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Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome

Viral infection had not been observed for amoebae, until the Acanthamoeba polyphaga mimivirus (APMV) was discovered in 2003. APMV belongs to the nucleocytoplasmatic large DNA virus (NCLDV) family and infects not only A. polyphaga, but also other professional phagocytes. Here, we review the Megaviral...

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Autores principales: Diesend, Jan, Kruse, Janis, Hagedorn, Monica, Hammann, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768912/
https://www.ncbi.nlm.nih.gov/pubmed/29376032
http://dx.doi.org/10.3389/fcimb.2017.00527
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author Diesend, Jan
Kruse, Janis
Hagedorn, Monica
Hammann, Christian
author_facet Diesend, Jan
Kruse, Janis
Hagedorn, Monica
Hammann, Christian
author_sort Diesend, Jan
collection PubMed
description Viral infection had not been observed for amoebae, until the Acanthamoeba polyphaga mimivirus (APMV) was discovered in 2003. APMV belongs to the nucleocytoplasmatic large DNA virus (NCLDV) family and infects not only A. polyphaga, but also other professional phagocytes. Here, we review the Megavirales to give an overview of the current members of the Mimi- and Marseilleviridae families and their structural features during amoebal infection. We summarize the different steps of their infection cycle in A. polyphaga and Acanthamoeba castellani. Furthermore, we dive into the emerging field of virophages, which parasitize upon viral factories of the Megavirales family. The discovery of virophages in 2008 and research in recent years revealed an increasingly complex network of interactions between cell, giant virus, and virophage. Virophages seem to be highly abundant in the environment and occupy the same niches as the Mimiviridae and their hosts. Establishment of metagenomic and co-culture approaches rapidly increased the number of detected virophages over the recent years. Genetic interaction of cell and virophage might constitute a potent defense machinery against giant viruses and seems to be important for survival of the infected cell during mimivirus infections. Nonetheless, the molecular events during co-infection and the interactions of cell, giant virus, and virophage have not been elucidated, yet. However, the genetic interactions of these three, suggest an intricate, multilayered network during amoebal (co-)infections. Understanding these interactions could elucidate molecular events essential for proper viral factory activity and could implicate new ways of treating viruses that form viral factories.
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spelling pubmed-57689122018-01-26 Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome Diesend, Jan Kruse, Janis Hagedorn, Monica Hammann, Christian Front Cell Infect Microbiol Microbiology Viral infection had not been observed for amoebae, until the Acanthamoeba polyphaga mimivirus (APMV) was discovered in 2003. APMV belongs to the nucleocytoplasmatic large DNA virus (NCLDV) family and infects not only A. polyphaga, but also other professional phagocytes. Here, we review the Megavirales to give an overview of the current members of the Mimi- and Marseilleviridae families and their structural features during amoebal infection. We summarize the different steps of their infection cycle in A. polyphaga and Acanthamoeba castellani. Furthermore, we dive into the emerging field of virophages, which parasitize upon viral factories of the Megavirales family. The discovery of virophages in 2008 and research in recent years revealed an increasingly complex network of interactions between cell, giant virus, and virophage. Virophages seem to be highly abundant in the environment and occupy the same niches as the Mimiviridae and their hosts. Establishment of metagenomic and co-culture approaches rapidly increased the number of detected virophages over the recent years. Genetic interaction of cell and virophage might constitute a potent defense machinery against giant viruses and seems to be important for survival of the infected cell during mimivirus infections. Nonetheless, the molecular events during co-infection and the interactions of cell, giant virus, and virophage have not been elucidated, yet. However, the genetic interactions of these three, suggest an intricate, multilayered network during amoebal (co-)infections. Understanding these interactions could elucidate molecular events essential for proper viral factory activity and could implicate new ways of treating viruses that form viral factories. Frontiers Media S.A. 2018-01-11 /pmc/articles/PMC5768912/ /pubmed/29376032 http://dx.doi.org/10.3389/fcimb.2017.00527 Text en Copyright © 2018 Diesend, Kruse, Hagedorn and Hammann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Diesend, Jan
Kruse, Janis
Hagedorn, Monica
Hammann, Christian
Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome
title Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome
title_full Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome
title_fullStr Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome
title_full_unstemmed Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome
title_short Amoebae, Giant Viruses, and Virophages Make Up a Complex, Multilayered Threesome
title_sort amoebae, giant viruses, and virophages make up a complex, multilayered threesome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768912/
https://www.ncbi.nlm.nih.gov/pubmed/29376032
http://dx.doi.org/10.3389/fcimb.2017.00527
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