Molecular characterization and differential expression analysis of interleukin 1 beta from Ovis aries

文献类型： 外文期刊

第一作者： Shui, Yi-Ming

作者： Shui, Yi-Ming;Lu, Shi-Ying;Guo, Xing;Liu, Xi-Lin;Hu, Pan;Qu, Lin-Lin;Liu, Nan-Nan;Li, Yan-Song;Wang, Lu-Lu;Zhai, Fei-Fei;Ju, Dan-Di;Liu, Zeng-Shan;Zhou, Yu;Ren, Hong-Lin;Fu, Bao-Quan;Guo, Xing

作者机构：

关键词： Ovis aries; Interleukin 1 beta; Monoclonal antibodies; Expression analysis; Brucella

期刊名称：MICROBIAL PATHOGENESIS （ 影响因子：3.738； 五年影响因子：3.663 ）

ISSN： 0882-4010

年卷期： 2018 年 116 卷

页码：

收录情况： SCI

摘要： The interleukin-1 family is an important component of the innate immune system and plays an important role in regulating immune responses on the invasion of intracellular parasites in the acquired immune system. Interleukin 1 beta (IL-1 beta) is one of the members of the IL-1 family that predominantly activates downstream signaling pathways to play immunological functions of stimulating T and B lymphocyte activation and promoting the various syntheses of inflammatory substances in conjunction with other cytokines. Here, a full-length IL-1 beta cDNA (OaIL-1 beta) of sheep (Ovis aries) was cloned using rapid amplification of cDNA ends (RACE), which consists of 1494 bp and contains a 5'-UTR region with a length of 83 bp, a complete ORF of 801 bp in length, and a 3'-UTR region with a length of 642 bp. Recombinant protein OalL-1 beta was expressed and purified, and the monoclonal antibody against IL-1 beta of sheep is prepared. Western blotting results showed that the sheep IL-1 beta protein was detected in the heart, liver, lung, kidney, stomach, intestine, muscle, lymph nodes and leukocytes with the highest expression in the muscle and the lowest expression in the lung. Different bacteria treating sheep white blood cells induced differential expression of OaIL-1 beta. Compared with the normal sheep, OaIL-1 beta in the buffy coat was differentially expressed in the Brucella melitensis-challenged group and the B. suis S2 strain- inoculated group. However, whether IL-1 beta may be considered as a molecular biomarker for differing Brucella-infected animals from brucellosis-vaccinated animals or not need to be further studied.

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