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<title>PLANT PHYSIOLOGY PLANTS INTERACTING WITH OTHER ORGANISMS</title>
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<prism:eIssn>1532-2548</prism:eIssn>
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<title>PLANT PHYSIOLOGY</title>
<url>http://www.plantphysiol.org/icons/banner/title.gif</url>
<link>http://www.plantphysiol.org</link>
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<item rdf:about="http://www.plantphysiol.org/cgi/content/short/151/3/1459?rss=1">
<title><![CDATA[Dual Roles of Reactive Oxygen Species and NADPH Oxidase RBOHD in an Arabidopsis-Alternaria Pathosystem]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/151/3/1459?rss=1</link>
<description><![CDATA[
<p>Arabidopsis (<I>Arabidopsis thaliana</I>) NADPH oxidases have been reported to suppress the spread of pathogen- and salicylic acid-induced cell death. Here, we present dual roles of RBOHD (for respiratory burst oxidase homolog D) in an Arabidopsis-<I>Alternaria</I> pathosystem, suggesting either initiation or prevention of cell death dependent on the distance from pathogen attack. Our data demonstrate that a <I>rbohD</I> knockout mutant exhibits increased spread of cell death at the macroscopic level upon inoculation with the fungus <I>Alternaria brassicicola</I>. However, the cellular patterns of reactive oxygen species accumulation and cell death are fundamentally different in the <I>AtrbohD</I> mutant compared with the wild type. Functional RBOHD causes marked extracellular hydrogen peroxide accumulation as well as cell death in distinct, single cells of <I>A. brassicicola</I>-infected wild-type plants. This single cell response is missing in the <I>AtrbohD</I> mutant, where infection triggers spreading-type necrosis preceded by less distinct chloroplastic hydrogen peroxide accumulation in large clusters of cells. While the salicylic acid analog benzothiadiazole induces the action of RBOHD and the development of cell death in infected tissues, the ethylene inhibitor aminoethoxyvinylglycine inhibits cell death, indicating that both salicylic acid and ethylene positively regulate RBOHD and cell death. Moreover, <I>A. brassicicola</I>-infected <I>AtrbohD</I> plants hyperaccumulate ethylene and free salicylic acid compared with the wild type, suggesting negative feedback regulation of salicylic acid and ethylene by RBOHD. We propose that functional RBOHD triggers death in cells that are damaged by fungal infection but simultaneously inhibits death in neighboring cells through the suppression of free salicylic acid and ethylene levels.</p>
]]></description>
<dc:creator><![CDATA[Pogany, M., von Rad, U., Grun, S., Dongo, A., Pintye, A., Simoneau, P., Bahnweg, G., Kiss, L., Barna, B., Durner, J.]]></dc:creator>
<dc:date>Tue, 03 Nov 2009 12:22:27 PST</dc:date>
<dc:identifier>info:doi/10.1104/pp.109.141994</dc:identifier>
<dc:title><![CDATA[Dual Roles of Reactive Oxygen Species and NADPH Oxidase RBOHD in an Arabidopsis-Alternaria Pathosystem]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>3</prism:number>
<prism:volume>151</prism:volume>
<prism:endingPage>1475</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1459</prism:startingPage>
<prism:section>PLANTS INTERACTING WITH OTHER ORGANISMS</prism:section>
</item>

<item rdf:about="http://www.plantphysiol.org/cgi/content/short/151/2/792?rss=1">
<title><![CDATA[Plant-Derived Sucrose Is a Key Element in the Symbiotic Association between Trichoderma virens and Maize Plants]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/151/2/792?rss=1</link>
<description><![CDATA[
<p>Fungal species belonging to the genus <I>Trichoderma</I> colonize the rhizosphere of many plants, resulting in beneficial effects such as increased resistance to pathogens and greater yield and productivity. However, the molecular mechanisms that govern the recognition and association between <I>Trichoderma</I> and their hosts are still largely unknown. In this report, we demonstrate that plant-derived sucrose (Suc) is an important resource provided to <I>Trichoderma</I> cells and is also associated with the control of root colonization. We describe the identification and characterization of an intracellular invertase from <I>Trichoderma virens</I> (TvInv) important for the mechanisms that control the symbiotic association and fungal growth in the presence of Suc. Gene expression studies revealed that the hydrolysis of plant-derived Suc in <I>T. virens</I> is necessary for the up-regulation of Sm1, the <I>Trichoderma</I>-secreted elicitor that systemically activates the defense mechanisms in leaves. We determined that as a result of colonization of maize (<I>Zea mays</I>) roots by <I>T. virens</I>, photosynthetic rate increases in leaves and the functional expression of <I>tvinv</I> is crucial for such effect. In agreement, the steady-state levels of mRNA for Rubisco small subunit and the oxygen-evolving enhancer 3-1 were increased in leaves of plants colonized by wild-type <I>T. virens</I>. We conclude that during the symbiosis, the sucrolytic activity in the fungal cells affects the sink activity of roots, directing carbon partitioning toward roots and increasing the rate of photosynthesis in leaves. A discussion of the role of Suc in controlling the fungal proliferation on roots and its pivotal role in the coordination of plant-microbe associations is provided.</p>
]]></description>
<dc:creator><![CDATA[Vargas, W. A., Mandawe, J. C., Kenerley, C. M.]]></dc:creator>
<dc:date>Thu, 01 Oct 2009 06:20:41 PDT</dc:date>
<dc:identifier>info:doi/10.1104/pp.109.141291</dc:identifier>
<dc:title><![CDATA[Plant-Derived Sucrose Is a Key Element in the Symbiotic Association between Trichoderma virens and Maize Plants]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>151</prism:volume>
<prism:endingPage>808</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>792</prism:startingPage>
<prism:section>PLANTS INTERACTING WITH OTHER ORGANISMS</prism:section>
</item>

<item rdf:about="http://www.plantphysiol.org/cgi/content/short/151/2/809?rss=1">
<title><![CDATA[Live-Cell Imaging Reveals Periarbuscular Membrane Domains and Organelle Location in Medicago truncatula Roots during Arbuscular Mycorrhizal Symbiosis]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/151/2/809?rss=1</link>
<description><![CDATA[
<p>In the arbuscular mycorrhizal symbiosis, the fungal symbiont colonizes root cortical cells, where it establishes differentiated hyphae called arbuscules. As each arbuscule develops, the cortical cell undergoes a transient reorganization and envelops the arbuscule in a novel symbiosis-specific membrane, called the periarbuscular membrane. The periarbuscular membrane, which is continuous with the plant plasma membrane of the cortical cell, is a key interface in the symbiosis; however, relatively little is known of its composition or the mechanisms of its development. Here, we used fluorescent protein fusions to obtain both spatial and temporal information about the protein composition of the periarbuscular membrane. The data indicate that the periarbuscular membrane is composed of at least two distinct domains, an "arbuscule branch domain" that contains the symbiosis-specific phosphate transporter, MtPT4, and an "arbuscule trunk domain" that contains MtBcp1. This suggests a developmental transition from plasma membrane to periarbuscular membrane, with biogenesis of a novel membrane domain associated with the repeated dichotomous branching of the hyphae. Additionally, we took advantage of available organelle-specific fluorescent marker proteins to further evaluate cells during arbuscule development and degeneration. The three-dimensional data provide new insights into relocation of Golgi and peroxisomes and also illustrate that cells with arbuscules can retain a large continuous vacuolar system throughout development.</p>
]]></description>
<dc:creator><![CDATA[Pumplin, N., Harrison, M. J.]]></dc:creator>
<dc:date>Thu, 01 Oct 2009 06:20:41 PDT</dc:date>
<dc:identifier>info:doi/10.1104/pp.109.141879</dc:identifier>
<dc:title><![CDATA[Live-Cell Imaging Reveals Periarbuscular Membrane Domains and Organelle Location in Medicago truncatula Roots during Arbuscular Mycorrhizal Symbiosis]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>151</prism:volume>
<prism:endingPage>819</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>809</prism:startingPage>
<prism:section>PLANTS INTERACTING WITH OTHER ORGANISMS</prism:section>
</item>

<item rdf:about="http://www.plantphysiol.org/cgi/content/short/151/2/820?rss=1">
<title><![CDATA[Extracellular DNA Is Required for Root Tip Resistance to Fungal Infection]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/151/2/820?rss=1</link>
<description><![CDATA[
<p>Plant defense involves a complex array of biochemical interactions, many of which occur in the extracellular environment. The apical 1- to 2-mm root tip housing apical and root cap meristems is resistant to infection by most pathogens, so growth and gravity sensing often proceed normally even when other sites on the root are invaded. The mechanism of this resistance is unknown but appears to involve a mucilaginous matrix or "slime" composed of proteins, polysaccharides, and detached living cells called "border cells." Here, we report that extracellular DNA (exDNA) is a component of root cap slime and that exDNA degradation during inoculation by a fungal pathogen results in loss of root tip resistance to infection. Most root tips (&gt;95%) escape infection even when immersed in inoculum from the root-rotting pathogen <I>Nectria haematococca</I>. By contrast, 100% of inoculated root tips treated with DNase I developed necrosis. Treatment with BAL31, an exonuclease that digests DNA more slowly than DNase I, also resulted in increased root tip infection, but the onset of infection was delayed. Control root tips or fungal spores treated with nuclease alone exhibited normal morphology and growth. Pea (<I>Pisum sativum</I>) root tips incubated with [<sup>32</sup>P]dCTP during a 1-h period when no cell death occurs yielded root cap slime containing <sup>32</sup>P-labeled exDNA. Our results suggest that exDNA is a previously unrecognized component of plant defense, an observation that is in accordance with the recent discovery that exDNA from white blood cells plays a key role in the vertebrate immune response against microbial pathogens.</p>
]]></description>
<dc:creator><![CDATA[Wen, F., White, G. J., VanEtten, H. D., Xiong, Z., Hawes, M. C.]]></dc:creator>
<dc:date>Thu, 01 Oct 2009 06:20:41 PDT</dc:date>
<dc:identifier>info:doi/10.1104/pp.109.142067</dc:identifier>
<dc:title><![CDATA[Extracellular DNA Is Required for Root Tip Resistance to Fungal Infection]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>151</prism:volume>
<prism:endingPage>829</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>820</prism:startingPage>
<prism:section>PLANTS INTERACTING WITH OTHER ORGANISMS</prism:section>
</item>

<item rdf:about="http://www.plantphysiol.org/cgi/content/short/151/2/925?rss=1">
<title><![CDATA[The Role of Specific Tomato Volatiles in Tomato-Whitefly Interaction]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/151/2/925?rss=1</link>
<description><![CDATA[
<p><I>Bemisia tabaci</I> (whitefly) infestations and the subsequent transfer of viruses are the cause of severe losses in crop production and horticultural practice. To improve biological control of <I>B. tabaci</I>, we investigated repellent properties of plant-produced semiochemicals. The mix of headspace volatiles, collected from naturally repellent wild tomato accessions, influenced <I>B. tabaci</I> initial choice behavior, indicating a role for plant semiochemicals in locating host plants. A collection of wild tomato accessions and introgression lines (<I>Solanum pennellii</I> LA716 <FONT FACE="arial,helvetica">x</FONT> <I>Solanum lycopersicum</I> &lsquo;Moneyberg&rsquo;) were extensively screened for attractiveness to <I>B. tabaci</I>, and their headspace profiles were determined by means of gas chromatography-mass spectrometry. Correlation analysis revealed that several terpenoids were putatively involved in tomato-whitefly interactions. Several of these candidate compounds conferred repellence to otherwise attractive tomato plants when applied to the plant's branches on paper cards. The sesquiterpenes zingiberene and curcumene and the monoterpenes <I>p</I>-cymene, <I></I>-terpinene, and <I></I>-phellandrene had the strongest effects in free-choice bioassays. These terpenes also elicited a response of receptors on the insect's antennae as determined by electroantennography. Conversely, the monoterpene <I>&beta;</I>-myrcene showed no activity in both assays. <I>B. tabaci</I> apparently uses, besides visual cues, specific plant volatile cues for the initial selection of a host. Altering whitefly choice behavior by manipulation of the terpenoid composition of the host headspace may therefore be feasible.</p>
]]></description>
<dc:creator><![CDATA[Bleeker, P. M., Diergaarde, P. J., Ament, K., Guerra, J., Weidner, M., Schutz, S., de Both, M. T.J., Haring, M. A., Schuurink, R. C.]]></dc:creator>
<dc:date>Thu, 01 Oct 2009 06:20:41 PDT</dc:date>
<dc:subject><![CDATA[Plant-Herbivore Interactions]]></dc:subject>
<dc:identifier>info:doi/10.1104/pp.109.142661</dc:identifier>
<dc:title><![CDATA[The Role of Specific Tomato Volatiles in Tomato-Whitefly Interaction]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>151</prism:volume>
<prism:endingPage>935</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>925</prism:startingPage>
<prism:section>PLANTS INTERACTING WITH OTHER ORGANISMS</prism:section>
</item>

<item rdf:about="http://www.plantphysiol.org/cgi/content/short/151/2/936?rss=1">
<title><![CDATA[A Pair of Allelic WRKY Genes Play Opposite Roles in Rice-Bacteria Interactions]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/151/2/936?rss=1</link>
<description><![CDATA[
<p>Although allelic diversity of genes has been reported to play important roles in different physiological processes, information on allelic diversity of defense-responsive genes in host-pathogen interactions is limited. Here, we report that a pair of allelic genes, <I>OsWRKY45-1</I> and <I>OsWRKY45-2</I>, which encode proteins with a 10-amino acid difference, play opposite roles in rice (<I>Oryza sativa</I>) resistance against bacterial pathogens. Bacterial blight caused by <I>Xanthomonas</I> <I>oryzae</I> pv <I>oryzae</I> (<I>Xoo</I>), bacterial streak caused by <I>Xanthomonas oryzae</I> pv <I>oryzicola</I> (<I>Xoc</I>), and fungal blast caused by <I>Magnaporthe grisea</I> are devastating diseases of rice worldwide. <I>OsWRKY45-1</I>-overexpressing plants showed increased susceptibility and <I>OsWRKY45-1</I>-knockout plants showed enhanced resistance to <I>Xoo</I> and <I>Xoc</I>. In contrast, <I>OsWRKY45-2</I>-overexpressing plants showed enhanced resistance and <I>OsWRKY45-2</I>-suppressing plants showed increased susceptibility to <I>Xoo</I> and <I>Xoc</I>. Interestingly, both <I>OsWRKY45-1-</I> and <I>OsWRKY45-2</I>-overexpressing plants showed enhanced resistance to <I>M. grisea</I>. OsWRKY45-1-regulated <I>Xoo</I> resistance was accompanied by increased accumulation of salicylic acid and jasmonic acid and induced expression of a subset of defense-responsive genes, while OsWRKY45-2-regulated <I>Xoo</I> resistance was accompanied by increased accumulation of jasmonic acid but not salicylic acid and induced expression of another subset of defense-responsive genes. These results suggest that both OsWRKY45-1 and OsWRKY45-2 are positive regulators in rice resistance against <I>M. grisea</I>, but the former is a negative regulator and the latter is a positive regulator in rice resistance against <I>Xoo</I> and <I>Xoc</I>. The opposite roles of the two allelic genes in rice-<I>Xoo</I> interaction appear to be due to their mediation of different defense signaling pathways.</p>
]]></description>
<dc:creator><![CDATA[Tao, Z., Liu, H., Qiu, D., Zhou, Y., Li, X., Xu, C., Wang, S.]]></dc:creator>
<dc:date>Thu, 01 Oct 2009 06:20:41 PDT</dc:date>
<dc:subject><![CDATA[The Grasses]]></dc:subject>
<dc:identifier>info:doi/10.1104/pp.109.145623</dc:identifier>
<dc:title><![CDATA[A Pair of Allelic WRKY Genes Play Opposite Roles in Rice-Bacteria Interactions]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>151</prism:volume>
<prism:endingPage>948</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>936</prism:startingPage>
<prism:section>PLANTS INTERACTING WITH OTHER ORGANISMS</prism:section>
</item>

<item rdf:about="http://www.plantphysiol.org/cgi/content/short/151/1/290?rss=1">
<title><![CDATA[The Arabidopsis RESURRECTION1 Gene Regulates a Novel Antagonistic Interaction in Plant Defense to Biotrophs and Necrotrophs]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/151/1/290?rss=1</link>
<description><![CDATA[
<p>We report a role for the Arabidopsis (<I>Arabidopsis thaliana</I>) <I>RESURRECTION1</I> (<I>RST1</I>) gene in plant defense. The <I>rst1</I> mutant exhibits enhanced susceptibility to the biotrophic fungal pathogen <I>Erysiphe cichoracearum</I> but enhanced resistance to the necrotrophic fungal pathogens <I>Botrytis cinerea</I> and <I>Alternaria brassicicola. RST1</I> encodes a novel protein that localizes to the plasma membrane and is predicted to contain 11 transmembrane domains. Disease responses in <I>rst1</I> correlate with higher levels of jasmonic acid (JA) and increased basal and <I>B. cinerea</I>-induced expression of the plant defensin <I>PDF1.2</I> gene but reduced <I>E. cichoracearum</I>-inducible salicylic acid levels and expression of pathogenesis-related genes <I>PR1</I> and <I>PR2</I>. These results are consistent with <I>rst1</I>'s varied resistance and susceptibility to pathogens of different life styles. Cuticular lipids, both cutin monomers and cuticular waxes, on <I>rst1</I> leaves were significantly elevated, indicating a role for <I>RST1</I> in the suppression of leaf cuticle lipid synthesis. The <I>rst1</I> cuticle exhibits normal permeability, however, indicating that the disease responses of <I>rst1</I> are not due to changes in this cuticle property. Double mutant analysis revealed that the <I>coi1</I> mutation (causing defective JA signaling) is completely epistatic to <I>rst1</I>, whereas the <I>ein2</I> mutation (causing defective ethylene signaling) is partially epistatic to <I>rst1</I>, for resistance to <I>B. cinerea</I>. The <I>rst1</I> mutation thus defines a unique combination of disease responses to biotrophic and necrotrophic fungi in that it antagonizes salicylic acid-dependent defense and enhances JA-mediated defense through a mechanism that also controls cuticle synthesis.</p>
]]></description>
<dc:creator><![CDATA[Mang, H. G., Laluk, K. A., Parsons, E. P., Kosma, D. K., Cooper, B. R., Park, H. C., AbuQamar, S., Boccongelli, C., Miyazaki, S., Consiglio, F., Chilosi, G., Bohnert, H. J., Bressan, R. A., Mengiste, T., Jenks, M. A.]]></dc:creator>
<dc:date>Wed, 02 Sep 2009 10:00:32 PDT</dc:date>
<dc:identifier>info:doi/10.1104/pp.109.142158</dc:identifier>
<dc:title><![CDATA[The Arabidopsis RESURRECTION1 Gene Regulates a Novel Antagonistic Interaction in Plant Defense to Biotrophs and Necrotrophs]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>1</prism:number>
<prism:volume>151</prism:volume>
<prism:endingPage>305</prism:endingPage>
<prism:publicationDate>2009-09-01</prism:publicationDate>
<prism:startingPage>290</prism:startingPage>
<prism:section>PLANTS INTERACTING WITH OTHER ORGANISMS</prism:section>
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