TLR4 and TLR21 expression, MIF, IFN-β, MD-2, CD14 activation, and sIgA production in chickens administered with EFAL41 strain challenged with Campylobacter jejuni
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27696326
DOI
10.1007/s12223-016-0475-6
PII: 10.1007/s12223-016-0475-6
Knihovny.cz E-zdroje
- MeSH
- Campylobacter jejuni růst a vývoj MeSH
- cékum imunologie mikrobiologie MeSH
- Enterococcus faecium růst a vývoj imunologie MeSH
- feces mikrobiologie MeSH
- imunoglobulin A sekreční genetika MeSH
- interakce hostitele a patogenu MeSH
- interferon beta genetika imunologie MeSH
- kampylobakterové infekce dietoterapie imunologie mikrobiologie veterinární MeSH
- kur domácí MeSH
- lipopolysacharidové receptory genetika imunologie MeSH
- lymfocytární antigen 96 genetika imunologie MeSH
- nemoci drůbeže dietoterapie genetika imunologie mikrobiologie MeSH
- novorozená zvířata MeSH
- probiotika farmakologie MeSH
- protein - isoformy genetika imunologie MeSH
- receptory imunologické genetika imunologie MeSH
- regulace genové exprese MeSH
- signální transdukce MeSH
- toll-like receptor 4 genetika imunologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- imunoglobulin A sekreční MeSH
- interferon beta MeSH
- lipopolysacharidové receptory MeSH
- lymfocytární antigen 96 MeSH
- macrophage migration inhibitory factor receptor MeSH Prohlížeč
- protein - isoformy MeSH
- receptory imunologické MeSH
- toll-like receptor 4 MeSH
The protective effect of Enterococcus faecium EFAL41 on chicken's caecum in relation to the TLR (TLR4 and TLR21) activation and production of luminal IgA challenged with Campylobacter jejuni CCM6191 was assessed. The activation of MIF, IFN-β, MD-2 and CD14 was followed-up after bacterial infection. Day-old chicks (40) were divided into four groups (n = 10): control (C), E. faecium AL41 (EFAL41), C. jejuni (CJ) and combined E. faecium AL41+C. jejuni (EFAL41+CJ). Relative mRNA expression of TLR4, TLR21 and CD14 was upregulated in the probiotic strain and infected (combined) group on day 4 and 7 post infection (p.i.). The caecal relative MD-2 mRNA expression was upregulated on day 4 p.i. in the EFAL41+CJ and CJ groups. MIF and IFN-β reached the highest levels in the combined groups on day 7 p.i. The concentration of the sIgA in intestinal flush was upregulated in EFAL41+CJ group on day 4 p.i. The results demonstrated that E. faecium EFAL41 probiotic strain can modulate the TLRs expression and modify the activation of MIF, IFN-β, MD-2 and CD14 molecules in the chickens caecum challenged with C. jejuni CCM 6191. The counts of EFAL41 were sufficient and high, similarly the counts of enterococci in both, caecum and faeces but without reduction of Campylobacter counts.
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