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Impact of poplar-based phytomanagement on soil properties and microbial communities in a metal-contaminated site.

Identifieur interne : 001816 ( Main/Exploration ); précédent : 001815; suivant : 001817

Impact of poplar-based phytomanagement on soil properties and microbial communities in a metal-contaminated site.

Auteurs : Julie Foulon [France] ; Cyril Zappelini [France] ; Alexis Durand [France] ; Benoit Valot [France] ; Damien Blaudez [France] ; Michel Chalot [France]

Source :

RBID : pubmed:27481257

Descripteurs français

English descriptors

Abstract

Despite a long history of use in phytomanagement strategies, the impacts of poplar trees on the structure and function of microbial communities that live in the soil remain largely unknown. The current study combined fungal and bacterial community analyses from different management regimes using Illumina-based sequencing with soil analysis. The poplar phytomanagement regimes led to a significant increase in soil fertility and a decreased bioavailability of Zn and Cd, in concert with changes in the microbial communities. The most notable changes in the relative abundance of taxa and operational taxonomic units unsurprisingly indicated that root and soil constitute distinct ecological microbial habitats, as exemplified by the dominance of Laccaria in root samples. The poplar cultivar was also an important driver, explaining 12% and 6% of the variance in the fungal and bacterial data sets, respectively. The overall dominance of saprophytic fungi, e.g. Penicillium canescens, might be related to the decomposition activities needed at the experimental site. Our data further highlighted that the mycorrhizal colonization of poplar cultivars varies greatly between the species and genotypes, which is exemplified by the dominance of Scleroderma under Vesten samples. Further interactions between fungal and bacterial functional groups stressed the potential of high-throughput sequencing technologies in uncovering the microbial ecology of disturbed environments.

DOI: 10.1093/femsec/fiw163
PubMed: 27481257


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Le document en format XML

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<term>High-Throughput Nucleotide Sequencing (MeSH)</term>
<term>Metals (analysis)</term>
<term>Metals (metabolism)</term>
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<term>Mycorrhizae (MeSH)</term>
<term>Plant Roots (microbiology)</term>
<term>Populus (MeSH)</term>
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<div type="abstract" xml:lang="en">Despite a long history of use in phytomanagement strategies, the impacts of poplar trees on the structure and function of microbial communities that live in the soil remain largely unknown. The current study combined fungal and bacterial community analyses from different management regimes using Illumina-based sequencing with soil analysis. The poplar phytomanagement regimes led to a significant increase in soil fertility and a decreased bioavailability of Zn and Cd, in concert with changes in the microbial communities. The most notable changes in the relative abundance of taxa and operational taxonomic units unsurprisingly indicated that root and soil constitute distinct ecological microbial habitats, as exemplified by the dominance of Laccaria in root samples. The poplar cultivar was also an important driver, explaining 12% and 6% of the variance in the fungal and bacterial data sets, respectively. The overall dominance of saprophytic fungi, e.g. Penicillium canescens, might be related to the decomposition activities needed at the experimental site. Our data further highlighted that the mycorrhizal colonization of poplar cultivars varies greatly between the species and genotypes, which is exemplified by the dominance of Scleroderma under Vesten samples. Further interactions between fungal and bacterial functional groups stressed the potential of high-throughput sequencing technologies in uncovering the microbial ecology of disturbed environments.</div>
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<AbstractText>Despite a long history of use in phytomanagement strategies, the impacts of poplar trees on the structure and function of microbial communities that live in the soil remain largely unknown. The current study combined fungal and bacterial community analyses from different management regimes using Illumina-based sequencing with soil analysis. The poplar phytomanagement regimes led to a significant increase in soil fertility and a decreased bioavailability of Zn and Cd, in concert with changes in the microbial communities. The most notable changes in the relative abundance of taxa and operational taxonomic units unsurprisingly indicated that root and soil constitute distinct ecological microbial habitats, as exemplified by the dominance of Laccaria in root samples. The poplar cultivar was also an important driver, explaining 12% and 6% of the variance in the fungal and bacterial data sets, respectively. The overall dominance of saprophytic fungi, e.g. Penicillium canescens, might be related to the decomposition activities needed at the experimental site. Our data further highlighted that the mycorrhizal colonization of poplar cultivars varies greatly between the species and genotypes, which is exemplified by the dominance of Scleroderma under Vesten samples. Further interactions between fungal and bacterial functional groups stressed the potential of high-throughput sequencing technologies in uncovering the microbial ecology of disturbed environments.</AbstractText>
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<Affiliation>Laboratoire Chrono-Environnement, UMR 6249, Université de Bourgogne Franche-Comté, Pôle Universitaire du Pays de Montbéliard, 4 place Tharradin, BP 71427, 25211 Montbéliard, France Université de Lorraine, Faculté des Sciences et Technologies, BP 70239, 54506 Vandoeuvre-les-Nancy, France michel.chalot@univ-fcomte.fr.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2016</Year>
<Month>07</Month>
<Day>31</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>FEMS Microbiol Ecol</MedlineTA>
<NlmUniqueID>8901229</NlmUniqueID>
<ISSNLinking>0168-6496</ISSNLinking>
</MedlineJournalInfo>
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<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D008670">Metals</NameOfSubstance>
</Chemical>
<Chemical>
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<NameOfSubstance UI="D012987">Soil</NameOfSubstance>
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<Chemical>
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<DescriptorName UI="D004777" MajorTopicYN="N">Environment</DescriptorName>
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<DescriptorName UI="D059014" MajorTopicYN="N">High-Throughput Nucleotide Sequencing</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D008670" MajorTopicYN="N">Metals</DescriptorName>
<QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D059013" MajorTopicYN="Y">Microbial Consortia</DescriptorName>
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<DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D012987" MajorTopicYN="N">Soil</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
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<MeshHeading>
<DescriptorName UI="D012988" MajorTopicYN="Y">Soil Microbiology</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012989" MajorTopicYN="N">Soil Pollutants</DescriptorName>
<QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="Y">Illumina-based sequencing</Keyword>
<Keyword MajorTopicYN="Y">bacterial 16S</Keyword>
<Keyword MajorTopicYN="Y">fungal ITS</Keyword>
<Keyword MajorTopicYN="Y">metal-contaminated soils</Keyword>
<Keyword MajorTopicYN="Y">phytomanagement, poplar cultivars</Keyword>
</KeywordList>
</MedlineCitation>
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<PubMedPubDate PubStatus="accepted">
<Year>2016</Year>
<Month>07</Month>
<Day>25</Day>
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<PubMedPubDate PubStatus="entrez">
<Year>2016</Year>
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<PubMedPubDate PubStatus="medline">
<Year>2017</Year>
<Month>6</Month>
<Day>16</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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</History>
<PublicationStatus>ppublish</PublicationStatus>
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<ArticleId IdType="pubmed">27481257</ArticleId>
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<ArticleId IdType="doi">10.1093/femsec/fiw163</ArticleId>
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<affiliations>
<list>
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<li>France</li>
</country>
<region>
<li>Bourgogne-Franche-Comté</li>
<li>Franche-Comté</li>
<li>Grand Est</li>
<li>Lorraine (région)</li>
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<li>Montbéliard</li>
<li>Vandœuvre-lès-Nancy</li>
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<orgName>
<li>Université de Lorraine</li>
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<country name="France">
<region name="Bourgogne-Franche-Comté">
<name sortKey="Foulon, Julie" sort="Foulon, Julie" uniqKey="Foulon J" first="Julie" last="Foulon">Julie Foulon</name>
</region>
<name sortKey="Blaudez, Damien" sort="Blaudez, Damien" uniqKey="Blaudez D" first="Damien" last="Blaudez">Damien Blaudez</name>
<name sortKey="Chalot, Michel" sort="Chalot, Michel" uniqKey="Chalot M" first="Michel" last="Chalot">Michel Chalot</name>
<name sortKey="Durand, Alexis" sort="Durand, Alexis" uniqKey="Durand A" first="Alexis" last="Durand">Alexis Durand</name>
<name sortKey="Valot, Benoit" sort="Valot, Benoit" uniqKey="Valot B" first="Benoit" last="Valot">Benoit Valot</name>
<name sortKey="Zappelini, Cyril" sort="Zappelini, Cyril" uniqKey="Zappelini C" first="Cyril" last="Zappelini">Cyril Zappelini</name>
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</record>

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