Garg Priyanka, Vanamamalai Venkata Krishna, Sharma Shailesh
National Institute of Animal Biotechnology (NIAB), Opp. Journalist Colony, Near Gowlidoddi, Extended Q City Road, Gachibowli, Hyderabad, Telangana, 500032, India.
Regional Centre for Biotechnology, Faridabad-Gurgaon Expressway, Faridabad Rd, Faridabad, Haryana, 121001, India.
Sci Rep. 2024 Jul 17;14(1):16537. doi: 10.1038/s41598-024-67001-0.
Long noncoding RNAs (lncRNAs) are RNA molecules with a length greater than 200 nucleotides that do not code for functional proteins. Although, genes play a vital role in immune response against a disease, it is less known that lncRNAs also contribute through gene regulation. Bovine tuberculosis is a significant zoonotic disease caused by Mycobacterium bovis (M. bovis) in cattle. Here, we report the in-silico analysis of the publicly available transcriptomic data of calves infected with M. bovis. A total of 51,812 lncRNAs were extracted across all the samples. A total of 216 genes and 260 lncRNAs were found to be differentially expressed across all the 4 conditions-infected vs uninfected at 8- and 20-week post-infection (WPI), 8 vs 20-WPI of both infected and uninfected. Gene Ontology and Functional annotation showed that 8 DEGs were annotated with immune system GOs and 2 DEGs with REACTOME immune system pathways. Co-expression analysis of DElncRNAs with DEGs revealed the involvement of lncRNAs with the genes annotated with Immune related GOs and pathways. Overall, our study sheds light on the dynamic transcriptomic changes in response to M. bovis infection, particularly highlighting the involvement of lncRNAs with immune-related genes. The identified immune pathways and gene-lncRNA interactions offer valuable insights for further research in understanding host-pathogen interactions and potential avenues for genetic improvement strategies in cattle.
长链非编码RNA(lncRNAs)是长度大于200个核苷酸的RNA分子,不编码功能性蛋白质。虽然基因在针对疾病的免疫反应中起着至关重要的作用,但人们对lncRNAs也通过基因调控发挥作用却知之甚少。牛结核病是由牛分枝杆菌(M. bovis)引起的一种重要的人畜共患病。在此,我们报告了对感染牛分枝杆菌的犊牛公开可用转录组数据的电子分析。在所有样本中总共提取了51,812个lncRNAs。发现在所有4种条件下——感染组与未感染组在感染后8周和20周(WPI),以及感染组和未感染组的8周WPI与20周WPI——共有216个基因和260个lncRNAs差异表达。基因本体论和功能注释显示,8个差异表达基因(DEGs)被注释为免疫系统基因本体,2个DEGs被注释为REACTOME免疫系统途径。对差异表达lncRNAs与差异表达基因的共表达分析揭示了lncRNAs与注释有免疫相关基因本体和途径的基因之间的关联。总体而言,我们的研究揭示了对牛分枝杆菌感染的动态转录组变化,特别强调了lncRNAs与免疫相关基因的关联。所确定的免疫途径和基因-lncRNA相互作用为进一步研究宿主-病原体相互作用以及牛遗传改良策略的潜在途径提供了有价值的见解。