Bacterial Canker and Dieback Disease of Apricots (Pseudomonas syringae van Hall)

Bacterial canker and dieback (Pseudomonas syringae van Hall) of apricot is a widespread disease in Europe, except for the Mediterranean areas. Cankers usually develop at pruning wounds or other points of injury. Phloem and cambium become susceptible from just after leaf drop until budding. If the phloem necrosis does not girdle the branch or trunk, cankers develop by the middle or the end of summer. In early summer, the bacterium actually dies out in the infected tissue, and the tree remains resistant during the summer. During this period, the pathogen lives epiphytically on the surface of the leaves, without causing any symptoms. The extent of bacterial necrosis of the phloem depends on the severity of winter frost. Without winter frost, bacterial induced tissue necrosis does not occur. Necrosis is found only if P. syringae has enough time to proliferate before the onset of frost. The most effective method of control is to carry out spring rather than winter pruning.     

Cytospora Canker and Dieback of Apricots

Cytosporal canker and dieback (Cytospora cincta Sacc.) is a widespread disease in apricot growing areas of Europe, excluding the Mediterranean. The pathogen attacks xylem and phloem. If the necrotic phloem completely girdles the branches or trunk, the section above the girdled region dies. When cambium necrosis does not girdle the branch or trunk, canker development ensues. Apricot trees are susceptible to Cytospora infection between July and the next bud opening.     

Infection of cucumber seedling roots by Pseudomonas amygdali pv. lachrymans following artificial substrate inoculation

European Journal of Plant Pathology - There are few studies of cucumber roots at the seedling stage infected by Pseudomonas amygdali pv. lachrymans (Pal). We used growth chamber assays to determine...     

Infection of horse chestnut (Aesculus hippocastanum) by Pseudomonas syringae pv. aesculi and its detection by quantitative real-time PCR

Pseudomonas syringae pv. aesculi is a pathogenic bacterium causing bleeding canker disease of horse chestnut ( Aesculus hippocastanum ). This is a serious disease which has been affecting horse chestnut in several European countries over the last five years; however, very little is known about the biology of the causal agent. One of the obstacles to studying this pathogen is the lengthy procedure associated with confirming its presence on the host. In this study, P. syringae pv. aesculi was isolated from lesions on different parts of horse chestnut and its pathogenicity confirmed on horse chestnut saplings using two inoculation techniques. Real-time PCR primers were developed based on gyrase B gene sequence data for the specific detection of P. syringae pv. aesculi . Primer specificity was tested on isolates of the target pathogen as well as on a broad range of related non-target bacteria and other bacterial spp. which inhabit horse chestnut. The real-time primers reliably amplified P. syringae pv. aesculi down to 1 pg of extracted DNA, with and without the presence of host DNA, and also amplified unextracted DNA in whole cells of the bacterium down to at least 160 colony forming units. Detection and quantification of the target pathogen in phloem and xylem of both naturally infected and inoculated horse chestnut tissues was also demonstrated. This quantitative real-time PCR assay provides the facility to study several important aspects of the biology of P. syringae pv. aesculi on horse chestnut including its potential for dissemination in different substrates.     

假单胞菌产生的抗生素

假单胞菌属Pseudomonas群体庞大,广泛分布于土壤、水体和动植物中,并产生大量的次生代谢产物以适应环境的变化。抗生素为假单胞菌在自然生态条件下的生存提供了重要的竞争手段,同时也是生防假单胞菌防治植物病害的主要机制之一。本文介绍假单胞菌产生的抗生素种类、作用机制、不同浓度下抗生素的生物学功能,以及假单胞菌抗生素在医学和农业病害防治中的应用。     

皱果赤瓟白绢病病原的生物学特征与防治

在对野生珍稀食用植物皱果赤的引种驯化中发现白绢病是皱果赤生长期的主要病害。本文研究了皱果赤白绢病的症状、病原及其生物学特征和发生规律,提出了防治措施。     

枸杞炭疽病菌毒素的初步研究

枸杞炭疽病菌(Colletotrichum gloeosporioides Penz)可产生有致病力的外毒素,其毒素可引起枸杞叶片形成黑色坏死斑,类似于病原菌侵染形成的症状。Czapek-Dox培养液适于枸杞炭疽病菌的生长和产毒,其适宜温度为25～28℃,初始pH为6,通气条件促进其生长和产生毒素。试验结果表明该毒素为多聚糖类物质,毒素液对不同品种枸杞的致病作用存在明显差异,与品种对枸杞炭疽病的抗性有关。     

Production of syringomycins and syringopeptins by Pseudomonas syringae pv. atrofaciens

All virulent strains of Pseudomonas syringae pv. atrofaciens produce in vitro substances with syringomycin-like features. All strains inhibited the growth of Geotrichum candidum in the plate assay although the extent of their growth inhibition was variable.
Purification of bioactive culture extracts of a highly virulent strain by ion exchange chromatography (Whatman CM52) yielded a main fraction which inhibited the growth of Rhodotorula pilimanae and Bacillus megaterium , and was phytotoxic to tobacco and wheat plants. In particular, the injection of this fraction in the culm of wheat plants caused phytotoxic symptoms on leaves similar to those caused in nature by the pathogen. The further purification by HPLC of the above fraction gave rise to four main bioactive substances which have been identified by spectroscopic methods (FAB-MS) and amino acid analysis as syringomycin E, syringomycin G, syringopeptin 25A and syringopeptin 25B, toxic lipodepsipeptides thus far recognized to be produced by most strains of P. syringae pv. syringae . The injection of both syringomycin E and syringopeptin 25A in wheat leaves caused necrotic symptoms; however, syringopeptin 25A was at least six times more active than syringomycin E. The possible role of the toxins in the disease development on cereals and the need for a careful examination of pathogenetic and biochemical features of P. syringae pv. atrofaciens to establish the relationships of the two pathovars in the 'syringae group' are discussed.     

Bacterial brown spot on Avena storigosa Schereb. caused by Pseudomonas syringae pv. alisalensis

Avena storigosa Schereb. (bristle oat) is used as a green manure in crop rotations and as an antagonist of nematodes in Nagano Prefecture, Japan. In 2011, necrotic, brown, water-soaked lesions were observed on young bristle oat plants. A pathogenic bacterium was isolated from symptomatic leaves of infected plants and produced the same symptoms after inoculation. Bacteriological properties of the bacterial isolates from bristle oat matched those of Pseudomonas syringae pathovars. The host range of the bristle oat isolates was identical to that of P. syringae pv. alisalensis. This is the first report of bristle oat disease caused by P. syringae pv. alisalensis.     

Induced systemic resistance in arabidopsis thaliana against Pseudomonas syringae pv. tomato by 2,4-diacetylphloroglucinol-producing Pseudomonas fluorescens

Pseudomonas fluorescens strains that produce the polyketide antibiotic 2,4-diacetylphloroglucinol (2,4-DAPG) are among the most effective rhizobacteria that suppress root and crown rots, wilts, and damping-off diseases of a variety of crops, and they play a key role in the natural suppressiveness of some soils to certain soilborne pathogens. Root colonization by 2,4-DAPG-producing P. fluorescens strains Pf-5 (genotype A), Q2-87 (genotype B), Q8r1-96 (genotype D), and HT5-1 (genotype N) produced induced systemic resistance (ISR) in Arabidopsis thaliana accession Col-0 against bacterial speck caused by P. syringae pv. tomato. The ISR-eliciting activity of the four bacterial genotypes was similar, and all genotypes were equivalent in activity to the well-characterized strain P. fluorescens WCS417r. The 2,4-DAPG biosynthetic locus consists of the genes phlHGF and phlACBDE. phlD or phlBC mutants of Q2-87 (2,4-DAPG minus) were significantly reduced in ISR activity, and genetic complementation of the mutants restored ISR activity back to wild-type levels. A phlF regulatory mutant (overproducer of 2,4-DAPG) had ISR activity equivalent to the wild-type Q2-87. Introduction of DAPG into soil at concentrations of 10 to 250 μM 4 days before challenge inoculation induced resistance equivalent to or better than the bacteria. Strain Q2-87 induced resistance on transgenic NahG plants but not on npr1-1, jar1, and etr1 Arabidopsis mutants. These results indicate that the antibiotic 2,4-DAPG is a major determinant of ISR in 2,4-DAPG-producing P. fluorescens, that the genotype of the strain does not affect its ISR activity, and that the activity induced by these bacteria operates through the ethylene- and jasmonic acid-dependent signal transduction pathway.     

三环唑对稻瘟病菌再侵染的抑制作用初探

在实验室条件下模拟稻瘟病菌Magnaporthe grisea再侵染发生的全过程,研究了三环唑对稻瘟病菌再侵染的抑制作用及其机制。在接种稻瘟病菌48 h后喷雾处理,10 μg/mL三环唑的防病效果只有28.58%,表明三环唑对稻瘟病的治疗效果较差;10 μg/mL三环唑处理过的发病植株作为再侵染源引起周围未经药剂处理的健康水稻的发病程度要比未经药剂处理的病株作为再侵染源引起的低63.28%。进一步的研究表明,三环唑抑制稻瘟病菌再侵染的主要机制是抑制再侵染源的孢子产生和降低分生孢子的释放及致病能力。     

Knot Formation Caused by Pseudomonas syringae subsp. savastanoi on Olive Plants Is hrp-Dependent

ABSTRACT The virulence of Pseudomonas syringae subsp. savastanoi, which causes hyperplastic symptoms (knots) on olive plants, is associated with secreted phytohormones. We identified a Tn5-induced mutant of P. syringae subsp. savastanoi that did not cause disease symptoms on olive plants although it was still able to produce phytohormones. In addition, the mutant failed to elicit a hypersensitive response in a nonhost plant. Molecular characterization of the mutant revealed that a single Tn5 insertion occurred within an open reading frame encoding a protein 92% identical to the HrcC protein of P. syringae pv. syringae. Moreover, sequence analysis revealed that the gene encoding the HrcC protein in P. syringae subsp. savastanoi was part of an operon that included five genes arranged as in other phytopathogenic bacteria. These results imply that hrp/hrc genes are functional in P. syringae subsp. savastanoi and that they play a key role in the pathogenicity of this plant pathogen.