The research findings, published in Nature Communications, revealed the workings of a ‘hidden code’ within the genome of Human Parechovirus, a member of the Picornavirus family that includes the common cold, polio, and hand, foot and mouth disease.
The work builds on a discovery made in 2015 when scientists at the Universities of Leeds and York identified a set of encrypted signals in a plant virus with a single-stranded ribonucleic acid (RNA) genome.
This is not too dissimilar to the structure of the Parechovirus that infect humans and can cause sepsis-like illness and meningitis in children.
They found that the details of the decoding mechanism appear identical in all strains of the virus, potentially allowing a single drug to treat them all, something that is not possible with a vaccine.
Professor Reidun Twarock, a mathematical biologist at the University of York’s Departments of Mathematics, Biology, and the York Centre for Complex Systems Analysis, explained: “Previously scientists have assumed that the signals regulating the assembly of a virus were located in a unique area of the genome.
“Using a combination of biological insight and mathematical modelling, our study suggests that, by contrast, the mechanism relies on multiple dispersed sites in the genome that act together in a cooperative way to enable efficient virus formation.
“The common cold infects more than two billion people annually, making it one of the most successful viral pathogens, so we are excited to make this crucial step forward.”
Scientists had previously attempted to detect assembly signals by genetically recoding these viruses, but failed to find any.
The latest results solve this mystery; they show that the additional, ‘hidden’ code responsible for virus formation is robust against such genome changes, and is conserved across different viruses in the same family.
The team is now working to screen for potential anti-viral drugs that target this decoding mechanism. Successful future partnerships with the pharmaceutical industry and further funding support could potentially see drug development results within the next 10 years.
“We need to move away from a vaccine approach, which is what we have for flu and polio. Vaccines, although our best source of defence against polio at the moment, can result in the release of more virulent strains of the disease.
"Protecting against infection therefore relies on continued worldwide vaccination, which is both very expensive and logistically difficult.”
The World Health Organisation has a goal of eliminating polio infections worldwide via vaccination but recognises that before vaccination can be terminated there is a need to develop anti-polio drugs to cure residual infections.
Professor Sarah Butcher, from the University of Helsinki, said: “This new research means that treatment would be less likely to trigger drug resistance, which is currently one of the major problems in anti-viral therapy. This discovery could be a great leap forward in curing a host of conditions.”
The research, funded by Wellcome and is published in Nature Communications.
Professor Stockley is available for interview – contact Peter Le Riche in the University of Leeds press office on 0113 343 2049 or email firstname.lastname@example.org.
The image above shows the structure of the virus particles of human parechovirus (HPEV) and the closely related Ljungan virus. The top row shows the outside of the virus whilst the bottom row shows the inside of the virus where the RNA genome, the genetic code of the virus, is found. The images were important for the study as they show that the RNA genome, shown in red/pink, is structured within the virus. This was the first clue that the RNA genome plays an important role in the assembly of these viruses.
Helen Miller, Innovate UK (Apr 2018), £999,960
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