Nod factor and elicitors activate different phospholipid signaling pathways in suspension-cultured alfalfa cells

Lipo-chitooligosaccharides (Nod factors) are produced by symbiotic Rhizobium sp. bacteria to elicit Nod responses on their legume hosts. One of the earliest responses is the formation of phosphatidic acid (PA), a novel second messenger in plant cells. Remarkably, pathogens have also been reported to...

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Veröffentlicht in:Plant physiology (Bethesda) 2003-05, Vol.132 (1), p.311-317
Hauptverfasser: Hartog, M. den, Verhoef, N, Munnik, T
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description Lipo-chitooligosaccharides (Nod factors) are produced by symbiotic Rhizobium sp. bacteria to elicit Nod responses on their legume hosts. One of the earliest responses is the formation of phosphatidic acid (PA), a novel second messenger in plant cells. Remarkably, pathogens have also been reported to trigger the formation of PA in nonlegume plants. To investigate how host plants can distinguish between symbionts and pathogens, the effects of Nod factor and elicitors (chitotetraose and xylanase) on the formation of PA were investigated in suspension-cultured alfalfa (Medicago sativa) cells. Theoretically, PA can be synthesized via two signaling pathways, i.e. via phospholipase D (PLD) and via phospholipase C in combination with diacylglycerol (DAG) kinase. Therefore, a strategy involving differential radiolabeling with [32P]orthophosphate was used to determine the contribution of each pathway to PA formation. In support, PLD activity was specifically measured by using the ability of the enzyme to transfer the phosphatidyl group of its substrate to a primary alcohol. In practice, Nod factor, chitotetraose, and xylanase induced the formation of PA and its phosphorylated product DAG pyrophosphate within 2 min of treatment. However, whereas phospholipase C and DAG kinase were activated during treatment with all three different compounds, PLD was only activated by Nod factor. No evidence was obtained for the activation of phospholipase A2.
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One of the earliest responses is the formation of phosphatidic acid (PA), a novel second messenger in plant cells. Remarkably, pathogens have also been reported to trigger the formation of PA in nonlegume plants. To investigate how host plants can distinguish between symbionts and pathogens, the effects of Nod factor and elicitors (chitotetraose and xylanase) on the formation of PA were investigated in suspension-cultured alfalfa (Medicago sativa) cells. Theoretically, PA can be synthesized via two signaling pathways, i.e. via phospholipase D (PLD) and via phospholipase C in combination with diacylglycerol (DAG) kinase. Therefore, a strategy involving differential radiolabeling with [32P]orthophosphate was used to determine the contribution of each pathway to PA formation. In support, PLD activity was specifically measured by using the ability of the enzyme to transfer the phosphatidyl group of its substrate to a primary alcohol. In practice, Nod factor, chitotetraose, and xylanase induced the formation of PA and its phosphorylated product DAG pyrophosphate within 2 min of treatment. However, whereas phospholipase C and DAG kinase were activated during treatment with all three different compounds, PLD was only activated by Nod factor. No evidence was obtained for the activation of phospholipase A2.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.102.017954</identifier><identifier>PMID: 12746536</identifier><identifier>CODEN: PPHYA5</identifier><language>eng</language><publisher>Rockville, MD: American Society of Plant Biologists</publisher><subject>Agronomy. Soil science and plant productions ; Alfalfa ; Biological and medical sciences ; biosynthesis ; Calcium ; Cell Biology and Signal Transduction ; Cell physiology ; cell suspension culture ; Cells, Cultured ; chitotetraose ; diacylglycerol kinase ; Diacylglycerol Kinase - metabolism ; diacylglycerol pyrophosphate ; Diglycerides ; Diphosphates - metabolism ; Economic plant physiology ; forage legumes ; Fundamental and applied biological sciences. Psychology ; fungal diseases of plants ; Fungal plant pathogens ; Glycerol - analogs &amp; derivatives ; Glycerol - metabolism ; Glycerophospholipids - biosynthesis ; Lipids ; lipo-chitooligosaccharide ; Lipopolysaccharides - metabolism ; Lipopolysaccharides - pharmacology ; Medicago sativa ; Medicago sativa - cytology ; Medicago sativa - drug effects ; Medicago sativa - metabolism ; Molecular and cellular biology ; Nod factor ; nodulation factor ; oligosaccharides ; Oligosaccharides - pharmacology ; Parasitism and symbiosis ; Pathology, epidemiology, host-fungus relationships. Damages, economic importance ; phosphatidic acid ; Phosphatidic acids ; Phosphatidic Acids - biosynthesis ; phospholipase C ; phospholipase D ; Phospholipase D - metabolism ; Phospholipids ; Phospholipids - biosynthesis ; phosphotransferases (phosphomutases) ; Phytopathology. Animal pests. Plant and forest protection ; Plant cells ; plant pathogenic fungi ; Plant physiology and development ; Plants ; Rhizobium ; Signal Transduction ; Symbiosis ; Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...) ; Type C Phospholipases - metabolism ; Xylan Endo-1,3-beta-Xylosidase ; Xylosidases - pharmacology</subject><ispartof>Plant physiology (Bethesda), 2003-05, Vol.132 (1), p.311-317</ispartof><rights>Copyright 2003 American Society of Plant Biologists</rights><rights>2003 INIST-CNRS</rights><rights>Copyright © 2003, American Society of Plant Biologists 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-167498dd758e0e82657bafbb9b4a4c73a88f71dafa84d256f48eed691fca99d73</citedby><cites>FETCH-LOGICAL-c524t-167498dd758e0e82657bafbb9b4a4c73a88f71dafa84d256f48eed691fca99d73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4281099$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4281099$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,780,784,803,885,27915,27916,58008,58241</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14817973$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12746536$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hartog, M. den</creatorcontrib><creatorcontrib>Verhoef, N</creatorcontrib><creatorcontrib>Munnik, T</creatorcontrib><title>Nod factor and elicitors activate different phospholipid signaling pathways in suspension-cultured alfalfa cells</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>Lipo-chitooligosaccharides (Nod factors) are produced by symbiotic Rhizobium sp. bacteria to elicit Nod responses on their legume hosts. One of the earliest responses is the formation of phosphatidic acid (PA), a novel second messenger in plant cells. Remarkably, pathogens have also been reported to trigger the formation of PA in nonlegume plants. To investigate how host plants can distinguish between symbionts and pathogens, the effects of Nod factor and elicitors (chitotetraose and xylanase) on the formation of PA were investigated in suspension-cultured alfalfa (Medicago sativa) cells. Theoretically, PA can be synthesized via two signaling pathways, i.e. via phospholipase D (PLD) and via phospholipase C in combination with diacylglycerol (DAG) kinase. Therefore, a strategy involving differential radiolabeling with [32P]orthophosphate was used to determine the contribution of each pathway to PA formation. In support, PLD activity was specifically measured by using the ability of the enzyme to transfer the phosphatidyl group of its substrate to a primary alcohol. In practice, Nod factor, chitotetraose, and xylanase induced the formation of PA and its phosphorylated product DAG pyrophosphate within 2 min of treatment. However, whereas phospholipase C and DAG kinase were activated during treatment with all three different compounds, PLD was only activated by Nod factor. No evidence was obtained for the activation of phospholipase A2.</description><subject>Agronomy. Soil science and plant productions</subject><subject>Alfalfa</subject><subject>Biological and medical sciences</subject><subject>biosynthesis</subject><subject>Calcium</subject><subject>Cell Biology and Signal Transduction</subject><subject>Cell physiology</subject><subject>cell suspension culture</subject><subject>Cells, Cultured</subject><subject>chitotetraose</subject><subject>diacylglycerol kinase</subject><subject>Diacylglycerol Kinase - metabolism</subject><subject>diacylglycerol pyrophosphate</subject><subject>Diglycerides</subject><subject>Diphosphates - metabolism</subject><subject>Economic plant physiology</subject><subject>forage legumes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>fungal diseases of plants</subject><subject>Fungal plant pathogens</subject><subject>Glycerol - analogs &amp; derivatives</subject><subject>Glycerol - metabolism</subject><subject>Glycerophospholipids - biosynthesis</subject><subject>Lipids</subject><subject>lipo-chitooligosaccharide</subject><subject>Lipopolysaccharides - metabolism</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Medicago sativa</subject><subject>Medicago sativa - cytology</subject><subject>Medicago sativa - drug effects</subject><subject>Medicago sativa - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Nod factor</subject><subject>nodulation factor</subject><subject>oligosaccharides</subject><subject>Oligosaccharides - pharmacology</subject><subject>Parasitism and symbiosis</subject><subject>Pathology, epidemiology, host-fungus relationships. Damages, economic importance</subject><subject>phosphatidic acid</subject><subject>Phosphatidic acids</subject><subject>Phosphatidic Acids - biosynthesis</subject><subject>phospholipase C</subject><subject>phospholipase D</subject><subject>Phospholipase D - metabolism</subject><subject>Phospholipids</subject><subject>Phospholipids - biosynthesis</subject><subject>phosphotransferases (phosphomutases)</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>Plant cells</subject><subject>plant pathogenic fungi</subject><subject>Plant physiology and development</subject><subject>Plants</subject><subject>Rhizobium</subject><subject>Signal Transduction</subject><subject>Symbiosis</subject><subject>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</subject><subject>Type C Phospholipases - metabolism</subject><subject>Xylan Endo-1,3-beta-Xylosidase</subject><subject>Xylosidases - pharmacology</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk2PFCEQhonRuLOjR29GueitR6CBhsMezMZVk40edM-kho8ZNj3dCN1r9t_LpCe7ejKBUEU9VaniBaFXlGwoJfxDShtK2IbQTgv-BK2oaFnDBFdP0YqQahOl9Bk6L-WWEEJbyp-jM8o6LkUrVyh9Gx0OYKcxYxgc9n20sToF17t4B5PHLobgsx8mnPZjqbuPKTpc4m6APg47nGDa_4b7guOAy1ySH0och8bO_TRn7zD04biw9X1fXqBn1Sv-5elco5urTz8vvzTX3z9_vfx43VjB-NRQ2XGtnOuE8sQrJkW3hbDd6i0HbrsWlAoddRBAcceEDFx576SmwYLWrmvX6GKpm-btwTtb-8_Qm5TjAfK9GSGafyND3JvdeGeolLqTNf_9KT-Pv2ZfJnOI5TgBDH6ci-naljAuxH9BqhWVrVAVbBbQ5rGU7MNDM5SYo5YmpWoys2hZ-Td_T_BIn8SrwLsTAMXWF84w2FgeOa5qodrnGr1euNtSlX2Ic6Yo0bqG3y7hAKOBXa4lbn6w-lUIJYpQJds_zxu92A</recordid><startdate>20030501</startdate><enddate>20030501</enddate><creator>Hartog, M. den</creator><creator>Verhoef, N</creator><creator>Munnik, T</creator><general>American Society of Plant Biologists</general><general>American Society of Plant Physiologists</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030501</creationdate><title>Nod factor and elicitors activate different phospholipid signaling pathways in suspension-cultured alfalfa cells</title><author>Hartog, M. den ; Verhoef, N ; Munnik, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-167498dd758e0e82657bafbb9b4a4c73a88f71dafa84d256f48eed691fca99d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Agronomy. Soil science and plant productions</topic><topic>Alfalfa</topic><topic>Biological and medical sciences</topic><topic>biosynthesis</topic><topic>Calcium</topic><topic>Cell Biology and Signal Transduction</topic><topic>Cell physiology</topic><topic>cell suspension culture</topic><topic>Cells, Cultured</topic><topic>chitotetraose</topic><topic>diacylglycerol kinase</topic><topic>Diacylglycerol Kinase - metabolism</topic><topic>diacylglycerol pyrophosphate</topic><topic>Diglycerides</topic><topic>Diphosphates - metabolism</topic><topic>Economic plant physiology</topic><topic>forage legumes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>fungal diseases of plants</topic><topic>Fungal plant pathogens</topic><topic>Glycerol - analogs &amp; derivatives</topic><topic>Glycerol - metabolism</topic><topic>Glycerophospholipids - biosynthesis</topic><topic>Lipids</topic><topic>lipo-chitooligosaccharide</topic><topic>Lipopolysaccharides - metabolism</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Medicago sativa</topic><topic>Medicago sativa - cytology</topic><topic>Medicago sativa - drug effects</topic><topic>Medicago sativa - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Nod factor</topic><topic>nodulation factor</topic><topic>oligosaccharides</topic><topic>Oligosaccharides - pharmacology</topic><topic>Parasitism and symbiosis</topic><topic>Pathology, epidemiology, host-fungus relationships. Damages, economic importance</topic><topic>phosphatidic acid</topic><topic>Phosphatidic acids</topic><topic>Phosphatidic Acids - biosynthesis</topic><topic>phospholipase C</topic><topic>phospholipase D</topic><topic>Phospholipase D - metabolism</topic><topic>Phospholipids</topic><topic>Phospholipids - biosynthesis</topic><topic>phosphotransferases (phosphomutases)</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>Plant cells</topic><topic>plant pathogenic fungi</topic><topic>Plant physiology and development</topic><topic>Plants</topic><topic>Rhizobium</topic><topic>Signal Transduction</topic><topic>Symbiosis</topic><topic>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</topic><topic>Type C Phospholipases - metabolism</topic><topic>Xylan Endo-1,3-beta-Xylosidase</topic><topic>Xylosidases - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hartog, M. den</creatorcontrib><creatorcontrib>Verhoef, N</creatorcontrib><creatorcontrib>Munnik, T</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hartog, M. den</au><au>Verhoef, N</au><au>Munnik, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nod factor and elicitors activate different phospholipid signaling pathways in suspension-cultured alfalfa cells</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>2003-05-01</date><risdate>2003</risdate><volume>132</volume><issue>1</issue><spage>311</spage><epage>317</epage><pages>311-317</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>Lipo-chitooligosaccharides (Nod factors) are produced by symbiotic Rhizobium sp. bacteria to elicit Nod responses on their legume hosts. One of the earliest responses is the formation of phosphatidic acid (PA), a novel second messenger in plant cells. Remarkably, pathogens have also been reported to trigger the formation of PA in nonlegume plants. To investigate how host plants can distinguish between symbionts and pathogens, the effects of Nod factor and elicitors (chitotetraose and xylanase) on the formation of PA were investigated in suspension-cultured alfalfa (Medicago sativa) cells. Theoretically, PA can be synthesized via two signaling pathways, i.e. via phospholipase D (PLD) and via phospholipase C in combination with diacylglycerol (DAG) kinase. Therefore, a strategy involving differential radiolabeling with [32P]orthophosphate was used to determine the contribution of each pathway to PA formation. In support, PLD activity was specifically measured by using the ability of the enzyme to transfer the phosphatidyl group of its substrate to a primary alcohol. In practice, Nod factor, chitotetraose, and xylanase induced the formation of PA and its phosphorylated product DAG pyrophosphate within 2 min of treatment. However, whereas phospholipase C and DAG kinase were activated during treatment with all three different compounds, PLD was only activated by Nod factor. No evidence was obtained for the activation of phospholipase A2.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Biologists</pub><pmid>12746536</pmid><doi>10.1104/pp.102.017954</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; JSTOR
subjects Agronomy. Soil science and plant productions
Alfalfa
Biological and medical sciences
biosynthesis
Calcium
Cell Biology and Signal Transduction
Cell physiology
cell suspension culture
Cells, Cultured
chitotetraose
diacylglycerol kinase
Diacylglycerol Kinase - metabolism
diacylglycerol pyrophosphate
Diglycerides
Diphosphates - metabolism
Economic plant physiology
forage legumes
Fundamental and applied biological sciences. Psychology
fungal diseases of plants
Fungal plant pathogens
Glycerol - analogs & derivatives
Glycerol - metabolism
Glycerophospholipids - biosynthesis
Lipids
lipo-chitooligosaccharide
Lipopolysaccharides - metabolism
Lipopolysaccharides - pharmacology
Medicago sativa
Medicago sativa - cytology
Medicago sativa - drug effects
Medicago sativa - metabolism
Molecular and cellular biology
Nod factor
nodulation factor
oligosaccharides
Oligosaccharides - pharmacology
Parasitism and symbiosis
Pathology, epidemiology, host-fungus relationships. Damages, economic importance
phosphatidic acid
Phosphatidic acids
Phosphatidic Acids - biosynthesis
phospholipase C
phospholipase D
Phospholipase D - metabolism
Phospholipids
Phospholipids - biosynthesis
phosphotransferases (phosphomutases)
Phytopathology. Animal pests. Plant and forest protection
Plant cells
plant pathogenic fungi
Plant physiology and development
Plants
Rhizobium
Signal Transduction
Symbiosis
Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)
Type C Phospholipases - metabolism
Xylan Endo-1,3-beta-Xylosidase
Xylosidases - pharmacology
title Nod factor and elicitors activate different phospholipid signaling pathways in suspension-cultured alfalfa cells
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