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Bacterial Canker (bacterial + canker)

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Screening wild cherry (Prunus avium) for resistance to bacterial canker by laboratory and field tests

FOREST PATHOLOGY, Issue 6 2004
F. Santi
Summary Currently, bacterial canker caused by Pseudomonas syringae is a major cause of dieback and tree death in wild cherry (Prunus avium) plantations. The evaluation of breeding collections is needed to produce less susceptible clones or cultivars. Resistance tests were performed using excised shoots (1 and 2 years old) from 79 clones in the laboratory. A subset of 10 clones was also tested in the field. The clones were inoculated with four to seven isolates of a set of 15 isolates of P. s. pv. morsprunorum, P. s. pv. syringae, P. s. pv. persicae, P. syringae pv. avii and P. fluorescens. In the laboratory tests, older and larger shoots were more susceptible. In the field test, size and age of the shoots were not related to girdling by the bacterial canker. Two-year-old shoots were best for clonal discrimination. Correlations between 1 and 2-year-old shoots were significant but not high. The isolates varied a lot between experiments, but as the clone × isolate interactions were always low, breeding could thus be facilitated. The ranking of clones was conserved quite well between two laboratory tests, but not between two others. Good agreement was found for the best clones in the laboratory tests and in the field test. However, the two worst clones in the latter were among the best in one laboratory test. At least two independent tests in the laboratory are needed to evaluate resistance/susceptibility of clones. Broad sense heritability for resistance varied from 0.27 to 0.51. Although moderate, such heritability clearly encourages a breeding approach to reduce the problem of bacterial canker. Résumé Le chancre bactérien (Pseudomonas syringae) est une cause majeure de dépérissement dans les plantations de merisier du nord de la France. Nous devons évaluer les collections pour produire des variétés moins sensibles. Des branches coupées de un ou deux ans de 79 clones ont été testées au laboratoire. Dix de ces clones ont également été testés dans un test en extérieur. Les clones ont été inoculés avec un total de 15 isolats de P. s. pv. morsprunorum, P. s. pv. syringae, P. s. pv. persicae, P. s. pv. avii et P. fluorescens. Les plus fortes infections, mesurées par la longueur du chancre, ont été observées sur les branches les plus âgées et les plus épaisses, mais la taille et l'âge des branches n'ont eu aucune influence sur la note de ceinturation du test au champ. Les branches de deux ans se sont révélées meilleures pour discriminer les clones. Les corrélations entre moyennes de clones avec les branches de un et deux ans étaient significatives mais pas très élevées. Les isolats variaient beaucoup entre expériences, mais comme les interactions clone × bactérie étaient toujours faibles, la sélection clonale en devrait être facilitée. Le classement des clones était bien conservé entre deux tests de laboratoire, mais pas entre deux autres. Le classement entre tests au laboratoire et au champ se trouvait conservé, mais les deux plus mauvais clones dans ce dernier ont été bien classés dans un test de laboratoire, ce qui signifie qu'un seul test a laboratoire est insuffisant pour l'évaluation des clones. Les héritabilités au sens large variaient de 0.27 à 0.51. Bien que modérées, de telles héritabilités encouragent clairement à sélectionner des génotypes moins sensibles pour solutionner le problème du chancre bactérien. Zusammenfassung Der durch Pseudomonas syringae verursachte Bakterienkrebs ist eine der häufigsten Ursachen für das Absterben von Süsskirschen (Prunus avium) in Pflanzungen. Die Prüfung von Zuchtformen auf Resistenz ist nötig, um weniger anfällige Klone und Sorten zu fördern. Die Resistenz von 79 Klonen wurde im Labor an abgeschnittenen ein- und zweijährigen Trieben getestet. Zehn Klone wurden auch im Feld getestet. Die Klone wurden mit je vier bis sieben von insgesamt 15 Isolaten von P. s. pv. morsprunorum, P. s. pv. syringae, P. s. pv. persicae, P. s. pv. avii und P. fluorescens inokuliert. In den Labortests waren die älteren, dickeren Triebe anfälliger, währenddem in den Feldversuchen weder Alter noch Dicke der Triebe eine Rolle spielten. Zweijährige Triebe eigneten sich zur Differenzierung der Klone hinsichtlich ihrer Resistenz besser. Korrelationen zwischen ein- und zweijährigen Trieben waren signifikant aber nicht hoch. Die Reaktionen auf die Isolate variierten stark zwischen den Experimenten, aber die statistisch nachgewiesenen Wechselwirkungen zwischen Klonen und Isolaten waren stets schwach, was die Züchtung neuer Klone erleichtern dürfte. In zwei Labortests erzielten die Klone analoge Bewertungen, währenddem sie in zwei anderen Labortests unterschiedlich reagierten. Die Resultate aus Labor- und Feldversuchen stimmten für die resistentesten Klone gut überein, die anfälligsten Klone im Feldversuch waren jedoch unter den resistentesten in den Laborversuchen. Es sind also mindestens zwei unabhängige Labortests nötig, um den Grad der Resistenz eines Klones zu bestimmen. Der Vererbarkeit der Resistenz variierte zwischen 0.27 und 0.51. Obschon diese Werte moderat sind, sollen sie dazu ermuntern, mittels Züchtung auf eine Reduktion von durch den Bakterienkrebs bedingten Ausfällen hinzuarbeiten. [source]

Season-long mating disruption of citrus leafminer, Phyllocnistis citrella Stainton, with an emulsified wax formulation of pheromone

JOURNAL OF APPLIED ENTOMOLOGY, Issue 6 2010
L. L. Stelinski
Abstract The citrus leafminer, Phyllocnistis citrella Stainton (Lepidoptera: Gracillariidae), is a major worldwide pest of citrus. Larval feeding by this insect facilitates proliferation of citrus bacterial canker, Xanthomonas axonopodis pv. citri. Herein, we describe a season-long disruption trial of P. citrella with a newly developed, emulsified wax dispenser of pheromone (SPLAT-CLMTM). A formulation containing a 3 : 1 blend of (Z,Z,E)-7,11,13-hexadecatrienal:(Z,Z)-7,11-hexadecadienal at a 0.2% loading rate of active ingredient by weight and deployed twice per season (24 weeks total) at 490 g of formulation/ha caused season-long disruption of male moth catch in pheromone traps as well as reduced leaf infestation. Analysis of pheromone release from dispensers by gas chromatography revealed that effective disruption of P. citrella occurred at a deployment rate of 126 ,g of (Z,Z,E)-7,11,13-hexadecatrienal/ha/h. Direct observation of moth behaviour in the field suggested that disruption by this formulation occurred by a non-competitive mechanism. A formulation of the 3 : 1 attractive blend at a 0.02% pheromone loading rate caused only 2,6 weeks of disruption per deployment and did not reduce leaf infestation during mid and end of the season evaluations. A formulation containing 0.2% of (Z,Z)-7,11-hexadecadienal alone and deployed at 490 g/ha caused 6,7 weeks of moth disruption to pheromone traps and did not prevent leaf infestation, while an identical formulation loaded with 0.02% (w/w) of (Z,Z)-7,11-hexadecadienal alone had no effect on P. citrella orientation to pheromone traps. The SPLAT formulation evaluated herein appears to be an excellent release device for (Z,Z,E)-7,11,13-hexadecatrienal given that approximately 100 days of steady release occurred following an initial brief (ca. 7 days) burst of higher release. The advantages of SPLAT as a formulation for P. citrella disruption include low cost of manufacturing, biodegradable and weather resistant characteristics, and flowability allowing machine application. Mating disruption should be an effective alternative to insecticides for management of P. citrella and may reduce the incidence of citrus canker. [source]

Physiological and Biochemical Characteristics of Iranian Strains of Xanthomonas axonopodis pv. citri, the Causal Agent of Citrus bacterial Canker Disease

JOURNAL OF PHYTOPATHOLOGY, Issue 2 2001
M. Mohammadi
Twenty-four strains of Xanthomonas axonopodis pv. citri (Xac), the causal agent of bacterial canker of citrus, isolated from Mexican lime (Citrus aurantifolia) and lemon (Citrus limon) in southern Iran, were characterized phenotypically. Strains were all pathogenic on C. aurantifolia. Sodium dodecyl sulphate-polyacrylamide gel electrophoresis analysis revealed slight differences in soluble protein profiles among the strains. Based on host range specificity and phenotypic characteristics, representative strains were differentiated into two groups of Asiatic (A) and atypical Asiatic (aA) forms. DNA fingerprinting analysis using EcoRI as the restriction endonuclease showed a negligible difference in restriction pattern between the two groups. On the basis of isozymic analysis, the two groups were distinct with respect to superoxide dismutase (SOD) and esterase (EST) banding patterns. Plasmid DNA profile analysis showed that the bacterial strains were different from each other in terms of plasmid number and molecular weight. Phage typing study revealed that most of group A strains were susceptible to Cp1 and/or Cp2 and some were resistant to both phage types including the strain in aA group. Bacteriocin production test indicated that there was a variation among Xac strains using different indicators for each bacteriocin producer. It is concluded that the Iranian strains of Xac are heterogeneous and constitute a subgroup(s) within the pathotype A. Physiologische und biochemische Merkmale iranischer Stämme von Xanthomonas axonopodis pv. citri, dem Erreger des bakteriellen Zitruskrebses Vierundzwanzig Stämme von Xanthomonas axonopodis pv. citri, dem Erreger des bakteriellen Zitruskrebses, wurden von mexikanischen Sauren Limetten (Citrus aurantifolia) und Zitronen (Citrus limon) im Südiran isoliert und phänotypisch charakterisiert. Alle Stämme waren für C. aurantifolia pathogen. Eine SDS-PAGE-Analyse zeigte, daß zwischen den Stämmen geringfügige Unterschiede bei den Profilen der löslichen Proteine bestanden. Auf Grundlage der Spezifität des Wirtsspektrums und phänotypischer Merkmale wurden repräsentative Stämme in die zwei Gruppen asiatische (A) und atypische asiatische (aA) Formen eingeteilt. Eine Analyse mit DNA-Fingerabdrücken, wobei EcoRI als Restriktionsendonuclease diente, zeigte einen vernachlässigbar kleinen Unterschied bei den Restriktionsmustern der beiden Gruppen. Die Isoenzymanalyse ergab Unterschiede zwischen beiden Gruppen bezüglich der Bandenmuster von Superoxiddismutase (SOD) und Esterase (EST). Eine Analyse der Plasmid-DNA-Profile zeigte, daß die Bakterienstämme unterschiedliche Plasmidzahlen und verschiedene Molekülmassen aufwiesen. Eine Phagentypisierung ergab, daß die meisten Stämme der Gruppe A anfällig für Cp1 und/oder Cp2 waren; einige waren resistent gegen beide Phagentypen, darunter der Stamm in der aA-Gruppe. Ein Test der Bacteriocinproduktion ergab, daß die Xac -Stämme variierten; hier wurden verschiedene Indikatoren für jeden Bakteriocinbildner verwendet. Es wird gefolgert, daß die iranischen Stämme von Xac heterogen sind und eine oder mehrere Untergruppen innerhalb des Pathotyps A bilden. [source]

Occurrence of Pseudomonas avellanae (Psallidas) Janse et al. and related pseudomonads on wild Corylus avellana trees and genetic relationships with strains isolated from cultivated hazelnuts

JOURNAL OF PHYTOPATHOLOGY, Issue 9-10 2000
M. Scortichini
Surveys in submediterranean forests of central Italy were carried out during 1996,98 to verify the possible presence of bacterial canker caused by Pseudomonas avellanae in wild hazelnut trees (Corylus avellana L.). Wilted twigs were noticed several times especially in summer. In other cases, wild C. avellana trees growing near to hazelnut orchards appeared completely wilted. Isolates that were pathogenic to C. avellana, showing a different degree of virulence, were obtained in both situations. Biochemical, physiological and nutritional tests as well as the comparison of whole-cell protein profiles, revealed the presence of 16 isolates identical to P. avellanae reference strains that had previously been isolated in the same area and five deviating isolates. Repetitive-PCR genomic fingerprinting performed by using BOX (Box elements), ERIC (Enterobacterial Repetitive Interkingdom Consensus) and REP (Repetitive Extragenic Palindromic) primer sets and analysed by means of upgma, revealed the existence of two main groups of pseudomonads pathogenic to C. avellana. Group A includes P. avellanae strains isolated in northern Greece and central Italy as well as the isolates obtained from the wild C. avellana trees grown near the cultivated hazelnut orchards. Group B includes strains previously isolated in northern, southern and other areas of central Italy as well as the isolates obtained from C. avellana wild trees showing twig dieback. Control measures should be taken to avoid the spread of bacterial canker of hazelnut in the forests of central Italy. [source]