Curtis A. Suttle: Effect of viral infection on sinking rates of Heterosigma akashiwo and its implications for bloom termination. In: Aquatic Microbial Ecology (AME), Band 37, Nr. 1, 2004, S. 1–7; doi:10.3354/ame037001, Academia (PDF), Abstract.
Christopher R.Schvarcz, Grieg F.Steward: A giant virus infecting green algae encodes key fermentation genes. In: Virology, Band 518, Mai 2018, S. 423–433; doi:10.1016/j.virol.2018.03.010 (englisch).
Yuji Tomaru, Yoko Shirai, Keizo Nagasaki: Ecology, physiology and genetics of a phycodnavirus infecting the noxious bloom-forming raphidophyte Heterosigma akashiwo. In: Fisheries Science. 74. Jahrgang, Nr.4, 1. August 2008, S.701–711, doi:10.1111/j.1444-2906.2008.01580.x (englisch).
Fumito Maruyama, Shoko Ueki: Evolution and Phylogeny of Large DNA Viruses, Mimiviridae and Phycodnaviridae Including Newly Characterized Heterosigma akashiwo Virus. In: Frontiers in Microbiology, Band 7, 30. November 2016, S. 1942; doi:10.3389/fmicb.2016.01942, PMC 5127864 (freier Volltext), PMID 27965659 (englisch).
Vera Tai, Janice E Lawrence, Andrew S Lang, Amy M Chan, Alexander I Culley, Curtis A Suttle: Characterization of HaRNAV, a single-stranded RNA virus causing lysis of Heterosigma akashiwo (Raphidophyceae). In: Journal of Phycology. 39. Jahrgang, Nr.2, 2003, S.343–352, doi:10.1046/j.1529-8817.2003.01162.x (englisch).
Janice E. Lawrence, Corina P. D. Brussaard, Curtis A. Suttle: Virus-Specific Responses of Heterosigma akashiwo to Infection. In: Appl Environ Microbiol, Band 72, Nr. 12, Dezember 2006, S. 7829–7834; doi:10.1128/AEM.01207-06, PMC 1694243 (freier Volltext), PMID 17041155.
Janice E Lawrence, Amy M Chan, Curtis A Suttle: A novel virus (HaNIV) causes lysis of the toxic bloom-forming alga Heterosigma akashiwo (Raphidophyceae). In: Journal of Phycology. 37. Jahrgang, Nr.2, 2001, S.216–222, doi:10.1046/j.1529-8817.2001.037002216.x (englisch).
Y. Bettarel, J. Kan, K. Wang, Kurt E. Williamson, S. Cooney, S. Ribblett, F. Chen, K. Wommack, D. Coats: Isolation and preliminary characterisation of a small nuclear inclusion virus infecting the diatom Chaetoceros cf. gracilis. In: Aquatic Microbial Ecology (AME), Band 40, Nr. 2, 2005; doi:10.3354/AME040103, Abstract. Zitat: „Chaetoceros nuclear inclusion virus: CspNIV“, „CspNIV shows some strong similarities with Heterosigma akashiwo nuclear inclusion virus (HaNIV)“
Keizo Nagasaki: Dinoflagellates, diatoms, and their viruses. In: The Journal of Microbiology, Band 46, Nr. 3, Juli 2008, S. 235–243; doi:10.1007/s12275-008-0098-y, ResearchGate. Zitat: „CspNIV shows some strong similarities with Heterosigma akashiwo nuclear inclusion virus (HaNIV)“.
Curtis A. Suttle: Effect of viral infection on sinking rates of Heterosigma akashiwo and its implications for bloom termination. In: Aquatic Microbial Ecology (AME), Band 37, Nr. 1, 2004, S. 1–7; doi:10.3354/ame037001, Academia (PDF), Abstract.
Jean-Michel Claverie, Chantal Abergel: Mimiviridae: An Expanding Family of Highly Diverse Large dsDNA Viruses Infecting a Wide Phylogenetic Range of Aquatic Eukaryotes. In: Viruses, Band 10, Nr. 9, 18. September 2018, S. 506; doi:10.3390/v10090506, PMC 6163669 (freier Volltext), PMID 30231528. Siehe insbes. Tab. 2.
Kenji Tarutani, Keizo Nagasaki, Mineo Yamaguchi: Virus adsorption process determines virus susceptibility in Heterosigma akashiwo (Raphidophyceae). In: Aquatic Microbial Ecolology (AME), Band 42, S. 209–213, 29. März 2006; doi:10.3354/ame042209, ResearchGate, PDF.
Yoshitoshi Ogura, Tetsuya Hayashi, Shoko Ueki: Complete Genome Sequence of a Phycodnavirus, Heterosigma akashiwo Virus Strain 53. In: Microbiology, September 2016; doi:10.1128/genomeA.01279-16, PMID 27834719 (englisch).
Eugene V. Koonin, Natalya Yutin: Evolution of the Large Nucleocytoplasmatic DNA Viruses of Eukaryotes and Convergent Origins of Viral Gigantism. In: Advances in Virus research, Band 103, AP 21. Januar 2019, doi:10.1016/bs.aivir.2018.09.002, S. 167–202. In Fig. 4 ist phycodnaviruses wohl im engeren Sinne (s. s.) zu verstehen und dürfte der Chlorovirus/Prasinovirus/‚YLPV‘-Gruppe bei Schulz et al. (2018) entsprechen.
Clara Rolland, Julien Andreani, Amina Cherif Louazani, Sarah Aherfi, Rania Francis, Rodrigo Rodrigues, Ludmila Santos Silva, Dehia Sahmi, Said Mougari, Nisrine Chelkha, Meriem Bekliz, Lorena Silva, Felipe Assis, Fábio Dornas, Jacques Yaacoub Bou Khalil, Isabelle Pagnier, Christelle Desnues, Anthony Levasseur, Philippe Colson, Jônatas Abrahão, Bernard La Scola: Discovery and Further Studies on Giant Viruses at the IHU Mediterranee Infection That Modified the Perception of the Virosphere. In: MDPI: Viruses, Band 11, Nr. 4, März/April 2019, pii: E312; doi:10.3390/v11040312, PMC 6520786 (freier Volltext), PMID 30935049, MDPI (englisch); siehe Fig. 2a.
Clara Rolland, Julien Andreani, Dehia Sahmi-Bounsiar, Mart Krupovic, Bernard La Scola, Anthony Levasseur: Clandestinovirus: A Giant Virus With Chromatin Proteins and a Potential to Manipulate the Cell Cycle of Its Host Vermamoeba vermiformis. In: Frontiers in Microbiology, Band 12, 10. August 2021, Nr. 715608; doi:10.3389/fmicb.2021.715608, PMID 34447361, PMC 8383183 (freier Volltext) (englisch).
Shengzhong Xu, Liang Zhou, Xiaosha Liang, Yifan Zhou, Hao Chen, Shuling Yan, Yongjie Wang; Julie K. Pfeiffer (Hrsg.): Novel Cell-Virus-Virophage Tripartite Infection Systems Discovered in the Freshwater Lake Dishui Lake in Shanghai, China. In: Journal of Virology, 18. Mai 2020; doi:10.1128/JVI.00149-20, PMID 32188734 (englisch).
Frank O. Aylward, Mohammad Moniruzzaman, Anh D. Ha, Eugene V. Koonin: A phylogenomic framework for charting the diversity and evolution of giant viruses. In: PLOS Biology, 27. Oktober 2021; doi:10.1371/journal.pbio.3001430 (englisch).
Ruixuan Zhang, Masaharu Takemura, Kazuyoshi Murata, Hiroyuki Ogata: “Mamonoviridae”, a proposed new family of the phylum Nucleocytoviricota. In: Archives of Virology, Band 168, Nr. 80, 5. Februar 2023; doi:10.1007/s00705-022-05633-1, PMID 36740641 (englisch).
Kenji Tarutani, Keizo Nagasaki, Mineo Yamaguchi: Virus adsorption process determines virus susceptibility in Heterosigma akashiwo (Raphidophyceae). In: Aquatic Microbial Ecolology (AME), Band 42, S. 209–213, 29. März 2006; doi:10.3354/ame042209, ResearchGate, PDF.
mdpi.com
Clara Rolland, Julien Andreani, Amina Cherif Louazani, Sarah Aherfi, Rania Francis, Rodrigo Rodrigues, Ludmila Santos Silva, Dehia Sahmi, Said Mougari, Nisrine Chelkha, Meriem Bekliz, Lorena Silva, Felipe Assis, Fábio Dornas, Jacques Yaacoub Bou Khalil, Isabelle Pagnier, Christelle Desnues, Anthony Levasseur, Philippe Colson, Jônatas Abrahão, Bernard La Scola: Discovery and Further Studies on Giant Viruses at the IHU Mediterranee Infection That Modified the Perception of the Virosphere. In: MDPI: Viruses, Band 11, Nr. 4, März/April 2019, pii: E312; doi:10.3390/v11040312, PMC 6520786 (freier Volltext), PMID 30935049, MDPI (englisch); siehe Fig. 2a.
Fumito Maruyama, Shoko Ueki: Evolution and Phylogeny of Large DNA Viruses, Mimiviridae and Phycodnaviridae Including Newly Characterized Heterosigma akashiwo Virus. In: Frontiers in Microbiology, Band 7, 30. November 2016, S. 1942; doi:10.3389/fmicb.2016.01942, PMC 5127864 (freier Volltext), PMID 27965659 (englisch).
Janice E. Lawrence, Corina P. D. Brussaard, Curtis A. Suttle: Virus-Specific Responses of Heterosigma akashiwo to Infection. In: Appl Environ Microbiol, Band 72, Nr. 12, Dezember 2006, S. 7829–7834; doi:10.1128/AEM.01207-06, PMC 1694243 (freier Volltext), PMID 17041155.
Jean-Michel Claverie, Chantal Abergel: Mimiviridae: An Expanding Family of Highly Diverse Large dsDNA Viruses Infecting a Wide Phylogenetic Range of Aquatic Eukaryotes. In: Viruses, Band 10, Nr. 9, 18. September 2018, S. 506; doi:10.3390/v10090506, PMC 6163669 (freier Volltext), PMID 30231528. Siehe insbes. Tab. 2.
Keizo Nagasaki, Kenji Tarutani, Mineo Yamaguchi: Growth Characteristics of Heterosigma akashiwo Virus and Its Possible Use as a Microbiological Agent for Red Tide Control. In: Applied and Environmental Microbiology. 65. Jahrgang, Nr.3, 1. März 1999, S.898–902, PMID 10049839, PMC 91120 (freier Volltext) – (englisch).
Yoshitoshi Ogura, Tetsuya Hayashi, Shoko Ueki: Complete Genome Sequence of a Phycodnavirus, Heterosigma akashiwo Virus Strain 53. In: Microbiology, September 2016; doi:10.1128/genomeA.01279-16, PMID 27834719 (englisch).
Clara Rolland, Julien Andreani, Amina Cherif Louazani, Sarah Aherfi, Rania Francis, Rodrigo Rodrigues, Ludmila Santos Silva, Dehia Sahmi, Said Mougari, Nisrine Chelkha, Meriem Bekliz, Lorena Silva, Felipe Assis, Fábio Dornas, Jacques Yaacoub Bou Khalil, Isabelle Pagnier, Christelle Desnues, Anthony Levasseur, Philippe Colson, Jônatas Abrahão, Bernard La Scola: Discovery and Further Studies on Giant Viruses at the IHU Mediterranee Infection That Modified the Perception of the Virosphere. In: MDPI: Viruses, Band 11, Nr. 4, März/April 2019, pii: E312; doi:10.3390/v11040312, PMC 6520786 (freier Volltext), PMID 30935049, MDPI (englisch); siehe Fig. 2a.
Clara Rolland, Julien Andreani, Dehia Sahmi-Bounsiar, Mart Krupovic, Bernard La Scola, Anthony Levasseur: Clandestinovirus: A Giant Virus With Chromatin Proteins and a Potential to Manipulate the Cell Cycle of Its Host Vermamoeba vermiformis. In: Frontiers in Microbiology, Band 12, 10. August 2021, Nr. 715608; doi:10.3389/fmicb.2021.715608, PMID 34447361, PMC 8383183 (freier Volltext) (englisch).
Shengzhong Xu, Liang Zhou, Xiaosha Liang, Yifan Zhou, Hao Chen, Shuling Yan, Yongjie Wang; Julie K. Pfeiffer (Hrsg.): Novel Cell-Virus-Virophage Tripartite Infection Systems Discovered in the Freshwater Lake Dishui Lake in Shanghai, China. In: Journal of Virology, 18. Mai 2020; doi:10.1128/JVI.00149-20, PMID 32188734 (englisch).
Ruixuan Zhang, Masaharu Takemura, Kazuyoshi Murata, Hiroyuki Ogata: “Mamonoviridae”, a proposed new family of the phylum Nucleocytoviricota. In: Archives of Virology, Band 168, Nr. 80, 5. Februar 2023; doi:10.1007/s00705-022-05633-1, PMID 36740641 (englisch).
researchgate.net
Keizo Nagasaki: Dinoflagellates, diatoms, and their viruses. In: The Journal of Microbiology, Band 46, Nr. 3, Juli 2008, S. 235–243; doi:10.1007/s12275-008-0098-y, ResearchGate. Zitat: „CspNIV shows some strong similarities with Heterosigma akashiwo nuclear inclusion virus (HaNIV)“.
Kenji Tarutani, Keizo Nagasaki, Mineo Yamaguchi: Virus adsorption process determines virus susceptibility in Heterosigma akashiwo (Raphidophyceae). In: Aquatic Microbial Ecolology (AME), Band 42, S. 209–213, 29. März 2006; doi:10.3354/ame042209, ResearchGate, PDF.
semanticscholar.org
Y. Bettarel, J. Kan, K. Wang, Kurt E. Williamson, S. Cooney, S. Ribblett, F. Chen, K. Wommack, D. Coats: Isolation and preliminary characterisation of a small nuclear inclusion virus infecting the diatom Chaetoceros cf. gracilis. In: Aquatic Microbial Ecology (AME), Band 40, Nr. 2, 2005; doi:10.3354/AME040103, Abstract. Zitat: „Chaetoceros nuclear inclusion virus: CspNIV“, „CspNIV shows some strong similarities with Heterosigma akashiwo nuclear inclusion virus (HaNIV)“
Curtis A. Suttle: Effect of viral infection on sinking rates of Heterosigma akashiwo and its implications for bloom termination. In: Aquatic Microbial Ecology (AME), Band 37, Nr. 1, 2004, S. 1–7; doi:10.3354/ame037001, Academia (PDF), Abstract.
