» Articles » PMID: 34460066

Characterization of Episomal Replication of Bovine Papillomavirus Type 1 DNA in Long-Term Virion-Infected Saccharomyces Cerevisiae Culture

Overview
Journal Virol Sin
Specialty Microbiology
Date 2021 Aug 30
PMID 34460066
Authors
Affiliations
Soon will be listed here.
Abstract

We have previously reported that bovine papillomavirus type 1 (BPV-1) DNA can replicate its genome and produce infectious virus-like particles in short term virion-infected S. cerevisiae (budding yeast) cultures (Zhao and Frazer 2002, Journal of Virology, 76:3359-64 and 76:12265-73). Here, we report the episomal replications of BPV-1 DNA in long term virion-infected S. cerevisiae culture up to 108 days. Episomal replications of the BPV-1 DNA could be divided into three patterns at three stages, early active replication (day 3-16), middle weak replication (day 23-34/45) and late stable replication (day 45-82). Two-dimensional gel electrophoresis analysis and Southern blot hybridization have revealed further that multiple replication intermediates of BPV-1 DNA including linear form, stranded DNA, monomers and higher oligomers were detected in the virion-infected yeast cells over the time course. Higher oligomers shown as covalently closed circular DNAs (cccDNAs) are the most important replication intermediates that serve as the main nuclear transcription template for producing all viral RNAs in the viral life cycle. In this study, the cccDNAs were generated at the early active replication stage with the highest frequencies and then at late stable replication, but they appeared to be suppressed at the middle weak replication. Our data provided a novel insight that BPV-1 genomic DNA could replicate episomally for the long period and produce the key replication intermediates cccDNAs in S. cerevisiae system.

References
1.
Thomson N, Dunowska M, Munday J . The use of quantitative PCR to detect Felis catus papillomavirus type 2 DNA from a high proportion of queens and their kittens. Vet Microbiol. 2014; 175(2-4):211-7. DOI: 10.1016/j.vetmic.2014.11.028. View

2.
Zhao K, Frazer I . Replication of bovine papillomavirus type 1 (BPV-1) DNA in Saccharomyces cerevisiae following infection with BPV-1 virions. J Virol. 2002; 76(7):3359-64. PMC: 136048. DOI: 10.1128/jvi.76.7.3359-3364.2002. View

3.
Schvartzman J, Adolph S, Martin-Parras L, SCHILDKRAUT C . Evidence that replication initiates at only some of the potential origins in each oligomeric form of bovine papillomavirus type 1 DNA. Mol Cell Biol. 1990; 10(6):3078-86. PMC: 360672. DOI: 10.1128/mcb.10.6.3078-3086.1990. View

4.
Zhang L, Zhao Y, Tu Q, Xue X, Zhu X, Zhao K . The Roles of Programmed Cell Death Ligand-1/ Programmed Cell Death-1 (PD-L1/PD-1) in HPV-induced Cervical Cancer and Potential for their Use in Blockade Therapy. Curr Med Chem. 2020; 28(5):893-909. DOI: 10.2174/0929867327666200128105459. View

5.
Amtmann E, Sauer G . Bovine papilloma virus transcription: polyadenylated RNA species and assessment of the direction of transcription. J Virol. 1982; 43(1):59-66. PMC: 256096. DOI: 10.1128/JVI.43.1.59-66.1982. View