. We first repaired the gE (ORF74) coding region, since the parental virus used for BAC cloning specifies a truncated version of the gene, and then created gE-tagged and gE-null versions of the virus. Our results demonstrated that: (i) EHV-3 can be efficiently cloned as a BAC allowing easy manipulation of its genome; (ii) gE is dispensable for EHV-3 growth in vitro and is expressed as a product of approximately 110-kDa in infected cells; (iii) viruses having a deletion compromising gE expression or with a truncation of the cytoplasmic and transmembrane domains are significantly compromised with regard cell-to-cell spread. The cloning of EHV-3 as a BAC simplifies future studies to identify the role of its coding genes in viral pathogenesis and host immune responses.