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Molecular Identification of C-type Lectin Receptor Gene CD302 from Japanese sea bass (Lateolabrax japonicus) and Its Expression upon Vibrio harveyi Infection |
ZHANG Yi-Rong, LI Chang-Hong*, CHEN Jiong |
Laboratory of Biochemistry and Molecular Biology, School of Marine Sciences, Ningbo University, Ningbo 315832, China |
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Abstract Cluster of differentiation 302 (CD302), also known as DEC-205-associated C-type lectin-1 (DCL-1), is a type I transmembrane C-type lectin receptor. It participates in the processes of cell adhesion, migration, endocytosis and phagocytosis, and plays an important role in resisting pathogenic infection. In this study, the LjCD302 cDNA sequence (GenBank No. MT468568) was obtained from Japanese sea bass (Lateolabrax Japonicus) tissue transcriptome. It spanned 2 280 nucleotides (nts) and comprised an open reading frame of 729 nts, which encoded a polypeptide of 242 amino acids (aa) with a molecular weight of 26.9 kD and an isoelectric point of 4.97. LjCD302 composed of a signal peptide sequence (aa 1-27), a C-type lectin-like domain (CTLD) (aa 30-165), a transmembrane domain (aa 179-201) and a cytoplasmic tail (aa 202-242). The aa sequence homology analysis showed that LjCD302 shared the highest homology with that of the barramundi perch (Lates calcarifer) (82.0%). Phylogenetic tree analysis showed that CD302 from fish, amphibians, reptiles and mammals grouped into different clusters, and LjCD302 belonged to the fish cluster and had the closest evolutionary relationship with the barramundi perch CD302. Real-time quantitative PCR analysis showed that LjCD302 mRNA in healthy Japanese sea bass was mainly expressed in the liver, followed by the head kidney, and its expression was significantly up-regulated in head kidney, gill, intestine, spleen, and liver of Japanese sea bass after Vibrio harveyi infection (P<0.05). The CTLD domain of LjCD302 was prokaryotically expressed, and its antiserum was prepared. Western blot analysis showed that LjCD302 expression was significantly up-regulated in the head kidney of V. harveyi-infected Japanese sea bass (P<0.05). In summary, the expression of LjCD302 mRNA and protein was positively correlated with V. harveyi infection, suggesting that it may play a crucial role in the antibacterial immune response in fish. The results provide a basis for further research on the function of fish CLR and its mechanism of action in antibacterial immunity.
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Received: 17 June 2020
Published: 01 March 2021
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Corresponding Authors:
*lichanghong0716@163.com
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[1] 林星. 2013. 花鲈皮肤溃疡病病原菌的分离与鉴定[J]. 中国农学通报, 29(32): 100-104. (Lin X.2013. Isolation and identification of the pathogens of the skin ulceration disease in Lateolabrax japonicus[J]. Chinese Agricultural Science Bulletin, 29(32): 100-104.) [2] 乔丹, 丁斐斐, 李长红, 等. 2019. 花鲈结合珠蛋白基因的克隆及其在哈维氏弧菌感染下的表达分析[J]. 农业生物技术学报, 27(11): 2042-2051. (Qiao D, Ding F F, Li C H, et al.2019. Cloning of Lateolabrax japonicus haptoglobin gene and its expression analysis upon Vibrio harveyi infection[J]. Journal of Agricultural Biotechnology, 27(11): 2042-2051.) [3] 张静, 施慧, 谢建军, 等. 2009. 网箱养殖鲈鱼内脏白点病病原的分离与鉴定[J]. 浙江海洋学院学报 (自然科学版), 28(2): 176-182. (Zhang J, Shi H, Xie J, et al.2009. Isolation and identification of causative pathogen for visceral white spot in Lateolabrax japonicus stocked in sea-cage[J]. Journal of Zhejiang Ocean University (Natural Science Edition), 28(2): 176-182.) [4] Ao J, Ding Y, Chen Y, et al.2015. Molecular characterization and biological effects of a C-type lectin-like receptor in large yellow croaker (Larimichthys crocea)[J]. International Journal of Molecular Sciences, 16(12): 29631-29642. [5] Bradford M M.1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding[J]. Analytical Biochemistry, 72(1-2): 248-254. [6] Chen S X, Ma H L, Shi Y H, et al.2016. Molecular and functional characterization of a novel CD302 gene from ayu (Plecoglossus altivelis)[J]. Fish and Shellfish Immunology, 55: 140-148. [7] Du X, Wang G H, Su Y L, et al.2018. Black rockfish C-type lectin, SsCTL4: A pattern recognition receptor that promotes bactericidal activity and virus escape from host immune defense[J]. Fish and Shellfish Immunology, 79: 340-350. [8] Kato M, Khan S, d' Aniello E, et al.2007. The novel endocytic and phagocytic C-type lectin receptor DCL-1/CD302 on macrophages is colocalized with F-actin, suggesting a role in cell adhesion and migration[J]. The Journal of Immunology, 179(9): 6052-6063. [9] Kato M, Khan S, Gonzalez N, et al.2003. Hodgkin's lymphoma cell lines express a fusion protein encoded by intergenically spliced mRNA for the multilectin receptor DEC-205 (CD205) and a novel C-type lectin receptor DCL-1[J]. The Journal of Biological Chemistry, 278(36): 34035-34041. [10] Kerrigan A M, Brown G D.2009. C-type lectins and phagocytosis[J]. Immunobiology, 214(7): 562-575. [11] Liu L, Dang Y F.2020. Antimicrobial activity of mannose binding lectin in grass carp (Ctenopharyngodon idella) in vivo and in vitro[J]. Fish and Shellfish Immunology, 98: 25-33. [12] Liu X L, Tang X C, Wang L, et al.2014. Molecular cloning and expression analysis of mannose receptor in blunt snout bream (Megalobrama amblycephala)[J]. Molecular Biology Reports, 41(7): 4601-4611. [13] Livak K J, Schmittgen T D.2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCt method[J]. Methods, 25(4): 402-408. [14] Mayer S, Raulf M K, Lepenies B.2017. C-type lectins: Their network and roles in pathogen recognition and immunity[J]. Histochemistry and Cell Biology, 147(2): 223-237. [15] Pyz E, Marshall A S, Gordon S, et al.2006. C-type lectin-like receptors on myeloid cells[J]. Annals of Medicine, 38(4): 242-251. [16] Secombes C J, Wang T.2012. The innate and adaptive immune system of fish[J]. Infectious Disease in Aquaculture, 14(7): 3-68. [17] Soanes K H, Figuereido K, Richards R C, et al.2004. Sequence and expression of C-type lectin receptors in Atlantic salmon (Salmo salar)[J]. Immunogenetics, 56(8): 572-584. [18] Xu F, Li M Y, Chen J.2020. D-dopachrome tautomerase from Japanese sea bass (Lateolabrax japonicus) is a chemokine-like cytokine and functional homolog of macrophage migration inhibitory factor[J]. Zoological Research, 41(1): 39-50. [19] Yang G J, Lu X J, Chen Q, et al.2015. Molecular characterization and functional analysis of a novel C-type lectin receptor-like gene from a teleost fish, Plecoglossus altivelis[J]. Fish and Shellfish Immunology, 44(2): 603-610. [20] Zelensky A N, Gready J E.2005. The C‐type lectin‐like domain superfamily[J]. FEBS Journal, 272(24): 6179-6217. [21] Zhang X H, Shi Y H, Chen J.2015. Molecular characterization of a transmembrane C-type lectin receptor gene from ayu (Plecoglossus altivelis) and its effect on the recognition of different bacteria by monocytes/macrophages[J]. Fish and Shellfish Immunology, 66(2): 439-450. [22] Zheng F, Asim M, Lan J, et al.2015. Molecular cloning and functional characterization of mannose receptor in zebrafish (Danio rerio) during infection with Aeromonas sobria[J]. International Journal of Molecular Sciences, 16(5): 10997-11012. |
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