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
Authors: Verdonck, F ×
Cox, E
van Gog, K
Van der Stede, Y
Duchateau, L
Deprez, P
Goddeeris, Bruno #
Issue Date: Jul-2002
Publisher: Elsevier sci ltd
Series Title: Vaccine vol:20 issue:23-24 pages:2995-3004
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. (C) 2002 Elsevier Science Ltd. All rights reserved.
ISSN: 0264-410X
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Division of Gene Technology (-)
× corresponding author
# (joint) last author

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