{"title":"采用R10.4.1纳米孔测序技术对禽大肠杆菌菌株基因组和表观基因组进行解码。","authors":"Jingyao Wang, Xudong Liu, Yanwen Shao, Runsheng Li, Surya Paudel","doi":"10.3389/fvets.2025.1541964","DOIUrl":null,"url":null,"abstract":"<p><p>Avian pathogenic <i>Escherichia coli</i> (APEC) causes colibacillosis in poultry, which is a very important disease worldwide. Despite well-documented genomic traits and diversity of APEC, its epigenomic characteristics are less understood. This study utilized the high throughput and long-read capabilities of Oxford Nanopore Technology (ONT) to elucidate the genome structures and methylation modifications of three <i>E. coli</i> isolates of avian origin: one intestinal isolate from a healthy wild bird and two systemic isolates from clinically affected chickens. Three complete genomes, each comprising a single chromosome and multiple plasmids were assembled. Diverse virulence-associated genes, antimicrobial resistance genes, mobile genetic elements plasmids and integrons were characterized from the genomes. Despite a limited sample size, our whole genome sequencing (WGS) data highlighted significant genomic diversity among the <i>E. coli</i> strains and enriched repertoire of gene clusters related to APEC pathogenicity. From the epigenetic analysis, multiple methylation modifications, including three N5-methylcytosine (5mC), eight N6-methyladenine (6mA) and two N4-methylcytosine (4mC) modification motifs were identified within all three isolates. Furthermore, common GATC and CCWGG methylation motifs were predominantly distributed within regulatory regions, suggesting a role in epigenetic transcription regulation. This study opens the avenue for future research into pathogenesis, diagnostic and therapeutic strategies of APEC considering epigenetic analysis.</p>","PeriodicalId":12772,"journal":{"name":"Frontiers in Veterinary Science","volume":"12 ","pages":"1541964"},"PeriodicalIF":2.6000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11963381/pdf/","citationCount":"0","resultStr":"{\"title\":\"Decoding the genome and epigenome of avian <i>Escherichia coli</i> strains by R10.4.1 nanopore sequencing.\",\"authors\":\"Jingyao Wang, Xudong Liu, Yanwen Shao, Runsheng Li, Surya Paudel\",\"doi\":\"10.3389/fvets.2025.1541964\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Avian pathogenic <i>Escherichia coli</i> (APEC) causes colibacillosis in poultry, which is a very important disease worldwide. Despite well-documented genomic traits and diversity of APEC, its epigenomic characteristics are less understood. This study utilized the high throughput and long-read capabilities of Oxford Nanopore Technology (ONT) to elucidate the genome structures and methylation modifications of three <i>E. coli</i> isolates of avian origin: one intestinal isolate from a healthy wild bird and two systemic isolates from clinically affected chickens. Three complete genomes, each comprising a single chromosome and multiple plasmids were assembled. Diverse virulence-associated genes, antimicrobial resistance genes, mobile genetic elements plasmids and integrons were characterized from the genomes. Despite a limited sample size, our whole genome sequencing (WGS) data highlighted significant genomic diversity among the <i>E. coli</i> strains and enriched repertoire of gene clusters related to APEC pathogenicity. From the epigenetic analysis, multiple methylation modifications, including three N5-methylcytosine (5mC), eight N6-methyladenine (6mA) and two N4-methylcytosine (4mC) modification motifs were identified within all three isolates. Furthermore, common GATC and CCWGG methylation motifs were predominantly distributed within regulatory regions, suggesting a role in epigenetic transcription regulation. This study opens the avenue for future research into pathogenesis, diagnostic and therapeutic strategies of APEC considering epigenetic analysis.</p>\",\"PeriodicalId\":12772,\"journal\":{\"name\":\"Frontiers in Veterinary Science\",\"volume\":\"12 \",\"pages\":\"1541964\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-03-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11963381/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Veterinary Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.3389/fvets.2025.1541964\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"VETERINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Veterinary Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.3389/fvets.2025.1541964","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
Decoding the genome and epigenome of avian Escherichia coli strains by R10.4.1 nanopore sequencing.
Avian pathogenic Escherichia coli (APEC) causes colibacillosis in poultry, which is a very important disease worldwide. Despite well-documented genomic traits and diversity of APEC, its epigenomic characteristics are less understood. This study utilized the high throughput and long-read capabilities of Oxford Nanopore Technology (ONT) to elucidate the genome structures and methylation modifications of three E. coli isolates of avian origin: one intestinal isolate from a healthy wild bird and two systemic isolates from clinically affected chickens. Three complete genomes, each comprising a single chromosome and multiple plasmids were assembled. Diverse virulence-associated genes, antimicrobial resistance genes, mobile genetic elements plasmids and integrons were characterized from the genomes. Despite a limited sample size, our whole genome sequencing (WGS) data highlighted significant genomic diversity among the E. coli strains and enriched repertoire of gene clusters related to APEC pathogenicity. From the epigenetic analysis, multiple methylation modifications, including three N5-methylcytosine (5mC), eight N6-methyladenine (6mA) and two N4-methylcytosine (4mC) modification motifs were identified within all three isolates. Furthermore, common GATC and CCWGG methylation motifs were predominantly distributed within regulatory regions, suggesting a role in epigenetic transcription regulation. This study opens the avenue for future research into pathogenesis, diagnostic and therapeutic strategies of APEC considering epigenetic analysis.
期刊介绍:
Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy.
Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field.
Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.