Biological pathways via which the anthocyanin malvidin alleviated the murine colitis induced by Citrobacter rodentium
Enteropathogenic (EPEC) is a causal agent for diarrheal diseases and contributes to morbidity and mortality in children under the age of five years. The emergence and rapid spread of antibiotic resistant EPEC strains necessitate the search for novel alternatives to antibiotics. In this study, we use...
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creator | Liu, Fang Smith, Allen D Wang, Thomas T Y Pham, Quynhchi Cheung, Lumei Yang, Haiyan Li, Robert W |
description | Enteropathogenic
(EPEC) is a causal agent for diarrheal diseases and contributes to morbidity and mortality in children under the age of five years. The emergence and rapid spread of antibiotic resistant EPEC strains necessitate the search for novel alternatives to antibiotics. In this study, we used
, a natural mouse pathogen that mimics many aspects of human EPEC infections, to investigate the antimicrobial properties of the blueberry anthocyanin malvidin 3-glucoside (MG) using a multi-omics approach. MG supplementation reversed the bodyweight loss induced by
infection and improved colonic hyperplasia and histopathological scores. In the colon tissue, MG supplementation significantly increased the expression of Hace1, a key regulator of TNFα-driven signaling, and impacted multiple pathways, such as TGFβ signaling. MG partially restored
-induced microbial dysbiosis and significantly enhanced the abundance of the probiotic
. Moreover, MG disrupted the interactions of
with other gut microbes. MG significantly mediated several host- and microbiota-derived metabolites, such as cytosine, ureidopropionic acid, and glutaric acid. MG normalized the bioactive lipid oleoylethanolamine, a member of the endocannabinoid system, from the dysregulated level in infected mice, directly contributing to its overall beneficial effects. Our findings provided novel insights into molecular processes
which the flavonoid malvidin exerts its biological effects in the gastrointestinal tract. |
doi_str_mv | 10.1039/d2fo02873e |
format | Article |
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(EPEC) is a causal agent for diarrheal diseases and contributes to morbidity and mortality in children under the age of five years. The emergence and rapid spread of antibiotic resistant EPEC strains necessitate the search for novel alternatives to antibiotics. In this study, we used
, a natural mouse pathogen that mimics many aspects of human EPEC infections, to investigate the antimicrobial properties of the blueberry anthocyanin malvidin 3-glucoside (MG) using a multi-omics approach. MG supplementation reversed the bodyweight loss induced by
infection and improved colonic hyperplasia and histopathological scores. In the colon tissue, MG supplementation significantly increased the expression of Hace1, a key regulator of TNFα-driven signaling, and impacted multiple pathways, such as TGFβ signaling. MG partially restored
-induced microbial dysbiosis and significantly enhanced the abundance of the probiotic
. Moreover, MG disrupted the interactions of
with other gut microbes. MG significantly mediated several host- and microbiota-derived metabolites, such as cytosine, ureidopropionic acid, and glutaric acid. MG normalized the bioactive lipid oleoylethanolamine, a member of the endocannabinoid system, from the dysregulated level in infected mice, directly contributing to its overall beneficial effects. Our findings provided novel insights into molecular processes
which the flavonoid malvidin exerts its biological effects in the gastrointestinal tract.</description><identifier>ISSN: 2042-6496</identifier><identifier>EISSN: 2042-650X</identifier><identifier>DOI: 10.1039/d2fo02873e</identifier><identifier>PMID: 36562464</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Animals ; Anthocyanins ; Anthocyanins - metabolism ; Antibiotic resistance ; Antibiotics ; Antiinfectives and antibacterials ; Bifidobacterium animalis ; Biological effects ; Citrobacter ; Citrobacter rodentium ; Colitis ; Colitis - metabolism ; Colon - metabolism ; Cytosine ; Diarrhea ; Dysbacteriosis ; E coli ; Endocannabinoid system ; Enteropathogenic Escherichia coli ; Escherichia coli ; Flavonoids ; Gastrointestinal system ; Gastrointestinal tract ; Humans ; Hyperplasia ; Infections ; Lipids ; Metabolites ; Mice ; Mice, Inbred C57BL ; Microorganisms ; Morbidity ; Probiotics ; Signal transduction ; Signaling ; Supplements ; Tumor necrosis factor-α ; Ubiquitin-Protein Ligases - metabolism</subject><ispartof>Food & function, 2023-01, Vol.14 (2), p.1048-1061</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-c723f96182725a872b8a8c78e3246a0f1109f14669dc1aaad0d2021d138f0f323</citedby><cites>FETCH-LOGICAL-c315t-c723f96182725a872b8a8c78e3246a0f1109f14669dc1aaad0d2021d138f0f323</cites><orcidid>0000-0001-9220-7049</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36562464$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Fang</creatorcontrib><creatorcontrib>Smith, Allen D</creatorcontrib><creatorcontrib>Wang, Thomas T Y</creatorcontrib><creatorcontrib>Pham, Quynhchi</creatorcontrib><creatorcontrib>Cheung, Lumei</creatorcontrib><creatorcontrib>Yang, Haiyan</creatorcontrib><creatorcontrib>Li, Robert W</creatorcontrib><title>Biological pathways via which the anthocyanin malvidin alleviated the murine colitis induced by Citrobacter rodentium</title><title>Food & function</title><addtitle>Food Funct</addtitle><description>Enteropathogenic
(EPEC) is a causal agent for diarrheal diseases and contributes to morbidity and mortality in children under the age of five years. The emergence and rapid spread of antibiotic resistant EPEC strains necessitate the search for novel alternatives to antibiotics. In this study, we used
, a natural mouse pathogen that mimics many aspects of human EPEC infections, to investigate the antimicrobial properties of the blueberry anthocyanin malvidin 3-glucoside (MG) using a multi-omics approach. MG supplementation reversed the bodyweight loss induced by
infection and improved colonic hyperplasia and histopathological scores. In the colon tissue, MG supplementation significantly increased the expression of Hace1, a key regulator of TNFα-driven signaling, and impacted multiple pathways, such as TGFβ signaling. MG partially restored
-induced microbial dysbiosis and significantly enhanced the abundance of the probiotic
. Moreover, MG disrupted the interactions of
with other gut microbes. MG significantly mediated several host- and microbiota-derived metabolites, such as cytosine, ureidopropionic acid, and glutaric acid. MG normalized the bioactive lipid oleoylethanolamine, a member of the endocannabinoid system, from the dysregulated level in infected mice, directly contributing to its overall beneficial effects. Our findings provided novel insights into molecular processes
which the flavonoid malvidin exerts its biological effects in the gastrointestinal tract.</description><subject>Animals</subject><subject>Anthocyanins</subject><subject>Anthocyanins - metabolism</subject><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Antiinfectives and antibacterials</subject><subject>Bifidobacterium animalis</subject><subject>Biological effects</subject><subject>Citrobacter</subject><subject>Citrobacter rodentium</subject><subject>Colitis</subject><subject>Colitis - metabolism</subject><subject>Colon - metabolism</subject><subject>Cytosine</subject><subject>Diarrhea</subject><subject>Dysbacteriosis</subject><subject>E coli</subject><subject>Endocannabinoid system</subject><subject>Enteropathogenic Escherichia coli</subject><subject>Escherichia coli</subject><subject>Flavonoids</subject><subject>Gastrointestinal system</subject><subject>Gastrointestinal tract</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Infections</subject><subject>Lipids</subject><subject>Metabolites</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microorganisms</subject><subject>Morbidity</subject><subject>Probiotics</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>Supplements</subject><subject>Tumor necrosis factor-α</subject><subject>Ubiquitin-Protein Ligases - metabolism</subject><issn>2042-6496</issn><issn>2042-650X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0UtLxDAQB_Agiop68QNIwIsIq3m0aXLU9QmCFwVvZTZJbSRt1iRV9tsbnwfnMgP58WfIILRPyQklXJ0a1gXCZMPtGtpmpGIzUZOn9d-5UmIL7aX0QkpxpaSSm2iLi1qwSlTbaDp3wYdnp8HjJeT-HVYJvznA773TPc69xTDmPugVjG7EA_g3Z8oA3tvCsjVfZpiiGy3WwbvsEnajmXR5Wqzw3OUYFqCzjTgGY8fspmEXbXTgk9376Tvo8eryYX4zu7u_vp2f3c00p3We6YbxTgkqWcNqkA1bSJC6kZaX5YF0lBLV0UoIZTQFAEMMI4waymVHOs74Djr6zl3G8DrZlNvBJW29h9GGKbWsqWUJqRta6OE_-hKmOJbtihKSNqqmdVHH30rHkFK0XbuMboC4ailpP-_RXrCr-697XBZ88BM5LQZr_ujv7_MPTeWF-w</recordid><startdate>20230123</startdate><enddate>20230123</enddate><creator>Liu, Fang</creator><creator>Smith, Allen D</creator><creator>Wang, Thomas T Y</creator><creator>Pham, Quynhchi</creator><creator>Cheung, Lumei</creator><creator>Yang, Haiyan</creator><creator>Li, Robert W</creator><general>Royal Society of Chemistry</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>7T5</scope><scope>7T7</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9220-7049</orcidid></search><sort><creationdate>20230123</creationdate><title>Biological pathways via which the anthocyanin malvidin alleviated the murine colitis induced by Citrobacter rodentium</title><author>Liu, Fang ; Smith, Allen D ; Wang, Thomas T Y ; Pham, Quynhchi ; Cheung, Lumei ; Yang, Haiyan ; Li, Robert W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-c723f96182725a872b8a8c78e3246a0f1109f14669dc1aaad0d2021d138f0f323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Anthocyanins</topic><topic>Anthocyanins - metabolism</topic><topic>Antibiotic resistance</topic><topic>Antibiotics</topic><topic>Antiinfectives and antibacterials</topic><topic>Bifidobacterium animalis</topic><topic>Biological effects</topic><topic>Citrobacter</topic><topic>Citrobacter rodentium</topic><topic>Colitis</topic><topic>Colitis - metabolism</topic><topic>Colon - metabolism</topic><topic>Cytosine</topic><topic>Diarrhea</topic><topic>Dysbacteriosis</topic><topic>E coli</topic><topic>Endocannabinoid system</topic><topic>Enteropathogenic Escherichia coli</topic><topic>Escherichia coli</topic><topic>Flavonoids</topic><topic>Gastrointestinal system</topic><topic>Gastrointestinal tract</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Infections</topic><topic>Lipids</topic><topic>Metabolites</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microorganisms</topic><topic>Morbidity</topic><topic>Probiotics</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>Supplements</topic><topic>Tumor necrosis factor-α</topic><topic>Ubiquitin-Protein Ligases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Fang</creatorcontrib><creatorcontrib>Smith, Allen D</creatorcontrib><creatorcontrib>Wang, Thomas T Y</creatorcontrib><creatorcontrib>Pham, Quynhchi</creatorcontrib><creatorcontrib>Cheung, Lumei</creatorcontrib><creatorcontrib>Yang, Haiyan</creatorcontrib><creatorcontrib>Li, Robert W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology 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>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Food & function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Fang</au><au>Smith, Allen D</au><au>Wang, Thomas T Y</au><au>Pham, Quynhchi</au><au>Cheung, Lumei</au><au>Yang, Haiyan</au><au>Li, Robert W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biological pathways via which the anthocyanin malvidin alleviated the murine colitis induced by Citrobacter rodentium</atitle><jtitle>Food & function</jtitle><addtitle>Food Funct</addtitle><date>2023-01-23</date><risdate>2023</risdate><volume>14</volume><issue>2</issue><spage>1048</spage><epage>1061</epage><pages>1048-1061</pages><issn>2042-6496</issn><eissn>2042-650X</eissn><abstract>Enteropathogenic
(EPEC) is a causal agent for diarrheal diseases and contributes to morbidity and mortality in children under the age of five years. The emergence and rapid spread of antibiotic resistant EPEC strains necessitate the search for novel alternatives to antibiotics. In this study, we used
, a natural mouse pathogen that mimics many aspects of human EPEC infections, to investigate the antimicrobial properties of the blueberry anthocyanin malvidin 3-glucoside (MG) using a multi-omics approach. MG supplementation reversed the bodyweight loss induced by
infection and improved colonic hyperplasia and histopathological scores. In the colon tissue, MG supplementation significantly increased the expression of Hace1, a key regulator of TNFα-driven signaling, and impacted multiple pathways, such as TGFβ signaling. MG partially restored
-induced microbial dysbiosis and significantly enhanced the abundance of the probiotic
. Moreover, MG disrupted the interactions of
with other gut microbes. MG significantly mediated several host- and microbiota-derived metabolites, such as cytosine, ureidopropionic acid, and glutaric acid. MG normalized the bioactive lipid oleoylethanolamine, a member of the endocannabinoid system, from the dysregulated level in infected mice, directly contributing to its overall beneficial effects. Our findings provided novel insights into molecular processes
which the flavonoid malvidin exerts its biological effects in the gastrointestinal tract.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>36562464</pmid><doi>10.1039/d2fo02873e</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-9220-7049</orcidid></addata></record> |
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subjects | Animals Anthocyanins Anthocyanins - metabolism Antibiotic resistance Antibiotics Antiinfectives and antibacterials Bifidobacterium animalis Biological effects Citrobacter Citrobacter rodentium Colitis Colitis - metabolism Colon - metabolism Cytosine Diarrhea Dysbacteriosis E coli Endocannabinoid system Enteropathogenic Escherichia coli Escherichia coli Flavonoids Gastrointestinal system Gastrointestinal tract Humans Hyperplasia Infections Lipids Metabolites Mice Mice, Inbred C57BL Microorganisms Morbidity Probiotics Signal transduction Signaling Supplements Tumor necrosis factor-α Ubiquitin-Protein Ligases - metabolism |
title | Biological pathways via which the anthocyanin malvidin alleviated the murine colitis induced by Citrobacter rodentium |
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