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Cardiovascular involvement in human and experimental leptospirosis: pathologic findings and immunohistochemical

T de Brito1, C F Morais, P H Yasuda

  • 1Faculty of Medicine, Department of Pathology, University of São Paulo, Brazil.

Insights

Leptospirosis causes inflammation in heart tissues, including myocarditis and coronary arteritis, and affects major blood vessels. These findings suggest leptospirosis is a systemic vasculitis impacting the cardiovascular system.

Area of Science:

  • Cardiovascular Pathology
  • Infectious Diseases
  • Medical Microbiology

Background:

  • Leptospirosis is a zoonotic disease with potential systemic manifestations.
  • The cardiovascular impact of leptospirosis, particularly in severe cases, requires further elucidation.

Purpose of the Study:

  • To investigate the cardiac and vascular pathology in human leptospirosis cases.
  • To correlate histopathological findings with the presence of Leptospira interrogans.
  • To examine the effects of experimental Leptospira infection on cardiac tissue.

Main Methods:

  • Human autopsy hearts (n=20) were examined for myocarditis, conduction tissue inflammation, coronary arteritis, and aortitis.
  • Immunohistochemistry was used to detect Leptospira antigen deposits.
  • Experimental model using guinea pigs (n=12) inoculated with L. interrogans serovar icterohaemorrhagiae.

Main Results:

  • Interstitial myocarditis observed in 50% of cases, correlating with conduction tissue inflammation.
  • Acute coronary arteritis found in 70% of cases, significantly associated with myocarditis.
  • Aortitis present in 57.8% of cases; Leptospira antigen deposits identified in coronary arteries and aorta.
  • Experimental infection induced focal myocarditis and antigen deposition in guinea pigs.

Conclusions:

  • Leptospirosis can manifest as a systemic vasculitis affecting the heart and major vessels.
  • Inflammation of the myocardium and vasculature is a significant feature of severe leptospirosis.
  • Bacterial components or toxins likely contribute to endothelial damage and inflammation during the septicaemic phase.

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