Sorghum Downy Mildew of Maize – a Review

Total Page:16

File Type:pdf, Size:1020Kb

Sorghum Downy Mildew of Maize – a Review Int.J.Curr.Microbiol.App.Sci (2018) 7(8): 1472-1488 International Journal of Current Microbiology and Applied Sciences ISSN: 2319-7706 Volume 7 Number 08 (2018) Journal homepage: http://www.ijcmas.com Review Article https://doi.org/10.20546/ijcmas.2018.708.168 Sorghum Downy Mildew of Maize – A Review S. Arulselvi1*, B. Selvi2 and M. Pandiyan1 1Agricultural College and Research Institute, Tamil Nadu Agricultural University, Eachangkottai, Thanjavur – 614 902, Tamil Nadu, India 2Department of Millets, Tamil Nadu Agricultural University, Coimbatore – 641 003, Tamil Nadu, India *Corresponding author ABSTRACT Corn ranks one of the four principal crops of the world. It has greater adaptability and is K e yw or ds grown throughout the world, over a range of climatic conditions. Maize breeding Sorghum downy, programmes generally focus on yield improvement. However, several diseases are Mildew, Maize responsible for major economic losses in maize. Sorghum downy mildew is one of the most serious diseases in maize producing areas throughout the world. Although effective Article Info chemical measures are available, breeding resistant cultivars is more cost effective and Accepted: environmentally safe alternative for controlling sorghum downy mildew. Effective 10 July 2018 breeding methods for producing sorghum downy mildew resistant inbreds and hybrids Available Online: would depend primarily on the mode of inheritance of resistance or susceptibility to the 10 August 2018 disease. Introduction The average area under this crop of the world is 177.37 m ha with a world average Maize or corn (Zea mays L.) is an important production and productivity is around 872.06 cereal crop of the world after wheat and rice. million tonnes and 4.9 tonnes per hectare It is an annual, herbaceous, monoecious and respectively (FAO, 2012). After the discovery protandrous plant (Dhillon, 1998). of America by Europeans in Columbus‟ time its cultivation spread rapidly to all suitable It probably originated in Mexico and evolved parts of the world. The important maize from teosinte (Zea mexicana) (de Wet and growing countries are the USA, China, Brazil, Harlan, 1972). Being a C4 plant, it is Mexico, India, Philippines, South Africa and physiologically more efficient and has higher Indonesia. Maize is a relatively new crop to grain yield and wider adaptation over a range Asia, compared with other important cereals. of environmental conditions (Dowswell et al., This crop was introduced in the sixteenth 1996). Maize has a wider range of uses than century by European traders to Asia as an any other cereals as animal feed, human food ornamental garden plant and did not become and for hundreds of industrial purposes agriculturally important until 200 or 300 years (Dhillon, 1998). later (Moore and Renfro, 1971). 1472 Int.J.Curr.Microbiol.App.Sci (2018) 7(8): 1472-1488 In India, maize is grown in an area of 9.43 infected plants, deep ploughing and adjusting million hectares and the annual production is time of planting and by systemic fungicide, about 24.35 million tonnes with a productivity Metalaxyl either through seed treatment of 2.58 tonnes per hectare (Agricultural (Odvody and Frederiksen, 1984a) or foliar Statistics at a Glance, 2014). In Tamil Nadu, application (Odvody and Frederiksen, 1984b), maize occupies 3.21 lakh hectares with an their effectiveness on disease incidence is average production and productivity of 2.64 variable and in most cases, offer incomplete lakh tonnes and 8224 kg per hectare control. Moreover the economic costs of respectively (Department of EconoFmics and chemical control in maize production have Statistics, Chennai, 2014). It is expected to been a barrier. Considering the cost of increase in future to meet the growing chemicals and the emergence of chemical demands of poultry and other animals feed resistance in the downy mildew pathogens industry, industrial utilization and human (Raymundo, 2000) use of host plant resistance consumption. The demand for maize is seems to be the most effective, economical increasing every year. According to recent and environmentally safe way of controlling study (The Hindu Survey of Indian SDM disease in maize (Rathore and Jain, Agriculture, 2000), in 2015 the domestic 2000). The genetic information relating to host demand for maize will be about 12 million resistance is vital for making breeding tonnes and in 2030 it will be 13.5 million decisions. tonnes and for Tamil Nadu state it is about ten to twelve lakh tonnes. The commercial Downy mildew pathogens of maize exploitation of single cross hybrids in maize, initially suggested by Shull (1909), is Among the various maize diseases, downy emerging again because of their uniformity in mildews are considered to be the major plant ear characters than other types of hybrids diseases. In origin, the downy mildews are and high yield potential. Frey (1971) reported “old world” diseases that now are very that yield increases in the USA after 1957 damaging and prevalent on the “new world were mainly due to the wide cultivation of crop” – maize (Shaw, 1975). None of the single cross hybrids. Due to yield advantage, downy mildew diseases originated on maize hybrids dominate in maize cultivation over (Shaw, 1975) but they possessed the ability to varieties. Hence, high yielding single cross attack maize when maize was introduced from hybrids are the need to meet the growing the new world to old world. Heavy losses (as demand. To meet this demand it is necessary high as 100 per cent) in maize due to downy to increase the productivity of maize. One of mildew pathogens have been recorded in the major factors limiting productivity in Philippines, Taiwan, Indonesia, Thailand, maize is the increasing incidence of pest and India, West Africa, Venezuela, Japan, diseases. Of these, sorghum downy mildew Australia, Europe, North America and other (SDM) caused by Peronosclerospora sorghi parts of the world (Bonde, 1982 and Rifin, (Weston and Uppal) C.G. Shaw is the most 1983). Twenty one species of downy mildew prevalent downy mildew in the tropical and pathogens have been reported to attack the subtropical areas of the world (Frederiksen et graminae family (Shaw, 1975). Of these, ten al., 1969; Pupipat, 1975; Frederiksen and species of fungi belong to three genera (seven Renfro, 1977 and Williams, 1984). species of Peronosclerospora, one species of Sclerospora and two species of Though the disease can be controlled by Sclerophthora) have been reported to cause cultural practices such as eradication of different types of downy mildews in maize 1473 Int.J.Curr.Microbiol.App.Sci (2018) 7(8): 1472-1488 (Frederiksen and Renfro, 1977; Siradhana et Subsequently, Kulkarni (1913) in India al., 1980 and Rathore et al., 2002). The details observed that, in the asexual phase, are given in Table 1. germination was direct by means of a germ tube from conidia (rather than through Downy mildews such as Sorghum downy zoospores from sporangia) and primarily on mildew, Philippine downy mildew, Sugar cane the basis he recommended designation of downy mildew, Brown stripe downy mildew varietal rank as Sclerospora graminicola var and more recently identified Rajasthan downy Andropogonis-sorghi. Weston and Uppal mildew were reported from different agro- (1932) described this fungus in English and ecological regions in India (Payak, 1975a; further investigation of morphology and host Siradhana et al., 1980). Sorghum Downy range he named it as Sclerospora sorghi in Mildew (SDM) is particularly prevalent in the 1932. In 1978 C.G. Shaw proposed the new Peninsular India, in the states of Karnataka, genus Peronosclerospora as subgenus of Tamil Nadu and Andhra Pradesh reportedly Sclerospora based on conidial germination (by causing yield losses of 30 per cent and higher a germ tube) and he transferred genus name (Payak, 1975a, 1975b and Krishnappa et al., from Sclerospora in to Peronosclerospora that 1995). SDM became an internationally produce conidia which germinate directly by a important disease of maize during the years of germ tube (Shaw, 1978). From 1978 this SDM rapid expansion of the use of sorghum for pathogen has been named as grain and forage (Sabry et al., 2006; Lukman Peronosclerospora sorghi [(Weston and et al., 2013; Muis et al., 2015). Uppal) C.G. Shaw]. It infects both maize and sorghum in warm Symptoms of sorghum downy mildew on and humid areas of the world (Frederiksen, maize 1980). The pathogen infects the roots primarily by oospores and the leaves by Systemic infection in maize seedlings is conidia and reaches the meristem causing characterized by chlorosis which normally systemic infection. Systemically infected appears two weeks after sowing (Safeeulla, plants do not produce cobs. If at all produce 1974). The leaves of infected plants tend to be cobs they have only a few seeds and it causes narrower and more erect than those of healthy severe yield loss in maize. It is an obligate plants. Plants infected early usually die parasite (Cardwell et al., 1997) that cannot be approximately four weeks after infection cultured in the laboratory. The disease occurs (Ajala et al., 2003). In late infected plants, the in both maize and sorghum in warm and chlorosis may be more noticeable on the lower humid areas of the world (Sabry et al., 2006). half of the leaf which is often called half-leaf symptom. This chlorosis gradually covers the Taxonomy of P. sorghi entire leaf surface at later stage (Safeeulla, 1974). Under warm humid conditions, a white SDM has two crop hosts, sorghum and maize. downy growth is produced on the lower leaf It is a member of subdivision surface some times on both surfaces also. This Mastigomycotina, class Oomycetes, order growth is a combination of conidia and Peronosporales and family Peronosporaceae. conidiophores (Jeger et al., 1998). In maize, The widely prevalent SDM was first reported leaf shredding is rare but it is common in by Butler (1907) in Tamil Nadu and sorghum (Jeger et al., 1998).
Recommended publications
  • Bioimaging Structural Signatures of the Oomycete Pathogen Sclerospora Graminicola in Pearl Millet Using Different Microscopic Te
    www.nature.com/scientificreports OPEN Bioimaging structural signatures of the oomycete pathogen Sclerospora graminicola in pearl millet using diferent microscopic techniques Hunthrike Shekar Shetty1, Sharada Mysore Suryanarayan2, Sudisha Jogaiah3*, Aditya Rao Shimoga Janakirama1, Michael Hansen4, Hans Jørgen Lyngs Jørgensen 4 & Lam-Son Phan Tran5,6* In this case study, the mycelium growth of Sclerospora graminicola in the infected tissues of pearl millet and the process of sporulation and liberation of sporangia and zoospores were observed using four diferent microscopic techniques. The cotton blue-stained samples observed under light microscope revealed the formation of zoospores with germ tubes, appressoria and initiation of haustorium into the host cells, while the environmental scanning electron microscopy showed the rapid emergence of sporangiophores with dispersed sporangia around the stomata. For fuorescence microscopy, the infected leaf samples were stained with Fluorescent Brightener 28 and Calcofuor White, which react with β-glucans present in the mycelial walls, sporangiophores and sporangia. Calcofour White was found to be the most suitable for studying the structural morphology of the pathogen. Therefore, samples observed by confocal laser scanning microscopy (CLSM) were pre-treated with Calcofuor White, as well as with Syto-13 that can stain the cell nuclei. Among the four microscopic techniques, CLSM is ideal for observing live host-pathogen interaction and studying the developmental processes of the pathogen in the host tissues. The use of diferent microscopic bioimaging techniques to study pathogenesis will enhance our understanding of the morphological features and development of the infectious propagules in the host. Many oomycete plant pathogens cause a considerable loss in food crops, including cereals, legumes, oil seeds, vegetables, and fruit crops1.
    [Show full text]
  • AR TICLE Baobabopsis, a New Genus of Graminicolous Downy Mildews
    IMA FUNGUS · 6(2): 483–491 (2015) doi:10.5598/imafungus.2015.06.02.12 Baobabopsis, a new genus of graminicolous downy mildews from tropical ARTICLE Australia, with an updated key to the genera of downy mildews Marco Thines1,2,3,4, Sabine Telle1,2, Young-Joon Choi1,2,3, Yu Pei Tan5, and Roger G. Shivas5 1Integrative Fungal Research (IPF), Georg-oigt-Str. 14-16, D-60325 Frankfurt am Main, Germany; corresponding author e-mail: marco.thines@ senckenberg.de 2Biodiversity and Climate Research Centre (BiK-F), Georg-oigt-Str. 14-16, D-60325 Frankfurt am Main, Germany 3Senckenberg Gesellschaft für Naturkunde, Senckenberganlage 25, D-60325 Frankfurt am Main, Germany 4Goethe University, Faculty of Biosciences, Institute of Ecology, Evolution and Diversity, May-von-Laue-Str. 9, D-60483 Frankfurt am Main, Germany 5Plant Pathology Herbarium, Department of Agriculture and Fisheries, Ecosciences Precinct, GPO Box 267, Brisbane, Qld 4001, Australia Abstract: So far 19 genera of downy mildews have been described, of which seven are parasitic to grasses. Key words: Here, we introduce a new genus, Baobabopsis, to accommodate two distinctive downy mildews, B. donbarrettii cox2 sp. nov., collected on Perotis rara in northern Australia, and B. enneapogonis sp. nov., collected on Enneapogon genus key spp. in western and central Australia. Baobabopsis donbarrettii produced both oospores and sporangiospores that nrLSU are morphologically distinct from other downy mildews on grasses. Molecular phylogenetic analyses showed that phylogeny the two species of Baobabopsis occupied an isolated position among the known genera of graminicolous downy Peronosporaceae mildews. The importance of the Poaceae for the evolution of downy mildews is highlighted by the observation that Poaceae more than a third of the known genera of downy mildews occur on grasses, while more than 90 % of the known species of downy mildews infect eudicots.
    [Show full text]
  • Fantastic Downy Mildew Pathogens and How to Find Them: Advances in Detection and Diagnostics
    plants Review Fantastic Downy Mildew Pathogens and How to Find Them: Advances in Detection and Diagnostics Andres F. Salcedo 1 , Savithri Purayannur 1 , Jeffrey R. Standish 1 , Timothy Miles 2, Lindsey Thiessen 1 and Lina M. Quesada-Ocampo 1,* 1 Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC 27695-7613, USA; [email protected] (A.F.S.); [email protected] (S.P.); [email protected] (J.R.S.); [email protected] (L.T.) 2 Department of Plant, Soil and Microbial Sciences, Michigan State University, East Lansing, MI 48824, USA; [email protected] * Correspondence: [email protected] Abstract: Downy mildews affect important crops and cause severe losses in production worldwide. Accurate identification and monitoring of these plant pathogens, especially at early stages of the disease, is fundamental in achieving effective disease control. The rapid development of molecular methods for diagnosis has provided more specific, fast, reliable, sensitive, and portable alternatives for plant pathogen detection and quantification than traditional approaches. In this review, we provide information on the use of molecular markers, serological techniques, and nucleic acid amplification technologies for downy mildew diagnosis, highlighting the benefits and disadvantages of the technologies and target selection. We emphasize the importance of incorporating information on pathogen variability in virulence and fungicide resistance for disease management and how the Citation: Salcedo, A.F.; Purayannur, development and application of diagnostic assays based on standard and promising technologies, S.; Standish, J.R.; Miles, T.; Thiessen, including high-throughput sequencing and genomics, are revolutionizing the development of species- L.; Quesada-Ocampo, L.M. Fantastic specific assays suitable for in-field diagnosis.
    [Show full text]
  • An Overview on Philippine Estuarine Oomycetes
    REVIEW PAPER | Philippine Journal of Systematic Biology DOI 10.26757/pjsb2020a14007 An overview on Philippine estuarine oomycetes Reuel M. Bennett1 and Marco Thines2,3 Abstract Estuarine saprotrophic oomycetes are a group of eukaryotic, fungal-like protists of the Kingdom Straminipila. Species classified as estuarine oomycetes are commonly present on mangrove leaf litter and saltmarsh plant debris. They are distributed over several families (i.e. Peronosporaceae, Pythiaceae, Salisapiliaceae, and Salispinaceae). It is estimated that there are more than 100 species of estuarine oomycetes and, surprisingly, some supposedly terrestrial phytopathogenic hemibiotrophic oomycetes, e.g. Phytophthora elongata, Ph. insolita, and Ph. ramorum, are likewise present in the estuarine biome. In the Philippines, this group has been neglected for several decades as compared to the obligate biotrophic and hemibiotrophic members of Peronosporaceae and Albuginaceae. In this account, a general overview on the systematics and phylogeny of estuarine oomycetes is given. Further, the state of knowledge regarding thallus organization, taxonomy, habitat, and status of Philippine oomycetes are presented. Keywords: estuarine, mangroves, oomycetes, phylogeny, taxonomy History of knowledge on estuarine oomycetes from environments (Fig. 1). Nigrelli and Thines (2013) suggested that saltmarsh and mangrove habitats there are approximately 60 known species of marine oomycetes The Phylum Oomycota is a group of fungal-like recorded in the literature, and to date, 30 species are known eukaryotes of the Kingdom Straminipila and is composed of from mangrove and saltmarsh habitats (Hulvey et al. 2010, approximately 1,700 species grouped into 90 genera (Beakes Nigrelli and Thines 2013, Bennett and Thines 2017, 2019, and Thines 2017, Wijayawardene et al.
    [Show full text]
  • Production of Conidia by Peronosclerospora Sorghi on Sorghum Crops in Zimbabwe
    Plant Pathology (1998) 47, 243–251 Production of conidia by Peronosclerospora sorghi on sorghum crops in Zimbabwe C. H. Bocka*, M. J. Jegerb, L. K. Mughoghoc, E. Mtisid and K. F. Cardwelle aNatural Resources Institute, Central Avenue, Chatham Maritime, Chatham, Kent ME4 4TB, England, UK; bDepartment of Phytopathology, Agricultural University of Wageningen, P.O.B. 8025, 6700 EE, Wageningen, The Netherlands; cSouthern African Development Co-operation/International Crops Research Institute for the Semi-Arid Tropics/Sorghum and Millet Improvement Program, PO Box 776, Bulawayo; dPlant Protection Research Institute, Department of Research and Special Services, PO Box 8100, Causeway, Harare; Zimbabwe; and eInternational Institute of Tropical Agriculture, Oyo Road, PMB 5320, Ibadan, Nigeria Factors affecting the production of conidia of Peronosclerospora sorghi, causing sorghum downy mildew (SDM), were investigated during 1993 and 1994 in Zimbabwe. In the field conidia were detected on nights when the minimum temperature was in the range 10–198C. On 73% of nights when conidia were detected rain had fallen within the previous 72 h and on 64% of nights wind speed was < 2·0 m s¹1. The time period over which conidia were detected was 2–9 h. Using incubated leaf material, conidia were produced in the temperature range 10–268C. Local lesions and systemically infected leaf material produced 2·4–5·7 × 103 conidia per cm2. Under controlled conditions conidia were released from conidiophores for 2·5 h after maturation and were shown to be well adapted to wind dispersal, having a settling velocity of 1·5 × 10¹4 ms¹1. Conditions that are suitable for conidia production occur in Zimbabwe and other semi-arid regions of southern Africa during the cropping season.
    [Show full text]
  • Peronosclerospora Maydis Primary Pest of Corn Fungal-Like Java Downy Mildew
    Peronosclerospora maydis Primary Pest of Corn Fungal-like Java downy mildew Peronosclerospora maydis Scientific Name Peronosclerospora maydis (Racib.) C.G. Shaw Synonyms: Peronospora maydis and Sclerospora maydis Common Name Java downy mildew, downy mildew of corn, and corn downy mildew Type of Pest Fungal-like pathogen Taxonomic Position Phylum: Oomycota, Class: Oomycetes, Order: Sclerosporales, Family: Sclerosporaceae Reason for Inclusion in Manual CAPS Target: AHP Prioritized Pest List – 2009 Pest Description Java downy mildew, caused by Peronosclerospora maydis, was discovered by Raciborski (1897) in Java, Indonesia in 1897 and has the distinction of being the first downy mildew disease reported on corn (Bonde, 1982). Initially it was misidentified as Sclerospora maydis. The disease was reported in India by Butler (1913) and has continued to spread. Peronosclerospora maydis is an obligate parasite that will not grow on artificial media. The pathogen produces two kinds of hyphae: straight and sparsely branched, and lobed and irregularly branched. The mycelium has many haustoria with different forms (Semangoen, 1970). Clustered conidiophores arise from stomata and are dichotomously branched two to four times. The branches are robust and 150-550 µm long with basal cells 60-180 µm long. Conidia (17-23 x 27-39 µm) are hyaline and spherical to subspherical (Smith and Renfro, 1999). Semangoen (1970), however, indicated that the conidia are smaller (12-29 x 10-23 µm). Oospores have not been reported (Smith and Renfro, 1999). Biology and Ecology Infected corn plants grown during the dry season are the primary source of inoculum in Indonesia. The fungus may also survive as mycelium in kernels, but this is thought to be a minor source of inoculum.
    [Show full text]
  • Proceedings of the Global Conference on Ergot of Sorghum
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln International Sorghum and Millet Collaborative INTSORMIL Impacts and Bulletins Research Support Program (INTSORMIL CRSP) 6-8-1997 Proceedings of The Global Conference on Ergot of Sorghum Carlos R. Casela Jeffery A. Dahlberg Follow this and additional works at: https://digitalcommons.unl.edu/intsormilimpacts Part of the Agricultural Science Commons, and the Agronomy and Crop Sciences Commons This Article is brought to you for free and open access by the International Sorghum and Millet Collaborative Research Support Program (INTSORMIL CRSP) at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in INTSORMIL Impacts and Bulletins by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Global Conference on frgot of Sorghum ~............... The conference sponsors, EMBRAPA and INTSORMIL, gratefully acknowledge the contributions made to this conference by the following organizations. American Seed Trade Association ICRISAT National Grain Sorghum Producers Novartis Seeds, Inc. Pioneer Hi-Bred International, Inc. Texas A&M University Texas Seed Trade Association USDA Members of the Organizing Committee Robert Schaffert, Chair, EMBRAPA, Sete Lagoas, Brazil Gisela de Avellar, EMBRAPA, Sete Lagoas, Brazil Ranajit Bandyopadhyay, ICRISAT, Hyderabad, India Tania M.A. Barbosa, EMBRAPA, Sete Lagoas, Brazil Carlos R. Casela, EMBRAPA, Sete Lagoas, Brazil Alexandre S. Ferreira, EMBRAPA, Sete Lagoas, Brazil Richard Frederiksen,
    [Show full text]
  • Unraveling the Genetic Diversity of Maize Downy Mildew in Indonesia Rudy Lukman PT
    Agronomy Publications Agronomy 2013 Unraveling the Genetic Diversity of Maize Downy Mildew in Indonesia Rudy Lukman PT. BISI International Ahmad Afifuddin PT. BISI International Thomas Lubberstedt Iowa State University, [email protected] Follow this and additional works at: http://lib.dr.iastate.edu/agron_pubs Part of the Agronomy and Crop Sciences Commons The ompc lete bibliographic information for this item can be found at http://lib.dr.iastate.edu/ agron_pubs/283. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Agronomy at Iowa State University Digital Repository. It has been accepted for inclusion in Agronomy Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Unraveling the Genetic Diversity of Maize Downy Mildew in Indonesia Abstract Varying effectiveness of metalaxyl fungicides and disease incidences caused by downy mildew to maize in several places in Indonesia led to the speculation that genetic variation of Peronosclerospora species in Indonesia exists. Hence, we employed two molecular marker systems, namely SSR (Simple Sequence Repeat) and ARDRA A( mplified Ribosomal DNA Restriction Analysis) markers, to study the population structure and genetic diversity of downy mildew isolates collected from hotspot production areas of maize in Indonesia. Both molecular techniques grouped the isolates into three clusters with a genetic similarity between 66-98% and 58-100% for SSR and ARDRA am rkers, respectively. In general, SSRs yielded lower similarities among isolates compared to ARDRA. Combined analysis of data from both techniques resulted in genetic similarities of 64-98% for 31 downy mildew isolates grouped into three clusters, two clusters of Java, and one cluster of Lampung and Gorontalo isolates.
    [Show full text]
  • Phytosanitary Interventions for Safe Global Germplasm Exchange and the Prevention of Transboundary Pest Spread: the Role of CGIAR Germplasm Health Units
    plants Review Phytosanitary Interventions for Safe Global Germplasm Exchange and the Prevention of Transboundary Pest Spread: The Role of CGIAR Germplasm Health Units P. Lava Kumar 1,* , Maritza Cuervo 2, J. F. Kreuze 3 , Giovanna Muller 3, Gururaj Kulkarni 4, Safaa G. Kumari 5, Sebastien Massart 6, Monica Mezzalama 7,†, Amos Alakonya 7 , Alice Muchugi 8, Ignazio Graziosi 8,‡, Marie-Noelle Ndjiondjop 9, Rajan Sharma 10 and Alemayehu Teressa Negawo 11 1 International Institute of Tropical Agriculture (IITA), Oyo Road, PMB 5320, Ibadan 200001, Nigeria 2 The Alliance of Bioversity International and International Center for Tropical Agriculture (CIAT), Palmira 763537, Cali, Colombia; [email protected] 3 International Potato Center (CIP), Avenida La Molina 1895, Lima 15023, Peru; [email protected] (J.F.K.); [email protected] (G.M.) 4 International Rice Research Institute (IRRI), Los Banos 4031, Philippines; [email protected] 5 International Center for Agricultural Research in the Dry Areas (ICARDA), Terbol Station, Zahle 1801, Lebanon; [email protected] 6 The Alliance of Bioversity International-CIAT & University of Liège, Gembloux Agro-BioTech, Passage des déportés, 2, 5030 Gembloux, Belgium; [email protected] 7 International Maize and Wheat Improvement Center (CIMMYT), México-Veracruz, El Batán Km. 45, Citation: Kumar, P.L.; Cuervo, M.; Texcoco 56237, Mexico; [email protected] (M.M.); [email protected] (A.A.) 8 World Agroforestry Center (ICRAF), United Nations Avenue, Gigiri P.O. Box 30677, Nairobi 00100, Kenya; Kreuze, J.F.; Muller, G.; Kulkarni, G.; [email protected] (A.M.); [email protected] (I.G.) Kumari, S.G.; Massart, S.; 9 Africa Rice Center (AfricaRice), 01 BP 2551, Bouake 99326, Côte d’Ivoire; [email protected] Mezzalama, M.; Alakonya, A.; 10 International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru 502324, Hyderabad, Muchugi, A.; et al.
    [Show full text]
  • Index of Plant Diseases in South Carolina
    INDEX OF PLANT DISEASES IN SOUTH CAROLINA Third Edition James H. Blake, Ed.D. State Coordinator SC Master Gardener Program SC Master Naturalist Program Meg Williamson, M.S. Plant Disease Diagnostician PREFACE The first edition of the Index of Plant Diseases in South Carolina published in 2008 listed the plant diseases occurring on cultivated and native plants in SC as reported from plant samples submitted to the Clemson University Plant Problem Clinic between 1972 and 2006, with the addition of disease reports from Extension and research plant pathologists across SC. The second edition included data from 2007 through 2011, adding 85 new host plants and 634 new diagnoses. This third edition includes disease reports from 2012 through 2014, adding 54 new host plants and 350 new diagnoses. The Index now contains 1,041 genera and species of plants from 124 plant families with 1,573 common names. There are 5,727 disease reports with 4,712 diseases being caused by fungi, 442 diseases caused by nematodes, 380 diseases caused by bacteria, 247 diseases caused by viruses, 20 diseases caused by algae, 3 diseases caused lichens, 1 disease caused by a phytoplasma, and 1 disease caused by a viroid. No attempt has been made to update the binomial nomenclature of either plants or plant pathogens listed in this publication. This index lists the plants and their pathogens as taken from the sample submission forms and the reports generated by the various Clemson University plant pathologists. This index does not imply that it is a complete list of the diseases of plants in South Carolina.
    [Show full text]
  • 425 2009 IB81 Safe Movemen
    About ICRISAT Science with a human face The International Crops Research Institute for the Semi-Arid Tropics (ICRISAT) is a non-profit, non-political organization that does innovative agricultural research and capacity building for sustainable development with a wide array of partners across the globe. ICRISAT’s mission is to help empower 600 million poor people to overcome hunger, poverty and a degraded environment in the dry tropics through better agriculture. ICRISAT belongs to the Alliance of Centers of the Consultative Group on International Agricultural Research (CGIAR). Company Information ICRISAT-Patancheru ICRISAT-Liaison Office ICRISAT-Nairobi ICRISAT-Niamey (Headquarters) CG Centers Block (Regional hub ESA) (Regional hub WCA) Patancheru 502 324 NASC Complex PO Box 39063, Nairobi, Kenya BP 12404, Niamey, Niger (Via Paris) Andhra Pradesh, India Dev Prakash Shastri Marg Tel +254 20 7224550 Tel +227 20722529, 20722725 Tel +91 40 30713071 New Delhi 110 012, India Fax +254 20 7224001 Fax +227 20734329 Fax +91 40 30713074 Tel +91 11 32472306 to 08 [email protected] [email protected] [email protected] Fax +91 11 25841294 ICRISAT-Bamako ICRISAT-Bulawayo ICRISAT-Lilongwe ICRISAT-Maputo BP 320 Matopos Research Station Chitedze Agricultural Research Station c/o IIAM, Av. das FPLM No 2698 Bamako, Mali PO Box 776, PO Box 1096 Caixa Postal 1906 Tel +223 20223375 Bulawayo, Zimbabwe Lilongwe, Malawi Maputo, Mozambique Fax +223 20228683 Tel +263 383 311 to 15 Tel +265 1 707297/071/067/057 Tel +258 21 461657 [email protected] Fax +263 383 307 Fax +265 1 707298 Fax +258 21 461581 [email protected] [email protected] [email protected] www.icrisat.org ISBN 978-92-9066-524-3 Order code: IBE 081 425–2009 Citation: Thakur RP, Gunjotikar GA and Rao VP.
    [Show full text]
  • Peronosclerospora Philippinensis
    Peronosclerospora philippinensis Scientific Name Peronosclerospora philippinensis (W. Weston) C.G. Shaw Synonyms: Peronosclerospora sacchari, Sclerospora indica, Sclerospora maydis, and Sclerospora philippinensis Common Name Philippine downy mildew, Java downy mildew of corn, and sugarcane downy mildew Type of Pest Fungal-like Taxonomic Position Phylum: Oomycota, Class: Oomycetes, Order: Sclerosporales, Family: Sclerosporaceae Reason for Inclusion in Manual CAPS Target: AHP Prioritized Pest List – 2009; Agricultural Bioterrorism Protection Act of 2002 (Select Agent) Pest Description Philippine downy mildew, caused by Peronosclerospora philippinensis, was initially reported from India in 1913. The pathogen at this time, however, was misidentified as Sclerospora maydis and later as S. indica (Bonde, 1982). The disease in India has never caused large losses (Payak, 1975). In contrast, in the Philippines, where the disease has been present at least since 1916 (Weston, 1920), it is economically very damaging. Philippine downy mildew is confined to parts of Asia and has not been reported within the United States. Peronosclerospora philippinensis is an obligate parasite that will not grow on artificial media. The mycelia are branched, slender (8 µm in diameter), irregularly constricted, and inflated. Figure 1. Chlorotic symptoms of Erect conidiophores (15-26 x 150-400 µm) Philippine downy mildew. Photo grow out of stomata and are dichotomously courtesy of CIMMYT . branched two to four times. Branches are 1 robust. Sterigmata are ovoid to subulate, slightly curved, and 10 µm long. The conidia (17-21 x 27-39 µm) are elongate ovoid to round cylindrical, hyaline, and slightly rounded at the apex (Weston, 1920; Smith and Renfro, 1999). Haustoria are simple, vesiculiform to subdigitate, 8 x 2 µm.
    [Show full text]