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THE SEROLOGICAL DIAGNOSIS OF RELAPSING FEVER
1Department of Bacteriology, New York University College of Medicine, New York.
Abstract:
1. Spirochetes of relapsing fever have been separated from the blood of heavily infected mice and rats by hemolysing with saponin, followed by repeated washing of the spirochetal suspension with physiological saline. 2. Spirochetes obtained in this manner appear to have broad antigenic specificity. Antigens of this type fixed complement in the presence of serum obtained from man or animals infected with one or other of the recognized strains or "species" of relapsing fever spirochetes. Macroscopic agglutination of the antigens likewise was observed with sera from the same sources. 3. Positive serological reactions were not observed with convalescent sera obtained following infection with other diseases, for example, typhus fever, malaria, Rocky Mountain spotted fever, Weil's disease, syphilis, and typhoid fever. Hyperimmune sera prepared against other pathogens also failed to react with the relapsing fever antigens. 4. No apparent change in the antigen occurred following storage in the ice box for as long as 4 months. 5. The results indicate that treatment of the spirochetes of relapsing fever with saponin yields a relatively stable antigenic preparation which may prove useful in the serological diagnosis of this disease.
Insights
Researchers developed a stable relapsing fever spirochete antigen using saponin treatment. This antigen shows broad specificity and potential for accurate serological diagnosis of relapsing fever infections.
Area of Science:
- Microbiology
- Immunology
- Infectious Diseases
Background:
- Relapsing fever is caused by spirochetes, posing diagnostic challenges.
- Effective serological diagnostic tools are crucial for disease management.
Purpose of the Study:
- To develop a stable antigenic preparation from relapsing fever spirochetes.
- To evaluate the antigenic specificity and diagnostic utility of the preparation.
Main Methods:
- Spirochetes were isolated from infected animal blood using saponin hemolysis and saline washing.
- Antigenic properties were assessed through complement fixation and macroscopic agglutination tests.
- Specificity was confirmed using sera from various infectious diseases and hyperimmune sera.
Main Results:
- Saponin-treated spirochetes yielded a stable antigen, unchanged after 4 months of storage.
- The antigen demonstrated broad specificity, reacting with sera from relapsing fever patients and infected animals.
- No cross-reactivity was observed with sera from other diseases or hyperimmune sera against different pathogens.
Conclusions:
- Saponin treatment provides a robust method for preparing relapsing fever spirochete antigens.
- The resulting antigen is suitable for serological diagnostic applications.
- This preparation holds promise for improving the diagnosis of relapsing fever.
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