太平洋白鲉(Centropomus viridis)鳃部感染单基因寄生虫 Rhabdosynochus viridisi 后免疫相关基因的转录组分析。

IF 1.5 4区 医学 Q3 PARASITOLOGY
Marian Mirabent-Casals , Víctor Hugo Caña-Bozada , Francisco Neptalí Morales-Serna , Juan Manuel Martínez-Brown , Rosa María Medina-Guerrero , Rubí Hernández-Cornejo , Alejandra García-Gasca
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引用次数: 0

摘要

寄生虫 Rhabdosynochus viridisi(扁形动物:单膜虫)感染太平洋白塘鹅(Centropomus viridis)的鳃,可对水产养殖业造成不利影响。人们对太平洋白鲉对单膜虫感染的免疫反应知之甚少。因此,本研究旨在鉴定实验性感染 R. viridisi 的太平洋白鱖幼鱼鳃部的差异表达基因(DEGs),强调感染期间激活或抑制的免疫相关基因和途径。对未感染(对照组)和感染鱼鳃进行了 RNA 测序。在没有参考转录组的情况下,选择 Seq2Fun 算法将读数映射到基因直向同源物数据库(EcoOmics)中的鱼类转录本,并获得计数表。使用 ExpressAnalyst 软件进行差异表达和功能分析。共发现 20,106 个转录本,其中 1430 个(7%)是感染组和对照组之间的差异表达基因(DEGs)。我们发现了 860 个(60%)下调基因和 570 个(40%)上调基因。京都基因和基因组百科全书(KEGG)数据库中的 13 个典型通路的代表性过高,而大多数 DEGs 的表达量下降,表明这些通路失活。本研究中发现的大多数折叠变化较大的 DEGs 在鱼类中的功能尚不清楚。尽管病毒感染鱼鳃后,众所周知的促炎细胞因子没有变化,转化生长因子β(tgfβ)下调,但白细胞介素-17配体il17d和il17a/f1以及C-X-C motif趋化因子受体2(cxcr2)基因上调,表明病毒感染促进了Th17类免疫。本研究还检测到浆 B 细胞活性标志物的过表达,如免疫球蛋白轻链样基因和 v-set 前 B 细胞代用轻链 3(vpreb3)。本研究讨论了与钙失衡、缺氧适应、止血和免疫相关的 DEGs 的可能影响。这些结果将为今后的研究提供支持,以改进鱼类养殖中单克隆抗体感染的预防和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcriptomic analysis of immune-related genes in Pacific white snook (Centropomus viridis) gills infected with the monogenean parasite Rhabdosynochus viridisi

Transcriptomic analysis of immune-related genes in Pacific white snook (Centropomus viridis) gills infected with the monogenean parasite Rhabdosynochus viridisi
The parasite Rhabdosynochus viridisi (Platyhelminthes: Monogenea) infects the Pacific white snook Centropomus viridis gills and can cause adverse effects in the aquaculture industry. The immune responses of Pacific white snook to monogenean infections are poorly understood. Thus, this study aimed to identify differentially expressed genes (DEGs) in the gills of Pacific white snook juveniles experimentally infected with R. viridisi, emphasizing immune-related genes and pathways activated or suppressed during the infection. RNA sequencing was performed on the gills of uninfected (control) and infected fish. The algorithm Seq2Fun was selected without a reference transcriptome to map the reads to transcripts of fishes available from a database for gene orthologs (EcoOmics) and obtain the counting table. The ExpressAnalyst software was used for differential expression and functional analyses. A total of 20,106 transcripts were found, and 1430 (7 %) were differentially expressed genes (DEGs) between infected and control groups. We identified 860 (60 %) downregulated and 570 (40 %) upregulated genes. Thirteen canonical pathways after the Kyoto Encyclopedia of Genes and Genomes (KEGG) database were overrepresented, and most of the DEGs were downregulated, suggesting the inactivation of these pathways. The functions of most of the DEGs with higher fold change found in this study are poorly understood in fish. Even though the well-known pro-inflammatory cytokines remained unchanged in infected gills of C. viridis, and transforming growth factor β (tgfβ) was downregulated, interleukin-17 ligands il17d and il17a/f1, as well as C-X-C motif chemokine receptor 2 (cxcr2) genes were upregulated, indicating that the infection with R. viridisi promotes Th17-like immunity. Overexpression of plasma B cell activity markers such as immunoglobulin light chain-like genes and the v-set pre-B cell surrogate light chain 3 (vpreb3) was also detected in this study. The possible implications of DEGs related to calcium imbalance, hypoxia adaptation, hemostasis, and immunity are discussed. These results will support future studies to improve the prevention and treatment of monogenean infections in finfish aquaculture.
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来源期刊
Parasitology International
Parasitology International 医学-寄生虫学
CiteScore
4.00
自引率
10.50%
发文量
140
审稿时长
61 days
期刊介绍: Parasitology International provides a medium for rapid, carefully reviewed publications in the field of human and animal parasitology. Original papers, rapid communications, and original case reports from all geographical areas and covering all parasitological disciplines, including structure, immunology, cell biology, biochemistry, molecular biology, and systematics, may be submitted. Reviews on recent developments are invited regularly, but suggestions in this respect are welcome. Letters to the Editor commenting on any aspect of the Journal are also welcome.
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