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  1. Article: Mriyaviruses: Small Relatives of Giant Viruses.

    Yutin, Natalya / Mutz, Pascal / Krupovic, Mart / Koonin, Eugene V

    bioRxiv : the preprint server for biology

    2024  

    Abstract: ... The ... ...

    Abstract The phylum
    Language English
    Publishing date 2024-02-29
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.02.29.582850
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The crAss-like Phage Group: How Metagenomics Reshaped the Human Virome.

    Koonin, Eugene V / Yutin, Natalya

    Trends in microbiology

    2020  Volume 28, Issue 5, Page(s) 349–359

    Abstract: Metagenomics is currently the primary means for identifying new viruses. One of the most impactful metagenomic discoveries is that of crAssphage, the most abundant human-associated virus that is found in about 50% of human gut viromes where it can ... ...

    Abstract Metagenomics is currently the primary means for identifying new viruses. One of the most impactful metagenomic discoveries is that of crAssphage, the most abundant human-associated virus that is found in about 50% of human gut viromes where it can comprise up to 90% of the virus sequences. Although initial genome analysis of crAssphage failed to detect related phages, or functionally annotate most of the genes, subsequent reanalysis with powerful computational methods and larger databases led to the identification of an expansive group of crAss-like phages. The functions of most crAssphage proteins were predicted, including unusual ones such as giant RNA polymerase polyproteins. The host range of the crAss-like phages consists of various members of the bacterial phylum Bacteroidetes as demonstrated by CRISPR spacer analysis and by analysis of genes acquired by phages from the hosts. New metagenomic studies vastly expanded the crAss-like phage group and demonstrated its global spread and ancient association with primates. The first members of the crAss-like group was recently isolated and shown to infect the bacterium Bacteroides intestinales. Characterization of this phage validated the predicted podovirus-like virion structure and the identity of the major capsid protein and other predicted virion proteins, including three RNA polymerase subunits.
    MeSH term(s) Bacteriophages/classification ; Bacteriophages/genetics ; Bacteroides/virology ; Gastrointestinal Microbiome/genetics ; Genome, Viral/genetics ; Humans ; Metagenomics ; Viral Replicase Complex Proteins/genetics ; Viral Replicase Complex Proteins/metabolism ; Virome/genetics
    Chemical Substances Viral Replicase Complex Proteins
    Language English
    Publishing date 2020-02-28
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1158963-2
    ISSN 1878-4380 ; 0966-842X
    ISSN (online) 1878-4380
    ISSN 0966-842X
    DOI 10.1016/j.tim.2020.01.010
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The crAss-like Phage Group: How Metagenomics Reshaped the Human Virome

    Koonin, Eugene V / Yutin, Natalya

    Trends in microbiology. 2020 May, v. 28, no. 5

    2020  

    Abstract: Metagenomics is currently the primary means for identifying new viruses. One of the most impactful metagenomic discoveries is that of crAssphage, the most abundant human-associated virus that is found in about 50% of human gut viromes where it can ... ...

    Abstract Metagenomics is currently the primary means for identifying new viruses. One of the most impactful metagenomic discoveries is that of crAssphage, the most abundant human-associated virus that is found in about 50% of human gut viromes where it can comprise up to 90% of the virus sequences. Although initial genome analysis of crAssphage failed to detect related phages, or functionally annotate most of the genes, subsequent reanalysis with powerful computational methods and larger databases led to the identification of an expansive group of crAss-like phages. The functions of most crAssphage proteins were predicted, including unusual ones such as giant RNA polymerase polyproteins. The host range of the crAss-like phages consists of various members of the bacterial phylum Bacteroidetes as demonstrated by CRISPR spacer analysis and by analysis of genes acquired by phages from the hosts. New metagenomic studies vastly expanded the crAss-like phage group and demonstrated its global spread and ancient association with primates. The first members of the crAss-like group was recently isolated and shown to infect the bacterium Bacteroides intestinales. Characterization of this phage validated the predicted podovirus-like virion structure and the identity of the major capsid protein and other predicted virion proteins, including three RNA polymerase subunits.
    Keywords Bacteroides ; CRISPR sequences ; DNA-directed RNA polymerase ; Primates ; bacteria ; coat proteins ; computational methodology ; databases ; digestive system ; gene editing ; genes ; host range ; hosts ; humans ; metagenomics ; phages ; polyproteins ; sequence analysis ; virion
    Language English
    Dates of publication 2020-05
    Size p. 349-359.
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 1158963-2
    ISSN 1878-4380 ; 0966-842X
    ISSN (online) 1878-4380
    ISSN 0966-842X
    DOI 10.1016/j.tim.2020.01.010
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: Updated Virophage Taxonomy and Distinction from Polinton-like Viruses.

    Roux, Simon / Fischer, Matthias G / Hackl, Thomas / Katz, Laura A / Schulz, Frederik / Yutin, Natalya

    Biomolecules

    2023  Volume 13, Issue 2

    Abstract: Virophages are small dsDNA viruses that hijack the machinery of giant viruses during the co-infection of a protist (i.e., microeukaryotic) host and represent an exceptional case of "hyperparasitism" in the viral world. While only a handful of virophages ... ...

    Abstract Virophages are small dsDNA viruses that hijack the machinery of giant viruses during the co-infection of a protist (i.e., microeukaryotic) host and represent an exceptional case of "hyperparasitism" in the viral world. While only a handful of virophages have been isolated, a vast diversity of virophage-like sequences have been uncovered from diverse metagenomes. Their wide ecological distribution, idiosyncratic infection and replication strategy, ability to integrate into protist and giant virus genomes and potential role in antiviral defense have made virophages a topic of broad interest. However, one limitation for further studies is the lack of clarity regarding the nomenclature and taxonomy of this group of viruses. Specifically, virophages have been linked in the literature to other "virophage-like" mobile genetic elements and viruses, including polinton-like viruses (PLVs), but there are no formal demarcation criteria and proper nomenclature for either group, i.e., virophage or PLVs. Here, as part of the ICTV Virophage Study Group, we leverage a large set of genomes gathered from published datasets as well as newly generated protist genomes to propose delineation criteria and classification methods at multiple taxonomic ranks for virophages 'sensu stricto', i.e., genomes related to the prototype isolates Sputnik and mavirus. Based on a combination of comparative genomics and phylogenetic analyses, we show that this group of virophages forms a cohesive taxon that we propose to establish at the class level and suggest a subdivision into four orders and seven families with distinctive ecogenomic features. Finally, to illustrate how the proposed delineation criteria and classification method would be used, we apply these to two recently published datasets, which we show include both virophages and other virophage-related elements. Overall, we see this proposed classification as a necessary first step to provide a robust taxonomic framework in this area of the virosphere, which will need to be expanded in the future to cover other virophage-related viruses such as PLVs.
    MeSH term(s) Humans ; Virophages/genetics ; Phylogeny ; Genome, Viral ; Viruses/genetics ; Eukaryota/genetics
    Language English
    Publishing date 2023-01-19
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom13020204
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Evolution of the Large Nucleocytoplasmic DNA Viruses of Eukaryotes and Convergent Origins of Viral Gigantism.

    Koonin, Eugene V / Yutin, Natalya

    Advances in virus research

    2018  Volume 103, Page(s) 167–202

    Abstract: The Nucleocytoplasmic Large DNA Viruses (NCLDV) of eukaryotes (proposed order "Megavirales") comprise an expansive group of eukaryotic viruses that consists of the families Poxviridae, Asfarviridae, Iridoviridae, Ascoviridae, Phycodnaviridae, ... ...

    Abstract The Nucleocytoplasmic Large DNA Viruses (NCLDV) of eukaryotes (proposed order "Megavirales") comprise an expansive group of eukaryotic viruses that consists of the families Poxviridae, Asfarviridae, Iridoviridae, Ascoviridae, Phycodnaviridae, Marseilleviridae, Pithoviridae, and Mimiviridae, as well as Pandoraviruses, Molliviruses, and Faustoviruses that so far remain unaccounted by the official virus taxonomy. All these viruses have double-stranded DNA genomes that range in size from about 100 kilobases (kb) to more than 2.5 megabases. The viruses with genomes larger than 500kb are informally considered "giant," and the largest giant viruses surpass numerous bacteria and archaea in both particle and genome size. The discovery of giant viruses has been highly unexpected and has changed the perception of viral size and complexity, and even, arguably, the entire concept of a virus. Given that giant viruses encode multiple proteins that are universal among cellular life forms and are components of the translation system, the quintessential cellular molecular machinery, attempts have been made to incorporate these viruses in the evolutionary tree of cellular life. Moreover, evolutionary scenarios of the origin of giant viruses from a fourth, supposedly extinct domain of cellular life have been proposed. However, despite all the differences in the genome size and gene repertoire, the NCLDV can be confidently defined as monophyletic group, on the strength of the presence of about 40 genes that can be traced back to their last common ancestor. Using several most strongly conserved genes from this ancestral set, a well-resolved phylogenetic tree of the NCLDV was built and employed as the scaffold to reconstruct the history of gene gain and loss throughout the course of the evolution of this group of viruses. This reconstruction reveals extremely dynamic evolution that involved extensive gene gain and loss in many groups of viruses and indicates that giant viruses emerged independently in several clades of the NCLDV. Thus, these giants of the virus world evolved repeatedly from smaller and simpler viruses, rather than from a fourth domain of cellular life, and captured numerous genes, including those for translation system components, from eukaryotes, along with some bacterial genes. Even deeper evolutionary reconstructions reveal apparent links between the NCLDV and smaller viruses of eukaryotes, such as adenoviruses, and ultimately, derive all these viruses from tailless bacteriophages.
    MeSH term(s) Biological Evolution ; DNA ; DNA Viruses/classification ; DNA Viruses/physiology ; Eukaryotic Cells/virology ; Genome Size ; Genome, Viral ; Giant Viruses/physiology ; Phylogeny ; Protein Biosynthesis ; Viral Proteins/genetics
    Chemical Substances Viral Proteins ; DNA (9007-49-2)
    Language English
    Publishing date 2018-11-10
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 195-8
    ISSN 1557-8399 ; 0065-3527
    ISSN (online) 1557-8399
    ISSN 0065-3527
    DOI 10.1016/bs.aivir.2018.09.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Multiple evolutionary origins of giant viruses.

    Koonin, Eugene V / Yutin, Natalya

    F1000Research

    2018  Volume 7

    Abstract: The nucleocytoplasmic large DNA viruses (NCLDVs) are a monophyletic group of diverse eukaryotic viruses that reproduce primarily in the cytoplasm of the infected cells and include the largest viruses currently known: the giant mimiviruses, pandoraviruses, ...

    Abstract The nucleocytoplasmic large DNA viruses (NCLDVs) are a monophyletic group of diverse eukaryotic viruses that reproduce primarily in the cytoplasm of the infected cells and include the largest viruses currently known: the giant mimiviruses, pandoraviruses, and pithoviruses. With virions measuring up to 1.5 μm and genomes of up to 2.5 Mb, the giant viruses break the now-outdated definition of a virus and extend deep into the genome size range typical of bacteria and archaea. Additionally, giant viruses encode multiple proteins that are universal among cellular life forms, particularly components of the translation system, the signature cellular molecular machinery. These findings triggered hypotheses on the origin of giant viruses from cells, likely of an extinct fourth domain of cellular life, via reductive evolution. However, phylogenomic analyses reveal a different picture, namely multiple origins of giant viruses from smaller NCLDVs via acquisition of multiple genes from the eukaryotic hosts and bacteria, along with gene duplication. Thus, with regard to their origin, the giant viruses do not appear to qualitatively differ from the rest of the virosphere. However, the evolutionary forces that led to the emergence of virus gigantism remain enigmatic.
    MeSH term(s) Biological Evolution ; Evolution, Molecular ; Genome ; Giant Viruses/genetics ; Host Microbial Interactions/genetics
    Language English
    Publishing date 2018-11-22
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Intramural ; Review
    ZDB-ID 2699932-8
    ISSN 2046-1402 ; 2046-1402
    ISSN (online) 2046-1402
    ISSN 2046-1402
    DOI 10.12688/f1000research.16248.1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Evolution of a major virion protein of the giant pandoraviruses from an inactivated bacterial glycoside hydrolase.

    Krupovic, Mart / Yutin, Natalya / Koonin, Eugene

    Virus evolution

    2020  Volume 6, Issue 2, Page(s) veaa059

    Abstract: The diverse viruses in the ... ...

    Abstract The diverse viruses in the phylum
    Language English
    Publishing date 2020-11-30
    Publishing country England
    Document type Journal Article
    ZDB-ID 2818949-8
    ISSN 2057-1577
    ISSN 2057-1577
    DOI 10.1093/ve/veaa059
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Conservation and Evolution of the Sporulation Gene Set in Diverse Members of the

    Galperin, Michael Y / Yutin, Natalya / Wolf, Yuri I / Vera Alvarez, Roberto / Koonin, Eugene V

    Journal of bacteriology

    2022  Volume 204, Issue 6, Page(s) e0007922

    Abstract: The current classification of the ... ...

    Abstract The current classification of the phylum
    MeSH term(s) Bacillus ; Bacillus subtilis/genetics ; Bacterial Proteins/genetics ; Clostridium/genetics ; Firmicutes ; Humans ; Phylogeny ; Spores, Bacterial/genetics
    Chemical Substances Bacterial Proteins
    Language English
    Publishing date 2022-05-31
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2968-3
    ISSN 1098-5530 ; 0021-9193
    ISSN (online) 1098-5530
    ISSN 0021-9193
    DOI 10.1128/jb.00079-22
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Programmable RNA-guided endonucleases are widespread in eukaryotes and their viruses.

    Jiang, Kaiyi / Lim, Justin / Sgrizzi, Samantha / Trinh, Michael / Kayabolen, Alisan / Yutin, Natalya / Koonin, Eugene V / Abudayyeh, Omar O / Gootenberg, Jonathan S

    bioRxiv : the preprint server for biology

    2023  

    Abstract: TnpB proteins are RNA-guided nucleases that are broadly associated with IS200/605 family transposons in prokaryotes. TnpB homologs, named Fanzors, have been detected in genomes of some eukaryotes and large viruses, but their activity and functions in ... ...

    Abstract TnpB proteins are RNA-guided nucleases that are broadly associated with IS200/605 family transposons in prokaryotes. TnpB homologs, named Fanzors, have been detected in genomes of some eukaryotes and large viruses, but their activity and functions in eukaryotes remain unknown. We searched genomes of diverse eukaryotes and their viruses for TnpB homologs and identified numerous putative RNA-guided nucleases that are often associated with various transposases, suggesting they are encoded in mobile genetic elements. Reconstruction of the evolution of these nucleases, which we rename Horizontally-transferred Eukaryotic RNA-guided Mobile Element Systems (HERMES), revealed multiple acquisitions of TnpBs by eukaryotes and subsequent diversification. In their adaptation and spread in eukaryotes, HERMES proteins acquired nuclear localization signals, and genes captured introns, indicating extensive, long term adaptation to functioning in eukaryotic cells. Biochemical and cellular evidence show that HERMES employ non-coding RNAs encoded adjacent to the nuclease for RNA-guided cleavage of double-stranded DNA. HERMES nucleases contain a re-arranged catalytic site of the RuvC domain, similar to a distinct subset of TnpBs, and lack collateral cleavage activity. We demonstrate that HERMES can be harnessed for genome editing in human cells, highlighting the potential of these widespread eukaryotic RNA-guided nucleases for biotechnology applications.
    Language English
    Publishing date 2023-06-14
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.06.13.544871
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Varidnaviruses in the Human Gut: A Major Expansion of the Order Vinavirales

    Yutin, Natalya / Rayko, Mike / Antipov, Dmitry / Mutz, Pascal / Wolf, Yuri I. / Krupovic, Mart / Koonin, Eugene V.

    Viruses. 2022 Aug. 23, v. 14, no. 9

    2022  

    Abstract: Bacteriophages play key roles in the dynamics of the human microbiome. By far the most abundant components of the human gut virome are tailed bacteriophages of the realm Duplodnaviria, in particular, crAss-like phages. However, apart from duplodnaviruses, ...

    Abstract Bacteriophages play key roles in the dynamics of the human microbiome. By far the most abundant components of the human gut virome are tailed bacteriophages of the realm Duplodnaviria, in particular, crAss-like phages. However, apart from duplodnaviruses, the gut virome has not been dissected in detail. Here we report a comprehensive census of a minor component of the gut virome, the tailless bacteriophages of the realm Varidnaviria. Tailless phages are primarily represented in the gut by prophages, that are mostly integrated in genomes of Alphaproteobacteria and Verrucomicrobia and belong to the order Vinavirales, which currently consists of the families Corticoviridae and Autolykiviridae. Phylogenetic analysis of the major capsid proteins (MCP) suggests that at least three new families should be established within Vinavirales to accommodate the diversity of prophages from the human gut virome. Previously, only the MCP and packaging ATPase genes were reported as conserved core genes of Vinavirales. Here we report an extended core set of 12 proteins, including MCP, packaging ATPase, and previously undetected lysis enzymes, that are shared by most of these viruses. We further demonstrate that replication system components are frequently replaced in the genomes of Vinavirales, suggestive of selective pressure for escape from yet unknown host defenses or avoidance of incompatibility with coinfecting related viruses. The results of this analysis show that, in a sharp contrast to marine viromes, varidnaviruses are a minor component of the human gut virome. Moreover, they are primarily represented by prophages, as indicated by the analysis of the flanking genes, suggesting that there are few, if any, lytic varidnavirus infections in the gut at any given time. These findings complement the existing knowledge of the human gut virome by exploring a group of viruses that has been virtually overlooked in previous work.
    Keywords Corticoviridae ; Duplodnaviria ; Verrucomicrobia ; adenosinetriphosphatase ; alpha-Proteobacteria ; capsid ; digestive system ; genome ; humans ; microbiome ; mixed infection ; phylogeny
    Language English
    Dates of publication 2022-0823
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    ZDB-ID 2516098-9
    ISSN 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v14091842
    Database NAL-Catalogue (AGRICOLA)

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