Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)
The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesion...
Gespeichert in:
Veröffentlicht in: | Journal of bacteriology 2015-04, Vol.197 (8), p.1478-1491 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1491 |
---|---|
container_issue | 8 |
container_start_page | 1478 |
container_title | Journal of bacteriology |
container_volume | 197 |
creator | Caballero-Flores, Gustavo G Croxen, Matthew A Martóínez-Santos, Verónica I Finlay, B. Brett Puente, Josóíé L |
description | The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesions in the intestinal epithelium. During infection, these bacteria employ surface structures called fimbriae to adhere and colonize the host intestinal epithelium. For C. rodentium , the roles of only a small number of its genome-carried fimbrial operons have been evaluated. Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. The gcf operon possesses interesting novel traits that open future opportunities to expand our knowledge of the structure, regulation, and function during infection of these important bacterial structures. IMPORTANCE Fimbriae are surface bacterial structures implicated in a variety of biological processes. Some have been shown to play a critical role during host colonization and thus in disease. Pathogenic bacteria possess the genetic information for an assortment of fimbriae, but their function and regulation and the interplay between them have not been studied in detail. This work provides new insights into the function and regulation of a novel fimbria called Gcf that is important for early establishment of a successful infection by C. rodentium in mice, despite being poorly expressed under in vitro growth conditions. This discovery offers an opportunity to better understand the individual role and the regulatory mechanisms controlling the expression of specific fimbrial operons that are critical during infection. |
doi_str_mv | 10.1128/JB.02486-14 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4372744</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1666990487</sourcerecordid><originalsourceid>FETCH-LOGICAL-c499t-b0e730deba7fdf8c9ec38c366e976723936c7260caaa76a1aaf25b10adfecd3b3</originalsourceid><addsrcrecordid>eNqNkstrFEEQxhtRzBo9edcBLxGZ2O_HRTCLWROCgpqjNDU93WuHmemkeyagf72zmRjUU05FUb_6qMeH0HOCDwmh-u3p0SGmXMua8AdoRbDRtRAMP0QrjCmpDTFsDz0p5QJjwrmgj9EeFVJKwswKfT9p_TDGEB2MMQ0VDG31xW-nbklTqKD6lK59V63jmFMDbvS5yumma-qrzTRW69SlIf5aOo5j3-QI1cHGhddP0aMAXfHPbuM-Oj_-8G39sT77vDlZvz-rHTdmrBvsFcOtb0CFNmhnvGPaMSm9UVJRZph0ikrsAEBJIACBioZgaIN3LWvYPnq36F5OTe9bNw-XobOXOfaQf9oE0f5bGeIPu03XljNFFeezwMGtQE5Xky-j7WNxvutg8GkqlkjDBSaGq3ugSrL5AdTcA5XSGMz1TvXVf-hFmvIwH21HKS60wWym3iyUy6mU7MPdigTbnRns6ZG9MYMlu6Ve_H2VO_bP92fg5QIESBa2ORZ7_pViImanaE2oYL8BHR-4jA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1667458903</pqid></control><display><type>article</type><title>Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Caballero-Flores, Gustavo G ; Croxen, Matthew A ; Martóínez-Santos, Verónica I ; Finlay, B. Brett ; Puente, Josóíé L</creator><contributor>DiRita, V. J.</contributor><creatorcontrib>Caballero-Flores, Gustavo G ; Croxen, Matthew A ; Martóínez-Santos, Verónica I ; Finlay, B. Brett ; Puente, Josóíé L ; DiRita, V. J.</creatorcontrib><description>The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesions in the intestinal epithelium. During infection, these bacteria employ surface structures called fimbriae to adhere and colonize the host intestinal epithelium. For C. rodentium , the roles of only a small number of its genome-carried fimbrial operons have been evaluated. Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. The gcf operon possesses interesting novel traits that open future opportunities to expand our knowledge of the structure, regulation, and function during infection of these important bacterial structures. IMPORTANCE Fimbriae are surface bacterial structures implicated in a variety of biological processes. Some have been shown to play a critical role during host colonization and thus in disease. Pathogenic bacteria possess the genetic information for an assortment of fimbriae, but their function and regulation and the interplay between them have not been studied in detail. This work provides new insights into the function and regulation of a novel fimbria called Gcf that is important for early establishment of a successful infection by C. rodentium in mice, despite being poorly expressed under in vitro growth conditions. This discovery offers an opportunity to better understand the individual role and the regulatory mechanisms controlling the expression of specific fimbrial operons that are critical during infection.</description><identifier>ISSN: 0021-9193</identifier><identifier>EISSN: 1098-5530</identifier><identifier>DOI: 10.1128/JB.02486-14</identifier><identifier>PMID: 25666139</identifier><identifier>CODEN: JOBAAY</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animals ; bacteria ; Bacterial infections ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacteriology ; Citrobacter rodentium ; Citrobacter rodentium - genetics ; Citrobacter rodentium - metabolism ; Colonization ; E coli ; enterohemorrhagic Escherichia coli ; Escherichia coli ; Fimbria ; fimbriae ; Fimbriae, Bacterial - genetics ; Fimbriae, Bacterial - metabolism ; Gastrointestinal Tract - microbiology ; Gene expression ; Gene Expression Regulation, Bacterial - physiology ; Gram-negative bacteria ; Growth conditions ; humans ; intestinal mucosa ; Mice ; Multigene Family ; mutants ; Mutation ; open reading frames ; Operon ; Pathogens ; RNA, Bacterial - genetics ; RNA, Bacterial - metabolism ; start codon ; Virulence Factors - genetics ; Virulence Factors - metabolism</subject><ispartof>Journal of bacteriology, 2015-04, Vol.197 (8), p.1478-1491</ispartof><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright American Society for Microbiology Apr 2015</rights><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-b0e730deba7fdf8c9ec38c366e976723936c7260caaa76a1aaf25b10adfecd3b3</citedby><cites>FETCH-LOGICAL-c499t-b0e730deba7fdf8c9ec38c366e976723936c7260caaa76a1aaf25b10adfecd3b3</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/PMC4372744/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372744/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25666139$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>DiRita, V. J.</contributor><creatorcontrib>Caballero-Flores, Gustavo G</creatorcontrib><creatorcontrib>Croxen, Matthew A</creatorcontrib><creatorcontrib>Martóínez-Santos, Verónica I</creatorcontrib><creatorcontrib>Finlay, B. Brett</creatorcontrib><creatorcontrib>Puente, Josóíé L</creatorcontrib><title>Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)</title><title>Journal of bacteriology</title><addtitle>J Bacteriol</addtitle><description>The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesions in the intestinal epithelium. During infection, these bacteria employ surface structures called fimbriae to adhere and colonize the host intestinal epithelium. For C. rodentium , the roles of only a small number of its genome-carried fimbrial operons have been evaluated. Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. The gcf operon possesses interesting novel traits that open future opportunities to expand our knowledge of the structure, regulation, and function during infection of these important bacterial structures. IMPORTANCE Fimbriae are surface bacterial structures implicated in a variety of biological processes. Some have been shown to play a critical role during host colonization and thus in disease. Pathogenic bacteria possess the genetic information for an assortment of fimbriae, but their function and regulation and the interplay between them have not been studied in detail. This work provides new insights into the function and regulation of a novel fimbria called Gcf that is important for early establishment of a successful infection by C. rodentium in mice, despite being poorly expressed under in vitro growth conditions. This discovery offers an opportunity to better understand the individual role and the regulatory mechanisms controlling the expression of specific fimbrial operons that are critical during infection.</description><subject>Animals</subject><subject>bacteria</subject><subject>Bacterial infections</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>Citrobacter rodentium</subject><subject>Citrobacter rodentium - genetics</subject><subject>Citrobacter rodentium - metabolism</subject><subject>Colonization</subject><subject>E coli</subject><subject>enterohemorrhagic Escherichia coli</subject><subject>Escherichia coli</subject><subject>Fimbria</subject><subject>fimbriae</subject><subject>Fimbriae, Bacterial - genetics</subject><subject>Fimbriae, Bacterial - metabolism</subject><subject>Gastrointestinal Tract - microbiology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Bacterial - physiology</subject><subject>Gram-negative bacteria</subject><subject>Growth conditions</subject><subject>humans</subject><subject>intestinal mucosa</subject><subject>Mice</subject><subject>Multigene Family</subject><subject>mutants</subject><subject>Mutation</subject><subject>open reading frames</subject><subject>Operon</subject><subject>Pathogens</subject><subject>RNA, Bacterial - genetics</subject><subject>RNA, Bacterial - metabolism</subject><subject>start codon</subject><subject>Virulence Factors - genetics</subject><subject>Virulence Factors - metabolism</subject><issn>0021-9193</issn><issn>1098-5530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkstrFEEQxhtRzBo9edcBLxGZ2O_HRTCLWROCgpqjNDU93WuHmemkeyagf72zmRjUU05FUb_6qMeH0HOCDwmh-u3p0SGmXMua8AdoRbDRtRAMP0QrjCmpDTFsDz0p5QJjwrmgj9EeFVJKwswKfT9p_TDGEB2MMQ0VDG31xW-nbklTqKD6lK59V63jmFMDbvS5yumma-qrzTRW69SlIf5aOo5j3-QI1cHGhddP0aMAXfHPbuM-Oj_-8G39sT77vDlZvz-rHTdmrBvsFcOtb0CFNmhnvGPaMSm9UVJRZph0ikrsAEBJIACBioZgaIN3LWvYPnq36F5OTe9bNw-XobOXOfaQf9oE0f5bGeIPu03XljNFFeezwMGtQE5Xky-j7WNxvutg8GkqlkjDBSaGq3ugSrL5AdTcA5XSGMz1TvXVf-hFmvIwH21HKS60wWym3iyUy6mU7MPdigTbnRns6ZG9MYMlu6Ve_H2VO_bP92fg5QIESBa2ORZ7_pViImanaE2oYL8BHR-4jA</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Caballero-Flores, Gustavo G</creator><creator>Croxen, Matthew A</creator><creator>Martóínez-Santos, Verónica I</creator><creator>Finlay, B. Brett</creator><creator>Puente, Josóíé L</creator><general>American Society for Microbiology</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>7QL</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>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20150401</creationdate><title>Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)</title><author>Caballero-Flores, Gustavo G ; Croxen, Matthew A ; Martóínez-Santos, Verónica I ; Finlay, B. Brett ; Puente, Josóíé L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-b0e730deba7fdf8c9ec38c366e976723936c7260caaa76a1aaf25b10adfecd3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>bacteria</topic><topic>Bacterial infections</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacteriology</topic><topic>Citrobacter rodentium</topic><topic>Citrobacter rodentium - genetics</topic><topic>Citrobacter rodentium - metabolism</topic><topic>Colonization</topic><topic>E coli</topic><topic>enterohemorrhagic Escherichia coli</topic><topic>Escherichia coli</topic><topic>Fimbria</topic><topic>fimbriae</topic><topic>Fimbriae, Bacterial - genetics</topic><topic>Fimbriae, Bacterial - metabolism</topic><topic>Gastrointestinal Tract - microbiology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Bacterial - physiology</topic><topic>Gram-negative bacteria</topic><topic>Growth conditions</topic><topic>humans</topic><topic>intestinal mucosa</topic><topic>Mice</topic><topic>Multigene Family</topic><topic>mutants</topic><topic>Mutation</topic><topic>open reading frames</topic><topic>Operon</topic><topic>Pathogens</topic><topic>RNA, Bacterial - genetics</topic><topic>RNA, Bacterial - metabolism</topic><topic>start codon</topic><topic>Virulence Factors - genetics</topic><topic>Virulence Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caballero-Flores, Gustavo G</creatorcontrib><creatorcontrib>Croxen, Matthew A</creatorcontrib><creatorcontrib>Martóínez-Santos, Verónica I</creatorcontrib><creatorcontrib>Finlay, B. Brett</creatorcontrib><creatorcontrib>Puente, Josóíé L</creatorcontrib><collection>AGRIS</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>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>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bacteriology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caballero-Flores, Gustavo G</au><au>Croxen, Matthew A</au><au>Martóínez-Santos, Verónica I</au><au>Finlay, B. Brett</au><au>Puente, Josóíé L</au><au>DiRita, V. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)</atitle><jtitle>Journal of bacteriology</jtitle><addtitle>J Bacteriol</addtitle><date>2015-04-01</date><risdate>2015</risdate><volume>197</volume><issue>8</issue><spage>1478</spage><epage>1491</epage><pages>1478-1491</pages><issn>0021-9193</issn><eissn>1098-5530</eissn><coden>JOBAAY</coden><abstract>The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesions in the intestinal epithelium. During infection, these bacteria employ surface structures called fimbriae to adhere and colonize the host intestinal epithelium. For C. rodentium , the roles of only a small number of its genome-carried fimbrial operons have been evaluated. Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. The gcf operon possesses interesting novel traits that open future opportunities to expand our knowledge of the structure, regulation, and function during infection of these important bacterial structures. IMPORTANCE Fimbriae are surface bacterial structures implicated in a variety of biological processes. Some have been shown to play a critical role during host colonization and thus in disease. Pathogenic bacteria possess the genetic information for an assortment of fimbriae, but their function and regulation and the interplay between them have not been studied in detail. This work provides new insights into the function and regulation of a novel fimbria called Gcf that is important for early establishment of a successful infection by C. rodentium in mice, despite being poorly expressed under in vitro growth conditions. This discovery offers an opportunity to better understand the individual role and the regulatory mechanisms controlling the expression of specific fimbrial operons that are critical during infection.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>25666139</pmid><doi>10.1128/JB.02486-14</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9193 |
ispartof | Journal of bacteriology, 2015-04, Vol.197 (8), p.1478-1491 |
issn | 0021-9193 1098-5530 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4372744 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Animals bacteria Bacterial infections Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacteriology Citrobacter rodentium Citrobacter rodentium - genetics Citrobacter rodentium - metabolism Colonization E coli enterohemorrhagic Escherichia coli Escherichia coli Fimbria fimbriae Fimbriae, Bacterial - genetics Fimbriae, Bacterial - metabolism Gastrointestinal Tract - microbiology Gene expression Gene Expression Regulation, Bacterial - physiology Gram-negative bacteria Growth conditions humans intestinal mucosa Mice Multigene Family mutants Mutation open reading frames Operon Pathogens RNA, Bacterial - genetics RNA, Bacterial - metabolism start codon Virulence Factors - genetics Virulence Factors - metabolism |
title | Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T11%3A04%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Identification%20and%20Regulation%20of%20a%20Novel%20Citrobacter%20rodentium%20Gut%20Colonization%20Fimbria%20(Gcf)&rft.jtitle=Journal%20of%20bacteriology&rft.au=Caballero-Flores,%20Gustavo%20G&rft.date=2015-04-01&rft.volume=197&rft.issue=8&rft.spage=1478&rft.epage=1491&rft.pages=1478-1491&rft.issn=0021-9193&rft.eissn=1098-5530&rft.coden=JOBAAY&rft_id=info:doi/10.1128/JB.02486-14&rft_dat=%3Cproquest_pubme%3E1666990487%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1667458903&rft_id=info:pmid/25666139&rfr_iscdi=true |