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1.
Methods Mol Biol ; 1302: 1-16, 2015.
Article in English | MEDLINE | ID: mdl-25981242

ABSTRACT

Blackleg and soft rot of potato, caused by Pectobacterium and Dickeya spp., are major production constraints in many potato-growing regions of the world. Despite advances in our understanding of the causative organisms, disease epidemiology, and control, blackleg remains the principal cause of down-grading and rejection of potato seed in classification schemes across Northern Europe and many other parts of the world. Although symptom recognition is relatively straightforward and is applied universally in seed classification schemes, attributing disease to a specific organism is problematic and can only be achieved through the use of diagnostics. Similarly as disease spread is largely through the movement of asymptomatically infected seed tubers and, possibly in the case of Dickeya spp., irrigation waters, accurate and sensitive diagnostics are a prerequisite for detection. This chapter describes the diagnostic pathway that can be applied to identify the principal potato pathogens within the genera Pectobacterium and Dickeya.


Subject(s)
DNA, Bacterial/analysis , Enterobacteriaceae/genetics , Enterobacteriaceae/isolation & purification , Pectobacterium/genetics , Pectobacterium/isolation & purification , Real-Time Polymerase Chain Reaction/methods , Solanum tuberosum/microbiology , DNA, Bacterial/genetics , Enterobacteriaceae/pathogenicity , Pectobacterium/pathogenicity , Plant Diseases/genetics , Plant Diseases/microbiology , Plant Tubers/chemistry , Plant Tubers/microbiology , Species Specificity
2.
Methods Mol Biol ; 1302: 113-22, 2015.
Article in English | MEDLINE | ID: mdl-25981250

ABSTRACT

Phytoplasma infections are regularly reported worldwide, and concerns about their threats on agricultural production, especially in relation to global climate change, are increasing. Sensitive and reliable detection methods are important to ensure that propagation material is free of phytoplasma infection and for epidemiological studies that may provide information to limit the extent of phytoplasma diseases and to prevent large-scale crop losses. The detection method described here uses LNA chemistry in real-time PCR. It has been developed and validated for use on potatoes, and its sensitivity and specificity make it suitable for use in postentry potato quarantine and initiation of potato nuclear stocks to ensure that material is phytoplasma-free.


Subject(s)
DNA, Bacterial/analysis , Nucleic Acid Probes/chemistry , Oligonucleotides/chemistry , Phytoplasma/isolation & purification , Plant Diseases/microbiology , Real-Time Polymerase Chain Reaction/methods , Solanum tuberosum/microbiology , DNA, Bacterial/genetics , Phytoplasma/genetics , Phytoplasma/pathogenicity , Solanum tuberosum/genetics
3.
Int J Syst Evol Microbiol ; 64(Pt 3): 768-774, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24225027

ABSTRACT

Pectinolytic bacteria have been recently isolated from diseased potato plants exhibiting blackleg and slow wilt symptoms found in a number of European countries and Israel. These Gram-reaction-negative, motile, rods were identified as belonging to the genus Dickeya, previously the Pectobacterium chrysanthemi complex (Erwinia chrysanthemi), on the basis of production of a PCR product with the pelADE primers, 16S rRNA gene sequence analysis, fatty acid methyl esterase analysis, the production of phosphatases and the ability to produce indole and acids from α-methylglucoside. Differential physiological assays used previously to differentiate between strains of E. chrysanthemi, showed that these isolates belonged to biovar 3. Eight of the isolates, seven from potato and one from hyacinth, were analysed together with 21 reference strains representing all currently recognized taxa within the genus Dickeya. The novel isolates formed a distinct genetic clade in multilocus sequence analysis (MLSA) using concatenated sequences of the intergenic spacer (IGS), as well as dnaX, recA, dnaN, fusA, gapA, purA, rplB, rpoS and gyrA. Characterization by whole-cell MALDI-TOF mass spectrometry, pulsed field gel electrophoresis after digestion of whole-genome DNA with rare-cutting restriction enzymes, average nucleotide identity analysis and DNA-DNA hybridization studies, showed that although related to Dickeya dadantii, these isolates represent a novel species within the genus Dickeya, for which the name Dickeya solani sp. nov. (type strain IPO 2222(T) = LMG25993(T) = NCPPB4479(T)) is proposed.


Subject(s)
Enterobacteriaceae/classification , Pectins/metabolism , Phylogeny , Solanum tuberosum/microbiology , Bacterial Typing Techniques , DNA, Bacterial/genetics , Enterobacteriaceae/genetics , Enterobacteriaceae/isolation & purification , Europe , Fatty Acids/chemistry , Genes, Bacterial , Indoles/metabolism , Israel , Molecular Sequence Data , Multilocus Sequence Typing , Nucleic Acid Hybridization , Plant Diseases/microbiology , RNA, Ribosomal, 16S/genetics , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
4.
Genome Announc ; 1(6)2013 Nov 21.
Article in English | MEDLINE | ID: mdl-24265502

ABSTRACT

Dickeya (formerly Erwinia chrysanthemi) species cause diseases on a wide range of crops and ornamental plants worldwide. Here we present the draft sequences of 17 Dickeya isolates spanning four Dickeya species, including five isolates that are currently unassigned to a species.

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