综合研究鸡肺转录组,了解新城疫病毒挑战期间宿主的免疫反应

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Venkata Krishna Vanamamalai, E. Priyanka, T. R. Kannaki, Shailesh Sharma
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引用次数: 0

摘要

引言 新城疫是家禽业的重大问题之一,在全球范围内造成灾难性影响。肺是藏有支气管相关淋巴组织的重要器官之一,在免疫反应中起着至关重要的作用。众所周知,蛋鸡和法虞美鸡对新城疫的抵抗力存在差异。本研究分析了肺转录组数据,并确定了基因和长非编码 RNA 在不同免疫抵抗力中的作用。我们使用了之前分析硬腺体和气管转录组时使用的计算管道 FHSpipe 来识别基因和 lncRNA。随后进行了差异表达分析、基因和lncRNA的功能注释、转录因子和microRNA的鉴定,最后使用qRT-PCR进行了验证。其中,1263 个 lncRNA 和 281 个基因有差异表达。约66个基因被注释为免疫相关的GO术语或通路,12个基因同时被注释为免疫相关的GO术语或通路。在基于挑战和品种的分析中,这些基因中的大多数在法尤米鸡中比在莱格纳鸡中上调,而在基于时间点的分析中,莱格纳挑战鸡在不同时间点之间表现出下调。在 lncRNAs 的表达中也观察到类似的趋势。共表达分析显示,一些lncRNA与免疫基因共表达,且呈正相关。一些被注释为非免疫通路的基因也受到了影响,包括新陈代谢、信号转导、小分子转运、细胞外基质组织、发育生物学和细胞过程。由此,我们可以了解到,法尤米鸡在非挑战和 NDV 挑战条件下,即使组织中没有病毒转录本,也会出现免疫基因上调和 cis-lncRNAs 阳性的情况。这一发现表明,这些免疫注释基因和共表达顺式-lncRNA 在法虞美鸡对 NDV 的抵抗力高于莱格霍恩鸡方面发挥了重要作用。我们的研究肯定并扩展了之前的研究结果,并强调了 lncRNA 在对 NDV 的免疫反应过程中的关键作用。结论这项分析清楚地表明了莱格汉鸡和法优米鸡之间基因表达模式的差异以及 lncRNA 与基因的共表达,表明 lncRNA 和共表达基因可能在区分这些品种方面具有潜在作用。我们假设,这些基因和 lncRNA 在法优米对 NDV 的抗性高于莱格汉的过程中发挥了重要作用。这项研究可为未来研究揭示免疫相关基因调控背后的生物学机制铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrative study of chicken lung transcriptome to understand the host immune response during Newcastle disease virus challenge
IntroductionNewcastle disease is one of the significant issues in the poultry industry, having catastrophic effects worldwide. The lung is one of the essential organs which harbours Bronchus-associated lymphoid tissue and plays a vital role in the immune response. Leghorn and Fayoumi breeds are known to have differences in resistance to Newcastle disease. Along with genes and long non-coding RNAs (lncRNAs) are also known to regulate various biological pathways through gene regulation.MethodsThis study analysed the lung transcriptome data and identified the role of genes and long non-coding RNAs in differential immune resistance. The computational pipeline, FHSpipe, as used in our previous studies on analysis of harderian gland and trachea transcriptome was used to identify genes and lncRNAs. This was followed by differential expression analysis, functional annotation of genes and lncRNAs, identification of transcription factors, microRNAs and finally validation using qRT-PCR.Results and discussionA total of 8219 novel lncRNAs were identified. Of them, 1263 lncRNAs and 281 genes were differentially expressed. About 66 genes were annotated with either an immune-related GO term or pathway, and 12 were annotated with both. In challenge and breed-based analysis, most of these genes were upregulated in Fayoumi compared to Leghorn, and in timepoint-based analysis, Leghorn challenge chicken showed downregulation between time points. A similar trend was observed in the expression of lncRNAs. Co-expression analysis has revealed several lncRNAs co-expressing with immune genes with a positive correlation. Several genes annotated with non-immune pathways, including metabolism, signal transduction, transport of small molecules, extracellular matrix organization, developmental biology and cellular processes, were also impacted. With this, we can understand that Fayoumi chicken showed upregulated immune genes and positive cis-lncRNAs during both the non-challenged and NDV-challenge conditions, even without viral transcripts in the tissue. This finding shows that these immune-annotated genes and coexpressing cis-lncRNAs play a significant role in Fayoumi being comparatively resistant to NDV compared to Leghorn. Our study affirms and expands upon the outcomes of previous studies and highlights the crucial role of lncRNAs during the immune response to NDV.ConclusionThis analysis clearly shows the differences in the gene expression patterns and lncRNA co-expression with the genes between Leghorn and Fayoumi, indicating that the lncRNAs and co-expressing genes might potentially have a role in differentiating these breeds. We hypothesise that these genes and lncRNAs play a vital role in the higher resistance of Fayoumi to NDV than Leghorn. This study can pave the way for future studies to unravel the biological mechanism behind the regulation of immune-related genes.
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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