Virus production boosted in cells to generate more vectors for gene transfer

Virus production boosted in cells to generate more vectors for gene transfer
Co-transfection with a small amount of plasmid capable of expressing 'transcriptional activator' robustly enhances lentiviral production. Credit: Department of Molecular Virology,TMDU

The introduction of foreign genes into cells has a range of benefits, such as compensating for dysfunctional genes in cells and producing large amounts of specific gene products that can be harvested and used clinically. Viruses are useful tools for this purpose, as they have evolved to enter cells and express their genetic material there. However, it has been difficult and expensive to produce lentiviral vectors in sufficient quantities to apply this approach in practical contexts.

In a new study by a team based at Tokyo Medical and Dental University (TMDU), researchers have managed to boost the production and release of lentiviral particles from host by introducing two molecules into the viral culture. The findings should promote the use of lentiviral vectors for introducing exogenous genes into cells in a safe and efficient manner.

Viruses contain only a limited amount of , so they need to enter cells and hijack some of their hosts' machinery in order to survive and reproduce. In this latest work reported in the journal Scientific Reports, the team focused on some of the molecules that, when present in the host, can help viruses to do this, in this case for the HIV-1 virus.

Virus production boosted in cells to generate more vectors for gene transfer
Co-transfection with Tax expression plasmid augments transgene expression. Credit: Department of Molecular Virology,TMDU

"We first focused on the effects of the SPSB proteins, by expressing them in human embryonic kidney cells along with a plasmid for HIV-1," Shoji Yamaoka says. "SPSB1, but not SPSB2 and 3, boosted the release of HIV-1 from these cells, which was revealed by increased viral infection of indicator cells that exhibited bioluminescence upon infection."

The TMDU team then looked in detail at the mechanism behind this effect of SPSB1. Their findings showed that it activates a promoter in the HIV-1 genome to induce the transcription of the structural components that this virus uses to replicate. This in turn led the team to identify the Tax protein as another enhancer of virus production, given that it activates transcription factors that are also promoted by SPSB1. When Tax was co-expressed, was boosted by up to 12 times.

"It is often difficult to produce enough virus to achieve gene transfer at a high enough rate, especially for transfer in vivo or in non-dividing cells," lead author Naoto Suzuki says. "This new approach of promoter activation using should extend the range of applications in which viral vectors can be used."


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More information: Naoto Suzuki et al, Robust Enhancement of Lentivirus Production by Promoter Activation, Scientific Reports (2018). DOI: 10.1038/s41598-018-33042-5
Journal information: Scientific Reports

Provided by Tokyo Medical and Dental University
Citation: Virus production boosted in cells to generate more vectors for gene transfer (2018, October 30) retrieved 18 October 2019 from https://phys.org/news/2018-10-virus-production-boosted-cells-vectors.html
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