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马蹄蟹血细胞对脂多糖反应的比较转录组分析。

Comparative transcriptome profiling of horseshoe crab Tachypleus gigas hemocytes in response to lipopolysaccharides.

机构信息

School of Health Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, Kelantan, Malaysia.

Faculty of Medicine and Health Sciences, Universiti Malaysia Sabah, Kota Kinabalu, Sabah, Malaysia.

出版信息

Fish Shellfish Immunol. 2021 Oct;117:148-156. doi: 10.1016/j.fsi.2021.08.001. Epub 2021 Aug 3.

DOI:10.1016/j.fsi.2021.08.001
PMID:34358702
Abstract

Horseshoe crabs (HSCs) are living fossil species of marine arthropods with a long evolutionary history spanning approximately 500 million years. Their survival is helped by their innate immune system that comprises cellular and humoral immune components to protect them against invading pathogens. To help understand the genetic mechanisms involved, the present study utilised the Illumina HiSeq platform to perform transcriptomic analysis of hemocytes from the HSC, Tachypleus gigas, that were challenged with lipopolysaccharides (LPS). The high-throughput sequencing resulted in 352,077,208 and 386,749,136 raw reads corresponding to 282,490,910 and 305,709,830 high-quality mappable reads for the control and LPS-treated hemocyte samples, respectively. Based on the log-fold change of > 0.3 or < -0.3, 1338 genes were significantly upregulated and 215 genes were significantly downregulated following LPS stimulation. The differentially expressed genes (DEGs) were further identified to be associated with multiple pathways such as those related to immune defence, stress response, cytoskeleton function and signal transduction. This study provides insights into the underlying molecular and regulatory mechanisms in hemocytes exposed to LPS, which has relevance for the study of the immune response of HSCs to infection.

摘要

马蹄蟹(HSCs)是一种具有悠久进化历史的海洋节肢动物活化石,其历史可追溯至大约 5 亿年前。它们的先天免疫系统由细胞和体液免疫成分组成,可以保护它们免受入侵病原体的侵害,这有助于它们的生存。为了帮助理解所涉及的遗传机制,本研究利用 Illumina HiSeq 平台对 LPS 刺激的中国鲎(Tachypleus gigas)血细胞进行转录组分析。高通量测序分别得到 352,077,208 和 386,749,136 条原始读数,分别对应于对照和 LPS 处理血细胞样本的 282,490,910 和 305,709,830 条高质量可映射读数。基于 log2 倍变化>0.3 或<−0.3,1338 个基因在 LPS 刺激后显著上调,215 个基因显著下调。进一步鉴定差异表达基因(DEGs)与多种途径相关,如免疫防御、应激反应、细胞骨架功能和信号转导。本研究深入了解了暴露于 LPS 的血细胞中的潜在分子和调控机制,这对于研究 HSCs 对感染的免疫反应具有重要意义。

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