Serveur d'exploration sur la mycorhize

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Alleviation of drought stress by mycorrhizas is related to increased root H2O2 efflux in trifoliate orange.

Identifieur interne : 000D66 ( Main/Corpus ); précédent : 000D65; suivant : 000D67

Alleviation of drought stress by mycorrhizas is related to increased root H2O2 efflux in trifoliate orange.

Auteurs : Yong-Ming Huang ; Ying-Ning Zou ; Qiang-Sheng Wu

Source :

RBID : pubmed:28176859

English descriptors

Abstract

The Non-invasive Micro-test Technique (NMT) is used to measure dynamic changes of specific ions/molecules non-invasively, but information about hydrogen peroxide (H2O2) fluxes in different classes of roots by mycorrhiza is scarce in terms of NMT. Effects of Funneliformis mosseae on plant growth, H2O2, superoxide radical (O2·-), malondialdehyde (MDA) concentrations, and H2O2 fluxes in the taproot (TR) and lateral roots (LRs) of trifoliate orange seedlings under well-watered (WW) and drought stress (DS) conditions were studied. DS strongly inhibited mycorrhizal colonization in the TR and LRs, whereas mycorrhizal inoculation significantly promoted plant growth and biomass production. H2O2, O2·-, and MDA concentrations in leaves and roots were dramatically lower in mycorrhizal seedlings than in non-mycorrhizal seedlings under DS. Compared with non-mycorrhizal seedlings, mycorrhizal seedlings had relatively higher net root H2O2 effluxes in the TR and LRs especially under WW, as well as significantly higher total root H2O2 effluxes in the TR and LRs under WW and DS. Total root H2O2 effluxes were significantly positively correlated with root colonization but negatively with root H2O2 and MDA concentrations. It suggested that mycorrhizas induces more H2O2 effluxes of the TR and LRs, thus, alleviating oxidative damage of DS in the host plant.

DOI: 10.1038/srep42335
PubMed: 28176859
PubMed Central: PMC5296721

Links to Exploration step

pubmed:28176859

Le document en format XML

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<term>Biomass (MeSH)</term>
<term>Colony Count, Microbial (MeSH)</term>
<term>Droughts (MeSH)</term>
<term>Hydrogen Peroxide (metabolism)</term>
<term>Linear Models (MeSH)</term>
<term>Malondialdehyde (metabolism)</term>
<term>Mycorrhizae (growth & development)</term>
<term>Mycorrhizae (physiology)</term>
<term>Poncirus (microbiology)</term>
<term>Poncirus (physiology)</term>
<term>Stress, Physiological (MeSH)</term>
<term>Superoxides (metabolism)</term>
<term>Water (metabolism)</term>
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<term>Hydrogen Peroxide</term>
<term>Malondialdehyde</term>
<term>Superoxides</term>
<term>Water</term>
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<term>Poncirus</term>
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<term>Mycorrhizae</term>
<term>Poncirus</term>
</keywords>
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<term>Biomass</term>
<term>Colony Count, Microbial</term>
<term>Droughts</term>
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<div type="abstract" xml:lang="en">The Non-invasive Micro-test Technique (NMT) is used to measure dynamic changes of specific ions/molecules non-invasively, but information about hydrogen peroxide (H
<sub>2</sub>
O
<sub>2</sub>
) fluxes in different classes of roots by mycorrhiza is scarce in terms of NMT. Effects of Funneliformis mosseae on plant growth, H
<sub>2</sub>
O
<sub>2</sub>
, superoxide radical (O
<sub>2</sub>
<sup>·-</sup>
), malondialdehyde (MDA) concentrations, and H
<sub>2</sub>
O
<sub>2</sub>
fluxes in the taproot (TR) and lateral roots (LRs) of trifoliate orange seedlings under well-watered (WW) and drought stress (DS) conditions were studied. DS strongly inhibited mycorrhizal colonization in the TR and LRs, whereas mycorrhizal inoculation significantly promoted plant growth and biomass production. H
<sub>2</sub>
O
<sub>2</sub>
, O
<sub>2</sub>
<sup>·-</sup>
, and MDA concentrations in leaves and roots were dramatically lower in mycorrhizal seedlings than in non-mycorrhizal seedlings under DS. Compared with non-mycorrhizal seedlings, mycorrhizal seedlings had relatively higher net root H
<sub>2</sub>
O
<sub>2</sub>
effluxes in the TR and LRs especially under WW, as well as significantly higher total root H
<sub>2</sub>
O
<sub>2</sub>
effluxes in the TR and LRs under WW and DS. Total root H
<sub>2</sub>
O
<sub>2</sub>
effluxes were significantly positively correlated with root colonization but negatively with root H
<sub>2</sub>
O
<sub>2</sub>
and MDA concentrations. It suggested that mycorrhizas induces more H
<sub>2</sub>
O
<sub>2</sub>
effluxes of the TR and LRs, thus, alleviating oxidative damage of DS in the host plant.</div>
</front>
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<sub>2</sub>
O
<sub>2</sub>
efflux in trifoliate orange.</ArticleTitle>
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<AbstractText>The Non-invasive Micro-test Technique (NMT) is used to measure dynamic changes of specific ions/molecules non-invasively, but information about hydrogen peroxide (H
<sub>2</sub>
O
<sub>2</sub>
) fluxes in different classes of roots by mycorrhiza is scarce in terms of NMT. Effects of Funneliformis mosseae on plant growth, H
<sub>2</sub>
O
<sub>2</sub>
, superoxide radical (O
<sub>2</sub>
<sup>·-</sup>
), malondialdehyde (MDA) concentrations, and H
<sub>2</sub>
O
<sub>2</sub>
fluxes in the taproot (TR) and lateral roots (LRs) of trifoliate orange seedlings under well-watered (WW) and drought stress (DS) conditions were studied. DS strongly inhibited mycorrhizal colonization in the TR and LRs, whereas mycorrhizal inoculation significantly promoted plant growth and biomass production. H
<sub>2</sub>
O
<sub>2</sub>
, O
<sub>2</sub>
<sup>·-</sup>
, and MDA concentrations in leaves and roots were dramatically lower in mycorrhizal seedlings than in non-mycorrhizal seedlings under DS. Compared with non-mycorrhizal seedlings, mycorrhizal seedlings had relatively higher net root H
<sub>2</sub>
O
<sub>2</sub>
effluxes in the TR and LRs especially under WW, as well as significantly higher total root H
<sub>2</sub>
O
<sub>2</sub>
effluxes in the TR and LRs under WW and DS. Total root H
<sub>2</sub>
O
<sub>2</sub>
effluxes were significantly positively correlated with root colonization but negatively with root H
<sub>2</sub>
O
<sub>2</sub>
and MDA concentrations. It suggested that mycorrhizas induces more H
<sub>2</sub>
O
<sub>2</sub>
effluxes of the TR and LRs, thus, alleviating oxidative damage of DS in the host plant.</AbstractText>
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<Affiliation>Institute of Root Biology, Yangtze University, Jingzhou, Hubei 434025, China.</Affiliation>
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<Affiliation>Institute of Root Biology, Yangtze University, Jingzhou, Hubei 434025, China.</Affiliation>
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<MeshHeading>
<DescriptorName UI="D055864" MajorTopicYN="Y">Droughts</DescriptorName>
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</MeshHeading>
<MeshHeading>
<DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName>
<QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
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<CoiStatement>The authors declare no competing financial interests.</CoiStatement>
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