Diversity among field populations of Bradyrhizobium japonicum in Poland

Genetic structure in field populations of Bradyrhizobium japonicum isolated in Poland was determined by using several complementary techniques. Of the 10 field sites examined, only 4 contained populations of indigenous B. japonicum strains. The Polish bradyrhizobia were divided into at least two maj...

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Veröffentlicht in:Applied and Environmental Microbiology 1995-04, Vol.61 (4), p.1194-1200
Hauptverfasser: MADRZAK, C. J, GOLINSKA, B, KROLICZAK, J, PUDEŁKO, K, LAZEWSKA, D, LAMPKA, B, SADOWSKY, M. J
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container_issue 4
container_start_page 1194
container_title Applied and Environmental Microbiology
container_volume 61
creator MADRZAK, C. J
GOLINSKA, B
KROLICZAK, J
PUDEŁKO, K
LAZEWSKA, D
LAMPKA, B
SADOWSKY, M. J
description Genetic structure in field populations of Bradyrhizobium japonicum isolated in Poland was determined by using several complementary techniques. Of the 10 field sites examined, only 4 contained populations of indigenous B. japonicum strains. The Polish bradyrhizobia were divided into at least two major groups on the basis of protein profiles on polyacrylamide gels, serological reaction with polyclonal antisera, repetitive extragenic palindromic PCR fingerprints of genomic DNA, and Southern hybridization analyses with nif and nod gene probes. Serological analyses indicated that 87.5% of the Polish B. japonicum isolates tested were in serogroups 123 and 129, while seven (12.5%) of the isolates tested belonged to their own unique serogroup. These seven strains also could be grouped together on the basis of repetitive extragenic palindromic PCR fingerprints, protein profiles, and Southern hybridization analyses. Cluster analyses indicated that the seven serologically undefined isolates were genetically dissimilar from the majority of the Polish B. japonicum strains. Moreover, immuno-cross-adsorption studies indicated that although the Polish B. japonicum strains reacted with polyclonal antisera prepared against strain USDA123, the majority failed to react with serogroup 123- and 129-specific antisera, suggesting that Polish bradyrhizobia comprise a unique group of root nodule bacteria which have only a few antigens in common with strains USDA123 and USDA129. Nodulation studies indicated that members of the serologically distinct group were very competitive for nodulation of Glycine max cv. Nawiko. None of the Polish serogroup 123 or 129 isolates were restricted for nodulation by USDA123- and USDA129-restricting soybean plant introduction genotypes. Taken together, our results indicate that while genetically diverse B. japonicum strains were isolated from some Polish soils, the majority of field sites contained no soybean-nodulating bacteria.
doi_str_mv 10.1128/aem.61.4.1194-1200.1995
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J ; GOLINSKA, B ; KROLICZAK, J ; PUDEŁKO, K ; LAZEWSKA, D ; LAMPKA, B ; SADOWSKY, M. J</creator><creatorcontrib>MADRZAK, C. J ; GOLINSKA, B ; KROLICZAK, J ; PUDEŁKO, K ; LAZEWSKA, D ; LAMPKA, B ; SADOWSKY, M. J ; University of Agriculture, Poznan, Poland ; Ministere de l' Agriculture et de la Reforme Agraire, Rabat (Maroc). Institut Agronomique et Veterinaire Hassan 2</creatorcontrib><description>Genetic structure in field populations of Bradyrhizobium japonicum isolated in Poland was determined by using several complementary techniques. Of the 10 field sites examined, only 4 contained populations of indigenous B. japonicum strains. The Polish bradyrhizobia were divided into at least two major groups on the basis of protein profiles on polyacrylamide gels, serological reaction with polyclonal antisera, repetitive extragenic palindromic PCR fingerprints of genomic DNA, and Southern hybridization analyses with nif and nod gene probes. Serological analyses indicated that 87.5% of the Polish B. japonicum isolates tested were in serogroups 123 and 129, while seven (12.5%) of the isolates tested belonged to their own unique serogroup. These seven strains also could be grouped together on the basis of repetitive extragenic palindromic PCR fingerprints, protein profiles, and Southern hybridization analyses. Cluster analyses indicated that the seven serologically undefined isolates were genetically dissimilar from the majority of the Polish B. japonicum strains. Moreover, immuno-cross-adsorption studies indicated that although the Polish B. japonicum strains reacted with polyclonal antisera prepared against strain USDA123, the majority failed to react with serogroup 123- and 129-specific antisera, suggesting that Polish bradyrhizobia comprise a unique group of root nodule bacteria which have only a few antigens in common with strains USDA123 and USDA129. Nodulation studies indicated that members of the serologically distinct group were very competitive for nodulation of Glycine max cv. Nawiko. None of the Polish serogroup 123 or 129 isolates were restricted for nodulation by USDA123- and USDA129-restricting soybean plant introduction genotypes. Taken together, our results indicate that while genetically diverse B. japonicum strains were isolated from some Polish soils, the majority of field sites contained no soybean-nodulating bacteria.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/aem.61.4.1194-1200.1995</identifier><identifier>PMID: 16534985</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>adn ; Agronomy. Soil science and plant productions ; amplification chaine polymerase ; analytical methods ; Bacteria ; Bacteriology ; Biodiversity ; Biological and medical sciences ; biological competition ; biological differences ; bradyrhizobium ; Bradyrhizobium japonicum ; Classification ; competencia biologica ; competition biologique ; diferencias biologicas ; difference biologique ; dna ; Economic plant physiology ; electroforesis ; electrophorese ; electrophoresis ; formation de nodosites ; Fundamental and applied biological sciences. Psychology ; gene ; genes ; Genetics ; glycine max ; immunologie ; immunology ; inmunologia ; Microbiology ; nodulacion ; poland ; pologne ; polonia ; polymerase chain reaction ; proteinas ; proteine ; proteins ; reaccion de cadenas de polimerasa ; root nodulation ; serotipos ; serotype ; serotypes ; Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...) ; technique analytique ; tecnicas analiticas</subject><ispartof>Applied and Environmental Microbiology, 1995-04, Vol.61 (4), p.1194-1200</ispartof><rights>1995 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Apr 1995</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c670t-e0025db1967cfc4f251ac2ea8624c8a827fc2dc69e7778cfcde4b9e62cb75a283</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1388403/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1388403/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3492158$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16534985$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MADRZAK, C. J</creatorcontrib><creatorcontrib>GOLINSKA, B</creatorcontrib><creatorcontrib>KROLICZAK, J</creatorcontrib><creatorcontrib>PUDEŁKO, K</creatorcontrib><creatorcontrib>LAZEWSKA, D</creatorcontrib><creatorcontrib>LAMPKA, B</creatorcontrib><creatorcontrib>SADOWSKY, M. J</creatorcontrib><creatorcontrib>University of Agriculture, Poznan, Poland</creatorcontrib><creatorcontrib>Ministere de l' Agriculture et de la Reforme Agraire, Rabat (Maroc). Institut Agronomique et Veterinaire Hassan 2</creatorcontrib><title>Diversity among field populations of Bradyrhizobium japonicum in Poland</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Genetic structure in field populations of Bradyrhizobium japonicum isolated in Poland was determined by using several complementary techniques. Of the 10 field sites examined, only 4 contained populations of indigenous B. japonicum strains. The Polish bradyrhizobia were divided into at least two major groups on the basis of protein profiles on polyacrylamide gels, serological reaction with polyclonal antisera, repetitive extragenic palindromic PCR fingerprints of genomic DNA, and Southern hybridization analyses with nif and nod gene probes. Serological analyses indicated that 87.5% of the Polish B. japonicum isolates tested were in serogroups 123 and 129, while seven (12.5%) of the isolates tested belonged to their own unique serogroup. These seven strains also could be grouped together on the basis of repetitive extragenic palindromic PCR fingerprints, protein profiles, and Southern hybridization analyses. Cluster analyses indicated that the seven serologically undefined isolates were genetically dissimilar from the majority of the Polish B. japonicum strains. Moreover, immuno-cross-adsorption studies indicated that although the Polish B. japonicum strains reacted with polyclonal antisera prepared against strain USDA123, the majority failed to react with serogroup 123- and 129-specific antisera, suggesting that Polish bradyrhizobia comprise a unique group of root nodule bacteria which have only a few antigens in common with strains USDA123 and USDA129. Nodulation studies indicated that members of the serologically distinct group were very competitive for nodulation of Glycine max cv. Nawiko. None of the Polish serogroup 123 or 129 isolates were restricted for nodulation by USDA123- and USDA129-restricting soybean plant introduction genotypes. Taken together, our results indicate that while genetically diverse B. japonicum strains were isolated from some Polish soils, the majority of field sites contained no soybean-nodulating bacteria.</description><subject>adn</subject><subject>Agronomy. Soil science and plant productions</subject><subject>amplification chaine polymerase</subject><subject>analytical methods</subject><subject>Bacteria</subject><subject>Bacteriology</subject><subject>Biodiversity</subject><subject>Biological and medical sciences</subject><subject>biological competition</subject><subject>biological differences</subject><subject>bradyrhizobium</subject><subject>Bradyrhizobium japonicum</subject><subject>Classification</subject><subject>competencia biologica</subject><subject>competition biologique</subject><subject>diferencias biologicas</subject><subject>difference biologique</subject><subject>dna</subject><subject>Economic plant physiology</subject><subject>electroforesis</subject><subject>electrophorese</subject><subject>electrophoresis</subject><subject>formation de nodosites</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gene</subject><subject>genes</subject><subject>Genetics</subject><subject>glycine max</subject><subject>immunologie</subject><subject>immunology</subject><subject>inmunologia</subject><subject>Microbiology</subject><subject>nodulacion</subject><subject>poland</subject><subject>pologne</subject><subject>polonia</subject><subject>polymerase chain reaction</subject><subject>proteinas</subject><subject>proteine</subject><subject>proteins</subject><subject>reaccion de cadenas de polimerasa</subject><subject>root nodulation</subject><subject>serotipos</subject><subject>serotype</subject><subject>serotypes</subject><subject>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</subject><subject>technique analytique</subject><subject>tecnicas analiticas</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNp9kstu1DAUhiMEokPhFSAgBKsMvl82SFCgIFUCCbq2ThxnxqMkTu2kaHh6HGbUUhasfPvOfy6_i-IZRmuMiXoDrl8LvGb5pFmFCcr3WvN7xQojrSpOqbhfrBDSuiKEoZPiUUo7hBBDQj0sTrDglGnFV8X5B3_tYvLTvoQ-DJuy9a5ryjGMcweTD0MqQ1u-j9Ds49b_CrWf-3IHYxi8zTs_lN9CB0PzuHjQQpfck-N6Wlx--vjj7HN18fX8y9m7i8oKiabKIUR4U2MtpG0tawnHYIkDJQizChSRrSWNFdpJKVVGGsdq7QSxteRAFD0t3h50x7nuXWPdMEXozBh9D3FvAnhz92XwW7MJ1wZTpRiiWeD1USCGq9mlyfQ-WdflJlyYk5GUMo4J0Zl89V8SCykk0TKDL_4Bd2GOQx6DIYhrigklGZIHyMaQUnTtTc0YmcVTkz01AhtmFk_N4qlZPM2RT_9u-TbuaGIGXh4BSBa6NsJgfbrhMkQwX0b3_IBt_Wb700dnIPV3s97maiEY2MQsc_k9VyH-_B3G6G9_eMAG</recordid><startdate>19950401</startdate><enddate>19950401</enddate><creator>MADRZAK, C. 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Soil science and plant productions</topic><topic>amplification chaine polymerase</topic><topic>analytical methods</topic><topic>Bacteria</topic><topic>Bacteriology</topic><topic>Biodiversity</topic><topic>Biological and medical sciences</topic><topic>biological competition</topic><topic>biological differences</topic><topic>bradyrhizobium</topic><topic>Bradyrhizobium japonicum</topic><topic>Classification</topic><topic>competencia biologica</topic><topic>competition biologique</topic><topic>diferencias biologicas</topic><topic>difference biologique</topic><topic>dna</topic><topic>Economic plant physiology</topic><topic>electroforesis</topic><topic>electrophorese</topic><topic>electrophoresis</topic><topic>formation de nodosites</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gene</topic><topic>genes</topic><topic>Genetics</topic><topic>glycine max</topic><topic>immunologie</topic><topic>immunology</topic><topic>inmunologia</topic><topic>Microbiology</topic><topic>nodulacion</topic><topic>poland</topic><topic>pologne</topic><topic>polonia</topic><topic>polymerase chain reaction</topic><topic>proteinas</topic><topic>proteine</topic><topic>proteins</topic><topic>reaccion de cadenas de polimerasa</topic><topic>root nodulation</topic><topic>serotipos</topic><topic>serotype</topic><topic>serotypes</topic><topic>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</topic><topic>technique analytique</topic><topic>tecnicas analiticas</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MADRZAK, C. 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Institut Agronomique et Veterinaire Hassan 2</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</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>MADRZAK, C. J</au><au>GOLINSKA, B</au><au>KROLICZAK, J</au><au>PUDEŁKO, K</au><au>LAZEWSKA, D</au><au>LAMPKA, B</au><au>SADOWSKY, M. J</au><aucorp>University of Agriculture, Poznan, Poland</aucorp><aucorp>Ministere de l' Agriculture et de la Reforme Agraire, Rabat (Maroc). Institut Agronomique et Veterinaire Hassan 2</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diversity among field populations of Bradyrhizobium japonicum in Poland</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>1995-04-01</date><risdate>1995</risdate><volume>61</volume><issue>4</issue><spage>1194</spage><epage>1200</epage><pages>1194-1200</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>Genetic structure in field populations of Bradyrhizobium japonicum isolated in Poland was determined by using several complementary techniques. Of the 10 field sites examined, only 4 contained populations of indigenous B. japonicum strains. The Polish bradyrhizobia were divided into at least two major groups on the basis of protein profiles on polyacrylamide gels, serological reaction with polyclonal antisera, repetitive extragenic palindromic PCR fingerprints of genomic DNA, and Southern hybridization analyses with nif and nod gene probes. Serological analyses indicated that 87.5% of the Polish B. japonicum isolates tested were in serogroups 123 and 129, while seven (12.5%) of the isolates tested belonged to their own unique serogroup. These seven strains also could be grouped together on the basis of repetitive extragenic palindromic PCR fingerprints, protein profiles, and Southern hybridization analyses. Cluster analyses indicated that the seven serologically undefined isolates were genetically dissimilar from the majority of the Polish B. japonicum strains. Moreover, immuno-cross-adsorption studies indicated that although the Polish B. japonicum strains reacted with polyclonal antisera prepared against strain USDA123, the majority failed to react with serogroup 123- and 129-specific antisera, suggesting that Polish bradyrhizobia comprise a unique group of root nodule bacteria which have only a few antigens in common with strains USDA123 and USDA129. Nodulation studies indicated that members of the serologically distinct group were very competitive for nodulation of Glycine max cv. Nawiko. None of the Polish serogroup 123 or 129 isolates were restricted for nodulation by USDA123- and USDA129-restricting soybean plant introduction genotypes. Taken together, our results indicate that while genetically diverse B. japonicum strains were isolated from some Polish soils, the majority of field sites contained no soybean-nodulating bacteria.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>16534985</pmid><doi>10.1128/aem.61.4.1194-1200.1995</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source American Society for Microbiology; Open Access: PubMed Central; Alma/SFX Local Collection
subjects adn
Agronomy. Soil science and plant productions
amplification chaine polymerase
analytical methods
Bacteria
Bacteriology
Biodiversity
Biological and medical sciences
biological competition
biological differences
bradyrhizobium
Bradyrhizobium japonicum
Classification
competencia biologica
competition biologique
diferencias biologicas
difference biologique
dna
Economic plant physiology
electroforesis
electrophorese
electrophoresis
formation de nodosites
Fundamental and applied biological sciences. Psychology
gene
genes
Genetics
glycine max
immunologie
immunology
inmunologia
Microbiology
nodulacion
poland
pologne
polonia
polymerase chain reaction
proteinas
proteine
proteins
reaccion de cadenas de polimerasa
root nodulation
serotipos
serotype
serotypes
Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)
technique analytique
tecnicas analiticas
title Diversity among field populations of Bradyrhizobium japonicum in Poland
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