Clinical Microbiology Newsletter
Volume 31, Issue 16 , Pages 119-127, 15 August 2009

Buruli Ulcer (Mycobacterium ulcerans Infection): a Re-emerging Disease

  • Douglas S. Walsh, M.D.

      Affiliations

    • KEMRI/Walter Reed Project, United States Army Medical Research Unit-Kenya, Kisumu, Kenya
    • Corresponding Author InformationMailing address: Dr. Walsh, Walter Reed Project, PO Box 54, Kisumu, 10400, Kenya. TEL: +254-57-20-22942. FAX: +254-57-20-22903
  • ,
  • Françoise Portaels, Ph.D

      Affiliations

    • Department of Environmental and Infectious Disease Sciences, Armed Forces Institute of Pathology, Washington, D.C.
  • ,
  • Wayne M. Meyers, M.D., Ph.D.

      Affiliations

    • Department of Microbiology, Institute of Tropical Medicine, Antwerp, Belgium

Abstract 

Mycobacterium ulcerans infection is an emerging disease that causes indolent, necrotizing skin lesions known as Buruli ulcer (BU). Approximately 10% of patients develop reactive osteitis or osteomyelitis beneath skin lesions or metastatic osteomyelitis from lymphohematogenous spread of M. ulcerans. The most plausible mode of transmission is by skin trauma at sites contaminated by M. ulcerans. Pathogenesis is mediated by a necrotizing, immunosuppressive toxin produced by M. ulcerans called mycolactone. The incidence of BU is highest in children up to 15 years old and is a public health problem in countries of endemicity due to disabling scarring and bone destruction. Today, most BU occurs in West Africa, but the disease has been reported in over 30 countries. Treatment options for BU are antibiotics and surgery. BCG vaccination provides short-term protection against BU and prevents osteomyelitis. HIV seropositivity may increase the risk for BU and render BU osteomyeletis highly aggressive.

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PII: S0196-4399(09)00037-3

doi:10.1016/j.clinmicnews.2009.07.004

Clinical Microbiology Newsletter
Volume 31, Issue 16 , Pages 119-127, 15 August 2009