SARS-CoV-2 mutations do not increase transmissibility, research shows

New research has found that none of the mutations currently documented in the SARS-CoV-2 virus appear to increase its transmissibility in humans. The study was conducted at University College London, UK. 

The team analysed the virus genomes from over 46,723 people with COVID-19 from 99 countries.

First and corresponding author Dr Lucy van Dorp said: “The number of SARS-CoV-2 genomes being generated for scientific research is staggering. We realised early on in the pandemic that we needed new approaches to analyse enormous amounts of data in close to real time to flag new mutations in the virus that could affect its transmission or symptom severity. Fortunately, we found that none of these mutations are making COVID-19 spread more rapidly, but we need to remain vigilant and continue monitoring new mutations, particularly as vaccines get rolled out.”

According to the researchers, coronaviruses like SARS-CoV-2 are a type of RNA virus, which can develop mutations in three different ways:

• by mistake from copying errors during viral replication
• through interactions with other viruses infecting the same cell (recombination or reassortment)
• induced by host RNA modification systems which are part of host immunity.

From their analyses, the researchers identified 12,706 mutations in SARS-CoV-2. For 398 of the mutations, there is strong evidence that they have occurred repeatedly and independently. Of those, the researchers honed in on 185 mutations which have occurred at least three times independently during the course of the pandemic.

To test if the mutations increase transmission of the virus, the scientists modelled the virus’s evolution and analysed whether a particular mutation was becoming increasingly common. They tested whether, after a mutation first develops in a virus, descendants of that virus outperform closely-related SARS-CoV-2 viruses without that particular mutation.

They found no evidence that any of the common mutations are increasing the virus’s transmissibility. Instead, they found most common mutations are neutral for the virus. This includes one mutation in the virus Spike (S) protein called D614G, which has been widely reported as being a common mutation that may make the virus more transmissible. The new evidence finds that this mutation is in fact not associated with significantly increasing transmission.

The researchers found that most of the common mutations appear to have been induced by the human immune system, rather than being the result of the virus adapting to its novel human host. This situation is in contrast with another analysis by the same team of what happened when SARS-CoV-2 later jumped from humans into farmed minks.

Van Dorp said: “When we analysed virus genomes sourced from mink, we were amazed to see the same mutation appearing over and again in different mink farms, despite those same mutations having rarely been observed in humans before.”

Lead author Professor Francois Balloux added: “We may well have missed this period of early adaptation of the virus in humans. We previously estimated SARS-CoV-2 jumped into humans in October or November 2019, but the first genomes we have date to the very end of December. By that time, viral mutations crucial for the transmissibility in humans may have emerged and become fixed, precluding us from studying them.”

“The virus seems well adapted to transmission among humans and it may have already reached its fitness optimum in the human host by the time it was identified as a novel virus,” van Dorp said. 

The researchers caution that the imminent introduction of vaccines is likely to exert new selective pressures on the virus to escape recognition by the human immune system. This may lead to the emergence of vaccine-escape mutants. The team stressed that the computational framework they developed should prove useful for the timely identification of possible vaccine-escape mutations.

“The news on the vaccine front looks great. The virus may well acquire vaccine-escape mutations in the future, but we’re confident we’ll be able to flag them up promptly, which would allow updating the vaccines in time if required,” concluded Balloux. 

The findings were published in Nature Communications.