A dot-immunobinding assay for the serodiagnosis of Pasteurella multocida infection in laboratory rabbits
A dot-immunobinding assay was developed to detect serum IgG specific for lipopolysaccharide of rabbit isolates of P. multocida. The assay detected serum IgG as early as 1 week after experimental subclinical nasal infection, whereas 8 weeks were required to detect antibody by a gel diffusion precipit...
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Published in | Laboratory animal science (Chicago) Vol. 37; no. 5; p. 615 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
01.10.1987
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Abstract | A dot-immunobinding assay was developed to detect serum IgG specific for lipopolysaccharide of rabbit isolates of P. multocida. The assay detected serum IgG as early as 1 week after experimental subclinical nasal infection, whereas 8 weeks were required to detect antibody by a gel diffusion precipitin test. The assay was more reliable than nasal cultures, in that up to 46% of 16 weekly nasal washings of some infected rabbits failed to yield P. multocida. The bacterial antigen (proteinase k digested cell lysate) used in the assay reacted with IgG that did not cross-react with lipopolysaccharide antigens of B. bronchiseptica, P. pneumotropica or P. hemolytica. The assay is sensitive and specific, easily performed, cost effective, requires no special laboratory instruments and provides a permanent easily stored record. |
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AbstractList | A dot-immunobinding assay was developed to detect serum IgG specific for lipopolysaccharide of rabbit isolates of P. multocida. The assay detected serum IgG as early as 1 week after experimental subclinical nasal infection, whereas 8 weeks were required to detect antibody by a gel diffusion precipitin test. The assay was more reliable than nasal cultures, in that up to 46% of 16 weekly nasal washings of some infected rabbits failed to yield P. multocida. The bacterial antigen (proteinase k digested cell lysate) used in the assay reacted with IgG that did not cross-react with lipopolysaccharide antigens of B. bronchiseptica, P. pneumotropica or P. hemolytica. The assay is sensitive and specific, easily performed, cost effective, requires no special laboratory instruments and provides a permanent easily stored record. |
Author | Manning, P J Brackee, G Naasz, M A DeLong, D Leary, S L |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/3695396$$D View this record in MEDLINE/PubMed |
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Snippet | A dot-immunobinding assay was developed to detect serum IgG specific for lipopolysaccharide of rabbit isolates of P. multocida. The assay detected serum IgG as... |
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SubjectTerms | Animals Animals, Laboratory Cross Reactions Immunoassay - methods Immunoglobulin G - analysis Lipopolysaccharides - immunology Pasteurella Infections - diagnosis Pasteurella Infections - immunology Pasteurella Infections - veterinary Rabbits Serologic Tests |
Title | A dot-immunobinding assay for the serodiagnosis of Pasteurella multocida infection in laboratory rabbits |
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