Host-Specific Adaptive Diversification of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli
Crohn’s disease (CD) is an inflammatory bowel disease influenced by bacteria. Adherent-invasive E. coli (AIEC) is associated with CD, yet the adaptations facilitating AIEC gut colonization are unknown. AIEC isolates exhibit high genetic diversity, suggesting strains evolve independently across diffe...
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Veröffentlicht in: | Cell host & microbe 2019-02, Vol.25 (2), p.301-312.e5 |
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creator | Elhenawy, Wael Tsai, Caressa N. Coombes, Brian K. |
description | Crohn’s disease (CD) is an inflammatory bowel disease influenced by bacteria. Adherent-invasive E. coli (AIEC) is associated with CD, yet the adaptations facilitating AIEC gut colonization are unknown. AIEC isolates exhibit high genetic diversity, suggesting strains evolve independently across different gut environments. We tracked the adaptive evolution of AIEC in a murine model of chronic colonization across multiple hosts and transmission events. We detected evolved lineages that outcompeted the ancestral strain in the host through independent mechanisms. One lineage was hypermotile because of a mobile insertion sequence upstream of the master flagellar regulator, flhDC, which enhanced AIEC invasion and establishment of a mucosal niche. Another lineage outcompeted the ancestral strain through improved use of acetate, a short-chain fatty acid in the gut. The presence of hypermotile and acetate-consuming lineages discriminated E. coli isolated from CD patients from healthy controls, suggesting an evolutionary trajectory that distinguishes AIEC from commensal E. coli.
[Display omitted]
•Host-to-host transmission selects for AIEC with greater motility and acetate metabolism•Hypermotility mediates higher invasive and inflammatory host responses•Improved acetate utilization is a common trait for many hypomotile isolates•Crohn’s disease E. coli isolates also exhibit increased motility and acetate utilization
Crohn’s disease is associated with adherent-invasive E. coli (AIEC), but the factors promoting AIEC colonization are unclear. Elhenawy et al. show that murine host-to-host transmission selects for adaptive diversification of AIEC, with enhanced bacterial motility and acetate metabolism. E. coli isolates from Crohn’s disease patients similarly exhibit these adaptive features. |
doi_str_mv | 10.1016/j.chom.2018.12.010 |
format | Article |
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[Display omitted]
•Host-to-host transmission selects for AIEC with greater motility and acetate metabolism•Hypermotility mediates higher invasive and inflammatory host responses•Improved acetate utilization is a common trait for many hypomotile isolates•Crohn’s disease E. coli isolates also exhibit increased motility and acetate utilization
Crohn’s disease is associated with adherent-invasive E. coli (AIEC), but the factors promoting AIEC colonization are unclear. Elhenawy et al. show that murine host-to-host transmission selects for adaptive diversification of AIEC, with enhanced bacterial motility and acetate metabolism. E. coli isolates from Crohn’s disease patients similarly exhibit these adaptive features.</description><identifier>ISSN: 1931-3128</identifier><identifier>EISSN: 1934-6069</identifier><identifier>DOI: 10.1016/j.chom.2018.12.010</identifier><identifier>PMID: 30683582</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>adherent-invasive E. coli ; AIEC ; clinical isolates ; Crohn’s disease ; host-pathogen interactions ; within-host evolution</subject><ispartof>Cell host & microbe, 2019-02, Vol.25 (2), p.301-312.e5</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-8ecb9f731b11ce24539bf2b47ebb142b57cb74d466471a53a3346f4ede4cc8c3</citedby><cites>FETCH-LOGICAL-c466t-8ecb9f731b11ce24539bf2b47ebb142b57cb74d466471a53a3346f4ede4cc8c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1931312818306371$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30683582$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Elhenawy, Wael</creatorcontrib><creatorcontrib>Tsai, Caressa N.</creatorcontrib><creatorcontrib>Coombes, Brian K.</creatorcontrib><title>Host-Specific Adaptive Diversification of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli</title><title>Cell host & microbe</title><addtitle>Cell Host Microbe</addtitle><description>Crohn’s disease (CD) is an inflammatory bowel disease influenced by bacteria. Adherent-invasive E. coli (AIEC) is associated with CD, yet the adaptations facilitating AIEC gut colonization are unknown. AIEC isolates exhibit high genetic diversity, suggesting strains evolve independently across different gut environments. We tracked the adaptive evolution of AIEC in a murine model of chronic colonization across multiple hosts and transmission events. We detected evolved lineages that outcompeted the ancestral strain in the host through independent mechanisms. One lineage was hypermotile because of a mobile insertion sequence upstream of the master flagellar regulator, flhDC, which enhanced AIEC invasion and establishment of a mucosal niche. Another lineage outcompeted the ancestral strain through improved use of acetate, a short-chain fatty acid in the gut. The presence of hypermotile and acetate-consuming lineages discriminated E. coli isolated from CD patients from healthy controls, suggesting an evolutionary trajectory that distinguishes AIEC from commensal E. coli.
[Display omitted]
•Host-to-host transmission selects for AIEC with greater motility and acetate metabolism•Hypermotility mediates higher invasive and inflammatory host responses•Improved acetate utilization is a common trait for many hypomotile isolates•Crohn’s disease E. coli isolates also exhibit increased motility and acetate utilization
Crohn’s disease is associated with adherent-invasive E. coli (AIEC), but the factors promoting AIEC colonization are unclear. Elhenawy et al. show that murine host-to-host transmission selects for adaptive diversification of AIEC, with enhanced bacterial motility and acetate metabolism. E. coli isolates from Crohn’s disease patients similarly exhibit these adaptive features.</description><subject>adherent-invasive E. coli</subject><subject>AIEC</subject><subject>clinical isolates</subject><subject>Crohn’s disease</subject><subject>host-pathogen interactions</subject><subject>within-host evolution</subject><issn>1931-3128</issn><issn>1934-6069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kM9uEzEQhy0EoqXwAhzQHrns4rG9_yQuUWhppUoc6N2yZ2cVR8k6eDaRuPU1eD2eBG9TOHKxrfH3-0nzCfEeZAUSmk_bCjdxXykJXQWqkiBfiEvotSkb2fQvn95QalDdhXjDvJWyrmULr8WFlk2n605dinAbeS6_HwjDGLBYDe4whxMVX_KReJm5OcSpiGOxTnEz_X78xfmTyTGVK-aIwc005OCGEk1zeTedHC8N14x5FHATXIFxF96KV6PbMb17vq_Ew831w_q2vP_29W69ui_RNM1cdoS-H1sNHgBJmVr3flTetOQ9GOXrFn1rhsyaFlytndamGQ0NZBA71Ffi47n2kOKPI_Fs94GRdjs3UTyyVdD2RmmQMqPqjGKKzIlGe0hh79JPC9Iuhu3WLobtYtiCstlwDn147j_6PQ3_In-VZuDzGaC85ClQsoyBJqQhJMLZDjH8r_8PC8GO3A</recordid><startdate>20190213</startdate><enddate>20190213</enddate><creator>Elhenawy, Wael</creator><creator>Tsai, Caressa N.</creator><creator>Coombes, Brian K.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20190213</creationdate><title>Host-Specific Adaptive Diversification of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli</title><author>Elhenawy, Wael ; Tsai, Caressa N. ; Coombes, Brian K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-8ecb9f731b11ce24539bf2b47ebb142b57cb74d466471a53a3346f4ede4cc8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>adherent-invasive E. coli</topic><topic>AIEC</topic><topic>clinical isolates</topic><topic>Crohn’s disease</topic><topic>host-pathogen interactions</topic><topic>within-host evolution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elhenawy, Wael</creatorcontrib><creatorcontrib>Tsai, Caressa N.</creatorcontrib><creatorcontrib>Coombes, Brian K.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cell host & microbe</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elhenawy, Wael</au><au>Tsai, Caressa N.</au><au>Coombes, Brian K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Host-Specific Adaptive Diversification of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli</atitle><jtitle>Cell host & microbe</jtitle><addtitle>Cell Host Microbe</addtitle><date>2019-02-13</date><risdate>2019</risdate><volume>25</volume><issue>2</issue><spage>301</spage><epage>312.e5</epage><pages>301-312.e5</pages><issn>1931-3128</issn><eissn>1934-6069</eissn><abstract>Crohn’s disease (CD) is an inflammatory bowel disease influenced by bacteria. Adherent-invasive E. coli (AIEC) is associated with CD, yet the adaptations facilitating AIEC gut colonization are unknown. AIEC isolates exhibit high genetic diversity, suggesting strains evolve independently across different gut environments. We tracked the adaptive evolution of AIEC in a murine model of chronic colonization across multiple hosts and transmission events. We detected evolved lineages that outcompeted the ancestral strain in the host through independent mechanisms. One lineage was hypermotile because of a mobile insertion sequence upstream of the master flagellar regulator, flhDC, which enhanced AIEC invasion and establishment of a mucosal niche. Another lineage outcompeted the ancestral strain through improved use of acetate, a short-chain fatty acid in the gut. The presence of hypermotile and acetate-consuming lineages discriminated E. coli isolated from CD patients from healthy controls, suggesting an evolutionary trajectory that distinguishes AIEC from commensal E. coli.
[Display omitted]
•Host-to-host transmission selects for AIEC with greater motility and acetate metabolism•Hypermotility mediates higher invasive and inflammatory host responses•Improved acetate utilization is a common trait for many hypomotile isolates•Crohn’s disease E. coli isolates also exhibit increased motility and acetate utilization
Crohn’s disease is associated with adherent-invasive E. coli (AIEC), but the factors promoting AIEC colonization are unclear. Elhenawy et al. show that murine host-to-host transmission selects for adaptive diversification of AIEC, with enhanced bacterial motility and acetate metabolism. E. coli isolates from Crohn’s disease patients similarly exhibit these adaptive features.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30683582</pmid><doi>10.1016/j.chom.2018.12.010</doi><oa>free_for_read</oa></addata></record> |
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source | Cell Press Free Archives; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | adherent-invasive E. coli AIEC clinical isolates Crohn’s disease host-pathogen interactions within-host evolution |
title | Host-Specific Adaptive Diversification of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli |
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