Difference between revisions of "Epstein-Barr Virus"

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[[Category:Pages edited by students of Tyrrell Conway at the University of Oklahoma]][[Image:OULOGOBIANCO.JPEG|thumb|230px|left|University of Oklahoma Study Abroad Microbiology in Arezzo, Italy[http://cas.ou.edu/study-abroad/]]]
[[File:Epstein Barr B cell.gif|300px|thumb|right|Epstein-Barr budding in a B cell From: msdiscovery.org
[[File:Epstein Barr B cell.gif|300px|thumb|right|Epstein-Barr budding in a B cell From: msdiscovery.org

Latest revision as of 14:45, 11 February 2016

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University of Oklahoma Study Abroad Microbiology in Arezzo, Italy[1]
Epstein-Barr budding in a B cell From: msdiscovery.org [2]



| Order = Herpesvirales | Family = Herpesviridae | Subfamily = Gammaherpesvirinae | Genus = Lymphocryptovirus | Species = Human Herpesvirus 4

NCBI: [9] Genome: [10]


The Epstein-Barr virus (EBV) is one of the two human host-specific viruses in the subfamily Gammaherpesvirinae, along with Kaposi's Sarcoma, a virus normally associated with lesions in AIDS patients. It is the most common virus among the human population. More than 95% of the human population contain EBV antibodies, meaning that they have come into contact with the virus at some point in life and it is lying latent. Many people are asymptomatic when infected, but under certain stresses diseases, such as infectious mononucleosis (IM), can arise. EBV was found to be the main virus responsible for Burkitt's Lymphoma in 1964, and later on was found to be correlative with Hodgkin's Lymphoma and nasopharyngeal carcinoma. EBV is not the sole cause of these cancers, but it does play an important role in their development. A defining marker of a virus is that it requires a host to replicate and survive, and when EBV was discovered, it was very difficult to grow on any medium.

Herpesviruses are characteristically icosahedral, 20-sided, and 70-100 microns in diameter, which led Epstein to characterize EBV with this family, however because he could not run standard tests of the other herpesviruses at the time, he concluded it must be a new strain [1].


EBV is a double-stranded DNA virus, making it more stable and less likely for mutations than RNA viruses. EBV is 184 kb pairs in length. The genome shows around 70 predictable open reading frames and there are two different strains. The strains differ in their latent proteins, but they are not associated with any specific disease. Analyzing repeat genes can be used in studying outbreaks [2]. The genome codes for latent and lytic proteins, and there are RNA transcription proteins whose functions are still unknown. It is an enveloped herpes virus, which means it can cause a life-long latent infection. EBV is very large for a herpesvirus and is surrounded by an outer layer comprised of cellular membranes from infected cells, adding an extra 50-100 nm to its size. The envelope is necessary for infectivity and sensitivity.

There are two types of EBV: they are found in different geographic regions though both are common and neither correlate to specific diseases.

Genes required for proliferation of latently infected cells: EBNA2, LMP1, EBNA3A and EBNA3C. EBNA1 is responsible for maintenance of the EBV genome inside the host cell nucleus. There are 3 latent cycles that EBV can go through, each expressing different proteins. B cells can produce all three, but epithelial cells can only produce type II. Type I is found in Burkitt's Lymphoma tumors and only expresses EBNA1 showing minimum levels of virus activity. Type II is seen in nasopharyngeal carcinoma (NPC) tumors and expresses LMP proteins as well as EBNA1. Type III is common in non-cancerous cells and expresses all 11 latent viral genes [23].



Transmission of EBV From: mdpi.org [3]

EBV is transmitted through salivary contact. Mononucleosis is commonly called the "kissing disease" because it is often spread through the saliva when kissing. It is also possible to catch EBV from sharing eating utensils and drinks. Targets of primary infection are most likely B cells near the tonsillar epithelia or other lymphoid organs in that region. Though EBV can infect epithelial cells and B cells, it is imperative for EBV's replication cycle to infect B cells [17]. Epithelial cells enhance transmission from different hosts and may play a role in establishing latency. EBV has been discovered in the uterine lining and semen of IM patients, so EBV can likely be spread through sexual contact as well [2]. Transmission through blood and air are very rare. One study shows that vertical transmission through the mother is possible, but not definite. The study was done with HIV-positive women as well and having the disease does not increase the risk of transmission to a fetus [18]. The cell membrane contains glycoproteins that are essential for invasion of a host cell.

Infectious Dose and Incubation

The infectious dose is still not known for sure. There have been studies trying to quantify viral output in saliva, though the trial was inconclusive. The virus in the saliva was replenished at a very fast rate even after numerous mouth rinses [19]. The epithelial cells are those most known to cause infection and transmission, but they can be infected from other epithelial cells or B cells. Equations were created to quantify virus shedding in EBV positive individuals, but the amount it takes to infect another host is still unclear. Any contact with an infected person's saliva can cause transmission of EBV. If contact occurs after childhood, IM is likely to occur with uncomfortable symptoms.

Because the moment of infection is difficult to determine, it is hard to note exactly how long the incubation period is. Some accounts say 4 to 7 weeks and the consensus is usually 30 to 50 days before symptoms arise [2]. There is evidence to suggest that those with IM are contagious in the first six weeks, though EBV can be transmitted at any point in infection. That is only accurate for IM, EBV can lie latent for years and under certain conditions can cause tumors or other cancers.


Malaria and Burkitt's Lymphoma Belts From: National Cancer Institute [4]

The epidemiology of EBV is difficult to study as it is so prevalent in the human population all over the world. Certain cancers caused by EBV are seen in exclusive parts of the world, however. Burkitt's Lymphoma, for example, is almost always seen in Africa with a direct correlation to malaria outbreaks [20]. In fact, the epidemiological factors of Burkitt's Lymphoma is what led Michael Epstein to search for a viral component of the disease [21]. The same thought process was used for nasopharyngeal carcinoma (NPC), as the epidemiology factors were virtually the same as Burkitt's Lymphoma. Studying different serotypes of the virus can correlate with small outbreaks of IM or an unusual amount of tumors in an area.


The frequency of EBV transmission is between 95-100%. It is extremely infectious, as it only takes contact with saliva to cause latent or lytic infection. Most primary infections occur in the first 5 years of life, and the frequency of transmission after is the same, but the chance to develop dangerous symptoms is higher. If EBV is contracted in adolescence, it is more likely to cause IM or cancers if in certain parts of the world. It is almost impossible to avoid the virus; the frequency of transmission is too high. Obviously geographic location plays a large role in causing these EBV-stimulated cancers. Africa and Asia have increased risks of BL and NPC respectively as each deal with various cofactors aside from EBV.

Various factors in EBV infection have been studied, though are often inconclusive. Females often mount a larger immune response in general, so it's reasonable that antibody titres would be higher than those in males. In households and communities of low socioeconomic status, there is an increased risk of infection at an earlier age, 60%, compared to 20% in high socioeconomic backgrounds. In some of these cultures the mothers chew the food up before feeding their children, and this is a large reason infection is so high. Genetics and race have yet to be seen as factors for an increased risk of infection. IM infections are exclusively seen in high school and college (74%) students as EBV infections at an early age usually only result in flu-like symptoms if any [10].

Virulence Factors

The main virulence factor of EBV is its ability to remain latent for years. It replicates and survives in host B cells and evades the immune response. Even if a response is mounted, the virus is never truly eliminated because it injects its DNA into the host cell nucleus. EBV also uses glycoproteins, like many viruses, for cell entry. Glycoproteins gB, gH, and gL all form a dimer used to enter epithelial cells and release their nucleocapsid [22]. When entering B cells, other glycoproteins are used to bind to cell receptor CD21 and MHC II to fuse the viral envelope with the cell membrane. When entering epithelial cells, the lytic cycle is usually triggered, whereas with B cells latent proteins are secreted. EBV activates, proliferates, and immortalizes latent B cells [23]. Diseases arise from the immune system not being able to control the replication of latently infected cells.

Clinical Features

Clinical features can be hard to discern as most immunocompetent patients are asymptomatic [3]. In immunocompetent individuals, symptoms will mainly correspond to infectious mononucleosis (IM) in young adults, though these symptoms could also presuppose leukemia or lymphoma. In immunocompromised patients, EBV may exacerbate their autoimmunity; this results in high morbidity and mortality rates. Most symptoms in IM and other diseases caused by EBV are a direct result of cytotoxic T cells attacking the EBV in B cells.


Burkitt's Lymphoma Tumor From: Wikipedia [5]
Swollen Lymph Nodes From: Cancer-Oncology [6]
Nasopharyngeal Carcinoma From: MicrobeWiki [7]

Infectious Mononucleosis

The symptoms of IM can begin quickly and develop rapidly. The main, specific, symptoms to IM are sore throat and neck swelling, though there are non-specific symptoms such as vague discomfort, headaches, chills, and fever [2]. Spleen tenderness and rashes are some of the more commonly serious symptoms to suggest IM. EBV replicates in B cells and epithelial cells and the sore throat is usually caused by lysis of the oropharyngeal epithelial cells. The swollen neck is due to enlarged lymph nodes as the infected B cells replicate to normal cells. IM can be caused by a variety of pathogens, however EBV is the cause of over 90% of reported cases. Teenagers are at the highest risk of IM when exposed to EBV for the first time. Primary exposure of EBV in infants is usually accompanied by flu-like or no symptoms whatsoever. Chronic Fatigue Syndrome was once thought to be associated with EBV, but as of recent research, no correlation has ever been found [4]. IM caused by EBV has been shown to be a risk factor for those with Chronic Fatigue Syndrome, but EBV itself does not cause CFS.

Other Diseases/Cancers

EBV is an aggressor and stimulator of other, more serious and life-threatening, diseases and cancers. There is not always a direct correlation between EBV and these symptoms, but they can be worsened if EBV becomes lytic. Most of these ailments are found in the lymphatic system, as that is where the infected B cells reside.

  • Burkitt's Lymphoma: EBV is found in nearly all endemic patients in Africa. Chronic malaria is thought to reduce resistance to EBV, allowing it to cause tumors, mostly around the jaw and facial bones. This is one of the first cases of viral infections being correlated to cancers [5].
  • Hodgkin's Lymphoma: Being infected with IM increases your chance of contracting this cancer, but a precise correlation cannot be found. Symptoms include enlarged lymph nodes, spleen, and liver, as well as back pain and weight loss. This is a serious cancer that usually possesses a survival rate of 5 years, though treatments are always improving [6].
  • Nasopharyngeal Carcinoma: There are a variety of factors that can be attributed to this cancer, and the main viral component is associated with EBV. As stated previously, this is the most common virus among the human population, so there are many reasons this virus could be found in many cancer patients. EBV may aggravate the cancer, but it has not been proven to be a direct cause. Studies have only shown that patients produce a higher level of antibodies towards EBV, and this can be used as a marker for NPC [7]. Once again, main symptoms include swollen lymph nodes, a soft palate, pain, and hearing loss.
  • Autoimmune Complications:
    • Hairy Leukoplakia-This is a white lesion that cannot be scraped off in the oral cavity. It is directly caused by EBV and is usually seen in HIV or otherwise immunocompromised patients [8].
    • Multiple Sclerosis-Neurological functions are severely compromised, making everyday tasks challenging. It has been found that those infected with EBV during adolescence are more likely to develop MS than those exposed during childhood or not at all. Some hypothesize that MS could be a serious complication of IM, though there are some outlying patients that test negative for EBV. EBV has a mechanism that prevents infected B cells from being killed, and some of these errant cells could make it to the central nervous system, where antibodies could mistake the myelin sheath for EBV. Though much research still needs to be done to determine specific pathways that could link EBV to MS [9].
    • Pretty much any disease that can cause swelling in the lymph nodes could be associated with EBV in some way. Symptoms are relatively similar across these various diseases, and because so much of the population is infected with EBV, correlations are prevalent, but suspicious.


Starry Sky in Burkitt's Lymphoma From: Pathologystudent.com [8]

There are a variety of serological tests that can be used to detect for mononucleosis. A Paul-Bunnell monospot test can be performed to test for heterophil antibodies. Heterophils are associated with neutrophils in humans and the antibodies are present in over 90% of IM patients. However, these antibodies can also arise in Lupus and HIV patients and are also not present in children [10]. The monospot test has high specificity markers but low sensitivity, so unless the infection is caught at just the right point after onset of symptoms, false-negatives and false-postives are very common. If IM infections chronically occur, EBV antibodies can be studied for abnormalities. Elevated white blood cell counts and 10% abnormal lymphocytes are also sufficient to diagnose IM. Epstein-Barr virus antibody tests can test the viral capsid antibodies (VCA) which also successfully diagnoses EBV infections. IgM antibodies to VCA and the absence of IgG are diagnostic for IM [2].

The diagnosis of those aforementioned cancers are usually telling by swollen necks/tumors. Biopsy of lymph nodes and tumors can give a correct diagnosis of Burkitt's Lymphoma or NPC. Serum antibody titres of EBV antigen can give a diagnosis and progress of NPC. When dealing with immunocompromised individuals, finding any EBV DNA in cerebrospinal fluid is a known diagnostic marker. A starry sky pattern is commonly associated with Burkitt's Lymphoma. The name comes from the dark background produced by the tumor cells and the macrophages surrounding are turned white as they turnover the damaged cells. These macrophages are called scattered tingible body macrophages and cause the cytoplasm to fall away in the tumor cells, leaving the white "stars" [11]. When a section of the lymph is seen under a microscope and a "starry sky" is observed, a diagnosis of Burkitt's Lymphoma is certain.

Serology tests are always used to determine the specific diseases and EBV antigens are usually present in the aforementioned cancers/IM. The route of diagnosis varies for immunocompromised or immunocompetent patients, as a correct diagnosis is more pertinent in HIV and otherwise compromised patients. Just because a patient tests positive for EBV antibodies does not necessarily mean they are at risk or carry these diseases.


Any treatments used against infections/cancers linked to EBV can only be used to alleviate symptoms and there is no definitive cure. The overall goal in anti-EBV trials is to inhibit the replication cycle and growth of the virus in cells. Various trials have been performed, however, no significant advances have been made in truly getting rid of the virus. [12]. Once infected with EBV it will remain in your cells for the rest of your life, but IM usually resolves on its own within 4 to 6 weeks. Symptoms can last for 1-4 weeks, but it can often be months before normal activities may be resumed. The best treatment for IM is bed rest and minimal activity until symptoms are resolved. If the swelling is severe enough, corticosteroids can often be used to reduce inflammation, and NSAIDS can be taken for pain and fever. Anti-viral treatments have not been proven to alleviate symptoms or shorten the duration of illness [13].

For Burkitt's Lymphoma, one dose of chemotherapy is usually sufficient for regression of tumor cells, but a full course of treatment should be given to lessen the chance of a severe relapse [2]. Nasopharyngeal carcinoma is usually treated with radiotherapy, though chemotherapy and surgery are also options, though not recommended. The survival rate is significantly less compared to Burkitt's Lymphoma due to the area affected. For NPC and MS, immunotherapy trials are still being conducted. The purpose of immunotherapy is to trigger the immune system to work better against the infection or to introduce crucial proteins that aren't found in immunocompromised patients. These various immunotherapy trials are usually last-ditch efforts to eradicate a tumor or cancer and are not proven to fully eradicate EBV [14].


With the advent of an HPV vaccine, hopes for an EBV vaccine are high, but so far has just led to disappointment. With over 90% of the world's population infected with EBV, it is essentially impossible to prevent infection. Theoretically avoiding an infected person's saliva would prevent the infection, but it's usually too common during adolescence to avoid. An effort to develop a vaccine targeting the glycoprotein responsible for adherence showed a decreased incidence in IM but could not prevent EBV latency. This is troubling as it seems unlikely to ever prevent the dangerous cancers caused by EBV [15]. Developing a vaccine is also challenging because it is difficult to work with the virus and find suitable animal models to mimic a human host immune response. The virus will only replicate in human cells, making research incredibly difficult.

Though the virus is linked with these diseases, there are other factors to consider such as geographic location, other pathogens, genetics, and lifestyle. For instance, malaria works hand in hand with EBV to cause Burkitt's Lymphoma, and it has yet to be seen which is a stronger factor. Because the role of EBV in these cancers has not been fully elucidated, preventative measures are difficult to create. The best mode of prevention in immunocompromised patients and those that struggle with recurring illnesses is to watch the EBV load and stimulate the immune system to prevent further complications [16].

Host Immune Response

The immune response is what causes massive infections and tumors. Swollen lymph nodes are a main symptom in each type of cancer/IM. This is caused by the cytotoxic T cells and NK cells trying to kill the B cells infected with EBV. Unfortunately for the host, no matter how many B cells get killed, there are still more that are infected. As soon as you test positive for EBV, you have it for life. CD4 helper cells also try to trigger apoptosis in infected B cells. In otherwise healthy patients, EBV will result in no severe infection or disease. Immunocompromised patients are at greater risk for lymphomas and other cancerous tumors. There are no long-term symptoms associated with EBV, unless faced with chronic IM. The body will never get rid of the virus from every cell, though it has been shown that in blood marrow transplants involving an EBV free patient, results in the other patient being EBV free as well.


1. Cancer Virus: The Story of Epstein-Barr Virus

2. Principles and Practice of Clinical Virology Chapter 2D

3. Routine Epstein-Barr Virus Diagnostics

4. CDC Chronic Fatigue Syndrome

5. Burkitt's Lymphoma, Malaria, and Epstein-Barr

6. Hodgkin's Disease and Epstein-Barr Virus

7. Relationship Between Epstein-Barr and Nasopharyngeal Carcinoma

8. Managing HIV/AIDS

9. Epstein-Barr and Multiple Sclerosis

10. Epidemiology of EBV and Malignant Diseases

11. Differential Diagnosis of Burkitt's Lymphoma

12. Epstein-Barr Current Treatment Options

13. Epstein-Barr: A Complete Guide

14. Immunotherapy for Epstein-Barr Virus Associated Cancers

15. Epstein Barr Virus Turns 50

16. Prevention and Treatment for Epstein Barr Virus

17. Latency Strategies of Herpesviruses: Epstein Barr

18. Mother to Child Epstein Barr Transmission

19. Dynamics of Virus Shedding in Saliva

20. Co-Infection of Malaria and Epstein-Barr

21. Epstein-Barr and Pathogenesis of Burkitt's Lymphoma

22. Crystal Structure of Epstein-Barr Virus

23. DNA Viruses-Herpesviruses II

Created by Jordan Abney, student of Tyrell Conway at the University of Oklahoma.