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A reconstruction of the Binjari virus, which will help reimagine the architecture of immature flaviviruses. Image credit: Dr Natalee Newton
A reconstruction of the Binjari virus, which will help reimagine the architecture of immature flaviviruses. Image credit: Dr Natalee Newton
17 May 2021

Better designed vaccines for insect-spread viruses like dengue and Zika are likely after researchers discovered models of immature flavivirus particles were originally misinterpreted.

Researchers from Õ¬Äе¼º½ and Monash University have now determined the first complete 3D molecular structure of the immature flavivirus, revealing an unexpected organisation.

Õ¬Äе¼º½ researcher said the team was studying the insect-specific Binjari virus when they made the discovery.

“We were using Australia’s safe-to-handle Binjari virus, which we combine with more dangerous viral genes to make safer and more effective vaccines,” Dr Watterson said.

“But when analysing Binjari we could clearly see that the molecular structure we’ve all been working from since 2008 wasn’t quite correct.

“Imagine trying to build a house when your blueprints are wrong – that’s exactly what it’s like when you’re attempting to build effective vaccines and treatments and your molecular ‘map’ is not quite right.”

The team used a technique known as cryogenic electron microscopy to image the virus, generating high resolution data from Monash’s facility.

With thousands of collected two-dimensional images of the virus, the researchers then combined them using a high-performance computing platform called ‘MASSIVE’ to construct a high-resolution 3D structure.

Monash’s , a co-leader of the study, said the revelation could lead to new and better vaccines for flaviviruses, which have a huge disease burden globally.

“Flaviviruses are globally distributed and dengue virus alone infects around 400 million people annually,” Dr Coulibaly said.

“They cause a spectrum of potentially severe diseases including hepatitis, vascular shock syndrome, encephalitis, acute flaccid paralysis, congenital abnormalities and foetal death.

“This structure defines the exact wiring of the immature virus before it becomes infectious, and we now have a better understanding of the levers and pulleys involved in viral assembly.

 “This is a continuation of fundamental research by us and others and, without this hard-won basic knowledge, we wouldn’t have the solid foundation needed to design tomorrow’s treatments.”

The research has been published in (DOI: 10.1126/sciadv.abe4507).

The joint first authors are from Õ¬Äе¼º½’s Watterson lab and from  Coulibaly lab at the Monash Biomedicine Discovery Institute.

Image above: The cryo-electron microscopy reconstruction of Binjari virus provides the missing piece to correctly model the architecture of immature flaviviruses. The largest piece depicts the collapse of the spike required for the acquisition of infectivity. The smaller piece represents a previous model that does not fit with the new structure. Credit: Dr Fasseli Coulibaly.

Media: Dr Daniel Watterson, d.watterson@uq.edu.au, +61 422 098 299; Dr Fasseli Coulibaly, fasseli.coulibaly@monash.edu, +61 400 755 491; Dominic Jarvis, Õ¬Äе¼º½ Communications, dominic.jarvis@uq.edu.au, +61 413 334 924; Tania Ewing, Monash Communications, taniaewing@taniaewing.com, +61 408 681 293.