Autoregulation of Nodulation Interferes with Impacts of Nitrogen Fertilization Levels on the Leaf-Associated Bacterial Community in Soybeans
The diversities leaf-associated bacteria on nonnodulated (Nod⁻), wild-type nodulated (Nod⁺), and hypernodulated (Nod⁺⁺) soybeans were evaluated by clone library analyses of the 16S rRNA gene. To analyze the impact of nitrogen fertilization on the bacterial leaf community, soybeans were treated with...
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Veröffentlicht in: | Applied and Environmental Microbiology 2011-03, Vol.77 (6), p.1973-1980 |
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container_title | Applied and Environmental Microbiology |
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creator | Ikeda, Seishi Anda, Mizue Inaba, Shoko Eda, Shima Sato, Shusei Sasaki, Kazuhiro Tabata, Satoshi Mitsui, Hisayuki Sato, Tadashi Shinano, Takuro Minamisawa, Kiwamu |
description | The diversities leaf-associated bacteria on nonnodulated (Nod⁻), wild-type nodulated (Nod⁺), and hypernodulated (Nod⁺⁺) soybeans were evaluated by clone library analyses of the 16S rRNA gene. To analyze the impact of nitrogen fertilization on the bacterial leaf community, soybeans were treated with standard nitrogen (SN) (15 kg N ha⁻¹) or heavy nitrogen (HN) (615 kg N ha⁻¹) fertilization. Under SN fertilization, the relative abundance of Alphaproteobacteria was significantly higher in Nod⁻ and Nod⁺⁺ soybeans (82% to 96%) than in Nod⁺ soybeans (54%). The community structure of leaf-associated bacteria in Nod⁺ soybeans was almost unaffected by the levels of nitrogen fertilization. However, differences were visible in Nod⁻ and Nod⁺⁺ soybeans. HN fertilization drastically decreased the relative abundance of Alphaproteobacteria in Nod⁻ and Nod⁺⁺ soybeans (46% to 76%) and, conversely, increased those of Gammaproteobacteria and Firmicutes in these mutant soybeans. In the Alphaproteobacteria, cluster analyses identified two operational taxonomic units (OTUs) (Aurantimonas sp. and Methylobacterium sp.) that were especially sensitive to nodulation phenotypes under SN fertilization and to nitrogen fertilization levels. Arbuscular mycorrhizal infection was not observed on the root tissues examined, presumably due to the rotation of paddy and upland fields. These results suggest that a subpopulation of leaf-associated bacteria in wild-type Nod⁺ soybeans is controlled in similar ways through the systemic regulation of autoregulation of nodulation, which interferes with the impacts of N levels on the bacterial community of soybean leaves. |
doi_str_mv | 10.1128/AEM.02567-10 |
format | Article |
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To analyze the impact of nitrogen fertilization on the bacterial leaf community, soybeans were treated with standard nitrogen (SN) (15 kg N ha⁻¹) or heavy nitrogen (HN) (615 kg N ha⁻¹) fertilization. Under SN fertilization, the relative abundance of Alphaproteobacteria was significantly higher in Nod⁻ and Nod⁺⁺ soybeans (82% to 96%) than in Nod⁺ soybeans (54%). The community structure of leaf-associated bacteria in Nod⁺ soybeans was almost unaffected by the levels of nitrogen fertilization. However, differences were visible in Nod⁻ and Nod⁺⁺ soybeans. HN fertilization drastically decreased the relative abundance of Alphaproteobacteria in Nod⁻ and Nod⁺⁺ soybeans (46% to 76%) and, conversely, increased those of Gammaproteobacteria and Firmicutes in these mutant soybeans. In the Alphaproteobacteria, cluster analyses identified two operational taxonomic units (OTUs) (Aurantimonas sp. and Methylobacterium sp.) that were especially sensitive to nodulation phenotypes under SN fertilization and to nitrogen fertilization levels. Arbuscular mycorrhizal infection was not observed on the root tissues examined, presumably due to the rotation of paddy and upland fields. These results suggest that a subpopulation of leaf-associated bacteria in wild-type Nod⁺ soybeans is controlled in similar ways through the systemic regulation of autoregulation of nodulation, which interferes with the impacts of N levels on the bacterial community of soybean leaves.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AEM.02567-10</identifier><identifier>PMID: 21239540</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Abundance ; Alphaproteobacteria - growth & development ; Alphaproteobacteria - metabolism ; Bacteria ; Bacteria - growth & development ; Bacteria - metabolism ; Bacteriology ; Biological and medical sciences ; Cluster analysis ; Fundamental and applied biological sciences. Psychology ; Gammaproteobacteria - growth & development ; Gammaproteobacteria - metabolism ; Genotype & phenotype ; Glycine max - genetics ; Glycine max - metabolism ; Glycine max - microbiology ; Methylobacterium - growth & development ; Methylobacterium - metabolism ; Microbiology ; Nitrogen ; Nitrogen - metabolism ; Plant Leaves - genetics ; Plant Leaves - metabolism ; Plant Leaves - microbiology ; Plant Microbiology ; Plant reproduction ; Plant Root Nodulation - genetics ; Plant Root Nodulation - physiology ; Ribonucleic acid ; RNA ; Soybeans ; Symbiosis - genetics ; Symbiosis - physiology ; Taxonomy</subject><ispartof>Applied and Environmental Microbiology, 2011-03, Vol.77 (6), p.1973-1980</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Mar 2011</rights><rights>Copyright © 2011, American Society for Microbiology 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-ee561fe031d57ab29ce0a2cf66a8324aaff7f87dd789f5ceaeb39b7cbba80bfd3</citedby><cites>FETCH-LOGICAL-c522t-ee561fe031d57ab29ce0a2cf66a8324aaff7f87dd789f5ceaeb39b7cbba80bfd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3067336/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3067336/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3186,3187,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23960575$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21239540$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikeda, Seishi</creatorcontrib><creatorcontrib>Anda, Mizue</creatorcontrib><creatorcontrib>Inaba, Shoko</creatorcontrib><creatorcontrib>Eda, Shima</creatorcontrib><creatorcontrib>Sato, Shusei</creatorcontrib><creatorcontrib>Sasaki, Kazuhiro</creatorcontrib><creatorcontrib>Tabata, Satoshi</creatorcontrib><creatorcontrib>Mitsui, Hisayuki</creatorcontrib><creatorcontrib>Sato, Tadashi</creatorcontrib><creatorcontrib>Shinano, Takuro</creatorcontrib><creatorcontrib>Minamisawa, Kiwamu</creatorcontrib><title>Autoregulation of Nodulation Interferes with Impacts of Nitrogen Fertilization Levels on the Leaf-Associated Bacterial Community in Soybeans</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>The diversities leaf-associated bacteria on nonnodulated (Nod⁻), wild-type nodulated (Nod⁺), and hypernodulated (Nod⁺⁺) soybeans were evaluated by clone library analyses of the 16S rRNA gene. To analyze the impact of nitrogen fertilization on the bacterial leaf community, soybeans were treated with standard nitrogen (SN) (15 kg N ha⁻¹) or heavy nitrogen (HN) (615 kg N ha⁻¹) fertilization. Under SN fertilization, the relative abundance of Alphaproteobacteria was significantly higher in Nod⁻ and Nod⁺⁺ soybeans (82% to 96%) than in Nod⁺ soybeans (54%). The community structure of leaf-associated bacteria in Nod⁺ soybeans was almost unaffected by the levels of nitrogen fertilization. However, differences were visible in Nod⁻ and Nod⁺⁺ soybeans. HN fertilization drastically decreased the relative abundance of Alphaproteobacteria in Nod⁻ and Nod⁺⁺ soybeans (46% to 76%) and, conversely, increased those of Gammaproteobacteria and Firmicutes in these mutant soybeans. In the Alphaproteobacteria, cluster analyses identified two operational taxonomic units (OTUs) (Aurantimonas sp. and Methylobacterium sp.) that were especially sensitive to nodulation phenotypes under SN fertilization and to nitrogen fertilization levels. Arbuscular mycorrhizal infection was not observed on the root tissues examined, presumably due to the rotation of paddy and upland fields. These results suggest that a subpopulation of leaf-associated bacteria in wild-type Nod⁺ soybeans is controlled in similar ways through the systemic regulation of autoregulation of nodulation, which interferes with the impacts of N levels on the bacterial community of soybean leaves.</description><subject>Abundance</subject><subject>Alphaproteobacteria - growth & development</subject><subject>Alphaproteobacteria - metabolism</subject><subject>Bacteria</subject><subject>Bacteria - growth & development</subject><subject>Bacteria - metabolism</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Cluster analysis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gammaproteobacteria - growth & development</subject><subject>Gammaproteobacteria - metabolism</subject><subject>Genotype & phenotype</subject><subject>Glycine max - genetics</subject><subject>Glycine max - metabolism</subject><subject>Glycine max - microbiology</subject><subject>Methylobacterium - growth & development</subject><subject>Methylobacterium - metabolism</subject><subject>Microbiology</subject><subject>Nitrogen</subject><subject>Nitrogen - metabolism</subject><subject>Plant Leaves - genetics</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Leaves - microbiology</subject><subject>Plant Microbiology</subject><subject>Plant reproduction</subject><subject>Plant Root Nodulation - genetics</subject><subject>Plant Root Nodulation - physiology</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Soybeans</subject><subject>Symbiosis - genetics</subject><subject>Symbiosis - physiology</subject><subject>Taxonomy</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0ktv1DAQAOAIgeiycOMMAQlxIcV2Ho4vSEvVwkoLHErP1sQZ77pK7NZ2Wi2_gR-N292Wx4WTNfbnkT0zWfackkNKWft-cfzlkLC64QUlD7IZJaIt6rJsHmYzQoQoGKvIQfYkhHNCSEWa9nF2wCgrRV2RWfZzMUXncT0NEI2zudP5V9ffRUsb0Wv0GPJrEzf5crwAFcOtMtG7Ndr8BH00g_mxu7HCKxwSsHncYIpAF4sQnDIQsc8_ptvoDQz5kRvHyZq4zY3NT922Q7DhafZIwxDw2X6dZ2cnx9-PPherb5-WR4tVoWrGYoFYN1QjKWlfc-iYUEiAKd000JasAtCa65b3PW-FrhUCdqXouOo6aEmn-3KefdjlvZi6EXuFNnoY5IU3I_itdGDk3yfWbOTaXcmSNDyVNiV4u0_g3eWEIcrRBIXDABbdFGSqbVPTior_yjY1ThDOqyRf_yPP3eRtqkNCLa2qpr1B73ZIeReCR33_aErkzTjINA7ydhzSTuIv_vzoPb7rfwJv9gCCgkF7sMqE364UDal5ndyrnduY9ebaeJQQRgk4Ss5lI6lIZZlnL3dGg5Ow9inP2SkjtCRU1IzwtvwF9hHVmw</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Ikeda, Seishi</creator><creator>Anda, Mizue</creator><creator>Inaba, Shoko</creator><creator>Eda, Shima</creator><creator>Sato, Shusei</creator><creator>Sasaki, Kazuhiro</creator><creator>Tabata, Satoshi</creator><creator>Mitsui, Hisayuki</creator><creator>Sato, Tadashi</creator><creator>Shinano, Takuro</creator><creator>Minamisawa, Kiwamu</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110301</creationdate><title>Autoregulation of Nodulation Interferes with Impacts of Nitrogen Fertilization Levels on the Leaf-Associated Bacterial Community in Soybeans</title><author>Ikeda, Seishi ; Anda, Mizue ; Inaba, Shoko ; Eda, Shima ; Sato, Shusei ; Sasaki, Kazuhiro ; Tabata, Satoshi ; Mitsui, Hisayuki ; Sato, Tadashi ; Shinano, Takuro ; Minamisawa, Kiwamu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-ee561fe031d57ab29ce0a2cf66a8324aaff7f87dd789f5ceaeb39b7cbba80bfd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Abundance</topic><topic>Alphaproteobacteria - growth & development</topic><topic>Alphaproteobacteria - metabolism</topic><topic>Bacteria</topic><topic>Bacteria - growth & development</topic><topic>Bacteria - metabolism</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Cluster analysis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gammaproteobacteria - growth & development</topic><topic>Gammaproteobacteria - metabolism</topic><topic>Genotype & phenotype</topic><topic>Glycine max - genetics</topic><topic>Glycine max - metabolism</topic><topic>Glycine max - microbiology</topic><topic>Methylobacterium - growth & development</topic><topic>Methylobacterium - metabolism</topic><topic>Microbiology</topic><topic>Nitrogen</topic><topic>Nitrogen - metabolism</topic><topic>Plant Leaves - genetics</topic><topic>Plant Leaves - metabolism</topic><topic>Plant Leaves - microbiology</topic><topic>Plant Microbiology</topic><topic>Plant reproduction</topic><topic>Plant Root Nodulation - genetics</topic><topic>Plant Root Nodulation - physiology</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Soybeans</topic><topic>Symbiosis - genetics</topic><topic>Symbiosis - physiology</topic><topic>Taxonomy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikeda, Seishi</creatorcontrib><creatorcontrib>Anda, Mizue</creatorcontrib><creatorcontrib>Inaba, Shoko</creatorcontrib><creatorcontrib>Eda, Shima</creatorcontrib><creatorcontrib>Sato, Shusei</creatorcontrib><creatorcontrib>Sasaki, Kazuhiro</creatorcontrib><creatorcontrib>Tabata, Satoshi</creatorcontrib><creatorcontrib>Mitsui, Hisayuki</creatorcontrib><creatorcontrib>Sato, Tadashi</creatorcontrib><creatorcontrib>Shinano, Takuro</creatorcontrib><creatorcontrib>Minamisawa, Kiwamu</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikeda, Seishi</au><au>Anda, Mizue</au><au>Inaba, Shoko</au><au>Eda, Shima</au><au>Sato, Shusei</au><au>Sasaki, Kazuhiro</au><au>Tabata, Satoshi</au><au>Mitsui, Hisayuki</au><au>Sato, Tadashi</au><au>Shinano, Takuro</au><au>Minamisawa, Kiwamu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autoregulation of Nodulation Interferes with Impacts of Nitrogen Fertilization Levels on the Leaf-Associated Bacterial Community in Soybeans</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>77</volume><issue>6</issue><spage>1973</spage><epage>1980</epage><pages>1973-1980</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><eissn>1098-6596</eissn><coden>AEMIDF</coden><abstract>The diversities leaf-associated bacteria on nonnodulated (Nod⁻), wild-type nodulated (Nod⁺), and hypernodulated (Nod⁺⁺) soybeans were evaluated by clone library analyses of the 16S rRNA gene. To analyze the impact of nitrogen fertilization on the bacterial leaf community, soybeans were treated with standard nitrogen (SN) (15 kg N ha⁻¹) or heavy nitrogen (HN) (615 kg N ha⁻¹) fertilization. Under SN fertilization, the relative abundance of Alphaproteobacteria was significantly higher in Nod⁻ and Nod⁺⁺ soybeans (82% to 96%) than in Nod⁺ soybeans (54%). The community structure of leaf-associated bacteria in Nod⁺ soybeans was almost unaffected by the levels of nitrogen fertilization. However, differences were visible in Nod⁻ and Nod⁺⁺ soybeans. HN fertilization drastically decreased the relative abundance of Alphaproteobacteria in Nod⁻ and Nod⁺⁺ soybeans (46% to 76%) and, conversely, increased those of Gammaproteobacteria and Firmicutes in these mutant soybeans. In the Alphaproteobacteria, cluster analyses identified two operational taxonomic units (OTUs) (Aurantimonas sp. and Methylobacterium sp.) that were especially sensitive to nodulation phenotypes under SN fertilization and to nitrogen fertilization levels. Arbuscular mycorrhizal infection was not observed on the root tissues examined, presumably due to the rotation of paddy and upland fields. These results suggest that a subpopulation of leaf-associated bacteria in wild-type Nod⁺ soybeans is controlled in similar ways through the systemic regulation of autoregulation of nodulation, which interferes with the impacts of N levels on the bacterial community of soybean leaves.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>21239540</pmid><doi>10.1128/AEM.02567-10</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abundance Alphaproteobacteria - growth & development Alphaproteobacteria - metabolism Bacteria Bacteria - growth & development Bacteria - metabolism Bacteriology Biological and medical sciences Cluster analysis Fundamental and applied biological sciences. Psychology Gammaproteobacteria - growth & development Gammaproteobacteria - metabolism Genotype & phenotype Glycine max - genetics Glycine max - metabolism Glycine max - microbiology Methylobacterium - growth & development Methylobacterium - metabolism Microbiology Nitrogen Nitrogen - metabolism Plant Leaves - genetics Plant Leaves - metabolism Plant Leaves - microbiology Plant Microbiology Plant reproduction Plant Root Nodulation - genetics Plant Root Nodulation - physiology Ribonucleic acid RNA Soybeans Symbiosis - genetics Symbiosis - physiology Taxonomy |
title | Autoregulation of Nodulation Interferes with Impacts of Nitrogen Fertilization Levels on the Leaf-Associated Bacterial Community in Soybeans |
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