Cloning and expression analysis of a Toll-like receptor 22 (tlr22) gene from turbot, Scophthalmus maximus

• Published in: Fish & shellfish immunology 2015-06, Vol.44 (2), p.399-409
• Main Authors: Hu, Guo-Bin, Zhang, Shou-Feng, Yang, Xi, Liu, Da-Hai, Liu, Qiu-Ming, Zhang, Shi-Cui
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; Cloning, Molecular; Flatfishes - genetics; Flatfishes - immunology; Gene Components; Gene expression; Gene Expression Profiling; Gene Expression Regulation - physiology; Gills - virology; Iridoviridae; Iridovirus; Lipopolysaccharides; Marine; Molecular Sequence Data; PAMPs; Phylogeny; Pleuronectiformes; Poly I-C; Real-Time Polymerase Chain Reaction; Scophthalmus maximus; Sequence Analysis, DNA; Sequence Homology; Structural characteristics; Teleostei; Tlr22; Toll-Like Receptors - genetics; Toll-Like Receptors - metabolism
• ISSN: 1050-4648; 1095-9947
• DOI: 10.1016/j.fsi.2015.03.001

Toll-like receptor 22 (TLR22) exists exclusively in aquatic animals and recognizes double stranded RNA (dsRNA). In the present study, a tlr22 gene and its 5′-flanking sequence were cloned from turbot, Scophthalmus maximus, its immune responsive expression was subsequently studied in vivo. The turbot (sm)tlr22 gene spans over 5.6 kb with a structure of 4 exon-3 intron and encodes 962 amino acids. The deduced protein shows the highest sequence identity (76.7%) to Japanese flounder Tlr22 and possesses a signal peptide sequence, a leucine-rich repeat (LRR) domain composed of 27 LRR motifs, a transmembrane region and a Toll/interleukin-1 receptor (TIR) domain. Phylogenetic analysis grouped it with other teleost Tlr22s. The interferon-stimulated response element (ISRE) and signal transducer and activator of transcription (STAT) binding site important for the basal transcriptional activity of TLR3 were predicted in the 5′-flanking sequence of smtlr22 gene. Quantitative real-time PCR (qPCR) analysis demonstrated the constitutive expression of smtlr22 mRNA in all examined tissues with higher levels in the head kidney, kidney and spleen. Further, smtlr22 expression was significantly up-regulated following challenge with polyinosinic: polycytidylic acid (poly I:C), lipopolysaccharide (LPS) or turbot reddish body iridovirus (TRBIV) in the gills, head kidney, spleen and muscle, with maximum increases ranging from 2.56 to 6.24 fold upon different immunostimulants and organs. These findings suggest a possible role of Smtlr22 in the immune responses to the infections of a broad range of pathogens that include DNA and RNA viruses and Gram-negative bacteria. •A tlr22 gene and its 5′-flanking sequence were cloned from turbot.•tlr22 transcripts distributed ubiquitously.•The higher levels of tlr22 transcripts were detected in lymphomyeloid-rich tissues.•tlr22 mRNA levels were up-regulated by poly I:C, LPS and TRBIV in immune and non-immune organs.