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Changes to Virus Taxonomy 2004
Arch Virol (2005) 150: 189–198 DOI 10.1007/s00705-004-0429-1 Changes to virus taxonomy 2004 M. A. Mayo (ICTV Secretary) Scottish Crop Research Institute, Invergowrie, Dundee, U.K. Received July 30, 2004; accepted September 25, 2004 Published online November 10, 2004 c Springer-Verlag 2004 This note presents a compilation of recent changes to virus taxonomy decided by voting by the ICTV membership following recommendations from the ICTV Executive Committee. The changes are presented in the Table as decisions promoted by the Subcommittees of the EC and are grouped according to the major hosts of the viruses involved. These new taxa will be presented in more detail in the 8th ICTV Report scheduled to be published near the end of 2004 (Fauquet et al., 2004). Fauquet, C.M., Mayo, M.A., Maniloff, J., Desselberger, U., and Ball, L.A. (eds) (2004). Virus Taxonomy, VIIIth Report of the ICTV. Elsevier/Academic Press, London, pp. 1258. Recent changes to virus taxonomy Viruses of vertebrates Family Arenaviridae • Designate Cupixi virus as a species in the genus Arenavirus • Designate Bear Canyon virus as a species in the genus Arenavirus • Designate Allpahuayo virus as a species in the genus Arenavirus Family Birnaviridae • Assign Blotched snakehead virus as an unassigned species in family Birnaviridae Family Circoviridae • Create a new genus (Anellovirus) with Torque teno virus as type species Family Coronaviridae • Recognize a new species Severe acute respiratory syndrome coronavirus in the genus Coro- navirus, family Coronaviridae, order Nidovirales -
Aphid-Transmitted Viruses in Vegetable Crops Department of Departmentof Integrated Virus Disease Management
Agri-Science Queensland Employment, Economic Development and Innovation and Development Economic Employment, Aphid-transmitted viruses in vegetable crops Department of Departmentof Integrated virus disease management The majority of viruses infecting plants are spread by Non-persistent transmission insects, and aphids are the most common group of • It takes less than one minute of feeding for an virus vectors or carriers. All potyviruses (the largest aphid to acquire the virus and the same short time group of plant viruses) are transmitted by aphids. to infect another plant when feeding. Aphids are sap-sucking insects and have piercing, • Viruses remain viable on aphids mouthparts for a sucking mouthparts. Their mouthparts include a few hours only. needle-like stylet that allows the aphid to access • When an aphid loses the virus from its mouthparts and feed on the contents of plant cells. During when feeding it has to feed again on another feeding, aphids simultaneously ingest sap contents infected plant to obtain a new ‘charge’ of virus and inject saliva, which can contain viruses if the before it can infect other plants. aphid has previously fed on an infected plant. Persistent transmission The structure of aphid mouthparts, their searching • It takes several hours of feeding for an aphid to behaviour for host plants, the range of available acquire a virus. host plants and high reproductive rates contribute to • The virus must circulate through the aphid’s body the efficiency of aphids to act as virus carriers. to the salivary glands before transmission can Aphid transmission occur. This period is at least 12 hours. -
P. Lava Kumar, A. T. Jones and F. Waliyar
Methods Manual Edited by P. Lava Kumar, A. T. Jones and F. Waliyar Virology and Mycotoxin Diagnostics Laboratory International Crops Research Institute for the Semi-Arid Tropics © International Crops Research Institute for the Semi-Arid Tropics, 2004 AUTHORS P. LAVA KUMAR Special Project Scientist – Virology Virology and Mycotoxin Diagnostics ICRISAT, Patancheru 502 324, India e-mail: [email protected] A. T. JONES Senior Principal Virologist Scottish Crop Research Institute (SCRI) Invergowrie Dundee DD2 5DA Scotland, United Kingdom e-mail: [email protected] FARID WALIYAR Principal Scientist and Global Theme Leader – Biotechnology ICRISAT, Patancheru 502 324, India e-mail: [email protected] Material from this manual may be reproduced for the research use providing the source is acknowledged as: KUMAR, P.L., JONES, A. T. and WALIYAR, F. (Eds) (2004). Serological and nucleic acid based methods for the detection of plant viruses. International Crops Research Institute for the Semi-Arid Tropics, Patancheru 502 324, India. FOR FURTHER INFORMATION: International Crops Research Institute for the Semi-Arid Tropics (ICRISAT) Patancheru - 502 324, Andhra Pradesh, India Telephone: +91 (0) 40 23296161 Fax: +91 (0) 40 23241239 +91 (0) 40 23296182 Web site: http://www.icrisat.org Cover photo: Purified particles of PoLV-PP (©Kumar et al., 2001) This publication is an output from the United Kingdom Department for International Development (DFID) Crop Protection Programme for the benefit of developing countries. Views expressed are not necessarily those of DFID. Manual designed by P Lava Kumar Serological and Nucleic Acid Based Methods for the Detection of Plant Viruses Edited by P. -
Plant Pathology Circular No. 261 Fla. Dept. Agric. & Consumer Serv. July 1984 Division of Plant Industry PEANUT STRIPE VIRUS
Plant Pathology Circular No. 261 Fla. Dept. Agric. & Consumer Serv. July 1984 Division of Plant Industry PEANUT STRIPE VIRUS C. L. Schoultiesl During the 1982 peanut growing season, virus symptoms previously unknown to the United States were observed in new peanut germplasm obtained from the People's Republic of China (3). This germplasm was under observation at the regional plant introduction station at the University of Georgia at Experiment. J. W. Demski (2) identified this virus as peanut stripe virus (PStV), which may be synonymous with a virus described recently from the People's Republic of China (5). In 1983, surveys of some commercial fields and many experimental peanut plantings of universities from Texas to Virginia and Florida indicated that the virus problem was predominantly limited to breeding plots (4). In early 1984, at least 40 seed lots from the Florida peanut breeding programs at Marianna and Gainesville and a limited number from foundation seed lots were indexed by J. W. Demski in Georgia (4). Four of the 40 lots were positive for PStV and were not planted this year. The virus was not detected in foundation seed, however. Concurrent with seed indexing, infected peanut plants from Georgia were received in the quarantine greenhouse at the Florida Division of Plant Industry. D. E. Purcifull of the Institute of Food and Agricultural Sciences (IFAS), University of Florida, inoculated healthy peanuts with the virus. The virus was isolated and purified, and antiserum to the purified virus was produced (D. E. Purcifull and E. Hiebert, personal communication). During June 1984, PStV-infected plants were found in IFAS experimental plantings in Gainesville and Marianna. -
RNA-Based Technologies for Engineering Plant Virus Resistance
plants Review RNA-Based Technologies for Engineering Plant Virus Resistance Michael Taliansky 1,2,*, Viktoria Samarskaya 1, Sergey K. Zavriev 1 , Igor Fesenko 1 , Natalia O. Kalinina 1,3 and Andrew J. Love 2,* 1 Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, 117997 Moscow, Russia; [email protected] (V.S.); [email protected] (S.K.Z.); [email protected] (I.F.); [email protected] (N.O.K.) 2 The James Hutton Institute, Invergowrie, Dundee DD2 5DA, UK 3 Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Leninskie Gory, 119991 Moscow, Russia * Correspondence: [email protected] (M.T.); [email protected] (A.J.L.) Abstract: In recent years, non-coding RNAs (ncRNAs) have gained unprecedented attention as new and crucial players in the regulation of numerous cellular processes and disease responses. In this review, we describe how diverse ncRNAs, including both small RNAs and long ncRNAs, may be used to engineer resistance against plant viruses. We discuss how double-stranded RNAs and small RNAs, such as artificial microRNAs and trans-acting small interfering RNAs, either produced in transgenic plants or delivered exogenously to non-transgenic plants, may constitute powerful RNA interference (RNAi)-based technology that can be exploited to control plant viruses. Additionally, we describe how RNA guided CRISPR-CAS gene-editing systems have been deployed to inhibit plant virus infections, and we provide a comparative analysis of RNAi approaches and CRISPR-Cas technology. The two main strategies for engineering virus resistance are also discussed, including direct targeting of viral DNA or RNA, or inactivation of plant host susceptibility genes. -
Determining the Role of Seed and Soil in the Transmission Of
DETERMINING THE ROLE OF SEED AND SOIL IN THE TRANSMISSION OF VIRUSES CAUSING MAIZE LETHAL NECROSIS DISEASE By GATUNZI KITIRA FELIX (B.Sc. in Rural Development) A thesis submitted in partial fulfillment of requirements for the award of degree of Master of Science in Plant Pathology Department of Plant Science and Crop Protection Faculty of Agriculture University of Nairobi 2018 DECLARATION This thesis is a presentation of my original research work and has not been presented for a degree in any other University. Felix Gatunzi Kitira Date…................................................ This thesis has been submitted with our approval as University supervisors: Dr. Douglas Watuku Miano Department of Plant Science and Crop Protection University of Nairobi Signature ….…………………………. Date……………………………….. Prof. Daniel Mukunya Department of Plant Science and Crop Protection Signature ……………………………. Date……………………………….. Dr. Suresh Lingadahalli Mahabaleswara Global Maize Program (GMP), International Maize and Wheat Improvement Center CIMMYT Signature.…………………………………… Date……………………………… i PLAGIARISM DECLARATION I understand what plagiarism is and I am aware of the University’s policy. In this regard, I declare that this MSc Thesis is my original work. Where other people’s work or my own work has been used, it has properly been acknowledged and referenced in accordance with the University of Nairobi’s requirement. I have not allowed, and shall allow anyone to copy my work with the intention of passing it off as his or her own work. I understand that any false claim in respect of this work shall result in disciplinary action, in accordance with University Plagiarism Policy. Signature.................................................................Date.......................................................... ii DEDICATION To the almighty God for imparting me with his grace along this journey. -
Plant Pathology Circular No. 275 Fla. Dept. Agric. & Consumer Serv
Plant Pathology Circular No. 275 Fla. Dept. Agric. & Consumer Serv. September 1985 Division of Plant Industry LETTUCE MOSAIC VIRUS Gail C. Wislerl Lettuce mosaic virus (LMV) was first reported in 1921 in Florida by Jagger (6). Due to transmission of LMV through seed, it has now been reported in at least 14 countries (4) or wherever lettuce is commercially grown. Although specific leaf symptoms are difficult to detect in mature lettuce, the overall effect on lettuce production is significant in terms of stunting, the absence of heading, and early bolting. The 50-million dollar per year Florida lettuce industry was severely threatened during the early 1970's by an outbreak of LMV. Fortunately, the lettuce growers in California had already established a viable indexing program for control of LMV through years of observation, experimentation, and research. This program was designed to establish the minimum allowable percentage of infected seed in commercial seedlots. It had been demonstrated that even with 1-3% infected seed, the spread by aphids could lead to 100% infection by harvest time. Research has shown that seed infection greater than even 0.1% gives inadequate disease control (2). Therefore, the allowable tolerance under Florida law adopted in 1973 and by California at an earlier date is less than one infected seed in 30,000. If one seed in 30,000 is infected, the entire seedlot is rejected. SYMPTOMS: Symptoms of LMV are most easily detected in young plants. First seen is an inward rolling of the leaves along the long axis, and the first true leaf is irregularly shaped and slightly lobed. -
ICTV Code Assigned: 2011.001Ag Officers)
This form should be used for all taxonomic proposals. Please complete all those modules that are applicable (and then delete the unwanted sections). For guidance, see the notes written in blue and the separate document “Help with completing a taxonomic proposal” Please try to keep related proposals within a single document; you can copy the modules to create more than one genus within a new family, for example. MODULE 1: TITLE, AUTHORS, etc (to be completed by ICTV Code assigned: 2011.001aG officers) Short title: Change existing virus species names to non-Latinized binomials (e.g. 6 new species in the genus Zetavirus) Modules attached 1 2 3 4 5 (modules 1 and 9 are required) 6 7 8 9 Author(s) with e-mail address(es) of the proposer: Van Regenmortel Marc, [email protected] Burke Donald, [email protected] Calisher Charles, [email protected] Dietzgen Ralf, [email protected] Fauquet Claude, [email protected] Ghabrial Said, [email protected] Jahrling Peter, [email protected] Johnson Karl, [email protected] Holbrook Michael, [email protected] Horzinek Marian, [email protected] Keil Guenther, [email protected] Kuhn Jens, [email protected] Mahy Brian, [email protected] Martelli Giovanni, [email protected] Pringle Craig, [email protected] Rybicki Ed, [email protected] Skern Tim, [email protected] Tesh Robert, [email protected] Wahl-Jensen Victoria, [email protected] Walker Peter, [email protected] Weaver Scott, [email protected] List the ICTV study group(s) that have seen this proposal: A list of study groups and contacts is provided at http://www.ictvonline.org/subcommittees.asp . -
Characterization and Electron Microscopy of a Potyvirus Infecting Commelina Diffusa F
Etiology Characterization and Electron Microscopy of a Potyvirus Infecting Commelina diffusa F. J. Morales and F. W. Zettler Graduate Student and Professor, respectively, Department of Plant Pathology, University of Florida, Gainesville, FL 32611. The authors are grateful to Louise M. Russell, Entomologist, U.S. Department of Agriculture, Agricultural Research Service, Beltsville, Maryland, and to David Hall, Department of Botany, University of Florida, for the identification of the Aphis and Commelina species, respectively, used in this study. We also appreciate the assistance of T. A. Zitter, Univ. of Florida Agric. Res. and Educ. Center, Belle Glade, for assistance in making surveys in Palm Beach County. Journal Series Paper No. 6187 of the Florida Agricultural Experiment Station. Accepted for publication 11 January 1977. ABSTRACT MORALES, F. J. and F. W. ZETTLER. 1977. Characterization and eletron microscopy of a potyvirus infecting Commelina diffusa. Phytopathology 67: 839-843. A filamentous virus has been discovered that induces with ammonium molybdate. The dilution end-point of mosaic symptoms in Commelina diffusa distinguishable CoMV was 10-' to 10- , its longevity in vitro was 12-20 hr, from those caused by cucumber mosaic virus (CMV). This and the thermal inactivation point was 50-60 C. Leaf extracts virus, herein designated as commelina mosaic virus (CoMV), from CoMV-infected plants did not react in which appears to be a potyvirus, was readily transmitted immunodiffusion tests with antisera prepared to bidens mechanically to C. diffusa but not to 15 other species in nine mottle, blackeye cowpea mosaic, dasheen mosaic, lettuce plant families. Commelina mosaic virus was transmitted in a mosaic, pepper mottle, potato Y, tobacco etch, or turnip stylet-borne manner by Myzus persicaeand Aphis gossypii. -
Aphid Transmission of Potyvirus: the Largest Plant-Infecting RNA Virus Genus
Supplementary Aphid Transmission of Potyvirus: The Largest Plant-Infecting RNA Virus Genus Kiran R. Gadhave 1,2,*,†, Saurabh Gautam 3,†, David A. Rasmussen 2 and Rajagopalbabu Srinivasan 3 1 Department of Plant Pathology and Microbiology, University of California, Riverside, CA 92521, USA 2 Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC 27606, USA; [email protected] 3 Department of Entomology, University of Georgia, 1109 Experiment Street, Griffin, GA 30223, USA; [email protected] * Correspondence: [email protected]. † Authors contributed equally. Received: 13 May 2020; Accepted: 15 July 2020; Published: date Abstract: Potyviruses are the largest group of plant infecting RNA viruses that cause significant losses in a wide range of crops across the globe. The majority of viruses in the genus Potyvirus are transmitted by aphids in a non-persistent, non-circulative manner and have been extensively studied vis-à-vis their structure, taxonomy, evolution, diagnosis, transmission and molecular interactions with hosts. This comprehensive review exclusively discusses potyviruses and their transmission by aphid vectors, specifically in the light of several virus, aphid and plant factors, and how their interplay influences potyviral binding in aphids, aphid behavior and fitness, host plant biochemistry, virus epidemics, and transmission bottlenecks. We present the heatmap of the global distribution of potyvirus species, variation in the potyviral coat protein gene, and top aphid vectors of potyviruses. Lastly, we examine how the fundamental understanding of these multi-partite interactions through multi-omics approaches is already contributing to, and can have future implications for, devising effective and sustainable management strategies against aphid- transmitted potyviruses to global agriculture. -
Identification of Zinnia Leaf Curl Virus Infecting Zinnia Elegans in India
ISABB Journal of Biotechnology and Bioinformatics Vol. 2(1), pp. 6-10, April 2012 Available online at http://www.isabb.academicjournals.org/JBB DOI: 10.5897/ISAAB-JBB12.001 ISSN 1937-3244©2012 Academic Journals Full Length Research Paper Identification of Zinnia leaf curl virus infecting Zinnia elegans in India NAVEEN PANDAY1 and A. K. TIWARI2* 1Department of Botany, DDU University Gorakhpur, Uttar Pradesh, UP, -273008 India. 2Central Laboratory, U P Council of Sugarcane Research, Shahjahnapur-242001, Uttar Pradesh, India. Accepted 26 March, 2012 In a survey during 2007 to 2009 at Gorakhpur and nearby locations of North Eastern Uttar Pradesh, India leaf curling, foliar deformation and distortion symptoms were observed on Zinnia elegans plants. The associated White fly population indicated the possible presence of begomovirus in the field. Therefore, Polymerase chain reaction (PCR) was performed with the begomovirus specific primers (TLCV-CP). Total genomic DNA was isolated from infected as well as healthy leaf samples. In gel electrophoresis expected ~500 bp amplicons was obtained in symptomatic leaf sample while, no amplicon was found in healthy leaf samples. Amplicon obtained were directly sequenced and submitted in the GenBank (GQ412352) and phylogeny were constructed with the available identical sequences in the Genbank. Based on the highest similarity 97% at nucleotide and 99% at amino acid level and closest relationship with isolates of Zinnia leaf curl virus, the present study isolate was considered an isolate of Zinnia leaf curl virus. Key words: Zinnia elegans, Zinnia leaf curl virus, polymerase chain reaction (PCR), phylogenetic analysis. INTRODUCTION Zinnia is a common Mexican wildflower and members of reported virus on Zinnia (Storey, 1931). -
Quarantine Requirements for the Importation of Plants Or Plant Products Into the Republic of China
Quarantine Requirements for The Importation of Plants or Plant Products into The Republic of China Bureau of Animal and Plant Health Inspection and Quarantine Council of Agriculture Executive Yuan In case of any discrepancy between the Chinese text and the English translation thereof, the Chinese text shall govern. Individaual Quarantine Requirements please refer to BAPHIQ website(www.baphiq.gov.tw) Updated July 19, 2017 - 1 - Quarantine Requirements for The Importation of Plants or Plant Products into The Republic of China A. Prohibited Plants or Plant Products Pursuant to Paragraph 1, Article 14, Plant Protection and Quarantine Act 1. List of prohibited plants or plant products, countries or districts of origin and the reasons for prohibition: Plants or Plant Products Countries or Districts of Origin Reasons for Prohibition 1. Entire or any part of the All countries and districts 1. Rice hoja blanca virus following living plants (Tenuivirus) (excluding seeds): 2. Rice dwarf virus (1) Brachiaria spp. (Phytoreovirus) (2) Echinochloa spp. 3. Rice stem nematode (3) Leersia hexandra. (Ditylenchus angustus (4) Oryza spp Butler) (5) Panicum spp. (6) Rottboellia spp. (7) Paspalum spp. (8) Saccioleps interrupta (9) Triticum aestivum 2. Entire or any part of the Asia and Pacific Region West Indian sweet potato following living plants (1) Palau weevil (excluding seeds) (2) Mainland (Euscepes postfasciatus (1) Calystegia spp. (3) Cook Islands Fairmaire) (2) Dioscorea japonica (4) Federated States of Micronesia (3) Ipomoea spp. (5) Fiji (4) Pharbitis