Animal Models in Q Fever: Pathological Responses of Inbred Mice to Phase 1 Coxiella burnetti

Abstract

The susceptibility of inbred strains of mice to infection by phase 1 Coxiella burnetii, the aetiology agent of Q fever, was investigated by evaluating morbidity, mortality, antibody production and in vitro proliferative responses of splenic lymphocytes. Among the 47 strains of mice tested for morbidity and mortality to C. burnetii infection, 33 were resistant, 10 were of intermediate sensitivity, and four were sensitive. A/J mice exhibited the highest mortality, and surviving mice of this strain yielded high concentrations of viable rickettsiae from essentially all organs for more than 3 weeks after inoculation. However, A/J mice developed a protective immune response after vaccination with inactivated C. burnetii cells. Induction of gross pathological responses and antibody production were similar in sensitive mice (strain A/J) and resistant mice (strain C57BL/6J). The LD50 of phase 1 C. burnetii for A/J mice was about 1000-fold lower than that for the more resistant C57BL/6J mice. Mice of both strains developed antibody tires against phase 1 cells, phase 2 cells, and phase 1 lipopolysaccharide after the injection of one or more viable phase 1 organisms of C. burnetii; five or more rickettsiae caused splenomegaly that was almost proportional to the infecting dose. Suppression of in vitro proliferative responses of splenic lymphocytes to concanavalin A, a T-cell mitogen, was apparent after infection of sensitive A/J mice with as few as one to five phase 1 micro-organisms. However, suppression of proliferation of splenic lymphocytes from resistant C57BL/6J mice required 10 to the 7th power phase 1 C. burnetii.

Document Details

Document Type
Technical Report
Publication Date
Jan 01, 1987
Accession Number
ADA187295

Entities

People

  • Edward H. Stephenson
  • George H. Scott
  • Jim C. Williams

Organizations

  • United States Army Medical Research Institute of Infectious Diseases

Tags

DTIC Thesaurus Topics

  • Antibodies
  • Cells
  • Infection
  • Lymphocytes
  • Morbidity
  • Production
  • Q Fever
  • Wound Infections

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech