Escherichia coli lipopolysaccharides decrease molecular expression and activity of disaccharidases and aminopeptidases in weaned pigs

ABSTRACT: Escherichia coli populations in the gut increase after weaning, releasing cell wall lipopolysaccharides (LPS), which are potent pro-inflammatory substances. Objective: this study evaluated LPS intake effects on protein expression and activity of intestinal disaccharidases and aminopetidase...

Full description

Autores:
Agudelo Trujillo, Jorge Hernán
Parra Suescún, Jaime Eduardo
López Herrera, Albeiro
Tipo de recurso:
Article of investigation
Fecha de publicación:
2015
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/8005
Acceso en línea:
http://hdl.handle.net/10495/8005
Palabra clave:
Digestive enzymes
Intestinal villi
RT- PCR (Transcripción reversa-PCR)
Swine
Escherichia coli
Lipopolisacarido
Cerdos destetados
Enzimas digestivas
Rights
openAccess
License
Atribución-NoComercial-CompartirIgual 2.5 Colombia (CC BY-NC-SA 2.5 CO)
Description
Summary:ABSTRACT: Escherichia coli populations in the gut increase after weaning, releasing cell wall lipopolysaccharides (LPS), which are potent pro-inflammatory substances. Objective: this study evaluated LPS intake effects on protein expression and activity of intestinal disaccharidases and aminopetidases. Methods: sixty-four pigs (weaning age: 21 d) were fed a basal diet with added LPS (0.0, 0.3, 0.5, and 1.0 μg LPS/mg feed) during 10 days post-weaning. Pigs were slaughtered on days 1, 5, 7, and 10 post-weaning to assess small intestine molecular expression and enzyme activity. A randomized block design in a 4x4 factorial arrangement was used. Results: intestinal enzyme expression and activity was lower in pigs fed the highest LPS level (p < 0.01). Enzyme values were lowest at day 10 (p < 0.01). The highest gene expression and enzyme activity was observed in duodenum (p < 0.01). Conclusions: data from this study suggest that LPS from E. coli decreases intestinal enzyme expression and activity.