Literature DB >> 22805238

Pseudomonas savastanoi pv. savastanoi: some like it knot.

Cayo Ramos1, Isabel M Matas, Leire Bardaji, Isabel M Aragón, Jesús Murillo.   

Abstract

Pseudomonas savastanoi pv. savastanoi is the causal agent of olive (Olea europaea) knot disease and an unorthodox member of the P. syringae complex, causing aerial tumours instead of the foliar necroses and cankers characteristic of most members of this complex. Olive knot is present wherever olive is grown; although losses are difficult to assess, it is assumed that olive knot is one of the most important diseases of the olive crop. The last century witnessed a large number of scientific articles describing the biology, epidemiology and control of this pathogen. However, most P. savastanoi pv. savastanoi strains are highly recalcitrant to genetic manipulation, which has effectively prevented the pathogen from benefitting from the scientific progress in molecular biology that has elevated the foliar pathogens of the P. syringae complex to supermodels. A number of studies in recent years have made significant advances in the biology, ecology and genetics of P. savastanoi pv. savastanoi, paving the way for the molecular dissection of its interaction with other nonpathogenic bacteria and their woody hosts. The selection of a genetically pliable model strain was soon followed by the development of rapid methods for virulence assessment with micropropagated olive plants and the analysis of cellular interactions with the plant host. The generation of a draft genome of strain NCPPB 3335 and the closed sequence of its three native plasmids has allowed for functional and comparative genomic analyses for the identification of its pathogenicity gene complement. This includes 34 putative type III effector genes and genomic regions, shared with other pathogens of woody hosts, which encode metabolic pathways associated with the degradation of lignin-derived compounds. Now, the time is right to explore the molecular basis of the P. savastanoi pv. savastanoi-olive interaction and to obtain insights into why some pathovars like it necrotic and why some like it knot. SYNONYMS: Pseudomonas syringae pv. savastanoi. TAXONOMY: Kingdom Bacteria; Phylum Proteobacteria; Class Gammaproteobacteria; Family Pseudomonadaceae; Genus Pseudomonas; included in genomospecies 2 together with at least P. amygdali, P. ficuserectae, P. meliae and 16 other pathovars from the P. syringae complex (aesculi, ciccaronei, dendropanacis, eriobotryae, glycinea, hibisci, mellea, mori, myricae, phaseolicola, photiniae, sesami, tabaci, ulmi and certain strains of lachrymans and morsprunorum); when a formal proposal is made for the unification of these bacteria, the species name P. amygdali would take priority over P. savastanoi. MICROBIOLOGICAL PROPERTIES: Gram-negative rods, 0.4-0.8 × 1.0-3.0 μm, aerobic. Motile by one to four polar flagella, rather slow growing, optimal temperatures for growth of 25-30 °C; oxidase negative, arginine dihydrolase negative; elicits the hypersensitive response on tobacco; most isolates are fluorescent and levan negative, although some isolates are nonfluorescent and levan positive. HOST RANGE: P. savastanoi pv. savastanoi causes tumours in cultivated and wild olive and ash (Fraxinus excelsior). Although strains from olive have been reported to infect oleander (Nerium oleander), this is generally not the case; however, strains of P. savastanoi pv. nerii can infect olive. Pathovars fraxini and nerii are differentiated from pathovar savastanoi mostly in their host range, and were not formally recognized until 1996. Literature before about 1996 generally names strains of the three pathovars as P. syringae ssp. savastanoi or P. savastanoi ssp. savastanoi, contributing to confusion on the host range and biological properties. DISEASE SYMPTOMS: Symptoms of infected trees include hyperplastic growths (tumorous galls or knots) on the stems and branches of the host plant and, occasionally, on leaves and fruits. EPIDEMIOLOGY: The pathogen can survive and multiply on aerial plant surfaces, as well as in knots, from where it can be dispersed by rain, wind, insects and human activities, entering the plant through wounds. Populations are very unevenly distributed in the plant, and suffer drastic fluctuations throughout the year, with maximum numbers of bacteria occurring during rainy and warm months. Populations of P. savastanoi pv. savastanoi are normally associated with nonpathogenic bacteria, both epiphytically and endophytically, and have been demonstrated to form mutualistic consortia with Erwinia toletana and Pantoea agglomerans, which could result in increased bacterial populations and disease symptoms. DISEASE CONTROL: Based on preventive measures, mostly sanitary and cultural practices. Integrated control programmes benefit from regular applications of copper formulations, which should be maintained for at least a few years for maximum benefit. Olive cultivars vary in their susceptibility to olive knot, but there are no known cultivars with full resistance to the pathogen. USEFUL WEBSITES: http://www.pseudomonas-syringae.org/; http://genome.ppws.vt.edu/cgi-bin/MLST/home.pl; ASAP access to the P. savastanoi pv. savastanoi NCPPB 3335 genome sequence https://asap.ahabs.wisc.edu/asap/logon.php.
© 2012 THE AUTHORS. MOLECULAR PLANT PATHOLOGY © 2012 BSPP AND BLACKWELL PUBLISHING LTD.

Entities:  

Mesh:

Year:  2012        PMID: 22805238      PMCID: PMC6638699          DOI: 10.1111/j.1364-3703.2012.00816.x

Source DB:  PubMed          Journal:  Mol Plant Pathol        ISSN: 1364-3703            Impact factor:   5.663


  53 in total

Review 1.  Genomic insights into the contribution of phytopathogenic bacterial plasmids to the evolutionary history of their hosts.

Authors:  George W Sundin
Journal:  Annu Rev Phytopathol       Date:  2007       Impact factor: 13.078

2.  Recovery of Pseudomonas savastanoi pv. savastanoi from symptomless shoots of naturally infected olive trees.

Authors:  José M Quesada; Amparo García; Edson Bertolini; María M López; Ramón Penyalver
Journal:  Int Microbiol       Date:  2007-06       Impact factor: 2.479

3.  Effects of Timing of Copper Sprays, Defoliation, Rainfall, and Inoculum Concentration on Incidence of Olive Knot Disease.

Authors:  Beth L Teviotdale; William H Krueger
Journal:  Plant Dis       Date:  2004-02       Impact factor: 4.438

4.  Annotation and overview of the Pseudomonas savastanoi pv. savastanoi NCPPB 3335 draft genome reveals the virulence gene complement of a tumour-inducing pathogen of woody hosts.

Authors:  Pablo Rodríguez-Palenzuela; Isabel M Matas; Jesús Murillo; Emilia López-Solanilla; Leire Bardaji; Isabel Pérez-Martínez; Martín E Rodríguez-Moskera; Ramón Penyalver; Maria M López; José M Quesada; Bryan S Biehl; Nicole T Perna; Jeremy D Glasner; Eric L Cabot; Eric Neeno-Eckwall; Cayo Ramos
Journal:  Environ Microbiol       Date:  2010-04-01       Impact factor: 5.491

5.  The 73-kb pIAA plasmid increases competitive fitness of Pseudomonas syringae subspecies savastanoi in oleander.

Authors:  S E Silverstone; D G Gilchrist; R M Bostock; T Kosuge
Journal:  Can J Microbiol       Date:  1993-07       Impact factor: 2.419

Review 6.  Roadmap to new virulence determinants in Pseudomonas syringae: insights from comparative genomics and genome organization.

Authors:  Magdalen Lindeberg; Christopher R Myers; Alan Collmer; David J Schneider
Journal:  Mol Plant Microbe Interact       Date:  2008-06       Impact factor: 4.171

7.  Pseudomonas savastanoi pv. savastanoi contains two iaaL paralogs, one of which exhibits a variable number of a trinucleotide (TAC) tandem repeat.

Authors:  Isabel M Matas; Isabel Pérez-Martínez; José M Quesada; José J Rodríguez-Herva; Ramón Penyalver; Cayo Ramos
Journal:  Appl Environ Microbiol       Date:  2008-12-19       Impact factor: 4.792

8.  Comparison of Ethylene Production by Pseudomonas syringae and Ralstonia solanacearum.

Authors:  H Weingart; B Völksch; M S Ullrich
Journal:  Phytopathology       Date:  1999-05       Impact factor: 4.025

9.  Cotranscription of genes encoding indoleacetic acid production in Pseudomonas syringae subsp. savastanoi.

Authors:  C J Palm; T Gaffney; T Kosuge
Journal:  J Bacteriol       Date:  1989-02       Impact factor: 3.490

10.  Role of indoleacetic acid-lysine synthetase in regulation of indoleacetic acid pool size and virulence of Pseudomonas syringae subsp. savastanoi.

Authors:  N L Glass; T Kosuge
Journal:  J Bacteriol       Date:  1988-05       Impact factor: 3.490

View more
  22 in total

1.  The mangotoxin biosynthetic operon (mbo) is specifically distributed within Pseudomonas syringae genomospecies 1 and was acquired only once during evolution.

Authors:  Víctor J Carrión; José A Gutiérrez-Barranquero; Eva Arrebola; Leire Bardaji; Juan C Codina; Antonio de Vicente; Francisco M Cazorla; Jesús Murillo
Journal:  Appl Environ Microbiol       Date:  2012-11-09       Impact factor: 4.792

2.  Structure of the flavoprotein tryptophan 2-monooxygenase, a key enzyme in the formation of galls in plants.

Authors:  Helena M Gaweska; Alexander B Taylor; P John Hart; Paul F Fitzpatrick
Journal:  Biochemistry       Date:  2013-04-04       Impact factor: 3.162

Review 3.  The olive knot disease as a model to study the role of interspecies bacterial communities in plant disease.

Authors:  Roberto Buonaurio; Chiaraluce Moretti; Daniel Passos da Silva; Chiara Cortese; Cayo Ramos; Vittorio Venturi
Journal:  Front Plant Sci       Date:  2015-06-10       Impact factor: 5.753

4.  Draft Genome Sequence of Pseudomonas savastanoi pv. savastanoi Strain DAPP-PG 722, Isolated in Italy from an Olive Plant Affected by Knot Disease.

Authors:  Chiaraluce Moretti; Chiara Cortese; Daniel Passos da Silva; Vittorio Venturi; Cayo Ramos; Giuseppe Firrao; Roberto Buonaurio
Journal:  Genome Announc       Date:  2014-10-02

5.  The extent of genome flux and its role in the differentiation of bacterial lineages.

Authors:  Reuben W Nowell; Sarah Green; Bridget E Laue; Paul M Sharp
Journal:  Genome Biol Evol       Date:  2014-06-12       Impact factor: 3.416

6.  Arabidopsis thaliana as a tool to identify traits involved in Verticillium dahliae biocontrol by the olive root endophyte Pseudomonas fluorescens PICF7.

Authors:  M Mercedes Maldonado-González; Peter A H M Bakker; Pilar Prieto; Jesús Mercado-Blanco
Journal:  Front Microbiol       Date:  2015-04-07       Impact factor: 5.640

7.  Complete genome sequence of Pseudomonas fluorescens strain PICF7, an indigenous root endophyte from olive (Olea europaea L.) and effective biocontrol agent against Verticillium dahliae.

Authors:  Pedro Manuel Martínez-García; David Ruano-Rosa; Elisabetta Schilirò; Pilar Prieto; Cayo Ramos; Pablo Rodríguez-Palenzuela; Jesús Mercado-Blanco
Journal:  Stand Genomic Sci       Date:  2015-02-06

Review 8.  Plant tumors: a hundred years of study.

Authors:  Irina E Dodueva; Maria A Lebedeva; Kseniya A Kuznetsova; Maria S Gancheva; Svetlana S Paponova; Ludmila L Lutova
Journal:  Planta       Date:  2020-03-18       Impact factor: 4.116

9.  Contribution of the non-effector members of the HrpL regulon, iaaL and matE, to the virulence of Pseudomonas syringae pv. tomato DC3000 in tomato plants.

Authors:  Melissa G Castillo-Lizardo; Isabel M Aragón; Vivian Carvajal; Isabel M Matas; María Luisa Pérez-Bueno; María-Trinidad Gallegos; Matilde Barón; Cayo Ramos
Journal:  BMC Microbiol       Date:  2015-08-19       Impact factor: 3.605

10.  From the root to the stem: interaction between the biocontrol root endophyte Pseudomonas fluorescens PICF7 and the pathogen Pseudomonas savastanoi NCPPB 3335 in olive knots.

Authors:  M Mercedes Maldonado-González; Pilar Prieto; Cayo Ramos; Jesús Mercado-Blanco
Journal:  Microb Biotechnol       Date:  2013-02-20       Impact factor: 5.813

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.