This undated electron microscope image made available by the U.S. National Institutes of Health in February 2020 shows the Novel Coronavirus SARS-CoV-2, yellow, emerging from the surface of cells, blue/pink, cultured in the lab. Also known as 2019-nCoV, the virus causes COVID-19. Photo by: NIAID-RML via AP
This undated electron microscope image made available by the U.S. National Institutes of Health in February 2020 shows the Novel Coronavirus SARS-CoV-2, yellow, emerging from the surface of cells, blue/pink, cultured in the lab. Also known as 2019-nCoV, the virus causes COVID-19. Photo by: NIAID-RML via AP

SANBI scientists peek inside first South African Sars-CoV-2 Genome

By ANA Reporter Time of article published Apr 7, 2020

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CAPE TOWN- Covid-19 pandemic has emerged, wrecking havoc and taking a heavy toll around the world, researchers from the National Institute for Communicable Diseases (NICD) and University of the Western Cape (UWC)’s South African National Bioinformatics Institute (SANBI) have sequenced the first Sars-Cov-2 genome in the country, providing a genetic "fingerprint" that can help understand and contain the spread of the virus.

“Next-generation sequencing of pathogens allows us to perform genomic fingerprinting on viruses,” says Peter van Heusden, SANBI researcher and co-author of the new report presenting the sequence, phylogenetic analysis and modelling of non-synonymous mutations for a Sars-CoV-2 genome that was detected in a South African patient with Covid-19.

“Much like you look more similar to your siblings and cousins than you do to a person chosen at random, this fingerprint of viruses can be used to organise the samples into clusters and thus understand the spread of the disease,” he says.

Medical scientists, Arshad Ismail, Zamantungwa Khumalo, Phillip Senzo Mtshali, Florah Mnyameni, Mushal Allam, and Stanford Kwenda at the NICD Sequencing Core worked with Jinal Bhiman’s group at the NICD's Centre for Respiratory Diseases and Meningitis on doing the initial sample collection sequencing for this. 

Peter van Heusden, SANBI researcher and co-author of the new report presenting the sequence, phylogenetic analysis and modelling of non-synonymous mutations for a Sars-CoV-2 genome that was detected in a South African patient with Covid-19. Picture: Supplied

“The sample is from a patient's nose and throat so it is not ‘pure virus’. The only way to get a pure virus is to grow or culture the virus and no one wants to do that,” Van Heusden says. 

“It is thus challenging to get enough virus DNA from a sample to get a complete virus genome, but the NICD managed to do it.” 

SANBI researchers then compared the virus genome with a collection of virus genomes from around the world, sourced via the Global Initiative on Sharing All Influenza Data (GISAID) website, a global data sharing initiative for flu, and now for Covid-19 as well. 

“I examined each difference between our South African genome and other genomes to see if the evidence was there to support it. In the end we had six differences,” Van Heusden explains.

These differences are important for two reasons, he says.

“Firstly they give us a ‘fingerprint’ that is useful to understand the spread of the virus,” Van Heusden notes. 

“In this case the version of the virus found in South Africa looks like the ones found in Europe and the USA, suggesting that the virus is travelling alongside people travelling between SA and those places. We suspected that already, but this helps confirm it.”

Secondly, we can look at how the differences impact on the proteins the virus makes, according to Van Heusden.

“Genes don’t directly determine what happens in cells,” he further explains. 

“Proteins are the molecular machines that make cells work and the virus genome is like a recipe book for the proteins the virus needs to do its work, invading cells and making copies of itself.”

Another SANBI researcher, Ruben Cloete, helped with that part, confirming that the changes in the virus genome are mostly neutral, making very little difference in the proteins made by those particular genes. 

“It’s important to note that this is true for most changes in a virus, they don't create ‘super mutants’ but are just like the difference between your eye colour and that of someone else,” Van Heusden notes. 

“People sometimes panic when they hear that a virus is mutating, but that’s just natural and most mutations just don’t matter much.”

The work is a contribution to the global efforts to track and trace the ongoing coronavirus pandemic. As of April 1, more than 3,000 Sars-Cov-2 genomes were globally sequenced and uploaded to GISAID. 

The Nextstrain website provides real-time monitoring of the spread and evolution of the Sars-CoV-2 virus, drawing on sequence data stored in GISAID. 

“Ideally, you want to be able to analyse virus DNA samples to better understand the spread of disease or predict when an outbreak will occur,” says Van Heusden. “With a sufficient number of sequenced genomes, it is possible to reconstruct a phylogenetic tree of the mutation history of a family of viruses.”

African News Agency (ANA)

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