Amphiprion Percula(Lacepède,1802 年)在感染 Cryptocaryon Irritans Brown(布朗,1951 年)后的转录组变异。

IF 2.6 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jose Priya T. A., Charutha Karunakaran, Aishwarya Nath, Sudha Kappalli
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引用次数: 0

摘要

隐鞭毛虫(Cryptocaryon irritans)(布朗,1951 年)经常感染鲳鲉科鱼类,造成严重的经济损失。然而,这些鱼类抗C. irritans的分子机制在很大程度上仍然未知。为了解决这个问题,我们对小丑鱼Amphiprion percula(Lacepède 1802)在感染早期(第1天)和晚期(第3天)的鳃进行了RNA-Seq分析。共鉴定出 1655 个差异表达基因(DEG)。基因本体(GO)和京都基因组百科全书(KEGG)对 DEGs 的通路富集分析表明,遗传变异的巨大差异与以下方面有关:ECM-受体相互作用、P13K-Akt 信号传导、细胞因子-细胞因子受体相互作用以及内吞作用。在感染的早期阶段,参与 ATP 生成、能量平衡和应激控制的关键基因突然增加。然而,在晚期阶段,外周神经系统的急性反应分子(突触传递和局部免疫)、引发糖原合成的代谢系统、能量维持和渗透调节被发现是至关重要的。早期阶段恢复的上调基因(URGs)数量最多,属于 "生物过程 "类别,主要功能是对刺激做出反应、传递信号和进行生物调节。在晚期阶段,大部分上调基因与 "分子功能 "类别下的基因调控和免疫系统过程有关。早期感染中与免疫有关的URG包括主要组织相容性复合体(MHC)II类分子,它们显然触发了CD4+ T细胞激活的Th反应;晚期感染中的URG包括MHC1类分子,它们可能是CD8+ T细胞触发细胞毒性的顶点。感染晚期发现的高水平基因单核苷酸多态性(SNPs)很可能会影响它们对二次感染的易感性。总之,所发现的DEGs及其相关的代谢和免疫途径以及SNPs可能会为协调鱼类的免疫事件和提高鱼类对刺激性角叉菜绦虫的抵抗力提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcriptomic Variation of Amphiprion Percula (Lacepède, 1802) in Response to Infection with Cryptocaryon Irritans Brown, 1951

Transcriptomic Variation of Amphiprion Percula (Lacepède, 1802) in Response to Infection with Cryptocaryon Irritans Brown, 1951

Transcriptomic Variation of Amphiprion Percula (Lacepède, 1802) in Response to Infection with Cryptocaryon Irritans Brown, 1951

Cryptocaryon irritans (Brown 1951) frequently infect the Pomacentridae fishes causing severe economic losses. However, the anti-C. irritans’ molecular mechanism in these fishes remains largely unknown. To address this issue, we conducted RNA-Seq for C. irrtians-infected gills of the clownfish Amphiprion percula (Lacepède 1802) at the early (day 1) and late (day 3) stages of infection. A total of 1655 differentially expressed genes (DEGs) were identified. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses of DEGs showed a vast genetic variation related to the following aspects: ECM-receptor interaction, P13K-Akt signalling, cytokine-cytokine receptor interaction, and endocytosis. During the early phase of infection, key genes involved in ATP production, energy homeostasis, and stress control were abruptly increased. In the late phase, however, acute response molecules of the peripheral nervous system (synaptic transmission and local immunity), metabolic system triggering glycogen synthesis, energy maintenance, and osmoregulation were found to be critical. The highest number of upregulated genes (URGs) recovered during the early phase was included under the ‘biological process’ category, which primarily functions as response to stimuli, signalling, and biological regulation. In the late phase, most of the URGs were related to gene regulation and immune system processes under ‘molecular function’ category. The immune-related URGs of early infection include major histocompatibility complex (MHC) class-II molecules apparently triggering CD4+ T-cell–activated Th responses, and that of late infection include MHC class-1 molecules for the possible culmination of CD8+ T-cell triggered cytotoxicity. The high level of genic single nucleotide polymorphisms (SNPs) identified during the late phase of infection is likely to influence their susceptibility to secondary infection. In summary, the identified DEGs and their related metabolic and immune-related pathways and the SNPs may provide new insights into coordinating the immunological events and improving resistance in Pomacentridae fishes against C. irritans.

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来源期刊
Marine Biotechnology
Marine Biotechnology 工程技术-海洋与淡水生物学
CiteScore
4.80
自引率
3.30%
发文量
95
审稿时长
2 months
期刊介绍: Marine Biotechnology welcomes high-quality research papers presenting novel data on the biotechnology of aquatic organisms. The journal publishes high quality papers in the areas of molecular biology, genomics, proteomics, cell biology, and biochemistry, and particularly encourages submissions of papers related to genome biology such as linkage mapping, large-scale gene discoveries, QTL analysis, physical mapping, and comparative and functional genome analysis. Papers on technological development and marine natural products should demonstrate innovation and novel applications.
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