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The world is on alert as Ebola epidemic claimed several lives in Africa. The latest and the first outbreak of Ebola virus in west Africa is the worst ever and this is the deadliest (''zaire") strain to infect human beings say the experts. Guinea, Liberia and Sierra Leone all have confirmed cases. And it is spreading very fast.




Usually world alert will be given by WHO and asks the countries around to take precautions. So how is the world health organization dealing with it. This video shows the procedure followed:


Ebola virus disease (formerly known as Ebola haemorrhagic fever) is a severe, often fatal illness, with a case fatality rate that ranges from 50 to 90%. It is one of the world’s most virulent diseases. Ebola is a virus that is named after the Ebola River in the Democratic Republic of Congo, where it first was identified in 1976. There are currently 5 strains of the virus, with 4 out of the 5 causing disease in humans. It is suspected that it first originated from fruit bats, and then spread to humans. The infection is transmitted by direct contact with the blood, body fluids and tissues of infected animals or people. To become infected in the first place, a person's mucous membranes, or an area of broken skin, must come into contact with the bodily fluids of an infected person, such as blood, urine, saliva, vomit, semen or stools, materials contaminated with these fluids such as soiled clothing or bed linen, needles or non-sterilized medical equipment, contact with blood or fluids of infected animal meat. It is the cause of a very threatening illness called “hemorrhagic fever,” where the term “hemorrhagic” refers to bleeding that is often accompanied by a high fever. This bleeding is often caused by Ebola’s effects on the liver, which normally produces the necessary clotting factors to stop bleeding when it occurs. If the clotting factors are no longer being produced by the liver the way they should be, then the patient can experience excessive and prolonged bleeding. This bleeding can be external or internal, and can involve multiple organs, such as the kidneys, brain, and lungs. Unfortunately, Ebola has a high risk of mortality associated with it, and majority of those who contract it eventual die from organ failure, due to bleeding and/or shock.

Severely ill patients require intensive supportive care. This is difficult because they will have to be isolated to control the spread of the disease. During an outbreak, those at higher risk of infection are health workers, family members and others in close contact with sick people and deceased patients. Safe burial practices or safe preparation of the body for funeral is critical.

Ebola virus disease outbreaks can devastate families and communities, but the infection can be controlled through the use of recommended protective measures in clinics and hospitals, at community gatherings, or at home.

Experts are still unclear about where Ebola comes from. There are documented cases of contracting the virus after someone is exposed to a fruit bat, bush meat or encountering an infected porcupine, but it’s undeniable that once the chain of human-to-human transmission gets going, it is deadly.

The incubation period of Ebola virus disease (EVD) varies from 2 to 21 days. Person-to-person transmission by means of direct contact with infected persons or their body fluids/secretions is considered the principal mode of transmission. In a household study, secondary transmission took place only if direct physical contact occurred. No transmission was reported without this direct contact. Airborne transmission has not been documented during previous EVD outbreaks.
Therefore, the governments in countries this outbreaks occurs must restrict movement, get people into hospitals with proper hygiene practices and set up field hospitals where necessary.
The World Health Organisation estimates that there is a high risk of spread to countries bordering those with existing outbreaks, a moderate risk to countries further afield in the sub-region, but that there is little chance of spread overseas. There is no reason to assume that an exported case — be it to Lagos, a city of 17 million people, or any other place — will spark new outbreaks, because Ebola is not very highly contagious.
Ebola can look like flu at first, causing fever along with head and muscle aches. In latter stages it can progress into diarrhea, vomiting, rash and bleeding, ultimately leading to organ failure.

There is no risk of transmission during the incubation period and only low risk of transmission in the early phase of symptomatic patients. The risk of infection during transport of persons can be further reduced through use of infection control precautions

The Ebola virus is usually transmitted by close contact and the first cells it affects are cells important to your primary immune response—monocytes, macrophages and dendritic cells. These cells are important because they’re the first to recognize that something foreign has entered your body and the first cells to trigger your innate immune system to fight off the infection. By attacking the body's first responders, the virus cripples the immune system before it can mount an effective defense . This makes it hard to mount an effective immune response against the virus—your body has a tough time fighting the virus off, and the virus multiplies to the point that it takes over major organs in your body.

One of the greatest challenges with Ebola is that there is no cure. Like many other viruses, once contracted, it needs to run its course. Also, like other viruses, it requires certain supportive measures to mitigate its effects while it runs its course--like providing IV fluids, controlling the bleeding and low blood pressures, fever control, maintaining oxygenation, etc. No specific treatment for Ebola currently exists, but several investigational drugs are under development. It’s not very realistic for such a virus to spread as rapidly in developed countries and countries that take adequate preventive measures no matter how much drama and fear the media likes to create.

There are no effective vaccines or therapies for Ebola. It takes years to develop⁠ and bring a drug or vaccine through all phases of clinical treatment. So health care workers can only attempt to support patients’ immune systems (regulating fluids, oxygen levels, blood pressure and treating other infections) to help the afflicted fight off the virus as best they can.
A vaccine is a few years away. There are quite a few preventative vaccines in development, with three to five that have been shown to completely protect nonhuman primates against Ebola. The pharmaceutical companies are not much interested in developing a vaccine that treats little outbreaks every 3 or 4 years! Since Ebola first appeared in 1976, only 19 outbreaks have had more than 10 victims, and around 2,000 people in total have died from the disease.This is the main reason why there is no vaccine till now.
But how a vaccine, if developed, works in these cases? The vaccine VSV is probably one of the most promising, and it’s based on a viral vector related to the rabies virus. It’s a bullet-shaped particle, and on its surface is a structural protein called a “glycoprotein,” which allows a virus to recognize a host cell, bind to it and take over the host cell’s machinery. With a vaccine, we remove the gene that encodes the glycoprotein of the VSV virus and we replace it with a gene that encodes the glycoprotein of Ebola. You end up with a vaccine that has an Ebola glycoprotein on the surface. Now, it doesn’t behave like Ebola because the rest of its genome is not Ebola, but because it has the Ebola glycoprotein your body is going to recognize it as foreign and build up an immune response against Ebola.
An experimental drug given to two American patients with Ebola is made from tobacco leaves and is hard to produce on a large scale. Known as ZMapp, the serum consists of three antibodies manufactured in modified tobacco leaves, which take weeks to grow.
It was reportedly rushed to US missionaries Kent Brantly and Nancy Writebol, who were stricken with Ebola while treating patients in Liberia. Both have shown improvements in their health and are now being treated in isolation at an Atlanta, Georgia hospital. But we cannot say right now that this drug is particularly promising. The animal data during the experiments with them are very good and the use of it in the two patients is suggestive that it may have a favorable effect, but since there are only two patients, you have to be careful about making any definitive decision. With ZMapp, which was first identified as a drug candidate in January this year, there have been no safety tests yet in humans.
According to WHO, blood transfusions from survivors is one of the best way to fight Ebola.
A panel of experts from the World Health Organization says blood plasma and whole blood transfusions should have priority for now because survivors of an Ebola infection would typically have produced effective antibodies against the virus (otherwise they wouldn't have survived), transfusions of their blood into a newly infected individual may help that person survive the often fatal disease. Such blood preparations, drawn from volunteers, could be ready before the end of 2014.
Right now, though, all that people can do to protect themselves is take precautions, especially while traveling.
Ebola Declared a Public Health Emergency by WHO on August 8th, 2014.

Ebola survivors struggle with new symptoms like brain deficits, memory loss, depression, anxiety, throbbing headaches, hip and knee aches, muscle aches, sleep disorders, and hearing loss. Eye burning and pain are highly prevalent, sometimes they make  the world appear cloudy or foggy. Eyes also become sensitive to light. More than half of the patients who lived through an acute attack later reported muscle and joint problems. Two thirds had neurological difficulties and 60 percent reported eye problems - including blindness - approximately one year after Ebola infection.  A new study hints at hidden virus remnants or immune system overreaction. Doctors began referring to this constellation of symptoms as post-Ebola syndrome. 

Recent update: 6th Aug., 2015...from The Lancet

http://www.thelancet.com/journals/lancet/article/PIIS0140-6736%2815...

For the first time, there is evidence that a vaccine protects people from Ebola. The interim study results, unveiled by the World Health Organization on July 31 and published online by The Lancet, suggest that a single shot can protect people who were directly or indirectly exposed to individuals with the disease. The vaccine, which appears safe, could fundamentally alter how well humans contain future Ebola outbreaks.
This vaccine was being tested in people living in Guinea and is based on an animal virus that primarily affects rodents, cattle, swine and horses. One gene of that virus, however, was replaced with a segment of the gene for the outer protein of an Ebola virus species.
The only individuals in the trial were those who had been exposed to newly identified Ebola patients or were those contacts’ contacts. This unique study approach, called “ring” vaccination, is based on the smallpox eradication strategy. It effectively forms a “ring” of protection by targeting individuals directly around the infected person and the people around those contacts’ contacts as well.
WHO says that this is a highly effective vaccine.

Updates:

15th Oct., 2015

U.K. Ebola “Relapse” Case Takes Virus Specialists to Uncharted Waters according to Reuters

Scottish nurse Pauline Cafferkey is in critical condition following "totally unprecedented" return of symptoms. Her case is different now because she has Meningitis Caused by Persisting Virus.
The case of Pauline Cafferkey, the first person known to have recovered from Ebola and then suffer an apparently life-threatening relapse, is taking scientists into uncharted territory.

The Scottish nurse's critically ill situation, described as "staggering" by one British virologist, signals just how complex and formidable a foe the Ebola virus may turn out to be now that scientists have the chance to study its survivors.

Previous studies and preliminary data from research in survivors of the vast West African outbreak have detected Ebola virus in semen, breast milk, vaginal secretions, spinal fluid and fluids around the eyes.

But scientific literature has never documented an Ebola relapse case before, meaning Cafferkey's is likely to generate great fear and anxiety for the 17,000 or so other Ebola survivors across West Africa.
This has never been observed before. Is this a one off? A very rare event? Or is this going to be quite common? The honest answer is we don't know!
Until researchers can study in detail and in large numbers of people the virus's long-term effects, each survivor, be they healthy or sickly, will be able to teach virologists more.
Preliminary data published this week has already forced a re-think on how long male survivors should be advised to abstain from sex or use condoms, with a study showing traces of Ebola can be found in semen of some men at least nine months after they first became ill.

Even if you don't have the virus in your bloodstream it can be hiding out. And we need to be aware of that because it's setting up the stage for potentially new outbreaks.
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First known case of sexually transmitted Ebola reported
Oct., 2015
A Liberian woman contracted Ebola in March by having sex with a survivor of the viral disease, researchers report. Using studies of both people’s viral genomes and of the people’s contacts with any other possible sources of the virus, the researchers conclude that the woman’s disease represents the first known case of sexual transmission of Ebola.

People ordinarily catch the often-deadly virus through direct contact with blood or other body fluids.

In this case, the two people had unprotected sex six months after the man got Ebola, and 155 days after his second blood test showed him to be clear of the virus. The genomes of the Ebola virus from the man’s semen and woman’s blood were not only practically identical but also different from all other Western African Ebola viruses that had been sequenced, researchers report October 14 in the New England Journal of Medicine.

Also appearing in the journal is a preliminary report that genetic material from Ebola viruses can persist in semen nine months after infection.

Both findings suggest that Ebola remains in certain parts of the body long after the blood is clear of the virus. However, in an opinion piece that accompanies the two research reports, Armand Sprecher of Doctors Without Borders in Brussels notes that more than 17,000 people survived the West African Ebola outbreak. “If sexual transmission from survivors were an important means of disease propagation, we would have seen a number of cases by now,” he writes.
Source: http://www.nejm.org/doi/full/10.1056/NEJMoa1509773

Views: 416

Replies to This Discussion

303

Fact or Fiction?: The Ebola Virus Will Go Airborne

Why do some viruses go airborne? Will the pathogen causing the west African outbreak be one of them?

http://www.scientificamerican.com/article/fact-or-fiction-the-ebola...

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http://www.scientificamerican.com/article/ebola-an-eyewitness-accou...

Ebola: An Eyewitness Account from Sierra Leone, Dec. 7

Nature reports from the front line of the outbreak

Largest ever Ebola outbreak is not a global threat

Although the virus is exerting a heavy toll in West Africa, it does not spread easily
http://www.nature.com/news/largest-ever-ebola-outbreak-is-not-a-glo...

Science for a Complex World: The mathematics of stopping Ebola

http://www.santafe.edu/news/item/sfnm-scarpino-math-stopping-ebola/

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Ebola Free-for-All Could Trigger Bad Science and Wasted Efforts

Everybody and his uncle, it seems, has an idea of something that might work to cure people infected with the deadly virus

http://www.scientificamerican.com/article/ebola-free-for-all-could-...

What the doctors who treated the American patients successfully are saying about the condtions in Africa and why they think African doctors are failing:

We are not being critical of our colleagues in west Africa. They suffer from a terrible lack of infrastructure and the sort of testing that everyone in our society takes for granted, such as the ability to do a complete blood count—measuring your red blood cells, your white blood cells and your platelets—which is done as part of any standard checkup here. The facility in Liberia where our two patients were didn’t even have this simple thing, which everyone assumes is done as part of your annual physical.
 
What we found in general is that among our Ebola patients, because of the amount of fluid they lost through diarrhea and vomiting, they had a lot of electrolyte abnormalities. And so replacing that with standard fluids [used in hospital settings] without monitoring will not do a very good job of replacing things like sodium and potassium. In both of our patients we found those levels to be very low. One of the messages we will be sending back to our colleagues is even if you don’t have the equipment to measure these levels, do be aware this is occurring when patients are having a lot of body fluid loss.
 
Our two patients also gained an enormous amount of fluid in their tissues, what we call edema. In Ebola virus disease there is damage to the liver and the liver no longer makes sufficient amount of protein; the proteins in the blood are very low and there is an enormous amount of fluid leakage out into the tissues. So one of the takeaway messages is to pay closer attention to that and perhaps early on try to replace some of these proteins that patients’ livers lack.

We  think the world is becoming aware that issues like this are not going to go away. The developed countries of the world will have to do our part to assist our colleagues with less developed infrastructure to care for sick people. I think one of the messages that is going out from many sources is we really have to help countries such as the ones involved in this outbreak to develop their medical infrastructure. Hopefully in five years they will have this infrastructure.

Mostly the clinical course of the patients—much like any physician sending a patient to a referral center. They admitted they knew they were kind of flying blind. They’d say, “this is what we observed but we had no way to test it.”

There are data that go back several decades—over several outbreaks—that suggest when you have individuals that have recovered from Ebola virus infection they may still be shedding nuclear material [genetic material from the virus which could potentially help spread it] in semen in males and vaginal secretions in females and also, potentially in urine. People have done this by doing assays looking specifically at the nuclear material of the virus. There has been very little attempt to demonstrate if this is viable virus that these individuals are shedding. It’s important when looking at epidemiological investigations that no one has been able to show people shedding these nuclear materials as a source of infection after they are discharged.
 
Looking at Ebola survivors who were discharged and successfully resolved the infection, following up several months later and evaluating their family members, there has never been any evidence that family members became infected. A lot of the thinking now is this probably was not live and is not important in terms of control of infection. We did give both of our patients the standard recommendations, which are contained on the CDC [U.S. Centers for Disease Control] Web site—not having unprotected sex for three months.
  Given that there is no treatment for Ebola virus disease, the main intervention that will determine if someone lives or dies with this infection is supportive care: The ability to replace fluid and electrolytes if a patient is losing them. The ability to replace platelets if that count is low and a patient is starting to bleed. The ability to replace protein in the blood that may be deficient. A developed country has the capability because of our infrastructure to provide that level of support is at a much higher level than a hospital dealing with patients in west Africa.

http://www.scientificamerican.com/article/ebola-doctor-reveals-how-...

Epidemiological Dynamics of Ebola Outbreaks
Ebola is a deadly virus that causes frequent disease outbreaks in the human population. Here, we analyse its rate of new introductions, case fatality ratio, and potential to spread from person to person. The analysis is performed for all completed outbreaks, and for a scenario where these are augmented by a more severe outbreak of several thousand cases. The results show a fast rate of new outbreaks, a high case fatality ratio, and an effective reproductive ratio of just less than 1.
http://elifesciences.org/content/early/2014/09/12/eLife.03908

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Ebola: A Poem for the Living (English) from United Methodist Communications on Vimeo.

Can science and religion come together to improve global health?

On Friday, leaders from both scientific and religious communities will meet to discuss how they could work together to make the world a healthier place.
http://newsok.com/can-science-and-religion-come-together-to-improve...

Nightmare Scenario: Ebola 'Could Become Airborne'
Save the Children reports that Ebola is spreading at the rate of five new cases an hour in Sierra Leone.

Anthony Banbury, chief of the United Nations Ebola mission, admits that the international community has been "a bit late" to respond to the epidemic.

There are also worries Ebola could become airborne and spread in the United States and around the world through travel and other means.

"The longer it moves around in human hosts in the virulent melting pot that is West Africa, the more chances increase that it could mutate," Banbury told the Telegraph. "It is a nightmare scenario [that it could become airborne], and unlikely, but it can't be ruled out."
http://www.cbn.com/cbnnews/healthscience/2014/October/Nightmare-Sce...

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U.K. Nurse with Serious Ebola Complications Has Meningitis Caused by Persisting Virus

The Scottish patient, who first contracted Ebola in December 2014, is being treated with an experimental antiviral drug




The Ebola virus continues to linger in one Scottish nurse and fuel serious complications.




A Scottish nurse who contracted and initially recovered from Ebola, but then suffered relapsing illness, has meningitis caused by the virus persisting in her brain, doctors treating her said on Wednesday.

Pauline Cafferkey was not reinfected with the Ebola virus, doctors said, but it had remained in her body since her initial recovery and had re-emerged to cause life-threatening complications.

"The virus re-emerged around the brain and around the spinal column to cause meningitis," said Michael Jacobs, an infectious diseases consultant who has been treating Cafferkey in London.

He said Cafferkey had been critically ill and at one stage last week was at high risk of dying, but had now made a significant improvement and looked likely to be able to recover.

Cafferkey was transferred to an isolation unit at the Royal Free Hospital in London on Oct. 9 after suffering an apparent relapse.

She was the first person to have been diagnosed with Ebola on British soil when she contracted the disease in December 2014 and spent several weeks in an isolation unit at the Royal Free before making a recovery and being discharged.

Cafferkey's case has generated worldwide interest, as experts say there has never been a documented case like it.

The Ebola virus has killed more than 11,300 people in West Africa in an unprecedented epidemic over the past year, which also left some 17,000 survivors of the disease.

Jacobs said on Wednesday Cafferkey is now able to talk and eat a little, but is still in bed, faces a long recovery and will probably need to remain in hospital for some time.

The nurse, who originally contracted Ebola while working in Sierra Leone, is currently being treated with an experimental antiviral drug known as GS5734 being developed by the U.S. drugmaker Gilead Sciences.

Gilead confirmed that its compound "is currently being provided to a female patient in the United Kingdom".

Jacobs said this treatment was being carried out with Cafferkey's full consent, and added that he and his medical team did not yet know whether it would work.

"We're very hopeful that Pauline will slowly make a full recovery," he said, adding that he hoped Cafferkey's own immune system would eventually fight off and clear the virus.

The Ebola virus is known to be able to persist in various tissues in the body after it has cleared the bloodstream, but scientists are only now starting to find out more about how long it can survive and where, whether and when it might re-emerge.

Asked if Cafferkey posed a contagion risk, Jacobs stressed that her current illness was very different from the Ebola haemorrhagic fever she had in December 2014, with the virus far less likely to be shed and spread to others.

"The infection risk is completely different," he said. "But we can't call it zero, so we're taking a precautionary approach."

- Reuters

Ebola virus, which is transmitted from person to person via close and direct physical contact with infected bodily fluids. The most infectious fluids are blood, feces and vomit, although the virus has also been detected in breast milk, urine and semen, according to the World Health Organization. Saliva and tears may also carry some risk. Researchers have detected fragments of the virus in sweat, but the whole live virus has never been isolated in it, WHO reports, so the possibility of transmission by perspiration is unclear.

The Ebola virus can also be transmitted indirectly, through contact with previously contaminated surfaces and objects. The risk of transmission from these surfaces is low, according to WHO, and can be reduced even further by appropriate cleaning and disinfection. The health organization also emphasizes that Ebola virus disease is not an airborne infection. The organization, however, acknowledges the possibility that the virus could be transmitted a short distance if virus-laden droplets of vomit or mucus are directly “propelled onto the mucus membranes or skin with cuts or abrasions of another person.” WHO says it is not aware of any studies that actually document this mode of transmission.
http://www.scientificamerican.com/article/ebola-spread-shows-flaws-...

Ebola Gorilla Vaccine Could Prevent Human Outbreaks
Infected gorillas and chimps butchered for meat may be behind Ebola outbreaks.
http://www.scientificamerican.com/podcast/episode/ebola-gorilla-vac...

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When the World Health Organization recently named blood transfusions from Ebola survivors as its priority experimental therapy for the disease ravaging west Africa there was only one major problem: no data indicating that such transfusions work. Blood plasma from survivors contains antibodies that could potentially trigger an immune system response in patients, which would bolster their ability to fight the virus, but clinical data suggesting it has helped patients beat back the virus does not exist.

Is the Blood of Ebola Survivors an Effective Treatment?

http://blogs.scientificamerican.com/observations/2014/12/01/is-the-...

Ebola found to be at least 16 to 23 million years old.
A new study has re-written Ebola's family history.

Ebola's evolutionary roots more ancient than previously thought, the study has found.

The family of viruses housing Ebola and Marburg is ancient, and the two viruses last shared a common ancestor millions of years ago, scientists say.

The research shows that filoviruses — a family to which Ebola and its similarly lethal relative, Marburg, belong — are at least 16-23 million years old.

An experimental Ebola vaccine made using an Australian virus called Kunjin might help in the fight against the deadly Ebola virus, according to a study published in The Journal of Infectious Diseases. Lead researcher Professor Alexander Khromykh, from the University of Queensland, said the researchers from Australia, France and Russia found the engineered vaccine gave significant protection from Ebola infection.
Fighting Virus With Virus- A small pre-clinical trial suggests that the virus-like particles of the Kunjin virus could be used as an Ebola vaccine.
http://jid.oxfordjournals.org/content/early/2015/02/28/infdis.jiv019

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