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Ebola Evolved Into Deadlier Enemy During the African Epidemic

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Author: God_Eater_4       Show all posts   Read mode

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Post time 14-11-2016 02:52 AM | Show all posts |Read mode
Ebola Evolved Into Deadlier Enemy During the African Epidemic
Carl Zimmer
MATTER NOV. 3, 2016

A burial team in Bong County, Liberia, buried a suspected Ebola victim in October 2014. The Ebola epidemic that hit West Africa that year claimed 11,310 lives. Credit Daniel Berehulak for The New York Times

The Ebola epidemic that tore through West Africa in 2014 claimed 11,310 lives, far more than any previous outbreak. A combination of factors contributed to its savagery, among them a mobile population, crumbling public health systems, official neglect and hazardous burial practices.

But new research suggests another impetus: The virus may have evolved a new weapon against its human hosts. In studies published on Thursday in the journal Cell, two teams of scientists report that a genetic mutation may have made Ebola more deadly by improving the viruss ability to enter human cells.

The researchers do not yet understand exactly how it works, but several lines of evidence suggest it helped expand the scope of the epidemic. One alarming finding: Patients infected with the mutated version of Ebola were significantly more likely to die.

Its hard to escape the conclusion that its an adaptation to the human host, said Dr. Jeremy Luban, a virologist at the University of Massachusetts Medical School and an author of one of the new studies.

Normally, Ebola circulates among animal hosts, probably African bats. Scientists suspect that the West African epidemic began when a bat infected a boy in a village in Guinea in December 2013.

As reports of the outbreak surfaced, Dr. Pardis C. Sabeti, a computational biologist at Harvard, and her colleagues started a collaboration with doctors in Sierra Leone. The researchers quickly sequenced the genomes of 99 Ebola viruses isolated from 78 patients there.

Their analysis showed that Ebola was moving quickly from one victim to the next, and that the virus was gaining new mutations along the way. One worrying possibility was that those mutations somehow sped up Ebolas replication.

But it was also possible these changes didnt mean anything at all. We know that viruses mutate, Dr. Sabeti said. There was nothing revelatory in that.

Each of Ebolas seven genes encodes a protein. Even if a gene is altered with a mutation, it may end up making precisely the same protein as before, or one that works exactly the same way.

Last year computer simulations by Dr. Simon C. Lovell, an evolutionary biologist at the University of Manchester, and his colleagues did not find any important difference in Ebolas proteins caused by the new mutations. But that work was based only on what scientists knew about the molecular biology of Ebola at the time.

There was still a lot left to learn, it turned out. Dr. Sabeti and her colleagues went on to analyze 1,489 Ebola genomes, tracing the viruss development over the course of the epidemic in an evolutionary tree.

The tree showed that one mutation arose at a crucial point in the outbreak. Known as GPA82V, it was first observed in viral samples collected from a patient in Guinea on March 31, 2014.

Ebola viruses carrying GPA82V exploded across all three countries. The original version of the virus, by contrast, sputtered on at low levels in Guinea before disappearing in a couple of months.

The GPA82V mutation alters the gene that directs production of Ebolas surface proteins, called glycoproteins. The tips of these proteins contact human host cells, opening a passageway by which the virus enters.

To judge the effects of the mutation, Dr. Luban created a form of HIV studded with Ebolas surface proteins and observed as these hybrid viruses infected human cells. One set of hybrid viruses contained the GPA82V mutation; the other contained the original version of the Ebola gene.

The mutation, the scientists found, made the viruses much more successful at attacking human cells and those of other primates. Compared with the older gene, the mutated form infected four times as many primate cells.

But the mutation did not help the hybrid viruses infect the cells of other species, such as cats and dogs.

In a parallel study also published on Thursday, Jonathan K. Ball, a virologist at the University of Nottingham, and his colleagues analyzed 1,610 Ebola genomes and arrived at the same conclusion as Dr. Sabeti: The GPA82V mutation arose early in the West African epidemic and spread like wildfire.

Dr. Balls team also created hybrid viruses instead of HIV, they used mouse viruses and found that GPA82V made them twice as infectious to human cells.

The scientists also tried infecting cells from fruit bats, including an African species thought to be Ebolas natural host. The mutation actually made the viruses worse at infecting the bat cells.

Dr. Lovell said he and his colleagues had completed a study of their own, now under review at a journal, that produced similar findings. As a result, he is no longer a skeptic.

Now it seems there is a change, he said of the Ebola virus. What we dont know yet is the effect on people.

Dr. Sabeti and her colleagues have discovered some frightening clues in patient medical records. Among 194 cases, they found, people infected with mutated Ebola were significantly more likely to die than those with the older strain.

Collectively, Dr. Luban said, the evidence points strongly to the conclusion that Ebolas mutation helped it spread more effectively in people.

It looks like a duck, and so I think it probably is a duck, he said.

It is not clear what role the mutation played in West Africas epidemic. Perhaps it was only minor, compared with geography and the poor state of regions public health systems, Dr. Ball said.

But the fact that Ebola did gain at least one advantage that made it better at infecting human cells worries him anyway. We will almost certainly face another outbreak.

You will see that virus trying to adapt to its new host, he said. And the longer you let that spillover take place, the more chance it has to become better adapted.

http://www.nytimes.com/2016/11/04/science/ebola-evolution-african-epidemic.html

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Post time 15-11-2016 05:43 PM | Show all posts
Article yang interesting; mungkin agak ''dalam'' untuk forumer tetapi jika dibaca, dapat difahami dengan elok.
Mereka dah dapat kenal semua genomes dalam Ebola ni..semua 1489 genes dalam nye dah di study dan di kaji. Hebat mereka ni kerana mereka co-operate dan bersatu.. kita pulak hanya cari perbezaan antara sesama sendiri .
This new mutation pon depa dah dapat kenal ie GPA82V ini.
Ebola really is a very deadly virus..yg u tgk pakai tutup liptup dalam pics tu pon ada jugak yg mati; doctors and nurses pon mati because of this virus. Jika dah dapat genomic sequences nye, jap lagi ade lah military applications utk ini, eg dalam germ-warfare, sebab Ebola ni really guarantee to kill.
Jika sebarkan TB / hepatitis..lambat pulak satu satu populasi tu nak mati . Cynicism aside, this is a scary news that Ebola has evolved.
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 Author| Post time 15-11-2016 10:45 PM | Show all posts
ipes2 replied at 15-11-2016 05:43 PM
Article yang interesting; mungkin agak ''dalam'' untuk forumer tetapi jika dibaca, dapat difahami de ...

too deadly also not good...... tak sempat nak spread, host dah kojol   
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Post time 16-11-2016 03:49 AM | Show all posts
God_Eater_4 replied at 15-11-2016 10:45 PM
too deadly also not good...... tak sempat nak spread, host dah kojol

yes that is true; better is like a tapeworm, host wont die and there is only 1 tapeworm per person
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