Effect of Saccharomyces cerevisiae var. Boulardii and β-galactomannan oligosaccharide on porcine intestinal epithelial and dendritic cells challenged in vitro with Escherichia coli F4 (K88)

被引:55
作者
Badia, Roger [1 ,3 ]
Zanello, Galliano [2 ]
Chevaleyre, Claire [2 ]
Lizardo, Rosil [1 ]
Meurens, Francois [2 ]
Martinez, Paz [3 ]
Brufau, Joaquim [1 ]
Salmon, Henri [2 ]
机构
[1] IRTA, Constanti, Spain
[2] INRA, UR1282, F-37380 Tours, France
[3] UAB, IBB, Bellaterra, Spain
关键词
ENTERICA SEROVAR TYPHIMURIUM; COMMENSAL BACTERIA; FIMBRIAL ADHESIN; LINES; EXPRESSION; MATURATION; SWINE; POLYSACCHARIDES; ACTIVATION; ADHERENCE;
D O I
10.1186/1297-9716-43-4
中图分类号
S85 [动物医学(兽医学)];
学科分类号
090604 [动物药学];
摘要
Probiotic and prebiotics, often called "immune-enhancing" feed additives, are believed to deal with pathogens, preventing the need of an immune response and reducing tissue damage. In this study, we investigated if a recently developed beta-galactomannan (beta GM) had a similar protective role compared to Saccharomyces cerevisiae var. Boulardii (Scb), a proven probiotic, in the context of enterotoxigenic Escherichia coli (ETEC) infection. ETEC causes inflammation, diarrhea and intestinal damage in piglets, resulting in large economic loses worldwide. We observed that Scb and beta GM products inhibited in vitro adhesion of ETEC on cell surface of porcine intestinal IPI-2I cells. Our data showed that Scb and beta GM decreased the mRNA ETEC-induced gene expression of pro-inflammatory cytokines TNF-alpha, IL-6, GM-CSF and chemokines CCL2, CCL20 and CXCL8 on intestinal IPI-2I. Furthermore, we investigated the putative immunomodulatory role of Scb and beta GM on porcine monocyte-derived dendritic cells (DCs) per se and under infection conditions. We observed a slight up-regulation of mRNA for TNF-alpha and CCR7 receptor after co-incubation of DC with Scb and beta GM. However, no differences were found in DC activation upon ETEC infection and Scb or beta GM co-culture. Therefore, our results indicate that, similar to probiotic Scb, prebiotic beta GM may protect intestinal epithelial cells against intestinal pathogens. Finally, although these products may modulate DC activation, their effect under ETEC challenge conditions remains to be elucidated.
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页数:11
相关论文
共 54 条
[1]
Type 1 fimbriae of Salmonella enterica serovar typhimurium bind to enterocytes and contribute to colonization of swine in vivo [J].
Althouse, C ;
Patterson, S ;
Fedorka-Cray, P ;
Isaacson, RE .
INFECTION AND IMMUNITY, 2003, 71 (11) :6446-6452
[2]
[Anonymous], 1997, MED IMP US ANT FOOD
[3]
Innate immune activation of swine intestinal epithelial cell lines (IPEC-J2 and IPI-2I) in response to LPS from Salmonella typhimurium [J].
Arce, C. ;
Ramirez-Boo, M. ;
Lucena, C. ;
Garrido, J. J. .
COMPARATIVE IMMUNOLOGY MICROBIOLOGY AND INFECTIOUS DISEASES, 2010, 33 (02) :161-174
[4]
Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut [J].
Artis, David .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (06) :411-420
[5]
Differential activation and maturation of two porcine DC populations following TLR ligand stimulation [J].
Auray, Gael ;
Facci, Marina R. ;
van Kessel, Jill ;
Buchanan, Rachelle ;
Babiuk, Lorne A. ;
Gerdts, Volker .
MOLECULAR IMMUNOLOGY, 2010, 47 (11-12) :2103-2111
[6]
Food and feed components for gut health-promoting adhesion of E-coli and Salmonella enterica [J].
Becker, Petra M. ;
Galletti, Sara .
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2008, 88 (11) :2026-2035
[7]
Epithelial induction of porcine suppressor of cytokine signaling 2 (SOCS2) gene expression in response to Entamoeba histolytica [J].
Bruel, Timothee ;
Guibon, Roseline ;
Melo, Sandrine ;
Guillen, Nancy ;
Salmon, Henri ;
Girard-Misguich, Fabienne ;
Meurens, Francois .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2010, 34 (05) :562-571
[8]
Brufau J, 2003, NUTR BIOTECHNOLOGY F
[9]
Cloeckaert A, 2001, VET RES, V32, P301, DOI 10.1051/vetres:2001126
[10]
IL-10: The master regulator of immunity to infection [J].
Couper, Kevin N. ;
Blount, Daniel G. ;
Riley, Eleanor M. .
JOURNAL OF IMMUNOLOGY, 2008, 180 (09) :5771-5777