Hepatitis B ‘neutralised’ by cell sentinel

Hepatitis B ‘neutralised’ by cell sentinel

New research suggests the hepatitis B virus can be neutralised by a cell sentinel according to University of Geneva scientists

The hepatitis B virus (HBV) is responsible for one of the most serious and common infectious diseases.

Transmitted through biological fluids, it attacks the liver cells and the chronic form of the disease can lead to serious complications, including cirrhosis and liver cancer.

There is no effective treatment for the chronic form of the disease, which can only be prevented by vaccination.

After identifying a key protein complex that is active when our body is infected by the virus, a team from the University of Geneva (UNIGE) has deciphered the precise functioning of this protective mechanism, opening the way to new therapeutic targets.

See also: Fat cell hormone restrains liver tumours in mice

chronic hepatitis b

Hepatitis B is the most common form of hepatitis. It is a viral disease caused by the hepatitis B virus and is mainly blood or sexually transmitted. It is up to 100 times more contagious than HIV and by infecting the liver cells, this virus causes a transitory inflammation of this organ that can also evolve towards a chronic infection.

This can then lead to serious pathologies, such as cirrhosis or liver cancer and it is estimated that nearly one million people die each year from this disease worldwide.

There is no definitive treatment for chronic hepatitis B; he only way to prevent it is to be vaccinated before the disease appears.

In 2016, a UNIGE team led by Michel Strubin, an associate professor in the Department of Microbiology and Molecular Medicine and in the Geneva Centre for Inflammation Research at the UNIGE Faculty of Medicine, revealed a mechanism that is crucial for understanding this disease: when our immune system defends itself against it, a complex – i.e. an interdependent set – of six proteins called SMC5/6, present in our cells, detects the viral DNA and blocks it.

The virus then strikes back and produces a specific protein, the X protein. This protein enters the cell and degrades SMC5/6, which is no longer able to play its sentinel role.

A three-step mechanism

Before this discovery, the antiviral function of SMC5/6 was unknown; it was only identified as a key complex for the structural maintenance of our chromosomes.

Today, Strubin’s team has made a new breakthrough; in a recent study, conducted in collaboration with the American pharmaceutical company Gilead Sciences, the UNIGE researchers identified the three steps and the specific proteins required for SMC5/6 to play its antiviral role.

Fabian Abdul is a senior research and teaching assistant in the Department of Microbiology and Molecular Medicine at the UNIGE Faculty of Medicine, and first author of the study. He said: “In the first step, a protein of the SMC5/6 complex detects the virus’ DNA and traps it.

“Then, a second protein of the complex – SLF2 – takes the trapped DNA of the virus into a sub-compartment of the nucleus of the attacked cell, called the PML body. A third protein – Nse2 – then comes into play and inhibits the virus’ chromosome.”

As SMC is a large family of protein complexes, the researchers also wanted to know whether other ‘members’ of this family were able to bind to hepatitis B viral DNA.

“We discovered that this competence was unique to SMC5/6,” Abdul added.

To achieve these results, the research team worked on in vitro cell cultures.

Lead author Strubin said: “We used molecular biology techniques and more specifically genetic scissors called CRISPR-Cas9. This tool allowed us to cut the DNA strands within the cells and thus delete or modify the gene coding for each protein constituting the SMC5/6 complex.

“Thanks to this technique, we were able to make one or other of the proteins disappear and thus understand their respective functions within the complex.”

Based on these observations, the three steps of the antiviral mechanism could be established.

This discovery provides a better understanding of how the complex functions during its antiviral action. It could thus pave the way for the identification of new therapeutic targets to combat the hepatitis B virus.

These results can be read in the journalNature Structural and Molecular Biology.

Image: Confocal microscopy images showing in the cell nucleus (blue), the recruitment of Smc5/6 (green) by SLF2 (red) into PML bodies.

Credit: UNIGE – Laboratory of Professor Michel Strubin – Regulation of hepatitis B virus gene expression – Department of Microbiology and Molecular Medicine.

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