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An ELISA with Brucella lipopolysaccharide antigen for the diagnosis of B. melitensis infection in sheep and for the evaluation of serological responses following subcutaneous or conjunctival B. melitensis strain Rev 1 vaccination.

Abstract
An indirect enzyme-linked immunosorbent assay (ELISA) with unpurified Brucella melitensis smooth lipopolysaccharide (S-LPS) as antigen was evaluated for the serological diagnosis of B. melitensis infection in sheep in comparison with the Rose Bengal (RB), complement fixation (CF), radial immunodiffusion (RID), microplate agglutination (MA) and rivanol agglutination (RIV) tests. Tests RB and CF detected as positive each of the 77 sera from B. melitensis-infected animals tested, the RID (74), MA (76) and the RIV (72) were less sensitive. However, all tests compared were negative when 77 sera from Brucella-free rams were tested. While subcutaneous Rev 1 vaccination induced high response levels in any of the tests, low level responses were obtained upon conjunctival vaccination, particularly in ELISA and RID tests.
AuthorsM P Jiménez de Bagüés, C M Marín, J M Blasco, I Moriyón, C Gamazo
JournalVeterinary microbiology (Vet Microbiol) Vol. 30 Issue 2-3 Pg. 233-41 (Feb 1992) ISSN: 0378-1135 [Print] Netherlands
PMID1557898 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Bacterial
  • Brucella Vaccine
  • Lipopolysaccharides
  • Rose Bengal
Topics
  • Agglutination Tests
  • Animals
  • Antibodies, Bacterial (blood)
  • Brucella (immunology)
  • Brucella Vaccine (administration & dosage, immunology)
  • Brucellosis (diagnosis, veterinary)
  • Complement Fixation Tests
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Immunodiffusion
  • Injections, Subcutaneous (veterinary)
  • Lipopolysaccharides (immunology)
  • Male
  • Rose Bengal
  • Sheep
  • Sheep Diseases (diagnosis)
  • Vaccination (veterinary)

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