Adenoviruses cause respiratory illnesses in humans and have been used as vectors in vaccination for many years, for example against MERS and Ebola virus. Several Covid-19 vaccines are based on replication-defective adenoviruses, including products from AstraZeneca, Johnson & Johnson, CanSino Biologics and Sputnik V. The vaccinated cells produce the SARS-CoV-2 spike protein on their surface, and thereby trigger a protective immune response in the human body.
Viral protein increases stability of virus particle
Researchers are exploiting a key feature of adenoviruses, namely their ability to infect human cells and transfer foreign DNA into the nucleus of these cells. A new study led by Urs Greber, professor at the Department of Molecular Life Sciences at the University of Zurich (UZH), now shows that this process evolved a sophisticated mechanism. “The viral protein V plays a key role. It connects the DNA with the protein coat surrounding the genome. Protein V increases the stability of the virus particle outside the cell, and also in the cytoplasm of the infected cells,” explains Greber.
The protein coat prevents the cell from recognizing the invading foreign DNA and activating the alarm systems. Once the virus particle reaches the nuclear pore complex – the gateway into the nucleus – the viral DNA is released into the nucleus, where the genetic information is read by the cell’s machinery, resulting in the relevant proteins being produced. In Covid-19 vaccines, the cells produce the spike protein on the coronavirus’s surface. Presenting the viral protein on the outside of the cell then triggers the immune response in the human body.
Premature release of DNA activates anti-viral alarm systems
The UZH scientists have shown that an adenovirus that is missing the protein V is not only less stable than regular adenoviruses, but also releases its DNA prematurely, before reaching the nuclear pore complex. “This reduces infection and triggers reactions activating the immune system,” says Greber. Too many of these reactions trigger inflammation. Notably, both vector-based and mRNA vaccines against coronavirus require just the right amount of these reactions to induce a strong immune response.
In vector-based vaccines, the protective protein coat around the DNA enables the particle to reach the nuclear pore complex, where the viral DNA is released. This “uncoating” is absolutely essential for nuclear import, and success in vector-based vaccination, since the nuclear pore complex prevents large virus particles from invading the nucleus. “We were able to demonstrate that the protein V uses the activation by a cellular enzyme named Mind bomb 1, which changes its features and leads to the disruption of the protein coat. The enzyme thereby initiates the nuclear import of the viral DNA genome,” says Greber.
Stopping viral infection and improving gene therapy
To demonstrate this key function of Mind bomb1, the researchers used regular adenoviruses to infect human cells that lacked Mind bomb 1, as well as a virus mutant containing protein V, which cannot be modified by this enzyme. In both cases, nuclear import of the viral DNA was defective and the virus particles clustered at the nuclear pore complexes. In other words, the viral infection was stopped.
“Our results inspire the development of anti-viral strategies and enhance procedures to transfer genes into diseased cells for clinical therapy,” says Urs Greber. Notably, adenoviruses are employed in a variety of ways – including use as DNA carriers for gene editing in genetic and metabolic diseases as well as cancer.
Michael Bauer, Alfonso Gomez-Gonzalez, Maarit Suomalainen, Nicolas Schilling, Silvio Hemmi, Urs F. Greber. A viral ubiquitination switch attenuates innate immunity and triggers nuclear import of virion DNA and infection. Science Advances. December 17, 2021. DOI: 10.1126/sciadv.abl7150
The study received financial support from the Swiss National Science Foundation (SNSF).