{"title":"Unveiling the long non-coding RNA profile of Aeromonas veronii-infected mouse abdominal macrophages","authors":"Haichao Song, Meiqing Xu, Jinxiao Feng","doi":"10.1016/j.ygeno.2026.111328","DOIUrl":null,"url":null,"abstract":"<div><div>Long non-coding RNAs (lncRNAs) play key roles in the host's defense against pathogenic infection. <em>Aeromonas veronii</em> is a zoonotic pathogen capable of provoking severe inflammatory responses<em>.</em> However, the function of lncRNAs in <em>A. veronii</em> infected mouse abdominal macrophages (MAMs) remains poorly understood. MAMs serve as the primary defense against bacterial infection and play critical roles in the anti-infectious immune response. Here, we profiled lncRNAs from MAMs infected with <em>A. veronii</em>. RNA sequencing identified a total of 1628 differentially expressed lncRNAs (DElncRNAs), comprising 680 up-regulated and 948 down-regulated genes. An integrated analysis of lncRNA-mRNA interaction networks identified 4888 target genes of DElncRNAs (DETGs). Of these, 55 DElncRNAs were found to be involved in the regulation of seven immune pathways by regulating 41 DETGs. Furthermore, GO and KEGG enrichment analyses revealed that DETGs were significantly enriched in clusters or pathways associated with immune regulation. These findings provide the transcriptomic profile of MAMs. A comprehensive analysis of DElncRNAs in MAMs was conducted in response to <em>A. veronii</em> infection. Co-expression analysis indicates that lncRNAs are serving as vital regulators of immune gene activity through their critical influence on MAMs during <em>A. veronii</em> infection.</div></div>","PeriodicalId":12521,"journal":{"name":"Genomics","volume":"118 6","pages":"Article 111328"},"PeriodicalIF":3.6000,"publicationDate":"2026-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0888754326001369","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/18 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Long non-coding RNAs (lncRNAs) play key roles in the host's defense against pathogenic infection. Aeromonas veronii is a zoonotic pathogen capable of provoking severe inflammatory responses. However, the function of lncRNAs in A. veronii infected mouse abdominal macrophages (MAMs) remains poorly understood. MAMs serve as the primary defense against bacterial infection and play critical roles in the anti-infectious immune response. Here, we profiled lncRNAs from MAMs infected with A. veronii. RNA sequencing identified a total of 1628 differentially expressed lncRNAs (DElncRNAs), comprising 680 up-regulated and 948 down-regulated genes. An integrated analysis of lncRNA-mRNA interaction networks identified 4888 target genes of DElncRNAs (DETGs). Of these, 55 DElncRNAs were found to be involved in the regulation of seven immune pathways by regulating 41 DETGs. Furthermore, GO and KEGG enrichment analyses revealed that DETGs were significantly enriched in clusters or pathways associated with immune regulation. These findings provide the transcriptomic profile of MAMs. A comprehensive analysis of DElncRNAs in MAMs was conducted in response to A. veronii infection. Co-expression analysis indicates that lncRNAs are serving as vital regulators of immune gene activity through their critical influence on MAMs during A. veronii infection.
期刊介绍:
Genomics is a forum for describing the development of genome-scale technologies and their application to all areas of biological investigation.
As a journal that has evolved with the field that carries its name, Genomics focuses on the development and application of cutting-edge methods, addressing fundamental questions with potential interest to a wide audience. Our aim is to publish the highest quality research and to provide authors with rapid, fair and accurate review and publication of manuscripts falling within our scope.