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Polymerase Chain Reaction-Denaturing Gradient Gel Electrophoresis Analysis of Bacterial Community Structure in the Food, Intestines, and Feces of Earthworms
The bacterial communities in the food, intestines, and feces of earthworms were investigated by PCR-denaturing gradient gel electrophoresis (DGGE). In this study, PCR-DGGE was optimized by testing 6 universal primer sets for microbial 16S rRNA in 6 pure culture strains of intestinal microbes in eart...
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Published in: | The journal of microbiology 2011, 49(4), , pp.544-550 |
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description | The bacterial communities in the food, intestines, and feces of earthworms were investigated by PCR-denaturing gradient gel electrophoresis (DGGE). In this study, PCR-DGGE was optimized by testing 6 universal primer sets for microbial 16S rRNA in 6 pure culture strains of intestinal microbes in earthworms. One primer set effectively amplified 16S rRNA from bacterial populations that were found in the food, intestines, and feces of earthworms. Compared with the reference markers from the pure culture strains, the resulting DGGE profiles contained 28 unique DNA fragments. The dominant microorganisms in the food, intestines, and feces of earthworms included Rhodobacterales bacterium, Fusobacteria, Ferrimonas marina, Aeromonas popoffii, and soil bacteria. Other strains, such as Acinetobacter, Clostridium, and Veillonella, as well as rumen bacteria and uncultured bacteria also were present. These results demonstrated that PCR-DGGE analysis can be used to elucidate bacterial diversity and identify unculturable microorganisms. |
doi_str_mv | 10.1007/s12275-011-0423-8 |
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In this study, PCR-DGGE was optimized by testing 6 universal primer sets for microbial 16S rRNA in 6 pure culture strains of intestinal microbes in earthworms. One primer set effectively amplified 16S rRNA from bacterial populations that were found in the food, intestines, and feces of earthworms. Compared with the reference markers from the pure culture strains, the resulting DGGE profiles contained 28 unique DNA fragments. The dominant microorganisms in the food, intestines, and feces of earthworms included Rhodobacterales bacterium, Fusobacteria, Ferrimonas marina, Aeromonas popoffii, and soil bacteria. Other strains, such as Acinetobacter, Clostridium, and Veillonella, as well as rumen bacteria and uncultured bacteria also were present. These results demonstrated that PCR-DGGE analysis can be used to elucidate bacterial diversity and identify unculturable microorganisms.</description><identifier>ISSN: 1225-8873</identifier><identifier>EISSN: 1976-3794</identifier><identifier>DOI: 10.1007/s12275-011-0423-8</identifier><identifier>PMID: 21887635</identifier><language>eng</language><publisher>Heidelberg: The Microbiological Society of Korea</publisher><subject>16S rRNA ; Acinetobacter ; Aeromonas popoffii ; Animal Feed - microbiology ; Animals ; Bacteria ; Bacteria - classification ; Bacteria - genetics ; bacterial community ; Biomedical and Life Sciences ; Cattle ; Clostridium ; Community structure ; Denaturing Gradient Gel Electrophoresis ; DNA ; DNA, Bacterial - genetics ; Ecosystem ; Electrophoresis ; Feces ; Feces - microbiology ; Food ; Gel electrophoresis ; Intestine ; Intestines - microbiology ; Life Sciences ; Manures ; Microbiology ; Microorganisms ; OLIGOCHAETA ; Oligochaeta - microbiology ; Phylogeny ; Polymerase Chain Reaction ; Primers ; Pure culture ; RNA, Ribosomal, 16S - genetics ; rRNA 16S ; Rumen ; Soil microorganisms ; Veillonella ; Worms ; 생물학</subject><ispartof>The Journal of Microbiology, 2011, 49(4), , pp.544-550</ispartof><rights>The Microbiological Society of Korea and Springer-Verlag Berlin Heidelberg 2011</rights><rights>The Microbiological Society of Korea and Springer-Verlag Berlin Heidelberg 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-bcd9688af6fe8658eb58338ba5d87ee401438e969167913130c10690ad1a67143</citedby><cites>FETCH-LOGICAL-c524t-bcd9688af6fe8658eb58338ba5d87ee401438e969167913130c10690ad1a67143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21887635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001579518$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Hong, S.W., Yonsei University, Wonju, Republic of Korea</creatorcontrib><creatorcontrib>Lee, J.S., Yonsei University, Wonju, Republic of Korea</creatorcontrib><creatorcontrib>Chung, K.S., Yonsei University, Wonju, Republic of Korea</creatorcontrib><title>Polymerase Chain Reaction-Denaturing Gradient Gel Electrophoresis Analysis of Bacterial Community Structure in the Food, Intestines, and Feces of Earthworms</title><title>The journal of microbiology</title><addtitle>J Microbiol</addtitle><addtitle>J Microbiol</addtitle><description>The bacterial communities in the food, intestines, and feces of earthworms were investigated by PCR-denaturing gradient gel electrophoresis (DGGE). In this study, PCR-DGGE was optimized by testing 6 universal primer sets for microbial 16S rRNA in 6 pure culture strains of intestinal microbes in earthworms. One primer set effectively amplified 16S rRNA from bacterial populations that were found in the food, intestines, and feces of earthworms. Compared with the reference markers from the pure culture strains, the resulting DGGE profiles contained 28 unique DNA fragments. The dominant microorganisms in the food, intestines, and feces of earthworms included Rhodobacterales bacterium, Fusobacteria, Ferrimonas marina, Aeromonas popoffii, and soil bacteria. Other strains, such as Acinetobacter, Clostridium, and Veillonella, as well as rumen bacteria and uncultured bacteria also were present. These results demonstrated that PCR-DGGE analysis can be used to elucidate bacterial diversity and identify unculturable microorganisms.</description><subject>16S rRNA</subject><subject>Acinetobacter</subject><subject>Aeromonas popoffii</subject><subject>Animal Feed - microbiology</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>bacterial community</subject><subject>Biomedical and Life Sciences</subject><subject>Cattle</subject><subject>Clostridium</subject><subject>Community structure</subject><subject>Denaturing Gradient Gel Electrophoresis</subject><subject>DNA</subject><subject>DNA, Bacterial - genetics</subject><subject>Ecosystem</subject><subject>Electrophoresis</subject><subject>Feces</subject><subject>Feces - microbiology</subject><subject>Food</subject><subject>Gel electrophoresis</subject><subject>Intestine</subject><subject>Intestines - microbiology</subject><subject>Life Sciences</subject><subject>Manures</subject><subject>Microbiology</subject><subject>Microorganisms</subject><subject>OLIGOCHAETA</subject><subject>Oligochaeta - microbiology</subject><subject>Phylogeny</subject><subject>Polymerase Chain Reaction</subject><subject>Primers</subject><subject>Pure culture</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>rRNA 16S</subject><subject>Rumen</subject><subject>Soil microorganisms</subject><subject>Veillonella</subject><subject>Worms</subject><subject>생물학</subject><issn>1225-8873</issn><issn>1976-3794</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9ks2O0zAQgCMEYpeFB-AAsrjAYQP-iWPnWEpbKlYCleVsucmk9W5iF9sR6rvwsDjNwkpIcPLI_uazPTNZ9pzgtwRj8S4QSgXPMSE5LijL5YPsnFSizJmoiocpppTnUgp2lj0J4QbjkrCCPs7OKEm7JePn2c8vrjv24HUANN9rY9EGdB2Ns_kHsDoO3tgdWnndGLARraBDiw7q6N1h7zwEE9DM6u44Bq5F71MueKM7NHd9P1gTj-hr9EOdRICSPe4BLZ1rLtHaRgjRWAiXSNsGLaGGk2Ohfdz_cL4PT7NHre4CPLtbL7Jvy8X1_GN-9Xm1ns-u8prTIubbuqlKKXVbtiBLLmHLJWNyq3kjBUCBScEkVGVFSlERRhiuCS4rrBuiS5EOL7I3k9f6Vt3WRjltTuvOqVuvZpvrtZJEEC4S-npCD959H9IHVG9CDV2nLbghqFRXjmmB2b30HyRJzyK4YFQm9NVf6I0bfCrryYd5geXoIxNUexeCh1YdvOm1PyaTGsdBTeOg0jiocRzUKH55Jx62PTR_Mn73PwF0AsJhbDT4-5v_Z30xJbXaKb3zJqhPG4oJxRgzIdkv3VnILg</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Hong, S.W., Yonsei University, Wonju, Republic of Korea</creator><creator>Lee, J.S., Yonsei University, Wonju, Republic of Korea</creator><creator>Chung, K.S., Yonsei University, Wonju, Republic of Korea</creator><general>The Microbiological Society of Korea</general><general>Springer Nature B.V</general><general>한국미생물학회</general><scope>FBQ</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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TM</scope><scope>7TN</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>H95</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L.G</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>ACYCR</scope></search><sort><creationdate>20110801</creationdate><title>Polymerase Chain Reaction-Denaturing Gradient Gel Electrophoresis Analysis of Bacterial Community Structure in the Food, Intestines, and Feces of Earthworms</title><author>Hong, S.W., Yonsei University, Wonju, Republic of Korea ; Lee, J.S., Yonsei University, Wonju, Republic of Korea ; Chung, K.S., Yonsei University, Wonju, Republic of Korea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-bcd9688af6fe8658eb58338ba5d87ee401438e969167913130c10690ad1a67143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>16S rRNA</topic><topic>Acinetobacter</topic><topic>Aeromonas popoffii</topic><topic>Animal Feed - 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In this study, PCR-DGGE was optimized by testing 6 universal primer sets for microbial 16S rRNA in 6 pure culture strains of intestinal microbes in earthworms. One primer set effectively amplified 16S rRNA from bacterial populations that were found in the food, intestines, and feces of earthworms. Compared with the reference markers from the pure culture strains, the resulting DGGE profiles contained 28 unique DNA fragments. The dominant microorganisms in the food, intestines, and feces of earthworms included Rhodobacterales bacterium, Fusobacteria, Ferrimonas marina, Aeromonas popoffii, and soil bacteria. Other strains, such as Acinetobacter, Clostridium, and Veillonella, as well as rumen bacteria and uncultured bacteria also were present. These results demonstrated that PCR-DGGE analysis can be used to elucidate bacterial diversity and identify unculturable microorganisms.</abstract><cop>Heidelberg</cop><pub>The Microbiological Society of Korea</pub><pmid>21887635</pmid><doi>10.1007/s12275-011-0423-8</doi><tpages>7</tpages></addata></record> |
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subjects | 16S rRNA Acinetobacter Aeromonas popoffii Animal Feed - microbiology Animals Bacteria Bacteria - classification Bacteria - genetics bacterial community Biomedical and Life Sciences Cattle Clostridium Community structure Denaturing Gradient Gel Electrophoresis DNA DNA, Bacterial - genetics Ecosystem Electrophoresis Feces Feces - microbiology Food Gel electrophoresis Intestine Intestines - microbiology Life Sciences Manures Microbiology Microorganisms OLIGOCHAETA Oligochaeta - microbiology Phylogeny Polymerase Chain Reaction Primers Pure culture RNA, Ribosomal, 16S - genetics rRNA 16S Rumen Soil microorganisms Veillonella Worms 생물학 |
title | Polymerase Chain Reaction-Denaturing Gradient Gel Electrophoresis Analysis of Bacterial Community Structure in the Food, Intestines, and Feces of Earthworms |
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