Twin studies reveal specific imbalances in the mucosa‐associated microbiota of patients with ileal Crohn's disease
Background: Large interindividual variation in the composition of the intestinal microbiota between unrelated individuals has made it challenging to identify specific aspects of dysbiosis that lead to Crohn's disease (CD). Methods: To reduce variations in exposure during establishment of the gu...
Gespeichert in:
Veröffentlicht in: | INFLAMMATORY BOWEL DISEASES 2009-05, Vol.15 (5), p.653-660 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 660 |
---|---|
container_issue | 5 |
container_start_page | 653 |
container_title | INFLAMMATORY BOWEL DISEASES |
container_volume | 15 |
creator | Willing, Ben Halfvarson, Jonas Dicksved, Johan Rosenquist, Magnus Järnerot, Gunnar Engstrand, Lars Tysk, Curt Jansson, Janet K. |
description | Background: Large interindividual variation in the composition of the intestinal microbiota between unrelated individuals has made it challenging to identify specific aspects of dysbiosis that lead to Crohn's disease (CD).
Methods: To reduce variations in exposure during establishment of the gut flora and the influence of genotype, we studied the mucosa‐associated microbiota of monozygotic twin pairs that were discordant (n = 6) or concordant (n = 4) for CD. DNA was extracted from biopsies collected from 5 locations between the ileum and rectum. Bacterial 16S ribosomal RNA genes were amplified and community composition assessed by terminal‐restriction fragment length polymorphism, cloning and sequencing, and quantitative real‐time polymerase chain reaction (PCR).
Results: The microbial compositions at all biopsy locations for each individual were similar, regardless of disease state, but there were differences between individuals. In particular, individuals with predominantly ileal CD had a dramatically lower abundance (P < 0.001) of Faecalibacterium prausnitzii and increased abundance (P < 0.03) of Escherichia coli compared to healthy co‐twins and those with CD localized in the colon. This dysbiosis was significantly correlated to the disease phenotype rather than genotype.
Conclusions: The reduced abundance of F. prausnitzii and increased abundance of E. coli are indicative of an ileal CD phenotype, distinct from colonic CD, and the relative abundances of these specific bacterial populations are promising biomarker candidates for differential diagnosis of CD and eventually customized treatment.
(Inflamm Bowel Dis 2009) |
doi_str_mv | 10.1002/ibd.20783 |
format | Article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_slubar_slu_se_25694</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67122946</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5393-ba4c34ca3fce5a019b07d1a342473aef793d4ccbf3058d7fa6869d9c3a1f2bac3</originalsourceid><addsrcrecordid>eNqFkstu1TAQhiMEohdY8ALIKyoEae3YuXhZTgutVIlNYWuNnQnHkBwHO-aouz4Cz8iT1CFHdNUiL2Y0_vzJ0j9Z9orRY0ZpcWJ1e1zQuuFPsn1W8ioXjRBPU59mOZWy2csOQvie0HTk82yPSVpwSdl-Nl1v7YaEKbYWA_H4C6EnYURjO2uIHTT0sDHpKlHTGskQjQvw5_Y3hOCMhQlbMljjnbZuAuI6MsJkcTMFsrXTmth-Fq68W2-OAmltQAj4InvWQR_w5a4eZl8-nl-vLvKrz58uV6dXuSm55LkGYbgwwDuDJVAmNa1bBlwUouaAXS15K4zRHadl09YdVE0lW2k4sK7QYPhhli_esMUxajV6O4C_UQ6s2o1-pA5VWTFWlo_zfdTg5zI_KMpKisS_f5A_s19PlfPfVIyKUdHwIuHv_o87H1VN2Sw_WujRu58Rw6QGGwz2KQ90Mag5Qi5oM3vfPEpWNSsKKaoEvl3AlFcIHrt_X2BUzZuk0iapv5uU2Nc7adQDtvfkbnUScLIA25TxzcMmdfnhbFHeAZKY1zU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67122946</pqid></control><display><type>article</type><title>Twin studies reveal specific imbalances in the mucosa‐associated microbiota of patients with ileal Crohn's disease</title><source>MEDLINE</source><source>Wiley Journals</source><source>Oxford University Press</source><creator>Willing, Ben ; Halfvarson, Jonas ; Dicksved, Johan ; Rosenquist, Magnus ; Järnerot, Gunnar ; Engstrand, Lars ; Tysk, Curt ; Jansson, Janet K.</creator><creatorcontrib>Willing, Ben ; Halfvarson, Jonas ; Dicksved, Johan ; Rosenquist, Magnus ; Järnerot, Gunnar ; Engstrand, Lars ; Tysk, Curt ; Jansson, Janet K. ; Sveriges lantbruksuniversitet</creatorcontrib><description>Background: Large interindividual variation in the composition of the intestinal microbiota between unrelated individuals has made it challenging to identify specific aspects of dysbiosis that lead to Crohn's disease (CD).
Methods: To reduce variations in exposure during establishment of the gut flora and the influence of genotype, we studied the mucosa‐associated microbiota of monozygotic twin pairs that were discordant (n = 6) or concordant (n = 4) for CD. DNA was extracted from biopsies collected from 5 locations between the ileum and rectum. Bacterial 16S ribosomal RNA genes were amplified and community composition assessed by terminal‐restriction fragment length polymorphism, cloning and sequencing, and quantitative real‐time polymerase chain reaction (PCR).
Results: The microbial compositions at all biopsy locations for each individual were similar, regardless of disease state, but there were differences between individuals. In particular, individuals with predominantly ileal CD had a dramatically lower abundance (P < 0.001) of Faecalibacterium prausnitzii and increased abundance (P < 0.03) of Escherichia coli compared to healthy co‐twins and those with CD localized in the colon. This dysbiosis was significantly correlated to the disease phenotype rather than genotype.
Conclusions: The reduced abundance of F. prausnitzii and increased abundance of E. coli are indicative of an ileal CD phenotype, distinct from colonic CD, and the relative abundances of these specific bacterial populations are promising biomarker candidates for differential diagnosis of CD and eventually customized treatment.
(Inflamm Bowel Dis 2009)</description><identifier>ISSN: 1078-0998</identifier><identifier>ISSN: 1536-4844</identifier><identifier>EISSN: 1536-4844</identifier><identifier>DOI: 10.1002/ibd.20783</identifier><identifier>PMID: 19023901</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Colon - microbiology ; Crohn Disease - genetics ; Crohn Disease - microbiology ; Dermatologi och venerologi, klinisk genetik, invärtesmedicin ; Dermatology and venerology,clinical genetics, internal medicine ; Diseases in Twins - genetics ; Diseases in Twins - microbiology ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - isolation & purification ; Escherichia coli Infections - genetics ; Escherichia coli Infections - microbiology ; Faecalibacterium prausnitzii ; Female ; Gastroenterologi ; Gastroenterology ; Gastroenterology and Hepatology ; Gram-Positive Bacterial Infections - genetics ; Gram-Positive Bacterial Infections - microbiology ; Humans ; Ileal Crohn's disease ; Ileal Diseases - genetics ; Ileal Diseases - microbiology ; Internal medicine ; Invärtesmedicin ; Male ; MEDICIN ; MEDICINE ; Middle Aged ; Monozygotic discordant twins ; Mucosa-associated microbiota ; Polymorphism, Restriction Fragment Length ; Prognosis ; RNA, Ribosomal, 16S - genetics ; Ruminococcus - genetics ; Ruminococcus - isolation & purification ; Twins, Monozygotic</subject><ispartof>INFLAMMATORY BOWEL DISEASES, 2009-05, Vol.15 (5), p.653-660</ispartof><rights>Copyright © 2009 Crohn's & Colitis Foundation of America, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5393-ba4c34ca3fce5a019b07d1a342473aef793d4ccbf3058d7fa6869d9c3a1f2bac3</citedby><cites>FETCH-LOGICAL-c5393-ba4c34ca3fce5a019b07d1a342473aef793d4ccbf3058d7fa6869d9c3a1f2bac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fibd.20783$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fibd.20783$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19023901$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-7014$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-104832$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://res.slu.se/id/publ/25694$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:118685208$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Willing, Ben</creatorcontrib><creatorcontrib>Halfvarson, Jonas</creatorcontrib><creatorcontrib>Dicksved, Johan</creatorcontrib><creatorcontrib>Rosenquist, Magnus</creatorcontrib><creatorcontrib>Järnerot, Gunnar</creatorcontrib><creatorcontrib>Engstrand, Lars</creatorcontrib><creatorcontrib>Tysk, Curt</creatorcontrib><creatorcontrib>Jansson, Janet K.</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</creatorcontrib><title>Twin studies reveal specific imbalances in the mucosa‐associated microbiota of patients with ileal Crohn's disease</title><title>INFLAMMATORY BOWEL DISEASES</title><addtitle>Inflamm Bowel Dis</addtitle><description>Background: Large interindividual variation in the composition of the intestinal microbiota between unrelated individuals has made it challenging to identify specific aspects of dysbiosis that lead to Crohn's disease (CD).
Methods: To reduce variations in exposure during establishment of the gut flora and the influence of genotype, we studied the mucosa‐associated microbiota of monozygotic twin pairs that were discordant (n = 6) or concordant (n = 4) for CD. DNA was extracted from biopsies collected from 5 locations between the ileum and rectum. Bacterial 16S ribosomal RNA genes were amplified and community composition assessed by terminal‐restriction fragment length polymorphism, cloning and sequencing, and quantitative real‐time polymerase chain reaction (PCR).
Results: The microbial compositions at all biopsy locations for each individual were similar, regardless of disease state, but there were differences between individuals. In particular, individuals with predominantly ileal CD had a dramatically lower abundance (P < 0.001) of Faecalibacterium prausnitzii and increased abundance (P < 0.03) of Escherichia coli compared to healthy co‐twins and those with CD localized in the colon. This dysbiosis was significantly correlated to the disease phenotype rather than genotype.
Conclusions: The reduced abundance of F. prausnitzii and increased abundance of E. coli are indicative of an ileal CD phenotype, distinct from colonic CD, and the relative abundances of these specific bacterial populations are promising biomarker candidates for differential diagnosis of CD and eventually customized treatment.
(Inflamm Bowel Dis 2009)</description><subject>Colon - microbiology</subject><subject>Crohn Disease - genetics</subject><subject>Crohn Disease - microbiology</subject><subject>Dermatologi och venerologi, klinisk genetik, invärtesmedicin</subject><subject>Dermatology and venerology,clinical genetics, internal medicine</subject><subject>Diseases in Twins - genetics</subject><subject>Diseases in Twins - microbiology</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - isolation & purification</subject><subject>Escherichia coli Infections - genetics</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Faecalibacterium prausnitzii</subject><subject>Female</subject><subject>Gastroenterologi</subject><subject>Gastroenterology</subject><subject>Gastroenterology and Hepatology</subject><subject>Gram-Positive Bacterial Infections - genetics</subject><subject>Gram-Positive Bacterial Infections - microbiology</subject><subject>Humans</subject><subject>Ileal Crohn's disease</subject><subject>Ileal Diseases - genetics</subject><subject>Ileal Diseases - microbiology</subject><subject>Internal medicine</subject><subject>Invärtesmedicin</subject><subject>Male</subject><subject>MEDICIN</subject><subject>MEDICINE</subject><subject>Middle Aged</subject><subject>Monozygotic discordant twins</subject><subject>Mucosa-associated microbiota</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Prognosis</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Ruminococcus - genetics</subject><subject>Ruminococcus - isolation & purification</subject><subject>Twins, Monozygotic</subject><issn>1078-0998</issn><issn>1536-4844</issn><issn>1536-4844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstu1TAQhiMEohdY8ALIKyoEae3YuXhZTgutVIlNYWuNnQnHkBwHO-aouz4Cz8iT1CFHdNUiL2Y0_vzJ0j9Z9orRY0ZpcWJ1e1zQuuFPsn1W8ioXjRBPU59mOZWy2csOQvie0HTk82yPSVpwSdl-Nl1v7YaEKbYWA_H4C6EnYURjO2uIHTT0sDHpKlHTGskQjQvw5_Y3hOCMhQlbMljjnbZuAuI6MsJkcTMFsrXTmth-Fq68W2-OAmltQAj4InvWQR_w5a4eZl8-nl-vLvKrz58uV6dXuSm55LkGYbgwwDuDJVAmNa1bBlwUouaAXS15K4zRHadl09YdVE0lW2k4sK7QYPhhli_esMUxajV6O4C_UQ6s2o1-pA5VWTFWlo_zfdTg5zI_KMpKisS_f5A_s19PlfPfVIyKUdHwIuHv_o87H1VN2Sw_WujRu58Rw6QGGwz2KQ90Mag5Qi5oM3vfPEpWNSsKKaoEvl3AlFcIHrt_X2BUzZuk0iapv5uU2Nc7adQDtvfkbnUScLIA25TxzcMmdfnhbFHeAZKY1zU</recordid><startdate>200905</startdate><enddate>200905</enddate><creator>Willing, Ben</creator><creator>Halfvarson, Jonas</creator><creator>Dicksved, Johan</creator><creator>Rosenquist, Magnus</creator><creator>Järnerot, Gunnar</creator><creator>Engstrand, Lars</creator><creator>Tysk, Curt</creator><creator>Jansson, Janet K.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><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>7X8</scope><scope>7T5</scope><scope>H94</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D91</scope><scope>DF2</scope></search><sort><creationdate>200905</creationdate><title>Twin studies reveal specific imbalances in the mucosa‐associated microbiota of patients with ileal Crohn's disease</title><author>Willing, Ben ; Halfvarson, Jonas ; Dicksved, Johan ; Rosenquist, Magnus ; Järnerot, Gunnar ; Engstrand, Lars ; Tysk, Curt ; Jansson, Janet K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5393-ba4c34ca3fce5a019b07d1a342473aef793d4ccbf3058d7fa6869d9c3a1f2bac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Colon - microbiology</topic><topic>Crohn Disease - genetics</topic><topic>Crohn Disease - microbiology</topic><topic>Dermatologi och venerologi, klinisk genetik, invärtesmedicin</topic><topic>Dermatology and venerology,clinical genetics, internal medicine</topic><topic>Diseases in Twins - genetics</topic><topic>Diseases in Twins - microbiology</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - isolation & purification</topic><topic>Escherichia coli Infections - genetics</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Faecalibacterium prausnitzii</topic><topic>Female</topic><topic>Gastroenterologi</topic><topic>Gastroenterology</topic><topic>Gastroenterology and Hepatology</topic><topic>Gram-Positive Bacterial Infections - genetics</topic><topic>Gram-Positive Bacterial Infections - microbiology</topic><topic>Humans</topic><topic>Ileal Crohn's disease</topic><topic>Ileal Diseases - genetics</topic><topic>Ileal Diseases - microbiology</topic><topic>Internal medicine</topic><topic>Invärtesmedicin</topic><topic>Male</topic><topic>MEDICIN</topic><topic>MEDICINE</topic><topic>Middle Aged</topic><topic>Monozygotic discordant twins</topic><topic>Mucosa-associated microbiota</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Prognosis</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Ruminococcus - genetics</topic><topic>Ruminococcus - isolation & purification</topic><topic>Twins, Monozygotic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Willing, Ben</creatorcontrib><creatorcontrib>Halfvarson, Jonas</creatorcontrib><creatorcontrib>Dicksved, Johan</creatorcontrib><creatorcontrib>Rosenquist, Magnus</creatorcontrib><creatorcontrib>Järnerot, Gunnar</creatorcontrib><creatorcontrib>Engstrand, Lars</creatorcontrib><creatorcontrib>Tysk, Curt</creatorcontrib><creatorcontrib>Jansson, Janet K.</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Örebro universitet</collection><collection>SWEPUB Uppsala universitet</collection><jtitle>INFLAMMATORY BOWEL DISEASES</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Willing, Ben</au><au>Halfvarson, Jonas</au><au>Dicksved, Johan</au><au>Rosenquist, Magnus</au><au>Järnerot, Gunnar</au><au>Engstrand, Lars</au><au>Tysk, Curt</au><au>Jansson, Janet K.</au><aucorp>Sveriges lantbruksuniversitet</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Twin studies reveal specific imbalances in the mucosa‐associated microbiota of patients with ileal Crohn's disease</atitle><jtitle>INFLAMMATORY BOWEL DISEASES</jtitle><addtitle>Inflamm Bowel Dis</addtitle><date>2009-05</date><risdate>2009</risdate><volume>15</volume><issue>5</issue><spage>653</spage><epage>660</epage><pages>653-660</pages><issn>1078-0998</issn><issn>1536-4844</issn><eissn>1536-4844</eissn><abstract>Background: Large interindividual variation in the composition of the intestinal microbiota between unrelated individuals has made it challenging to identify specific aspects of dysbiosis that lead to Crohn's disease (CD).
Methods: To reduce variations in exposure during establishment of the gut flora and the influence of genotype, we studied the mucosa‐associated microbiota of monozygotic twin pairs that were discordant (n = 6) or concordant (n = 4) for CD. DNA was extracted from biopsies collected from 5 locations between the ileum and rectum. Bacterial 16S ribosomal RNA genes were amplified and community composition assessed by terminal‐restriction fragment length polymorphism, cloning and sequencing, and quantitative real‐time polymerase chain reaction (PCR).
Results: The microbial compositions at all biopsy locations for each individual were similar, regardless of disease state, but there were differences between individuals. In particular, individuals with predominantly ileal CD had a dramatically lower abundance (P < 0.001) of Faecalibacterium prausnitzii and increased abundance (P < 0.03) of Escherichia coli compared to healthy co‐twins and those with CD localized in the colon. This dysbiosis was significantly correlated to the disease phenotype rather than genotype.
Conclusions: The reduced abundance of F. prausnitzii and increased abundance of E. coli are indicative of an ileal CD phenotype, distinct from colonic CD, and the relative abundances of these specific bacterial populations are promising biomarker candidates for differential diagnosis of CD and eventually customized treatment.
(Inflamm Bowel Dis 2009)</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19023901</pmid><doi>10.1002/ibd.20783</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1078-0998 |
ispartof | INFLAMMATORY BOWEL DISEASES, 2009-05, Vol.15 (5), p.653-660 |
issn | 1078-0998 1536-4844 1536-4844 |
language | eng |
recordid | cdi_swepub_primary_oai_slubar_slu_se_25694 |
source | MEDLINE; Wiley Journals; Oxford University Press |
subjects | Colon - microbiology Crohn Disease - genetics Crohn Disease - microbiology Dermatologi och venerologi, klinisk genetik, invärtesmedicin Dermatology and venerology,clinical genetics, internal medicine Diseases in Twins - genetics Diseases in Twins - microbiology Escherichia coli Escherichia coli - genetics Escherichia coli - isolation & purification Escherichia coli Infections - genetics Escherichia coli Infections - microbiology Faecalibacterium prausnitzii Female Gastroenterologi Gastroenterology Gastroenterology and Hepatology Gram-Positive Bacterial Infections - genetics Gram-Positive Bacterial Infections - microbiology Humans Ileal Crohn's disease Ileal Diseases - genetics Ileal Diseases - microbiology Internal medicine Invärtesmedicin Male MEDICIN MEDICINE Middle Aged Monozygotic discordant twins Mucosa-associated microbiota Polymorphism, Restriction Fragment Length Prognosis RNA, Ribosomal, 16S - genetics Ruminococcus - genetics Ruminococcus - isolation & purification Twins, Monozygotic |
title | Twin studies reveal specific imbalances in the mucosa‐associated microbiota of patients with ileal Crohn's disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T19%3A46%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Twin%20studies%20reveal%20specific%20imbalances%20in%20the%20mucosa%E2%80%90associated%20microbiota%20of%20patients%20with%20ileal%20Crohn's%20disease&rft.jtitle=INFLAMMATORY%20BOWEL%20DISEASES&rft.au=Willing,%20Ben&rft.aucorp=Sveriges%20lantbruksuniversitet&rft.date=2009-05&rft.volume=15&rft.issue=5&rft.spage=653&rft.epage=660&rft.pages=653-660&rft.issn=1078-0998&rft.eissn=1536-4844&rft_id=info:doi/10.1002/ibd.20783&rft_dat=%3Cproquest_swepu%3E67122946%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=67122946&rft_id=info:pmid/19023901&rfr_iscdi=true |