Pox viruses are able to get a head start on infecting a host by delivering a package of proteins that directly interferes with the body’s innate immune system.
According to a new study by researchers at the University of Birmingham and ETH Zurich, the pox virus starts to do this immediately after infection -even before it has begun to replicate - using proteins specifically designed to target key components of a host’s immune response.
In a new paper, published in PLOS Pathogens, the interdisciplinary team have identified these proteins for the first time, uncovering the molecular mechanisms at work and in turn opening up new avenues for the development of anti- poxvirus treatments.
Co-Lead researcher Professor Jason Mercer, of the University of Birmingham, said: “Our current arsenal of pox anti-viral agents is limited and only available for emergency use, so new anti-viral treatments would be extremely valuable. Our research identifies a highly unusual ability to bring immunosuppressing proteins into the host right at the start of the infection. By understanding what proteins the virus brings and how they work, we can start to investigate how to exploit them for new treatments.”
In the study, the researchers used mass spectrometry-based proteotyping and super-resolution microscopy to identify and characterise relevant proteins in vaccinia virus, the smallpox vaccine, which is a member of the same virus family as monkeypox virus and the smallpox virus, variola.
While all viruses have the goal of invading cells and successfully replicating, they must also find ways to evade the body’s innate immune system – the broad-spectrum defences against invading pathogens. In most viruses, this is by producing proteins during replication which can evade and attack the immune system. Pox viruses, in contrast, are unusual in that they contain and deliver immune-modulating proteins right at the start.
The research team identified 15 new proteins within the viral delivery packets called lateral bodies. Importantly, they found five ‘redox’ proteins, which are designed to interact with immune system elements called Reactive Oxygen Species.
Reactive Oxygen Species (ROS) are highly reactive molecules which play a key role destroying pathogens identified by the body’s innate immune system. The redox proteins within the pox virus are released at the start of the infection specifically to seek out and suppress ROS.
“Identifying the precise nature of the proteins contained with the lateral bodies was a complicated process because poxviruses are highly complex molecular structures,” added Professor Bernd Wollscheid, of ETH Zurich. “This work represents a big step in advancing our understanding of the molecular mode of action of this important family of viruses which is timely/relevant considering the current multi-country monkeypox outbreak in non-endemic countries.”
Next steps for the UK & Swiss research team will include testing the protein mechanisms in animal models to find out how they work individually and together to combat the host immune response.
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Subject of Research
Poxviruses package viral redox proteins in lateral bodies and modulate the host oxidative response
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