Review Article Volume 22 Issue 9 - 2026

Ebola Disease: An Updated Review and the 2026 Bundibugyo Virus Disease Outbreak

Suleiman Al-Obeid1*, and Ruqaiyah J Hussain2

1Consultant of Clinical Microbiology, Paris, France
2Lab Medicine and Blood Bank, Mohammed Bin Khalifa Bin Salman AL Khalifa Specialist, Cardiac Center (MKCC), Kingdom of Bahrain

*Corresponding Author: Suleiman Al-Obeid, Consultant of Clinical Microbiology, Paris, France.
Received: August 03, 2026; Published: August 28, 2026



The 2014-2016 Ebola virus disease epidemic exposed major weaknesses in global preparedness for emerging infectious diseases, revealing critical gaps in outbreak response, coordination, and clinical management. The COVID-19 pandemic subsequently accelerated advances in diagnostics, therapeutics, vaccine development, and public health preparedness, thereby improving the management of high-consequence viral infections. Despite these advances, Orthoebolaviruses continue to cause recurrent outbreaks in Africa, with occasional international spread. Ebola disease (EBOD) is a severe viral haemorrhagic disease caused principally by Ebola virus, Sudan virus, or Bundibugyo virus, with an average case fatality rate of approximately 50%, although rates have ranged from 25% to 90% in previous outbreaks. Early intensive supportive care, including prompt rehydration, correction of electrolyte abnormalities, and symptomatic treatment, remains the cornerstone of management and significantly improves survival. Licensed vaccines and targeted monoclonal antibody therapies are currently available only for Ebola virus disease caused by Ebola virus, whereas effective countermeasures against Sudan virus disease and Bundibugyo virus disease remain under development. Successful outbreak control depends on rapid case detection, laboratory confirmation, infection prevention and control, surveillance and contact tracing, safe and dignified burials, vaccination where appropriate, and sustained community engagement. This review summarizes current evidence on the virology, pathogenesis, transmission, diagnosis, clinical management, prevention, and evolving epidemiology of Ebola disease, with particular emphasis on the ongoing Bundibugyo virus disease outbreak.

Keywords: Ebola Disease; Bundibugyo Virus; Filoviridae; Viral Haemorrhagic Fever; Pathogenesis; Diagnosis; Therapeutics; Vaccination

 

  1. International Committee on Taxonomy of Viruses. “ICTV report on virus classification and taxon nomenclature: Family Filoviridae, genus Orthoebolavirus”. ICTV website (2024).
  2. World Health Organization. “International Classification of Diseases, 11th Revision”. Geneva: WHO (2024).
  3. World Health Organization. “Ebola and Marburg virus disease outbreak toolbox”. Geneva: WHO (2024).
  4. Rougeron V., et al. “Ebola and Marburg haemorrhagic fever”. Journal of Clinical Virology 64 (2015): 111-119.
  5. World Health Organization. “Marburg virus disease: fact sheet”. Geneva: WHO (2024).
  6. World Health Organization. “Ebola disease: fact sheet”. Geneva: WHO updated 24 April 2025 (2025).
  7. World Health Organization. “Therapeutics for Ebola virus disease: living guideline”. Geneva: WHO (2022).
  8. World Health Organization. “Optimized supportive care for Ebola virus disease: clinical management standard operating procedures”. Geneva: WHO (2019).
  9. Grifoni A., et al. “Genetic diversity in Ebola virus: phylogenetic and in silico structural studies of Ebola viral proteins”. Asian Pacific Journal of Tropical Medicine 4 (2016): 337-343.
  10. Sanchez A., et al. “Filoviridae: Marburg and Ebola viruses”. In: Knipe DM, Howley PM, editors. Fields Virology. Philadelphia: Lippincott Williams & Wilkins (2007).
  11. Mehedi M., et al. “A new Ebola virus nonstructural glycoprotein expressed through RNA editing”. Journal of Virology11 (2011): 5406-5414.
  12. Ikegami T., et al. “Genome structure of Ebola virus subtype Reston: differences among Ebola subtypes”. Archives of Virology 10 (2001): 2021-2027.
  13. Dong S., et al. “Insight into the Ebola virus nucleocapsid assembly mechanism: crystal structure of Ebola virus nucleoprotein core domain at 1.8 Å resolution”. Protein Cell5 (2015): 351-362.
  14. Bharat TA., et al. “Structural dissection of Ebola virus and its assembly determinants using cryo-electron tomography”. Proceedings of the National Academy of Sciences of the United States of America11 (2012): 4275-4280.
  15. Chan SY., et al. “Folate receptor-alpha is a cofactor for cellular entry by Marburg and Ebola viruses”. Cell 1 (2001): 117-126.
  16. Côté M., et al. “Small-molecule inhibitors reveal Niemann-Pick C1 is essential for Ebola virus infection”. Nature7364 (2011): 344-348.
  17. Martin B., et al. “Filovirus proteins for antiviral drug discovery: structure-function bases of the replication cycle”. Antiviral Research 141 (2017): 48-61.
  18. Volchkov VE., et al. “Processing of the Ebola virus glycoprotein by the proprotein convertase furin”. Proceedings of the National Academy of Sciences of the United States of America 10 (1998): 5762-5767.
  19. Dolnik O., et al. “Ectodomain shedding of the glycoprotein GP of Ebola virus”. EMBO Journal 10 (2004): 2175-2184.
  20. Schudt G., et al. “Transport of ebolavirus nucleocapsids is dependent on actin polymerization: live-cell imaging analysis of ebolavirus-infected cells”. Journal of Infectious Diseases 2 (2015): S160-S166.
  21. Lu J., et al. “Host IQGAP1 and Ebola virus VP40 interactions facilitate virus-like particle egress”. Journal of Virology 13 (2013): 7777-7780.
  22. Centers for Disease Control and Prevention. “History of Ebola disease outbreaks”. Atlanta: CDC.
  23. Gross L., et al. “Ebola vaccine development: systematic review of preclinical and clinical studies and meta-analysis of determinants of antibody-response variability after vaccination”. International Journal of Infectious Diseases 74 (2018): 83-96.
  24. Jain S and Baranwal M. “Computational analysis in designing T-cell epitope-enriched peptides of Ebola glycoprotein exhibiting strong binding interactions with HLA molecules”. Journal of Theoretical Biology 465 (2019): 34-44.
  25. Ollmann Saphire E. “A vaccine against Ebola virus”. Cell1 (2020): 6.
  26. United States Food and Drug Administration. “Ervebo”. Silver Spring, MD: FDA (2019).
  27. Iversen PL., et al. “Recent successes in therapeutics for Ebola virus disease: no time for complacency”. Lancet Infectious Diseases 9 (2020): e231-e237.
  28. Fausther-Bovendo H and Kobinger G. “Vaccine innovation spurred by the long wait for an Ebola virus vaccine”. Lancet Infectious Diseases 4 (2021): 440-441.
  29. Leroy EM., et al. “Human asymptomatic Ebola infection and strong inflammatory response”. Lancet 9222 (2000): 2210-2215.
  30. World Health Organization. “Ebola haemorrhagic fever in Zaire, 1976: report of an international commission”. Bulletin of the World Health Organization 2 (1978): 271-293.
  31. Rowe AK., et al. “Clinical, virological, and immunological follow-up of convalescent Ebola haemorrhagic fever patients and their household contacts, Kikwit, Democratic Republic of the Congo”. Journal of Infectious Diseases 1 (1999): S28-S35.
  32. Baggi FM., et al. “Management of pregnant women infected with Ebola virus in a treatment centre in Guinea, June 2014”. Eurosurveillance 49 (2014): 20983.
  33. Judson S., et al. “Understanding Ebola virus transmission”. Viruses 2 (2015): 511-521.
  34. World Health Organization. “Infection prevention and control guideline for Ebola and Marburg diseases”. Geneva: WHO (2026).
  35. World Health Organization. “Guidelines for the collection of clinical specimens during field investigation of outbreaks”. Geneva: WHO. WHO/CDS/CSR/EDC/2000.4 (2000).
  36. World Health Organization. “Guidance on regulations for the transport of infectious substances”. Geneva: WHO current edition.
  37. Broadhurst MJ., et al. “Diagnosis of Ebola virus disease: past, present, and future”. Clinical Microbiology Reviews 4 (2016): 773-793.
  38. World Health Organization. “Therapeutics for Ebola virus disease: living guideline”. Geneva: WHO (2022).
  39. World Health Organization. “Ebola disease: fact sheet”. Geneva: WHO updated 24 April 2025 (2025).
  40. World Health Organization Strategic Advisory Group of Experts on Immunization. “SAGE Ebola vaccines working group report”. Geneva: WHO May 2024 (2024).
  41. World Health Organization. “Ebola vaccines and global vaccine stockpile recommendations”. Weekly Epidemiological Record 99 (2024).
  42. European Medicines Agency. “Ebola: authorised vaccines and therapeutics”. Amsterdam: EMA updated May 2026 (2026).
  43. World Health Organization. “Ebola disease caused by Sudan virus—Uganda. Disease Outbreak News”. Geneva: WHO 26 September 2022 (2022).
  44. World Health Organization. “Infection prevention and control guidance for the care of patients with suspected or confirmed filovirus disease in healthcare settings”. Geneva: WHO (2026).
  45. World Health Organization. “Clinical management of patients with viral haemorrhagic fever: a pocket guide for frontline health workers”. Geneva: WHO (2016).
  46. World Health Organization. “Ebola disease: fact sheet”. Geneva: WHO updated 24 April 2025 (2025).
  47. European Centre for Disease Prevention and Control. “Ebola disease outbreak in the Democratic Republic of the Congo and Uganda”. Stockholm: ECDC updated 20 July 2026 (2026).
  48. World Health Organization. “Ebola disease caused by Bundibugyo virus, Democratic Republic of the Congo and Uganda. Disease Outbreak News”. Geneva: WHO 17 July 2026 (2026).

Suleiman Al-Obeid and Ruqaiyah J Hussain. “Ebola Disease: An Updated Review and the 2026 Bundibugyo Virus Disease Out- break”. EC Microbiology 22.9 (2026): 01-08.