Saimin Zhai , Ruixue Li , Keying Liu , Huichao Gao , Xia Yang , Jun Zhao , Xiaozhan Zhang , Zeng Wang
{"title":"腺苷脱氨酶促进鹅星状病毒基因型II在GEF细胞中的复制","authors":"Saimin Zhai , Ruixue Li , Keying Liu , Huichao Gao , Xia Yang , Jun Zhao , Xiaozhan Zhang , Zeng Wang","doi":"10.1016/j.psj.2025.105176","DOIUrl":null,"url":null,"abstract":"<div><div>Goose astrovirus genotype II (<strong>GAstV-II</strong>), the causative agent of visceral and joint gout in goslings, has been widespread in China since 2016 and resulted in considerable economic losses to waterfowl industry. As an important enzyme involved in purine metabolism and uricogenesis, adenosine deaminase (<strong><em>ADA</em></strong>) is reported to be upregulated via GAstV infection. However, knowledge about the regulatory role of ADA played during virus replication is still limited. In the present work, goose ADA (<strong><em>gADA</em></strong>) was firstly cloned from goose embryo fibroblasts (<strong>GEF</strong>) and phylogenetic analysis showed that it was highly homologous with duck <em>ADA</em>, sharing 96.6 % identity in nucleotide sequences. Moreover, GAstV-II infection promoted the production of <em>gADA</em> but did not change its cellular distribution pattern, which was evenly dispersed in the cytoplasm and nucleus. Further results demonstrated that ectopic expression of <em>gADA</em> significantly enhanced viral capsid protein expression and virus loads in GEF cells. Conversely, knockdown of <em>gADA</em> by siRNA played the opposite role in virus replication. Notably, <em>gADA</em> could directly interact with viral capsid protein, particularly with its C-terminal domain. Our data elucidated the regulatory role of <em>gADA</em> during GAstV-II infection, thereby laying a solid foundation to further explore its pathogenesis.</div></div>","PeriodicalId":20459,"journal":{"name":"Poultry Science","volume":"104 7","pages":"Article 105176"},"PeriodicalIF":3.8000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Adenosine deaminase promotes goose astrovirus genotype II replication in GEF cells\",\"authors\":\"Saimin Zhai , Ruixue Li , Keying Liu , Huichao Gao , Xia Yang , Jun Zhao , Xiaozhan Zhang , Zeng Wang\",\"doi\":\"10.1016/j.psj.2025.105176\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Goose astrovirus genotype II (<strong>GAstV-II</strong>), the causative agent of visceral and joint gout in goslings, has been widespread in China since 2016 and resulted in considerable economic losses to waterfowl industry. As an important enzyme involved in purine metabolism and uricogenesis, adenosine deaminase (<strong><em>ADA</em></strong>) is reported to be upregulated via GAstV infection. However, knowledge about the regulatory role of ADA played during virus replication is still limited. In the present work, goose ADA (<strong><em>gADA</em></strong>) was firstly cloned from goose embryo fibroblasts (<strong>GEF</strong>) and phylogenetic analysis showed that it was highly homologous with duck <em>ADA</em>, sharing 96.6 % identity in nucleotide sequences. Moreover, GAstV-II infection promoted the production of <em>gADA</em> but did not change its cellular distribution pattern, which was evenly dispersed in the cytoplasm and nucleus. Further results demonstrated that ectopic expression of <em>gADA</em> significantly enhanced viral capsid protein expression and virus loads in GEF cells. Conversely, knockdown of <em>gADA</em> by siRNA played the opposite role in virus replication. Notably, <em>gADA</em> could directly interact with viral capsid protein, particularly with its C-terminal domain. Our data elucidated the regulatory role of <em>gADA</em> during GAstV-II infection, thereby laying a solid foundation to further explore its pathogenesis.</div></div>\",\"PeriodicalId\":20459,\"journal\":{\"name\":\"Poultry Science\",\"volume\":\"104 7\",\"pages\":\"Article 105176\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-04-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Poultry Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032579125004183\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURE, DAIRY & ANIMAL SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poultry Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032579125004183","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
Adenosine deaminase promotes goose astrovirus genotype II replication in GEF cells
Goose astrovirus genotype II (GAstV-II), the causative agent of visceral and joint gout in goslings, has been widespread in China since 2016 and resulted in considerable economic losses to waterfowl industry. As an important enzyme involved in purine metabolism and uricogenesis, adenosine deaminase (ADA) is reported to be upregulated via GAstV infection. However, knowledge about the regulatory role of ADA played during virus replication is still limited. In the present work, goose ADA (gADA) was firstly cloned from goose embryo fibroblasts (GEF) and phylogenetic analysis showed that it was highly homologous with duck ADA, sharing 96.6 % identity in nucleotide sequences. Moreover, GAstV-II infection promoted the production of gADA but did not change its cellular distribution pattern, which was evenly dispersed in the cytoplasm and nucleus. Further results demonstrated that ectopic expression of gADA significantly enhanced viral capsid protein expression and virus loads in GEF cells. Conversely, knockdown of gADA by siRNA played the opposite role in virus replication. Notably, gADA could directly interact with viral capsid protein, particularly with its C-terminal domain. Our data elucidated the regulatory role of gADA during GAstV-II infection, thereby laying a solid foundation to further explore its pathogenesis.
期刊介绍:
First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers.
An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.