Xanthomonas campestris pv. sesami. [Descriptions of Fungi and Bacteria].

Author(s):  
J. F. Bradbury

Abstract A description is provided for Xanthomonas campestris pv. sesami. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Sesamum indicum (Pedaliaceae). DISEASE: Bacterial blight of sesame or simsim; known as 'Marad ed Dum' in the Sudan. Mainly a leaf spot disease, this starts as tiny dark olive green spots, which increase in size, becoming dark red-brown to black, and about 2-3 mm. They may be rounded or angular, and may coalesce to involve larger areas of leaf. Stems and capsules may also be infected, having oval, slightly raised, dark red-brown lesions. GEOGRAPHICAL DISTRIBUTION: Sudan and India (CMI Map 494, ed 2, 1973) to which must be added Venezuela, now confirmed (54, 524; 56, 2615). TRANSMISSION: Within a crop by water splash, wind-driven rain etc. ; from one area to another by seed transmission (47, 593). Survival in seed is up to 16 months (51, 400), in soil up to 6 months.

Author(s):  
A. Sivanesan

Abstract A description is provided for Mycosphaerella populorum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Populus spp. DISEASE: Septoria canker, leaf spot disease. GEOGRAPHICAL DISTRIBUTION: North America: USA (east and central states). South America: Argentina (CMI Distribution Map 540, 1981). TRANSMISSION: By windborne conidia and ascospores.


Author(s):  
D. W. Minter

Abstract A description is provided for Lophomerum ponticum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Rhododendron ponticum. DISEASE: Leaf spot of rhododendron. In general Lophomerum ponticum appears to be saprophytic. Its ascocarps are usually not produced until the leaves have senesced, become detached and fallen to the litter. Occasionally, however, ascocarps can be found on browned regions of otherwise green leaves, and it seems possible, therefore, that the species is facultatively parasitic. It is important to distinguish this species from Lophodermium vagulum (CMI Descriptions 789) which is the causal agent of a leaf spot disease of chinese rhododendrons, but which does not occur on R. ponticum. GEOGRAPHICAL DISTRIBUTION: Europe (Great Britain), probably much more widespread. TRANSMISSION: By air-borne ascospores in wet or humid weather.


Plant Disease ◽  
2008 ◽  
Vol 92 (7) ◽  
pp. 1134-1134 ◽  
Author(s):  
W. P. Wechter ◽  
A. P. Keinath ◽  
J. P. Smith ◽  
M. W. Farnham

Severe outbreaks of leaf spot disease of leafy vegetable brassica crops have occurred from early spring to late fall for at least the past 7 years in Lexington County, South Carolina, the major growing region for leafy greens in the state. Significant economic losses to this disease totaling $1.7 million have been incurred by large and small growers. In 2005, Pseudomonas syringae pv. maculicola was reported as one of the causal organisms of leaf spot disease in South Carolina (2). Investigations during 2006 and 2007 have led to the isolation of another bacterium causing leaf spotting of brassica crops. Symptoms in the field were nearly identical to symptoms caused by P syringae pv. maculicola, i.e., small, brown necrotic spots, often with chlorotic halos that expand and coalesce to cover the leaves. Colonies recovered from diseased tissues were xanthomonad like, nonfluorescent on Pseudomonas Agar F, mucoid on yeast extract dextrose chalk medium, grew at 35°C, hydrolyzed starch, positive for protein digestion, alkaline in litmus milk, and produce acid from arabinose. Sequence data from the 16S rDNA and fatty acid methyl ester analysis gave the best homology to Xanthomonas campestris pv. campestris with a similarity score index of >0.98 and >0.70, respectively, confirming genus and species. Excised-cotyledon assays, used to differentiate between pathovars campestris and armoraciae, confirmed the pathovar as campestris (1). Pathogenicity assays with spray inoculations (1 × 107 CFU/ml) (3) on eight plants each of ‘Topper’ and ‘Alamo’ turnip, ‘Early Jersey Wakefield’ cabbage, and ‘Money maker’ tomato produced leaf-spot symptoms within 10 days in the greenhouse and growth chamber on the turnip and cabbage plants, but not the tomato. X. campestris pv. campestris, which is common throughout the world, also is the causal agent of black rot in brassica. Typical black rot symptoms are seen often in Lexington County fields in summer and are quite different from the leaf spot symptoms observed. Leaf-spotting X. campestris pv. campestris (LS) strains and black rot (BR) strains, recovered from black rot-symptomatic plants lacking leaf spots, from the same fields were compared in greenhouse pathogenicity assays on six plants each of ‘Topper’ turnip and ‘Early Jersey Wakefield’ cabbage. Spray inoculations with 20 individual LS strains and 10 individual BR strains, collected from 2005 to 2007, produced symptoms unique to each group. These symptoms included chlorotic ‘V’-shaped lesions initiating from the leaf margins with black veining when plants were inoculated with BR strains, versus rapid and severe leaf spotting followed by chlorotic ‘V’-shaped lesions typically lacking black-veining 10 to 16 days postinoculation associated with LS strains. Additional inoculation tests gave similar results. To our knowledge, this is the first report of a severe leaf spotting disease of field-grown brassica leafy greens caused by X. campestris pv. campestris in South Carolina. These findings may have importance in differentiation of bacterial leaf spot pathogens in brassica crops. References: (1) A. M. Alvarez et al. Phytopathology 84:1449, 1994. (2) A. P. Keinath et al. Plant Dis. 90:683, 2006. (3) W. P. Wechter et al. Hortic Sci. 42:1140, 2007.


Author(s):  
J. F. Bradbury

Abstract A description is provided for Xanthomonas campestris pv. corylina. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Corylus avellana, C. maxima and C. rostrata (syn. C. californica). On inoculation C. colurna is also infected. DISEASE: Bacterial blight or bacteriosis of filbert or hazel nut trees. Leaf spots, bud and twig necroses and stem cankers are produced. The cankers may girdle branches or even trunks of young trees and cause death above. GEOGRAPHICAL DISTRIBUTION: Turkey (Black Sea area 54, 578), Australia (Vict. 60, 6677), England (59, 3913), France (56, 86), Italy (64, 4520), Yugoslavia (37: 125), USA (OR, WA), Chile (culture received at CMI), and apparently USSR (58, 4044). TRANSMISSION: Bacteria overwinter in cankers on branches and in buds, and spread to other parts of the tree in wet weather. Limited spread from tree to tree takes place by water splash. Man is an important vector especially during pruning activities on young trees. He is also responsible for the introduction of the disease into new areas.


Plant Disease ◽  
2015 ◽  
Vol 99 (2) ◽  
pp. 282-282 ◽  
Author(s):  
J. Cruz ◽  
R. Tenreiro ◽  
L. Cruz

Representing over 25% of the vegetable production, Brassicaceae crops are very important for Portuguese agriculture. Xanthomonas campestris pv. raphani (Xcr) was first described as the causative agent of a leaf spot disease affecting radish and turnip (4). Despite its ability to infect Solanaceae hosts upon inoculation, this pathogen affects mostly Brassicaceae plants. Typical symptoms include circular dark spots that become lighter and are occasionally surrounded by a chlorotic halo. In severely affected leaves, spots were not limited by the veins and coalesced into irregular shapes that perforated the leaves, rendering the plants unsuitable for marketing. In the early 2000s, several isolates causing leaf spots on Brassica oleracea varieties (cauliflower, white cabbage, savoy cabbage, and tronchuda cabbage) were collected in Sintra, near Lisbon. The isolates, identified as putative X. campestris (Xc), formed typical yellow mucoid and convex colonies when grown on YDC medium. Biochemical characterization (2) showed their ability to produce levan and hydrolyze starch and esculin. Isolates were also able to use celobiose, trehalose, glucose, mannose, raffinose, and sucrose. Furthermore, the isolates were oxidase negative and were unable to hydrolyze arginine and to use rhamnose, indol, inositol, and sorbitol, confirming them as Xc. The expected 619-bp amplicon was obtained for all isolates, after PCR using primers DLH120/DLH125 (1). Koch's postulates were fulfilled through pathogenicity tests on B. oleracea cv. Wirosa and Raphanus sativus, hosts susceptible to Xcr as well as to X. campestris pv. campestris (Xcc). Inoculations on B. carinata (Assession No. PI199947) and Solanum lycopersicum, hosts susceptible only to Xcr, were performed to confirm pathovar identification (2). Four plants of each host were inoculated with each isolate by spraying bacterial water suspensions (OD600 = 0.1) onto leaf surfaces. Positive and negative controls were performed using Xcc type strain (CFBP 5241) and sterile distilled water, respectively. Plants were kept 15 days with 16-h light and 8-h dark photoperiods at 24 and 18°C, respectively, at RH >80% and checked daily for symptom development. Leaf spots typical of Xcr were observed for all isolates on all hosts 5 days after inoculation. All isolates were recovered after re-isolation from inoculated plants, retaining their initial features. Negative control plants showed no symptoms, while CFBP 5241 caused V-shaped lesions, typical of Xcc, on B. oleracea cv. Wirosa and R. sativus. Further confirmation of the identification was attained by partial sequencing of the gyrB gene, using primers X.gyr.fsp.s1/X.gyr.rsp3 (3). Sequences from four isolates (CPBF 143, Genbank KM094906; CPBF 207, GenBank KM094907; CPBF 209, GenBank GU596416; and CPBF 1171, GenBank GU596419) were compared by nucleotide blast at NCBI and displayed higher levels of DNA similarity (>98%) to NCPPB 1946, the type strain for Xcr, than to NCPPB 528, the type strain for Xcc. The polyphasic approach combining phenotypic and genomic data confirmed the presence of X. campestris pv. raphani in Portugal for the first time. References: (1) T. Berg et al. Plant Pathol. 54: 416, 2005. (2) R. Lelliot and D. Stead. Methods for the Diagnosis of Bacterial Diseases of Plants. Blackwell Scientific Publications, Oxford, England, 1987. (3) N. Parkinson et al. Int. J. Syst. Evol. Microbiol. 57:2881, 2007. (4) H. White. Phytopathology 20:653, 1930.


Author(s):  
J. F. Bradbury

Abstract A description is provided for Pseudomonas andropogonis[Burkholderia andropogonis]. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Sorghum vulgare[Sorghum bicolor] and its vars. sudanense, technicum, saccharatum, S. halepense and unspecified grain and grass varieties of Sorghum, Zea mays, Bougainvillea sp., Mucuna deeringiana, Trifolium repens, T. pratense, Euchlaena mexicana and Vicia saliva. The following have been infected artificially: Medicago sativa, Viciafaba, Trifolium subterraneum by spray inoculation, and Dolichos lablab, Lespedeza sp., Phaseolus vulgaris (Allen et al. ; 36, 408) and Saccharum officinarum (Elliott & Smith, 1929) after injury. DISEASE: Bacterial stripe of sorghum, bacterial leaf spot or blight of velvet bean, vetch and other legumes. usually a leaf spot disease. On species of Sorghum spots and stripes on leaves and sheaths vary in colour from reddish or purplish-brown to tan or brick red, depending on host reaction. On legumes the spots are usually small, angular, dark brown to dark reddish-brown or nearly black. Stem lesions are extensive in vetch, where they can result in death progressively from the base. GEOGRAPHICAL DISTRIBUTION: Argentina, Brazil, USA, Rhodesia, Uganda, Zambia, South Africa, Nigeria, Hungary, USSR, China, Australia (NSW), Japan, Taiwan (CMI Map 495, ed. 1, 1973). TRANSMISSION: In the field transmission is by wind and rain and can lead to very rapid development of the disease if conditions remain humid. Overwintering is thought to take place in plant debris, in soil and possibly in weed hosts (42, 194). There is some observational evidence for seed transmission in Sorghum (Elliott & Smith, 1929) and in Mucuna (Allen et al, 1970). This would explain the very scattered distribution. With Bougainvillea, when the new wet season starts, the young growth is infected by rain splash from old infected leaves that have lasted over from the previous wet season, either attached or on the ground.


2006 ◽  
Vol 96 (7) ◽  
pp. 735-745 ◽  
Author(s):  
J. G. Vicente ◽  
B. Everett ◽  
S. J. Roberts

Twenty-five Xanthomonas isolates, including some isolates received as either X. campestris pv. armoraciae or pv. raphani, caused discrete leaf spot symptoms when spray-inoculated onto at least one Brassica oleracea cultivar. Twelve of these isolates and four other Xanthomonas isolates were spray- and pin-inoculated onto 21 different plant species/cultivars including horseradish (Armoracia rusticana), radish (Raphanus sativus), and tomato (Lycopersicon esculentum). The remaining 13 leaf spot isolates were spray-inoculated onto a subset of 10 plant species/cultivars. The leaf spot isolates were very aggressive on several Brassica spp., radish, and tomato causing leaf spots and dark sunken lesions on the middle vein, petiole, and stem. Based on the differential reactions of several Brassica spp. and radish cultivars, the leaf spot isolates were divided into three races, with races 1 and 3 predominating. A differential series was established to determine the race-type of isolates and a gene-for-gene model based on the interaction of two avirulence genes in the pathogen races and two matching resistance genes in the differential hosts is proposed. Repetitive-DNA polymerase chain reaction-based fingerprinting was used to assess the genetic diversity of the leaf spot isolates and isolates of closely related Xanthomonas pathovars. Although there was variability within each race, the leaf spot isolates were clustered separately from the X. campestris pv. campestris isolates. We propose that X. campestris isolates that cause a nonvascular leaf spot disease on Brassica spp. should be identified as pv. raphani and not pv. armoraciae. Race-type strains and a neopathotype strain for X. campestris pv. raphani are proposed.


Plant Disease ◽  
2003 ◽  
Vol 87 (7) ◽  
pp. 873-873 ◽  
Author(s):  
K. Pernezny ◽  
J. B. Jones ◽  
P. D. Roberts ◽  
E. Dickstein

From October to December 2001, a leaf spot disease was observed in numerous commercial fields of red and green cabbage (Brassica oleracea var. capitata L.) in the Everglades Agricultural Area, south and east of Lake Okeechobee and in the environs of Immokalee in southwestern Florida. Discrete water-soaked to greasy appearing spots were observed in the leaf blades with no evidence of marginal V-shaped lesions characteristic of black rot caused by Xanthomonas campestris pv. campestris. Profuse bacterial streaming was observed when cut leaf sections were examined microscopically. A bacterium that formed yellow colonies on nutrient agar was consistently isolated from these lesions. Ten bacteria were isolated, purified, and characterized. All strains were aerobic, gram-negative rods. Strains were positive for esculin hydrolysis, proteolysis in litmus milk, and gelatin liquefaction. Strains were negative for urease production, nitrate reduction, oxidase, and utilization of asparagine as a sole source of carbon and nitrogen. Fatty acid methyl ester analysis indicated a match with Florida library strains of X. campestris pv. raphani (similarity indices 0.605–0.738). Suspensions (2 × 107 CFU/ml in phosphate-buffered saline) of two Oklahoma strains identified as X. campestris pv. armoraciae provided by J. P. Damicone (3) and four representative Florida strains were applied to plants using a hand-held sprayer. Pathogenicity of the strains was tested on three replicate greenhouse-grown plants of the following: green cabbage cv. Market Early; red cabbage cv. Salad Delight; radish cv. Red Silk; tomato cv. Sunny; sweet bell pepper cv. Jupiter; and fresh horseradish roots purchased from a retail grocery chain. A strain of X. campestris pv. campestris originally isolated from Homestead, FL was also included in pathogenicity tests. All Florida and Oklahoma strains produced leaf spots, but no V-shaped lesions, on leaves of green cabbage, red cabbage, radish, tomato, and horseradish. Typical black rot symptoms were observed only in radish and green and red cabbage inoculated with the X. campestris pv. campestris strain. On the basis of these results, we identify the Florida strains as X. campestris pv. armoraciae (1,2,3), recognizing the precedent of X. campestris pv. armoraciae over X. campestris pv. raphani based on extensive genetic and serological data (1). Our strains appear to be more similar to those causing outbreaks on crucifers in Oklahoma (3) than those in Ohio (2), because Florida strains were pathogenic on tomato. References: (1) A. M. Alvarez et al. Phytopathology 84:1449, 1994. (2) F. Sahin and S. A. Miller. Plant Dis. 81:1334, 1997. (3) Y. Zhao et al. Plant Dis. 84:1008, 2000.


Author(s):  
E. Punithalingam

Abstract A description is provided for Didymella bryoniae. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Cucurbits (Bryonia, Colocynthis, Cucumis, Cucurbita, Luffa, Momordica and Trichosanthes). DISEASE: Gummy stem blight of Cucurbitaceae, showing a variety of symptoms which are referred to as leaf spot, stem canker, vine wilt and black fruit rot. Lesions on leaves and fruit usually begin as spreading water-soaked areas; in the former these may have a chlorotic halo, become light brown and irregular in outline, leaves can be destroyed. On fruit, dark cracked sunken lesions form, beneath which an extensive rot is found. In the field the first symptoms may be plant collapse where sunken, girdling cankers lead to total loss. Infection also occurs on seedlings. The main characteristic features are the gummy exudate on stem and fruit lesions and the abundant pycnidia followed by perithecia, GEOGRAPHICAL DISTRIBUTION: Widespread (CMI Map 450, ed. 2, 1970). Records not yet mapped are: Brunei, Mexico, Netherlands, Pitcairn Islands, Republic of Ireland, Salvador. TRANSMISSION: Through conidia by water splash and aerially by ascospores which, in glasshouses in England, had a diurnal periodicity with a peak at 1800-2000 hr (46, 825; 48, 672); and in USA occurred mostly at night (50, 2621). Both spore types may serve as primary inoculum and between-crop survival is an important factor in the epidemiology. Reports on seed transmission are conflicting in cucumber, although seed could be inoculated successfully, no evidence for natural infection was found (48, 322). In the glasshouse transmission by pruning knives has been demonstrated (46, 825).


Author(s):  
P. W. Crous

Abstract A description is provided for Mycosphaerella parkii. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Eucalyptus grandis, E. saligna, E. globulus. DISEASE: Associated with a serious leaf spot disease of Eucalyptus in Brazil (72, 5535). GEOGRAPHICAL DISTRIBUTION: Brazil, Indonesia. TRANSMISSION: Spores are wind-borne.


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