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从感染高致病性禽流感病毒 H5N1 的白来亨鸡中提取的外泌体 miRNA 的分析和分析。

Profiling and analysis of exosomal miRNAs derived from highly pathogenic avian influenza virus H5N1-infected White Leghorn chickens.

机构信息

Department of Animal Science and Technology, Chung-Ang University, Anseong 17546, Republic of Korea.

Department of Biochemistry and Immunology, National Institute of Veterinary Research, Dong Da, Hanoi 100000, Vietnam.

出版信息

Poult Sci. 2022 Nov;101(11):102123. doi: 10.1016/j.psj.2022.102123. Epub 2022 Aug 8.

DOI:10.1016/j.psj.2022.102123
PMID:36087445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9468452/
Abstract

Exosomes are small cell membrane-derived vesicles; they play important roles as mediators of cell-to-cell communication via delivery of their contents, such as proteins and microRNAs (miRNAs). In particular, exosomal miRNAs regulate the gene expression of recipient cells by inhibiting the expression of target mRNAs. In this study, we investigated the miRNA expression profiles of highly pathogenic avian influenza virus (HPAIV) H5N1-infected White Leghorn chickens and analyzed the functions of their target genes. After 3 d of infection with A/chicken/Vietnam/NA-01/2019 (H5N1), exosomes were isolated from the blood serum of White Leghorn chickens for small RNA sequencing. We accordingly identified 10 differentially expressed miRNAs (DE miRNAs; 5 upregulated and 5 downregulated) by comparing the exosomes derived from infected and noninfected chickens. The target genes of DE miRNAs were predicted using miRDB and TargetScan for Gene Ontology and KEGG pathway enrichment analyses. A majority of the target genes was found to be associated with the MAPK signaling pathway; several immune-related genes were identified as being regulated by these DE miRNAs. Moreover, we predicted DE miRNA binding sites in HPAIV RNA segments using the RNAhybrid algorithm. The findings of this study provide a theoretical basis for gaining insights into the regulatory mechanisms of exosomal miRNAs in response to HPAIV H5N1 infection and the identification of novel vaccine candidates.

摘要

外泌体是由小细胞衍生的膜泡,它们通过传递内容物(如蛋白质和 microRNAs(miRNAs)),在细胞间通讯中发挥重要作用。特别是,外泌体 miRNAs 通过抑制靶 mRNA 的表达来调节受体细胞的基因表达。在这项研究中,我们研究了高致病性禽流感病毒(HPAIV)H5N1 感染的白来航鸡的 miRNA 表达谱,并分析了其靶基因的功能。在感染 A/chicken/Vietnam/NA-01/2019(H5N1)后的第 3 天,从白来航鸡的血清中分离出外泌体进行小 RNA 测序。因此,我们通过比较感染和未感染鸡的外泌体,鉴定了 10 个差异表达的 miRNA(DE miRNAs;5 个上调和 5 个下调)。使用 miRDB 和 TargetScan 预测 DE miRNAs 的靶基因,并进行 GO 和 KEGG 通路富集分析。发现大多数靶基因与 MAPK 信号通路有关;一些免疫相关基因被鉴定为受这些 DE miRNAs 调控。此外,我们使用 RNAhybrid 算法预测了 HPAIV RNA 片段中的 DE miRNA 结合位点。这项研究的结果为深入了解外泌体 miRNAs 对 HPAIV H5N1 感染的反应的调控机制以及鉴定新型疫苗候选物提供了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/4d484698b33a/gr9.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/4d484698b33a/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/2a22b7240a92/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/4a73a6bd5b10/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/577400757f95/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/2fdf625b1144/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/6c38247161b6/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/f874a3baf0a1/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38ad/9468452/46d7a24f57bf/gr7.jpg
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