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MicroRNAs profiles of Chinese Perch Brain (CPB) cells infected with Siniperca chuatsi rhabdovirus (SCRV)

机译:用Siniperca Chuatsi rhabdovirus(SCRV)感染的中国鲈鱼脑(CPB)细胞的MicroRNAS谱

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摘要

MicroRNAs are non-coding RNAs, which widely participate in biological processes. In recent years, Siniperca chuatsi rhabdovirus (SCRV) has caused mass mortality in Chinese perch (Siniperca chuatsi). To identify specific miRNAs involved in SCRV infection, deep sequencing of microRNA on Chinese perch brain cell line (CPB) with or without SCRV infection were performed at 6 and 12 h post of infection (hpi). Totally 382 miRNAs were identified, including 217 known miRNA aligned with zebrafish miRNAs and 165 novel miRNAs by MiRDeep2 program. Of which 15 and 35 differentially-expressed miRNAs were determined respectively to 6 and 12 hpi. Nine miRNAs were selected randomly from the differentially-expressed miRNAs and validated by quantitative real-time PCR (qRT-PCR). These results were consistent with the microRNA sequencing results. Besides, target genes of 98 differentially-expressed miRNAs were predicted. Three of miRNAs (miR-122, miR-214, miR-135a) were selected, and its effects were analyzed in CPC cells transfected with appropriate miRNA mimics/inhibitors to evaluate its regulation effects by qRT-PCR and western blot. The results demonstrated that miR-214 inhibited the replication of SCRV, while miR-122 promoted the replication of SCRV and there was no correlation between the iniR-135a and SCRV replication. These results will pave a new way for the development of effective strategies against the SCRV infection.
机译:MicroRNA是非编码RNA,广泛参与生物过程。近年来,Siniperca Chuatsi rhabdovirus(Scrv)引起了中国鲈鱼(Siniperca Chuatsi)的质量死亡率。为了鉴定参与SCRV感染的特异性miRNA,在6和12 H次的感染(HPI)中进行或不含SCRV感染的MicroRNA对中药细胞系(CPB)的微小序列。鉴定了382个miRNA,包括用斑马鱼miRNA和165个新的MiRNA对齐的217名已知的miRNA,并通过MIDDeep2程序。其中,分别测定15和35差异表达的miRNA至6和12 HPI。从差异表达的miRNA随机选择九个miRNA,并通过定量实时PCR(QRT-PCR)验证。这些结果与MicroRNA测序结果一致。此外,预测了98个差异表达的miRNA的靶基因。选择了三种miRNA(miR-122,miR-214,miR-135a),并在用适当的miRNA模仿/抑制剂转染的CPC细胞中分析其效果,以评估QRT-PCR和Western印迹的调节作用。结果表明miR-214抑制SCRV的复制,而MiR-122促进了SCRV的复制,并且inir-135a和scrv复制之间没有相关性。这些结果将对杂志感染的有效策略的发展铺平了新的方式。

著录项

  • 来源
    《Fish & Shellfish Immunology》 |2019年第2019期|共8页
  • 作者单位

    Huazhong Agr Univ Dept Aquat Anim Med Coll Fisheries Wuhan 430070 Hubei Peoples R China;

    Chinese Acad Fishery Sci Pearl River Fisheries Res Inst Key Lab Fishery Drug Dev Key Lab Aquat Anim Immune Technol Guangzhou 510380 Guangdong Peoples R China;

    Chinese Acad Fishery Sci Pearl River Fisheries Res Inst Key Lab Fishery Drug Dev Key Lab Aquat Anim Immune Technol Guangzhou 510380 Guangdong Peoples R China;

    Zhongkai Univ Agr &

    Engn Guangzhou Key Lab Aquat Anim Dis &

    Waterfowl Bree Guangdong Prov Key Lab Waterfowl Hlth Breeding Coll Anim Sci &

    Technol Guangzhou 510225 Guangdong Peoples R China;

    Chinese Acad Fishery Sci Pearl River Fisheries Res Inst Key Lab Fishery Drug Dev Key Lab Aquat Anim Immune Technol Guangzhou 510380 Guangdong Peoples R China;

    Chinese Acad Fishery Sci Pearl River Fisheries Res Inst Key Lab Fishery Drug Dev Key Lab Aquat Anim Immune Technol Guangzhou 510380 Guangdong Peoples R China;

    Chinese Acad Fishery Sci Pearl River Fisheries Res Inst Key Lab Fishery Drug Dev Key Lab Aquat Anim Immune Technol Guangzhou 510380 Guangdong Peoples R China;

    Huazhong Agr Univ Dept Aquat Anim Med Coll Fisheries Wuhan 430070 Hubei Peoples R China;

    Zhongkai Univ Agr &

    Engn Guangzhou Key Lab Aquat Anim Dis &

    Waterfowl Bree Guangdong Prov Key Lab Waterfowl Hlth Breeding Coll Anim Sci &

    Technol Guangzhou 510225 Guangdong Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 水产、渔业;
  • 关键词

    Siniperca chuatsi rhabdovirus; CPB cell; miRNA; Deep sequencing;

    机译:Siniperca Chuatsi rhabdovirus;CPB细胞;miRNA;深度测序;

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