Identification of Two Novel Amalgaviruses in the Common
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Molecular Identification and Characterization of Two Rubber Dandelion
Molecular Identification and Characterization of Two Rubber Dandelion Amalgaviruses Archives of Virology – Annotated Sequence Record Humberto Debat1*, Zinan Luo, Brian J. Iaffaldano, Xiaofeng Zhuang, Katrina Cornish 2 1 Instituto de Patología Vegetal, Centro de Investigaciones Agropecuarias, Instituto Nacional de Tecnología Agropecuaria (IPAVE-CIAP-INTA), 11 de setiembre 4755, Córdoba, Argentina, X5020ICA. 2 Department of Horticulture and Crop Science, The Ohio State University, Ohio Agricultural Research and Development Center, Williams Hall, 1680 Madison Avenue, Wooster, OH 44691. * Corresponding author: Humberto Debat, [email protected], Tel: +54 9 351 4973636, Fax: +54 9 351 4974330 Abstract The Amalgaviridae family is composed of persistent viruses that share the genome architecture of Totiviridae and gene evolutionary resemblance to Partitiviridae. A single Amalgavirus genus has been assigned to this family, harboring only four recognized species, corresponding to plant infecting viruses with dsRNA monopartite genomes of ca. 3.4 kb. Here, we present the genomic identification and characterization of two novel Amalgavirus detected in Rubber dandelion (Taraxacum kok-saghyz). The sequenced isolates presented a 3,409 and 3,413 nt long genome, harbouring two partially overlapping ORFs encoding a putative coat protein and an RNA-dependent RNA polymerase (RdRP). Multiple independent RNAseq data suggest that the identified viruses have a differential distribution and low relative RNA levels in infected plants. Virus presence was not associated with any apparent symptoms on the plant host. We propose the name rubber dandelion latent virus 1 & 2 to the detected Amalgavirus. Annotated sequence record Natural rubber is an essential material to the manufacture of 50,000 different rubber and latex products. -
A Virus of Hyperthermophilic Archaea with a Unique Architecture Among DNA Viruses
A virus of hyperthermophilic archaea with a unique architecture among DNA viruses Elena Ilka Rensena,1, Tomohiro Mochizukia,b,1, Emmanuelle Quemina, Stefan Schoutenc, Mart Krupovica,2, and David Prangishvilia,2 aDepartment of Microbiology, Institut Pasteur, 75015 Paris, France; bEarth-Life Science Institute, Tokyo Institute of Technology, Tokyo 152-8550, Japan; and cDepartment of Marine Organic Biogeochemistry, Royal Netherlands Institute for Sea Research, 1790 AB Den Burg, The Netherlands Edited by James L. Van Etten, University of Nebraska-Lincoln, Lincoln, NE, and approved January 19, 2016 (received for review September 23, 2015) Viruses package their genetic material in diverse ways. Most known shell consisting of two protein layers and an external envelope. strategies include encapsulation of nucleic acids into spherical or Our results provide new insights into the diversity of architec- filamentous virions with icosahedral or helical symmetry, respec- tural solutions used by filamentous viruses. tively. Filamentous viruses with dsDNA genomes are currently as- sociated exclusively with Archaea. Here, we describe a filamentous Results hyperthermophilic archaeal virus, Pyrobaculum filamentous virus 1 Virus and Host Isolation. From the environmental sample collected (PFV1), with a type of virion organization not previously observed at the Pozzuoli Solfatara, Italy, enrichment cultures were estab- in DNA viruses. The PFV1 virion, 400 ± 20 × 32 ± 3 nm, contains an lished in conditions known to favor the growth of aerobic mem- envelope and an inner core consisting of two structural units: a rod- bers of the archaeal genus Pyrobaculum (14). The virus-like particles shaped helical nucleocapsid formed of two 14-kDa major virion pro- (VLPs) were detected in the enrichment culture by transmission teins and a nucleocapsid-encompassing protein sheath composed electron microscopy (TEM). -
Origins and Evolution of the Global RNA Virome
bioRxiv preprint doi: https://doi.org/10.1101/451740; this version posted October 24, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Origins and Evolution of the Global RNA Virome 2 Yuri I. Wolfa, Darius Kazlauskasb,c, Jaime Iranzoa, Adriana Lucía-Sanza,d, Jens H. 3 Kuhne, Mart Krupovicc, Valerian V. Doljaf,#, Eugene V. Koonina 4 aNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA 5 b Vilniaus universitetas biotechnologijos institutas, Vilnius, Lithuania 6 c Département de Microbiologie, Institut Pasteur, Paris, France 7 dCentro Nacional de Biotecnología, Madrid, Spain 8 eIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious 9 Diseases, National Institutes of Health, Frederick, Maryland, USA 10 fDepartment of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, USA 11 12 #Address correspondence to Valerian V. Dolja, [email protected] 13 14 Running title: Global RNA Virome 15 16 KEYWORDS 17 virus evolution, RNA virome, RNA-dependent RNA polymerase, phylogenomics, horizontal 18 virus transfer, virus classification, virus taxonomy 1 bioRxiv preprint doi: https://doi.org/10.1101/451740; this version posted October 24, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 19 ABSTRACT 20 Viruses with RNA genomes dominate the eukaryotic virome, reaching enormous diversity in 21 animals and plants. The recent advances of metaviromics prompted us to perform a detailed 22 phylogenomic reconstruction of the evolution of the dramatically expanded global RNA virome. -
Meta-Transcriptomic Detection of Diverse and Divergent RNA Viruses
bioRxiv preprint doi: https://doi.org/10.1101/2020.06.08.141184; this version posted June 8, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Meta-transcriptomic detection of diverse and divergent 2 RNA viruses in green and chlorarachniophyte algae 3 4 5 Justine Charon1, Vanessa Rossetto Marcelino1,2, Richard Wetherbee3, Heroen Verbruggen3, 6 Edward C. Holmes1* 7 8 9 1Marie Bashir Institute for Infectious Diseases and Biosecurity, School of Life and 10 Environmental Sciences and School of Medical Sciences, The University of Sydney, 11 Sydney, Australia. 12 2Centre for Infectious Diseases and Microbiology, Westmead Institute for Medical 13 Research, Westmead, NSW 2145, Australia. 14 3School of BioSciences, University of Melbourne, VIC 3010, Australia. 15 16 17 *Corresponding author: 18 Marie Bashir Institute for Infectious Diseases and Biosecurity, School of Life and 19 Environmental Sciences and School of Medical Sciences, 20 The University of Sydney, 21 Sydney, NSW 2006, Australia. 22 Tel: +61 2 9351 5591 23 Email: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.06.08.141184; this version posted June 8, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. -
Metagenomic Analysis of the Enteric RNA Virome of Infants from the Oukasie Clinic, North West Province, South Africa, Reveals Diverse Eukaryotic Viruses
viruses Article Metagenomic Analysis of the Enteric RNA Virome of Infants from the Oukasie Clinic, North West Province, South Africa, Reveals Diverse Eukaryotic Viruses Milton T. Mogotsi 1,2, Peter N. Mwangi 1,3, Phillip A. Bester 3, M. Jeffrey Mphahlele 4,5, Mapaseka L. Seheri 4, Hester G. O’Neill 2 and Martin M. Nyaga 1,3,* 1 Next Generation Sequencing Unit, University of the Free State, Bloemfontein 9300, South Africa; [email protected] (M.T.M.); [email protected] (P.N.M.) 2 Department of Microbial, Biochemical and Food Biotechnology, University of the Free State, Bloemfontein 9300, South Africa; [email protected] 3 Division of Virology, School of Pathology, Faculty of Health Sciences, University of the Free State, Bloemfontein 9300, South Africa; [email protected] 4 Diarrhoeal Pathogens Research Unit, Department of Virology, Faculty of Health Sciences, Sefako Makgatho Health Sciences University, Medunsa, Pretoria 0204, South Africa; Jeff[email protected] (M.J.M.); [email protected] (M.L.S.) 5 South African Medical Research Council, 1 Soutpansberg Road, Pretoria 0001, South Africa * Correspondence: [email protected]; Tel.: +27-51-401-9158 Received: 18 September 2020; Accepted: 3 November 2020; Published: 5 November 2020 Abstract: Establishing a diverse gut microbiota after birth is essential for preventing illnesses later in life. However, little knowledge exists about the total viral population (virome) present in the gut of infants during the early developmental stage, with RNA viruses being generally overlooked. Therefore, this small pilot longitudinal study investigated the diversity and changes in the enteric RNA virome in healthy infants from South Africa. -
Discovery of New Mycoviral Genomes Within Publicly Available Fungal Transcriptomic Datasets
bioRxiv preprint doi: https://doi.org/10.1101/510404; this version posted January 3, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Discovery of new mycoviral genomes within publicly available fungal transcriptomic datasets 1 1 1,2 1 Kerrigan B. Gilbert , Emily E. Holcomb , Robyn L. Allscheid , James C. Carrington * 1 Donald Danforth Plant Science Center, Saint Louis, Missouri, USA 2 Current address: National Corn Growers Association, Chesterfield, Missouri, USA * Address correspondence to James C. Carrington E-mail: [email protected] Short title: Virus discovery from RNA-seq data bioRxiv preprint doi: https://doi.org/10.1101/510404; this version posted January 3, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Abstract The distribution and diversity of RNA viruses in fungi is incompletely understood due to the often cryptic nature of mycoviral infections and the focused study of primarily pathogenic and/or economically important fungi. As most viruses that are known to infect fungi possess either single-stranded or double-stranded RNA genomes, transcriptomic data provides the opportunity to query for viruses in diverse fungal samples without any a priori knowledge of virus infection. Here we describe a systematic survey of all transcriptomic datasets from fungi belonging to the subphylum Pezizomycotina. -
Multipartite Viruses: Organization, Emergence and Evolution
UNIVERSIDAD AUTÓNOMA DE MADRID FACULTAD DE CIENCIAS DEPARTAMENTO DE BIOLOGÍA MOLECULAR MULTIPARTITE VIRUSES: ORGANIZATION, EMERGENCE AND EVOLUTION TESIS DOCTORAL Adriana Lucía Sanz García Madrid, 2019 MULTIPARTITE VIRUSES Organization, emergence and evolution TESIS DOCTORAL Memoria presentada por Adriana Luc´ıa Sanz Garc´ıa Licenciada en Bioqu´ımica por la Universidad Autonoma´ de Madrid Supervisada por Dra. Susanna Manrubia Cuevas Centro Nacional de Biotecnolog´ıa (CSIC) Memoria presentada para optar al grado de Doctor en Biociencias Moleculares Facultad de Ciencias Departamento de Biolog´ıa Molecular Universidad Autonoma´ de Madrid Madrid, 2019 Tesis doctoral Multipartite viruses: Organization, emergence and evolution, 2019, Madrid, Espana. Memoria presentada por Adriana Luc´ıa-Sanz, licenciada en Bioqumica´ y con un master´ en Biof´ısica en la Universidad Autonoma´ de Madrid para optar al grado de doctor en Biociencias Moleculares del departamento de Biolog´ıa Molecular en la facultad de Ciencias de la Universidad Autonoma´ de Madrid Supervisora de tesis: Dr. Susanna Manrubia Cuevas. Investigadora Cient´ıfica en el Centro Nacional de Biotecnolog´ıa (CSIC), C/ Darwin 3, 28049 Madrid, Espana. to the reader CONTENTS Acknowledgments xi Resumen xiii Abstract xv Introduction xvii I.1 What is a virus? xvii I.2 What is a multipartite virus? xix I.3 The multipartite lifecycle xx I.4 Overview of this thesis xxv PART I OBJECTIVES PART II METHODOLOGY 0.5 Database management for constructing the multipartite and segmented datasets 3 0.6 Analytical -
Informative Regions in Viral Genomes
viruses Article Informative Regions In Viral Genomes Jaime Leonardo Moreno-Gallego 1,2 and Alejandro Reyes 2,3,* 1 Department of Microbiome Science, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany; [email protected] 2 Max Planck Tandem Group in Computational Biology, Department of Biological Sciences, Universidad de los Andes, Bogotá 111711, Colombia 3 The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, Saint Louis, MO 63108, USA * Correspondence: [email protected] Abstract: Viruses, far from being just parasites affecting hosts’ fitness, are major players in any microbial ecosystem. In spite of their broad abundance, viruses, in particular bacteriophages, remain largely unknown since only about 20% of sequences obtained from viral community DNA surveys could be annotated by comparison with public databases. In order to shed some light into this genetic dark matter we expanded the search of orthologous groups as potential markers to viral taxonomy from bacteriophages and included eukaryotic viruses, establishing a set of 31,150 ViPhOGs (Eukaryotic Viruses and Phages Orthologous Groups). To do this, we examine the non-redundant viral diversity stored in public databases, predict proteins in genomes lacking such information, and used all annotated and predicted proteins to identify potential protein domains. The clustering of domains and unannotated regions into orthologous groups was done using cogSoft. Finally, we employed a random forest implementation to classify genomes into their taxonomy and found that the presence or absence of ViPhOGs is significantly associated with their taxonomy. Furthermore, we established a set of 1457 ViPhOGs that given their importance for the classification could be considered as markers or signatures for the different taxonomic groups defined by the ICTV at the Citation: Moreno-Gallego, J.L.; order, family, and genus levels. -
Origins and Evolution of the Global RNA Virome Yuri Wolf, Darius Kazlauskas, Jaime Iranzo, Adriana Lucía-Sanz, Jens Kuhn, Mart Krupovic, Valerian Dolja, Eugene Koonin
Origins and Evolution of the Global RNA Virome Yuri Wolf, Darius Kazlauskas, Jaime Iranzo, Adriana Lucía-Sanz, Jens Kuhn, Mart Krupovic, Valerian Dolja, Eugene Koonin To cite this version: Yuri Wolf, Darius Kazlauskas, Jaime Iranzo, Adriana Lucía-Sanz, Jens Kuhn, et al.. Origins and Evo- lution of the Global RNA Virome. mBio, American Society for Microbiology, 2018, 9 (6), pp.e02329-18. 10.1128/mBio.02329-18. pasteur-01977324 HAL Id: pasteur-01977324 https://hal-pasteur.archives-ouvertes.fr/pasteur-01977324 Submitted on 10 Jan 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Copyright RESEARCH ARTICLE Ecological and Evolutionary Science crossm Origins and Evolution of the Global RNA Virome Yuri I. Wolf,a Darius Kazlauskas,b,c Jaime Iranzo,a Adriana Lucía-Sanz,a,d Jens H. Kuhn,e Mart Krupovic,c Valerian V. Dolja,f Eugene V. Koonina aNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Downloaded from Bethesda, Maryland, USA bInstitute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius, Lithuania cDépartement de Microbiologie, Institut Pasteur, Paris, France dCentro Nacional de Biotecnología, Madrid, Spain eIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, Maryland, USA fDepartment of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, USA http://mbio.asm.org/ ABSTRACT Viruses with RNA genomes dominate the eukaryotic virome, reaching enormous diversity in animals and plants. -
Effects of Plant Viruses on Vectors and Non-Vector Herbivores in Three
Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School March 2019 Effects of Plant Viruses on Vectors and Non-vector Herbivores in Three Different Pathosystems Sunil Paudel Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Part of the Entomology Commons Recommended Citation Paudel, Sunil, "Effects of Plant Viruses on Vectors and Non-vector Herbivores in Three Different Pathosystems" (2019). LSU Doctoral Dissertations. 4870. https://digitalcommons.lsu.edu/gradschool_dissertations/4870 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Doctoral Dissertations by an authorized graduate school editor of LSU Digital Commons. For more information, please [email protected]. EFFECTS OF PLANT VIRUSES ON VECTORS AND NON-VECTOR HERBIVORES IN THREE DIFFERENT PATHOSYSTEMS A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Entomology by Sunil Paudel B. S., Tribhuvan University, 2008 M.S., University of Idaho, 2013 May 2019 ACKNOWLEDGEMENTS I would like to express my sincere gratitude to my major advisor, Dr. Jeffrey A. Davis for his continuous support throughout my graduate studies, for his patience, encouragement, and guidance that helped me to grow as a researcher and a critical thinker. I am also thankful to my dissertation committee members, Drs. Michael J. Stout, Fangneng Huang, Jeffrey W. Hoy, and Dean’s representative Dr. -
Deep Roots and Splendid Boughs of the Global Plant Virome
PY58CH11_Dolja ARjats.cls May 19, 2020 7:55 Annual Review of Phytopathology Deep Roots and Splendid Boughs of the Global Plant Virome Valerian V. Dolja,1 Mart Krupovic,2 and Eugene V. Koonin3 1Department of Botany and Plant Pathology and Center for Genome Research and Biocomputing, Oregon State University, Corvallis, Oregon 97331-2902, USA; email: [email protected] 2Archaeal Virology Unit, Department of Microbiology, Institut Pasteur, 75015 Paris, France 3National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20894, USA Annu. Rev. Phytopathol. 2020. 58:11.1–11.31 Keywords The Annual Review of Phytopathology is online at plant virus, virus evolution, virus taxonomy, phylogeny, virome phyto.annualreviews.org https://doi.org/10.1146/annurev-phyto-030320- Abstract 041346 Land plants host a vast and diverse virome that is dominated by RNA viruses, Copyright © 2020 by Annual Reviews. with major additional contributions from reverse-transcribing and single- All rights reserved stranded (ss) DNA viruses. Here, we introduce the recently adopted com- prehensive taxonomy of viruses based on phylogenomic analyses, as applied to the plant virome. We further trace the evolutionary ancestry of distinct plant virus lineages to primordial genetic mobile elements. We discuss the growing evidence of the pivotal role of horizontal virus transfer from in- vertebrates to plants during the terrestrialization of these organisms, which was enabled by the evolution of close ecological associations between these diverse organisms. It is our hope that the emerging big picture of the forma- tion and global architecture of the plant virome will be of broad interest to plant biologists and virologists alike and will stimulate ever deeper inquiry into the fascinating field of virus–plant coevolution. -
High-Throughput Sequencing for Deciphering the Virome of Alfalfa (Medicago Sativa L.)
fmicb-11-553109 September 10, 2020 Time: 19:38 # 1 REVIEW published: 11 September 2020 doi: 10.3389/fmicb.2020.553109 High-Throughput Sequencing for Deciphering the Virome of Alfalfa (Medicago sativa L.) Nicolas Bejerman1, Philippe Roumagnac2,3 and Lev G. Nemchinov4* 1 IPAVE-CIAP-INTA and UFyMA-INTA-CONICET, Córdoba, Argentina, 2 CIRAD, BGPI, Montpellier, France, 3 BGPI, INRAE, CIRAD, Institut Agro, Université Montpellier, Montpellier, France, 4 Molecular Plant Pathology Laboratory, USDA-ARS-BARC, Beltsville, MD, United States Alfalfa (Medicago sativa L.), also known as lucerne, is a major forage crop worldwide. In the United States, it has recently become the third most valuable field crop, with an estimated value of over $9.3 billion. Alfalfa is naturally infected by many different pathogens, including viruses, obligate parasites that reproduce only inside living host cells. Traditionally, viral infections of alfalfa have been considered by breeders, growers, producers and researchers to be diseases of limited importance, although they are widespread in all major cultivation areas. However, over the past Edited by: Henryk Hanokh Czosnek, few years, due to the rapid development of high-throughput sequencing (HTS), viral The Hebrew University of Jerusalem, metagenomics, bioinformatics tools for interpreting massive amounts of HTS data and Israel the increasing accessibility of public data repositories for transcriptomic discoveries, Reviewed by: Xiao-Wei Wang, several emerging viruses of alfalfa with the potential to cause serious yield losses have Zhejiang University, China been described. They include alfalfa leaf curl virus (family Geminiviridae), alfalfa dwarf Elvira Fiallo-Olivé, virus (family Rhabdoviridae), alfalfa enamovirus 1 (family Luteoviridae), alfalfa virus S Institute for Mediterranean and Subtropical Horticulture La (family Alphaflexiviridae) and others.