Researchers have used a technique called X-ray crystallography to learn the precise structure of the original strain of EV-D68 on its own and when bound to an anti-viral compound called "pleconaril."
The research could lead to the development of drugs that inhibit infections caused by the most recent strains of the virus, said Michael G Rossmann, Hanley Distinguished Professor of Biological Sciences at Purdue University.
Researchers found that a molecule called a "pocket factor" is located within a pocket of the virus's protective shell, called the capsid.
The antiviral compound pleconaril also binds into the pocket, inhibiting infection.
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"The compound and the normal pocket factor compete with each other for binding into the pocket," Rossmann said.
"They are both hydrophobic, and they both like to get away from water by going into the pocket. But which of these is going to win depends on the pocket itself, the pocket factor and properties of the antiviral compound," he said.
Although pleconaril is not active against current strains of EV-D68 tested thus far, it is active against the original isolate. Small changes in the structure of pleconaril are likely to lead to anti EV-D68 inhibitors against a broader spectrum of isolates.
An upsurge of EV-D68 cases in the past few years has been seen in clusters of infections worldwide, researchers said.
In August 2014 an outbreak of mild-to-severe respiratory illnesses occurred among thousands of children in the US of which 1,149 cases have been confirmed to be caused by EV-D68.
Purdue researchers became interested in studying pleconaril's potential effectiveness against EV-D68 after an outbreak of about 20 cases of acute flaccid paralysis was reported in California between 2012 and 2014. Out of those cases, two tested positive for EV-D68.
"This suggests the potential association of EV-D68 with polio-like illness," Liu said.