Literature DB >> 9774590

Two-color hybridization assay for simultaneous detection of Bordetella bronchiseptica and toxigenic Pasteurella multocida from swine.

K B Register1, R M Lee, C Thomson.   

Abstract

Bordetella bronchiseptica and toxigenic Pasteurella multocida are the etiologic agents of swine atrophic rhinitis. Methods currently used for their identification are time-consuming and suffer from a lack of sensitivity. We describe a colony lift-hybridization assay for detection of B. bronchiseptica and toxigenic P. multocida that can be performed with a single colony lift derived from a primary isolation plate without the need for pure subcultures of suspect bacteria. Membranes are hybridized simultaneously to probes derived from the B. bronchiseptica alcA gene and the P. multocida toxA gene. A multicolor development procedure permits sequential detection of bound probes. The assay was tested with 84 primary isolation plates generated from nasal swabs from swine with clinical signs of atrophic rhinitis. Comparison of the results from the colony lift-hybridization assay with those from conventional testing, based on a combination of colony morphology, biochemical reactions, mouse lethality, and enzyme-linked immunosorbent assay, indicated that the colony lift assay has superior sensitivity and comparable specificity. This technique has wide application for diagnostic and experimental studies.

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Year:  1998        PMID: 9774590      PMCID: PMC105326          DOI: 10.1128/JCM.36.11.3342-3346.1998

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   11.677


  15 in total

Review 1.  Pasteurella multocida toxin. The characterisation of the toxin and its significance in the diagnosis and prevention of progressive atrophic rhinitis in pigs.

Authors:  N T Foged
Journal:  APMIS Suppl       Date:  1992

2.  Biotinylated proteins of Pasteurella multocida and Pasteurella haemolytica cause false-positive reactions with biotinylated probes in colony lift-hybridization assays.

Authors:  K B Register
Journal:  Anal Biochem       Date:  1998-03-15       Impact factor: 3.365

3.  Tonsil and turbinate colonization by toxigenic and nontoxigenic strains of Pasteurella multocida in conventionally raised swine.

Authors:  M R Ackermann; M C DeBey; K B Register; D J Larson; J M Kinyon
Journal:  J Vet Diagn Invest       Date:  1994-07       Impact factor: 1.279

4.  Fowl cholera: gel diffusion precipitin test for serotyping Pasteruella multocida from avian species.

Authors:  K L Heddleston; J E Gallagher; P A Rebers
Journal:  Avian Dis       Date:  1972 Jul-Sep       Impact factor: 1.577

5.  Specificity of DNA probes for the detection of toxigenic Pasteurella multocida subsp. multocida strains.

Authors:  A M Kamps; W E Buys; E M Kamp; M A Smits
Journal:  J Clin Microbiol       Date:  1990-08       Impact factor: 5.948

6.  Detection and enumeration of toxin-producing Pasteurella multocida with a colony-blot assay.

Authors:  T Magyar; R B Rimler
Journal:  J Clin Microbiol       Date:  1991-07       Impact factor: 5.948

7.  Cloning and expression of the dermonecrotic toxin gene of Pasteurella multocida ssp. multocida in Escherichia coli.

Authors:  A M Kamps; E M Kamp; M A Smits
Journal:  FEMS Microbiol Lett       Date:  1990-01-15       Impact factor: 2.742

8.  Characterization of toxin from different strains of Pasteurella multocida serotype A and D.

Authors:  P L Frandsen; N T Foged; S K Petersen; A Bording
Journal:  Zentralbl Veterinarmed B       Date:  1991-07

9.  Cloning and expression of the Pasteurella multocida toxin gene, toxA, in Escherichia coli.

Authors:  S K Petersen; N T Foged
Journal:  Infect Immun       Date:  1989-12       Impact factor: 3.441

10.  Differentiation of toxigenic from nontoxigenic isolates of Pasteurella multocida by PCR.

Authors:  S Nagai; S Someno; T Yagihashi
Journal:  J Clin Microbiol       Date:  1994-04       Impact factor: 11.677

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