Ectomycorrhizal symbiosis enhanced the efficiency of inoculation with two Bradyrhizobium strains and Acacia holosericea growth.
Identifieur interne : 003642 ( Main/Corpus ); précédent : 003641; suivant : 003643Ectomycorrhizal symbiosis enhanced the efficiency of inoculation with two Bradyrhizobium strains and Acacia holosericea growth.
Auteurs : S. André ; A. Galiana ; C. Le Roux ; Y. Prin ; M. Neyra ; R. DuponnoisSource :
- Mycorrhiza [ 0940-6360 ] ; 2005.
English descriptors
- KwdEn :
- Acacia (growth & development), Acacia (microbiology), Basidiomycota (growth & development), Basidiomycota (metabolism), Bradyrhizobium (classification), Bradyrhizobium (genetics), Bradyrhizobium (physiology), DNA, Bacterial (analysis), DNA, Ribosomal Spacer (analysis), Molecular Sequence Data (MeSH), Mycorrhizae (growth & development), Nitrogen Fixation (MeSH), Plant Roots (microbiology), Polymerase Chain Reaction (MeSH), Polymorphism, Restriction Fragment Length (MeSH), RNA, Ribosomal, 16S (genetics), RNA, Ribosomal, 23S (genetics), Symbiosis (MeSH).
- MESH :
- chemical , analysis : DNA, Bacterial, DNA, Ribosomal Spacer.
- classification : Bradyrhizobium.
- genetics : Bradyrhizobium, RNA, Ribosomal, 16S, RNA, Ribosomal, 23S.
- growth & development : Acacia, Basidiomycota, Mycorrhizae.
- metabolism : Basidiomycota.
- microbiology : Acacia, Plant Roots.
- physiology : Bradyrhizobium.
- Molecular Sequence Data, Nitrogen Fixation, Polymerase Chain Reaction, Polymorphism, Restriction Fragment Length, Symbiosis.
Abstract
Two strains of Bradyrhizobium sp., Aust 13C and Aust 11C, were dually or singly inoculated with an ectomycorrhizal fungus, Pisolithus albus to assess the interactions between ectomycorrhizal symbiosis and the nodulation process in glasshouse conditions. Sequencing of strains Aust 13C and Aust 11C confirmed their previous placement in the genus Bradyrhizobium. After 4 months' culture, the ectomycorrhizal symbiosis promoted plant growth and the nodulation process of both Bradyrhizobium strains, singly or dually inoculated. PCR/RFLP analysis of the nodules randomly collected in each treatment with Aust 13C and/or Aust 11C: (1) showed that all the nodules exhibited the same patterns as those of the Bradyrhizobium strains, and (2) did not detect contaminant rhizobia. When both Bradyrhizobium isolates were inoculated together, but without P. albus IR100, Aust 11C was recorded in 13% of the treated nodules compared to 87% for Aust 13C, whereas Aust 11C and Aust 13C were represented in 20 and 80% of the treated nodules, respectively, in the ectomycorrhizal treatment. Therefore Aust 13C had a high competitive ability and a great persistence in soil. The presence of the fungus did not significantly influence the frequencies of each Bradyrhizobium sp. root nodules. Although the mechanisms remain unknown, these results showed that the ectomycorrhizal and biological nitrogen-fixing symbioses were very dependent on each other. From a practical point of view, the role of ectomycorrhizal symbiosis is of great importance to N2 fixation and, consequently, these kinds of symbiosis must be associated in any controlled inoculation.
DOI: 10.1007/s00572-004-0340-3
PubMed: 15616831
Links to Exploration step
pubmed:15616831Le document en format XML
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Neyra</name></author><author><name sortKey="Duponnois, R" sort="Duponnois, R" uniqKey="Duponnois R" first="R" last="Duponnois">R. Duponnois</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2005">2005</date><idno type="RBID">pubmed:15616831</idno><idno type="pmid">15616831</idno><idno type="doi">10.1007/s00572-004-0340-3</idno><idno type="wicri:Area/Main/Corpus">003642</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">003642</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Ectomycorrhizal symbiosis enhanced the efficiency of inoculation with two Bradyrhizobium strains and Acacia holosericea growth.</title><author><name sortKey="Andre, S" sort="Andre, S" uniqKey="Andre S" first="S" last="André">S. André</name><affiliation><nlm:affiliation>UMR 113 CIRAD/INRA/IRD/AGRO-M/UM2, Laboratoire des Symbioses Tropicales et Méditerranéennes, TA10/J, Campus International de Baillarguet, 34398 Montpellier, France.</nlm:affiliation></affiliation></author><author><name sortKey="Galiana, A" sort="Galiana, A" uniqKey="Galiana A" first="A" last="Galiana">A. Galiana</name></author><author><name sortKey="Le Roux, C" sort="Le Roux, C" uniqKey="Le Roux C" first="C" last="Le Roux">C. Le Roux</name></author><author><name sortKey="Prin, Y" sort="Prin, Y" uniqKey="Prin Y" first="Y" last="Prin">Y. Prin</name></author><author><name sortKey="Neyra, M" sort="Neyra, M" uniqKey="Neyra M" first="M" last="Neyra">M. Neyra</name></author><author><name sortKey="Duponnois, R" sort="Duponnois, R" uniqKey="Duponnois R" first="R" last="Duponnois">R. Duponnois</name></author></analytic><series><title level="j">Mycorrhiza</title><idno type="ISSN">0940-6360</idno><imprint><date when="2005" type="published">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acacia (growth & development)</term><term>Acacia (microbiology)</term><term>Basidiomycota (growth & development)</term><term>Basidiomycota (metabolism)</term><term>Bradyrhizobium (classification)</term><term>Bradyrhizobium (genetics)</term><term>Bradyrhizobium (physiology)</term><term>DNA, Bacterial (analysis)</term><term>DNA, Ribosomal Spacer (analysis)</term><term>Molecular Sequence Data (MeSH)</term><term>Mycorrhizae (growth & development)</term><term>Nitrogen Fixation (MeSH)</term><term>Plant Roots (microbiology)</term><term>Polymerase Chain Reaction (MeSH)</term><term>Polymorphism, Restriction Fragment Length (MeSH)</term><term>RNA, Ribosomal, 16S (genetics)</term><term>RNA, Ribosomal, 23S (genetics)</term><term>Symbiosis (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>DNA, Bacterial</term><term>DNA, Ribosomal Spacer</term></keywords><keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Bradyrhizobium</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Bradyrhizobium</term><term>RNA, Ribosomal, 16S</term><term>RNA, Ribosomal, 23S</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Acacia</term><term>Basidiomycota</term><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Basidiomycota</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Acacia</term><term>Plant Roots</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Bradyrhizobium</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Molecular Sequence Data</term><term>Nitrogen Fixation</term><term>Polymerase Chain Reaction</term><term>Polymorphism, Restriction Fragment Length</term><term>Symbiosis</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Two strains of Bradyrhizobium sp., Aust 13C and Aust 11C, were dually or singly inoculated with an ectomycorrhizal fungus, Pisolithus albus to assess the interactions between ectomycorrhizal symbiosis and the nodulation process in glasshouse conditions. Sequencing of strains Aust 13C and Aust 11C confirmed their previous placement in the genus Bradyrhizobium. After 4 months' culture, the ectomycorrhizal symbiosis promoted plant growth and the nodulation process of both Bradyrhizobium strains, singly or dually inoculated. PCR/RFLP analysis of the nodules randomly collected in each treatment with Aust 13C and/or Aust 11C: (1) showed that all the nodules exhibited the same patterns as those of the Bradyrhizobium strains, and (2) did not detect contaminant rhizobia. When both Bradyrhizobium isolates were inoculated together, but without P. albus IR100, Aust 11C was recorded in 13% of the treated nodules compared to 87% for Aust 13C, whereas Aust 11C and Aust 13C were represented in 20 and 80% of the treated nodules, respectively, in the ectomycorrhizal treatment. Therefore Aust 13C had a high competitive ability and a great persistence in soil. The presence of the fungus did not significantly influence the frequencies of each Bradyrhizobium sp. root nodules. Although the mechanisms remain unknown, these results showed that the ectomycorrhizal and biological nitrogen-fixing symbioses were very dependent on each other. From a practical point of view, the role of ectomycorrhizal symbiosis is of great importance to N2 fixation and, consequently, these kinds of symbiosis must be associated in any controlled inoculation.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15616831</PMID><DateCompleted><Year>2007</Year><Month>03</Month><Day>27</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0940-6360</ISSN><JournalIssue CitedMedium="Print"><Volume>15</Volume><Issue>5</Issue><PubDate><Year>2005</Year><Month>Jul</Month></PubDate></JournalIssue><Title>Mycorrhiza</Title><ISOAbbreviation>Mycorrhiza</ISOAbbreviation></Journal><ArticleTitle>Ectomycorrhizal symbiosis enhanced the efficiency of inoculation with two Bradyrhizobium strains and Acacia holosericea growth.</ArticleTitle><Pagination><MedlinePgn>357-64</MedlinePgn></Pagination><Abstract><AbstractText>Two strains of Bradyrhizobium sp., Aust 13C and Aust 11C, were dually or singly inoculated with an ectomycorrhizal fungus, Pisolithus albus to assess the interactions between ectomycorrhizal symbiosis and the nodulation process in glasshouse conditions. Sequencing of strains Aust 13C and Aust 11C confirmed their previous placement in the genus Bradyrhizobium. After 4 months' culture, the ectomycorrhizal symbiosis promoted plant growth and the nodulation process of both Bradyrhizobium strains, singly or dually inoculated. PCR/RFLP analysis of the nodules randomly collected in each treatment with Aust 13C and/or Aust 11C: (1) showed that all the nodules exhibited the same patterns as those of the Bradyrhizobium strains, and (2) did not detect contaminant rhizobia. When both Bradyrhizobium isolates were inoculated together, but without P. albus IR100, Aust 11C was recorded in 13% of the treated nodules compared to 87% for Aust 13C, whereas Aust 11C and Aust 13C were represented in 20 and 80% of the treated nodules, respectively, in the ectomycorrhizal treatment. Therefore Aust 13C had a high competitive ability and a great persistence in soil. The presence of the fungus did not significantly influence the frequencies of each Bradyrhizobium sp. root nodules. Although the mechanisms remain unknown, these results showed that the ectomycorrhizal and biological nitrogen-fixing symbioses were very dependent on each other. From a practical point of view, the role of ectomycorrhizal symbiosis is of great importance to N2 fixation and, consequently, these kinds of symbiosis must be associated in any controlled inoculation.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>André</LastName><ForeName>S</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>UMR 113 CIRAD/INRA/IRD/AGRO-M/UM2, Laboratoire des Symbioses Tropicales et Méditerranéennes, TA10/J, Campus International de Baillarguet, 34398 Montpellier, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Galiana</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Le Roux</LastName><ForeName>C</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Prin</LastName><ForeName>Y</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Neyra</LastName><ForeName>M</ForeName><Initials>M</Initials></Author><Author 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