Abstract

Dietary supplementation of fish with β-glucans has been commonly associated with immunomodulation and generally accepted as beneficial for fish health. However, to date the exact mechanisms of immunomodulation by β-glucan supplementation in fish have remained elusive. In mammals, a clear relation between high-fibre diets, such as those including β-glucans, and diet-induced immunomodulation via intestinal microbiota and associated metabolites has been observed. In this study, first we describe by 16S rRNA sequencing the active naive microbiota of common carp intestine. Based on the abundance of the genus Bacteroides, well known for their capacity to degrade and ferment carbohydrates, we hypothesize that common carp intestinal microbiota could ferment dietary β-glucans. Indeed, two different β-glucan preparations (curdlan and MacroGard®) were both fermented in vitro, albeit with distinct fermentation dynamics and distinct production of short-chain fatty acids (SCFA). Second, we describe the potential immunomodulatory effects of the three dominant SCFAs (acetate, butyrate, and propionate) on head kidney leukocytes, showing effects on both nitric oxide production and expression of several cytokines (il-1b, il-6, tnfα, and il-10) in vitro. Interestingly, we also observed a regulation of expression of several gpr40L genes, which were recently described as putative SCFA receptors. Third, we describe how a single in vivo oral gavage of carp with MacroGard® modulated simultaneously, the expression of several pro-inflammatory genes (il-1b, il-6, tnfα), type I IFN-associated genes (tlr3.1, mx3), and three specific gpr40L genes. The in vivo observations provide indirect support to our in vitro data and the possible role of SCFAs in β-glucan-induced immunomodulation. We discuss how β-glucan-induced immunomodulatory effects can be explained, at least in part, by fermentation of MacroGard® by specific bacteria, part of the naive microbiota of common carp intestine, and how a subsequent production of SFCAs could possibly explain immunomodulation by β-glucan via SCFA receptors present on leukocytes.

Highlights

  • Effects of immunomodulation by b-glucans have been widely studied in teleost fish

  • The intestinal content of the third segment of the intestine from n = 5 individual fish was analysed by 16S rRNA sequencing, revealing a total of n = 55 active operational taxonomic units (OTUs) in the intestinal content of unhandled carp

  • We confirmed that the carp naive intestinal microbiota has b-glucan fermenting ability by using an b-Glucan-Induced Immuno-Modulation in vitro batch culture system to test fermentation of two different b-glucan preparations

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Summary

Introduction

Effects of immunomodulation by b-glucans have been widely studied in teleost fish. Regardless of administration route or fish species, b-glucans are often associated with immunomodulatory effects and increased resistance to both viral and bacterial infections [as reviewed by [1–3]]. Direct recognition of b-glucans is mediated by at least the C-type lectin receptor (CLR) Dectin-1 [4–6], whereas in invertebrates b-glucans can be recognised by bglucan-binding proteins [7]. For both mammals [8, 9] and invertebrates [7, 10], several non-exclusive pathways play a downstream role in the response to b-glucans, often mediating activation of the transcription factor NF-kB [11]. We proposed that the immuno-modulatory effects of bglucan in carp macrophages could include regulation of a downstream signalling pathway typical of CLR activation and confirmed our hypothesis by pathway analysis of differentially expressed genes (DEGs) [14]. As there is clear evidence for presence of macrophages and other antigen-sampling cells in the fish intestine [as reviewed by [15]], it is possible that recognition of b-glucans in the intestine occurs via a direct recognition mechanism of b-glucan receptors

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