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Quantitative proteomics and bioinformatic analysis provide new insight into the dynamic response of porcine intestine to Salmonella Typhimurium
The enteropathogen Salmonella Typhimurium (S. Typhimurium) is the most commonly non-typhoideal serotype isolated in pig worldwide. Currently, one of the main sources of human infection is by consumption of pork meat. Therefore, prevention and control of salmonellosis in pigs is crucial for minimizin...
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Published in: | Frontiers in cellular and infection microbiology 2015-09, Vol.5, p.64-64 |
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description | The enteropathogen Salmonella Typhimurium (S. Typhimurium) is the most commonly non-typhoideal serotype isolated in pig worldwide. Currently, one of the main sources of human infection is by consumption of pork meat. Therefore, prevention and control of salmonellosis in pigs is crucial for minimizing risks to public health. The aim of the present study was to use isobaric tags for relative and absolute quantification (iTRAQ) to explore differences in the response to Salmonella in two segment of the porcine gut (ileum and colon) along a time course of 1, 2, and 6 days post infection (dpi) with S. Typhimurium. A total of 298 proteins were identified in the infected ileum samples of which, 112 displayed significant expression differences due to Salmonella infection. In colon, 184 proteins were detected in the infected samples of which 46 resulted differentially expressed with respect to the controls. The higher number of changes in protein expression was quantified in ileum at 2 dpi. Further biological interpretation of proteomics data using bioinformatics tools demonstrated that the expression changes in colon were found in proteins involved in cell death and survival, tissue morphology or molecular transport at the early stages and tissue regeneration at 6 dpi. In ileum, however, changes in protein expression were mainly related to immunological and infection diseases, inflammatory response or connective tissue disorders at 1 and 2 dpi. iTRAQ has proved to be a proteomic robust approach allowing us to identify ileum as the earliest response focus upon S. Typhimurium in the porcine gut. In addition, new functions involved in the response to bacteria such as eIF2 signaling, free radical scavengers or antimicrobial peptides (AMP) expression have been identified. Finally, the impairment at of the enterohepatic circulation of bile acids and lipid metabolism by means the under regulation of FABP6 protein and FXR/RXR and LXR/RXR signaling pathway in ileum has been established for the first time in pigs. Taken together, our results provide a better understanding of the porcine response to Salmonella infection and the molecular mechanisms underlying Salmonella-host interactions. |
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Typhimurium) is the most commonly non-typhoideal serotype isolated in pig worldwide. Currently, one of the main sources of human infection is by consumption of pork meat. Therefore, prevention and control of salmonellosis in pigs is crucial for minimizing risks to public health. The aim of the present study was to use isobaric tags for relative and absolute quantification (iTRAQ) to explore differences in the response to Salmonella in two segment of the porcine gut (ileum and colon) along a time course of 1, 2, and 6 days post infection (dpi) with S. Typhimurium. A total of 298 proteins were identified in the infected ileum samples of which, 112 displayed significant expression differences due to Salmonella infection. In colon, 184 proteins were detected in the infected samples of which 46 resulted differentially expressed with respect to the controls. The higher number of changes in protein expression was quantified in ileum at 2 dpi. Further biological interpretation of proteomics data using bioinformatics tools demonstrated that the expression changes in colon were found in proteins involved in cell death and survival, tissue morphology or molecular transport at the early stages and tissue regeneration at 6 dpi. In ileum, however, changes in protein expression were mainly related to immunological and infection diseases, inflammatory response or connective tissue disorders at 1 and 2 dpi. iTRAQ has proved to be a proteomic robust approach allowing us to identify ileum as the earliest response focus upon S. Typhimurium in the porcine gut. In addition, new functions involved in the response to bacteria such as eIF2 signaling, free radical scavengers or antimicrobial peptides (AMP) expression have been identified. Finally, the impairment at of the enterohepatic circulation of bile acids and lipid metabolism by means the under regulation of FABP6 protein and FXR/RXR and LXR/RXR signaling pathway in ileum has been established for the first time in pigs. Taken together, our results provide a better understanding of the porcine response to Salmonella infection and the molecular mechanisms underlying Salmonella-host interactions.</description><identifier>ISSN: 2235-2988</identifier><identifier>EISSN: 2235-2988</identifier><identifier>DOI: 10.3389/fcimb.2015.00064</identifier><identifier>PMID: 26389078</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>Animals ; Colon ; Colon - immunology ; Colon - microbiology ; Computational Biology ; experimentally infected pigs ; Host-Pathogen Interactions ; Ileum ; Ileum - immunology ; Ileum - microbiology ; Intestinal response ; iTRAQ ; Microbiology ; Proteomics ; Salmonella Infections, Animal - pathology ; Salmonella typhimurium ; Salmonella typhimurium - physiology ; Swine ; Swine Diseases - microbiology ; Swine Diseases - pathology ; Time Factors</subject><ispartof>Frontiers in cellular and infection microbiology, 2015-09, Vol.5, p.64-64</ispartof><rights>Copyright © 2015 Collado-Romero, Aguilar, Arce, Lucena, Codrea, Morera, Bendixen, Moreno and Garrido. 2015 Collado-Romero, Aguilar, Arce, Lucena, Codrea, Morera, Bendixen, Moreno and Garrido</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-d799bb2743457b9d5224e15e86bd7e9f510359585cfc72950a8c442c848d91163</citedby><cites>FETCH-LOGICAL-c462t-d799bb2743457b9d5224e15e86bd7e9f510359585cfc72950a8c442c848d91163</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/PMC4558531/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558531/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26389078$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Collado-Romero, Melania</creatorcontrib><creatorcontrib>Aguilar, Carmen</creatorcontrib><creatorcontrib>Arce, Cristina</creatorcontrib><creatorcontrib>Lucena, Concepción</creatorcontrib><creatorcontrib>Codrea, Marius C</creatorcontrib><creatorcontrib>Morera, Luis</creatorcontrib><creatorcontrib>Bendixen, Emoke</creatorcontrib><creatorcontrib>Moreno, Ángela</creatorcontrib><creatorcontrib>Garrido, Juan J</creatorcontrib><title>Quantitative proteomics and bioinformatic analysis provide new insight into the dynamic response of porcine intestine to Salmonella Typhimurium</title><title>Frontiers in cellular and infection microbiology</title><addtitle>Front Cell Infect Microbiol</addtitle><description>The enteropathogen Salmonella Typhimurium (S. Typhimurium) is the most commonly non-typhoideal serotype isolated in pig worldwide. Currently, one of the main sources of human infection is by consumption of pork meat. Therefore, prevention and control of salmonellosis in pigs is crucial for minimizing risks to public health. The aim of the present study was to use isobaric tags for relative and absolute quantification (iTRAQ) to explore differences in the response to Salmonella in two segment of the porcine gut (ileum and colon) along a time course of 1, 2, and 6 days post infection (dpi) with S. Typhimurium. A total of 298 proteins were identified in the infected ileum samples of which, 112 displayed significant expression differences due to Salmonella infection. In colon, 184 proteins were detected in the infected samples of which 46 resulted differentially expressed with respect to the controls. The higher number of changes in protein expression was quantified in ileum at 2 dpi. Further biological interpretation of proteomics data using bioinformatics tools demonstrated that the expression changes in colon were found in proteins involved in cell death and survival, tissue morphology or molecular transport at the early stages and tissue regeneration at 6 dpi. In ileum, however, changes in protein expression were mainly related to immunological and infection diseases, inflammatory response or connective tissue disorders at 1 and 2 dpi. iTRAQ has proved to be a proteomic robust approach allowing us to identify ileum as the earliest response focus upon S. Typhimurium in the porcine gut. In addition, new functions involved in the response to bacteria such as eIF2 signaling, free radical scavengers or antimicrobial peptides (AMP) expression have been identified. Finally, the impairment at of the enterohepatic circulation of bile acids and lipid metabolism by means the under regulation of FABP6 protein and FXR/RXR and LXR/RXR signaling pathway in ileum has been established for the first time in pigs. Taken together, our results provide a better understanding of the porcine response to Salmonella infection and the molecular mechanisms underlying Salmonella-host interactions.</description><subject>Animals</subject><subject>Colon</subject><subject>Colon - immunology</subject><subject>Colon - microbiology</subject><subject>Computational Biology</subject><subject>experimentally infected pigs</subject><subject>Host-Pathogen Interactions</subject><subject>Ileum</subject><subject>Ileum - immunology</subject><subject>Ileum - microbiology</subject><subject>Intestinal response</subject><subject>iTRAQ</subject><subject>Microbiology</subject><subject>Proteomics</subject><subject>Salmonella Infections, Animal - pathology</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - physiology</subject><subject>Swine</subject><subject>Swine Diseases - microbiology</subject><subject>Swine Diseases - pathology</subject><subject>Time Factors</subject><issn>2235-2988</issn><issn>2235-2988</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkk1v1DAQhiMEolXpnRPykcsu_oztCxKq-KhUCSHK2XLsya6rxA52UrS_gr-Ms1uq9jSjmXcej0dv07wleMuY0h96F8ZuSzERW4xxy18055QysaFaqZdP8rPmspS7KsESU6XZ6-aMthWApTpv_v5YbJzDbOdwD2jKaYY0BleQjR51IYXYpzzWrqsVOxxKKKvqPnhAEf6gEEvY7eca54TmPSB_iLYCUIYypVgApR5NKbsQYRVBmdesin_aYUwRhsGi28O0D-OSwzK-aV71dihw-RAvml9fPt9efdvcfP96ffXpZuN4S-eNl1p3HZWccSE77QWlHIgA1XZegu4FwUxooYTrnaRaYKsc59QprrwmpGUXzfWJ65O9M1MOo80Hk2wwx0LKO2Nz_fUARuJeEu2ZaLHjFrzmzjrlW2o1xa6zlfXxxJqWbgTvIM7ZDs-gzzsx7M0u3Rsu6oaMVMD7B0BOv5d6IjOG4tbTREhLMUSSVjMpCa1SfJK6nErJ0D8-Q7BZbWGOtjCrLczRFnXk3dP1Hgf-m4D9A3uyuLc</recordid><startdate>20150903</startdate><enddate>20150903</enddate><creator>Collado-Romero, Melania</creator><creator>Aguilar, Carmen</creator><creator>Arce, Cristina</creator><creator>Lucena, Concepción</creator><creator>Codrea, Marius C</creator><creator>Morera, Luis</creator><creator>Bendixen, Emoke</creator><creator>Moreno, Ángela</creator><creator>Garrido, Juan J</creator><general>Frontiers Media S.A</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>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150903</creationdate><title>Quantitative proteomics and bioinformatic analysis provide new insight into the dynamic response of porcine intestine to Salmonella Typhimurium</title><author>Collado-Romero, Melania ; Aguilar, Carmen ; Arce, Cristina ; Lucena, Concepción ; Codrea, Marius C ; Morera, Luis ; Bendixen, Emoke ; Moreno, Ángela ; Garrido, Juan J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-d799bb2743457b9d5224e15e86bd7e9f510359585cfc72950a8c442c848d91163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Colon</topic><topic>Colon - immunology</topic><topic>Colon - microbiology</topic><topic>Computational Biology</topic><topic>experimentally infected pigs</topic><topic>Host-Pathogen Interactions</topic><topic>Ileum</topic><topic>Ileum - immunology</topic><topic>Ileum - microbiology</topic><topic>Intestinal response</topic><topic>iTRAQ</topic><topic>Microbiology</topic><topic>Proteomics</topic><topic>Salmonella Infections, Animal - pathology</topic><topic>Salmonella typhimurium</topic><topic>Salmonella typhimurium - physiology</topic><topic>Swine</topic><topic>Swine Diseases - microbiology</topic><topic>Swine Diseases - pathology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Collado-Romero, Melania</creatorcontrib><creatorcontrib>Aguilar, Carmen</creatorcontrib><creatorcontrib>Arce, Cristina</creatorcontrib><creatorcontrib>Lucena, Concepción</creatorcontrib><creatorcontrib>Codrea, Marius C</creatorcontrib><creatorcontrib>Morera, Luis</creatorcontrib><creatorcontrib>Bendixen, Emoke</creatorcontrib><creatorcontrib>Moreno, Ángela</creatorcontrib><creatorcontrib>Garrido, Juan J</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>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in cellular and infection microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Collado-Romero, Melania</au><au>Aguilar, Carmen</au><au>Arce, Cristina</au><au>Lucena, Concepción</au><au>Codrea, Marius C</au><au>Morera, Luis</au><au>Bendixen, Emoke</au><au>Moreno, Ángela</au><au>Garrido, Juan J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative proteomics and bioinformatic analysis provide new insight into the dynamic response of porcine intestine to Salmonella Typhimurium</atitle><jtitle>Frontiers in cellular and infection microbiology</jtitle><addtitle>Front Cell Infect Microbiol</addtitle><date>2015-09-03</date><risdate>2015</risdate><volume>5</volume><spage>64</spage><epage>64</epage><pages>64-64</pages><issn>2235-2988</issn><eissn>2235-2988</eissn><abstract>The enteropathogen Salmonella Typhimurium (S. Typhimurium) is the most commonly non-typhoideal serotype isolated in pig worldwide. Currently, one of the main sources of human infection is by consumption of pork meat. Therefore, prevention and control of salmonellosis in pigs is crucial for minimizing risks to public health. The aim of the present study was to use isobaric tags for relative and absolute quantification (iTRAQ) to explore differences in the response to Salmonella in two segment of the porcine gut (ileum and colon) along a time course of 1, 2, and 6 days post infection (dpi) with S. Typhimurium. A total of 298 proteins were identified in the infected ileum samples of which, 112 displayed significant expression differences due to Salmonella infection. In colon, 184 proteins were detected in the infected samples of which 46 resulted differentially expressed with respect to the controls. The higher number of changes in protein expression was quantified in ileum at 2 dpi. Further biological interpretation of proteomics data using bioinformatics tools demonstrated that the expression changes in colon were found in proteins involved in cell death and survival, tissue morphology or molecular transport at the early stages and tissue regeneration at 6 dpi. In ileum, however, changes in protein expression were mainly related to immunological and infection diseases, inflammatory response or connective tissue disorders at 1 and 2 dpi. iTRAQ has proved to be a proteomic robust approach allowing us to identify ileum as the earliest response focus upon S. Typhimurium in the porcine gut. In addition, new functions involved in the response to bacteria such as eIF2 signaling, free radical scavengers or antimicrobial peptides (AMP) expression have been identified. Finally, the impairment at of the enterohepatic circulation of bile acids and lipid metabolism by means the under regulation of FABP6 protein and FXR/RXR and LXR/RXR signaling pathway in ileum has been established for the first time in pigs. Taken together, our results provide a better understanding of the porcine response to Salmonella infection and the molecular mechanisms underlying Salmonella-host interactions.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>26389078</pmid><doi>10.3389/fcimb.2015.00064</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Colon Colon - immunology Colon - microbiology Computational Biology experimentally infected pigs Host-Pathogen Interactions Ileum Ileum - immunology Ileum - microbiology Intestinal response iTRAQ Microbiology Proteomics Salmonella Infections, Animal - pathology Salmonella typhimurium Salmonella typhimurium - physiology Swine Swine Diseases - microbiology Swine Diseases - pathology Time Factors |
title | Quantitative proteomics and bioinformatic analysis provide new insight into the dynamic response of porcine intestine to Salmonella Typhimurium |
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