Mycorrhiza-induced lower oxidative burst is related with higher antioxidant enzyme activities, net H2O2 effluxes, and Ca2+ influxes in trifoliate orange roots under drought stress.
Identifieur interne : 001778 ( Main/Corpus ); précédent : 001777; suivant : 001779Mycorrhiza-induced lower oxidative burst is related with higher antioxidant enzyme activities, net H2O2 effluxes, and Ca2+ influxes in trifoliate orange roots under drought stress.
Auteurs : Ying-Ning Zou ; Yong-Ming Huang ; Qiang-Sheng Wu ; Xin-Hua HeSource :
- Mycorrhiza [ 1432-1890 ] ; 2015.
English descriptors
- KwdEn :
- Antioxidants (metabolism), Biological Transport (MeSH), Calcium (metabolism), Catalase (metabolism), Citrus (enzymology), Citrus (metabolism), Citrus (microbiology), Droughts (MeSH), Glomeromycota (growth & development), Hydrogen Peroxide (metabolism), Mycorrhizae (growth & development), Plant Proteins (metabolism), Respiratory Burst (MeSH), Superoxide Dismutase (metabolism).
- MESH :
- chemical , metabolism : Antioxidants, Calcium, Catalase, Hydrogen Peroxide, Plant Proteins, Superoxide Dismutase.
- enzymology : Citrus.
- growth & development : Glomeromycota, Mycorrhizae.
- metabolism : Citrus.
- microbiology : Citrus.
- Biological Transport, Droughts, Respiratory Burst.
Abstract
Mechanisms of arbuscular mycorrhiza (AM)-induced lower oxidative burst of host plants under drought stress (DS) are not elucidated. A noninvasive microtest technology (NMT) was used to investigate the effects of Funneliformis mosseae on net fluxes of root hydrogen peroxide (H2O2) and calcium ions (Ca2+) in 5-month-old Poncirus trifoliata, in combination with catalase (CAT) and superoxide dismutase (SOD) activities as well as tissue superoxide radical (O2•-) and H2O2 concentrations under DS and well-watered (WW) conditions. A 2-month DS (55% maximum water holding capacity of growth substrates) significantly inhibited AM fungal root colonization, while AM symbiosis significantly increased plant biomass production, irrespective of water status. F. mosseae inoculation generally increased SOD and CAT activity but decreased O2•- and H2O2 concentrations in leaves and roots under WW and DS. Compared with non-AM seedlings, roots of AM seedlings had significantly higher net H2O2 effluxes and net Ca2+ influxes, especially in the meristem zone, but lower net H2O2 efflux in the elongation zone. Net Ca2+ influxes into roots were significantly positively correlated with root net H2O2 effluxes but negatively with root H2O2 concentrations. Results from this study suggest that AM-induced lower oxidative burst is related with higher antioxidant enzyme activities, root net H2O2 effluxes, and Ca2+ influxes under WW and DS.
DOI: 10.1007/s00572-014-0598-z
PubMed: 25085218
Links to Exploration step
pubmed:25085218Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Mycorrhiza-induced lower oxidative burst is related with higher antioxidant enzyme activities, net H2O2 effluxes, and Ca2+ influxes in trifoliate orange roots under drought stress.</title><author><name sortKey="Zou, Ying Ning" sort="Zou, Ying Ning" uniqKey="Zou Y" first="Ying-Ning" last="Zou">Ying-Ning Zou</name><affiliation><nlm:affiliation>College of Horticulture and Gardening/Institute of Root Biology, Yangtze University, 88 Jingmi Road, Jingzhou, Hubei, 434025, People's Republic of China.</nlm:affiliation></affiliation></author><author><name sortKey="Huang, Yong Ming" sort="Huang, Yong Ming" uniqKey="Huang Y" first="Yong-Ming" last="Huang">Yong-Ming Huang</name></author><author><name sortKey="Wu, Qiang Sheng" sort="Wu, Qiang Sheng" uniqKey="Wu Q" first="Qiang-Sheng" last="Wu">Qiang-Sheng Wu</name></author><author><name sortKey="He, Xin Hua" sort="He, Xin Hua" uniqKey="He X" first="Xin-Hua" last="He">Xin-Hua He</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2015">2015</date><idno type="RBID">pubmed:25085218</idno><idno type="pmid">25085218</idno><idno type="doi">10.1007/s00572-014-0598-z</idno><idno type="wicri:Area/Main/Corpus">001778</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">001778</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Mycorrhiza-induced lower oxidative burst is related with higher antioxidant enzyme activities, net H2O2 effluxes, and Ca2+ influxes in trifoliate orange roots under drought stress.</title><author><name sortKey="Zou, Ying Ning" sort="Zou, Ying Ning" uniqKey="Zou Y" first="Ying-Ning" last="Zou">Ying-Ning Zou</name><affiliation><nlm:affiliation>College of Horticulture and Gardening/Institute of Root Biology, Yangtze University, 88 Jingmi Road, Jingzhou, Hubei, 434025, People's Republic of China.</nlm:affiliation></affiliation></author><author><name sortKey="Huang, Yong Ming" sort="Huang, Yong Ming" uniqKey="Huang Y" first="Yong-Ming" last="Huang">Yong-Ming Huang</name></author><author><name sortKey="Wu, Qiang Sheng" sort="Wu, Qiang Sheng" uniqKey="Wu Q" first="Qiang-Sheng" last="Wu">Qiang-Sheng Wu</name></author><author><name sortKey="He, Xin Hua" sort="He, Xin Hua" uniqKey="He X" first="Xin-Hua" last="He">Xin-Hua He</name></author></analytic><series><title level="j">Mycorrhiza</title><idno type="eISSN">1432-1890</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antioxidants (metabolism)</term><term>Biological Transport (MeSH)</term><term>Calcium (metabolism)</term><term>Catalase (metabolism)</term><term>Citrus (enzymology)</term><term>Citrus (metabolism)</term><term>Citrus (microbiology)</term><term>Droughts (MeSH)</term><term>Glomeromycota (growth & development)</term><term>Hydrogen Peroxide (metabolism)</term><term>Mycorrhizae (growth & development)</term><term>Plant Proteins (metabolism)</term><term>Respiratory Burst (MeSH)</term><term>Superoxide Dismutase (metabolism)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Antioxidants</term><term>Calcium</term><term>Catalase</term><term>Hydrogen Peroxide</term><term>Plant Proteins</term><term>Superoxide Dismutase</term></keywords><keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Citrus</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Glomeromycota</term><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Citrus</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Citrus</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Biological Transport</term><term>Droughts</term><term>Respiratory Burst</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Mechanisms of arbuscular mycorrhiza (AM)-induced lower oxidative burst of host plants under drought stress (DS) are not elucidated. A noninvasive microtest technology (NMT) was used to investigate the effects of Funneliformis mosseae on net fluxes of root hydrogen peroxide (H2O2) and calcium ions (Ca2+) in 5-month-old Poncirus trifoliata, in combination with catalase (CAT) and superoxide dismutase (SOD) activities as well as tissue superoxide radical (O2•-) and H2O2 concentrations under DS and well-watered (WW) conditions. A 2-month DS (55% maximum water holding capacity of growth substrates) significantly inhibited AM fungal root colonization, while AM symbiosis significantly increased plant biomass production, irrespective of water status. F. mosseae inoculation generally increased SOD and CAT activity but decreased O2•- and H2O2 concentrations in leaves and roots under WW and DS. Compared with non-AM seedlings, roots of AM seedlings had significantly higher net H2O2 effluxes and net Ca2+ influxes, especially in the meristem zone, but lower net H2O2 efflux in the elongation zone. Net Ca2+ influxes into roots were significantly positively correlated with root net H2O2 effluxes but negatively with root H2O2 concentrations. Results from this study suggest that AM-induced lower oxidative burst is related with higher antioxidant enzyme activities, root net H2O2 effluxes, and Ca2+ influxes under WW and DS.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25085218</PMID><DateCompleted><Year>2015</Year><Month>09</Month><Day>16</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1432-1890</ISSN><JournalIssue CitedMedium="Internet"><Volume>25</Volume><Issue>2</Issue><PubDate><Year>2015</Year><Month>Feb</Month></PubDate></JournalIssue><Title>Mycorrhiza</Title><ISOAbbreviation>Mycorrhiza</ISOAbbreviation></Journal><ArticleTitle>Mycorrhiza-induced lower oxidative burst is related with higher antioxidant enzyme activities, net H2O2 effluxes, and Ca2+ influxes in trifoliate orange roots under drought stress.</ArticleTitle><Pagination><MedlinePgn>143-52</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s00572-014-0598-z</ELocationID><Abstract><AbstractText>Mechanisms of arbuscular mycorrhiza (AM)-induced lower oxidative burst of host plants under drought stress (DS) are not elucidated. A noninvasive microtest technology (NMT) was used to investigate the effects of Funneliformis mosseae on net fluxes of root hydrogen peroxide (H2O2) and calcium ions (Ca2+) in 5-month-old Poncirus trifoliata, in combination with catalase (CAT) and superoxide dismutase (SOD) activities as well as tissue superoxide radical (O2•-) and H2O2 concentrations under DS and well-watered (WW) conditions. A 2-month DS (55% maximum water holding capacity of growth substrates) significantly inhibited AM fungal root colonization, while AM symbiosis significantly increased plant biomass production, irrespective of water status. F. mosseae inoculation generally increased SOD and CAT activity but decreased O2•- and H2O2 concentrations in leaves and roots under WW and DS. Compared with non-AM seedlings, roots of AM seedlings had significantly higher net H2O2 effluxes and net Ca2+ influxes, especially in the meristem zone, but lower net H2O2 efflux in the elongation zone. Net Ca2+ influxes into roots were significantly positively correlated with root net H2O2 effluxes but negatively with root H2O2 concentrations. Results from this study suggest that AM-induced lower oxidative burst is related with higher antioxidant enzyme activities, root net H2O2 effluxes, and Ca2+ influxes under WW and DS.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zou</LastName><ForeName>Ying-Ning</ForeName><Initials>YN</Initials><AffiliationInfo><Affiliation>College of Horticulture and Gardening/Institute of Root Biology, Yangtze University, 88 Jingmi Road, Jingzhou, Hubei, 434025, People's Republic of China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Huang</LastName><ForeName>Yong-Ming</ForeName><Initials>YM</Initials></Author><Author ValidYN="Y"><LastName>Wu</LastName><ForeName>Qiang-Sheng</ForeName><Initials>QS</Initials></Author><Author ValidYN="Y"><LastName>He</LastName><ForeName>Xin-Hua</ForeName><Initials>XH</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>08</Month><Day>03</Day></ArticleDate></Article><MedlineJournalInfo><Country>Germany</Country><MedlineTA>Mycorrhiza</MedlineTA><NlmUniqueID>100955036</NlmUniqueID><ISSNLinking>0940-6360</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000975">Antioxidants</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>BBX060AN9V</RegistryNumber><NameOfSubstance UI="D006861">Hydrogen Peroxide</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.11.1.6</RegistryNumber><NameOfSubstance UI="D002374">Catalase</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.15.1.1</RegistryNumber><NameOfSubstance UI="D013482">Superoxide Dismutase</NameOfSubstance></Chemical><Chemical><RegistryNumber>SY7Q814VUP</RegistryNumber><NameOfSubstance UI="D002118">Calcium</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000975" MajorTopicYN="N">Antioxidants</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001692" MajorTopicYN="N">Biological Transport</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002118" MajorTopicYN="N">Calcium</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002374" MajorTopicYN="N">Catalase</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002957" MajorTopicYN="N">Citrus</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D055864" MajorTopicYN="N">Droughts</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D055137" MajorTopicYN="N">Glomeromycota</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006861" MajorTopicYN="N">Hydrogen Peroxide</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000378" 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