Recognition of purified beta 1,3/1,6 glucan and molecular signalling in the intestine of Atlantic salmon

Atlantic salmon was orally intubated with a highly purified β-glucan product (MacroGard®) to study the recognition of the molecule by the receptor genes, the regulation of the downstream signalling genes and global proteins, and the micromorphological changes in the intestine. The β-glucan receptor...

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Veröffentlicht in:Developmental and comparative immunology 2016-03, Vol.56, p.57-66
Hauptverfasser: Kiron, Viswanath, Kulkarni, Amod, Dahle, Dalia, Vasanth, Ghana, Lokesh, Jep, Elvebo, Odd
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Sprache:eng
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Zusammenfassung:Atlantic salmon was orally intubated with a highly purified β-glucan product (MacroGard®) to study the recognition of the molecule by the receptor genes, the regulation of the downstream signalling genes and global proteins, and the micromorphological changes in the intestine. The β-glucan receptor genes of Atlantic salmon, sclra, sclrb, sclrc and cr3, seem to recognize the molecule, and initiate the downstream ITAM-motif signalling, as evident from the significantly high mRNA levels of ksyk, mapkin2, il1b and mip2a levels. Among the altered proteins, the Apoa4 (involved in carbohydrate and lipid metabolism); Tagln, Actb (uptake of β-glucan); Psma2 (associated with substrate recognition); and Ckt (energy metabolism-related) were the overexpressed ones. The underexpressed proteins included the Uk114, Rpl9, Ctsb and Lgal that are connected to proliferation, LPS-stimulation, Il1b and lactose recognition, respectively. Furthermore, the mRNA levels of igt and the number of immune cells in the distal intestine were found to increase upon β-glucan uptake by the fish. This study provides some clues on the mechanisms by which the β-glucan evokes response in Atlantic salmon, particularly at the intestinal level. •Recognition and responses of purified β-glucan product at the intestinal level.•Upregulation of genes of C-type lectin receptors.•Overexpression of proteins linked to uptake and substrate recognition.•Presence of more immune cells.
ISSN:0145-305X
1879-0089
DOI:10.1016/j.dci.2015.11.007