Bundibugyo virus disease: Transmission dynamics, infectiousness and viral persistence - Report - MDSpire
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Transmission Patterns, Infectiousness, and Viral Longevity in Bundibugyo Virus Disease

  • By

  • Andrea Bongiovanni

  • Erica Binetti

  • Francesca Colavita

  • Ilaria Mussetto

  • Laura Scorzolini

  • Eleonora Lalle

  • Andrea Antinori

  • Enrico Girardi

  • Fabrizio Maggi

  • Emanuele Nicastri

  • Francesco Vairo

  • September 1, 2026

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Clinical Report: Transmission Patterns, Infectiousness, and Viral Longevity in Bundibugyo Virus Disease

Background

Bundibugyo virus disease (BVD) is a severe hemorrhagic fever caused by Bundibugyo virus (BDBV), first identified during Uganda’s 2007–2008 outbreak. Only two outbreaks had been reported before the ongoing 2026 outbreak, leaving limited BDBV-specific evidence on transmission, infectiousness, viral persistence, and survivor management.

Data Highlights

  • Incubation period: The average interval from contact to clinical onset was 6.3 days during the 2007–2008 Uganda outbreak.

  • Burial-related exposure: Direct contact with deceased persons during burial-related activities was associated with increased infection risk (adjusted odds ratio, 3.83; 95% CI, 1.78–8.23).

  • Previous case fatality rates: Approximately 30% to 50%.

  • Ongoing outbreak: As of June 6, 2026, the Democratic Republic of the Congo had reported 515 laboratory-confirmed cases and 91 confirmed deaths, corresponding to a case fatality rate of 17.7%. This estimate required cautious interpretation because the outbreak was ongoing.

Key Findings

  • BDBV transmission occurs primarily through direct contact with the blood or body fluids of symptomatic or deceased individuals.

  • Prolonged transmission chains have occurred in household and healthcare settings.

  • Burial-related contact with deceased individuals represents a significant risk factor for infection.

  • No human cases of presymptomatic BDBV transmission have been documented, although limited evidence prevents this possibility from being definitively excluded.

  • Healthcare settings carry substantial transmission risk when adequate personal protective equipment and infection-control measures are not used.

Clinical Implications

Rigorous infection prevention and control measures, appropriate personal protective equipment, safe burial practices, symptom-based surveillance, contact monitoring, and prompt isolation of symptomatic individuals are central to outbreak control. Survivor guidance remains largely extrapolated from evidence involving other orthoebolaviruses because BDBV-specific evidence on viral persistence and post-recovery transmission is unavailable.

Conclusion

The ongoing outbreak underscores the need for prospective epidemiological, clinical, and laboratory investigations, including longitudinal survivor follow-up, to better characterize BDBV transmission, viral persistence, and the determinants of recrudescence and to strengthen species-specific public health recommendations.

Related Resources & Content

  1. Wamala JF, Lukwago L, Malimbo M, et al. Ebola hemorrhagic fever associated with novel virus strain, Uganda, 2007–2008. Emerg Infect Dis. 2010;16(7):1087–1092.

  2. MacNeil A, Farnon EC, Morgan OW, et al. Filovirus outbreak detection and surveillance: Lessons from Bundibugyo. J Infect Dis. 2011;204(suppl 3):S761–S767.

  3. Kratz T, Roddy P, Tshomba Oloma A, et al. Ebola virus disease outbreak in Isiro, Democratic Republic of the Congo, 2012: Signs and symptoms, management and outcomes. PLoS One. 2015;10(6):e0129333.

  4. Lewis CE, Nishiura H, Furuyama W, et al. Experimental infection of Bundibugyo virus in domestic swine leads to viral shedding with evidence of intraspecies transmission. Transbound Emerg Dis. 2024;2024:5350769.

  5. Clark DV, Kibuuka H, Millard M, et al. Long-term sequelae after Ebola virus disease in Bundibugyo, Uganda: A retrospective cohort study. Lancet Infect Dis. 2015;15(8):905–912.

  6. Vetter P, Kaiser L, Schibler M, Ciglenecki I, Bausch DG. Ebola virus shedding and transmission: Review of current evidence. J Infect Dis. 2016;214(suppl 3):S177–S184.

  7. World Health Organization. Infection prevention and control for Ebola disease and Marburg disease. World Health Organization; 2026.

  8. World Health Organization. Clinical care for survivors of Ebola virus disease: Interim guidance. World Health Organization; 2016.

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