One of the big mysteries in the Ebola
outbreak in West Africa is where the virus came from in the first
place — and whether it's changed in
any significant ways. These unanswered questions could be making it more
difficult to diagnose the disease and find treatment.
Now scientists are
starting to get some answers. In a new paper in Science,
researchers reveal that they have sequenced the genomes of Ebola from 78
patients in Sierra
Leone who contracted the disease in May and June. Those sequences
revealed some 300 mutationsspecific
to this outbreak.
The new analysis could
help determine if the virus' behavior has changed — and
provide information for future diagnostic tests and treatments.
Among their findings, the researchers discovered that the current viral
strains come from a related strain that left Central
Africa within the past ten years. And the research confirms that the virus
likely spread into Sierra Leone when women became infected after attending
the funeral of
a traditional healer who had been treating Guinean Ebola patients.
The current Ebola
outbreak in West Africa is the worst on
record. It has hit four countries, including Sierra Leone, infected
approximately 3,000, and killed about 1,500 people. And so far, there is no
sign of it slowing down.
The fact that the
researchers published the sequence of the Ebola genomes in mere months
contrasts with the typically slow pace of scientific research. "We’re
trying to do this as fast as possible," says co-senior author Pardis
Sabeti, a biologist at MIT and Harvard. This new data increases the number
of public Ebola virus sequences fourfold.
The paper is also
a sad reminder of the toll that the virus has taken on those working
on the front lines. Five of the authors died of Ebola before it
was published. All were affiliated with Kenema Government Hospital in
Sierra Leone.
Viruses randomly mutate over time. This is
completely normal for viruses, and there's no reason to think that
Ebola's mutation
rate is anything weird or unusual.
Scientists can use
these mutations as markers to piece together how the Ebola virus has traveled
from person to person. Because they know the general mutation rate of the
virus, they can also pin down the dates of when the disease spread.
So what has this
analysis revealed? Using genetic sequences from current and previous outbreaks,
the researchers mapped out a family tree that puts a common ancestor of the
recent West African outbreak some place in Central Africa roughly
around 2004. This contradicts an earlier hypothesis that the virus had been
hanging around West Africa for much longer than that.
The data, on the
whole, supports what epidemiologists have already deduced about how the virus
spread into Sierra Leone. More than a dozen women became infected after
attending the funeral of
a traditional healer who had been treating Guinean Ebola patients and contracted
the disease.
One surprise from the
paper is that two different strains of Ebola came out of that funeral.
This suggests that either the healer was infected with two different strains or
that another person at the funeral was already infected.
As Ebola then traveled
across Sierra Leone, a third strain of the virus appeared.
Why having Ebola gene
sequences is helpful
Some Ebola diagnostic
tests have been designed to detect areas that have mutated in the Ebola virus
samples from this outbreak, raising the possibility these tests might be losing
accuracy. One of the things Sabeti plans to do next is test whether that's
actually the case.
Diagnosing Ebola can
actually be more difficult than it might sound. The disease often looks like a
lot of other feverish illnesses that can be common. And at a later stage, only
some patients end up bleeding.
However, it's
essential to know who has it as soon as possible, especially so that
health-care workers can use appropriate procedures to
prevent transmission to themselves and others. So accurate diagnostic tests are
absolutely needed.
Researchers are also
planning to study the mutations to see if any of them are affecting Ebola's
recent behavior. The number of mutations found is completely normal, and it
isn't necessarily the case that they'll have a big effect. But it's possible
that something intriguing could turn up.
For example, this
outbreak has had a higher transmission rate and lower death rate than
others, and researchers are curious if any of these mutations are related to
that. (Right now, social factors are thought to be the main causes of these two
changes.)
"It sets the
stage for the next few years of research that will reveal the differences
between this virus and previous versions of Ebola virus," says Erica
Ollmann Saphire, who researches Ebola and similar viruses at The Scripps
Research Institute in La Jolla, California.
"My laboratory
will be using this sequence information to understand the molecular effects of
these mutations," she says. "We will also be looking at our pool of
antibody therapeutics beyond ZMapp to
ensure that candidate cocktails are optimally effective against these
circulating strains."
Those working on other
long-term projects involving vaccines should
also find this information helpful.
The longer Ebola
circulates, the more opportunities it has to change — possibly for the worse
Although Ebola's mutation
rate itself isn't anything unusual, the longer it's circulating in
people, the more chances it will have to randomly come up with a mutation that
it will find beneficial — possibly to the detriment of human health.
"You never want
to give a virus that kind of opportunity," Sabeti says. "We hope that
this work opens up new doors for more people to work together to stop this
virus now."




No comments:
Post a Comment