We Study Virus Evolution. Here’s Where We Think the Coronavirus Is Going.
https://www.nytimes.com/interactive/2022/03/28/opinion/coronavirus-mutation-future.html?action=click&algo=bandit-all-surfaces-time-cutoff-30_filter_new_arm_10_1&alpha=0.05&block=trending_recirc&fellback=false&imp_id=561475047&impression_id=0152db95-ae8a-11ec-9959-1732caa73b57&index=2&pgtype=Article&pool=pool%2F91fcf81c-4fb0-49ff-bd57-a24647c85ea1®ion=footer&req_id=995734146&surface=eos-most-popular-story&variant=1_bandit-all-surfaces-time-cutoff-30_filter_new_arm_10_1
The charts are easy to understand.
March 28, 2022
By Sarah Cobey, Jesse Bloom and Tyler Starr and Nathaniel Lash
Dr. Cobey studies the interaction of immunity, virus evolution and transmission at the University of Chicago. Dr. Bloom and Dr. Starr study virus evolution at Fred Hutchinson Cancer Research Center in Seattle. Mr. Lash is a graphics editor for Opinion.
As scientists who study how viruses evolve, we are often asked about the future of the coronavirus. Will it go away? Get worse? Fade into the background of our lives? Become seasonal like the flu?
Here’s what we know: The virus’s Omicron variant was significantly more infectious and more resistant to vaccines than the original strain that first emerged in Wuhan, China. There’s no reason, at least biologically, that the virus won’t continue to evolve. The coronavirus variants that have emerged thus far sample only a fraction of the genetic space that is most likely available for evolutionary exploration.
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Many coronavirus vaccines train the immune system to recognize a particular section of the original virus: the 201 amino acids that allow the virus to latch onto human cells.
Only two of those amino acids were mutated in the Delta variant. The mutations weren’t enough to make vaccines ineffective.
Fifteen of the 201 amino acids that vaccines target were mutated in Omicron.The mutations helped Omicron evade the immune system and infect people who had been vaccinated or previously infected.
But the virus can mutate much further than the handful of changes seen in Omicron. Each amino acid can mutate 19 different ways.
Scientists have already documented more than 400 other mutations in the amino acids that vaccines target.
By our count, there are nearly 2,000 other ways that the 201 targeted amino acids could mutate and still be able to attach to human cells.
Source: Bloom Lab (Fred Hutchinson Cancer Research Center) research and analysis of GISAID viral genetic sequence data. Note: Figures for Omicron mutations show only the mutations present in the BA.1 lineage.
A virus like SARS-CoV-2 faces one overriding pressure: to become better at spreading. Viruses that cause more infections will be more successful. The virus can do this by becoming more contagious and by skirting around the immune system. This coronavirus has undergone several adaptations that make it better at spreading in humans.
But although many scientists, including us, expected SARS-CoV-2 would be under evolutionary pressure to transmit better, it’s been remarkable just how well the virus has responded to that pressure. Recent variants like Omicron and Delta are several times more transmissible than the strain that first spread around the globe in early 2020. That’s a huge increase, and makes SARS-CoV-2 more contagious than many other human respiratory viruses. These big jumps in contagiousness have played a major role in driving the pandemic so far.
Chart showing properties of certain SARS-CoV-2 variants. Along the X axis, reductions in antibody effectiveness for variants is shown. Along the Y axis are figures on how much more contagious the variant is compared to the original SARS-CoV-2.
How the coronavirus has mutated
Comparing coronavirus variants to early 2020 strains.
Omicron
4× as contagious
Delta
2×
Mu
Gamma
Alpha
Beta
Antibodies are
less effective
Epsilon
1×
Early 2020 strains
1×
2×
5×
10×
20×
40×
Estimated reduction in antibody effectiveness
Sources: Contagiousness is based on estimates of growth advantage by Marlin Figgins and Trevor Bedford. Antibody escape is based on antibody sera collected from patients treated with the Moderna vaccine. Note: Figures are approximate. Figures for Omicron reflect the variant’s BA.1 lineage and are extrapolated based on findings of a 105 percent growth advantage by Omicron compared to Delta.
How much more transmissible SARS-CoV-2 can become is an open question, but there are limits. Even evolution is constrained: a cheetah can’t evolve to be infinitely fast, and SARS-CoV-2 won’t become infinitely transmissible.
Other viruses have reached plateaus in their ability to spread. Some respiratory viruses such as measles are more contagious than today’s SARS-CoV-2. Others, such as influenza, are generally not as contagious as SARS-CoV-2. We don’t know when this coronavirus will hit its transmissibility plateau, but it will happen eventually.
Viruses such as this one can also spread better by “escaping” immunity to prior variants. Early in the pandemic, few people had immunity to SARS-CoV-2. But now much of the world has antibodies from vaccination or prior infection. Because these antibodies can block infection, variants with mutations that skirt around them have an increasing advantage.
The importance of immune escape has become apparent with Omicron. Prior variants like Delta were only modestly able to sidestep antibodies, but Omicron has many mutations that reduce the ability of antibodies to recognize it. This, coupled with how contagious Omicron is, has enabled it to cause a huge wave of infections.
The fact that the virus developed the ability to infect people who had been vaccinated or previously infected shouldn’t have been a surprise, but how it happened with Omicron certainly was. Evolution often proceeds stepwise, with new successful variants descended from recent successful ones. That’s why six months ago many scientists, including us, thought the next variant would descend from Delta, which was dominant at the time. But evolution defied our expectations, and we got Omicron, which has a huge number of mutations and isn’t descended from Delta. It’s not known exactly how the virus made the big evolutionary jump that led to Omicron, although many scientists (including us) suspect the variant may have emerged from someone who couldn’t fight off the virus well, allowing it time to mutate.
It’s impossible to say whether future variants will have more big Omicron-like jumps or more typical stepwise changes, but we are confident SARS-CoV-2 will continue to evolve to escape immunity.
While transmissibility of viruses does plateau at a certain point, other human viruses that escape immunity keep doing so. The influenza vaccine has been updated annually for decades to chase viral evolution, and some influenza viruses show no sign of slowing down. Immune escape is an endless evolutionary arms race, because the immune system can always make new antibodies and the virus has a vast set of mutations to explore in response. For instance, Omicron has just a tiny fraction of the many mutations that have been observed in SARS-CoV-2 or related bat viruses, which are in turn just a small fraction of what lab experiments suggest the virus could potentially explore.
Taking all this together, we expect SARS-CoV-2 will continue to cause new epidemics, but they will increasingly be driven by the ability to skirt around the immune system. In this sense, the future may look something like the seasonal flu, where new variants cause waves of cases each year. If this happens, which we expect it will, vaccines may need to be updated regularly similar to the flu vaccines unless we develop broader variant-proof vaccines.
And of course, how much all this matters for public health depends on how sick the virus makes us. That is the hardest prediction to make, because evolution selects for viruses that spread well, and whether that makes disease severity go up or down is mostly a matter of luck. But we do know that immunity reduces disease severity even when it doesn’t fully block infections and spread, and immunity gained from vaccination and prior infections has helped blunt the impact of the Omicron wave in many countries. Updated or improved vaccines and other measures that slow transmission remain our best strategies for handling an uncertain evolutionary future.
Sarah Cobey (@sarahcobey) runs a computational group at the University of Chicago that investigates the interaction of immunity, viral evolution and transmission. Jesse Bloom (@jbloom_lab) leads a lab at Fred Hutchinson Cancer Research Center in Seattle that uses a mix of experiments and computation to study the evolution of viruses such as SARS-CoV-2. Tyler Starr (@tylernstarr) is a postdoctoral fellow in Dr. Bloom's lab. Nathaniel Lash (@nat_lash) is a graphics editor for Opinion.