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Applied microbiology1970; 19(6); 894-897; doi: 10.1128/am.19.6.894-897.1970

Preparation of agglutinating antisera and fluorescent-antibody conjugates against Pasteurella tularensis in equines.

Abstract: The serological response in burros and horses to the viable LVS strain of Pasteurella tularensis was studied. High-titered agglutinating antisera and fluorescent-antibody conjugates were obtained in both groups of animals. Maximum titers were obtained in horses 14 to 21 days after the start of vaccination and in burros 21 to 28 days after the start of vaccination. The use of Woodhour's adjuvants or booster inoculations did not result in increased titers.
Publication Date: 1970-06-01 PubMed ID: 4917187PubMed Central: PMC376818DOI: 10.1128/am.19.6.894-897.1970Google Scholar: Lookup
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  • Journal Article

Summary

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The research article explores the immune response in horses and burros to the LVS strain of Pasteurella tularensis bacteria, demonstrating that successful, high-titered antisera and fluorescent-antibody conjugates are generated after specific vaccination periods.

Background

  • Pasteurella tularensis is a type of bacteria known to cause tularemia, a disease that affects several species, including humans and horses, among others.
  • The researchers set out to study the serological response, or the body’s immune response as measured in the blood, to a live virus strain (LVS) of the bacteria in burros and horses. The LVS strain is attenuated and is often used in vaccinations because it stimulates an immune response without causing severe disease.

Methodology

  • Horses and burros were given a vaccination containing the LVS strain of Pasteurella tularensis.
  • The researchers monitored the animals over a period of time, testing their blood for the presence of agglutinating antisera (antibodies that can cause foreign cells to clump together) and fluorescent-antibody conjugates (special antibodies tagged with a fluorescent dye to make them visible under a fluorescent microscope).

Findings

  • Both species developed high levels of agglutinating antisera and fluorescent-antibody conjugates, showing that their immune systems successfully responded to the vaccination.
  • Maximum immune response (highest titers of antibodies) occurred 14-21 days post-vaccination in horses, and 21-28 days post-vaccination in burros.
  • The use of adjuvants which are substances that aid vaccines by boosting immune response, in this case, Woodhour’s adjuvants, or additional booster shots did not result in a stronger or quicker immune response.

Conclusion

  • This study highlights that the immune system in both horses and burros effectively responds to the LVS strain of Pasteurella tularensis.
  • The research provides critical insights into understanding the optimum timeline for the maximum immune response in these animals after vaccination. This can help in designing effective vaccination schedules for disease prevention in equines.
  • The ineffectiveness of the adjuvants or booster inoculations in enhancing the immune response suggests that the immune systems of these animals naturally respond robustly to the vaccine.

Cite This Article

APA
Green JH, Bolin RC, Carver RK, Gross H, Pigott N, Harrell WK. (1970). Preparation of agglutinating antisera and fluorescent-antibody conjugates against Pasteurella tularensis in equines. Appl Microbiol, 19(6), 894-897. https://doi.org/10.1128/am.19.6.894-897.1970

Publication

ISSN: 0003-6919
NlmUniqueID: 7605802
Country: United States
Language: English
Volume: 19
Issue: 6
Pages: 894-897

Researcher Affiliations

Green, J H
    Bolin, R C
      Carver, R K
        Gross, H
          Pigott, N
            Harrell, W K

              MeSH Terms

              • Adjuvants, Immunologic
              • Agglutination Tests
              • Animals
              • Antibodies / analysis
              • Antigens
              • Bacterial Vaccines
              • Blood Protein Electrophoresis
              • Densitometry
              • Fluorescent Antibody Technique
              • Francisella tularensis / immunology
              • Horses
              • Immune Sera / analysis
              • Immunization Schedule
              • Immunochemistry
              • Perissodactyla

              References

              This article includes 6 references
              1. Pittman B, Herbert GA, Cherry WB, Taylor GC. The quantitation of nonspecific staining as a guide for improvement of fluorescent antibody conjugates.. J Immunol 1967 Jun;98(6):1196-203.
                pubmed: 4165503
              2. Nutter JE. Effect of vaccine, route, and schedule on antibody response of rabbits to Pasteurella tularensis.. Appl Microbiol 1969 Mar;17(3):355-9.
                pubmed: 4976322doi: 10.1128/am.17.3.355-359.1969google scholar: lookup
              3. YAGER RH, SPERTZEL RO, JAEGER RF, TIGERTT WD. Domestic fowl--source of high titer P. tularensis serum for the fluorescent antibody technic.. Proc Soc Exp Biol Med 1960 Dec;105:651-4.
                pubmed: 13787043doi: 10.3181/00379727-105-26206google scholar: lookup
              4. EIGELSBACH HT, DOWNS CM. Prophylactic effectiveness of live and killed tularemia vaccines. I. Production of vaccine and evaluation in the white mouse and guinea pig.. J Immunol 1961 Oct;87:415-25.
                pubmed: 13889609
              5. BOWMER EJ. PREPARATION AND ASSAY OF THE INTERNATIONAL STANDARDS FOR CLOSTRIDIUM BOTULINUM TYPES A, B, C, D AND E ANTITOXINS.. Bull World Health Organ 1963;29(6):701-9.
                pubmed: 14107742
              6. WOODHOUR AF, METZGAR DP, STIM TB, TYTELL AA, HILLEMAN MR. NEW METABOLIZABLE IMMUNOLOGIC ADJUVANT FOR HUMAN USE. I. DEVELOPMENT AND ANIMAL IMMUNE RESPONSE.. Proc Soc Exp Biol Med 1964 Jun;116:516-23.
                pubmed: 14193390doi: 10.3181/00379727-116-29295google scholar: lookup

              Citations

              This article has been cited 1 times.
              1. Green JH, Gray SB Jr, Harrell WK. Stability of fluorescent antibody conjugates stored under various conditions. J Clin Microbiol 1976 Jan;3(1):1-4.
                doi: 10.1128/jcm.3.1.1-4.1976pubmed: 3516google scholar: lookup