{"title":"Changes in ORF4 of HCoV-229E under different culture conditions.","authors":"Yuki Kitai, Shohei Kojima, Aikeda Aishajiang, Miyuki Kawase, Oshi Watanabe, Haruka Yabukami, Rina Hashimoto, Yukiko Akahori, Hiroshi Katoh, Kazuo Takayama, Hidekazu Nishimura, Kazuya Shirato, Makoto Takeda","doi":"10.1099/jgv.0.002131","DOIUrl":null,"url":null,"abstract":"<p><p>The genome of human coronavirus 229E (HCoV-229E), a causative agent of human respiratory infections, encodes a unique accessory gene, ORF4. Analysis of laboratory strains and clinical specimens has suggested that HCoV-229E acquires truncating mutations in ORF4 under standard laboratory culture conditions. This study confirmed that HCoV-229E from patients with acute respiratory infections harboured a full-length ORF4 (219 amino acids). In contrast, virus stocks derived from the same patients and passaged in conventional cultured cells [LLC-MK2, human embryonic fibroblast (HEF); HEF, HeLa] exhibited truncated ORF4 of various lengths, such as 168, 143 and 16 amino acids. However, when these virus stocks were propagated in human bronchial/tracheal epithelial cells (HBTECs) cultured at the air-liquid interface (ALI), the full-length ORF4 was selected and stably maintained throughout a prolonged observation period. These findings highlight the importance of ORF4 in patients and under physiologically relevant conditions, and the HBTEC-ALI culture system is valuable for analyzing the native properties of HCoV-229E with an intact full-length ORF4.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12282251/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of General Virology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1099/jgv.0.002131","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The genome of human coronavirus 229E (HCoV-229E), a causative agent of human respiratory infections, encodes a unique accessory gene, ORF4. Analysis of laboratory strains and clinical specimens has suggested that HCoV-229E acquires truncating mutations in ORF4 under standard laboratory culture conditions. This study confirmed that HCoV-229E from patients with acute respiratory infections harboured a full-length ORF4 (219 amino acids). In contrast, virus stocks derived from the same patients and passaged in conventional cultured cells [LLC-MK2, human embryonic fibroblast (HEF); HEF, HeLa] exhibited truncated ORF4 of various lengths, such as 168, 143 and 16 amino acids. However, when these virus stocks were propagated in human bronchial/tracheal epithelial cells (HBTECs) cultured at the air-liquid interface (ALI), the full-length ORF4 was selected and stably maintained throughout a prolonged observation period. These findings highlight the importance of ORF4 in patients and under physiologically relevant conditions, and the HBTEC-ALI culture system is valuable for analyzing the native properties of HCoV-229E with an intact full-length ORF4.
期刊介绍:
JOURNAL OF GENERAL VIROLOGY (JGV), a journal of the Society for General Microbiology (SGM), publishes high-calibre research papers with high production standards, giving the journal a worldwide reputation for excellence and attracting an eminent audience.