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dc.contributor.authorDorati, F
dc.contributor.authorBarrett, GA
dc.contributor.authorSanchez-Contreras, M
dc.contributor.authorArseneault, T
dc.contributor.authorJosé, MS
dc.contributor.authorStudholme, DJ
dc.contributor.authorMurillo, J
dc.contributor.authorCaballero, P
dc.contributor.authorWaterfield, NR
dc.contributor.authorArnold, DL
dc.contributor.authorShaw, LJ
dc.contributor.authorJackson, RW
dc.date.accessioned2018-10-26T10:49:45Z
dc.date.issued2018-04-21
dc.description.abstractUnderstanding the molecular mechanisms underpinning the ecological success of plant pathogens is critical to develop strategies for controlling diseases and protecting crops. Recent observations have shown that plant pathogenic bacteria, particularly Pseudomonas, exist in a range of natural environments away from their natural plant host e.g., water courses, soil, non-host plants. This exposes them to a variety of eukaryotic predators such as nematodes, insects and amoebae present in the environment. Nematodes and amoeba in particular are bacterial predators while insect herbivores may act as indirect predators, ingesting bacteria on plant tissue. We therefore postulated that bacteria are probably under selective pressure to avoid or survive predation and have therefore developed appropriate coping mechanisms. We tested the hypothesis that plant pathogenic Pseudomonas syringae are able to cope with predation pressure and found that three pathovars show weak, but significant resistance or toxicity. To identify the gene systems that contribute to resistance or toxicity we applied a heterologous screening technique, called Rapid Virulence Annotation (RVA), for anti-predation and toxicity mechanisms. Three cosmid libraries for P. syringae pv. aesculi, pv. tomato and pv. phaseolicola, of approximately 2000 cosmids each, were screened in the susceptible/non-toxic bacterium Escherichia coli against nematode, amoebae and an insect. A number of potential conserved and unique genes were identified which included genes encoding haemolysins, biofilm formation, motility and adhesion. These data provide the first multi-pathovar comparative insight to how plant pathogens cope with different predation pressures and infection of an insect gut and provide a foundation for further study into the function of selected genes and their role in ecological success.en_GB
dc.description.sponsorshipAll work was funded by the University of Reading to which we are extremely grateful.en_GB
dc.identifier.citationVol. 6 (2), article 32en_GB
dc.identifier.doi10.3390/microorganisms6020032
dc.identifier.urihttp://hdl.handle.net/10871/34489
dc.language.isoenen_GB
dc.publisherMDPIen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/29690522en_GB
dc.rights© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en_GB
dc.subjectAcanthamoeba polyphagaen_GB
dc.subjectCaenorhabditis elegansen_GB
dc.subjectGalleria mellonellaen_GB
dc.subjectPseudomonas syringaeen_GB
dc.subjectRVAen_GB
dc.subjectanti-predationen_GB
dc.subjectpathogenen_GB
dc.subjectrapid virulence annotationen_GB
dc.titleCoping with Environmental Eukaryotes; Identification of Pseudomonas syringae Genes during the Interaction with Alternative Hosts or Predatorsen_GB
dc.typeArticleen_GB
dc.date.available2018-10-26T10:49:45Z
dc.identifier.issn2076-2607
exeter.place-of-publicationSwitzerlanden_GB
dc.descriptionThis is the final version. Available on open access from MDPI via the DOI in this recorden_GB
dc.identifier.journalMicroorganismsen_GB


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