Rome News-Tribune

Scientists scramble to determine if mutant strain will deepen pandemic

- By Gary Robbins

The COVID-19 vaccines rolling out across the nation are lifting spirits over the holidays. But there’s also budding concern about new strains of the virus that have been discovered in Great Britain, South Africa and possibly in Nigeria.

Scientists say they are hopeful, but unsure, that the vaccines will repel the mutants. The variant found in Great Britain may be more contagious than the original virus. And it’s unclear if the pathogens will take hold in the U.S., where nearly 19 million people have already been infected.

There’s lots of uncertaint­y because things are happening quickly. Researcher­s also say the U.S. hasn’t done enough to search for mutant strains of the virus and to figure out whether they’ll worsen the pandemic.

To get a better sense of what’s happening, the San Diego Union-Tribune posed questions to scientists who are involved in fighting the virus. They offered differing perspectiv­es, particular­ly on the nature of B.1.1.7, the mutant strain that helped lead to a lockdown in much of Great Britain.

The scientists are: Richard Scheuerman­n, director of the La Jolla campus of the J. Craig

Venter Institute, Nancy Binkin, professor of public health at the University of California, San Diego, and Greg Lemke, a molecular neurobiolo­gist at the Salk Institute.

Question: Let’s begin with a gut check. The public has been upset about the coronaviru­s for nearly a year. Does a mutant version of the virus pose a much deeper level of trouble?

Lemke:

Not necessaril­y. All viruses mutate during infection cycles, and most mutations are either of no impact or actually weaken a virus. SARS-CoV-2 has mutated repeatedly during this infection cycle. Concerns arise when mutations enhance virus infectivit­y, lethality or transmissi­bility.

Binkin: The rapid rise of cases in Southern England, despite all the measures undertaken to control spread, is alarming. If these mutations have made the virus more infectious by increasing the viral load or by shortening the incubation period or prolonging how long people remain infectious, this would have serious implicatio­ns for stopping further spread.

If the mutations also made the currently available treatments such as monoclonal antibodies less effective or the new vaccines less protective, this would also be very serious.

Scheuerman­n: I am not really worried about this strain, mainly because infections are running rampant in the United States already. So if another strain comes in maybe it will increase tranmissib­ility rates a bit. But they’re already high and it doesn’t appear that the virus is more virulent than the original. If it was, I would be more worried.

Q: The U.S. has not been routinely sequencing the genes of virus specimens to help determine what’s going on. Why not?

Binkin:

We have lagged behind some countries, especially Great Britain, which got its act together early. They have sequenced 157,000 virus specimens by working with their National Health Service and a consortium of universiti­es. The U.S. has sequenced about 51,000 specimens, and those have mostly come from 37 states. We are going to begin sequencing in all 50 states. But we’ll still be far behind the British, who plan to double the number of specimens they sequence, moving to 16,000 to 20,000 per week. We have been doing about 1,600 per week.

I don’t know whether the issue for us is funding or a lack of will or the fact that we don’t have the kind of centralize­d system the British have for pulling samples from its hospitals.

People are concerned that the mutation might be more lethal. That is an issue. But even if it is not, you could have more hospitaliz­ations and more deaths because a greater number of people become infected. We need to do more. Scheuerman­n: Public health labs are overwhelme­d with doing routine testing for the presence and absence of the coronaviru­s. They’re kind of under-funded and understaff­ed. When the outbreak spread, it became clear that doing genetic sequencing on the virus could be valuable. We weren’t as prepared for this as we should have been. But the CDC is rolling out a surveillan­ce program now.

Q: Does the lack of gene sequencing pose a major health risk? For example, could it make it harder to contain a mutant that is more contagious than the original virus?

Scheuerman­n:

It’s fair to say that without sequencing it would be harder to detect mutants that have the characteri­stics of the one we’re seeing in the U.K., where it seems to be highly transmissi­ble.

We would not recognize it right away. What you would have to see is a geographic region where all of a sudden the rates of infection increased dramatical­ly. That’s what they initially saw in the U.K. In parallel, they were doing surveillan­ce sequencing and recognized that the higher infection rates correspond to this new variant.

They saw it pretty rapidly.

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