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      Genomes and Virulence Factors of Novel Bacterial Pathogens Causing Bleaching Disease in the Marine Red Alga Delisea pulchra

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          Abstract

          Nautella sp. R11, a member of the marine Roseobacter clade, causes a bleaching disease in the temperate-marine red macroalga, Delisea pulchra. To begin to elucidate the molecular mechanisms underpinning the ability of Nautella sp. R11 to colonize, invade and induce bleaching of D. pulchra, we sequenced and analyzed its genome. The genome encodes several factors such as adhesion mechanisms, systems for the transport of algal metabolites, enzymes that confer resistance to oxidative stress, cytolysins, and global regulatory mechanisms that may allow for the switch of Nautella sp. R11 to a pathogenic lifestyle. Many virulence effectors common in phytopathogenic bacteria are also found in the R11 genome, such as the plant hormone indole acetic acid, cellulose fibrils, succinoglycan and nodulation protein L. Comparative genomics with non-pathogenic Roseobacter strains and a newly identified pathogen, Phaeobacter sp. LSS9, revealed a patchy distribution of putative virulence factors in all genomes, but also led to the identification of a quorum sensing (QS) dependent transcriptional regulator that was unique to pathogenic Roseobacter strains. This observation supports the model that a combination of virulence factors and QS-dependent regulatory mechanisms enables indigenous members of the host alga's epiphytic microbial community to switch to a pathogenic lifestyle, especially under environmental conditions when innate host defence mechanisms are compromised.

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          Plant pathogens and integrated defence responses to infection.

          Plants cannot move to escape environmental challenges. Biotic stresses result from a battery of potential pathogens: fungi, bacteria, nematodes and insects intercept the photosynthate produced by plants, and viruses use replication machinery at the host's expense. Plants, in turn, have evolved sophisticated mechanisms to perceive such attacks, and to translate that perception into an adaptive response. Here, we review the current knowledge of recognition-dependent disease resistance in plants. We include a few crucial concepts to compare and contrast plant innate immunity with that more commonly associated with animals. There are appreciable differences, but also surprising parallels.
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            Consed: a graphical tool for sequence finishing.

            Sequencing of large clones or small genomes is generally done by the shotgun approach (Anderson et al. 1982). This has two phases: (1) a shotgun phase in which a number of reads are generated from random subclones and assembled into contigs, followed by (2) a directed, or finishing phase in which the assembly is inspected for correctness and for various kinds of data anomalies (such as contaminant reads, unremoved vector sequence, and chimeric or deleted reads), additional data are collected to close gaps and resolve low quality regions, and editing is performed to correct assembly or base-calling errors. Finishing is currently a bottleneck in large-scale sequencing efforts, and throughput gains will depend both on reducing the need for human intervention and making it as efficient as possible. We have developed a finishing tool, consed, which attempts to implement these principles. A distinguishing feature relative to other programs is the use of error probabilities from our programs phred and phrap as an objective criterion to guide the entire finishing process. More information is available at http:// www.genome.washington.edu/consed/consed. html.
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              H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response.

              Microbial elicitors or attempted infection with an avirulent pathogen strain causes the rapid production of reactive oxygen intermediates. We report here that H2O2 from this oxidative burst not only drives the cross-linking of cell wall structural proteins, but also functions as a local trigger of programmed death in challenged cells and as a diffusible signal for the induction in adjacent cells of genes encoding cellular protectants such as glutathione S-transferase and glutathione peroxidase. Thus, H2O2 from the oxidative burst plays a key role in the orchestration of a localized hypersensitive response during the expression of plant disease resistance.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2011
                5 December 2011
                : 6
                : 12
                : e27387
                Affiliations
                [1 ]The Centre for Marine Bio-Innovation (CMB), University of New South Wales, Sydney, Australia
                [2 ]School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia
                [3 ]Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts, United States of America
                [4 ]School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, Australia
                [5 ]Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts, United States of America
                [6 ]Singapore Centre on Environmental Life Sciences Engineering, Nanyang Technological University, Singapore, Singapore
                Rutgers University, United States of America
                Author notes

                Conceived and designed the experiments: NF RJC PDS SK TT. Performed the experiments: NF RJC MRS TT. Analyzed the data: NJ RJC MRS TT. Contributed reagents/materials/analysis tools: SRL. Wrote the paper: NF TT.

                [¤]

                Current address: Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada

                Article
                PONE-D-11-14147
                10.1371/journal.pone.0027387
                3230580
                22162749
                da4c772c-d233-44ef-91c5-1a4ef19d9174
                Fernandes et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 25 July 2011
                : 15 October 2011
                Page count
                Pages: 12
                Categories
                Research Article
                Biology
                Ecology
                Marine Ecology
                Microbial Ecology
                Genomics
                Comparative Genomics
                Microbiology
                Bacterial Pathogens
                Host-Pathogen Interaction
                Microbial Ecology
                Microbial Pathogens
                Pathogenesis
                Model Organisms
                Plant and Algal Models
                Prokaryotic Models
                Plant Science
                Plant Pathology
                Plant Pathogens
                Plants
                Algae

                Uncategorized
                Uncategorized

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