转录组分析揭示虎河豚(Takifugu rubripes)在隐鞭毛虫感染下的免疫抑制状况

Animals Pub Date : 2024-07-13 DOI:10.3390/ani14142058
Yong Chi, Robert Mukiibi, Hongxiang Zhang, Haien Zhang, Weidong Li, Diego Robledo, Songlin Chen, Yangzhen Li
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引用次数: 0

摘要

虎河豚(Takifugu rubripes)又称河豚,最近在水产养殖环境中遭受了严重的C. irritans感染,但人们对其潜在的免疫机制仍然知之甚少。在这项研究中,我们利用 PacBio 长序列(严重感染和健康个体各一个样本池)和 Illumina 短序列(轻度感染、严重感染和健康个体各三个样本池)RNA 测序技术,对感染和未感染鱼鳃组织进行了全面的转录组分析。将序列数据与河豚的参考基因组进行比对后,在健康鱼和感染鱼体内分别鉴定和分析了 47,307 和 34,413 个已知的全长转录本。同样,我们从健康鱼和感染鱼身上分别鉴定和分析了 1126 个和 803 个新基因。有趣的是,我们发现感染恼怒弧菌后,替代剪接(AS)事件和长非编码 RNA(lncRNA)的数量有所减少,这表明它们可能参与了河豚免疫反应的调控。与未感染的鱼类相比,中度和重度感染的鱼类分别有687个和1535个差异表达基因(DEGs)。京都基因组百科全书》(KEGG)分析表明,两组中与免疫相关的 DEGs 主要富集在细胞因子-细胞因子受体相互作用、ECM-受体相互作用、T 细胞受体信号通路、Th1 和 Th2 细胞分化以及 Th17 细胞分化通路中。进一步分析表明,与未感染的鱼类相比,感染鱼类体内大量免疫相关基因被下调,如CCR7、IL7R、TNFRSF21、CD4、COL2A1、FOXP3B和ITGA8。我们的研究表明,C. irritans 是一种潜在的高效寄生虫,可能会破坏河豚对其的防御机制。此外,结合短读 RNA 测序和之前的全基因组关联分析,我们发现了五个可能与 C. irritans 抗性密切相关的关键基因(NDUFB6、PRELID1、SMOX、SLC25A4 和 DENND1B)。这项研究不仅为进一步的研究提供了宝贵的新基因转录本资源,而且为了解养殖河豚对C. irritans感染反应的免疫机制提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptome Analysis Reveals the Immunosuppression in Tiger Pufferfish (Takifugu rubripes) under Cryptocaryon irritans Infection
The tiger pufferfish (Takifugu rubripes), also known as fugu, has recently suffered from severe C. irritans infections under aquaculture environment, yet the underlying immune mechanisms against the parasite remain poorly understood. In this study, we conducted a comprehensive transcriptome analysis of the gill tissue from infected and uninfected fish using PacBio long-read (one pooled sample each for seriously infected and healthy individuals, respectively) and Illumina short-read (three pools for mildly infected, seriously infected, and healthy individuals, respectively) RNA sequencing technologies. After aligning sequence data to fugu’s reference genome, 47,307 and 34,413 known full-length transcripts were identified and profiled in healthy and infected fish, respectively. Similarly, we identified and profiled 1126 and 803 novel genes that were obtained from healthy and infected fish, respectively. Interestingly, we found a decrease in the number of alternative splicing (AS) events and long non-coding RNAs (lncRNAs) after infection with C. irritans, suggesting that they may be involved in the regulation of the immune response in fugu. There were 687 and 1535 differentially expressed genes (DEGs) in moderately and heavily infected fish, respectively, compared to uninfected fish. Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses showed that immune-related DEGs in the two comparison groups were mainly enriched in cytokine-cytokine receptor interactions, ECM-receptor interactions, T-cell receptor signaling pathways, Th1 and Th2 cell differentiation, and Th17 cell differentiation pathways. Further analysis revealed that a large number of immune-related genes were downregulated in infected fish relative to uninfected ones, such as CCR7, IL7R, TNFRSF21, CD4, COL2A1, FOXP3B, and ITGA8. Our study suggests that C. irritans is potentially a highly efficient parasite that may disrupt the defense mechanisms of fugu against it. In addition, in combination of short-read RNA sequencing and previous genome-wide association analyses, we identified five key genes (NDUFB6, PRELID1, SMOX, SLC25A4, and DENND1B) that might be closely associated with C. irritans resistance. This study not only provides valuable resources of novel genic transcripts for further research, but also provides new insights into the immune mechanisms underlying C. irritans infection response in farmed fugu.
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