Use of recombinant BP26 protein in serological diagnosis of Brucella melitensis infection in sheep

Clinical and Diagnostic Laboratory Immunology

Volumn 8, Issue 4, 2001, Pages 772-775

  Cloeckaert, A ^a   Baucheron, S ^a   Vizcaino, N ^a   Zygmunt, M S ^a  

^a Ctr Rech Tours Inst Natl R   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL POLYSACCHARIDE; BACTERIAL PROTEIN; RECOMBINANT PROTEIN;

ANTIBODY RESPONSE; ARTICLE; BACTERIOLOGY; BRUCELLA MELITENSIS; BRUCELLOSIS; DELAYED HYPERSENSITIVITY; ENZYME LINKED IMMUNOSORBENT ASSAY; ESCHERICHIA COLI; GENE DELETION; NONHUMAN; PRIORITY JOURNAL; SERODIAGNOSIS; SHEEP;

ANIMALS; ANTIGENS, BACTERIAL; BACTERIAL PROTEINS; BRUCELLA MELITENSIS; BRUCELLOSIS; ENZYME-LINKED IMMUNOSORBENT ASSAY; MEMBRANE PROTEINS; RECOMBINANT FUSION PROTEINS; SENSITIVITY AND SPECIFICITY; SHEEP; SHEEP DISEASES;

EID: 0034974160     PISSN: 1071412X     EISSN: None     Source Type: Journal    
DOI: 10.1128/CDLI.8.4.772-775.2001     Document Type: Article

References (15)

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4. Cloning, nucleotide sequence, and expression of the Brucella melitensis bp26 gene coding for a protein immunogenic in infected sheep
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11. Enzyme-linked immunosorbent assay with partially purified cytosoluble 28-kilodalton protein for serological differentiation between Brucella melitensis-infected and B. melitensis Rev. l-vaccinated sheep
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14. Antibody response to Brucella melitensis outer membrane antigens in naturally infected and Rev1 vaccinated sheep
15. Purified native hapten of Brucella abortus B19 and B. melitensis 16M reveal the lipopolysaccharide origin of the antigens