Phylogenomic evidence for host specialization and genetic divergence in OsHV-1 infecting Magallana gigas and Ostrea edulis

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
Camille Pelletier , Germain Chevignon , Nicole Faury , Isabelle Arzul , Céline Garcia , Bruno Chollet , Tristan Renault , Benjamin Morga , Maude Jacquot
{"title":"Phylogenomic evidence for host specialization and genetic divergence in OsHV-1 infecting Magallana gigas and Ostrea edulis","authors":"Camille Pelletier ,&nbsp;Germain Chevignon ,&nbsp;Nicole Faury ,&nbsp;Isabelle Arzul ,&nbsp;Céline Garcia ,&nbsp;Bruno Chollet ,&nbsp;Tristan Renault ,&nbsp;Benjamin Morga ,&nbsp;Maude Jacquot","doi":"10.1016/j.meegid.2025.105803","DOIUrl":null,"url":null,"abstract":"<div><div>Understanding how pathogens adapt to new hosts is critical to elucidating the evolutionary mechanisms driving disease emergence. This study investigates the evolutionary dynamics of <em>Ostreid herpesvirus 1</em> (OsHV-1) in two host species—the Pacific oyster <em>Magallana gigas</em> and the European flat oyster <em>Ostrea edulis</em>—to address the question of host specificity and cross-species transmission. While OsHV-1 is primarily associated with mortality in <em>M. gigas</em>, its detection in <em>O. edulis</em> raises concerns about its potential host range and evolutionary trajectory. We aimed to determine whether viral populations in these two hosts show genetic differentiation and to identify the evolutionary forces shaping this divergence. Using high-throughput sequencing, we assembled 40 OsHV-1 genomes from both oyster species and applied comparative genomics, population genetics, and phylodynamic approaches. Our results show that host species significantly influence viral genetic structure, with two distinct lineages emerging after a cross-species transmission event likely following the introduction of <em>M. gigas</em> into Europe. Selection signals were detected in viral genes related to host interaction, replication, and membrane-associated functions, suggesting host-driven adaptation. These findings underscore the importance of host-specific evolutionary pressures in shaping viral diversity and provide a framework for future studies on host-virus coevolution in marine ecosystems.</div></div>","PeriodicalId":54986,"journal":{"name":"Infection Genetics and Evolution","volume":"134 ","pages":"Article 105803"},"PeriodicalIF":2.6000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection Genetics and Evolution","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1567134825000929","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Understanding how pathogens adapt to new hosts is critical to elucidating the evolutionary mechanisms driving disease emergence. This study investigates the evolutionary dynamics of Ostreid herpesvirus 1 (OsHV-1) in two host species—the Pacific oyster Magallana gigas and the European flat oyster Ostrea edulis—to address the question of host specificity and cross-species transmission. While OsHV-1 is primarily associated with mortality in M. gigas, its detection in O. edulis raises concerns about its potential host range and evolutionary trajectory. We aimed to determine whether viral populations in these two hosts show genetic differentiation and to identify the evolutionary forces shaping this divergence. Using high-throughput sequencing, we assembled 40 OsHV-1 genomes from both oyster species and applied comparative genomics, population genetics, and phylodynamic approaches. Our results show that host species significantly influence viral genetic structure, with two distinct lineages emerging after a cross-species transmission event likely following the introduction of M. gigas into Europe. Selection signals were detected in viral genes related to host interaction, replication, and membrane-associated functions, suggesting host-driven adaptation. These findings underscore the importance of host-specific evolutionary pressures in shaping viral diversity and provide a framework for future studies on host-virus coevolution in marine ecosystems.
宿主特化和OsHV-1感染麦哲龙和毛豆的遗传分化的系统基因组证据。
了解病原体如何适应新宿主对于阐明驱动疾病出现的进化机制至关重要。本研究研究了Ostreid herpesvirus 1 (OsHV-1)在两种宿主物种(太平洋牡蛎Magallana gigas和欧洲扁平牡蛎Ostrea edulis)中的进化动力学,以解决宿主特异性和跨物种传播的问题。虽然OsHV-1主要与M. gigas的死亡率有关,但它在O. edulis中的检测引起了对其潜在宿主范围和进化轨迹的关注。我们的目的是确定这两种宿主的病毒种群是否表现出遗传分化,并确定形成这种分化的进化力量。通过高通量测序,我们从两个牡蛎物种中组装了40个OsHV-1基因组,并应用了比较基因组学、群体遗传学和系统动力学方法。我们的研究结果表明,宿主物种显著影响病毒的遗传结构,在将M. gigas引入欧洲后可能发生的跨物种传播事件后出现了两个不同的谱系。在与宿主相互作用、复制和膜相关功能相关的病毒基因中检测到选择信号,表明宿主驱动的适应。这些发现强调了宿主特异性进化压力在形成病毒多样性方面的重要性,并为海洋生态系统中宿主-病毒共同进化的未来研究提供了框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信