East Coast Fever Caused by Theileria parva Is Characterized by Macrophage Activation Associated with Vasculitis and Respiratory Failure

PLoS One. 2016 May 19;11(5):e0156004. doi: 10.1371/journal.pone.0156004. eCollection 2016.

Abstract

Respiratory failure and death in East Coast Fever (ECF), a clinical syndrome of African cattle caused by the apicomplexan parasite Theileria parva, has historically been attributed to pulmonary infiltration by infected lymphocytes. However, immunohistochemical staining of tissue from T. parva infected cattle revealed large numbers of CD3- and CD20-negative intralesional mononuclear cells. Due to this finding, we hypothesized that macrophages play an important role in Theileria parva disease pathogenesis. Data presented here demonstrates that terminal ECF in both Holstein and Boran cattle is largely due to multisystemic histiocytic responses and resultant tissue damage. Furthermore, the combination of these histologic changes with the clinical findings, including lymphadenopathy, prolonged pyrexia, multi-lineage leukopenia, and thrombocytopenia is consistent with macrophage activation syndrome. All animals that succumbed to infection exhibited lymphohistiocytic vasculitis of small to medium caliber blood and lymphatic vessels. In pulmonary, lymphoid, splenic and hepatic tissues from Holstein cattle, the majority of intralesional macrophages were positive for CD163, and often expressed large amounts of IL-17. These data define a terminal ECF pathogenesis in which parasite-driven lymphoproliferation leads to secondary systemic macrophage activation syndrome, mononuclear vasculitis, pulmonary edema, respiratory failure and death. The accompanying macrophage phenotype defined by CD163 and IL-17 is presented in the context of this pathogenesis.

Publication types

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

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / genetics
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Blood Vessels / pathology
  • Cattle
  • Fever / etiology
  • Fever / veterinary*
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism
  • Lymphatic Vessels / pathology
  • Macrophage Activation*
  • Macrophages / immunology
  • Monocytes / immunology
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Theileriasis / complications
  • Theileriasis / immunology
  • Theileriasis / pathology*
  • Vasculitis / etiology
  • Vasculitis / veterinary

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD163 antigen
  • Interleukin-17
  • Receptors, Cell Surface

Grants and funding

This work was supported by USAID AID-BFS-P-13-00002 and the Bill and Melinda Gates Foundation grant OPP1078791. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.