F4+ ETEC infection and oral immunization with F4 fimbriae elicits an IL-17-dominated immune response
Enterotoxigenic Escherichia coli (ETEC) are an important cause of post-weaning diarrhea (PWD) in piglets. Porcine-specific ETEC strains possess different fimbrial subtypes of which F4 fimbriae are the most frequently associated with ETEC-induced diarrhea in piglets. These F4 fimbriae are potent oral...
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description | Enterotoxigenic Escherichia coli (ETEC) are an important cause of post-weaning diarrhea (PWD) in piglets. Porcine-specific ETEC strains possess different fimbrial subtypes of which F4 fimbriae are the most frequently associated with ETEC-induced diarrhea in piglets. These F4 fimbriae are potent oral immunogens that induce protective F4-specific IgA antibody secreting cells at intestinal tissues. Recently, T-helper 17 (Th17) cells have been implicated in the protection of the host against extracellular pathogens. However, it remains unknown if Th17 effector responses are needed to clear ETEC infections. In the present study, we aimed to elucidate if ETEC elicits a Th17 response in piglets and if F4 fimbriae trigger a similar response. F4(+) ETEC infection upregulated IL-17A, IL-17F, IL-21 and IL-23p19, but not IL-12 and IFN-γ mRNA expression in the systemic and mucosal immune system. Similarly, oral immunization with F4 fimbriae triggered a Th17 signature evidenced by an upregulated mRNA expression of IL-17F, RORγt, IL-23p19 and IL-21 in the peripheral blood mononuclear cells (PBMCs). Intriguingly, IL-17A mRNA levels were unaltered. To further evaluate this difference between systemic and mucosal immune responses, we assayed the cytokine mRNA profile of F4 fimbriae stimulated PBMCs. F4 fimbriae induced IL-17A, IL-17F, IL-22 and IL-23p19, but downregulated IL-17B mRNA expression. Altogether, these data indicate a Th17 dominated response upon oral immunization with F4 fimbriae and F4(+) ETEC infection. Our work also highlights that IL-17B and IL-17F participate in the immune response to protect the host against F4(+) ETEC infection and could aid in the design of future ETEC vaccines. |
doi_str_mv | 10.1186/s13567-015-0264-2 |
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Porcine-specific ETEC strains possess different fimbrial subtypes of which F4 fimbriae are the most frequently associated with ETEC-induced diarrhea in piglets. These F4 fimbriae are potent oral immunogens that induce protective F4-specific IgA antibody secreting cells at intestinal tissues. Recently, T-helper 17 (Th17) cells have been implicated in the protection of the host against extracellular pathogens. However, it remains unknown if Th17 effector responses are needed to clear ETEC infections. In the present study, we aimed to elucidate if ETEC elicits a Th17 response in piglets and if F4 fimbriae trigger a similar response. F4(+) ETEC infection upregulated IL-17A, IL-17F, IL-21 and IL-23p19, but not IL-12 and IFN-γ mRNA expression in the systemic and mucosal immune system. Similarly, oral immunization with F4 fimbriae triggered a Th17 signature evidenced by an upregulated mRNA expression of IL-17F, RORγt, IL-23p19 and IL-21 in the peripheral blood mononuclear cells (PBMCs). Intriguingly, IL-17A mRNA levels were unaltered. To further evaluate this difference between systemic and mucosal immune responses, we assayed the cytokine mRNA profile of F4 fimbriae stimulated PBMCs. F4 fimbriae induced IL-17A, IL-17F, IL-22 and IL-23p19, but downregulated IL-17B mRNA expression. Altogether, these data indicate a Th17 dominated response upon oral immunization with F4 fimbriae and F4(+) ETEC infection. Our work also highlights that IL-17B and IL-17F participate in the immune response to protect the host against F4(+) ETEC infection and could aid in the design of future ETEC vaccines.</description><identifier>ISSN: 1297-9716</identifier><identifier>ISSN: 0928-4249</identifier><identifier>EISSN: 1297-9716</identifier><identifier>DOI: 10.1186/s13567-015-0264-2</identifier><identifier>PMID: 26490738</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Animals ; Antigens, Bacterial - immunology ; Cytokines - metabolism ; Enterotoxigenic Escherichia coli - immunology ; Escherichia coli Infections - immunology ; Escherichia coli Infections - microbiology ; Escherichia coli Infections - veterinary ; Escherichia coli Proteins - immunology ; Fimbriae Proteins - immunology ; Gene Expression ; Immunity, Innate ; Immunity, Mucosal ; Interleukin-17 - immunology ; Life Sciences ; Medical research ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Swine ; Swine Diseases - immunology ; Swine Diseases - microbiology ; Th17 Cells - immunology ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Veterinary medicine</subject><ispartof>Veterinary research (Paris), 2015-10, Vol.46 (1), p.121-121, Article 121</ispartof><rights>Copyright BioMed Central 2015</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Luo et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-7910f40bfcc122ba3865c99957b7b5b2e44c388aee3248cc9f7a7fd8c9d79c2b3</citedby><cites>FETCH-LOGICAL-c509t-7910f40bfcc122ba3865c99957b7b5b2e44c388aee3248cc9f7a7fd8c9d79c2b3</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/PMC4618862/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618862/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26490738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01341430$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, Yu</creatorcontrib><creatorcontrib>Van Nguyen, Ut</creatorcontrib><creatorcontrib>de la Fe Rodriguez, Pedro Y</creatorcontrib><creatorcontrib>Devriendt, Bert</creatorcontrib><creatorcontrib>Cox, Eric</creatorcontrib><title>F4+ ETEC infection and oral immunization with F4 fimbriae elicits an IL-17-dominated immune response</title><title>Veterinary research (Paris)</title><addtitle>Vet Res</addtitle><description>Enterotoxigenic Escherichia coli (ETEC) are an important cause of post-weaning diarrhea (PWD) in piglets. Porcine-specific ETEC strains possess different fimbrial subtypes of which F4 fimbriae are the most frequently associated with ETEC-induced diarrhea in piglets. These F4 fimbriae are potent oral immunogens that induce protective F4-specific IgA antibody secreting cells at intestinal tissues. Recently, T-helper 17 (Th17) cells have been implicated in the protection of the host against extracellular pathogens. However, it remains unknown if Th17 effector responses are needed to clear ETEC infections. In the present study, we aimed to elucidate if ETEC elicits a Th17 response in piglets and if F4 fimbriae trigger a similar response. F4(+) ETEC infection upregulated IL-17A, IL-17F, IL-21 and IL-23p19, but not IL-12 and IFN-γ mRNA expression in the systemic and mucosal immune system. Similarly, oral immunization with F4 fimbriae triggered a Th17 signature evidenced by an upregulated mRNA expression of IL-17F, RORγt, IL-23p19 and IL-21 in the peripheral blood mononuclear cells (PBMCs). Intriguingly, IL-17A mRNA levels were unaltered. To further evaluate this difference between systemic and mucosal immune responses, we assayed the cytokine mRNA profile of F4 fimbriae stimulated PBMCs. F4 fimbriae induced IL-17A, IL-17F, IL-22 and IL-23p19, but downregulated IL-17B mRNA expression. Altogether, these data indicate a Th17 dominated response upon oral immunization with F4 fimbriae and F4(+) ETEC infection. Our work also highlights that IL-17B and IL-17F participate in the immune response to protect the host against F4(+) ETEC infection and could aid in the design of future ETEC vaccines.</description><subject>Animals</subject><subject>Antigens, Bacterial - immunology</subject><subject>Cytokines - metabolism</subject><subject>Enterotoxigenic Escherichia coli - immunology</subject><subject>Escherichia coli Infections - immunology</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Escherichia coli Infections - veterinary</subject><subject>Escherichia coli Proteins - immunology</subject><subject>Fimbriae Proteins - immunology</subject><subject>Gene Expression</subject><subject>Immunity, Innate</subject><subject>Immunity, Mucosal</subject><subject>Interleukin-17 - immunology</subject><subject>Life Sciences</subject><subject>Medical research</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Swine</subject><subject>Swine Diseases - immunology</subject><subject>Swine Diseases - microbiology</subject><subject>Th17 Cells - immunology</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Veterinary medicine</subject><issn>1297-9716</issn><issn>0928-4249</issn><issn>1297-9716</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkUtv1DAUhS0Eog_4AWyQJTZUKOD3Y4NUjWZopZHYlLXlOA7jKrEHOymCX49DSlW6snX93XPP9QHgDUYfMVbiU8GUC9kgzBtEBGvIM3CKiZaNllg8f3Q_AWel3CKEBeXsJTipsEaSqlPQ7dgHuL3ZbmCIvXdTSBHa2MGU7QDDOM4x_LZ_qz_DdIA7BvswtjlYD_0QXJhKxeH1vsGy6dIYop18tzZ6mH05plj8K_Cit0Pxr-_Pc_Btt73ZXDX7r1-uN5f7xnGkp0ZqjHqG2t45TEhrqRLcaa25bGXLW-IZc1Qp6z0lTDmne2ll3ymnO6kdaek5-LzqHud29J3zcaprmGMOo82_TLLB_P8Sw8F8T3eGCayUIFXgYhU4PGm7utybpYYwZZhRdIcr-_5-WE4_Zl8mM4bi_DDY6NNcDJZEMiqUFBV99wS9TXOO9SsqJQmRhLNFEK-Uy6mU7PsHBxiZJW-z5l1NcLPkbRbDbx9v_NDxL2D6BzGepOw</recordid><startdate>20151021</startdate><enddate>20151021</enddate><creator>Luo, Yu</creator><creator>Van Nguyen, Ut</creator><creator>de la Fe Rodriguez, Pedro Y</creator><creator>Devriendt, Bert</creator><creator>Cox, Eric</creator><general>BioMed Central</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope></search><sort><creationdate>20151021</creationdate><title>F4+ ETEC infection and oral immunization with F4 fimbriae elicits an IL-17-dominated immune response</title><author>Luo, Yu ; Van Nguyen, Ut ; de la Fe Rodriguez, Pedro Y ; Devriendt, Bert ; Cox, Eric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-7910f40bfcc122ba3865c99957b7b5b2e44c388aee3248cc9f7a7fd8c9d79c2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Antigens, Bacterial - immunology</topic><topic>Cytokines - metabolism</topic><topic>Enterotoxigenic Escherichia coli - immunology</topic><topic>Escherichia coli Infections - immunology</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Escherichia coli Infections - veterinary</topic><topic>Escherichia coli Proteins - immunology</topic><topic>Fimbriae Proteins - immunology</topic><topic>Gene Expression</topic><topic>Immunity, Innate</topic><topic>Immunity, Mucosal</topic><topic>Interleukin-17 - immunology</topic><topic>Life Sciences</topic><topic>Medical research</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Swine</topic><topic>Swine Diseases - immunology</topic><topic>Swine Diseases - microbiology</topic><topic>Th17 Cells - immunology</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Veterinary medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Yu</creatorcontrib><creatorcontrib>Van Nguyen, Ut</creatorcontrib><creatorcontrib>de la Fe Rodriguez, Pedro Y</creatorcontrib><creatorcontrib>Devriendt, Bert</creatorcontrib><creatorcontrib>Cox, Eric</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Veterinary research (Paris)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Yu</au><au>Van Nguyen, Ut</au><au>de la Fe Rodriguez, Pedro Y</au><au>Devriendt, Bert</au><au>Cox, Eric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>F4+ ETEC infection and oral immunization with F4 fimbriae elicits an IL-17-dominated immune response</atitle><jtitle>Veterinary research (Paris)</jtitle><addtitle>Vet Res</addtitle><date>2015-10-21</date><risdate>2015</risdate><volume>46</volume><issue>1</issue><spage>121</spage><epage>121</epage><pages>121-121</pages><artnum>121</artnum><issn>1297-9716</issn><issn>0928-4249</issn><eissn>1297-9716</eissn><abstract>Enterotoxigenic Escherichia coli (ETEC) are an important cause of post-weaning diarrhea (PWD) in piglets. Porcine-specific ETEC strains possess different fimbrial subtypes of which F4 fimbriae are the most frequently associated with ETEC-induced diarrhea in piglets. These F4 fimbriae are potent oral immunogens that induce protective F4-specific IgA antibody secreting cells at intestinal tissues. Recently, T-helper 17 (Th17) cells have been implicated in the protection of the host against extracellular pathogens. However, it remains unknown if Th17 effector responses are needed to clear ETEC infections. In the present study, we aimed to elucidate if ETEC elicits a Th17 response in piglets and if F4 fimbriae trigger a similar response. F4(+) ETEC infection upregulated IL-17A, IL-17F, IL-21 and IL-23p19, but not IL-12 and IFN-γ mRNA expression in the systemic and mucosal immune system. Similarly, oral immunization with F4 fimbriae triggered a Th17 signature evidenced by an upregulated mRNA expression of IL-17F, RORγt, IL-23p19 and IL-21 in the peripheral blood mononuclear cells (PBMCs). Intriguingly, IL-17A mRNA levels were unaltered. To further evaluate this difference between systemic and mucosal immune responses, we assayed the cytokine mRNA profile of F4 fimbriae stimulated PBMCs. F4 fimbriae induced IL-17A, IL-17F, IL-22 and IL-23p19, but downregulated IL-17B mRNA expression. Altogether, these data indicate a Th17 dominated response upon oral immunization with F4 fimbriae and F4(+) ETEC infection. Our work also highlights that IL-17B and IL-17F participate in the immune response to protect the host against F4(+) ETEC infection and could aid in the design of future ETEC vaccines.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>26490738</pmid><doi>10.1186/s13567-015-0264-2</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens, Bacterial - immunology Cytokines - metabolism Enterotoxigenic Escherichia coli - immunology Escherichia coli Infections - immunology Escherichia coli Infections - microbiology Escherichia coli Infections - veterinary Escherichia coli Proteins - immunology Fimbriae Proteins - immunology Gene Expression Immunity, Innate Immunity, Mucosal Interleukin-17 - immunology Life Sciences Medical research RNA, Messenger - genetics RNA, Messenger - metabolism Swine Swine Diseases - immunology Swine Diseases - microbiology Th17 Cells - immunology Transcription Factors - genetics Transcription Factors - metabolism Veterinary medicine |
title | F4+ ETEC infection and oral immunization with F4 fimbriae elicits an IL-17-dominated immune response |
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