Jenny C M Chan, Rachel H H Ching, Hermione H M Kock, Teng Long, John M Nicholls, J S Malik Peiris, Kenrie P Y Hui, Michael C W Chan
Recent studies have reported a genotype 4 (G4) reassortant Eurasian avian-like (EA) H1N1 virus in swine, demonstrating a potential pandemic threat in humans. Here, we have compared the tropism, replication competence and pro-inflammatory cytokine and chemokine induction of the two G4 EA H1N1 strains in parallel with 2009 pandemic H1N1 (H1N1/pdm/09) and A/Quail/HK/G1/1997 H9N2 (G1) using ex vivo culture of the human respiratory tract and in vitro culture of human peripheral blood-derived macrophages. Our results showed that G4 strains could replicate in ex vivo cultures of human lung and bronchus with a similar replication competence to H1N1/pdm/09. The cytokine induction levels of G4 were similar to H1N1/pdm/09 in macrophages. Taken together, we could extrapolate that the G4 EA H1N1 swine influenza may pose a notable public health threat towards human and should not underestimate this threat.
最近的研究报告了一种基因型4 (G4)重组的欧亚鸟样(EA) H1N1病毒在猪身上,显示了对人类的潜在大流行威胁。本研究采用人呼吸道离体培养和人外周血源性巨噬细胞体外培养的方法,比较了2009年H1N1大流行(H1N1/pdm/09)和A/Quail/HK/G1/1997 H9N2 (G1)两株G4 EA H1N1毒株的趋向性、复制能力以及促炎因子和趋化因子诱导。结果表明,G4菌株能够在人肺和支气管离体培养物中复制,复制能力与H1N1/pdm/09相似。巨噬细胞中G4的诱导水平与H1N1/pdm/09相似。综上所述,我们可以推断G4 EA H1N1猪流感可能对人类构成显著的公共卫生威胁,不应低估这一威胁。
{"title":"Evaluation of pandemic potential of the genotype 4 (G4) swine influenza virus using <i>ex vivo</i> and <i>in vitro</i> cultures of the human respiratory tract.","authors":"Jenny C M Chan, Rachel H H Ching, Hermione H M Kock, Teng Long, John M Nicholls, J S Malik Peiris, Kenrie P Y Hui, Michael C W Chan","doi":"10.1099/jgv.0.002133","DOIUrl":"10.1099/jgv.0.002133","url":null,"abstract":"<p><p>Recent studies have reported a genotype 4 (G4) reassortant Eurasian avian-like (EA) H1N1 virus in swine, demonstrating a potential pandemic threat in humans. Here, we have compared the tropism, replication competence and pro-inflammatory cytokine and chemokine induction of the two G4 EA H1N1 strains in parallel with 2009 pandemic H1N1 (H1N1/pdm/09) and A/Quail/HK/G1/1997 H9N2 (G1) using <i>ex vivo</i> culture of the human respiratory tract and <i>in vitro</i> culture of human peripheral blood-derived macrophages. Our results showed that G4 strains could replicate in <i>ex vivo</i> cultures of human lung and bronchus with a similar replication competence to H1N1/pdm/09. The cytokine induction levels of G4 were similar to H1N1/pdm/09 in macrophages. Taken together, we could extrapolate that the G4 EA H1N1 swine influenza may pose a notable public health threat towards human and should not underestimate this threat.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12313140/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144760296","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sead Sabanadzovic, Chantal Abergel, Marı́a A Ayllón, Leticia Botella, Marta Canuti, Yuto Chiba, JeanMichel Claverie, Robert H A Coutts, Stefania Daghino, Livia Donaire, Marco Forgia, Ondřej Hejna, Jichun Jia, Daohong Jiang, Ioly Kotta-Loizou, Mart Krupovic, Andrew S Lang, Matthieu Legendre, Shin-Yi Lee Marzano, Fan Mu, Uri Neri, Luca Nerva, Judit Pénzes, Anna Poimala, Sofia Rigou, Yukiyo Sato, Wajeeha Shamsi, Suvi Sutela, Nobuhiro Suzuki, Massimo Turina, Syun-Ichi Urayama, Eeva J Vainio, Jiatao Xie, Ictv Taxonomy Summary Consortium
The Fungal and Protist Viruses Subcommittee (SC) of the International Committee on Taxonomy of Viruses (ICTV) has received a total of eight taxonomic proposals for the 2024 annual cycle. The extent of proposed changes varied, including nomenclatural updates, creation of new taxa and reorganization of established taxa. Following the ICTV procedures, all proposals were reviewed and voted upon by the members of the Executive Committee with ratification in March 2025. As a result, a total of 52 species in the families Botourmiaviridae and Marnaviridae were renamed to comply with the mandated binomial format. A new genus has been added to the dsRNA virus family Amalgaviridae, while two new families, Splipalmiviridae (Wolframvirales) and Mycoalphaviridae (Hepelivirales), were created to classify new groups of positive-sense (+) RNA mycoviruses. The class Arfiviricetes (Cressdnaviricota) was expanded by a new order Lineavirales and a new family Oomyviridae of ssDNA viruses. Additionally, a new class Orpoviricetes was created in the kingdom Orthornavirae to classify a group of bisegmented (+)RNA viruses reported from fungi and oomycetes. Finally, the order Pimascovirales was reorganized to better depict evolutionary relationships of pithoviruses and related viruses with large dsDNA genomes. The summary of updates in the taxonomy of fungal and protist viruses presented here is limited to taxa within the remit of this Subcommittee. For information on taxonomy changes on other fungal viruses closely related to animal and/or plant viruses, please see reports from sister ICTV Subcommittees (i.e. Plant Virus SC and Animal dsRNA and ssRNA(-) Viruses SC).
{"title":"Summary of taxonomy changes ratified by the International Committee on Taxonomy of Viruses (ICTV) from the Fungal and Protist Viruses Subcommittee, 2025.","authors":"Sead Sabanadzovic, Chantal Abergel, Marı́a A Ayllón, Leticia Botella, Marta Canuti, Yuto Chiba, JeanMichel Claverie, Robert H A Coutts, Stefania Daghino, Livia Donaire, Marco Forgia, Ondřej Hejna, Jichun Jia, Daohong Jiang, Ioly Kotta-Loizou, Mart Krupovic, Andrew S Lang, Matthieu Legendre, Shin-Yi Lee Marzano, Fan Mu, Uri Neri, Luca Nerva, Judit Pénzes, Anna Poimala, Sofia Rigou, Yukiyo Sato, Wajeeha Shamsi, Suvi Sutela, Nobuhiro Suzuki, Massimo Turina, Syun-Ichi Urayama, Eeva J Vainio, Jiatao Xie, Ictv Taxonomy Summary Consortium","doi":"10.1099/jgv.0.002115","DOIUrl":"10.1099/jgv.0.002115","url":null,"abstract":"<p><p>The Fungal and Protist Viruses Subcommittee (SC) of the International Committee on Taxonomy of Viruses (ICTV) has received a total of eight taxonomic proposals for the 2024 annual cycle. The extent of proposed changes varied, including nomenclatural updates, creation of new taxa and reorganization of established taxa. Following the ICTV procedures, all proposals were reviewed and voted upon by the members of the Executive Committee with ratification in March 2025. As a result, a total of 52 species in the families <i>Botourmiaviridae</i> and <i>Marnaviridae</i> were renamed to comply with the mandated binomial format. A new genus has been added to the dsRNA virus family <i>Amalgaviridae</i>, while two new families, <i>Splipalmiviridae</i> (<i>Wolframvirales</i>) and <i>Mycoalphaviridae</i> (<i>Hepelivirales</i>), were created to classify new groups of positive-sense (+) RNA mycoviruses. The class <i>Arfiviricetes</i> (<i>Cressdnaviricota</i>) was expanded by a new order <i>Lineavirales</i> and a new family <i>Oomyviridae</i> of ssDNA viruses. Additionally, a new class <i>Orpoviricetes</i> was created in the kingdom <i>Orthornavirae</i> to classify a group of bisegmented (+)RNA viruses reported from fungi and oomycetes. Finally, the order <i>Pimascovirales</i> was reorganized to better depict evolutionary relationships of pithoviruses and related viruses with large dsDNA genomes. The summary of updates in the taxonomy of fungal and protist viruses presented here is limited to taxa within the remit of this Subcommittee. For information on taxonomy changes on other fungal viruses closely related to animal and/or plant viruses, please see reports from sister ICTV Subcommittees (i.e. Plant Virus SC and Animal dsRNA and ssRNA(-) Viruses SC).</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12451638/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144707726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
As intracellular parasites, viruses must hijack and often rewire organelles, signalling pathways and the bioenergetics machinery of the infected cell to replicate their genome, produce viral proteins and assemble new viral particles. Mitochondria are key eukaryotic organelles often referred to as the cell's powerhouse. They control many fundamental cellular processes, from metabolism and energy production to calcium homeostasis and programmed cell death. Importantly, mitochondrial membranes are also critical sites for the integration and amplification of antiviral innate immune responses. Overall, mitochondria are therefore both supporting the virus life cycle by sustaining energy production, metabolism and synthesis of macromolecules and part of the cell's first line of defence against viruses. This review summarizes recent findings on viral manipulations of mitochondria and their functions. We explore the evolving understanding of how mitochondrial dynamics is targeted to regulate innate immunity, evasion strategies used to avoid mitochondrial-associated mechanisms that impair replication and the role of mitochondrial functions such as generating reactive oxygen species or regulating the electron transport chain during infection. Overall, we provide a comprehensive view of how viruses modulate mitochondrial function to promote replication.
{"title":"Understanding the mechanisms of mitochondrial rewiring during viral infections.","authors":"Marta Lopez-Nieto, Nicolas Locker","doi":"10.1099/jgv.0.002128","DOIUrl":"10.1099/jgv.0.002128","url":null,"abstract":"<p><p>As intracellular parasites, viruses must hijack and often rewire organelles, signalling pathways and the bioenergetics machinery of the infected cell to replicate their genome, produce viral proteins and assemble new viral particles. Mitochondria are key eukaryotic organelles often referred to as the cell's powerhouse. They control many fundamental cellular processes, from metabolism and energy production to calcium homeostasis and programmed cell death. Importantly, mitochondrial membranes are also critical sites for the integration and amplification of antiviral innate immune responses. Overall, mitochondria are therefore both supporting the virus life cycle by sustaining energy production, metabolism and synthesis of macromolecules and part of the cell's first line of defence against viruses. This review summarizes recent findings on viral manipulations of mitochondria and their functions. We explore the evolving understanding of how mitochondrial dynamics is targeted to regulate innate immunity, evasion strategies used to avoid mitochondrial-associated mechanisms that impair replication and the role of mitochondrial functions such as generating reactive oxygen species or regulating the electron transport chain during infection. Overall, we provide a comprehensive view of how viruses modulate mitochondrial function to promote replication.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":3.6,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12282254/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144584121","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
F Murilo Zerbini, Anya Crane, Jens H Kuhn, Peter Simmonds, Elliot J Lefkowitz, Ictv Taxonomy Summary Consortium
During the 56th annual meeting of the International Committee on Taxonomy of Viruses (ICTV), held in Bari, Italy, in August 2024, two technical proposals were presented. The first called for amended versions of accepted taxonomic proposals to be named in such a way to ensure that they are readily accessible on the ICTV website (2024.001G). The second proposed a substantial reformatting of the ICTV statutes and codes to produce a more unified text after the numerous changes made to both documents in previous years (2024.002G). Finally, the ICTV Executive Committee (EC) nominated Professor Stuart Siddell as a Life Member of the ICTV for his work over four decades on virus taxonomy, including 16 years as a member of the EC (2024.003G).
{"title":"Summary of taxonomy changes ratified by the International Committee on Taxonomy of Viruses (ICTV) - General taxonomy proposals, 2025.","authors":"F Murilo Zerbini, Anya Crane, Jens H Kuhn, Peter Simmonds, Elliot J Lefkowitz, Ictv Taxonomy Summary Consortium","doi":"10.1099/jgv.0.002116","DOIUrl":"10.1099/jgv.0.002116","url":null,"abstract":"<p><p>During the 56th annual meeting of the International Committee on Taxonomy of Viruses (ICTV), held in Bari, Italy, in August 2024, two technical proposals were presented. The first called for amended versions of accepted taxonomic proposals to be named in such a way to ensure that they are readily accessible on the ICTV website (2024.001G). The second proposed a substantial reformatting of the ICTV statutes and codes to produce a more unified text after the numerous changes made to both documents in previous years (2024.002G). Finally, the ICTV Executive Committee (EC) nominated Professor Stuart Siddell as a Life Member of the ICTV for his work over four decades on virus taxonomy, including 16 years as a member of the EC (2024.003G).</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12446860/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144715086","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jillian C Carmichael, Christian S Stevens, Kristina E Atanasoff, Shreyas Kowdle, Rebecca A Reis, Domenico Tortorella, Benhur Lee
Human cytomegalovirus (HCMV) genetic manipulation traditionally relies on bacterial artificial chromosome (BAC) recombineering, necessitated by its large ~236 kb genome. This approach is limited by the scarcity of HCMV strains engineered into BACs and often requires the deletion of 'non-essential' genes to accommodate the BAC cassette. We developed a novel approach using temperature-sensitive Sendai virus (SeV) vectors to deliver CRISPR/Cas9 for targeted HCMV genome editing without these constraints. This system achieves high editing efficiency (80-90%) in fibroblasts, epithelial cells and endothelial cells without BAC intermediates. As proof of principle, we targeted the HCMV (TB40/E strain) pentamer complex (PC) genes UL128 and UL130, crucial for viral entry into non-fibroblast cells. Edited viruses showed significantly reduced infectivity in epithelial cells, confirming functional disruption of the PC. Plaque purification yielded isogenic clones with phenotypes comparable to AD169, a naturally PC-deficient strain. Furthermore, multiplexed editing created precise 663 bp deletions in over 60% of viral genomes. Importantly, this method enables HCMV editing in physiologically relevant cell types without fibroblast passaging, which typically introduces mutations. This SeV-Cas9 system represents a significant advancement for studying HCMV biology in diverse cell types.
{"title":"Precision engineering of human cytomegalovirus without BAC constraints: a Sendai virus-delivered CRISPR/Cas9 approach.","authors":"Jillian C Carmichael, Christian S Stevens, Kristina E Atanasoff, Shreyas Kowdle, Rebecca A Reis, Domenico Tortorella, Benhur Lee","doi":"10.1099/jgv.0.002126","DOIUrl":"10.1099/jgv.0.002126","url":null,"abstract":"<p><p>Human cytomegalovirus (HCMV) genetic manipulation traditionally relies on bacterial artificial chromosome (BAC) recombineering, necessitated by its large ~236 kb genome. This approach is limited by the scarcity of HCMV strains engineered into BACs and often requires the deletion of 'non-essential' genes to accommodate the BAC cassette. We developed a novel approach using temperature-sensitive Sendai virus (SeV) vectors to deliver CRISPR/Cas9 for targeted HCMV genome editing without these constraints. This system achieves high editing efficiency (80-90%) in fibroblasts, epithelial cells and endothelial cells without BAC intermediates. As proof of principle, we targeted the HCMV (TB40/E strain) pentamer complex (PC) genes UL128 and UL130, crucial for viral entry into non-fibroblast cells. Edited viruses showed significantly reduced infectivity in epithelial cells, confirming functional disruption of the PC. Plaque purification yielded isogenic clones with phenotypes comparable to AD169, a naturally PC-deficient strain. Furthermore, multiplexed editing created precise 663 bp deletions in over 60% of viral genomes. Importantly, this method enables HCMV editing in physiologically relevant cell types without fibroblast passaging, which typically introduces mutations. This SeV-Cas9 system represents a significant advancement for studying HCMV biology in diverse cell types.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12311846/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144642753","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mart Krupovic, Diana P Baquero, Eduardo A Bignon, Ariane Bize, Guillaume Borrel, Mingwei Cai, Lanming Chen, Marion Coves, Changhai Duan, Simonetta Gribaldo, Eugene V Koonin, Meng Li, Lirui Liu, Yang Liu, Ying Liu, Sofia Medvedeva, Yimin Ni, Apoorva Prabhu, Christian Rinke, Yongjie Wang, Tianqi Xu, Shuling Yan, Qinglu Zeng, Rui Zhang, Ictv Taxonomy Summary Consortium
The International Committee on Taxonomy of Viruses (ICTV) holds a ratification vote annually following the review of newly proposed taxa by ICTV Study Groups and members of the virology community. This article reports changes to the taxonomy of viruses infecting archaea that were approved and ratified by the ICTV in March 2025. Six new families of head-tailed viruses expanded the order Caudoviricetes (realm Duplodnaviria); one new family of filamentous viruses was added to the order Ligamenvirales (realm Adnaviria); one new family of viruses with pleomorphic virions was included within a new phylum, new order and new class in the kingdom Trapavirae (realm Monodnaviria); finally, three new families were created for spindle-shaped viruses that remain unassigned to higher level taxa. The 25 new species represent viruses infecting a broad range of archaea, including members of the classes Archaeoglobi, Bathyarchaeia, Methanobacteria, Methanomicrobia, Nitrososphaeria and Poseidoniia. Most of these viruses have been discovered by metagenomics in samples derived from diverse environments, including ambient and extreme marine ecosystems, the gastrointestinal tract of humans and animals, anaerobic digesters and terrestrial hot springs. Following this taxonomic update, archaeal viruses are officially classified into a total of 163 virus species in 94 genera within 62 families.
{"title":"Summary of taxonomy changes ratified by the International Committee on Taxonomy of Viruses (ICTV) from the Archaeal Viruses Subcommittee, 2025.","authors":"Mart Krupovic, Diana P Baquero, Eduardo A Bignon, Ariane Bize, Guillaume Borrel, Mingwei Cai, Lanming Chen, Marion Coves, Changhai Duan, Simonetta Gribaldo, Eugene V Koonin, Meng Li, Lirui Liu, Yang Liu, Ying Liu, Sofia Medvedeva, Yimin Ni, Apoorva Prabhu, Christian Rinke, Yongjie Wang, Tianqi Xu, Shuling Yan, Qinglu Zeng, Rui Zhang, Ictv Taxonomy Summary Consortium","doi":"10.1099/jgv.0.002117","DOIUrl":"10.1099/jgv.0.002117","url":null,"abstract":"<p><p>The International Committee on Taxonomy of Viruses (ICTV) holds a ratification vote annually following the review of newly proposed taxa by ICTV Study Groups and members of the virology community. This article reports changes to the taxonomy of viruses infecting archaea that were approved and ratified by the ICTV in March 2025. Six new families of head-tailed viruses expanded the order <i>Caudoviricetes</i> (realm <i>Duplodnaviria</i>); one new family of filamentous viruses was added to the order <i>Ligamenvirales</i> (realm <i>Adnaviria</i>); one new family of viruses with pleomorphic virions was included within a new phylum, new order and new class in the kingdom <i>Trapavirae</i> (realm <i>Monodnaviria</i>); finally, three new families were created for spindle-shaped viruses that remain unassigned to higher level taxa. The 25 new species represent viruses infecting a broad range of archaea, including members of the classes Archaeoglobi, Bathyarchaeia, Methanobacteria, Methanomicrobia, Nitrososphaeria and Poseidoniia. Most of these viruses have been discovered by metagenomics in samples derived from diverse environments, including ambient and extreme marine ecosystems, the gastrointestinal tract of humans and animals, anaerobic digesters and terrestrial hot springs. Following this taxonomic update, archaeal viruses are officially classified into a total of 163 virus species in 94 genera within 62 families.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12451623/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144715087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Holly R Hughes, Matthew J Ballinger, Yiming Bao, Nicolas Bejerman, Kim R Blasdell, Thomas Briese, Julia Brignone, Jean Paul Carrera, Lander De Coninck, William Marciel de Souza, Humberto Debat, Ralf G Dietzgen, Ralf Dürrwald, Mert Erdin, Anthony R Fooks, Kristian M Forbes, Juliana Freitas-Astúa, Jorge B Garcia, Jemma L Geoghegan, Rebecca M Grimwood, Masayuki Horie, Timothy H Hyndman, Reimar Johne, John D Klena, Hideki Kondo, Eugene V Koonin, Alexei Y Kostygov, Mart Krupovic, Jens H Kuhn, Michael Letko, Jun-Min Li, Yiyun Liu, Maria Laura Martin, Nathaniel Mull, Yael Nazar, Norbert Nowotny, Márcio Roberto Teixeira Nunes, Arnfinn Lodden Økland, Dennis Rubbenstroth, Brandy J Russell, Eric Schott, Stephanie Seifert, Carina Sen, Elizabeth Shedroff, Tarja Sironen, Teemu Smura, Camila Prestes Dos Santos Tavares, Robert B Tesh, Natasha L Tilston, Noël Tordo, Nikos Vasilakis, Peter J Walker, Fei Wang, Anna E Whitfield, Shannon L M Whitmer, Yuri I Wolf, Han Xia, Gong-Yin Ye, Zhuangxin Ye, Vyacheslav Yurchenko, Mingli Zhao, Ictv Taxonomy Summary Consortium
RNA viruses are ubiquitous in the environment and are important pathogens of humans, animals and plants. In 2024, the International Committee on Taxonomy of Viruses Animal dsRNA and ssRNA(-) Viruses Subcommittee submitted 18 taxonomic proposals for consideration. These proposals expanded the known virosphere by classifying 9 new genera and 88 species for newly detected virus genomes. Of note, newly established species expand the large family of Rhabdoviridae to 580 species. A new species in the family Arenaviridae includes a virus detected in Antarctic fish with a unique split nucleoprotein ORF. Additionally, four new species were established for historically isolated viruses with previously unsequenced genomes. Furthermore, three species were abolished due to incomplete genome sequence information, and one family was moved from being unassigned in the phylum Negarnaviricota into a subphylum and order. Herein, we summarize the 18 ratified taxonomic proposals and the general features of the current taxonomy, thereby supporting public and animal health responses.
{"title":"Summary of taxonomy changes ratified by the International Committee on Taxonomy of Viruses (ICTV) from the Animal dsRNA and ssRNA(-) Viruses Subcommittee, 2025.","authors":"Holly R Hughes, Matthew J Ballinger, Yiming Bao, Nicolas Bejerman, Kim R Blasdell, Thomas Briese, Julia Brignone, Jean Paul Carrera, Lander De Coninck, William Marciel de Souza, Humberto Debat, Ralf G Dietzgen, Ralf Dürrwald, Mert Erdin, Anthony R Fooks, Kristian M Forbes, Juliana Freitas-Astúa, Jorge B Garcia, Jemma L Geoghegan, Rebecca M Grimwood, Masayuki Horie, Timothy H Hyndman, Reimar Johne, John D Klena, Hideki Kondo, Eugene V Koonin, Alexei Y Kostygov, Mart Krupovic, Jens H Kuhn, Michael Letko, Jun-Min Li, Yiyun Liu, Maria Laura Martin, Nathaniel Mull, Yael Nazar, Norbert Nowotny, Márcio Roberto Teixeira Nunes, Arnfinn Lodden Økland, Dennis Rubbenstroth, Brandy J Russell, Eric Schott, Stephanie Seifert, Carina Sen, Elizabeth Shedroff, Tarja Sironen, Teemu Smura, Camila Prestes Dos Santos Tavares, Robert B Tesh, Natasha L Tilston, Noël Tordo, Nikos Vasilakis, Peter J Walker, Fei Wang, Anna E Whitfield, Shannon L M Whitmer, Yuri I Wolf, Han Xia, Gong-Yin Ye, Zhuangxin Ye, Vyacheslav Yurchenko, Mingli Zhao, Ictv Taxonomy Summary Consortium","doi":"10.1099/jgv.0.002112","DOIUrl":"10.1099/jgv.0.002112","url":null,"abstract":"<p><p>RNA viruses are ubiquitous in the environment and are important pathogens of humans, animals and plants. In 2024, the International Committee on Taxonomy of Viruses Animal dsRNA and ssRNA(-) Viruses Subcommittee submitted 18 taxonomic proposals for consideration. These proposals expanded the known virosphere by classifying 9 new genera and 88 species for newly detected virus genomes. Of note, newly established species expand the large family of <i>Rhabdoviridae</i> to 580 species. A new species in the family <i>Arenaviridae</i> includes a virus detected in Antarctic fish with a unique split nucleoprotein ORF. Additionally, four new species were established for historically isolated viruses with previously unsequenced genomes. Furthermore, three species were abolished due to incomplete genome sequence information, and one family was moved from being unassigned in the phylum <i>Negarnaviricota</i> into a subphylum and order. Herein, we summarize the 18 ratified taxonomic proposals and the general features of the current taxonomy, thereby supporting public and animal health responses.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12451637/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144707725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Arvind Varsani, Adly M M Abd-Alla, Niklas Arnberg, Kelly S Bateman, Mária Benkő, Annie Bézier, Philippe Biagini, Jamie Bojko, Anamarija Butkovic, Marta Canuti, Vladimír Celer, Jean-Michel Drezen, Laszlo Egyed, Matthias G Fischer, Sarah François, Benjamin Guinet, Balázs Harrach, Robert L Harrison, Elisabeth A Herniou, Michael Hess, Jia Hu, Johannes A Jehle, Győző L Kaján, Adrianna E Kajon, Eugene V Koonin, Simona Kraberger, Peter J Krell, Mart Krupovic, Jens H Kuhn, Chengfeng Lei, Matthieu Leobold, Fabrizio Maggi, Suresh K Mittal, Hiroaki Okamoto, Tanja Opriessnig, Xiaowei Peng, Judit Pénzes, Iva I Podgorski, Thomas S Postler, Bergmann M Ribeiro, Carmen San Martín, Maria Söderlund-Venermo, Xiulian Sun, András Surján, Zoltán L Tarján, Julien Varaldi, Márton Z Vidovszky, Göran Wadell, Hidemi Watanabe, Natalya Yutin, Monique M van Oers, Ictv Taxonomy Summary Consortium
The International Committee on Taxonomy of Viruses (ICTV) holds a ratification vote annually after review of newly proposed taxa by ICTV Study Groups and members of the virology community. In March 2025, the vote outcome of the 11 proposals within the mandate of the Animal DNA Viruses and Retroviruses Subcommittee was made public. Here, we provide a summary of the newly accepted proposals. These include reorganization of taxa in the realm Varidnaviria, classification of the 'polinton-like' viruses into a new family (Phypoliviridae) within a new order Archintovirales; establishment of a new phylum (Commensaviricota) in the kingdom Shotokuvirae; the establishment of a new family called Filamentoviridae with two new genera and three new species; the addition of four new genera in the family Anelloviridae with 70 new species; and the addition of 85 new species in the families Adenoviridae (n=16), Baculoviridae (n=5), Circoviridae (n=5), Parvoviridae (n=55) and Polyomaviridae (n=4). Also, in the family Belpaoviridae, 11 species were renamed to comply with the binomial requirement for species names.
{"title":"Summary of taxonomy changes ratified by the International Committee on Taxonomy of Viruses (ICTV) from the Animal DNA Viruses and Retroviruses Subcommittee, 2025.","authors":"Arvind Varsani, Adly M M Abd-Alla, Niklas Arnberg, Kelly S Bateman, Mária Benkő, Annie Bézier, Philippe Biagini, Jamie Bojko, Anamarija Butkovic, Marta Canuti, Vladimír Celer, Jean-Michel Drezen, Laszlo Egyed, Matthias G Fischer, Sarah François, Benjamin Guinet, Balázs Harrach, Robert L Harrison, Elisabeth A Herniou, Michael Hess, Jia Hu, Johannes A Jehle, Győző L Kaján, Adrianna E Kajon, Eugene V Koonin, Simona Kraberger, Peter J Krell, Mart Krupovic, Jens H Kuhn, Chengfeng Lei, Matthieu Leobold, Fabrizio Maggi, Suresh K Mittal, Hiroaki Okamoto, Tanja Opriessnig, Xiaowei Peng, Judit Pénzes, Iva I Podgorski, Thomas S Postler, Bergmann M Ribeiro, Carmen San Martín, Maria Söderlund-Venermo, Xiulian Sun, András Surján, Zoltán L Tarján, Julien Varaldi, Márton Z Vidovszky, Göran Wadell, Hidemi Watanabe, Natalya Yutin, Monique M van Oers, Ictv Taxonomy Summary Consortium","doi":"10.1099/jgv.0.002113","DOIUrl":"10.1099/jgv.0.002113","url":null,"abstract":"<p><p>The International Committee on Taxonomy of Viruses (ICTV) holds a ratification vote annually after review of newly proposed taxa by ICTV Study Groups and members of the virology community. In March 2025, the vote outcome of the 11 proposals within the mandate of the Animal DNA Viruses and Retroviruses Subcommittee was made public. Here, we provide a summary of the newly accepted proposals. These include reorganization of taxa in the realm <i>Varidnaviria</i>, classification of the 'polinton-like' viruses into a new family (<i>Phypoliviridae</i>) within a new order <i>Archintovirales</i>; establishment of a new phylum (<i>Commensaviricota</i>) in the kingdom <i>Shotokuvirae</i>; the establishment of a new family called <i>Filamentoviridae</i> with two new genera and three new species; the addition of four new genera in the family <i>Anelloviridae</i> with 70 new species; and the addition of 85 new species in the families <i>Adenoviridae</i> (<i>n</i>=16), <i>Baculoviridae</i> (<i>n</i>=5), <i>Circoviridae</i> (<i>n</i>=5), <i>Parvoviridae</i> (<i>n</i>=55) and <i>Polyomaviridae</i> (<i>n</i>=4). Also, in the family <i>Belpaoviridae</i>, 11 species were renamed to comply with the binomial requirement for species names.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12451622/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144707724","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Simon P Jeeves, Jonathon D Kotwa, David L Pearl, Bradley S Pickering, Jeff Bowman, Samira Mubareka, Claire M Jardine
Coronaviruses are abundant and diverse RNA viruses with broad vertebrate host ranges. These viruses include agents of human seasonal respiratory illness, such as human coronaviruses OC43 and HKU1; important pathogens of livestock and domestic animals such as swine acute diarrhoea syndrome coronavirus and feline coronavirus; and human pathogens of epidemic potential such as SARS-CoV, MERS-CoV and SARS-CoV-2. Most coronavirus surveillance has been conducted in bat species. However, small terrestrial mammals such as rodents and eulipotyphlans are important hosts of coronaviruses as well. Although fewer studies of rodent and eulipotyphlan coronaviruses exist compared to those of bats, notable diversity of coronaviruses has been reported in the former. No literature synthesis for this area of research has been completed despite (a) growing evidence for a small mammal origin of certain human coronaviruses and (b) global abundance of small mammal species. In this review, we present an overview of the current state of coronavirus research in wild terrestrial small mammals. We conducted a literature search for studies that investigated coronaviruses infecting rodent and eulipotyphlan hosts, which returned 63 studies published up to and including 2024. We describe trends in coronavirus diversity and surveillance for these studies. To further the examination of the interrelatedness of these viruses, we conducted a phylogenetic analysis of coronavirus whole genomes recovered from rodent and eulipotyphlan hosts. We discuss important facets of terrestrial small mammal coronaviruses, including evolutionary aspects and zoonotic spillover risk. Lastly, we present important recommendations and considerations for further surveillance and viral characterization efforts in this field.
{"title":"Coronaviruses in wild rodent and eulipotyphlan small mammals: a review of diversity, ecological implications and surveillance considerations.","authors":"Simon P Jeeves, Jonathon D Kotwa, David L Pearl, Bradley S Pickering, Jeff Bowman, Samira Mubareka, Claire M Jardine","doi":"10.1099/jgv.0.002130","DOIUrl":"10.1099/jgv.0.002130","url":null,"abstract":"<p><p>Coronaviruses are abundant and diverse RNA viruses with broad vertebrate host ranges. These viruses include agents of human seasonal respiratory illness, such as human coronaviruses OC43 and HKU1; important pathogens of livestock and domestic animals such as swine acute diarrhoea syndrome coronavirus and feline coronavirus; and human pathogens of epidemic potential such as SARS-CoV, MERS-CoV and SARS-CoV-2. Most coronavirus surveillance has been conducted in bat species. However, small terrestrial mammals such as rodents and eulipotyphlans are important hosts of coronaviruses as well. Although fewer studies of rodent and eulipotyphlan coronaviruses exist compared to those of bats, notable diversity of coronaviruses has been reported in the former. No literature synthesis for this area of research has been completed despite (a) growing evidence for a small mammal origin of certain human coronaviruses and (b) global abundance of small mammal species. In this review, we present an overview of the current state of coronavirus research in wild terrestrial small mammals. We conducted a literature search for studies that investigated coronaviruses infecting rodent and eulipotyphlan hosts, which returned 63 studies published up to and including 2024. We describe trends in coronavirus diversity and surveillance for these studies. To further the examination of the interrelatedness of these viruses, we conducted a phylogenetic analysis of coronavirus whole genomes recovered from rodent and eulipotyphlan hosts. We discuss important facets of terrestrial small mammal coronaviruses, including evolutionary aspects and zoonotic spillover risk. Lastly, we present important recommendations and considerations for further surveillance and viral characterization efforts in this field.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":3.6,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12282219/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144608507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bhavya Shukla, J Michael Moore, Theodore McAvoy, Nino Brown, Albert K Culbreath, Sudeep Bag
Orthotospovirus tomatomaculae [tomato spotted wilt virus (TSWV)] is a major pathogen in horticultural and row crops worldwide including the USA. In this study, tomato spotted wilt disease incidence was monitored in Arachis hypogaea (peanut; year 1990 to 2024) and Nicotiana tabacum (tobacco; year 2000 to 2024) in commercial farmers' fields in the Southeastern USA. Furthermore, nucleocapsid (N), nonstructural movement (NSm) and nonstructural silencing suppressor (NSs) protein gene sequences of TSWV global populations from North America, South America, Europe, Asia-Pacific, Africa and Australia were compared with local US population and analysed to understand the genetic variability in the virus genome. In our study, full-length sequences of 94 N, 111 NSm and 78 NSs genes were amplified from TSWV-infected A. hypogaea (peanut), Capsicum annuum (pepper), N. tabacum (tobacco) and Solanum lycopersicum (tomato). nt-based phylogenetic analysis of N, NSm and NSs genes correlated with the geographical location of the TSWV isolates, with notably higher substitution rates in the population of recent years. In addition, the least genetic variability was observed in the N gene of the local population upon comparison with other global TSWV population. The neutrality test of TSWV suggested a non-neutral evolution of the virus genome. Low variation among the selected genes might be attributed to strong purifying selection pressure in the populations. Furthermore, estimation of selection pressure (dN/dS) on small (S) segment-encoded N protein and nonstructural protein showed higher purifying selection than the movement protein encoded by the medium (M) segment of the TSWV isolates. Single-likelihood ancestor counting suggested an overall negative selection pressure on several codons of the selected genes, which indicated that natural selection and population bottleneck events might have influenced the evolution of TSWV. Our study also deciphered high gene flow and low genetic differentiation amid the different TSWV population sets. Additionally, BEAST analysis of TSWV N gene sequences from GA predicted the most common recent ancestor existed ~25 years ago. This data was further correlated with disease incidence data from peanut and tobacco crops obtained in the last three decades. These findings suggest the intermixing of TSWV isolates between peanut, pepper, tobacco and tomato crops, while the virus genome has undergone strong purifying selection.
{"title":"Molecular genetic analyses of the N, NSm and NSs genes of a local population of <i>Orthotospovirus tomatomaculae</i> reveal purifying selection in crops in the southeastern USA.","authors":"Bhavya Shukla, J Michael Moore, Theodore McAvoy, Nino Brown, Albert K Culbreath, Sudeep Bag","doi":"10.1099/jgv.0.002119","DOIUrl":"10.1099/jgv.0.002119","url":null,"abstract":"<p><p><i>Orthotospovirus tomatomaculae</i> [tomato spotted wilt virus (TSWV)] is a major pathogen in horticultural and row crops worldwide including the USA. In this study, tomato spotted wilt disease incidence was monitored in <i>Arachis hypogaea</i> (peanut; year 1990 to 2024) and <i>Nicotiana tabacum</i> (tobacco; year 2000 to 2024) in commercial farmers' fields in the Southeastern USA. Furthermore, nucleocapsid (N), nonstructural movement (NSm) and nonstructural silencing suppressor (NSs) protein gene sequences of TSWV global populations from North America, South America, Europe, Asia-Pacific, Africa and Australia were compared with local US population and analysed to understand the genetic variability in the virus genome. In our study, full-length sequences of 94 N, 111 NSm and 78 NSs genes were amplified from TSWV-infected <i>A. hypogaea</i> (peanut), <i>Capsicum annuum</i> (pepper), <i>N. tabacum</i> (tobacco) and <i>Solanum lycopersicum</i> (tomato). nt-based phylogenetic analysis of N, NSm and NSs genes correlated with the geographical location of the TSWV isolates, with notably higher substitution rates in the population of recent years. In addition, the least genetic variability was observed in the N gene of the local population upon comparison with other global TSWV population. The neutrality test of TSWV suggested a non-neutral evolution of the virus genome. Low variation among the selected genes might be attributed to strong purifying selection pressure in the populations. Furthermore, estimation of selection pressure (dN/dS) on small (S) segment-encoded N protein and nonstructural protein showed higher purifying selection than the movement protein encoded by the medium (M) segment of the TSWV isolates. Single-likelihood ancestor counting suggested an overall negative selection pressure on several codons of the selected genes, which indicated that natural selection and population bottleneck events might have influenced the evolution of TSWV. Our study also deciphered high gene flow and low genetic differentiation amid the different TSWV population sets. Additionally, BEAST analysis of TSWV N gene sequences from GA predicted the most common recent ancestor existed ~25 years ago. This data was further correlated with disease incidence data from peanut and tobacco crops obtained in the last three decades. These findings suggest the intermixing of TSWV isolates between peanut, pepper, tobacco and tomato crops, while the virus genome has undergone strong purifying selection.</p>","PeriodicalId":15880,"journal":{"name":"Journal of General Virology","volume":"106 7","pages":""},"PeriodicalIF":3.6,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12282330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144584120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}