Clinical Veterinary Microbiology

Random Amplified Polymorphic DNA and Amplified Fragment Length Polymorphism Analyses of Pasteurella multocida Isolates from Fatal Fowl Cholera Infections

Brad S. Huber, Darin V. Allred, John C. Carmen, David D. Frame, David G. Whiting, Jason R. Cryan, Terry R. Olson, Paul J. Jackson, Karen Hill, Miriam T. Laker, Richard A. Robison
DOI: 10.1128/JCM.40.6.2163-2168.2002

Article Figures & Data

Figures

  • FIG. 1.
    FIG. 1.

    Contour map of Sanpete County, Utah, showing the geographic distributions of isolates color coded by serotype. See Fig. 3 for serotype key.

  • FIG. 2.
    FIG. 2.

    Portions of three electropherograms generated from AFLP analysis of three P. multocida isolates. The M-9 vaccine strain and isolate T29 are genetically similar. Isolate T25 is genetically dissimilar to the M-9 vaccine strain.

  • FIG. 3.
    FIG. 3.

    Cluster analysis tree of the concatenated AFLP analysis data generated by the neighbor-joining method. Isolates from vaccinated turkeys are identified by a V prefix, while unvaccinated turkeys are identified by a T prefix. Isolates are color coded according to serotype (see key).

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KEYWORDS

Pasteurella Infections
Pasteurella multocida
Polymorphism, Restriction Fragment Length
Poultry Diseases
Random Amplified Polymorphic DNA Technique

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