Specific oligonucleotide primers for the identification ofPseudomonas syringaepv.pisiyield one of two possible DNA fragments by PCR amplification: evidence for phylogenetic divergence

Arnold, D. L., Athey-Pollard, A., Gibbon, M., Taylor, J. D. and Vivian, A. (1996) Specific oligonucleotide primers for the identification ofPseudomonas syringaepv.pisiyield one of two possible DNA fragments by PCR amplification: evidence for phylogenetic divergence. Physiological and Molecular Plant Pathology, 49 (4). pp. 233-245. ISSN 0885-5765

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Publisher's URL: http://dx.doi.org/10.1006/pmpp.1996.0051

Abstract

Two unique DNA fragments, generated by RAPD-PCR, were used as probes against dot-blots of representative isolates of the seven races ofPseudomonas syringaepv.pisi. DNA from each isolate hybridized only to one of the two probes. Fragments identified from isolates 1691 (race 7) and 203 (race 2), were cloned into pUC18 and sequenced. The resulting sequences were used to design two pairs of oligonucleotide primers which when used in PCR reactions withP. syringaepv.pisicells gave specific amplification products (either a 272 bp or a 132 bp fragment) corresponding to the original cloned fragments. When all four primers were used in combination with specific DNA amplification reactions in 51 isolates ofP. syringaepv.pisithey produced one of the two PCR bands. No bands were detected in a range of closely relatedP. syringaepathovars following PCR amplification. These results suggest thatP. syringaepv.pisican be unambiguously identified using specific oligonucleotide primers and that isolates can be classified into two phylogenetic groups, I and II.

Item Type:Article
Faculty/Department:Faculty of Health and Applied Sciences > Department of Biological, Biomedical and Analytical Sciences
ID Code:7059
Deposited By: H. Hammond
Deposited On:29 Jul 2010 07:45
Last Modified:12 Aug 2013 07:59

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