Production of reactive oxygen species in Arabidopsis thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum: implications for basal resistance
The present understanding of ROS generation in the defence response of Arabidopsis thaliana is reviewed. Evidence suggests that the apoplastic oxidative burst generated during basal resistance is peroxidase-dependent. The ROS generated during this basal resistance may serve to activate NADPH oxidase...
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description | The present understanding of ROS generation in the defence response of Arabidopsis thaliana is reviewed. Evidence suggests that the apoplastic oxidative burst generated during basal resistance is peroxidase-dependent. The ROS generated during this basal resistance may serve to activate NADPH oxidase during the R-gene-mediated hypersensitive response. The processes involved in the production of reactive oxygen species in A. thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum are investigated in the present work. This system appears analogous to the production of ROS during the basal resistance response in French bean, which is peroxidase-dependent. A panel of modulators effective in other pathogen elicitor and plant cell systems has been used to investigate the Arabidopsis signalling pathways and the plant cell responses involved. Thus as in other systems, an early calcium influx into the cytosolic compartment, a rapid efflux of K⁺ and Cl⁻, and extracellular alkalinization of elicited cell cultures has been found. However the alkalinization is not sufficient to stimulate the apoplastic oxidative burst by itself, unlike in French bean, although vectorial ion fluxes are needed. A secretory component which is sensitive to monensin and N-ethylmaleimide and insensitive to brefeldin A may also be necessary for the release and provision of substrates for peroxidase-dependent generation of H₂O₂. |
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A panel of modulators effective in other pathogen elicitor and plant cell systems has been used to investigate the Arabidopsis signalling pathways and the plant cell responses involved. Thus as in other systems, an early calcium influx into the cytosolic compartment, a rapid efflux of K⁺ and Cl⁻, and extracellular alkalinization of elicited cell cultures has been found. However the alkalinization is not sufficient to stimulate the apoplastic oxidative burst by itself, unlike in French bean, although vectorial ion fluxes are needed. A secretory component which is sensitive to monensin and N-ethylmaleimide and insensitive to brefeldin A may also be necessary for the release and provision of substrates for peroxidase-dependent generation of H₂O₂.</description><identifier>ISSN: 0022-0957</identifier><identifier>EISSN: 1460-2431</identifier><identifier>DOI: 10.1093/jxb/erj216</identifier><identifier>PMID: 16720603</identifier><identifier>CODEN: JEBOA6</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>alkalinization ; Arabidopsis - metabolism ; Arabidopsis - microbiology ; Arabidopsis thaliana ; biochemical pathways ; Calcium ; Calcium - physiology ; Cell culture techniques ; Cell Death - physiology ; cell suspension culture ; Cell walls ; Cells, Cultured ; chlorides ; cultured cells ; Cyclic AMP - physiology ; cytosol ; disease resistance ; elicitation ; Exocytosis - physiology ; fungal diseases of plants ; fungal elicitors ; Fusarium ; Fusarium - physiology ; Fusarium oxysporum ; hydrogen peroxide ; Hydrogen-Ion Concentration ; hypersensitive response ; ion transport ; Modulated signal processing ; NADH or NADPH oxidoreductases ; Oxidases ; oxidative burst ; Pathogens ; peroxidases ; Plant cells ; Plant Diseases ; plant pathogenic fungi ; Plants ; potassium ; Potassium - physiology ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; resistance mechanisms ; secretion ; Signal Transduction</subject><ispartof>Journal of experimental botany, 2006-01, Vol.57 (8), p.1817-1827</ispartof><rights>Society for Experimental Biology 2006</rights><rights>Copyright Oxford University Press(England) May 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-90e4113570d8aa07c9088d19659c4125047d7d288c539f71456853968ee8cd643</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24036140$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24036140$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16720603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Davies, Dewi R</creatorcontrib><creatorcontrib>Bindschedler, Laurence V</creatorcontrib><creatorcontrib>Strickland, Tony S</creatorcontrib><creatorcontrib>Bolwell, G. Paul</creatorcontrib><title>Production of reactive oxygen species in Arabidopsis thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum: implications for basal resistance</title><title>Journal of experimental botany</title><addtitle>J Exp Bot</addtitle><description>The present understanding of ROS generation in the defence response of Arabidopsis thaliana is reviewed. Evidence suggests that the apoplastic oxidative burst generated during basal resistance is peroxidase-dependent. The ROS generated during this basal resistance may serve to activate NADPH oxidase during the R-gene-mediated hypersensitive response. The processes involved in the production of reactive oxygen species in A. thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum are investigated in the present work. This system appears analogous to the production of ROS during the basal resistance response in French bean, which is peroxidase-dependent. A panel of modulators effective in other pathogen elicitor and plant cell systems has been used to investigate the Arabidopsis signalling pathways and the plant cell responses involved. Thus as in other systems, an early calcium influx into the cytosolic compartment, a rapid efflux of K⁺ and Cl⁻, and extracellular alkalinization of elicited cell cultures has been found. However the alkalinization is not sufficient to stimulate the apoplastic oxidative burst by itself, unlike in French bean, although vectorial ion fluxes are needed. A secretory component which is sensitive to monensin and N-ethylmaleimide and insensitive to brefeldin A may also be necessary for the release and provision of substrates for peroxidase-dependent generation of H₂O₂.</description><subject>alkalinization</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis - microbiology</subject><subject>Arabidopsis thaliana</subject><subject>biochemical pathways</subject><subject>Calcium</subject><subject>Calcium - physiology</subject><subject>Cell culture techniques</subject><subject>Cell Death - physiology</subject><subject>cell suspension culture</subject><subject>Cell walls</subject><subject>Cells, Cultured</subject><subject>chlorides</subject><subject>cultured cells</subject><subject>Cyclic AMP - physiology</subject><subject>cytosol</subject><subject>disease resistance</subject><subject>elicitation</subject><subject>Exocytosis - physiology</subject><subject>fungal diseases of plants</subject><subject>fungal elicitors</subject><subject>Fusarium</subject><subject>Fusarium - physiology</subject><subject>Fusarium oxysporum</subject><subject>hydrogen peroxide</subject><subject>Hydrogen-Ion Concentration</subject><subject>hypersensitive response</subject><subject>ion transport</subject><subject>Modulated signal processing</subject><subject>NADH or NADPH oxidoreductases</subject><subject>Oxidases</subject><subject>oxidative burst</subject><subject>Pathogens</subject><subject>peroxidases</subject><subject>Plant cells</subject><subject>Plant Diseases</subject><subject>plant pathogenic fungi</subject><subject>Plants</subject><subject>potassium</subject><subject>Potassium - physiology</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>resistance mechanisms</subject><subject>secretion</subject><subject>Signal Transduction</subject><issn>0022-0957</issn><issn>1460-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGL1DAUxoso7jh68a4GDx6Eui9JkybelsF1hAUFd0W8hEyarhnbpps0Mvs_-Uea2mEFL17yHny_fMl7X1E8xfAGg6Sn-8Pu1IY9wfxescIVh5JUFN8vVgCElCBZfVI8inEPAAwYe1icYF4T4EBXxa9PwTfJTM4PyLcoWJ37nxb5w-21HVAcrXE2Ijegs6B3rvFjdBFN33Xn9KCRsV2HYsrYEGcLk7opheVCLqMfokWTR3pAtnPGTT6gNvgenaeog0v9_FDGQurfItePmdHzXyJqM7nTUXezj4uTHox9XDxodRftk2NdF1fn7y432_Li4_sPm7OL0jAip1KCrTCmrIZGaA21kSBEgyVn0lSYMKjqpm6IEIZR2da4YlzkjgtrhWl4RdfFq8V3DP4m2Tip3sV5VD1Yn6LiAiosSP1fEEsiJP3j-PIfcO9TGPIQilAGmAHhGXq9QCb4GINt1Rhcr8OtwqDmpFVOWi1JZ_j50THtetv8RY_RZuDZAuxj3vqdTiqgHOdjXZSLnpdrD3e6Dj8Ur2nN1PbrNyUF-UI2l1s18y8WvtVe6evgorr6TABTwFBLRgj9DfcWyV4</recordid><startdate>20060101</startdate><enddate>20060101</enddate><creator>Davies, Dewi R</creator><creator>Bindschedler, Laurence V</creator><creator>Strickland, Tony S</creator><creator>Bolwell, G. Paul</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>FBQ</scope><scope>BSCLL</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>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>20060101</creationdate><title>Production of reactive oxygen species in Arabidopsis thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum: implications for basal resistance</title><author>Davies, Dewi R ; Bindschedler, Laurence V ; Strickland, Tony S ; Bolwell, G. Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-90e4113570d8aa07c9088d19659c4125047d7d288c539f71456853968ee8cd643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>alkalinization</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis - microbiology</topic><topic>Arabidopsis thaliana</topic><topic>biochemical pathways</topic><topic>Calcium</topic><topic>Calcium - physiology</topic><topic>Cell culture techniques</topic><topic>Cell Death - physiology</topic><topic>cell suspension culture</topic><topic>Cell walls</topic><topic>Cells, Cultured</topic><topic>chlorides</topic><topic>cultured cells</topic><topic>Cyclic AMP - physiology</topic><topic>cytosol</topic><topic>disease resistance</topic><topic>elicitation</topic><topic>Exocytosis - physiology</topic><topic>fungal diseases of plants</topic><topic>fungal elicitors</topic><topic>Fusarium</topic><topic>Fusarium - physiology</topic><topic>Fusarium oxysporum</topic><topic>hydrogen peroxide</topic><topic>Hydrogen-Ion Concentration</topic><topic>hypersensitive response</topic><topic>ion transport</topic><topic>Modulated signal processing</topic><topic>NADH or NADPH oxidoreductases</topic><topic>Oxidases</topic><topic>oxidative burst</topic><topic>Pathogens</topic><topic>peroxidases</topic><topic>Plant cells</topic><topic>Plant Diseases</topic><topic>plant pathogenic fungi</topic><topic>Plants</topic><topic>potassium</topic><topic>Potassium - physiology</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>resistance mechanisms</topic><topic>secretion</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Davies, Dewi R</creatorcontrib><creatorcontrib>Bindschedler, Laurence V</creatorcontrib><creatorcontrib>Strickland, Tony S</creatorcontrib><creatorcontrib>Bolwell, G. 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Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of reactive oxygen species in Arabidopsis thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum: implications for basal resistance</atitle><jtitle>Journal of experimental botany</jtitle><addtitle>J Exp Bot</addtitle><date>2006-01-01</date><risdate>2006</risdate><volume>57</volume><issue>8</issue><spage>1817</spage><epage>1827</epage><pages>1817-1827</pages><issn>0022-0957</issn><eissn>1460-2431</eissn><coden>JEBOA6</coden><abstract>The present understanding of ROS generation in the defence response of Arabidopsis thaliana is reviewed. Evidence suggests that the apoplastic oxidative burst generated during basal resistance is peroxidase-dependent. The ROS generated during this basal resistance may serve to activate NADPH oxidase during the R-gene-mediated hypersensitive response. The processes involved in the production of reactive oxygen species in A. thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum are investigated in the present work. This system appears analogous to the production of ROS during the basal resistance response in French bean, which is peroxidase-dependent. A panel of modulators effective in other pathogen elicitor and plant cell systems has been used to investigate the Arabidopsis signalling pathways and the plant cell responses involved. Thus as in other systems, an early calcium influx into the cytosolic compartment, a rapid efflux of K⁺ and Cl⁻, and extracellular alkalinization of elicited cell cultures has been found. However the alkalinization is not sufficient to stimulate the apoplastic oxidative burst by itself, unlike in French bean, although vectorial ion fluxes are needed. A secretory component which is sensitive to monensin and N-ethylmaleimide and insensitive to brefeldin A may also be necessary for the release and provision of substrates for peroxidase-dependent generation of H₂O₂.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>16720603</pmid><doi>10.1093/jxb/erj216</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alkalinization Arabidopsis - metabolism Arabidopsis - microbiology Arabidopsis thaliana biochemical pathways Calcium Calcium - physiology Cell culture techniques Cell Death - physiology cell suspension culture Cell walls Cells, Cultured chlorides cultured cells Cyclic AMP - physiology cytosol disease resistance elicitation Exocytosis - physiology fungal diseases of plants fungal elicitors Fusarium Fusarium - physiology Fusarium oxysporum hydrogen peroxide Hydrogen-Ion Concentration hypersensitive response ion transport Modulated signal processing NADH or NADPH oxidoreductases Oxidases oxidative burst Pathogens peroxidases Plant cells Plant Diseases plant pathogenic fungi Plants potassium Potassium - physiology Reactive oxygen species Reactive Oxygen Species - metabolism resistance mechanisms secretion Signal Transduction |
title | Production of reactive oxygen species in Arabidopsis thaliana cell suspension cultures in response to an elicitor from Fusarium oxysporum: implications for basal resistance |
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