Virus, Viroids and Mycoplasma
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The Variability of Hop Latent Viroid As Induced Upon Heat Treatment
Virology 287, 349–358 (2001) doi:10.1006/viro.2001.1044, available online at http://www.idealibrary.com on View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector The Variability of Hop Latent Viroid as Induced upon Heat Treatment Jaroslav Matousˇek,* Josef Patzak,† Lidmila Orctova´,* Jo¨rg Schubert,‡ Luka´sˇ Vrba,* Gerhard Steger,§ and Detlev Riesner§,1 *Department of Molecular Genetics, Institute of Plant Molecular Biology Czech Academy of Sciences, Branisˇovska´31, 37005 Cˇ eske´Bude˘jovice, Czech Republic; †Department of Virology, Institute of Hop Research and Breeding, Kadanˇska´2525, 438 46 Zˇatec, Czech Republic; ‡Federal Centre for Breeding Research, Institute for Resistance Research and Pathogen Diagnostics, Theodor-Roemer-Weg 4, 06449 Aschersleben, Germany; and §Institute of Physical Biology, Heinrich-Heine Universita¨t Du¨sseldorf, Universita¨tsstraße 1, D-40225 Du¨sseldorf, Germany Received March 28, 2001; returned to author for revision March 30, 2001; accepted June 11, 2001; published online August 2, 2001 We have previously shown that heat treatment of hop plants infected by hop latent viroid (HLVd) reduces viroid levels. Here we investigate whether such heat treatment leads to the accumulation of sequence variability in HLVd. We observed a negligible level of mutated variants in HLVd under standard cultivation conditions. In contrast, the heat treatment of hop led to HLVd degradation and, simultaneously, to a significant increase in sequence variations, as judged from temperature gradient–gel electrophoresis analysis and cDNA library screening by DNA heteroduplex analysis. Thirty-one cDNA clones (9.8%) were identified as deviating forms. -
Hammerhead Ribozymes Against Virus and Viroid Rnas
Hammerhead Ribozymes Against Virus and Viroid RNAs Alberto Carbonell, Ricardo Flores, and Selma Gago Contents 1 A Historical Overview: Hammerhead Ribozymes in Their Natural Context ................................................................... 412 2 Manipulating Cis-Acting Hammerheads to Act in Trans ................................. 414 3 A Critical Issue: Colocalization of Ribozyme and Substrate . .. .. ... .. .. .. .. .. ... .. .. .. .. 416 4 An Unanticipated Participant: Interactions Between Peripheral Loops of Natural Hammerheads Greatly Increase Their Self-Cleavage Activity ........................... 417 5 A New Generation of Trans-Acting Hammerheads Operating In Vitro and In Vivo at Physiological Concentrations of Magnesium . ...... 419 6 Trans-Cleavage In Vitro of Short RNA Substrates by Discontinuous and Extended Hammerheads ........................................... 420 7 Trans-Cleavage In Vitro of a Highly Structured RNA by Discontinuous and Extended Hammerheads ........................................... 421 8 Trans-Cleavage In Vivo of a Viroid RNA by an Extended PLMVd-Derived Hammerhead ........................................... 422 9 Concluding Remarks and Outlooks ........................................................ 424 References ....................................................................................... 425 Abstract The hammerhead ribozyme, a small catalytic motif that promotes self- cleavage of the RNAs in which it is found naturally embedded, can be manipulated to recognize and cleave specifically -
Virus World As an Evolutionary Network of Viruses and Capsidless Selfish Elements
Virus World as an Evolutionary Network of Viruses and Capsidless Selfish Elements Koonin, E. V., & Dolja, V. V. (2014). Virus World as an Evolutionary Network of Viruses and Capsidless Selfish Elements. Microbiology and Molecular Biology Reviews, 78(2), 278-303. doi:10.1128/MMBR.00049-13 10.1128/MMBR.00049-13 American Society for Microbiology Version of Record http://cdss.library.oregonstate.edu/sa-termsofuse Virus World as an Evolutionary Network of Viruses and Capsidless Selfish Elements Eugene V. Koonin,a Valerian V. Doljab National Center for Biotechnology Information, National Library of Medicine, Bethesda, Maryland, USAa; Department of Botany and Plant Pathology and Center for Genome Research and Biocomputing, Oregon State University, Corvallis, Oregon, USAb Downloaded from SUMMARY ..................................................................................................................................................278 INTRODUCTION ............................................................................................................................................278 PREVALENCE OF REPLICATION SYSTEM COMPONENTS COMPARED TO CAPSID PROTEINS AMONG VIRUS HALLMARK GENES.......................279 CLASSIFICATION OF VIRUSES BY REPLICATION-EXPRESSION STRATEGY: TYPICAL VIRUSES AND CAPSIDLESS FORMS ................................279 EVOLUTIONARY RELATIONSHIPS BETWEEN VIRUSES AND CAPSIDLESS VIRUS-LIKE GENETIC ELEMENTS ..............................................280 Capsidless Derivatives of Positive-Strand RNA Viruses....................................................................................................280 -
Impact of Nucleic Acid Sequencing on Viroid Biology
International Journal of Molecular Sciences Review Impact of Nucleic Acid Sequencing on Viroid Biology Charith Raj Adkar-Purushothama * and Jean-Pierre Perreault * RNA Group/Groupe ARN, Département de Biochimie, Faculté de médecine des sciences de la santé, Pavillon de Recherche Appliquée au Cancer, Université de Sherbrooke, 3201 rue Jean Mignault, Sherbrooke, QC J1E 4K8, Canada * Correspondence: [email protected] (C.R.A.-P.); [email protected] (J.-P.P.) Received: 5 July 2020; Accepted: 30 July 2020; Published: 1 August 2020 Abstract: The early 1970s marked two breakthroughs in the field of biology: (i) The development of nucleotide sequencing technology; and, (ii) the discovery of the viroids. The first DNA sequences were obtained by two-dimensional chromatography which was later replaced by sequencing using electrophoresis technique. The subsequent development of fluorescence-based sequencing method which made DNA sequencing not only easier, but many orders of magnitude faster. The knowledge of DNA sequences has become an indispensable tool for both basic and applied research. It has shed light biology of viroids, the highly structured, circular, single-stranded non-coding RNA molecules that infect numerous economically important plants. Our understanding of viroid molecular biology and biochemistry has been intimately associated with the evolution of nucleic acid sequencing technologies. With the development of the next-generation sequence method, viroid research exponentially progressed, notably in the areas of the molecular mechanisms of viroids and viroid diseases, viroid pathogenesis, viroid quasi-species, viroid adaptability, and viroid–host interactions, to name a few examples. In this review, the progress in the understanding of viroid biology in conjunction with the improvements in nucleotide sequencing technology is summarized. -
Introduction to Viroids and Prions
Harriet Wilson, Lecture Notes Bio. Sci. 4 - Microbiology Sierra College Introduction to Viroids and Prions Viroids – Viroids are plant pathogens made up of short, circular, single-stranded RNA molecules (usually around 246-375 bases in length) that are not surrounded by a protein coat. They have internal base-pairs that cause the formation of folded, three-dimensional, rod-like shapes. Viroids apparently do not code for any polypeptides (proteins), but do cause a variety of disease symptoms in plants. The mechanism for viroid replication is not thoroughly understood, but is apparently dependent on plant enzymes. Some evidence suggests they are related to introns, and that they may also infect animals. Disease processes may involve RNA-interference or activities similar to those involving mi-RNA. Prions – Prions are proteinaceous infectious particles, associated with a number of disease conditions such as Scrapie in sheep, Bovine Spongiform Encephalopathy (BSE) or Mad Cow Disease in cattle, Chronic Wasting Disease (CWD) in wild ungulates such as muledeer and elk, and diseases in humans including Creutzfeld-Jacob disease (CJD), Gerstmann-Straussler-Scheinker syndrome (GSS), Alpers syndrome (in infants), Fatal Familial Insomnia (FFI) and Kuru. These diseases are characterized by loss of motor control, dementia, paralysis, wasting and eventually death. Prions can be transmitted through ingestion, tissue transplantation, and through the use of comtaminated surgical instruments, but can also be transmitted from one generation to the next genetically. This is because prion proteins are encoded by genes normally existing within the brain cells of various animals. Disease is caused by the conversion of normal cell proteins (glycoproteins) into prion proteins. -
Potato Spindle Tuber Viroid
This diagnostic protocol was adopted by the Standards Committee on behalf of the Commission on Phytosanitary Measures in January 2015. The annex is a prescriptive part of ISPM 27. ISPM 27 Annex 7 INTERNATIONAL STANDARDS FOR PHYTOSANITARY MEASURES ISPM 27 DIAGNOSTIC PROTOCOLS DP 7: Potato spindle tuber viroid (2015) Contents 1. Pest Information ............................................................................................................................... 3 2. Taxonomic Information .................................................................................................................... 4 3. Detection ........................................................................................................................................... 4 3.1 Sampling ........................................................................................................................... 6 3.2 Biological detection .......................................................................................................... 6 3.3 Molecular detection ........................................................................................................... 7 3.3.1 Sample preparation ............................................................................................................ 7 3.3.2 Nucleic acid extraction ...................................................................................................... 8 3.3.3 Generic molecular methods for pospiviroid detection ..................................................... -
The Simple Emergence of Complex Molecular Function
The simple emergence of complex molecular function Susanna Manrubia Department of Systems Biology, National Centre for Biotechnology (CSIC). c/ Darwin 3, 28049 Madrid, Spain Interdisciplinary Group of Complex Systems (GISC), Madrid, Spain (Dated: May 26, 2021) At odds with a traditional view of molecular evolution that seeks a descent-with-modification relationship between functional sequences, new functions can emerge de novo with relative ease. At early times of molecular evolution, random polymers could have sufficed for the appearance of incipi- ent chemical activity, while the cellular environment harbors a myriad of proto-functional molecules. The emergence of function is facilitated by several mechanisms intrinsic to molecular organization, such as redundant mapping of sequences into structures, phenotypic plasticity, modularity, or co- operative associations between genomic sequences. It is the availability of niches in the molecular ecology that filters new potentially functional proposals. New phenotypes and subsequent levels of molecular complexity could be attained through combinatorial explorations of currently available molecular variants. Natural selection does the rest. I. INTRODUCTION ble genotypes coding for comparable phenotypes [20, 21]. Further, function is flexible, so phenotypes admit a range Half a century ago, the idea that gene specificity could of variation, and phenotypes are plastic, so their ex- rely on a unique protein sequence raised concerns regard- pression adapts to different environments [22, 23]. Be- ing the come into being of functional genes. Natural se- yond multiple inconsequential variations in genotypes, lection would be ineffective if the raw material on which also changes in molecular structure or composition might it had to act were random sequences, given that a myriad be irrelevant for the functionality of a phenotype. -
Autonomously Replicating RNA in Mitochondria of Maize Plants with S
Proc. Natl. Acad. Sci. USA Vol. 83, pp. 5175-5179, July 1986 Genetics Autonomously replicating RNA in mitochondria of maize plants with S-type cytoplasm (cytoplasmnic male sterility/genetic RNA/RNA plasmids/double-stranded RNA/in organello RNA synthesis) PATRICK M. FINNEGAN AND GREGORY G. BROWN Centre for Plant Molecular Biology, Department of Biology, McGill University, Montreal, PQ, Canada H3A iB1 Communicated by Hewson Swift, March 17, 1986 ABSTRACT Mitochondria isolated from maize plants with in organello RNA synthesis system to search for differences S-type male-sterile cytoplasms are capable of synthesizing four in mitochondrial gene expression among the various maize species of RNA at concentrations of actinomycin D that cytoplasmic types. We have made the surprising discovery eliminate all DNA-directed RNA synthesis. No RNA synthesis that several R$As unique to the S cytoplasm are synthesized occurs under the same conditions with mitochondria from in a DNA-independent manner. Our observations indicate plants possessing normal (N) cytoplasm or with other that these RNAs represent an RNA-based genetic system subcellular fractions from plants with S cytoplasm. The that is endogenous to the mitochondnron. No other such actinomycin D-resistant RNA synthesis occurs within the system has been found in an organelle. Because these RNAs mitochondria since the labeling ofthese species is unaffected by replicate independently of cellular chromosomes, we have inclusion of RNase in the incubation medium and since they termed them RNA plasmids. become completely sensitive to RNase upon lysis of the mitochondria with low concentrations of Triton'X-100. Two of the actinomycin D-resistant products are double stranded. -
Temporal Dynamics of Uncultured Viruses: a New Dimension in Viral Diversity
The ISME Journal (2018) 12, 199–211 © 2018 International Society for Microbial Ecology All rights reserved 1751-7362/18 www.nature.com/ismej ORIGINAL ARTICLE Temporal dynamics of uncultured viruses: a new dimension in viral diversity Ksenia Arkhipova1,2, Timofey Skvortsov1,3, John P Quinn1, John W McGrath1,3, Christopher CR Allen1,3, Bas E Dutilh2,4, Yvonne McElarney5 and Leonid A Kulakov1 1School of Biological Sciences, The Queen’s University of Belfast, Belfast, UK; 2Theoretical Biology and Bioinformatics, Utrecht University, Utrecht, The Netherlands; 3Institute for Global Food Security, The Queen’s University of Belfast, Belfast, UK; 4Centre for Molecular and Biomolecular Informatics, Radboud University Medical Centre, Nijmegen, The Netherlands and 5Agri-Food and Biosciences Institute, Belfast, UK Recent work has vastly expanded the known viral genomic sequence space, but the seasonal dynamics of viral populations at the genome level remain unexplored. Here we followed the viral community in a freshwater lake for 1 year using genome-resolved viral metagenomics, combined with detailed analyses of the viral community structure, associated bacterial populations and environ- mental variables. We reconstructed 8950 complete and partial viral genomes, the majority of which were not persistent in the lake throughout the year, but instead continuously succeeded each other. Temporal analysis of 732 viral genus-level clusters demonstrated that one-fifth were undetectable at specific periods of the year. Based on host predictions for a subset of reconstructed viral genomes, we for the first time reveal three distinct patterns of host–pathogen dynamics, where the viruses may peak before, during or after the peak in their host’s abundance, providing new possibilities for modelling of their interactions. -
Participation of Multifunctional RNA in Replication, Recombination and Regulation of Endogenous Plant Pararetroviruses (Eprvs)
fpls-12-689307 June 18, 2021 Time: 16:5 # 1 MINI REVIEW published: 21 June 2021 doi: 10.3389/fpls.2021.689307 Participation of Multifunctional RNA in Replication, Recombination and Regulation of Endogenous Plant Pararetroviruses (EPRVs) Katja R. Richert-Pöggeler1*, Kitty Vijverberg2,3, Osamah Alisawi4, Gilbert N. Chofong1, J. S. (Pat) Heslop-Harrison5,6 and Trude Schwarzacher5,6 1 Julius Kühn-Institut, Federal Research Centre for Cultivated Plants, Institute for Epidemiology and Pathogen Diagnostics, Braunschweig, Germany, 2 Naturalis Biodiversity Center, Evolutionary Ecology Group, Leiden, Netherlands, 3 Radboud University, Institute for Water and Wetland Research (IWWR), Nijmegen, Netherlands, 4 Department of Plant Protection, Faculty of Agriculture, University of Kufa, Najaf, Iraq, 5 Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom, 6 Key Laboratory of Plant Resources Conservation and Sustainable Utilization, Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China Edited by: Jens Staal, Pararetroviruses, taxon Caulimoviridae, are typical of retroelements with reverse Ghent University, Belgium transcriptase and share a common origin with retroviruses and LTR retrotransposons, Reviewed by: Jie Cui, presumably dating back 1.6 billion years and illustrating the transition from an RNA Institut Pasteur of Shanghai (CAS), to a DNA world. After transcription of the viral genome in the host nucleus, viral DNA China Marco Catoni, synthesis occurs in the cytoplasm on the generated terminally redundant RNA including University of Birmingham, inter- and intra-molecule recombination steps rather than relying on nuclear DNA United Kingdom replication. RNA recombination events between an ancestral genomic retroelement with *Correspondence: exogenous RNA viruses were seminal in pararetrovirus evolution resulting in horizontal Katja R. -
In Vivo Generated Citrus Exocortis Viroid Progeny Variants Display a Range of Phenotypes with Altered Levels of Replication, Systemic Accumulation and Pathogenicity
CORE Metadata, citation and similar papers at core.ac.uk Provided by Elsevier - Publisher Connector Virology 417 (2011) 400–409 Contents lists available at ScienceDirect Virology journal homepage: www.elsevier.com/locate/yviro In vivo generated Citrus exocortis viroid progeny variants display a range of phenotypes with altered levels of replication, systemic accumulation and pathogenicity Subhas Hajeri a,1, Chandrika Ramadugu b, Keremane Manjunath c, James Ng a, Richard Lee c, Georgios Vidalakis a,⁎ a Department of Plant Pathology and Microbiology, University of California, Riverside CA 92521, USA b Department of Botany and Plant Sciences, University of California, Riverside CA 92521, USA c USDA ARS National Clonal Germplasm Repository for Citrus and Dates, Riverside, CA 92507, USA article info abstract Article history: Citrus exocortis viroid (CEVd) exists as populations of heterogeneous variants in infected hosts. In vivo Received 26 January 2011 generated CEVd progeny variants (CEVd-PVs) populations from citrus protoplasts, seedlings and mature Accepted 13 June 2011 plants, following inoculation with transcripts of a single CEVd cDNA-clone (wild-type, WT), were studied. The Available online 22 July 2011 CEVd-PVs population in protoplasts was heterogeneous and became progressively more homogeneous in seedlings and mature plants. The infectivity and pathogenicity of selected CEVd-PVs was evaluated in citrus Keywords: Viroid RNA evolution and herbaceous experimental hosts. The CEVd-PVs U30C, G128A and U182C were not infectious; G50A and Population composition 108U+ were infectious but reverted back to WT and 62A+, U129A and U278A were infectious, genetically Genomic diversity stable and more severe than WT. The 62A+ and U278A and U129A accumulated at higher levels than WT in Infectivity protoplasts and seedlings respectively. -
Parsimonious Scenario for the Emergence of Viroid-Like Replicons De Novo
bioRxiv preprint doi: https://doi.org/10.1101/593640; this version posted March 30, 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. Article Parsimonious scenario for the emergence of viroid-like replicons de novo Pablo Catalán 1,2 , Santiago F. Elena 3,4 , José A. Cuesta 2,5,6,7 and Susanna Manrubia 2,8* 1 Biosciences, College of Life and Environmental Sciences, University of Exeter, Exeter EX4 4QD, UK; [email protected] 2 Grupo Interdisciplinar de Sistemas Complejos (GISC), Madrid, Spain 3 Instituto de Biología Integrativa de Sistemas (I2SysBio), CSIC-Universitat de València, Paterna, 46980 València, Spain; [email protected] 4 The Santa Fe Institute, Santa Fe NM 87501, USA 5 Departamento de Matemáticas, Universidad Carlos III de Madrid, Leganés, Spain; [email protected] 6 Instituto de Biocomputación y Física de Sistemas Complejos (BiFi), Universidad de Zaragoza, Spain 7 Institute of Financial Big Data (IFiBiD), Universidad Carlos III de Madrid–Banco de Santander, Getafe, Spain 8 National Biotechnology Centre (CSIC), Madrid, Spain * Correspondence: [email protected]; Tel.: +34-91-585-4618 Version March 29, 2019 submitted to Viruses 1 Abstract: Viroids are small, non-coding, circular RNA molecules that infect plants. Different 2 hypotheses for their evolutionary origin have been put forward, such as an early emergence in a 3 precellular RNA World or several de novo independent evolutionary origins in plants. Here we discuss 4 the plausibility of de novo emergence of viroid-like replicons by giving theoretical support to the 5 likelihood of different steps along a parsimonious evolutionary pathway.