Human adenovirus type 5 vectors deleted of early region 1 (E1) undergo limited expression of early replicative E2 proteins and DNA replication in non-permissive cells

• Published in: PloS one 2017-07, Vol.12 (7), p.e0181012-e0181012
• Main Authors: Saha, Bratati, Parks, Robin J
• Format: Article
• Language: English
• Subjects: Adenoviruses; Adenoviruses, Human - genetics; Adenoviruses, Human - physiology; Biochemistry; Biology and life sciences; Cell Line; Cellular proteins; Copy number; Deoxyribonucleic acid; DNA; DNA biosynthesis; DNA polymerase; DNA Replication - genetics; DNA Replication - physiology; DNA-binding protein; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; DNA-directed DNA polymerase; Early region; Epitopes; Expression vectors; Gene expression; Gene Products, pol - genetics; Gene Products, pol - metabolism; Gene therapy; Genetic vectors; Genetic Vectors - genetics; Genomes; Hep G2 Cells; Humans; Immunology; Immunoprecipitation; Infections; Lysates; Neuromuscular diseases; Permissive cells; Proteins; Replication; Research and Analysis Methods; Terminal protein; Viral Proteins - genetics; Viral Proteins - metabolism; Virology; Virus replication; Viruses
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0181012

Adenovirus (Ad) vectors deleted of the early region 1 (E1) are widely used for transgene delivery in preclinical and clinical gene therapy studies. Although proteins encoded within the E1 region are required for efficient virus replication, previous studies have suggested that certain viral or cellular proteins can functionally compensate for E1, leading to expression of the early region 2 (E2)-encoded replicative proteins and subsequent virus replication. We have generated a series of E1-encoding and E1-deficient Ad vectors containing a FLAG-epitope tag on each of the E2-encoded proteins: DNA-binding protein (DBP), terminal protein (TP) and DNA polymerase (Pol). Using these constructs, we show that for the replication-competent virus, the expression level of each E2-encoded protein declines with increasing distance from the E2 promoter, with E2A-encoded DBP expression being ~800-fold higher than E2B-encoded TP. Pol was expressed at extremely low levels in infected cells, and immunoprecipitation from cell lysates was required prior to its detection by immunoblot. We further show that DBP was expressed 200- to 400-fold less efficiently from an E1-deficient virus compared to a replication-competent virus in A549 and HepG2 cells, which was accompanied by a very small increase in genome copy number. For the E1-deficient virus, late gene expression (a marker of virus replication) was only observed at very high multiplicities of infection. These data show that E1-deleted Ad gives rise to limited expression of the E2-encoded genes and replication in infected cells, but highlight the importance of considering viral dose-dependent effects in gene therapy studies.