Animal model of fatal human monocytotropic ehrlichiosis

Am J Pathol. 2001 Feb;158(2):757-69. doi: 10.1016/S0002-9440(10)64018-7.

Abstract

Human monocytotropic ehrlichiosis caused by Ehrlichia chaffeensis is a life-threatening, tick-borne, emerging infectious disease for which no satisfactory animal model has been developed. Strain HF565, an ehrlichial organism closely related to E. chaffeensis isolated from Ixodes ovatus ticks in Japan, causes fatal infection of mice. C57BL/6 mice became ill on day 7 after inoculation and died on day 9. The liver revealed confluent necrosis, ballooning cell injury, apoptosis, poorly formed granulomas, Kupffer cell hyperplasia, erythrophagocytosis, and microvesicular fatty metamorphosis. The other significant histological findings consisted of marked expansion of the marginal zone and infiltration of the red pulp of the spleen by macrophages, interstitial pneumonitis, and increased numbers of immature myeloid cells and areas of necrosis in the bone marrow. Ehrlichiae were detected by immunohistology and electron microscopy in the liver, lungs, and spleen. The main target cells were macrophages, including Kupffer cells, hepatocytes, and endothelial cells. Apoptosis was detected in Kupffer cells, hepatocytes, and macrophages in the lungs and spleen. This tropism for macrophages and the pathological lesions closely resemble those of human monocytotropic ehrlichiosis for which it is a promising model for investigation of immunity and pathogenesis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / metabolism
  • Apoptosis
  • Bone Marrow / microbiology
  • Bone Marrow / pathology
  • Disease Models, Animal
  • Ehrlichia chaffeensis / immunology
  • Ehrlichia* / immunology
  • Ehrlichiosis / metabolism
  • Ehrlichiosis / microbiology
  • Ehrlichiosis / pathology*
  • Humans
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Leukocyte Count
  • Liver / microbiology
  • Liver / pathology
  • Liver / ultrastructure
  • Lung / microbiology
  • Lung / pathology
  • Lung / ultrastructure
  • Mice
  • Mice, Inbred C57BL
  • Platelet Count
  • Spleen / microbiology
  • Spleen / pathology
  • Spleen / ultrastructure
  • Tissue Distribution

Substances

  • Antibodies, Monoclonal