Molecular Cloning and characterization in immune response of a novel C-type lectin gene (LvLc2) from Litopenaeus vannamei
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Affiliation:

1.Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University;2.Tianjin Fisheries Research Institute

Clc Number:

Q786;S945.1

Fund Project:

Natural Science Foundation of Tianjin (19JCYBJC29700, 15JCZDJC33800); Open Research Funding of Tianjin Key Lab of Aqua-Ecology and Aquaculture (TJAE2015005); National Natural Science Foundation of China (31472299)

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    Abstract:

    Litopenaeus vannamei is the largest economic shrimp breed in the world at present. However, with the expansion of shrimp culture, diseases and other problems are exposed gradually. Shrimp culture industry was affected seriously by diseases all over the world. Shrimp belongs to invertebrate, and has no typical acquired immune system. They mainly rely on the innate immune system for defense and protection when pathogens invade. In innate immune response, crustaceans recognize non-self components through pattern recognition receptors (PRRs). The components recognized by PRRs are mainly constitutive and conserved polysaccharide molecules on the surface of microorganisms, which are not produced by eukaryotic cell hosts and are necessary for the survival of pathogenic microorganisms. They are called pathogen associated molecular patterns (PAMPs). The recognition and binding of PRRs to PAMPs is the beginning of humoral immunity. The recognition of PRRS to pathogens can directly or indirectly activate proteases, hemocytes and intracellular signal pathways related to humoral immunity. A variety of immune defense reactions were triggered. It produce antibacterial substances and effective molecules to inhibit and eliminate pathogens. As a pattern recognition receptor and terminal effector, C-type lectin participates in the process of “non self” recognition and elimination of invasive pathogens, which is crucial in the innate immune defense mechanism of crustaceans. In this study, a novel C-type lectin gene (LvLc2, GenBank accession number: KR020738) was cloned from hemocytes of Litopenaeus vannamei according to our previous transcriptome results. Bioinformatics analysis showed that the ORF region of LvLc2 gene was 465 bp encoding 154 aa with 11 bp 5'-UTR and 126 bp 3'-UTR. The predicted molecular weight was 17.16 ku and the theoretical isoelectric point was 4.54. The deduced amino acid sequence contained a signal peptide sequence with 17 amino acids at the amino end and a conserved carbohydrate recognition domain (CRD) at the carboxyl end. LvLc2 gene was expressed in different tissues of L. vannamei. The main expression was in intestine, followed by stomach, hepatopancrease, hemocytes, and the lowest expression level was in muscle. After shrimps were challenged by LPS and PGN, the expression profiles of LvLc2 gene were analyzed by qPCR. Different pathogen-associated molecular patterns (PAMP) could induce response changes of LvLc2 gene after stimulation, which indicated that it had a potential broad-spectrum response pattern. At the same time, it had different expression profiles for different pathogens, which showed the differences of recognition, combination and indirect immune effects. The research of its characterization and function are helpful to better understand the mechanism of shrimp C-type lectin during the process of pathogen infection.

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Hao Shaoyan, Yin Siyu, Gong Chen, Zhang Yichen, Geng Xuyun, Liu Yichen, Sun Jinsheng. Molecular Cloning and characterization in immune response of a novel C-type lectin gene (LvLc2) from Litopenaeus vannamei[J]. Journal of Fisheries of China,2021,45(06):948~957

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History
  • Received:January 16,2021
  • Revised:March 12,2021
  • Adopted:March 16,2021
  • Online: August 04,2021
  • Published: