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United States Department of Agriculture

Agricultural Research Service

Title: Analytical Verification of a Multiplex Pcr for Identification of Bordetella Bronchiseptica and Pasteurella Multocida from Swine

item Register, Karen
item Dejong, Keith - IOWA STATE UNIVERSITY

Submitted to: American Society for Microbiology
Publication Type: Abstract Only
Publication Acceptance Date: February 17, 2006
Publication Date: May 21, 2006
Citation: Register, K.B., Dejong, K.D. 2006. Analytical Verification of a Multiplex PCR for Identification of Bordetella bronchiseptica and Pasteurella multocida from Swine [abstract]. American Society for Microbiology Meeting, May 21-25,2006, Orlando, Flordia. Z042:643.

Technical Abstract: Bordetella bronchiseptica and Pasteurella multocida are etiologic agents of progressive atrophic rhinitis (PAR) and bronchopneumonia in swine. Only dermonecrotic toxin-producing strains of P. multocida play a role in atrophic rhinitis while both toxigenic and nontoxigenic strains have been associated with pneumonia. Monitoring and investigation of outbreaks involving these bacteria require sensitive and accurate identification and reliable determination of the toxigenic status of P. multocida isolates. In the present study we report the development, optimization, and performance characteristics of a multiplex PCR assay for simultaneous amplification of up to 3 different targets, one common to all P. multocida strains, one found only in toxigenic P. multocida strains, and one common to B. bronchiseptica strains. Based on analysis of 94 P. multocida isolates (31 toxigenic) and 90 B. bronchiseptica isolates assay sensitivity is 100% for all amplicons. Evaluation of 22 isolates of other bacterial genera and species commonly found in the swine respiratory tract demonstrated a specificity of 100% for all gene targets. However, considering data previously reported by others for the P. multocida gene target a specificity of 98.2% is more accurate. The limit of detection for simultaneous amplification of all targets is 1-10pg of DNA per target, corresponding to a few hundred genomes or less. Amplicon mobility in agarose gels and sequence analysis indicate the amplicons are highly stable. The data presented establish this multiplex PCR as a reliable method for identification of B. bronchiseptica and both toxigenic and nontoxigenic P. multocida that may greatly simplify investigations of swine PAR and bronchopneumonia.

Last Modified: 4/19/2015
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