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Journal of Clinical Microbiology, February 1998, p. 443-448, Vol. 36, No. 2
Danish Veterinary Laboratory, DK-1790
Copenhagen V, Denmark
Received 24 June 1997/Accepted 12 November 1997
The gene (omlA) coding for an outer membrane protein of
Actinobacillus pleuropneumoniae serotypes 1 and 5 has been
described earlier and has formed the basis for development of a
specific PCR assay. The corresponding regions of all 12 A. pleuropneumoniae reference strains of biovar 1 were sequenced.
Alignment of the sequences revealed conserved terminal and variable
middle regions, which divided the reference strains into four distinct
groups. Primers were selected from the conserved 5' and 3' termini of the gene. A 950-bp amplicon was obtained from each of 102 tested field
isolates of A. pleuropneumoniae obtained from lungs. Their identity was verified by sequencing approximately 500 bp of the amplification product from 50 of the A. pleuropneumoniae
isolates, which all showed the expected DNA sequence characteristic of
the serotype. To test the specificity of the reaction, 23 other
bacterial species related to A. pleuropneumoniae or
isolated from pigs were assayed. They were all found negative in the
PCR, as were tonsil cultures from 50 pigs of an A. pleuropneumoniae-negative herd. The sensitivity assessed by
agarose gel analysis of the PCR product was 102 CFU/PCR
test tube. The specificity and sensitivity of this PCR compared to
those of culture suggest the use of this PCR for routine identification
of A. pleuropneumoniae.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Improved Diagnostic PCR Assay for Actinobacillus
pleuropneumoniae Based on the Nucleotide Sequence of an Outer
Membrane Lipoprotein
*
Corresponding author. Mailing address: Danish
Veterinary Laboratory, Bülowsvej 27, DK-1790 Copenhagen V,
Denmark. Phone: 45 35300100. Fax: 45 35300120. E-mail:
tg{at}svs.dk.
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