Comparisons of ectomycorrhizal colonization of transgenic american chestnut with those of the wild type, a conventionally bred hybrid, and related fagaceae species.
Identifieur interne : 001687 ( Main/Curation ); précédent : 001686; suivant : 001688Comparisons of ectomycorrhizal colonization of transgenic american chestnut with those of the wild type, a conventionally bred hybrid, and related fagaceae species.
Auteurs : Katherine M. D'Amico [États-Unis] ; Thomas R. Horton [États-Unis] ; Charles A. Maynard [États-Unis] ; Stephen V. Stehman [États-Unis] ; Allison D. Oakes [États-Unis] ; William A. Powell [États-Unis]Source :
- Applied and environmental microbiology [ 1098-5336 ] ; 2015.
Descripteurs français
- KwdFr :
- ADN fongique (composition chimique), ADN fongique (génétique), Analyse de séquence d'ADN (MeSH), Données de séquences moléculaires (MeSH), Fagaceae (microbiologie), Mycorhizes (classification), Mycorhizes (croissance et développement), Mycorhizes (isolement et purification), Oxidoreductases (génétique), Oxidoreductases (métabolisme), Polymorphisme de restriction (MeSH), Protéines recombinantes (génétique), Protéines recombinantes (métabolisme), Racines de plante (microbiologie), Végétaux génétiquement modifiés (microbiologie).
- MESH :
- composition chimique : ADN fongique, Mycorhizes.
- croissance et développement : Mycorhizes.
- génétique : ADN fongique, Oxidoreductases, Protéines recombinantes.
- isolement et purification : Mycorhizes.
- microbiologie : Fagaceae, Racines de plante, Végétaux génétiquement modifiés.
- métabolisme : Oxidoreductases, Protéines recombinantes.
- Analyse de séquence d'ADN, Données de séquences moléculaires, Polymorphisme de restriction.
English descriptors
- KwdEn :
- DNA, Fungal (chemistry), DNA, Fungal (genetics), Fagaceae (microbiology), Molecular Sequence Data (MeSH), Mycorrhizae (classification), Mycorrhizae (growth & development), Mycorrhizae (isolation & purification), Oxidoreductases (genetics), Oxidoreductases (metabolism), Plant Roots (microbiology), Plants, Genetically Modified (microbiology), Polymorphism, Restriction Fragment Length (MeSH), Recombinant Proteins (genetics), Recombinant Proteins (metabolism), Sequence Analysis, DNA (MeSH).
- MESH :
- chemical , chemistry : DNA, Fungal.
- chemical , genetics : DNA, Fungal, Oxidoreductases, Recombinant Proteins.
- classification : Mycorrhizae.
- growth & development : Mycorrhizae.
- isolation & purification : Mycorrhizae.
- chemical , metabolism : Oxidoreductases, Recombinant Proteins.
- microbiology : Fagaceae, Plant Roots, Plants, Genetically Modified.
- Molecular Sequence Data, Polymorphism, Restriction Fragment Length, Sequence Analysis, DNA.
Abstract
American chestnut (Castanea dentata [Marsh.] Borkh.) dominated the eastern forests of North America, serving as a keystone species both ecologically and economically until the introduction of the chestnut blight, Cryphonectria parasitica, functionally eradicated the species. Restoration efforts include genetic transformation utilizing genes such as oxalate oxidase to produce potentially blight-resistant chestnut trees that could be released back into the native range. However, before such a release can be undertaken, it is necessary to assess nontarget impacts. Since oxalate oxidase is meant to combat a fungal pathogen, we are particularly interested in potential impacts of this transgene on beneficial fungi. This study compares ectomycorrhizal fungal colonization on a transgenic American chestnut clone expressing enhanced blight resistance to a wild-type American chestnut, a conventionally bred American-Chinese hybrid chestnut, and other Fagaceae species. A greenhouse bioassay used soil from two field sites with different soil types and land use histories. The number of colonized root tips was counted, and fungal species were identified using morphology, restriction fragment length polymorphism (RFLP), and DNA sequencing. Results showed that total ectomycorrhizal colonization varied more by soil type than by tree species. Individual fungal species varied in their colonization rates, but there were no significant differences between colonization on transgenic and wild-type chestnuts. This study shows that the oxalate oxidase gene can increase resistance against Cryphonectria parasitica without changing the colonization rate for ectomycorrhizal species. These findings will be crucial for a potential deregulation of blight-resistant American chestnuts containing the oxalate oxidase gene.
DOI: 10.1128/AEM.02169-14
PubMed: 25326296
PubMed Central: PMC4272724
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Restoration efforts include genetic transformation utilizing genes such as oxalate oxidase to produce potentially blight-resistant chestnut trees that could be released back into the native range. However, before such a release can be undertaken, it is necessary to assess nontarget impacts. Since oxalate oxidase is meant to combat a fungal pathogen, we are particularly interested in potential impacts of this transgene on beneficial fungi. This study compares ectomycorrhizal fungal colonization on a transgenic American chestnut clone expressing enhanced blight resistance to a wild-type American chestnut, a conventionally bred American-Chinese hybrid chestnut, and other Fagaceae species. A greenhouse bioassay used soil from two field sites with different soil types and land use histories. The number of colonized root tips was counted, and fungal species were identified using morphology, restriction fragment length polymorphism (RFLP), and DNA sequencing. Results showed that total ectomycorrhizal colonization varied more by soil type than by tree species. Individual fungal species varied in their colonization rates, but there were no significant differences between colonization on transgenic and wild-type chestnuts. This study shows that the oxalate oxidase gene can increase resistance against Cryphonectria parasitica without changing the colonization rate for ectomycorrhizal species. These findings will be crucial for a potential deregulation of blight-resistant American chestnuts containing the oxalate oxidase gene. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25326296</PMID><DateCompleted><Year>2015</Year><Month>08</Month><Day>03</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1098-5336</ISSN><JournalIssue CitedMedium="Internet"><Volume>81</Volume><Issue>1</Issue><PubDate><Year>2015</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Applied and environmental microbiology</Title><ISOAbbreviation>Appl Environ Microbiol</ISOAbbreviation></Journal><ArticleTitle>Comparisons of ectomycorrhizal colonization of transgenic american chestnut with those of the wild type, a conventionally bred hybrid, and related fagaceae species.</ArticleTitle><Pagination><MedlinePgn>100-8</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1128/AEM.02169-14</ELocationID><Abstract><AbstractText>American chestnut (Castanea dentata [Marsh.] Borkh.) dominated the eastern forests of North America, serving as a keystone species both ecologically and economically until the introduction of the chestnut blight, Cryphonectria parasitica, functionally eradicated the species. Restoration efforts include genetic transformation utilizing genes such as oxalate oxidase to produce potentially blight-resistant chestnut trees that could be released back into the native range. However, before such a release can be undertaken, it is necessary to assess nontarget impacts. Since oxalate oxidase is meant to combat a fungal pathogen, we are particularly interested in potential impacts of this transgene on beneficial fungi. This study compares ectomycorrhizal fungal colonization on a transgenic American chestnut clone expressing enhanced blight resistance to a wild-type American chestnut, a conventionally bred American-Chinese hybrid chestnut, and other Fagaceae species. A greenhouse bioassay used soil from two field sites with different soil types and land use histories. The number of colonized root tips was counted, and fungal species were identified using morphology, restriction fragment length polymorphism (RFLP), and DNA sequencing. Results showed that total ectomycorrhizal colonization varied more by soil type than by tree species. Individual fungal species varied in their colonization rates, but there were no significant differences between colonization on transgenic and wild-type chestnuts. This study shows that the oxalate oxidase gene can increase resistance against Cryphonectria parasitica without changing the colonization rate for ectomycorrhizal species. These findings will be crucial for a potential deregulation of blight-resistant American chestnuts containing the oxalate oxidase gene. </AbstractText><CopyrightInformation>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>D'Amico</LastName><ForeName>Katherine M</ForeName><Initials>KM</Initials><AffiliationInfo><Affiliation>Department of Environmental and Forest Biology, State University of New York College of Environmental Science and Forestry, Syracuse, New York, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Horton</LastName><ForeName>Thomas R</ForeName><Initials>TR</Initials><AffiliationInfo><Affiliation>Department of Environmental and Forest Biology, State University of New York College of Environmental Science and Forestry, Syracuse, New York, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Maynard</LastName><ForeName>Charles A</ForeName><Initials>CA</Initials><AffiliationInfo><Affiliation>Department of Forest and Natural Resources Management, State University of New York College of Environmental Science and Forestry, Syracuse, New York, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Stehman</LastName><ForeName>Stephen V</ForeName><Initials>SV</Initials><AffiliationInfo><Affiliation>Department of Forest and Natural Resources Management, State University of New York College of Environmental Science and Forestry, Syracuse, New York, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Oakes</LastName><ForeName>Allison D</ForeName><Initials>AD</Initials><AffiliationInfo><Affiliation>Department of Environmental and Forest Biology, State University of New York College of Environmental Science and Forestry, Syracuse, New York, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Powell</LastName><ForeName>William A</ForeName><Initials>WA</Initials><AffiliationInfo><Affiliation>Department of Environmental and Forest Biology, State University of New York College of Environmental Science and Forestry, Syracuse, New York, USA wapowell@esf.edu.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><DataBankList CompleteYN="Y"><DataBank><DataBankName>GENBANK</DataBankName><AccessionNumberList><AccessionNumber>KM464680</AccessionNumber><AccessionNumber>KM464681</AccessionNumber><AccessionNumber>KM464682</AccessionNumber><AccessionNumber>KM464683</AccessionNumber><AccessionNumber>KM464684</AccessionNumber><AccessionNumber>KM464685</AccessionNumber><AccessionNumber>KM464686</AccessionNumber></AccessionNumberList></DataBank></DataBankList><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>10</Month><Day>17</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Appl Environ 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MajorTopicYN="N">Fagaceae</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName><QualifierName UI="Q000145" MajorTopicYN="N">classification</QualifierName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010088" MajorTopicYN="N">Oxidoreductases</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName><QualifierName UI="Q000382" 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