Solutions for Plant Disease Diagnostics

Total Page:16

File Type:pdf, Size:1020Kb

Solutions for Plant Disease Diagnostics LOEWE® Solutions for Plant Disease Diagnostics Catalog 2017 Molecular Diagnostics Rapid Tests ELISA Products Immuno Fluorescence Dear Partners and Colleagues, we invite you to browse our new Catalog for Plant Disease Diagnostics for the year 2017. Although ELISA tests still constitute the majority of our products, our objective is to present to you a choice of high-quality diagnostic tools, that will satisfy your specific needs for pathogen testing. These tools include: • A range of more almost 150 ELISA antisera for the detection of plant viruses, bacteria, and fungi • PCR complete reaction kits and RNA PCR complete reaction kits for easy and convenient molecular detection of plant bacteria and RNA-Viruses • Antisera and supplements for Immuno Fluorescence assays • LOEWE®FAST rapid tests for fast and easy assessment of suspicious plant material Our focus remains on the expansion of our range of molecular diagnostic kits for PCR detection of bacteria, phytoplasms, fungi, and RNA-Viruses. Thanks to our busy R&D team, this product line now already encompasses close to 30 pathogens. NEW: As an additional service for you, we are now also providing kits for easy extraction of high quality DNA and RNA, which are provided by our German partner Analytic Jena AG. A detailed description of our molecular diagnostics can be found on pages 3 and 4. Contact and Order Information Direct and immediate contact to our customers is one of our main goals. Our products can be ordered directly from LOEWE® Biochemica GmbH, Sauerlach, Germany. For ordering please contact us by e-mail to [email protected] or register with our web-shop at: www.loewe-info.com In addition our products are available through a worldwide net of authorized distributors. Please visit our website: www.loewe-info.com/delivery.html for ordering information in your region. The team of LOEWE® Biochemica is looking forward to help you with any questions and inquiries! Sincerely, Dr. Caroline Freye-Minks and Dr. Renate Loewe LOEWE® Mühlweg 2a 82054 Sauerlach Germany Phone: (+49) 8104 61620 Fax: : (+49) 8104 61648 E-Mail: [email protected] LOEWE® Content Product Information Page 3 - 5 NEW: Molecular Extraction Kits Page 6 One-Tube One-Step RNA PCR - Viruses Page 6 - 7 DNA PCR Products Page 8 - 10 DNA PCR Products – Phytoplasma Page 8 DNA PCR Products – Bacteria Page 9 - 10 DNA PCR Products – Fungi Page 10 LOEWE®FAST Rapid Tests Page 11 - 13 ELISA Products Page 14 - 55 ELISA Products – Viruses Page 14 - 47 ELISA Products– Bacteria Page 48 - 54 ELISA Products - Fungi Page 54 - 55 Immuno Fluorescence Products Page 55 - 57 Immuno Fluorescence - Antisera Page 55 - 57 Immuno Fluorescence - Secondary Antibodies Page 57 Immuno Fluorescence - Disposables Page 57 ELISA Chemicals Page 57 - 58 ELISA Disposables Page 58 AGB - General Terms for Sales and Delivery Appendix ® LOEWE Product Information One-Tube One-Step RNA PCR - Viruses The PCR technique allows specific and sensitive detection of plant pathogens, when serological reagents are not available or a second method is needed for confirmation of test results. We are offering a continously growing range of RNA PCR complete reaction kits for reverse transcriptase PCR of RNA plant viruses. Kits Content: All components have been optimized regarding concentrations Premix (Primers, dNTPs) and reaction conditions for reliable and repeatable test results DNA-Polymerase and are accompanied by a comprehensive test protocol. Reverse Transcriptase (M-MLV, RNase H-) The reagents are mixed in one tube on the bench top and the Reaction Buffer reverse transpcription and cDNA amplification take place in one PCR-grade Water reaction step without additional pipetting step, minimalizing the Dithiothreitol (DTT) risk of cross contamination. Positive Control (DNA based) Enzymes are thermostable and kits can be shipped at room Negative Control (DNA based) temperature without the need of dry-ice! Procedure: • extract virus RNA from your sample with your favorite method or our new extraction kits (see below) • run the reverse transcription and cDNA amplification in one tube and one step • run an agarose gel and analyse results Virus-RNA from infected plant 1. Reverse Transcription 2. cDNA Amplification 3 Hours Amplified cDNA Detection in agarose gel NEW: Molecular Extraction Kits * DNA Extraction Kit for Plants RNA Extraction Kit for Plants Kits are specially optimized for the extraction Kits are specially optimized for the extraction and purification of DNA from plant material and purification of RNA from plant material (leaves, stems, roots, flowers). The process (leaves, stems, roots, flowers). Due to its involves a prefiltering step, which effectively chemistry, lysis is highly efficient and two lysis removes non-lysed plant material. Subsequent buffers are included in the kit, in order to enable binding with a novel binding buffer to a spin- processing of a wide range of different plant filter column and elution to a tube enables fast matrices. Within only 30 minutes, total RNA of and easy purification of DNA, which can be used excellent quality can be extracted, which can be directly in downstream applications or stored used directly in downstream applications. One for later use. One kit is sufficient for 50 DNA kit is sufficient for 50 RNA extractions and extractions and contains: contains: lysis buffers 2 different lysis buffers precipitation buffer washing solutions binding and washing solution, proteinase K RNase-free water prefilters, spin filters with receiver and spin filters with receiver and elution tubes elution tubes and manual manual 3 * Kits and descriptions provided by our German partner Analytik Jena AG ® LOEWE Product Information DNA PCR Products Our DNA PCR kits and sets for the detection of bacteria, fungi, and phytoplasms are the perfect tool to establish PCR analysis in your lab! Your sample DNA is subjected to a pre-tested and evaluated PCR system, without the hassle of optimizing reaction- and cycle conditions. DNA PCR Sets The PCR sets contain a premix, including pathogen specific primers and dNTPs for 100 PCR reactions and positive and negative controls for 10 reactions. All components are pre-tested and each product is accompanied by a lot-specific certificate and a working protocol. Complete PCR Reaction Kits DNA PCR Complete Reaction Kits Premix (Primers, dNTPs) Included are a vaildated premix with pathogen specific primers DNA-Polymerase and dNTPs, DNA-based positive and negative controls, 10 x Reaction Buffer thermostable DNA-Polymerase and a detailed protocol. The kits PCR-grade Water can be shipped at room temperature. Positive Control (DNA based) Negative Control (DNA based) LOEWE®FAST Rapid Tests The LOEWE®FAST rapid test series is designed for reliable and specific detection of plant pathogens within minutes. You will be able to assess suspicious plant material in the field or greenhouse without the need of an analytical laboratory. Available for a series of viruses and bacteria like the quarantine pests C.m.s and Ralstonia solanacearum. Fast - easy - on the spot Specific detection of plant pathogens within minutes No laboratory needed Visit our A LOEWE®FAST basic kit includes: You-Tube • 5 single-use test cassettes Channel for a ‘How-to- • 5 pre-filled tubes with sample buffer do Video’ • 5 single-use pipettes Immuno Fluorescence Products Especially if testing a large number of samples, immuno fluorescence still is a very popular and straightforward technique. We are offering a wide range of polyclonal antisera against plant bacteria from goat and rabbit, secondary fluorescence labelled antibodies, as well as multiwell slides and cover slides for immuno fluorescence studies: Antisera and Controls Fluorescence labelled Secondary Antibodies (FITC or Cy3TM) Multiwell Slides Cover Slides 4 ® LOEWE Product Information ELISA Products ELISA (Enzyme-linked Immunosorbent Assay) is the most common test method for the detection of plant pathogens, like viruses and bacteria. LOEWE® offers a range of 150 high quality ELISA products for specific and sensitive detection. ELISA reagents can be supplied as sets or complete kits. All necessary reagents, buffers and plates are also available separately (see pages 57-58, ELISA Chemicals and Disposables). ELISA Sets contain Coating-IgG and AP-Conjugate and are supplied as 100, 300, 500, and for many pathogens as 1000 and 5000 test units. One test corresponds to one well in the ELISA plate. The reagents are optimized and evaluated for a test volume of 200 µl, if not indicated otherwise in the test manual, ensuring highest accuracy, repeatability and sensitivity. ELISA Complete Kits are available for 96, 480, and for many pathogens as 960 test kits. The kits contain all ELISA reagents, positive and negative controls, buffers and ELISA plates or modules to perform the ELISA assay. Components 96 test kits 480 test kits 960 test kits Antibody (IgG) 0.1 ml 0.5 ml 1.0 ml Antibody-AP-conjugate 0.1 ml 0.5 ml 1.0 ml Positive Control 10 tests 10 tests 20 tests Negative Control 10 tests 10 tests 20 tests Coating Buffer 1 liter 1 liter 1 liter Wash Buffer 1 x 5 liter 1 x 5 liter 2 x 5 liter Conjugate/Sample Buffer 1 x 1 liter 2 x 1 liter 4 x 1 liter Substrate Buffer (5x) 1 x 25 ml 1 x 25 ml 2 x 25 ml Substrate Tablets 4 x 5 mg 5 x 20 mg 10 x 20 mg Tween 20 10 ml 10 ml 10 ml High-binding ELISA plates 12 Modules à 8 wells 5 plates 10 plates Sealing Cover 1 sheet 5 sheets 10 sheets ELISA Positive and Negative Controls Negative controls are made from a healthy host plant and are tested for the absence of the respective pathogen. They are lyophilized and sufficient for 10 test wells. Positive controls are made from infected plant material or bacterial cultures, if not stated otherwise. They are lyophilized and sufficient for 10 test wells.
Recommended publications
  • Monitoring Plum Pox Virus in Austria, Greece and Hungary September
    September 2017 Monitoring Plum pox virus in Austria, Greece and Hungary Plum pox virus (PPV), syn. Sharka disease, is the most important and devastating virus disease causing the highest economic impact in stone fruits worldwide. The virus, classified as a quarantine pest (EPPO A2 list, EU 2000/29 EEC, annex II), was first detected in Bulgaria in the early 1900s, and is now widespread in most European countries. The hosts of PPV are fruit-producing, ornamental and wild species of Prunus. Nine strains have been identified based on their biological, serological and molecular properties. One example of the biological relevance of this intraspecific diversity is the PPV-M strain, causing more severe symptoms in peaches than the PPV-D strain. For an effective control and surveillance strategy, it is important to use PPV-free plant material, tolerant/resistant cultivars and quick identification and eradication of diseased plants. One of the objectives of the project is to develop an improved control and surveillance strategy which requires a correlation between the presence and absence of typical PPV symptoms in diseased and healthy plants. In Greece, surveys were carried out in six apricot nurseries in the Peloponnese, the most important apricot production area. A total of about 46.000 grafted saplings were visually inspected and PPV symptoms were only observed in propagation material of the old local apricot varieties (i.e. ‘Bebecou’, ‘Early of Tyrinth´, ‘Diamantopoulou’) and in one sapling of a local PPV tolerant variety (Nostos; Karayiannis et al., 2008). A total of 974 samples were randomly collected and tested by ELISA (Loewe Biochemica GmbH) for the presence of PPV.
    [Show full text]
  • 03001770.Pdf
    Serotyping of Albanian Plum Pox Virus isolates Stamo B., Myrta A., Boscia D. in Myrta A. (ed.), Di Terlizzi B. (ed.), Savino V. (ed.). Virus and virus-like diseases of stone fruits, with particular reference to the Mediterranean region Bari : CIHEAM Options Méditerranéennes : Série B. Etudes et Recherches; n. 45 2003 pages 57-60 Article available on line / Article disponible en ligne à l’adresse : -------------------------------------------------------------------------------------------------------------------------------------------------------------------------- http://om.ciheam.org/article.php?IDPDF=3001770 -------------------------------------------------------------------------------------------------------------------------------------------------------------------------- To cite this article / Pour citer cet article -------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Stamo B., Myrta A., Boscia D. Serotyping of Albanian Plum Pox Virus isolates. In : Myrta A. (ed.), Di Terlizzi B. (ed.), Savino V. (ed.). Virus and virus-like diseases of stone fruits, with particular reference to the Mediterranean region. Bari : CIHEAM, 2003. p. 57-60 (Options Méditerranéennes : Série B. Etudes et Recherches; n. 45) -------------------------------------------------------------------------------------------------------------------------------------------------------------------------- http://www.ciheam.org/ http://om.ciheam.org/ SEROTYPING
    [Show full text]
  • Biotech/GM Crops in Horticulture: Plum Cv. Honeysweet Resistant to Plum Pox Virus
    Plant Protect. Sci. Vol. 48, 2012, Special Issue: S43–S48 Biotech/GM Crops in Horticulture: Plum cv. HoneySweet Resistant to Plum Pox Virus Jaroslav POLÁK 1, Jiban KUMAR1, Boris KRŠKA2 and Michel RAVELONANDRO3 1Department of Virology, Division of Plant Health, Crop Research Institute, Prague, Czech Republic; 2Mendel University inBrno, Faculty of Horticulture, Lednice, Czech Republic; 3INRA-Bordeaux, Villenave d’Ornon, France Abstract Polák J., Kumar J., Krška B., Ravelonandro M. (2012): Biotech/GM crops in horticulture: Plum cv. Honey- Sweet resistant to Plum pox virus. Plant Protect. Sci., 48 (Special Issue): S43–S48. Commercialisation of Biotech/GM (Biotech) crops started in 1995. Not only field crops, but also horticultural transgenic crops are under development and are beginning to be commercialised. Genetic engineering has the potential to revolutionise fruit tree breeding. The development of transgenic fruit cultivars is in progress. Over the past 20 years an international public sector research team has collaborated in the development of HoneySweet plum which is highly resistant to Plum pox virus (PPV) the most devastating disease of plums and other stone fruits. HoneySweet was deregulated in the USA in 2010. HoneySweet (aka C5) has been evaluated for eleven years (2002–2012) in a regulated field trial in the Czech Republic for the resistance to PPV, Prune dwarf virus (PDV), and Apple chlorotic leaf spot virus (ACLSV), all of them being serious diseases of plum. Even under the high and permanent infection pressure produced through grafting, PPV has only been detected in HoneySweet trees in several leaves and fruits situated close to the point of inoculum grafting.
    [Show full text]
  • Barley Yellow Dwarf Virus Infection Leads to Higher Chemical Defense
    fpls-09-00145 March 3, 2018 Time: 16:29 # 1 ORIGINAL RESEARCH published: 06 March 2018 doi: 10.3389/fpls.2018.00145 Barley yellow dwarf virus Infection Leads to Higher Chemical Defense Signals and Lower Electrophysiological Reactions in Susceptible Compared to Tolerant Barley Genotypes Maria K. Paulmann1,2, Grit Kunert2, Matthias R. Zimmermann1, Nina Theis2,3, Anatoli Ludwig1, Doreen Meichsner1, Ralf Oelmüller1, Jonathan Gershenzon2, Antje Habekuss4, Frank Ordon4, Alexandra C. U. Furch1* and Torsten Will4 1 Department of Plant Physiology, Matthias-Schleiden-Institute for Genetics, Bioinformatics and Molecular Botany, Faculty of Biological Sciences, Friedrich Schiller University Jena, Jena, Germany, 2 Department of Biochemistry, Max Planck Institute for Chemical Ecology, Jena, Germany, 3 Department of Biology, Elms College, Chicopee, MA, United States, 4 Institute for Edited by: Resistance Research and Stress Tolerance, Federal Research Centre for Cultivated Plants, Julius Kuehn-Institute, Vicenta Salvador Recatala, Quedlinburg, Germany Ronin Institute, United States Reviewed by: Barley yellow dwarf virus (BYDV) is a phloem limited virus that is persistently Michael Robert Thorpe, Australian National University, transmitted by aphids. Due to huge yield losses in agriculture, the virus is of high Australia economic relevance. Since the control of the virus itself is not possible, tolerant Stefanie Wienkoop, University of Vienna, Austria barley genotypes are considered as the most effective approach to avoid yield *Correspondence: losses. Although several genes and quantitative trait loci are known and used in Alexandra C. U. Furch barley breeding for virus tolerance, little is known about molecular and physiological [email protected] backgrounds of this trait. Therefore, we compared the anatomy and early defense Specialty section: responses of a virus susceptible to those of a virus-tolerant cultivar.
    [Show full text]
  • Strain Identification and Sequence Variability of Plum Pox Virus in Turkey
    Turkish Journal of Agriculture and Forestry Turk J Agric For (2016) 40: 746-760 http://journals.tubitak.gov.tr/agriculture/ © TÜBİTAK Research Article doi:10.3906/tar-1509-97 Strain identification and sequence variability of plum pox virus in Turkey 1,2, 1,3 Kahraman GÜRCAN *, Ahmet CEYLAN 1 Genome and Stem Cell Research Center, Erciyes University, Kayseri, Turkey 2 Department of Agricultural Biotechnology, Erciyes University, Kayseri, Turkey 3 Department of Biology, Erciyes University, Kayseri, Turkey Received: 29.09.2015 Accepted/Published Online: 22.06.2016 Final Version: 02.11.2016 Abstract: Plum pox virus (PPV) is the causal agent of sharka disease of stone fruit trees. Since the late 1960s, PPV infection has been reported in different regions of Turkey. In this study, we aim to discover PPV strains in infected regions and determine its genetic variability in Turkey. For this reason, 612 samples were collected from distant locations, where PPV was previously detected in most cases. First, PPV presence in the samples was tested with serological and molecular methods to confirm the disease. Then 314 positive samples were sequence analyzed at a 664-nucleotide length, including the P3-6K1 gene region, one of the most variable regions among Potyvirus species and quite conserved among different strains of a viral species. PPV-D and PPV-T strains were identified mostly in residential gardens, whereas PPV-M was mostly detected in the orchards, except one isolate that was identified as PPV-Rec in Bursa. PPV-T was found to be dominant in the Turkish PPV pool. Estimates of average evolutionary divergence over sequence pairs of P3-6K1 gene regions revealed that the mean intragroup diversity was 0.049 for W; 0.017 for Rec, T, and M; 0.14 for C; 0.012 for Turkish D; 0.009 for global D; and 0.007 for CR.
    [Show full text]
  • Coat Protein Gene of Plum Pox Virus
    BIOPESTICIDES REGISTRATION ACTION DOCUMENT Coat Protein Gene of Plum Pox Virus PC Code: 006354 U.S. Environmental Protection Agency Office of Pesticide Programs Biopesticides and Pollution Prevention Division Coat Protein Gene of Plum Pox Virus Biopesticides Registration Action Document May 07, 2010 TABLE OF CONTENTS BIOPESTICIDES REGISTRATION ACTION DOCUMENT TEAM 4 GLOSSARY OF ACRONYMS AND ABBREVIATIONS 5 I. OVERVIEW A. Executive Summary 6 B. Use Profile 7 C. Regulatory Background 8 II. RISK ASSESSMENT SUMMARIES A. Product Characterization 9 B. Human Health Assessment 10 C. Environmental Effects Assessment 11 III. ENVIRONMENTAL JUSTICE 12 IV. BENEFITS AND PUBLIC INTEREST FINDING 12 V. RISK MANAGEMENT AND PROPOSED REGISTRATION DECISION A. Determination of Eligibility 13 B. Proposed Regulatory Decision 14 VI. ACTIONS REQUIRED BY THE APPLICANT A. Satisfaction of the Conditions of Registration 14 B. Reporting Requirements 14 APPENDIX A: Product Characterization I. Manufacturing Process 16 A. Inert Ingredients 17 B. Active Ingredient 18 II. Plum Pox Virus Resistance and Mode of Action 18 III. Enforcement Analytical Method 19 2 Coat Protein Gene of Plum Pox Virus Biopesticides Registration Action Document May 07, 2010 APPENDIX B: Human Health Assessment I. Toxicological Profile 20 A. Data Waivers – Justification 20 B. Previous Scientific Findings 21 C. Toxicity and Allergenicity Assessment 23 II. Aggregate Exposures 23 III. Cumulative Effects 24 IV. Endocrine Disruptors 24 APPENDIX C: Environmental Effects Assessment I. Non-Target Species Effects 26 A. Data Waivers – Justification 26 II. Endangered Species Consideration 28 BIBLIOGRAPHY I. Data Submissions Received and Reviewed by the Agency 29 II. EPA Risk Assessment Memoranda 30 III. Other References 30 3 Coat Protein Gene of Plum Pox Virus Biopesticides Registration Action Document May 07, 2010 BIOPESTICIDES REGISTRATION ACTION DOCUMENT TEAM Office of Pesticide Programs Biopesticides and Pollution Prevention Division Microbial Pesticides Branch Science Reviews Joel V.
    [Show full text]
  • Recovery Plan for Plum Pox Virus (Sharka) of Stone Fruits
    Recovery Plan for Plum Pox Virus (Sharka) of Stone Fruits July 17, 2014 Contents page Executive Summary 2 Contributors and List of Experts 4 I. Introduction 6 II. Symptoms 6 III. History and Spread of PPV in the United States 9 IV. Economic Impact and Compensation 13 V. Surveys and Detection 15 VI. Monitoring and Identification of Aphid Populations in the Vicinity of PA Prunus 19 VII. References: Educational Program Materials and Research Publications 20 VIII. Fruit Grower Observations and Recommendations 24 IX. Mitigation and Disease Management 26 X. Research and Extension Priorities 27 _________________________________________________________________ This recovery plan is one of several disease-specific documents produced as part of the National Plant Disease Recovery System (NPDRS) called for in Homeland Security Presidential Directive Number 9 (HSPD-9). The purpose of the NPDRS is to insure that the tools, infrastructure, communication networks, and capacity required to mitigate the impact of high consequence plant disease outbreaks are such that a reasonable level of crop production is maintained. Each disease-specific plan is intended to provide a brief primer on the disease, assess the status of critical recovery components, and identify disease management research, extension and education needs. These documents are not intended to be stand-alone documents that address all of the many and varied aspects of plant disease outbreak and all of the decisions that must be made and actions taken to achieve effective response and recovery. They are, however, documents that will help USDA guide further efforts directed toward plant disease recovery. Executive Summary Plum pox virus (PPV) causes the most devastating viral disease of stone fruits.
    [Show full text]
  • Plum Pox Virus in the United States
    UNDERSTANDING AND PREPARING FOR THE THREAT OF PLUM POX VIRUS SPREADING TO CALIFORNIA AND THE WESTERN STATES An international conference was held at the UC Davis campus on September 29-30, 2014, to address the treat to the U.S. stone fruit industry of Plum Pox Virus (aka sharka disease). A summary of the history of this disease in the US is presented below, followed by the listing of conference speakers and topics. Plum Pox Virus in the United States Gary Obenauf, Director, California Dried Plum Board The U.S. stone-fruit industry is under threat from Plum pox virus (PPV) (aka sharka disease). This exotic invasive pathogen, spread by aphids, compromises tree health, causes premature fruit drop and reduces fruit quality. Infected fruit of most stone fruit is neither suitable for fresh or for most processed products. First identified in Europe in the early 20th century, PPV has rapidly spread world-wide since the late 1980s, likely due to the globalization of trade and travel. PPV is now present in all major fruit growing countries except the U.S., Australia, New Zealand, and South Africa. It is estimated that PPV has caused $13 billion in losses over the last 30 years in Europe alone. Current losses in Europe, where the virus is most prevalent, amount to $180 million each year. Virus control consists of tree removal. The U.S. is highly vulnerable to this disease with few resistant cultivars and few resistant germplasm resources. In 1999 PPV was detected in Pennsylvania. After 10 years, an expenditure of over $65 M, and the almost complete destruction of the Pennsylvania stone fruit industry, the virus was declared eradicated in that state.
    [Show full text]
  • 175 Section 6 Stone Fruits (Prunus Spp.)
    SECTION 6 STONE FRUITS (PRUNUS SPP.) 1. Introduction A. General Background The genus of Prunus sensu latu comprises more domesticated (also cultivated) species of temperate fruits than the other genera in the family of Rosaceae (Malus, Pyrus, Sorbus, Cydonia, Rubus, Fragaria). One of the obvious reasons for the abundant domestication might have been the coincidence between the location of the centre of variability of Prunus and the site of human evolution and/or of the first ancient high civilisations of human history. Improvement of fruit trees through traditional breeding methods is a long-term effort because of their lengthy generation time. Thus, new approaches are researched to attain the envisaged breeding goals in a reasonable time frame. Genetic transformation is potentially useful, because specific genetic changes can be made. In the last few years successful examples of resistance breeding against viruses from different plant virus families have been reported, using the coat protein-mediated cross protection approach (Beachy et al., 1990). However, only very few fruit trees have been among these experiments due to the difficulties in transformation protocols. “Cross protection” was originally described as the phenomenon of protection of a plant against the invasion of a severe disease-causing virus due to prior inoculation of the plant with an attenuated virus strain (McKinney, 1929). Hamilton postulated in 1980 that the expression of sequences from the viral genome, if expressed in transgenic plants, could possibly cause a protection against viruses. In fact by the expression of the viral coat protein gene in transgenic plants, similar effects could be obtained, and it was therefore distinguished as coat protein mediated protection (Beachy et al., 1990).
    [Show full text]
  • Gene Expression Analysis of Induced Plum Pox Virus (Sharka) Resistance in Peach (Prunus Persica) by Almond (P
    International Journal of Molecular Sciences Article Gene Expression Analysis of Induced Plum pox virus (Sharka) Resistance in Peach (Prunus persica) by Almond (P. dulcis) Grafting Manuel Rubio 1,† , Pedro J. Martínez-García 1,† , Azam Nikbakht-Dehkordi 2, Ángela S. Prudencio 1, Eva M. Gómez 1, Bernardo Rodamilans 3 , Federico Dicenta 1, Juan A. García 3 and Pedro Martínez-Gómez 1,* 1 Department of Plant Breeding, CEBAS-CSIC, P.O. Box 164, 30100 Murcia, Spain; [email protected] (M.R.); [email protected] (P.J.M.-G.); [email protected] (Á.S.P.); [email protected] (E.M.G.); [email protected] (F.D.) 2 Department of Plant Breeding and Biotechnology, Faculty of Crop Sciences, Sari Agricultural Sciences and Natural Resources University, P.O. Box 578, Sari, Iran; [email protected] 3 Department of Plant Molecular Genetics, CNB-CSIC, 28049 Madrid, Spain; [email protected] (B.R.); [email protected] (J.A.G.) * Correspondence: [email protected]; Tel.: +34-968-396-200 † These authors contributed equally to this work. Abstract: No natural sources of resistance to Plum pox virus (PPV, sharka disease) have been identified in peach. However, previous studies have demonstrated that grafting a “Garrigues” almond scion onto “GF305” peach rootstock seedlings heavily infected with PPV can progressively reduce disease Citation: Rubio, M.; Martínez-García, symptoms and virus accumulation. Furthermore, grafting a “Garrigues” scion onto the “GF305” P.J.; Nikbakht-Dehkordi, A.; rootstock has been shown to completely prevent virus infection. This study aims to analyse the Prudencio, Á.S.; Gómez, E.M.; rewiring of gene expression associated with this resistance to PPV transmitted by grafting through Rodamilans, B.; Dicenta, F.; García, the phloem using RNA-Seq and RT-qPCR analysis.
    [Show full text]
  • Reporting Service 2003, No
    ORGANISATION EUROPEENNE EUROPEAN AND MEDITERRANEAN ET MEDITERRANEENNE PLANT PROTECTION POUR LA PROTECTION DES PLANTES ORGANIZATION EPPO Reporting Service Paris, 2003-04-01 Reporting Service 2003, No. 04 CONTENTS 2003/049 - New data on quarantine pests and pests of the EPPO Alert List 2003/050 - Situation of several quarantine pests in Lithuania in 2002 2003/051 - First report of Xanthomonas axonopodis pv. dieffenbachiae in Turkey 2003/052 - Isolated finding of Citrus tristeza closterovirus in Algeria 2003/053 - Results of the 2002 survey on Plum pox potyvirus in Canada 2003/054 - Plum pox potyvirus isolated from Prunus spinosa in Hungary 2003/055 - Studies on Plum pox potyvirus recombinants 2003/056 - First report of Beet necrotic yellow vein benyvirus (rhizomania) in Egypt 2003/057 - First report of Chrysanthemum stem necrosis tospovirus in United Kingdom 2003/058 - Situation of Grapevine flavescence dorée phytoplasma in Italy 2003/059 - Grapevine flavescence dorée is suspected in Serbia (YU) 2003/060 - First report of Cameraria ohridella in the United Kingdom 2003/061 - Introduction of Dryocosmus kuriphilus into Piemonte, Italy: Addition to the EPPO Alert List 2003/062 - Phyllonorycter issikii (Lime leaf miner): addition to the EPPO Alert List 2003/063 - Introduction of Paratachardina lobata lobata into Florida, US 2003/064 - Further findings of Ralstonia solanacearum on Pelargonium in USA 2003/065 - Detection methods for Ralstonia solanacearum 2003/066 - EPPO report on notifications of non-compliance (detection of regulated pests) 1, rue Le Nôtre Tel. : 33 1 45 20 77 94 E-mail : [email protected] 75016 Paris Fax : 33 1 42 24 89 43 Web : www.eppo.org EPPO Reporting Service 2003/049 New data on quarantine pests and pests of the EPPO Alert List By browsing through the literature, the EPPO Secretariat has extracted the following new data concerning quarantine pests and pests included on the EPPO Alert List.
    [Show full text]
  • Plum Pox Virus (PPV) Potyvirus Sp
    Rhode Island Department of Environmental Management/Division of Agriculture Cooperative Agricultural Pest Survey (CAPS) Plum Pox Virus (PPV) Potyvirus sp. Native of Europe, Plum Pox Virus was first introduced to Pennsylvania in 1999 and recently found in New York and Michigan in 2006. A pest of Prunus species, only PPV-D (one of four strains of PPV) has been found in North America as of 2008. An eradication plan has been set forth in the U.S. and Canada. Plum Pox Virus is not yet present in Rhode Island. R. Scorza Symptoms: PPV-D infects multiples varieties of fruits. General symptoms include; early fruit drop, reduced sugar content in fruit and vein yellowing. Symptoms that may be visible on Plum: Blotchy leaves, with speckles or ring spots. “Shot holes,” from • brown, dead areas forming and falling out. R. Scorza • Dark brown rings on unripe fruit. Maturing fruit show these rings turning red. Fruits are deformed and bumpy. Severely infected fruit will be shriveled with brown spots. • White rings or line patterns may be visible in pits. • Brown cankers with purple borders in the fall may be visible on the green shoots of infected trees. Symptoms that may be visible on Peach: R. Scorza • Pink stripes or streaking on petals of large flowers. • Yellow rings or netting on leaves, veinal chlorosis, speckling or blotches. Deformed leaves with brown patches. • Yellow or red rings/blotches on skin of fruit. When rings run together, line patterns may be evident. Symptoms that may be visible on Apricot: • Yellow or light green ring spots on leaves.
    [Show full text]