Ebola

views updated May 11 2018

Ebola

Introduction

Disease History, Characteristics, and Transmission

Scope and Distribution

Treatment and Prevention

Impacts and Issues

Primary Source Connection

BIBLIOGRAPHY

Introduction

Ebola is a type of hemorrhagic fever that is caused by four subtypes of a virus called the Ebola virus. The virus is one of two members of Filoviridae, a family of RNA viruses. The name of the virus comes from a river located in the Democratic Republic of the Congo, formerly called Zaire, where the virus was first discovered during an outbreak of the disease.

Ebola is a terrifying disease that can progress steadily towards death. The destruction of internal organs caused by the infecting virus produces a great deal of internal bleeding and can cause bleeding from various parts of the body such as the eyes, gums, and nose. The disease caused by Ebola-Zaire, the first of the four types of the virus yet discovered, is fatal over 90% of the time.

The progression from health to death within a few weeks for those unlucky enough to contract the infection is one terrifying aspect of Ebola. The other is, essentially, a fear of the unknown. Even though the disease has been known since the late 1980s, the origin of Ebola, its reservoir, and how the disease can be prevented are still largely mysterious. The main reason for this is the infrequency of outbreaks and the speed of their appearance and disappearance. The infection quickly spreads from person to person through a local population and, because of the high death rate, soon disappears after running out of new hosts to infect. This pattern has made the study of Ebola difficult.

It is thought that Ebola is transmitted to humans from a natural host by a vector. This route of transmission occurs in some other diseases. One example is malaria, which is transferred to a susceptible person from an infected animal or person via mosquitoes. Ebola may be naturally present in chimpanzees. At least two outbreaks of Ebola-Zaire were determined to be due to contact between humans and infected chimpanzees. However, it may be that chimpanzees are not the natural host, but are themselves infected by the virus, which is transmitted to them from another host. As discussed below, the natural host may be bats, although this has not been proven. Likewise, studies by the World Health Organization (WHO) and the U.S. Centers for Disease Control and Prevention (CDC) have not yet identified the vector that carries the virus from that host to humans. What is clear from the ferocity of past outbreaks is that once someone has been infected with Ebola, the virus is easily transferred from person to person.

Disease History, Characteristics, and Transmission

As of 2007, four subtypes of Ebola virus have been identified. Three of the subtypes cause disease in humans. The four subtypes of Ebola are slightly different in the sequence of their genetic material and in the composition of the proteins that are present on their surfaces. Analysis of blood obtained from people infected by one of the four viral subtypes has revealed slightly different antibody patterns. (An antibody is a protein produced by the immune system in response to the presence of a specific protein, which is termed an antigen.) The four subtypes of virus may have originated from a single virus that mutated to create the four slightly different subtypes over time, but this hypothesis has not yet been confirmed.

The first Ebola virus to be discovered was Ebola-Zaire. It was isolated near the Ebola River in the Democratic Republic of the Congo during an outbreak in 1976. There were 318 reported cases. Of these, 280 people died, a mortality rate of 88%. Other known occurrences of Ebola due to Ebola-Zaire include:

  • Democratic Republic of the Congo, 1977 (one case, one death)
  • Gabon, 1994 (52 cases, 31 deaths)
  • Democratic Republic of the Congo, 1995 (315 cases, 250 deaths)
  • Gabon, January to April 1996 (37 cases, 21 deaths)
  • Gabon, July 1996 to January 1997 (60 cases, 45 deaths)
  • South Africa, 1996 (two cases, one death; the disease was contracted in the Democratic Republic of the Congo)
  • Gabon and the Democratic Republic of the Congo, October 2001 to March 2002 (53 cases, 53 deaths in the Gabon outbreak; 57 cases, 43 deaths in the Congo outbreak)
  • Democratic Republic of Congo, December 2002 to April 2003 (143 cases, 128 deaths)
  • Democratic Republic of Congo, 2003 (35 cases, 29 deaths).

WORDS TO KNOW

AMPLIFICATION: A process by which something is made larger, or the quantity increased.

ANTIBODY: Antibodies, or Y-shaped immunoglobulins, are proteins found in the blood that help to fight against foreign substances called antigens. Antigens, which are usually proteins or polysaccharides, stimulate the immune system to produce antibodies. The antibodies inactivate the antigen and help to remove it from the body. While antigens can be the source of infections from pathogenic bacteria and viruses, organic molecules detrimental to the body from internal or environmental sources also act as antigens. Genetic engineering and the use of various mutational mechanisms allow the construction of a vast array of antibodies (each with a unique genetic sequence).

ANTIGEN: Antigens, which are usually proteins or polysaccharides, stimulate the immune system to produce antibodies. The antibodies inactivate the antigen and help to remove it from the body. While antigens can be the source of infections from pathogenic bacteria and viruses, organic molecules detrimental to the body from internal or environmental sources also act as antigens. Genetic engineering and the use of various mutational mechanisms allow the construction of a vast array of antibodies (each with a unique genetic sequence).

ANTISENSE DRUG: An antisense drug binds to mRNA, thereby blocking gene activity. Some viruses have mRNA as their genetic material, so an antisense drug could inhibit their replication

BUSH MEAT: The meat of terrestrial wild and exotic animals, typically those that live in parts of Africa, Asia, and the Americas; also known as wild meat.

HEMORRHAGIC FEVER: A hemorrhagic fever is caused by viral infection and features a high fever and a high volume of (copious) bleeding. The bleeding is caused by the formation of tiny blood clots throughout the bloodstream. These blood clots—also called microthrombi—deplete platelets and fibrinogen in the bloodstream. When bleeding begins, the factors needed for the clotting of the blood are scarce. Thus, uncontrolled bleeding (hemorrhage) ensues.

HOST: Organism that serves as the habitat for a parasite, or possibly for a symbiont. A host may provide nutrition to the parasite or symbiont, or simply a place in which to live.

RESERVOIR: The animal or organism in which the virus or parasite normally resides.

VECTOR: Any agent, living or otherwise, that carries and transmits parasites and diseases. Also, an organism or chemical used to transport a gene into a new host cell.

The second type of Ebola virus to be discovered was Ebola-Sudan. It was discovered in 1976 during an outbreak that occurred in Sudan (284 cases, 151 deaths). Other outbreaks involving Ebola-Sudan include:

  • England, 1976 (one case; when a lab technician studying the virus accidentally contracted the virus from a needle puncture)
  • Sudan, 1979 (34 cases, 22 deaths)
  • Uganda, 2000–2001 (425 cases, 224 deaths)
  • Sudan, 2004 (17 cases, 7 deaths).

The third type of Ebola virus to be discovered was Ebola-Reston. Outbreaks of Ebola occurred simultaneously in 1989 in three animal facilities in the United States that had received monkeys imported from the Philippines. One of the facilities was in Reston, Virginia, and the virus took its name from the outbreak among the primates at this facility. No humans died in the outbreak, although four people were infected, as shown by the antibodies that they developed to the virus. This outbreak formed the basis for a bestselling book by Richard Preston called The Hot Zone and a motion picture called Outbreak Other outbreaks of Ebola-Reston in 1990, 1992, and 1996 involved deaths among other primates, but no human fatalities (although some people had produced antibodies to the virus). Thus far, Ebola-Reston has not caused human illness.

The final subtype of Ebola virus, as of 2007, is Ebola-Ivory Coast, which was discovered in 1994 in Ivory Coast. It caused one non-lethal case involving a scientist who contracted the infection after conducting an autopsy on a chimpanzee.

IN CONTEXT: DISEASE IN DEVELOPING NATIONS

As of May 2007, the natural reservoir of the Ebola virus remained unknown. The World Health Organization (WHO) states that “the natural reservoir of the Ebola virus is unknown despite extensive studies, but seems to reside in the rain forests on the African continent and in the Western Pacific.”

“Although non-human primates have been a source of infection for humans, they are not thought to be the reservoir. They, like humans, are argued to be infected directly from the natural reservoir or through a chain of transmission from the natural reservoir. On the African continent, Ebola infections of human cases have been linked to direct contact with gorillas, chimpanzees, monkeys, forest antelope and porcupines found dead in the rainforest. So far, the Ebola virus has been detected in the wild in carcasses of chimpanzees (in Côte-d'Ivoire and Republic of Congo), gorillas (Gabon and Republic of Congo) and duikers (Republic of Congo).”

“Because bats deliberated infected with Ebola do not die there is continued scientific speculation that bats or mammals may play a role in harboring the virus in the wild.”

SOURCE: World Health Organization

The various types of Ebola virus are all filoviruses. One characteristic of filoviruses is their long, stringlike shape. When observed using the high magnification power of the electron microscope, the viruses can be coiled, circular, U-shaped, or even shaped like a cane (or a shepherd's crook). The different shapes may not be natural, but rather may be formed artificially during purification of the virus.

The molecular details of the Ebola infection have been clarified. This work can only be done in a few laboratories in the world that are designed for research involving highly dangerous and infectious microorganisms. The infection begins when a protein on the surface of the virus recognizes a host molecule. It is not known whether the host molecule is another protein, lipid, or carbohydrate. Following the linkage between the viral protein and the host receptor, the viral genetic material enters the host cell. It is not known how this occurs. Increased understanding of these early steps is vital, since by blocking the viral attachment to the host cell and/or the transfer of the genetic material into the host cell, the subsequent infection could be stopped. Efforts to develop a vaccine are focusing on these steps. For example, blocking the adherence of a microbe to a host cell has proven successful in the development of a preliminary vaccine for cattle against a bacterium called Escherichia coli O157:H7, which can cause a lethal infection in humans, popularly known as “hamburger disease.”

Ebola viruses contain RNA. For the manufacture of a new virus, the infecting virus must use the host cell's genetic machinery to read the viral payload of RNA and to manufacture one of the viral proteins. Once this so-called nonstructural protein is made, it can decode the remaining viral genetic material to manufacture seven other proteins. These proteins are described as being structural— they are used to form the new virus. The new virus particles are eventually released from the host cell when the cell bursts, and another cycle of infection begins as new cells are infected. How the virus, with just eight proteins, manages to make new copies of itself and evade the attempts by the hosts’ immune system to stop the infection is unclear.

In their natural host, the Ebola virus presumably does not cause a serious infection. If it did, it would not persist, since the host would be killed. However, in humans the resulting infection can be devastating. Within days, Ebola-Zaire and Ebola-Sudan produce a high fever, headache, generalized muscle aches (myalgia), abdominal pain, tiredness, and diarrhea. Cells lining the intestinal tract and stomach can be damaged, causing bloody diarrhea and vomiting of blood. At this stage some people do recover. But, for many, the infection worsens. Massive internal bleeding sends a person into shock and can cause heart damage. Death soon follows.

One of the challenges of combating an Ebola outbreak is the fact that the early symptoms of the infection are similar to those of the flu, malaria, typhoid fever, and several bacterial infections, which occur more often and are not as serious. By the time the true nature of the infection becomes known, many people in a community could have been infected.

The swiftness of the infection has been noted by some authors. Others feel, however, that the two-week course of the infection is not unusually quick. The latter view is true when a patient is near medical care in a developed country. However, in rural regions of Africa where Ebola is most common, medical care may be days in coming and even then may not be capable of dealing with a severe infection. In that situation, even a disease that develops within a week is swift and serious.

In some Ebola outbreaks, the initial infection has been traced to contact between humans and an animal (usually a primate) that harbors the virus. However, it is still unclear whether the primate is the natural host or becomes infected through contact with another animal. What is now clear is that the contagious person-to-person transmission of the virus subsequently occurs via infected blood or body fluids. This transfer can occur directly, with someone coming into contract with blood or body fluids during handling and care of a patient. Accidental infection during study of the virus also has occurred.

The rapid spread of Ebola is also aided by the location of most of the outbreaks. The areas in Africa where Ebola appears are poor, rural, and do not have medical facilities close by. The health care facilities that are available are not likely to have space available to isolate the infected patient from other patients, which can contribute to the spread of the infection.

The pattern of the Ebola-Reston outbreak that occurred in Virginia in 1989 indicates that the virus may be capable of airborne spread. In that outbreak, at least one of the primates who became ill was never in contact or even in the same room as the other sick primates. Lab studies have demonstrated that aerosols of the virus can infect test animals. Whether this route plays a major role in Ebola is unclear, but the general feeling is that airborne transmission is not as important as transmission by body fluids.

IN CONTEXT: CULTURAL CONNECTIONS

Because the Ebola virus is transmitted by direct contact with the body fluids (blood, secretions, etc.) of infected persons, living or dead, various cultural practices can facilitate Ebola transmission. The World Health Organization (WHO) states “Burial ceremonies where mourners have direct contact with the body of the deceased person can play a significant role in the transmission of Ebola.”

WHO also reports that “the infection of human cases with Ebola virus has been documented through the handling of infected chimpanzees, gorillas, and forest antelopes—both dead and alive—as was documented in Côte d'Ivoire, the Republic of Congo and Gabon.”

SOURCE: World Health Organization

Scope and Distribution

Almost all confirmed cases of Ebola through 2007 have been in Africa. However, the infection may also occur in the Western Pacific because the Reston, Virginia, outbreaks were caused by monkeys imported from the Philippines.

The rapid deterioration of a person following the appearance of symptoms and the fact that the affected villages can be difficult to reach has meant that response to infections by disease control officials from organizations such as the WHO and the CDC occurs long after the disease has begun. This has made the discovery of Ebola's origin difficult. As of 2007, the source of the Ebola viruses is still unknown. The general agreement among scientists who study Ebola is that, because other filoviruses can infect African monkeys, macaques, and chimpanzees without causing harm to these hosts, the host for the Ebola viruses may be similar. However, Ebola does harm some primates. Furthermore, an intensive 12-year-long sampling of tens of thousands of amphibians, mammals, birds, reptiles, and insects failed to detect the viruses.

Bats have also been considered as Ebola's natural host. The people who first became ill in two of the outbreaks worked in buildings where bats lived and may have come into contact with the bats. Furthermore, in a study that deliberately introduced Ebola virus into a number of vertebrates, the virus persisted only in bats. More evidence supporting the involvement of bats was published in Nature in 2006. The study reported on a survey of over 1,000 animals from Gabon and Republic of the Congo, including over 650 bats. Of these, Ebola virus RNA was found in 13 fruit bats. Bats also can harbor several other viruses that are related to Ebola. This evidence for the involvement of bats as the natural host of Ebola is still circumstantial. To date, there is no evidence that an infected bat is capable of infecting another animal, such as a primate.

Treatment and Prevention

Currently, there is no cure for Ebola. Treatment consists of keeping the patient as comfortable and pain-free as possible and minimizing the spread of infection. Additional treatment measures include restoring lost fluids, trying to minimize bleeding, and dealing with any secondary infections that might occur.

As of 2007, prevention of Ebola is impossible, but research is underway on several fronts. Antisense drugs have been used successfully in a small number of infected Rhesus monkeys. Antisense therapy uses genetic material that is complimentary to the region of interest in the virus. Because the added stretch of genetic material is complimentary, it binds with the target region. This prevents the target region from being used in the viral replication process. Put another way, antisense drugs can shut down the infectious process. Whether this approach will prove successful as a prevention strategy for Ebola is unclear, and much research still remains to be done.

Vaccines are another preventative strategy that is being actively explored. In the case of Ebola, several other viruses have been engineered to contain one of the Ebola proteins that is present on the surface of the virus. This bioengineered virus is then administered to monkeys, and the monkeys produce antibodies to the Ebola surface protein. When an intact Ebola virus is given to the monkeys, the anti-Ebola antibody can block the attachment of the Ebola surface protein to the host cell. This approach has shown enough promise to warrant giving the vaccine to humans to see if they produce the anti-Ebola antibody. As of 2007, this vaccine is still being studied.

Impacts and Issues

Ebola affects people in the most basic way. It strikes with little warning and can sweep through a village in a short time. In the rural settings where the disease usually occurs, medical care is minimal and health care providers are stretched to their limits to contain the infection and provide basic comforts to those who are ill.

Though the best selling book The Hot Zone and the movie Outbreak were somewhat sensational, they address the lethality of Ebola. These popular depictions of Ebola served a useful purpose in making the average person more aware of Ebola specifically and infectious diseases in general.

Ebola is a striking example of how human encroachment on regions that were previously uninhabited can bring people into contact with microorganisms to which they had not been previously exposed. Another example of this phenomenon is the emergence of avian influenza in humans. Long a disease transferred between some species of poultry, closer human contact with poultry has enabled the avian flu virus to adapt so that it is capable of, initially, bird-to-human transmission and, within the past several years, human-to-human transmission.

In the case of Ebola, human encroachment on previously uninhabited areas includes increased contact with the natural host of the disease. The blurring of the boundaries between the human and the natural world has brought people into closer contact with primates, who are either the natural reservoir of the virus or who acquire the infection from the natural reservoir, possibly a fruit bat. The virus can spread to humans who kill and eat apes or chimpanzees. Bush meat, including the meat of primates, has long been eaten by rural Africans, and its sale is still an important part of the rural economy. In addition, bush meat has become increasingly popular as a delicacy in the western world.

The link between the consumption of bush meat and the spread of Ebola has spurred efforts to restrict poaching. A 2005 meeting involving 23 African nations and representatives of the United Nations addressed the problem of the declining great ape population and urged stricter controls on poaching and deforestation (which increases the access of people to ape territory). While admirable, the effectiveness of the campaign is debatable. Ape meat is still available for sale in many local markets in regions of Africa and is sought by buyers in western countries.

While some species may naturally harbor the Ebola virus without harm, other species are being decimated. Beginning in 2002, conservationists in some regions of Africa began to note a die-off of western gorillas and common chimpanzees. The great ape population in the African nation of Gabon has declined by half since the 1990s, with Ebola and poaching cited as the most likely causes. Without a concerted effort, these near-human creatures may become extinct within decades.

Part of the reason for the ferocity of an Ebola outbreak is a lack of understanding of the disease among those who are most affected by it. More education targeting those who are at risk of acquiring the infection is still needed. For example, burial customs in many African cultures include an open viewing of the deceased, which potentially exposes the mourners to the virus. This practice can amplify the spread of the virus—that is, the virus can affect more people than it otherwise would. Amplification is an important means by which a variety of viral and bacterial diseases can spread. In the case of Ebola and mourning customs, learning to pay respect to the deceased person without touching or even seeing them would help reduce the spread of Ebola.

During some initial outbreaks, well-meaning medical personnel helped spread the virus. The infection of health care workers is, unfortunately, a common aspect of Ebola outbreaks. The use of protective measures, such as masks and gloves, lessens the risk of passing the infection to caregivers. In some rural clinics, however, such measures—commonplace in medical clinics in developed countries—are a luxury.

Development of a vaccine is a primary goal of those concerned with the control of Ebola. In 2003, researchers at the Dale and Betty Bumpers Vaccine Research Center and the U.S. Army Medical Research Institute reported the development of a vaccine that protects monkeys from injected Ebola virus. The vaccine involves a two-stage process in which immunity results from the injection of non-infectious genetic material from the Ebola virus followed a few weeks later by the introduction of another virus that carries genes of the Ebola virus, which are vital to the establishment of an infection. The resulting immune response can stop the Ebola infection.

As of 2007, the DNA vaccine is still undergoing evaluation. Small-scale human trials have been done. However, one stumbling block in its development concerns the ethical issue of testing the vaccine in humans on the large scale required for approval processes, since this would involve exposing people to the virus. In addition, it is not clear whether a vaccine will work in people whose immune systems are not functioning normally. This is an important consideration, since Africa is also home to millions of people who suffer from acquired immunodeficiency syndrome (AIDS, also cited as acquired immune deficiency syndrome), a disease whose hallmark is the deterioration in immune system function.

Another issue concerning serious infections, including Ebola, is the potential of the microbe to be used as a weapon. Indeed, Ebola has been considered for development as a biological weapon by both the United States and Russia (then the Soviet Union). More recently, members of the Japanese cult Aum Shinrikyo—who released sarin gas in the Tokyo subway system in 1995, killing 12 people and injuring almost 1,000—visited Zaire in 1992. Under the guise of offering medical aid to victims of an Ebola outbreak, cult members instead tried to acquire some virus to use as a terrorist weapon.

Primary Source Connection

The following press release from the World Health Organization details its field response to a 2004 Ebola outbreak in southern Sudan. Along with mobilizing supplies and health workers, education of local villagers at the center of the outbreak was crucial in containing the spread of the disease.

WHO Announces End of Ebola Outbreak in Southern Sudan

Geneva—Today marks the 42nd day since the last person identified as infected with Ebola haemorrhagic fever died on 26 June 2004 in Yambio Hospital, southern Sudan. As 42 days is twice the maximum incubation period for Ebola, and as no further cases have been identified, WHO declares today that the outbreak in southern Sudan is over.

“The rapid containment of this outbreak was a tremendous success for the health authorities, WHO, and the international community involved in the control operations,” said Dr Abdullah Ahmed, head of WHO, southern Sudan, and coordinator of the response.

As of today, the health authorities of Yambio County have reported a total of 17 cases, including seven deaths from Ebola. Ebola haemorrhagic fever is a febrile illness which causes death in 50–90% of all clinically ill cases. It is transmitted by direct contact with the blood, secretions, organs or bodily fluids of infected persons.

“In Yambio, WHO and our partners were able to apply lessons learned during responses to the five Ebola outbreaks that have occurred since 2000,” said Dr. Pierre Formenty, who worked as part of WHO's response team. Ebola outbreaks have been detected more frequently in recent years, making local and international collaboration essential.

During this outbreak, Ebola virus (sub-type Sudan) was confirmed by laboratory tests at the Kenya Medical Research Institute and the Centers for Disease Control and Prevention in the United States. When the outbreak was first reported in late May, a response team including members from WHO southern Sudan Early Warning and Response Network (EWARN), and WHO headquarters was formed to work with local health authorities in creating a Crisis Committee to control the outbreak.

The committee included UNICEF, Médecins Sans Frontières-France and other non-governmental organizations and churches working in public health. The international response to the outbreak also included partners from WHO's Regional Office for the Eastern Mediterranean, the Global Outbreak Alert and Response Network (GOARN) as well as experts from the CDC, the European Programme for Intervention Epidemiology Training, Field Epidemiology Training Programme, Egypt and the Health Protection Agency in the United Kingdom.

Intensive social mobilization for Ebola was essential to the outbreak's containment. Key messages about the disease and behaviour-specific precautionary advice were passed on to the people in and around Yambio by local community advocates.

“Once the people of Yambio were convinced of the very real risks Ebola posed and they understood what they could do to protect themselves and their families the outbreak response was greatly accelerated,” said Ms. Asiya Odugleh from the WHO Mediterranean Centre for Vulnerability Reduction, Tunis, who assisted the county social mobilization team.

The control efforts included, for example, an isolation ward at Yambio Hospital with a low fence so that patients were effectively isolated, yet still able to see and talk to their family and friends over the fence at a safe distance. Such simple adaptations of disease control measures made it easier for families to accept the case management of patients in the isolation unit, while ensuring maximum protection for the medical team and patients.

“The lessons we learned in Yambio from this outbreak will strengthen our responses to future outbreaks,” said Dr. Hassan El Bushra from the WHO Regional Office for the Eastern Mediterranean in Cairo. The Yambio experience has proven the value of rapid outbreak detection, local response capacities, active community involvement, and the coordination of specialized international assistance to the outbreak's containment.

“WHO cannot predict where or when the next Ebola outbreak will happen,” said Dr. El Bushra, “But we can continue laying the groundwork by building on what we have learned in Yambio.”

World Health Organization. Epidemic and Pandemic Alert and Response.

WORLD HEALTH ORGANIZATION. “WHO ANNOUNCES END OF EBOLA OUTBREAK IN SOUTHERN SUDAN.” PRESS RELEASE, AUGUST 7, 2004. AVAILABLE ONLINE AT <HTTP://WWW.WHO.INT/CSR/DON/2004_08_07/EN/INDEX.HTML>

See AlsoAntiviral Drugs; Emerging Infectious Diseases; Hemorrhagic Fevers; Vector-borne Disease.

BIBLIOGRAPHY

Books

Hirschmann, Kris. The Ebola Virus. San Diego: Lucent Books, 2006.

Regis, Ed. Virus Ground Zero: Stalking the Killer Viruses with the Centers for Disease Control. New York: Pocket Books, 2003.

Smith, Tara. Ebola. London: Chelsea House Publications, 2005.

Periodicals

Leroy, E.M., et al. “Fruits Bats as Reservoirs of Ebola Virus.” Nature 438 (December 1, 2005): 575–576.

Brian Hoyle

Ebola

views updated May 21 2018

Ebola


Ebola is a highly deadly viral hemorrhagic disease. As the disease progresses, the walls of blood vessels break down and blood gushes from every tissue and organ. The disease is caused by the Ebola virus , named after the river in Zaire (now the Democratic Republic of Congo) where the first known outbreak occurred. The disease is extremely contagious and exceptionally lethal. Where a 10% mortality rate is considered high for most infectious diseases, Ebola can kill up to 90% of its victims, usually within only a few days after exposure. It seems to take direct contact with contaminated blood or bodily fluids to catch the disease. Health personnel and caregivers are often the most likely to be infected. Even after a patient has died, preparing the body for a funeral can be deadly for families members.

The Ebola virus is one of two members of a family of RNA viruses called the Filoviridae. The other filovirus causes Marburg fever, an equally contagious and lethal hemorrhagic disease, named after a German town where it was first contracted by laboratory workers who handled imported monkeys infected with the virus. Together with members of three other families (arenaviruses, bunyanviruses, and flaviviruses), these viruses cause a group of deadly, episodic diseases including Lassa fever, Rift Valley fever, Bolivian fever, and Hanta or Four-Corners fever (named after the region of the southwestern United States where it was first reported).

The viruses associated with most of these emergent, hemorrhagic fevers are zoonotic. That means a reservoir of pathogens naturally resides in an animal host or arthropod vector. We don't know the specific host or vector for Ebola, but monkeys and other primates can contract related diseases. People who initially become infected with Ebola often have been involved in killing, butchering, and eating gorillas, chimps, or other primates. Why the viruses remain peacefully in their hosts for many years without causing much more trouble than a common cold, but then erupt sporadically and unpredictably into terrible human epidemics, is a new and growing question in environmental health .

The geographical origin for Ebola is unknown, but all recorded outbreaks have occurred in or around Central Africa, or in animals or people from this area. Ebola appears every few years in Africa. Confirmed cases have occurred in the Democratic Republic of the Congo, Gabon, Sudan, Uganda, and the Ivory Coast. No case of the disease in humans has ever been reported in the United States, but a variant called Ebola-Reston virus killed a number of monkeys in a research facility in Reston, Virginia. A fictionalized account of this outbreak was made into a movie called "Hot Zone." There probably are isolated cases in remote areas that go unnoticed. In fact, the disease may have been occurring in secluded villages deep in the jungle for a long time without outside attention. The most recent Ebola outbreak was in 2002 when about 100 people died in a remote part of Gabon and an adjacent area in Congo.

The worst epidemic of Ebola in humans occurred in 1995, in Kikwit, Zaire (now the Democratic Republic of Congo). Although many more people died in Kikwit that in any other outbreak, in many ways, the medical and social effects of the epidemic there was typical of what happens elsewhere. The first Kikwit victim was a 36-year-old laboratory technician named Kimfumu, who checked into a medical clinic complaining of a severe headache, stomach pains, fever, dizziness, weakness, and exhaustion. Surgeons did an exploratory operation to try to find the cause of his illness. To their horror, they found his entire gastrointestinal tract was necrotic and putrefying. He bled uncontrollably, and within hours was dead. By the next day, the five medical workers who had cared for Kimfumu, including an Italian nun who assisted in the operation, began to show similar symptoms, including high fevers, fatigue, bloody diarrhea, rashes, red and itchy eyes, vomiting, and bleeding from every body orifice. Less than 48 hours later, they, too, were dead, and the disease was spread throughout the city of 600,000.

As panicked residents fled into the bush, government officials responded to calls for help by closing off all travelincluding humanitarian aidinto or out of Kikwit, about 250 mi (400 km) from Kinshasa, the national capitol. Fearful neighboring villages felled trees across the roads to seal off the pestilent city. No one dared enter houses where dead corpses rotted in the intense tropical heat. Boats plying the adjacent Kwilu River refused to stop to take on or discharge passengers or cargo. Food and clean water became scarce. Hospitals could hardly function as medicines and medical personal became scarce. Within a few weeks, about 400 people in Kikwit had contracted the disease and at least 350 were dead. Eventually, the epidemic dissipated and disappeared. It isn't known why the infection rate dropped or what residents might do to prevent a further reappearance of the terrible disease.

Because health professionals are among the most likely to be exposed to Ebola when an outbreak occurs, it is important for them to have access to rapid antigen or antibody assays and isolation facilities to prevent further spread of the virus. Unfortunately, these advanced medical procedures generally are lacking in the African hospitals where the disease is most likely to occur. There is no standard treatment for Ebola other than supportive therapy. Patients are given replacement fluids and electrolytes, and oxygen levels and blood pressure are stabilized as much as possible. During the Kikwit outbreak, eight patients were given blood of individuals who had been infected with the virus but who had recovered. It was hoped that their blood might have antibodies to fight the infection. Seven of the eight transfusion patients survived, but the number tested is too small to be sure this was statistically significant. There is no vaccine or other antiviral drug available to prevent or halt an infection.

Several factors seem to be contributing to the appearance and spread of highly contagious diseases such as Ebola and Marburg fevers. With 6 billion people now inhabiting the planet, human densities are much higher enabling germs to spread further and faster than ever before. Expanding populations push people into remote areas where they encounter new pathogens and parasites . Environmental change is occurring on a larger scale: cutting forests, creating unhealthy urban surroundings, and causing global-climate change, among other things. Elimination of predators and habitat changes favor disease-carrying organisms such as mice, rats, cockroaches, and mosquitoes.

Another important factor in the spread of many diseases is the speed and frequency of modern travel. Millions of people go every day from one place to another by airplane, boat, train, or automobile . Very few places on earth are more than 24 hours by jet plane from any other place. In 2001, a woman flying from the Congo arrived in Canada delirious with a high fever. She didn't, in fact, have Ebola, but Canadian officials were concerned about the potential spread of the disease. Finding ways to cure Ebola and prevent its spread may be more than simply a humanitarian concern for its victims in Central Africa. It might be very much in our own self-interest to make sure that this terrible disease doesn't cross our borders either accidentally or intentionally through actions of a terrorist organization.

[William P. Cunningham Ph.D. ]


RESOURCES

BOOKS

Close, William T. Ebola: Through the Eyes of the People. London: Meadowlark Springs Productions, 2001.

Drexler, Madeline. Secret Agents: the Menace of Emerging Infections. Joseph Henry Press, 2002.

Preston, Richard. The Hot Zone. Anchor Books, 1995.

OTHER

Disease Information Fact Sheets: Ebola hemorrhagic fever. 2002. Center for Disease Control and Prevention. [cited July 9, 2002]. <http://www.cdc.gov/ncidod/dvrd/spb/mnpages/dispages/ebola.html>.

PERIODICALS

Daszak, P. et al. 2000."Emerging Infectious Diseases of Wildlife-Threats to Biodiversity and Human Health." Science(US) 287: 443-449.

Hughes, J.M. "Emerging infectious diseases: a CDC perspective." Emerging Infectious Diseases. 7(2001):494-6.

Osterholm, M. T. "Emerging InfectionsAnother Warning." The New England Journal of Medicine 342(17): 4-5.

Ebola Virus

views updated May 18 2018

Ebola virus

The Ebola virus is one of a number of viruses that cause a devastating disease in humans and closely related species such as monkeys , gorillas , and chimpanzees . The disease is known as a hemorrhagic fever because of the massive internal bleeding caused by the viral infection . Most strains of Ebola hemorrhagic fever progresses quickly from the initial appearance of symptoms to resolution, which is often death.

The name of the Ebola virus comes from a river located in the Democratic Republic of the Congo, where the virus was discovered in 1976. At that time, the country was known as Zaire. The virus was designated Ebola Zaire. Over 300 cases were associated with this initial outbreak. That same year, another type of Ebola virus, named Ebola Sudan, caused an outbreak in another African country, Sudan. Outbreaks also occurred in 1979, 1995, and 1996. In the latest outbreak, which has been ongoing in Gabon since late 2001, 54 people have died as of February of 2002.

The Ebola virus is a species in one group in a collection of viruses classified as Filoviridae. They were originally classified as rhabdoviruses. However, genome sequencing revealed more of a similarity to paramyxoviruses. However, filoviruses are sufficiently distinct from the other nonsegmented negative-stranded RNA viruses to warrant taxonomic status as a separate virus family. This family of viruses causes a disease that is typified by copious internal bleeding and bleeding from various orifices of the body, including the eyes. The disease can be swiftly devastating and results in death in about 90% of cases.

As of 2003, four species of Ebola virus have been identified. The species differ slightly in their genetic sequences and in the immune reaction they elicit in those who become infected. A different immune reaction means that the protein components that cause the immune reaction (antigens) are different.

Three of the Ebola virus species cause disease in humans. These are Ebola-Zaire (isolated in 1976), Ebola-Sudan (also isolated in 1976), and Ebola-Ivory Coast (isolated in 1994). The fourth species, called Ebola-Reston, causes disease only in primates .

Ebola Reston is named for the United States military primate research facility where the virus was isolated, during a 1989 outbreak of the disease caused by infected monkeys that had been imported from the Philippines. Until the non-human involvement of the disease was proven, the outbreak was thought to be the first outside of Africa . This incident brought the virus and the disease it causes to prominent public attention, particularly in the United States.

The appearance of the Ebola virus only dates back to 1976. The explosive onset of the illness and the fact that the outbreaks tend to occur in underdeveloped and remote regions of Africa have complicated both the treatment of the disease and the tracking of its habitat and origin. Indeed, the source of the Ebola virus is still unknown. However, the related filovirus, which produces similar effects, establishes a latent infection (one that does not always produce symptoms, but which is infectious and capable of being spread) in African monkeys, macaques , and chimpanzees. A credible theory, therefore, is that the Ebola virus normally resides in an animal that lives in Africa. As of 2002, the Ebola virus has not been isolated from live primates in the wild. Chimpanzees found dead and infected with the Ebola virus, however, were responsible for the initiation of Ebola outbreaks in 1996 in two regions of Gabon when local residents ate infected meat from the dead chimpanzees.

Almost all confirmed cases of Ebola from 1976 to 2002 have been in Africa. In the past, one individual in Liberia presented immunological evidence of exposure to Ebola, but had no symptoms. As well, a laboratory worker in England developed Ebola fever as a result of a laboratory accident in which the worker was punctured by an Ebola-contaminated needle. No human case has been reported in North America . A suspected case in Hamilton, Ontario, Canada in early 2001 turned out not to be Ebola, although the exact cause of this illness remains unresolved.

Infection with the Ebola virus produces a high fever, headache, muscle aches, abdominal pain , tiredness and diarrhea within a few days. Some people will also display bloody diarrhea and vomit blood . At this stage of the disease some people do recover. But, for most of those who are infected, the disease progresses within days to produce copious internal bleeding, shock, and death.

The initial infection is presumably by contact between the person and the animal that harbors the virus . Subsequent person-to-person spread likely occurs by contamination with the infected blood or body tissues of an infected person in the home or hospital setting, or via contaminated needles. Following the initial human infection, spread occurs from direct contact with the blood and/or secretions of the infected person. Within a few days of infection, symptoms that typically develop include a fever, headache, muscle aches, fatigue, and diarrhea. Within one week of infection, hemorrhaging causes blood to flow from the eyes, nose, and ears. Death usually occurs within nine or 10 days of the onset of infection.

The severity and lethality of Ebola hemorrhagic fever effectively limit the outbreaks to a relatively few individuals. Outbreaks of infection with the Ebola virus appear sporadically, rapidly move through the population, and usually end just as suddenly. The high death rate associated with infection is likely the limiting factor in the infection's spread. Viruses require a host cell in which to reproduce. Killing the host eliminates the use of the host's cells as a reproductive factory for the virus. In other words, death is so rapid that the virus has a limited chance to spread to other victims.

That infected people tend to be in more under-developed regions, where even the health care facilities are not as likely to be equipped with isolation wards, furthers the risk of spread. The person-to-person passage is immediate. Unlike the animal host, people do not harbor the virus for lengthy periods of time.

Whether Ebola viruses can be transmitted through the air is not known. In the outbreak at the Reston facility, Ebola Reston may well have been transmitted from monkey to monkey via the air distribution system. Indeed, some of the monkeys that were infected were never in physical contact with the other infected monkeys. However, if the other species of the Ebola virus are capable of similar transmission has not yet been documented. Laboratory studies have shown that Ebola virus can remain infectious when aerosolized. But the current consensus is that airborne transmission, although possible, plays a minor role in the spread of the virus.

Similarly, the natural reservoir of the Ebola viruses is not known. Between the sporadic outbreaks, the Ebola virus probably is resident in this natural reservoir, whatever that reservoir may be.

Currently there is no cure for the infection caused by the Ebola virus. However, near the end of a 1995 outbreak in Kikwit, Africa, blood products from survivors of the infection were transfused into those actively experiencing the disease. Of those eight people who received the blood, only one person died. Whether or not the transfused blood conveyed a protective factor was not established, as resources were being devoted to bedside care rather than research. A detailed examination of this possibility awaits another outbreak. With the advent of recombinant DNA technology, the molecular structure of Ebola viruses, the details of their replication and interaction with the host are under intense study.

The molecular basis for the establishment of an infection by the Ebola virus is still also more theoretical than fact. One clue has been the finding of a glycoprotein in the circulating fluid of infected humans and monkeys that is a shortened version of a viral component. It may be that this protein acts as a decoy for the immune system , diverting the immune defenses from the actual site of viral infection. It has also been proposed that the virus suppresses the immune system, via the selective invasion and damage of the spleen and the lymph nodes (which are vital in the functioning of the human immune system).

The devastating infection caused by the Ebola virus is all the more remarkable given the very small size of the viral genome. Fewer than a dozen genes have been detected. How the virus establishes an infection and evades the host immune system with only the capacity to code for less than twelve proteins is unknown.

See also Epidemiology.


Resources

books

Peters, C. J., and M. Olshaker. Virus Hunter: Thirty Years ofBattling Hot Viruses Around the World. New York: Doubleday, 1998.

periodicals

Sanchez, A., M. P. Kiley, B. P. Holloway, et al. "Sequence Analysis of the Ebola Virus Genome: Organization, Genetic Elements, and Comparison with the Genome of Marburg Virus." Virus Research 29 (1993): 215–240.

organizations

United States Centers for Disease Control and Prevention, Special Pathogens Branch. 1600 Clifton Road, Atlanta, GA 30333. (404) 639–3311. <http://www.cdc.gov/ncidod/dvrd/spb/mnpages/dispages/ebola.htm>.


Brian Hoyle

KEY TERMS

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Epidemiologist

—A physician or scientist who studies the distribution, sources, and control of diseases in populations.

Ebola Virus

views updated May 18 2018

Ebola Virus

BRIAN D. HOYLE

The Ebola virus is one of two members of a family of viruses that is designated as the Filoviridae. The name of the virus comes from a river located in the Democratic Republic of the Congo, where the virus was discovered. Although naturally occurring, some public health experts worry that the lethality of the virus makes it an attractive potential bioterrorism agent. Under natural circumstances Ebola induced hemorrhagic fever carriers have such high death rates that their rapid death actually acts to limit the spread of the virus. Deliberate spread of the virus would counteract this natural limiting factor.

The species of Ebola virus are among a number of viruses that cause a disease, hemorrhagic fever, that is typified by copious internal bleeding and bleeding from various orifices of the body, including the eyes. The disease can be swiftly devastating and results in death in over 90 per cent of cases.

To date, four species of Ebola virus have been identified, based on differences in their genetic sequences and in the immune reaction they elicit in infected individuals. Three of the species cause disease in humans. These are Ebola-Zaire (isolated in 1976), Ebola-Sudan (also isolated in 1976), and Ebola-Ivory Coast (isolated in 1994). The fourth species, called Ebola-Reston, causes disease in primates. The latter species is capable of infecting humans but so far has not caused disease in humans. Ebola-Reston is named for the United States military primate research facility where the virus was isolated, during a 1989 outbreak of the disease caused by infected monkeys that had been imported from the Philippines. Until the non-human involvement of the disease was proven, the outbreak was thought to be the first outside of Africa.

The appearance of the Ebola virus only dates back to 1976. The explosive onset of the illness and the underdeveloped and wild nature of the African region of the virus's appearance have complicated the definitive determinations of the origin and natural habitat of Ebola. The source of the Ebola virus is still unknown. However, given that filovirus, which produce similar effects, establish a latent infection in African monkeys, macaques, and chimpanzees, scientists consider the possibility that the Ebola virus likewise normally resides in an animal that lives in Africa. A search for Ebola virus in such primates has so far not revealed evidence of the virus.

Almost all confirmed cases of Ebola from 1976 to 2002 have been in Africa. In the latest outbreak, which has been ongoing since late in 2001, 54 people have died in the Gabon as of February of 2002. In the past, one individual in Liberia presented immunological evidence of exposure to Ebola, but had no symptoms. As well, a laboratory worker in England developed Ebola fever as a result of a laboratory accident in which the worker was punctured by an Ebola-containing needle.

The Ebola virus produces a high fever, headache, muscle aches, abdominal pain, tiredness and diarrhea within a few days after infecting a person. Some people will also display bloody diarrhea and vomit blood. At this stage of the disease some people recover. But, for most of those who are infected, the disease progresses within days to produce copious internal bleeding, shock and death.

Outbreaks of infection with the Ebola virus appear sporadically and suddenly. The outbreak rapidly moves through the local population and often just as quickly ends. The initial infection is presumable by contact between the person and the animal that harbors the virus. Subsequent person-to-person spread likely occurs by contamination with the infected blood or body tissues of an infected person in the home or hospital setting, or via contaminated needles. The fact that infected people tend to be in more under-developed regions, where even the health care facilities are not as likely to be equipped with isolation wards, furthers the risk of spread. The person-to-person passage is immediate; unlike the animal host, people do not harbor the virus for lengthy periods of time.

The possibility of air-borne transmission of the virus is debatable. Ebola-Reston may well have been transmitted from monkey to monkey in the Reston military facility via the air distribution system, since some of the monkeys that were infected were never in physical contact with the other infected monkeys. However, if the other species of the virus are capable of similar transmission, this has not yet been documented. Laboratory studies have shown that Ebola virus can remain infectious when aerosolized. But the current consensus is that airborne transmission is possible but plays a minor role in the spread of the virus.

In the intervening years between the sporadic outbreaks, the Ebola virus probably is resident in the natural reservoir.

Currently there is no cure for the infection caused by the Ebola virus. However, near the end of an outbreak of the virus in 1995 in Kikwit, Africa, blood products from survivors of the infection were transfused into those actively experiencing the disease. Of those eight people who received the blood, only one person died. Whether or not the transfused blood conveyed protective factor was not ascertained. A detailed examination of this possibility awaits another outbreak.

The molecular basis for the establishment of an infection by the Ebola virus is still also more in the realm of proposal than fact. One clue has been the finding of a glycoprotein that is a shortened version of the viral constituent in the in the circulating fluid of humans and monkeys. This protein has been suggested to function as a decoy for the immune system, diverting the immune defenses from the actual site of viral infection. Another immunosuppressive mechanism may be the selective invasion and damage of the spleen and the lymph nodes, which are vital in the functioning of the immune system.

The devastating infection caused by the Ebola virus is all the more remarkable given the very small size of the viral genome, or complement of genetic material. Fewer than a dozen genes have been detected. How the virus establishes an infection and evades the host immune system with only the capacity to code for less than twelve proteins is unknown.

FURTHER READING:

BOOKS:

Cormican, M. G. and M. A. Pfaller. "Molecular Pathology of Infectious Diseases," in Clinical Diagnosis and Management by Laboratory Methods, 20th ed. Philadelphia: W. B. Saunders, 2001.

PERIODICALS:

Peters, C. J., and J. W. LeDuc. "An Introduction to Ebola: The Virus and the Disease." The Journal of Infectious Diseases no. 179 (Supplement 1, February 1999): ixxvi.

ELECTRONIC:

Centers for Disease Control. "Ebola Hemorrhagic Fever." 2001. <http://www.cdc.gov/ncidod/dvrd/spb/mnpages/dispages/ebola.htm> (March 12, 2003).

. "Viral Hemorrhagic Fevers." 2000. <http://www.cdc.gov/ncidod/dvrd/spb/mnpages/dispages/vhf.htm> (March 12, 2003).

SEE ALSO

Biological Warfare
Biological Weapons, Genetic Identification
Bioshield Project
Bioterrorism
CDC (United States Centers for Disease Control and Prevention)
Hemorrhagic Fevers and Diseases
Viral Biology

Ebola Virus

views updated May 17 2018

Ebola Virus

Since the mid-1970s, scientists from organizations that include the Centers for Disease Control and prevention (CDC) have periodically been pressed into action to help quell disease outbreaks caused by the Ebola virus. One facet of their responsibilities has been forensic investigations that involve determining the origins of the outbreaks.

Although naturally occurring, the swift and high lethality of the Ebola virus makes it an attractive potential bioterrorism agent. This high lethality characteristic can actually work against a large outbreak, as it limits the natural spread of the virus. Deliberate spread of the virus in multiple population areas could counteract the natural limiting factor.

The Ebola virus is one of two members of a family of viruses that is designated as the Filoviridae. The name of the virus comes from a river located in the Democratic Republic of the Congo. It was near this river that the virus was discovered.

The species of Ebola virus are among a number of viruses that cause hemorrhagic fever, which is typified by copious internal bleeding and bleeding from various orifices of the body, including the eyes. The disease can be swift and devastating, resulting in death in up to 90% of cases.

To date, four species of Ebola virus have been identified, based on differences in their genetic sequences and in the immune reaction they elicit in infected individuals. Three of the species cause disease in humans. These are Ebola-Zaire (isolated in 1976), Ebola-Sudan (also isolated in 1976), and Ebola-Ivory Coast (isolated in 1994). The fourth species, called Ebola-Reston, causes disease in primates. The latter species is capable of infecting humans but so far has not caused disease in humans. Ebola-Reston is named for the United States military primate research facility where the virus was isolated during a 1989 outbreak of the disease caused by infected monkeys that had been imported from the Philippines. Until the non-human involvement of the disease was proven, the outbreak was thought to be the first outside of Africa.

The explosive onset of the illness and the under-developed and wild nature of the African region of the virus's appearance has complicated forensic investigations into the origin and natural habitat of Ebola. The source of the Ebola virus is still unknown. However, given that filovirus, which produces similar effects, can establish a latent infection in African monkeys, macaques, and chimpanzees, it seems reasonable that the Ebola virus could reside normally in a similar host. However, direct evidence is so far lacking.

Almost all confirmed cases of Ebola from 1976 to 2003 have been in Africa. In the latest outbreaks, which persisted in Gabon through 2003, 122 people were known to have been infected and 96 died, according to data from the CDC. A smaller outbreak killed 7 of 17 infected people in 2004 in Sudan. In the past, one individual in Liberia presented immunological evidence of exposure to Ebola, but had no symptoms. As well, in 1976 a laboratory worker in England developed Ebola fever as a result of a laboratory accident in which the worker was punctured by an Ebola-containing needle.

The Ebola virus produces a high fever, headache, muscle aches, abdominal pain, tiredness, and diarrhea within a few days after infecting a person. Some people will also display bloody diarrhea and vomit blood. At this stage of the disease, some people recover. But for most of those who are infected, the disease progresses within days to produce copious internal bleeding, shock, and death.

Outbreaks of infection with the Ebola virus appear sporadically and suddenly. The outbreak rapidly moves through the local population and often just as quickly ends. The initial infection is presumably by contact between the person and an animal that harbors the virus. Subsequent person-to-person spread likely occurs by contamination with the infected blood or body tissues of an infected person in the home or hospital setting, or via contaminated needles. The fact that infected people tend to be in more under-developed regions, where even the health care facilities are not as likely to be equipped with isolation wards, furthers the risk of spread. The person-to-person passage is immediate; unlike the animal host; people do not harbor the virus for lengthy periods of time.

The possibility of air-borne transmission of the virus is debatable. Ebola-Reston may have been transmitted from monkey to monkey in the Reston military facility via the air distribution system, since some of the monkeys that were infected were never in physical contact with the other infected monkeys. However, if the other species of the virus are capable of similar transmission, this has not yet been documented. Laboratory studies have shown that Ebola virus can remain infectious when aerosolized. But the current consensus is that airborne transmission is possible but plays a minor role in the spread of the virus.

In the intervening years between the sporadic outbreaks, the Ebola virus probably resides in its natural reservoir. Whether that reservoir is an animal or plant, or resides in the soil or other environment is unknown, although scientists suspect the reservoir is a mammal.

Currently there is no cure for the infection caused by the Ebola virus. However, near the end of an outbreak of the virus in 1995 in Kikwit, Africa, blood products from survivors of the infection were transfused into those actively experiencing the disease. Of those eight people who received the blood, only one person died. Whether or not the transfused blood conveyed protective factor was not ascertained. A detailed examination of this possibility awaits another outbreak.

The molecular basis for the establishment of an infection by the Ebola virus is still also more in the realm of proposal than fact. One clue has been the finding of a glycoprotein that is a shortened version of the viral constituent in the circulating fluid of humans and monkeys. This protein has been suggested to function as a decoy for the immune system , diverting the immune defenses from the actual site of viral infection. Another immunosuppressive mechanism may be the selective invasion and damage of the spleen and the lymph nodes, which are vital in the functioning of the immune system.

The devastating infection caused by the Ebola virus is all the more remarkable given the very small size of the viral genome, or complement of genetic material. Fewer than a dozen genes have been detected. How the virus establishes an infection and evades the host immune system with only the capacity to code for less than twelve proteins is unknown.

see also Bioterrorism; Hemorrhagic fevers and diseases.

Ebola Virus

views updated Jun 11 2018

Ebola virus

The Ebola (pronounced ee-BO-luh) virus is the common name for a severe, often-fatal bleeding or hemorrhagic (pronounced hem-or-RAD-jik) fever that first appeared in 1976. It is caused by a new kind of virus called a filovirus (pronounced FY-low-vye-russ) that kills most of its victims with frightening speed. The source of the virus is unknown and there is no cure.

A deadly disease

As a viral hemorrhagic fever, the Ebola virus infects its host and causes sudden fever, muscle aches, and weakness followed by vomiting, diarrhea, breathing and kidney problems, shock, internal and external bleeding, and usually death. It is one of the most deadly disease-causing agents known, and is classified as a Level 4 pathogen (pronounced PATH-o-jen). For comparison, the disease known as AIDS (acquired immunodeficiency syndrome) is only a Level 2 pathogen. This new disease is particularly horrible and has been described by one author as a "molecular shark" that can turn "virtually every part of the body into a digested slime of virus particles." This means that the victim's internal organs break down, with blood oozing eventually from every part of the body.

First outbreak

The first time the new, thread-shaped filovirus was ever seen was in 1967 in Germany and Yugoslavia. In both those countries, research laboratory workers became violently and desperately ill. Seven of thirty-one workers died. All had one thing in common: they had been exposed to the tissues and blood of several African green monkeys. Doctors soon examined the victims's blood and discovered a virus resembling a tangled rope that was unlike any virus they had ever seen. Following this incident, which gave the name Marburg virus to the new microorganism, there were a few cases in the African countries of Zimbabwe, South Africa, and Kenya.

Words to Know

Filovirus: A family of lethal thread-shaped viruses that includes Ebola and Marburg.

Virus: A package of chemicals that are far smaller than the living cells they infect. Viruses are not classified as living organisms, since they cannot grow and reproduce on their own, but rely on a host cell to make copies of themselves.

However, in the summer of 1976, a new version of the filovirus appeared in two major outbreaks that occurred almost at the same time. The first of these emerged in the country of Sudan, and the other in the country of Zaire (now known as the Democratic Republic of the Congo), some 500 miles (800 kilometers) away. In both places it was as if a deadly biological bomb had gone off, with hundreds of people becoming ill and dying at a terrible rate. These large outbreaks resulted in more than 550 cases and 340 deaths. Examination of the virus showed that it was similar to the Marburg virus, but not the same. In fact, it was even deadlier. It came to be called the Ebola virus, named after the river in Zaire where it was first recognized.

Four sub-types

Since that first outbreak in 1976, four subtypes or versions of the Ebola virus have been identified so far. The first three, called Ebola-Zaire, Ebola-Sudan, and Ebola-Ivory Coast, are known to have caused disease in humans. The fourth, called Ebola-Reston after the Reston, Virginia, primate laboratory where it was first discovered, seems to only be transmitted by monkeys to monkeys, although it may be the only one of the four viruses that is airborne (meaning it can be spread through particles floating in the air).

Ebola symptoms

People can get the first three Ebola fevers through direct contact with a sick person. This usually happens to hospital workers or family members who are caring for a severely ill victim and who somehow become infected by coming in contact with the victim's blood or other body fluids. In very poor countries, people often are infected when needles are reused instead of thrown away. Within a few days of being infected, most new victims experience a high fever, headache, muscle and stomach pain, fatigue, and diarrhea. Within one week of being infected, most patients experience chest pain, shock, bleeding, and death. Researchers have no explanation for why some people are able to recover from this devastating illness.

Treatment

There is currently no standard treatment for the Ebola virus that results in anything more than making the patient comfortable. The one standard therapy in use is to make sure that patients receive enough proper fluids, as well as maintaining their blood pressure and providing a good supply of oxygen. In hospitals, Ebola patients receive what are called barrier nursing techniques, meaning that they are isolated from other patients and only are tended to by workers who wear protective clothing, masks, gloves, gowns, and goggles. Complete sterilization procedures are also strictly followed.

Although the filovirus family has been known since 1967, scientists still have no idea where the virus lives in nature. So far, every case has been a secondary one, meaning that it was caused by contact from another. Nor do we know the exact mechanism the virus uses to enter the host cell. No drug is known that will work against the virus, nor is there any immunization (pronounced im-mew-nih-ZAY-shun) technique available to protect someone from exposure. No vaccines (pronounced vax-SEENZ) have yet been developed. During the late 1990s and into the new millennium, minor outbreaks had been reported with some regularity in different parts of Africa.

Although there is a great deal to learn about this terrible new disease, we do know that Ebola viruses are found only in Central Africa. Although the source in nature is not yet known, it appears that monkeys are susceptible to infection. The very deadliness of the disease has so far worked against any really massive health disaster because it kills its victims so quickly that they do not have a great chance to infect many others. In some ways, the virus burns itself out before it can spread to a major population center. No case of Ebola fever has ever been reported in the United States.

[See also Disease ]

Ebola Virus

views updated May 14 2018

Ebola Virus

Resources

The Ebola virus is one of two members of a family of viruses that is designated as the Filoviridae. The name of the virus comes from a river located in the Democratic Republic of the Congo, where the virus was discovered.

The species of Ebola virus are among a number of viruses that cause a disease that is typified by copious internal bleeding and bleeding from various orifices of the body, including the eyes. The disease can be swiftly devastating and results in death in over 90% of cases.

As of 2006, four species of Ebola virus have been identified, based on differences in their genetic sequences and in the immune reaction they elicit in infected individuals. Three of the species cause disease in humans. These are Ebola-Zaire (isolated in 1976), Ebola-Sudan (also isolated in 1976), and Ebola-Ivory Coast (isolated in 1994). The fourth species, called Ebola-Reston, causes disease in primates. The latter species is capable of infecting humans but so far has not caused disease in humans. Ebola-Reston is named for the United States military primate research facility where the virus was isolated, during a 1989 outbreak

of the disease caused by infected monkeys that had been imported from the Philippines. Until the nonhuman involvement of the disease was proven, the outbreak was thought to be the first outside of Africa.

The appearance of the Ebola virus only dates back to 1976. The explosive onset of the illness and the under-developed and remote nature of the African region of the viruss appearance, has complicated the definitive determinations of the origin and natural habitat of Ebola. The source of the Ebola virus is still unknown. However, given that filovirus, which produce similar effects, establish a latent infection in African monkeys, macaques, and chimpanzees, scientists consider the possibility that the Ebola virus likewise normally resides in an animal that lives in Africa. A search for Ebola virus in such primates has so far not revealed evidence of the virus.

Almost all confirmed cases of Ebola from 1976 to 2002 have been in Africa. In the latest outbreak, which has been ongoing since late in 2001, 54 people died in the Gabon by February of 2002. In the past, one individual in Liberia presented immunological evidence of exposure to Ebola, but had no symptoms. As well, a laboratory worker in England developed Ebola fever as a result of a laboratory accident in which the worker was punctured by an Ebola-containing needle.

The Ebola virus produces a high fever, headache, muscle aches, abdominal pain, tiredness, and diarrhea within a few days after infecting a person. Some people will also display bloody diarrhea and vomit blood. At this stage of the disease some people recover. But, for most of those who are infected, the disease progresses within days to produce copious internal bleeding, shock, and death.

Outbreaks of infection with the Ebola virus appear sporadically and suddenly. The outbreak rapidly moves through the local population and often just as quickly ends. The initial infection is presumable by contact between the person and the animal that harbors the virus. Subsequent person-to-person spread likely occurs by contamination with the infected blood or body tissues of an infected person in the home or hospital setting, or via contaminated needles. The fact that infected people tend to be in more under-developed regions, where even the health care facilities are not as likely to be equipped with isolation wards, furthers the risk of spread. The person-to-person passage is immediate; unlike the animal host, people do not harbor the virus for lengthy periods of time.

The possibility of air-borne transmission of the virus is debatable. Ebola-Reston may well have been transmitted from monkey to monkey in the Reston military facility via the air distribution system, since some of the monkeys that were infected were never in physical contact with the other infected monkeys. However, if the other species of the virus are capable of similar transmission, this has not yet been documented. Laboratory studies have shown that Ebola virus can remain infectious when aerosolized. But the current consensus is that airborne transmission is possible but plays a minor role in the spread of the virus.

In the intervening years between the sporadic outbreaks, the Ebola virus probably is resident in the natural reservoir.

Currently there is no cure for the infection caused by the Ebola virus. However, near the end of an outbreak of the virus in 1995 in Kikwit, Africa, blood products from survivors of the infection were trans-fused into those actively experiencing the disease. Of those eight people who received the blood, only one person died. Whether or not the transfused blood conveyed protective factor was not ascertained. A detailed examination of this possibility awaits another outbreak.

The molecular basis for the establishment of an infection by the Ebola virus is still also more in the realm of proposal than fact. One clue has been the finding of a glycoprotein that is a shortened version of the viral constituent in the in the circulating fluid of humans and monkeys. This protein has been suggested to function as a decoy for the immune system, diverting the immune defenses from the actual site of viral infection. Another immunosuppressive mechanism may be the selective invasion and damage of the spleen and the lymph nodes, which are vital in the functioning of the immune system.

The devastating infection caused by the Ebola virus is all the more remarkable given the very small size of the viral genome, or complement of genetic material. Fewer than a dozen genes have been detected. How the virus establishes an infection and evades the host immune system with only the capacity to code for less than twelve proteins is unknown.

Resources

BOOKS

Ryabchikova, Elena, and Barbara S. Price. Ebola and Marburg Viruses: A View of Infection Using Electron Microscopy. Columbus: Battelle Press, 2002.

Smith, Tara C. Ebola (Deadly Diseases and Epidemics). New York: Chelsea House Publications, 2005.

Willett, Edward. Ebola Virus (Diseases and People). Berkeley Heights, NJ: Enslow Publishers, 2003.

Brian Hoyle

Ebola Virus

views updated May 23 2018

Ebola virus

The Ebola virus is one of two members of a family of viruses that is designated as the Filoviridae. The name of the virus comes from a river located in the Democratic Republic of the Congo, where the virus was discovered.

The species of Ebola virus are among a number of viruses that cause a disease that is typified by copious internal bleeding and bleeding from various orifices of the body, including the eyes. The disease can be swiftly devastating and results in death in over 90% of cases.

To date, four species of Ebola virus have been identified, based on differences in their genetic sequences and in the immun reaction they elicit in infected individuals. Three of the species cause disease in humans. These are Ebola-Zaire (isolated in 1976), Ebola-Sudan (also isolated in 1976), and EbolaIvory Coast (isolated in 1994). The fourth species, called Ebola-Reston, causes disease in primates. The latter species is capable of infecting humans but so far has not caused disease in humans. Ebola-Reston is named for the United States military primate research facility where the virus was isolated, during a 1989 outbreak of the disease caused by infected monkeys that had been imported from the Philippines. Until the non-human involvement of the disease was proven, the outbreak was thought to be the first outside of Africa.

The appearance of the Ebola virus only dates back to 1976. The explosive onset of the illness and the under-developed and wild nature of the African region of the virus's appearance, has complicated the definitive determinations of the origin and natural habitat of Ebola. The source of the Ebola virus is still unknown. However, given that filovirus, which produce similar effects, establish a latent infection in African monkeys, macaques, and chimpanzees, scientists consider the possibility that the Ebola virus likewise normally resides in an animal that lives in Africa. A search for Ebola virus in such primates has so far not revealed evidence of the virus.

Almost all confirmed cases of Ebola from 1976 to 2002 have been in Africa. In the latest outbreak, which has been ongoing since late in 2001, 54 people have died in the Gabon as of February of 2002. In the past, one individual in Liberia presented immunological evidence of exposure to Ebola, but had no symptoms. As well, a laboratory worker in England developed Ebola fever as a result of a laboratory accident in which the worker was punctured by an Ebola-containing needle.

The Ebola virus produces a high fever, headache, muscle aches, abdominal pain, tiredness and diarrhea within a few days after infecting a person. Some people will also display bloody diarrhea and vomit blood. At this stage of the disease some people recover. But, for most of those who are infected, the disease progresses within days to produce copious internal bleeding, shock and death.

Outbreaks of infection with the Ebola virus appear sporadically and suddenly. The outbreak rapidly moves through the local population and often just as quickly ends. The initial infection is presumable by contact between the person and the animal that harbors the virus. Subsequent person-to-person spread likely occurs by contamination with the infected blood or body tissues of an infected person in the home or hospital setting, or via contaminated needles. The fact that infected people tend to be in more under-developed regions, where even the health care facilities are not as likely to be equipped with isolation wards, furthers the risk of spread. The person-to-person passage is immediate; unlike the animal host, people do not harbor the virus for lengthy periods of time.

The possibility of air-borne transmission of the virus is debatable. Ebola-Reston may well have been transmitted from monkey to monkey in the Reston military facility via the air distribution system, since some of the monkeys that were infected were never in physical contact with the other infected monkeys. However, if the other species of the virus are capable of similar transmission, this has not yet been documented. Laboratory studies have shown that Ebola virus can remain infectious when aerosolized. But the current consensus is that airborne transmission is possible but plays a minor role in the spread of the virus.

In the intervening years between the sporadic outbreaks, the Ebola virus probably is resident in the natural reservoir.

Currently there is no cure for the infection caused by the Ebola virus. However, near the end of an outbreak of the virus in 1995 in Kikwit, Africa, blood products from survivors of the infection were transfused into those actively experiencing the disease. Of those eight people who received the blood, only one person died. Whether or not the transfused blood conveyed protective factor was not ascertained. A detailed examination of this possibility awaits another outbreak.

The molecular basis for the establishment of an infection by the Ebola virus is still also more in the realm of proposal than fact. One clue has been the finding of a glycoprotein that is a shortened version of the viral constituent in the in the circulating fluid of humans and monkeys. This protein has been suggested to function as a decoy for the immune system , diverting the immune defenses from the actual site of viral infection. Another immunosuppressive mechanism may be the selective invasion and damage of the spleen and the lymph nodes, which are vital in the functioning of the immune system.

The devastating infection caused by the Ebola virus is all the more remarkable given the very small size of the viral genome, or complement of genetic material. Fewer than a dozen genes have been detected. How the virus establishes an infection and evades the host immune system with only the capacity to code for less than twelve proteins is unknown.

See also Hemorrhagic fevers and diseases; Zoonoses

Ebola virus

views updated May 23 2018

Ebola virus (i-boh-lă) n. a virus responsible for an acute infection in humans with features similar to those of Marburg disease. Transmission is by contact with infected blood and other body fluids. The mortality rate is 53–88%, but intensive treatment (including rehydration) in the early stages of the disease can halt its rapid and usually irreversible progression to haemorrhaging of internal organs.

ebola

views updated Jun 11 2018

ebola Virus that causes haemorrhagic fever. Thought to have been long present in animals, the ebola virus was first identified in humans during an outbreak in Congo in 1976. It is acquired through contact with contaminated body fluids. Death rates can be as high as 90%.