Hop Downy Mildew Caused by Pseudoperonospora humuli: A Diagnostic Guide

2020 ◽  
Vol 21 (3) ◽  
pp. 173-179 ◽  
Author(s):  
Savithri Purayannur ◽  
Timothy D. Miles ◽  
David H. Gent ◽  
Stacey Pigg ◽  
Lina M. Quesada-Ocampo

Downy mildew, caused by Pseudoperonospora humuli, is one of the most destructive diseases of hop. The purpose of this article is to provide an overview of the pathogen, the host range and geographical distribution, and the means to diagnose the disease. It is important to be able to diagnose downy mildew and distinguish it from other diseases for the timely application of suitable management practices. The procedures for laboratory propagation and maintenance of isolates are also presented.

Author(s):  
S. M. Francis

Abstract A description is provided for Pseudoperonospora humuli. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOST: Humulus lupulus. DISEASE: Downy mildew of hops. The first sign of infection, seen early in the year, is the development of spindly, stunted, shoots with pale, crowded and down-curled, leaves. These are known as 'primary basal spikes' and are shoots with a systemic infection developed from mycelium which has overwintered in the rootstock. The undersurfaces of the leaves of these shoots bear large crops of sporangia which in moist and humid conditions can soon spread the disease in the growing crop. Secondary infections may occur on leaves, growing tips, flowers and cones. On the leaves they are seen either as small discrete spots or larger, more angular, brown areas. The diseased shoots arising from secondary infections and depending upon the position of the infected bud are known as 'terminal' or 'lateral' spikes. They resemble basal spikes in appearance. Infection of the flowers can inhibit cone production. If cones do develop, and become infected, the brown spots and lesions of the fungus can make them unsaleable. GEOGRAPHICAL DISTRIBUTION: CMI Map No. 14, ed. 4, 1976, with the addition of Belorussia, Estonia, India, Kinghizia, Kazakhstan, Latvia, Lithuania, Moldavia, Ukraine and Uzebekistan. TRANSMISSION: Ware (1926) demonstrated the presence of mycelium in diseased rootstocks but its significance in the overwintering of the pathogen was not fully recognized until Coley Smith (1962) showed that the primary basal spikes which develop in spring originate from infected buds on the rootstocks. Oospores, which are often produced in abundance, were at one time thought to be responsible for infection of the shoots in spring but there is no convincing evidence to support this theory.


2021 ◽  
pp. 125-131
Author(s):  
Edward J. Sikora

Abstract This chapter focuses on the economic importance, host range, geographical distribution, symptoms of damage and biology and life cycle of root-knot and reniform nematodes (Meloidogyne spp. and Rotylenchulus reniformis) infesting soyabeans in southern USA. Some information on the efficacy and optimization of some recommended integrated nematode management practices and future outlook and research requirements are also presented.


Author(s):  
S. M. Francis

Abstract A description is provided for Peronospora dianthicola. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOST: Dianthus caryophyllus. DISEASE: Downy mildew of carnation. Early symptoms are seen on the leaves which have pale green to yellowish transverse bands and may bend at these lesions. Infected plants are stunted and become withered. Infection of the growing point may result in the development of axillary buds giving the plants a bushy appearance. Barthelet describes the shoots which can develop in some resistant varieties as resembling the basal spikes of Pseudoperonospora humuli on hops, i.e., shoots with smaller leaves, thickened stem and shortened internodes. GEOGRAPHICAL DISTRIBUTION: Europe (Britain*, Denmark, France, Greece, Turkey); N. America (California, USA); S. America (Colombia). *no herbarium material, but recorded by F.A. Mason, The Naturalist no. 848: 270, 1927; on leaves of carnation under glass, Duncombe Park, Helmsley, Yorks. (Sept. 1920). TRANSMISSION: Oospores, which are formed abundantly in the tissues of diseased plants, are thought to be important in disease transmission. A small amount of infection is often seen on the plants in the autumn and these foci can allow the pathogen to overwinter until more favourable weather conditions permit the spread of the disease the following spring. Possible weed hosts for the pathogen such as Cerastium and Stellaria, growing in the vicinity, were examined and found to be infected with a different species of Peronospora belonging to the P. alsinearum group (33, 230).


2020 ◽  
Vol 20 (12) ◽  
pp. 1118-1132
Author(s):  
Sidra Saleem ◽  
Haroon Ahmed ◽  
Tooba Siddiqui ◽  
Seyma Gunyakti Kilinc ◽  
Aisha Khan ◽  
...  

Schistosomiasis is a chronic parasitic disease caused by a trematode blood fluke of the genus Schistosoma that belongs to the Schistosomatidae family. It is a neglected disease in different regions of Asia. In this review, 218 articles (between 2000 and 2017) related to the topic were collected from PubMed and Google scholar and reviewed. After thoroughly reading collected articles, due to irrelevant topic requirements, 94 articles were excluded. Articles that have data associated with Asian regions are considered. In Asia, the disease is prevalent in China, Philippines, Indonesia, Yemen, Nepal and Laos, etc. While in Pakistan, India and Bangladesh, the disease is not endemic and very few cases were reported. The disease was eliminated from Japan and Iran. The current review highlights the geographical distribution among Asian countries, transmission patterns, diagnosis, control strategies based on the use of anthelmintic plants and management practices implemented in Asia for the control of schistosomiasis. However, new implementations to treat schistosomiasis in humans should be proved to eliminate the disease finally in the future. This review emphasizes the biological control of schistosomiasis for the eradication of the disease from Asia in the near future.


2021 ◽  
Author(s):  
Savithri Purayannur ◽  
David H. Gent ◽  
Timothy D. Miles ◽  
Sebastjan Radišek ◽  
Lina M. Quesada‐Ocampo

Plant Disease ◽  
2019 ◽  
Vol 103 (10) ◽  
pp. 2592-2598
Author(s):  
Anthony P. Keinath

The objective of this study was to evaluate fungicide applications, host resistance, and trellising, alone and in combination, as management practices for downy mildew on slicing cucumber. A split-split plot experimental design was used with three and four replications in spring and fall 2017, respectively. The whole-plot treatment was fungicide, four applications of chlorothalonil (Bravo Weather Stik 6SC) alternated with three applications of cyazofamid (Ranman 400SC), or water. Split plots were nontrellised or trellised with four strings supported by stakes. Split-split plots were cultivar Bristol, which is intermediately resistant to downy mildew, or cultivar Speedway, which is susceptible to downy mildew with similar parentage as Bristol. In both seasons, area under the disease progress curve (AUDPC) values were lower with fungicides than water for both cultivars. In the spring, AUDPC for Bristol was lower than for Speedway regardless of fungicide treatment. In the fall, Bristol had a lower AUDPC than Speedway with fungicides, but the AUDPC did not differ between the two cultivars with water. The mean AUDPC for trellised plants (376.2) was lower than for nontrellised plants (434.0; P = 0.007). Fungicide applications increased marketable and total fruit weights in both seasons (P ≤ 0.0002). Marketable weight with fungicides was almost double (93% greater) the marketable weight with water. Marketable weight was 55% greater for Bristol than for Speedway in spring, but yields did not differ between cultivars in fall (season-by-cultivar interaction, P ≤ 0.0003). Because trellising had no effect on marketable yields (P = 0.11), trellising is not recommended for managing downy mildew on slicing cucumber. Of the three management techniques examined, fungicides had the largest effects on disease and yields, followed by cultivar resistance.


Author(s):  
Z. Kozakiewicz

Abstract A description is provided for Eurotium rubrum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: A xerotolerant species with the same host range as E. repens (IMI Sheet 1255). DISEASES: Not known to be a pathogen of animals or man, but the species has been isolated from human nails (Smith, 1989). GEOGRAPHICAL DISTRIBUTION: World-wide.


Author(s):  
D. W. Minter

Abstract C. sphaerale is described and illustrated. Information on host range (Manilkara bidentata, insects and artefacts), geographical distribution (Japan; Ontario, Canada; Massachusetts, USA; and Puerto Rico), and transmission is provided.


Author(s):  
D. W. Minter

Abstract C. strumarium is described and illustrated. Information on diseases caused by C. strumarium, host range (field and horticultural crops, trees, dung, man and artefacts), geographical distribution (Algeria, Canary Islands, Democratic Republic of Congo, Egypt, Gambia, Kenya, Namibia, Nigeria, South Africa, Tanzania, USA, India, Nepal, Pakistan, Thailand, Western Australia, Germany, Great Britain, the Netherlands, Cyprus, Israel, Kuwait and Saudi Arabia), and transmission is provided.


Author(s):  
P. F. Cannon

Abstract A description is provided for P. liliacearum. Information on the transmission of the disease caused by the pathogen is included, along with details on geographical distribution (Alberta, Canada; New York and Pennsylvania, USA; Iran; Iraq; Austria; Belgium; Bulgaria; Czech Republic; Denmark; Finland; France; Germany; Hungary; Italy; Norway; Poland; Romania; mainland and Balearic Islands, Spain; Sweden; Switzerland; Ukraine; and England and Scotland, UK) and host range (Ornithogalum species, including O. amphibolum, O. collinum, O. fimbriatum, O. gussonei, O. montanum, O. narbonense, O. nutans, O. orthophyllum subsp. kochii, O. ponticum, O. pyramidale, O. pyrenaicum, O. refractum, O. sigmoideum and O. umbellatum).


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