A change of heart: New drug for HCM reduces heart mass

For the first time, a medication has impacted heart muscle thickness and function for patients with the most common inherited heart condition, rather than simply addressing their symptoms.

“This is the first study to show a favorable impact of a medication on cardiac structure and function in any form of hypertrophic cardiomyopathy,” says Sara Saberi, M.D., an assistant professor of internal medicine and a cardiologist at the Michigan Medicine Frankel Cardiovascular Center.

Current options, Saberi explains, might help patients feel better today, but they don’t help them live longer, nor do they prevent people from experiencing heart failure down the road. They also don’t affect any of the heart structural abnormalities that define the disease: thickness of the heart muscle, resultant stiffness and abnormalities in other cardiac structures.

“There’s a huge void. HCM is a chronic progressive disease that still does not have a cure,” Saberi says.

She presented the results of her team’s EXPLORER-HCM CMR sub-study at the 2020 American Heart Association Scientific Sessions, which published simultaneously in Circulation.

Addressing the underlying cause of HCM

In HCM, the motor proteins interact with each other too much, causing over-vigorous squeeze of the muscle and causing stiffness of the muscle.

A medication designed specifically for HCM, mavacamten, is currently being studied in a variety of clinical trials. It’s part of a new class of drugs called cardiac myosin inhibitors. The medication works by blocking a protein called myosin from interacting too much with other motor proteins, which then allows the heart muscle to squeeze and relax more normally, Saberi explains. It is effective at reducing obstruction to blood flow within the heart that can occur with the disease.

“It’s the first class of medications that actually targets the underlying pathophysiology of HCM.”

The primary measure for this study, the mass of the heart, was significantly reduced in those patients taking the drug as opposed to those taking placebo, Saberi says.

In September, Saberi and colleagues published findings from the EXPLORER-HCM randomized controlled trial in The Lancet. The patients had significant improvements in obstruction to blood flow in the heart and said they felt better after taking the drug for 30 weeks. They showed improvements in markers like exercise capacity. Now, this substudy explores some of the reason why people may be feeling better, Saberi says.

Results from cardiac imaging

The substudy was done using imaging of the study participants’ hearts.

“Cardiac MRI has such incredible visual and spatial resolution that you can accurately examine the heart’s mass, volume, ejection fraction, or how well the blood is pumping, and fibrosis, which is the scar burden in the heart muscle,” Saberi says.

Her team observed these encouraging results after just 30 weeks of treatment, which would be a plus for patients, Saberi says.

“It’s also encouraging that we don’t see a worsening in fibrosis along with the normalization in ejection fraction,” she says. Patients originally had a very high ejection fraction, but after treatment it moved into the normal range.

Although HCM is considered a rare disease, it affects about one in 500 people, Saberi says, so there’s a large need for more effective therapeutics.

The EXPLORER-HCM trial was a phase three trial that studied the use of mavacamten in obstructive HCM, and has moved into a five-year open-label extension. A concurrent phase two trial, MAVERICK-HCM, investigated safety and tolerability in non-obstructive HCM. Those participants are also in the five-year open-label extension study now. Saberi says a phase three trial that would look at how well it works for those patients with non-obstructive HCM would be the next step.

The medication is not currently available outside of a clinical trial setting, Saberi says.

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Henderson island fossils reveal new Polynesian sandpiper species

Fossil bones collected in the early 1990s on Henderson Island, part of the Pitcairn Group, have revealed a new species of Polynesian sandpiper.

The Henderson Sandpiper, a small wading bird that has been extinct for centuries, is described in an article in the Zoological Journal of the Linnean Society published last week.

The newly-described bird is formally named Prosobonia sauli after Cook Islands-based ornithologist and conservationist Edward K Saul.

A team of researchers from New Zealand, Australia, Denmark, Switzerland, the Netherlands and China, led by Canterbury Museum Research Curator Natural History Dr Vanesa De Pietri, described the Henderson Sandpiper from 61 fossilised bones cared for by the Natural History Museum at Tring in England.

Canterbury Museum Visiting Researcher Dr Graham Wragg collected the bones from caves and overhangs on Henderson Island in 1991 and 1992 during the Sir Peter Scott Commemorative Expedition to the Pitcairn Islands.

Prosobonia sauli is the fifth known species of Polynesian sandpiper. All but one of the species, the endangered Tuamotu Sandpiper (Prosobonia parvirostris), are extinct.

“We think Prosobonia sauli probably went extinct soon after humans arrived on Henderson Island, which archaeologists estimate happened no earlier than the eleventh century,” says Dr De Pietri.

“It’s possible these humans brought with them the Polynesian rat, which Polynesian sandpiper populations are very vulnerable to.”

DNA of the living Tuamotu Sandpiper and the extinct Tahiti Sandpiper (Prosobonia leucoptera), which is known only from a skin in the Naturalis Biodiversity Center in the Netherlands, was used to determine how Polynesian sandpipers are related to other wading birds.

“We found that Polynesian sandpipers are early-diverging members of a group that includes calidrine sandpipers and turnstones. They are unlike other sandpipers in that they are restricted to islands of the Pacific and do not migrate,” says Dr De Pietri.

Comparisons with the other two extinct Polynesian sandpiper species, the Kiritimati Sandpiper (Prosobonia cancellata) and the Mo’orea Sandpiper (Prosobonia ellisi), are complicated. These birds are known only from illustrations primarily by William Wade Ellis, an artist and Surgeon’s Mate on Captain James Cook’s third expedition, who probably saw the birds alive in the 1770s.

Compared to the Tuamotu Sandpiper, its geographically closest cousin, the Henderson Sandpiper had longer legs and a wider, straighter bill, indicating how it foraged for food. It probably adapted to the habitats available on Henderson Island, which are different to those on other islands where Polynesian sandpipers were found.

Henderson Island is the largest island in the Pitcairn Group, in the middle of the South Pacific Ocean. It has been uninhabited since around the fifteenth century and was designated a World Heritage Site by the United Nations in 1988.

Dr Paul Scofield, Canterbury Museum Senior Curator Natural History and one of the study’s co-authors, says Henderson Island is home to a number of unique species, a handful of which are landbirds like the Henderson Sandpiper.

“The island is really quite remarkable because every landbird species that lives there, or that we know used to live there, is not found anywhere else,” he says.

Dr De Pietri says the study shows the need to protect the one remaining Polynesian sandpiper species, the Tuamotu Sandpiper.

“We know that just a few centuries ago there were at least five Polynesian sandpiper species scattered around the Pacific. Now there’s only one, and its numbers are declining, so we need to ensure we look after the remaining populations.”

This research was supported by a grant from the Marsden Fund Council, managed by the Royal Society Te Ap?rangi, as well as the R S Allan Fund managed by Canterbury Museum.

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Health24.com | Cold truth: South Africa won’t be able to store these Covid vaccines. Here’s why.

  • The first results for a Covid vaccine are out, with Pfizer and BioNTech reporting 90% efficacy and Moderna reporting almost 95% efficacy based on early data
  • Despite its promise, cold chain requirements mean this jab wouldn’t be the first choice for countries like South Africa
  • The vaccine needs to be kept at minus 70 degrees Celsius, well below other vaccines used in South Africa, which poses a huge challenge to its delivery and storage

The world’s first hope for a Covid-19 vaccine – the jab developed by drug companies Pfizer and BioNTech, showing 90% efficacy in preventing Covid-19 in early results, and Moderna’s candidate showing almost 95% efficacy – is highly unlikely to become widely available in South Africa.

This is because Pfizer’s vaccine needs to be stored below freezing temperatures – at minus 70 degrees Celsius — that the country doesn’t have the capacity to do on a large scale. If the shots are kept at temperatures too high or too low, they can spoil and become less effective.

In the United States, large city hospitals are already “rushing to buy the expensive ultra-cold freezers” that cost between R150 000 and R235 000 each, to store the shots, for which Pfizer and BioNTech will apply for an emergency license from the US regulator, the Food and Drug Administration (FDA), later this month, Statnews reports.

And just three days after the announcement of the BNT162b2 vaccine’s first interim results, the European Union signed an agreement with the manufacturers to supply it with 200 million doses and an option to request an additional 100 million doses, “with deliveries anticipated to start by the end of 2020, subject to regulatory approval”.

But South Africa doesn’t have the required ultra-cold freezers to store the vaccine – except for a few at large research institutions such as the National Institute for Communicable Diseases, says director of Vaccines for Africa at the University of Cape Town, Gregory Hussey.

And, along with less well-off rural hospitals in developed countries, the country is unlikely to be able to afford to buy enough of the freezers to be able to make the vaccine available at community health centres or clinics, or pay for the cold chain systems that are necessary to maintain the vaccines.

Most vaccines that are part of South Africa’s immunisation programme have to be kept at temperatures between two and eight degrees Celsius. The country’s system – including vaccine transportation, storage, and monitoring – is therefore not suitable for vaccines that need to be kept below freezing temperatures.

And the Pfizer/BioNTech vaccine is not the only Covid-19 frontrunner that is likely to pose a problem to South Africa. The biotechnology company, Moderna’s mRNA-1273 jab, which released its first results on Monday, needs to be stored at minus 20 degrees Celsius.

Although, the pharmaceutical company released new data on Monday showing that their candidate could be stored at a standard temperature of between two and eight degrees Celsius for up to 30 days – compared to its shelf life of six months when kept frozen. Despite this revised storage temperature, the jab still needs to be shipped and transported at minus 20 degrees Celsius.

Pfizer/BioNTech and Moderna’s vaccine both use mRNA technology. Such vaccines use pieces of man-made genetic material known as messenger ribonucleic acid, or mRNA, that instructs our bodies to produce proteins, in the form of antibodies and killer cells, to fight off SARS-CoV-2, the virus that causes Covid-19.

But the snag is that these two mRNA vaccines need to be kept at extremely low temperatures, or they risk becoming damaged. 

And to complicate things even further, mRNA vaccine technology is new – not a single vaccine using mRNA messengers has been licensed for human use up to date.

“I don’t know if we could really even contemplate an mRNA vaccine with our present setup,”  explains Barry Schoub, chair of South Africa’s ministerial advisory committee on coronavirus vaccines. “Things may change, but with our present setup, the places where we could actually utilise it would be so limited that it would be a major challenge.”

South Africa’s challenge of keeping vaccines cool    

Maintaining a cold chain – where a product must be consistently stored at a low temperature – is important to ensure that vaccines don’t degrade or lose their efficacy. A 2018 paper in the journal Vaccine, showed that although this deterioration did not pose a safety risk to people receiving the vaccine, the jabs offered less protection after being stored at the wrong temperature.

This is a major risk for rural hospitals and clinics or those facilities that lack adequate infrastructure to properly store doses when a Covid vaccine becomes available, according to Hussey, who also serves on the Covid vaccines ministerial advisory committee.

Schoub, who is also a virologist and former director of the National Institute for Communicable Diseases, agrees: “You can’t really store vaccines reliably and sustainably at minus 20 degrees Celsius anywhere outside the bigger cities. Especially if you’re looking at places with a hotter climate, like the Northern Cape or KwaZulu-Natal, even maintaining a freezer at minus 20 is going to be a question mark.”

This means that even with Moderna’s stability at lower temperatures, South Africa’s cold chain system may be unable to handle maintaining the vaccine at its required minus 20 degrees Celsius during transport. Fluctuations in the temperature along the way could cause the jab to become less effective and offer less protection to the person being vaccinated. 

According to Schoub, Pfizer/BioNTech are considering freeze-dried vaccines – in the form of frozen powders to which liquid is later added – which could potentially ease cold chain requirements for the jab, because they can be stored between two and eight degrees Celsius. But the timeline for this, he says, is still unclear.  

But even without taking into account the additional obstacles that will arise with maintaining a vaccine at well below 0 degrees Celsius, just regulating the temperature for our existing vaccines is already a challenge.

An assessment of vaccine management in 18 countries done by the World Health Organisation Regional Office for Africa in 2001 found that “only 47% of the indicators were satisfactorily met for buildings, cold chain equipment, and transport at the national level”.

In the Western Cape, a 2015 study published in Vaccine found that government-managed vaccine supply chains were often unable to manage the temperatures at which vaccines need to be stored, adequately. 

The average temperature of health centre fridges in the study ranged from 0.9 to 9.2 degrees Celsius, meaning that the jabs could have potentially been stored at temperatures both too low or too high and been damaged.

Why does 90% efficacy matter? 

Despite the delivery challenges of the Pfizer/BioNTech vaccine, its 90% potential efficacy has physicians and scientists, who mostly expected a much lower efficiency, excited.

Although it is only initial data that could still change as the trial progresses, this kind of efficacy puts the jab in the same category as the world’s most effective vaccines, such as the measles shot.  

Schoub explains: “If it does turn out to be true then that is a major, giant step forward, but at this stage it’s very difficult to assess how accurate that figure is because it’s still early in the trial.”

A higher efficacy rate means that the jab is able to offer more protection to a population. This is important when it comes to the role of a vaccine in offering immunity to a community.

If only half the people receiving a vaccine are going to be protected, you need to vaccinate a much larger portion of the population in order for it to make a difference and properly contain an outbreak.

With herd immunity as the end goal – where enough of the population is protected or resistant to the virus that it stops spreading – the measles vaccine, which is 97% effective at preventing measles, is often held up as the ideal.

But until now, scientists have been skeptical that we would be able to reach the same level when it came to Covid-19.

As Schoub explains, it was speculated that a Covid vaccine would be unlikely to offer the same level of protection as the measles shot because of the differences between the two diseases. While both are spread in a similar manner, through coughs or sneezes, they fundamentally differ in how they affect a person’s body.

Measles is a systemic disease, meaning it affects the whole body, while Covid is initally a pulmonary disease that mainly targets the lungs. In that respect, Covid is more similar to influenza, which is what has been used as the sort of benchmark when it comes to vaccine efficacy, says Schoub.

The distinction in how the disease works matters, because it influences the type of immune response – with measles requiring the production of antibodies in the blood to fight off the measles virus and influenza needing a more complicated immune response through antibodies in respiratory secretions.

The type of immune response needed to fight off influenza is hard to get through vaccinations, with most flu jabs only offering around a 60% chance of protection from the infection.

Most Covid vaccine trials are therefore designed to pick up around 60% efficacy in a vaccine candidate, the director of the American government’s National Institute of Allergy and Infectious Diseases, Anthony Fauci, explained in a Medical Brief webinar in October.  

But regardless of whether the Pfizer/BioNTech candidate is suitable for South Africa, the issue of delivering a vaccine is something we need to begin working on now, says Hussey.

He concludes: “There is a huge cost involved in delivering a vaccine, the World Health Organisation has estimated that cost of delivery of vaccines could be up to two or three-fold greater than the cost of the vaccines alone.

“There is also the additional operational costs of conducting immunization campaigns during the Covid-19 pandemic. We have to ensure that the facilities, the staff administering vaccines and the recipients of vaccines are kept ‘Covid safe’. That’s something we need to factor into our planning.”

And even though South Africa is only expecting to get enough Covid vaccines for around 5% of its population by next year, and a large rollout to the general public will likely only come in the next two years, Hussey cautions: “I think getting the vaccine is a simple thing.

“Getting the vaccine out to the people who need it is the challenge and we don’t have a great track record in even getting routine vaccines to the communities that need them most.”

*This story was produced by the Bhekisisa Centre for Health Journalism. Sign up for the newsletter.

*This story has been updated with latest information related to the Moderna vaccine candidate,

Image credit: Getty Images

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NaNoWriMo – Days 13-15

We’re halfway through NaNoWriMo 2020, and my novel is now at 26,344 words.

Since this is the halfway point – with 50K words in 30 days being the goal – I should be at 25K words now, so I’m 1344 words ahead.

I think it was a wise decision to get ahead of the 1667 words per day pacing and then to pad that lead by a small amount each day, so I always feel like I’m ahead of schedule.

Many people get behind on their desired pacing and end up having to write 10-20K words in the last few days to catch up (or even on the final day). While I don’t think it’s such a big deal to do a marathon catch-up session at the end, I don’t think the Nano experience is quite as fun and motivating if you spend most or all of it feeling like you’re behind. I very much prefer to feel slightly ahead for the entire month.

It’s nice to just do 1700 or 1800 words and call my writing done for the day, knowing that I’m padding my lead by a modest amount each day. I can do that all month long with relative ease.

It’s especially nice to know that all I have to do is continue the same pacing I’ve been using for the first 15 days for the second 15 days, and I’ll coast across the finish line, likely reaching 50K words on Day 28 or 29.

Enjoyment

Some people talk about hitting a wall around this point. I’m presently experiencing the opposite.

Even when I hit my word target for the day and think, “I could do another 500 words right now,” I still stop. I prefer to leave something in the tank for the next day. This approach is working well. I’m feeling more motivated as I go along instead of feeling drained.

The writing is so much easier now than it was when I started, especially since I know the characters better after writing 20+ scenes with them. The dialogue feels more natural as it flows onto the screen, like real people communicating with wit, charm, humor, sass, and occasional silliness. It’s nice to be past the stiffness and shallowness of the dialogue that I began with in the first week. Now it’s easy to tell characters apart just from their speech patterns.

I didn’t know that it would be so much fun to breathe life into characters and then see how they respond to different situations. As I gradually build more detailed representations for these characters somewhere in my brain, it’s easier to discern how they’ll respond and react.

I still have to think through a lot of the plot, but now I’m able to write decent scenes just by grabbing a few characters and putting them into a fresh situation. They naturally seem to say and do things in accordance with their goals.

This is giving me the capacity to focus on other aspects of the story. I can now write scenes with more detail, nuance, and subtlety than when I first started, mainly because I don’t have to expend so much mental energy figuring out what the characters will say and do.

Sexuality

One aspect I’m wondering about is how sexual to make the story. There is a lot of sexuality in some scenes as I’m currently writing them, and I’m just running with that for now because it’s a first draft. But I am thinking ahead to whether I may end up cutting a lot of that material later.

I don’t recall ever reading any erotica (other than what people occasionally send in the form of naughty emails), and I’m not really trying to write that kind of book.

The story doesn’t have to go too much in a sexual direction, but for now there’s a certain pull with some characters and situations to take it there, and it would be weird not to let those characters have at it when they seem inclined. This is definitely a sci-fi story, but there’s an unusual romance at the core of it too.

None of the sexual aspects are vanilla, so they’re not like what you’d see in a typical R-rated movie with a sex scene or two. There are sexual situations in the book that don’t currently exist today, mainly due to the melding of sexuality and AI in the story.

One concept that Robert McKee emphasized in his Story seminar last year was to “Write the truth.” I think I grasp what he means by this. There’s an inauthentic way to have characters behave, so as to force some predetermined plot points to occur. But well-developed characters have their own authenticity to uphold.

Another way to write the truth is to share something deep and real that rings true. “Write the truth” is a call to courage – to be honest in expressing the story’s themes and not to water down the ideas. So I take that to mean that if the sexual aspects are honest expressions of the themes, then they very much belong in the story.

It feels aligned to have characters behave like real humans would, not to steer them away from sex if they’d actually be inclined to nudge things in that direction.

The competing force is thinking about selling the book to readers when it’s done. I’ve only done a little research on the book market so far, but I see a lot of potential for this story to be made into a movie someday. As it stands now, this novel would surely be an X-rated movie. At this point I don’t know if the story has to go that route to be authentically told though.

I could tone it down in future drafts to make it R or PG-13. I’m not sure if I’ll want to though. I think the story is likely to be more honest with more sexual situations intact or even expanded. The sexual situations are far from gratuitous. They naturally fit the flow of the story. And they help to raise the stakes as the story progresses.

Personally I think the story will be more fun to read if the sexual aspects are included instead of artificially censored. So my current preference is to write the book for readers who will appreciate authentic sexuality that fits the honest story without feeling like it should be more prudish.

I just don’t think it would feel as good to me to publish a story where I felt like I held back a lot just to appeal to a broader market. I don’t think I want to be that kind of writer.

However, if I can make the book appeal to a broader market without sacrificing anything that’s really important to the story, I may consider that, but my priority is to tell an interesting and meaningful story.

Instead of getting emails that say “cool story,” I’d honestly rather get emails that say, “That was hot! More please!” combined with other emails that say, “You will rot in hell for this, foul demon!”

There are plenty of vanilla books for vanilla readers. I think it would be more rewarding to write a book that scares away vanilla readers and pleases the non-vanilla ones. This isn’t due to being overly rebellious. I think honesty will suffice.

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Coronavirus: Dentists warn millions of treatments have been missed

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Health24.com | Weight loss and timing of meals – does it matter?

  • Eating more at breakfast and less at dinner was previously seen as beneficial
  • Studies were conducted indicating that this could help with weight loss
  • Recent research, however, shows otherwise

There are many theories around when and what one should eat in order to lose or maintain weight. One widely-accepted belief is that we must eat breakfast and that most of our daily calories should be consumed at breakfast. 

This idea is backed by numerous studies, one of which concluded: “High-calorie breakfast with reduced intake at dinner is beneficial and might be a useful alternative for the management of obesity and metabolic syndrome.”

Ground-breaking research presented on 13 November at the American Heart Association’s Scientific Sessions 2020, however, proves otherwise.

Author of the study and associate professor at John Hopkins University, Nisa M. Maruthur stated: “We have wondered for a long time if when one eats during the day affects the way the body uses and stores energy.” 

This led Maruthur and a team of her colleagues to conduct a study investigating whether restricting meals to early in the day would facilitate weight loss.

Time-restricted eating patterns

The study involved 41 adults with a BMI that classified them as being overweight. Ninety percent of the participants were Black women who were either diabetic or prediabetic. Twenty-one of the participants were assigned to a time-restricted eating plan which limited them to eating at specific hours only, and they had to eat 80% of their daily calories before 13:00.

The remaining 20 adults ate at usual times but consumed 50% of their daily calories after 17:00. Weight and blood pressure of the participants were measured at four-week intervals.

The researchers hypothesised that participants following a time-restricted feeding pattern would lose more weight than those following a more traditional eating pattern.

Eating times not deciding factors for weight loss

Researchers were stunned by the results of the study, which found that across both groups people lost weight and their blood pressure decreased regardless of when they ate. 

According to Maruthur, “Most prior studies have not controlled the number of calories, so it wasn’t clear if people who ate earlier just ate fewer calories. In this study, the only thing we changed was the time of day of eating.”

These results prove that you won’t necessarily gain weight if you were to eat bigger meals later in the day compared to eating a larger number of calories in the morning.

Image credit: iStock

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Health24.com | A common Covid-19 virus mutation may make it more susceptible to vaccines

  • It’s been confirmed that SARS-CoV-2 has mutated in a way that’s enabled it to spread more quickly 
  • However, the spike mutation may also make the virus more susceptible to a vaccine
  • As the study was not carried out on humans, additional studies are needed to track the consequences of these mutations 

The new coronavirus has a complex biology, and, according to ScienceMag, accumulates about two changes per month in its genome (the genetic material).

Now, a new study by scientists from the University of North Carolina at Chapel Hill and the University of Wisconsin-Madison has revealed that, while SARS-CoV-2 has mutated in a way that’s enabled it to be more infectious than other coronaviruses, the spike mutation may also make it more susceptible to a vaccine.

The findings, published in Science, note that the new strain, called D614G, emerged in Europe and has become the most common in the world. 

Strain more sensitive to neutralisation 

“The D614G virus outcompetes and outgrows the ancestral strain by about 10-fold and replicates extremely efficiently in primary nasal epithelial cells, which are a potentially important site for person-to-person transmission,” study author Ralph Baric, professor of epidemiology at the UNC-Chapel Hill Gillings School of Global Public Health and professor of microbiology and immunology at the UNC School of Medicine, said in a UNC news release.

However, despite the D614G strain replicating faster and becoming the most common worldwide, the research team found that it is slightly more sensitive to neutralisation by antibody drugs.

Baric has studied coronaviruses for more than three decades. He was also integral in the development of remdesivir, the first FDA-approved treatment for Covid-19. 

Why does the strain dominate?

Researchers believe the D614G strain dominates because it increases the spike protein’s ability to open cells for the virus to enter.

“The original spike protein had a ‘D’ at this position, and it was replaced by a ‘G’,” said Yoshihiro Kawaoka, a virologist at the University of Wisconsin-Madison.” Several papers had already described that this mutation makes the protein more functional and more efficient at getting into cells.”

The newly discovered mutation causes a flap on the tip of one spike to pop open, the researchers explained, thereby allowing the virus to infect cells more efficiently. It also creates a pathway to the virus’s vulnerable core, they said.

On the bright side, with one flap open, it’s also easier for antibodies, such as the ones currently being tested in vaccines, to infiltrate and disable the virus.

For this study, the researchers ran hamster experiments and performed replication and airborne transmission studies with both the original virus and the mutated version created by the team.

“We saw that the mutant virus transmits better airborne than the [original] virus, which may explain why this virus dominated in humans,” said Kawaoka.

Pathology also examined

In addition to the above, the researchers also looked at the pathology of the two coronavirus strains.

After infection, the hamsters displayed more or less the same viral load and symptoms, suggesting that while the mutant virus is much better at infecting hosts, it doesn’t cause significantly worse illness.

However, the researchers caution that these results may not reflect in human studies.

“SARS-CoV-2 is an entirely new human pathogen and its evolution in human populations is hard to predict,” Baric said.

“New variants are continually emerging, like the recently discovered mink SARS-CoV-2 cluster 5 variant in Denmark that also encodes D614G.

“To maximally protect public health, we must continue to track and understand the consequences of these new mutations on disease severity, transmission, host range and vulnerability to vaccine-induced immunity,” he commented.

READ | Does it matter that the Covid-19 virus is mutating?

READ | Mutation helps coronavirus infect more human cells, study shows

READ | How genetic mutations in healthy young men made them susceptible to severe Covid-19

Image credit: Getty/Peter Zelei Images

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