Premium
Development of a 23S rRNA‐based PCR assay for the identification of Pasteurella multocida
Author(s) -
Miflin J.K.,
Blackall P.J.
Publication year - 2001
Publication title -
letters in applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.698
H-Index - 110
eISSN - 1472-765X
pISSN - 0266-8254
DOI - 10.1046/j.1472-765x.2001.00985.x
Subject(s) - pasteurella multocida , library science , agency (philosophy) , identification (biology) , veterinary medicine , biology , medicine , sociology , social science , ecology , computer science , genetics , bacteria
Aims: The aim of this work was to develop a rapid diagnostic test for Pasteurella multocida . Methods and Results: A polymerase chain reaction (PCR) assay using primers derived from the 23S rRNA gene sequence of Past. multocida was developed. The PCR assay correctly identified all 144 isolates of Past. multocida tested, including type strains of the three subspecies as well as the reference strains for the Heddleston and Carter typing schemes. Of 20 closely related bacteria from the family Pasteurellaceae tested, only the type strains of Past. canis biovar 2 and Past. avium biovar 2 were positive. These two bacteria, formerly known as Bisgaard Taxon 13, are the closest phylogenetic relatives of Past. multocida based on 16S ribosomal rRNA. All phylogenetically unrelated avian and porcine organisms tested were negative. Conclusions: This PCR enables rapid identification of Past. multocida colonies from avian or porcine origin. Significance and Impact of the Study: Veterinary diagnostic laboratories can use this PCR to rapidly and accurately diagnose fowl cholera and porcine pasteurellosis.