African swine fever genome mapped

Research could provide vital information for those developing vaccines and antiviral drugs to prevent ASF.

February 20, 2020

2 Min Read
Pirbright ASF genome.jpg
The process of gene activation through transcription. RNA polymerase (yellow/orange) unwinds DNA (violet) and uses the code to build an RNA strand (red). The RNA can then be used to create viral proteins that have many different functions.The Pirbright Institute

Scientists from The Pirbright Institute have worked with University College London to map the expression of genes across the entire African swine fever virus (ASFV) genome, which helped establish their order of activation as well as uncovered new genes.

The research could provide vital information for those developing vaccines and antiviral drugs to prevent the deadly pig disease caused by this virus, Pirbright said.

ASFV causes an often lethal hemorrhagic fever in domesticated pigs and wild boars. Major African swine fever outbreaks continue to spread across Eastern Europe, Asia and Africa and resulted in the death of nearly 7 million pigs in 2019, Pirbright said. In the absence of a vaccine or antivirals, the only way to prevent outbreaks is through biosecurity measures.

In their study, published in the Journal of Virology, the researchers used next-generation sequencing to analyze genes expressed by ASFV. From this, they created the first complete genetic road map, which reveals the order that different sets of genes are turned on throughout the ASFV infection cycle, according to the institute.

Genes, including those in ASFV, are activated through a process called transcription. This is carried out by a molecular machine called RNA polymerase, which serves as "gatekeeper" by ensuring that the information coded in the DNA is expressed at the correct time during infection, Pirbright explained. The RNA polymerase finds genes based on specific DNA sequences, or "promoters," that are located before a gene.

The team demonstrated that genes expressed during early infection have different promoters to those expressed later, allowing the virus to shift the pattern of activated genes according to the stage of infection, Pirbright said. Genes used for DNA replication and immune system evasion are switched on early in the infection cycle, whereas those involved in creating proteins for the new virus particles are activated later.

“ASFV has a very large DNA genome. For comparison, the influenza virus expresses eight genes, whereas ASFV expresses between 150 and 190, which has so far made it difficult for scientists to identify and determine the significance of each gene. Our study helps to untangle which genes are important during different stages of infection to better understand their functions,” said Dr. Linda Dixon, head of the African Swine Fever Virus Group at Pirbright.

University College London professor of molecular biophysics Finn Werner added, “Our data shows ASFV has a complex and mammalian-like method for controlling gene expression that uses specific promoters to enable RNA polymerase to differentiate between which genes it should express when during viral infection. Our study has also uncovered over 30 novel genes that were previously unknown.”

By advancing knowledge of ASFV fundamental biology, this study provides vital information that will help progress research into desperately needed disease control methods.

This research was supported by funding from Wellcome.

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