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Different kinetic of antibody responses following infection of newly weaned pigs with an F4 enterotoxigenic Escherichia coli strain or an F18 verotoxigenic Escherichia coli strain
To develop a vaccine against Escherichia coli-induced post-weaning diarrhea and edema disease, insights in the induction of the protective immune response following infection with these pathogenic E. coli is needed. Therefore, the fimbriae-specific antibody response of newly weaned pigs following in...
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Published in: | Vaccine 2002-07, Vol.20 (23), p.2995-3004 |
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container_title | Vaccine |
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creator | Verdonck, F Cox, E van Gog, K Van der Stede, Y Duchateau, L Deprez, P Goddeeris, B.M |
description | To develop a vaccine against
Escherichia coli-induced post-weaning diarrhea and edema disease, insights in the induction of the protective immune response following infection with these pathogenic
E. coli is needed. Therefore, the fimbriae-specific antibody response of newly weaned pigs following infection with the Shiga-like toxin type II variant (SLT-IIv) producing F18
+ verotoxigenic
E. coli (VTEC) (strain 107/86) was compared with the response following an infection with LT producing F4
+ enterotoxigenic
E. coli (ETEC) (strain GIS 26). F4
+ ETEC were able to colonize the gut very soon after infection, as peak excretion of F4
+
E. coli bacteria was seen 2 days post-infection (dpi), but had already disappeared 7
dpi. On the other hand, F18
+ VTEC infection resulted in a slower colonization of the gut as the peak excretion of F18
+
E. coli was observed between 3 and 5
dpi, but this colonization remained longer as F18
+
E. coli were detected till 9
dpi in feces. Furthermore, this fast colonization pattern of F4
+ ETEC is accompanied with the presence of F4-specific antibodies in mucosal tissues and serum from 4
dpi onward, with maximal amounts of F4-specific IgA in the jejunal lamina propria and serum 7
dpi. In contrast, F18-specific IgA was only readily detected in the jejunal lamina propria 15
dpi and showed a maximum serum titer 21
dpi. Besides this faster induction and higher antibody response, the switch from IgM to IgA and IgG was also earlier following the F4
+ ETEC infection. |
doi_str_mv | 10.1016/S0264-410X(02)00220-7 |
format | article |
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Escherichia coli-induced post-weaning diarrhea and edema disease, insights in the induction of the protective immune response following infection with these pathogenic
E. coli is needed. Therefore, the fimbriae-specific antibody response of newly weaned pigs following infection with the Shiga-like toxin type II variant (SLT-IIv) producing F18
+ verotoxigenic
E. coli (VTEC) (strain 107/86) was compared with the response following an infection with LT producing F4
+ enterotoxigenic
E. coli (ETEC) (strain GIS 26). F4
+ ETEC were able to colonize the gut very soon after infection, as peak excretion of F4
+
E. coli bacteria was seen 2 days post-infection (dpi), but had already disappeared 7
dpi. On the other hand, F18
+ VTEC infection resulted in a slower colonization of the gut as the peak excretion of F18
+
E. coli was observed between 3 and 5
dpi, but this colonization remained longer as F18
+
E. coli were detected till 9
dpi in feces. Furthermore, this fast colonization pattern of F4
+ ETEC is accompanied with the presence of F4-specific antibodies in mucosal tissues and serum from 4
dpi onward, with maximal amounts of F4-specific IgA in the jejunal lamina propria and serum 7
dpi. In contrast, F18-specific IgA was only readily detected in the jejunal lamina propria 15
dpi and showed a maximum serum titer 21
dpi. Besides this faster induction and higher antibody response, the switch from IgM to IgA and IgG was also earlier following the F4
+ ETEC infection.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/S0264-410X(02)00220-7</identifier><identifier>PMID: 12126913</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Animals ; Antibodies, Bacterial - biosynthesis ; Antibodies, Bacterial - blood ; Bacterial Adhesion ; Escherichia coli ; Escherichia coli - growth & development ; Escherichia coli - immunology ; Escherichia coli - pathogenicity ; Escherichia coli Infections - immunology ; Escherichia coli Infections - microbiology ; Escherichia coli Proteins - immunology ; Fimbriae Proteins - immunology ; Immunity, Mucosal ; Immunoglobulin A - biosynthesis ; In Vitro Techniques ; Intestinal Mucosa - immunology ; Intestinal Mucosa - microbiology ; Kinetics ; Mucosal immune response ; Pig ; Species Specificity ; Sus scrofa</subject><ispartof>Vaccine, 2002-07, Vol.20 (23), p.2995-3004</ispartof><rights>2002 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-8cd8c34332dfa3a0812b8ff1209a1b6ee7b9303c2ecbb2e8c1d0dc224dd37f4c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12126913$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Verdonck, F</creatorcontrib><creatorcontrib>Cox, E</creatorcontrib><creatorcontrib>van Gog, K</creatorcontrib><creatorcontrib>Van der Stede, Y</creatorcontrib><creatorcontrib>Duchateau, L</creatorcontrib><creatorcontrib>Deprez, P</creatorcontrib><creatorcontrib>Goddeeris, B.M</creatorcontrib><title>Different kinetic of antibody responses following infection of newly weaned pigs with an F4 enterotoxigenic Escherichia coli strain or an F18 verotoxigenic Escherichia coli strain</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>To develop a vaccine against
Escherichia coli-induced post-weaning diarrhea and edema disease, insights in the induction of the protective immune response following infection with these pathogenic
E. coli is needed. Therefore, the fimbriae-specific antibody response of newly weaned pigs following infection with the Shiga-like toxin type II variant (SLT-IIv) producing F18
+ verotoxigenic
E. coli (VTEC) (strain 107/86) was compared with the response following an infection with LT producing F4
+ enterotoxigenic
E. coli (ETEC) (strain GIS 26). F4
+ ETEC were able to colonize the gut very soon after infection, as peak excretion of F4
+
E. coli bacteria was seen 2 days post-infection (dpi), but had already disappeared 7
dpi. On the other hand, F18
+ VTEC infection resulted in a slower colonization of the gut as the peak excretion of F18
+
E. coli was observed between 3 and 5
dpi, but this colonization remained longer as F18
+
E. coli were detected till 9
dpi in feces. Furthermore, this fast colonization pattern of F4
+ ETEC is accompanied with the presence of F4-specific antibodies in mucosal tissues and serum from 4
dpi onward, with maximal amounts of F4-specific IgA in the jejunal lamina propria and serum 7
dpi. In contrast, F18-specific IgA was only readily detected in the jejunal lamina propria 15
dpi and showed a maximum serum titer 21
dpi. Besides this faster induction and higher antibody response, the switch from IgM to IgA and IgG was also earlier following the F4
+ ETEC infection.</description><subject>Animals</subject><subject>Antibodies, Bacterial - biosynthesis</subject><subject>Antibodies, Bacterial - blood</subject><subject>Bacterial Adhesion</subject><subject>Escherichia coli</subject><subject>Escherichia coli - growth & development</subject><subject>Escherichia coli - immunology</subject><subject>Escherichia coli - pathogenicity</subject><subject>Escherichia coli Infections - immunology</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Escherichia coli Proteins - immunology</subject><subject>Fimbriae Proteins - immunology</subject><subject>Immunity, Mucosal</subject><subject>Immunoglobulin A - biosynthesis</subject><subject>In Vitro Techniques</subject><subject>Intestinal Mucosa - immunology</subject><subject>Intestinal Mucosa - microbiology</subject><subject>Kinetics</subject><subject>Mucosal immune response</subject><subject>Pig</subject><subject>Species Specificity</subject><subject>Sus scrofa</subject><issn>0264-410X</issn><issn>1873-2518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqNks1uEzEURi0EoqHwCCCvUFkM3GvPZDwrhEoLSJVYABI7a8a-TgwTO9iThjwXL4jzI9hRVt6ce67t72PsKcJLBJy_-gRiXlc1wtcLEC8AhICqvcdmqFpZiQbVfTb7g5yxRzl_A4BGYveQnaFAMe9Qztivt945ShQm_t0Hmrzh0fE-TH6IdscT5XUMmTJ3cRzj1ocF98GRmXwMezLQdtzxLfWBLF_7ReZbPy2LgF_XvFgpxSn-9AsKxXyVzZKSN0vfcxNHz_OUel886TCAit_-D_-YPXD9mOnJ6TxnX66vPl--r24-vvtw-eamMrVopkoZq4yspRTW9bIHhWJQzqGArsdhTtQOnQRpBJlhEKQMWrBGiNpa2brayHP2_Ohdp_hjQ3nSK58NjWN5bNxk3WJXC4ntnSCquu1AyQJe_BtsANp23iAUtDmiJsWcEzm9Tn7Vp51G0PsG6EMD9D5eDUIfGqD3d3l2WrEZVmT_Tp0iL8DrI0Dl6249JZ2Np2DI-lRy1Tb6O1b8BhIkxH0</recordid><startdate>20020726</startdate><enddate>20020726</enddate><creator>Verdonck, F</creator><creator>Cox, E</creator><creator>van Gog, K</creator><creator>Van der Stede, Y</creator><creator>Duchateau, L</creator><creator>Deprez, P</creator><creator>Goddeeris, B.M</creator><general>Elsevier Ltd</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>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20020726</creationdate><title>Different kinetic of antibody responses following infection of newly weaned pigs with an F4 enterotoxigenic Escherichia coli strain or an F18 verotoxigenic Escherichia coli strain</title><author>Verdonck, F ; Cox, E ; van Gog, K ; Van der Stede, Y ; Duchateau, L ; Deprez, P ; Goddeeris, B.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-8cd8c34332dfa3a0812b8ff1209a1b6ee7b9303c2ecbb2e8c1d0dc224dd37f4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Antibodies, Bacterial - biosynthesis</topic><topic>Antibodies, Bacterial - blood</topic><topic>Bacterial Adhesion</topic><topic>Escherichia coli</topic><topic>Escherichia coli - growth & development</topic><topic>Escherichia coli - immunology</topic><topic>Escherichia coli - pathogenicity</topic><topic>Escherichia coli Infections - immunology</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Escherichia coli Proteins - immunology</topic><topic>Fimbriae Proteins - immunology</topic><topic>Immunity, Mucosal</topic><topic>Immunoglobulin A - biosynthesis</topic><topic>In Vitro Techniques</topic><topic>Intestinal Mucosa - immunology</topic><topic>Intestinal Mucosa - microbiology</topic><topic>Kinetics</topic><topic>Mucosal immune response</topic><topic>Pig</topic><topic>Species Specificity</topic><topic>Sus scrofa</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Verdonck, F</creatorcontrib><creatorcontrib>Cox, E</creatorcontrib><creatorcontrib>van Gog, K</creatorcontrib><creatorcontrib>Van der Stede, Y</creatorcontrib><creatorcontrib>Duchateau, L</creatorcontrib><creatorcontrib>Deprez, P</creatorcontrib><creatorcontrib>Goddeeris, B.M</creatorcontrib><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>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Verdonck, F</au><au>Cox, E</au><au>van Gog, K</au><au>Van der Stede, Y</au><au>Duchateau, L</au><au>Deprez, P</au><au>Goddeeris, B.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different kinetic of antibody responses following infection of newly weaned pigs with an F4 enterotoxigenic Escherichia coli strain or an F18 verotoxigenic Escherichia coli strain</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2002-07-26</date><risdate>2002</risdate><volume>20</volume><issue>23</issue><spage>2995</spage><epage>3004</epage><pages>2995-3004</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><abstract>To develop a vaccine against
Escherichia coli-induced post-weaning diarrhea and edema disease, insights in the induction of the protective immune response following infection with these pathogenic
E. coli is needed. Therefore, the fimbriae-specific antibody response of newly weaned pigs following infection with the Shiga-like toxin type II variant (SLT-IIv) producing F18
+ verotoxigenic
E. coli (VTEC) (strain 107/86) was compared with the response following an infection with LT producing F4
+ enterotoxigenic
E. coli (ETEC) (strain GIS 26). F4
+ ETEC were able to colonize the gut very soon after infection, as peak excretion of F4
+
E. coli bacteria was seen 2 days post-infection (dpi), but had already disappeared 7
dpi. On the other hand, F18
+ VTEC infection resulted in a slower colonization of the gut as the peak excretion of F18
+
E. coli was observed between 3 and 5
dpi, but this colonization remained longer as F18
+
E. coli were detected till 9
dpi in feces. Furthermore, this fast colonization pattern of F4
+ ETEC is accompanied with the presence of F4-specific antibodies in mucosal tissues and serum from 4
dpi onward, with maximal amounts of F4-specific IgA in the jejunal lamina propria and serum 7
dpi. In contrast, F18-specific IgA was only readily detected in the jejunal lamina propria 15
dpi and showed a maximum serum titer 21
dpi. Besides this faster induction and higher antibody response, the switch from IgM to IgA and IgG was also earlier following the F4
+ ETEC infection.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>12126913</pmid><doi>10.1016/S0264-410X(02)00220-7</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Antibodies, Bacterial - biosynthesis Antibodies, Bacterial - blood Bacterial Adhesion Escherichia coli Escherichia coli - growth & development Escherichia coli - immunology Escherichia coli - pathogenicity Escherichia coli Infections - immunology Escherichia coli Infections - microbiology Escherichia coli Proteins - immunology Fimbriae Proteins - immunology Immunity, Mucosal Immunoglobulin A - biosynthesis In Vitro Techniques Intestinal Mucosa - immunology Intestinal Mucosa - microbiology Kinetics Mucosal immune response Pig Species Specificity Sus scrofa |
title | Different kinetic of antibody responses following infection of newly weaned pigs with an F4 enterotoxigenic Escherichia coli strain or an F18 verotoxigenic Escherichia coli strain |
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