scholarly journals Paraphoma Crown Rot of Pyrethrum (Tanacetum cinerariifolium)

Plant Disease ◽  
2016 ◽  
Vol 100 (12) ◽  
pp. 2363-2369 ◽  
Author(s):  
Azin Moslemi ◽  
Peter K. Ades ◽  
Tim Groom ◽  
Pedro W. Crous ◽  
Marc E. Nicolas ◽  
...  

Pyrethrum (Tanacetum cinerariifolium) is commercially cultivated for the extraction of natural pyrethrin insecticides from the oil glands inside seed. Yield decline has caused significant yield losses in Tasmania during the last decade. A new pathogen of pyrethrum causing crown rot and reduced growth of the plants in yield decline affected fields of northern Tasmania was isolated from necrotic crown tissue and described as Paraphoma vinacea. Multigene phylogenetic identification of the pathogen also revealed that P. vinacea was a new species different from other Paraphoma type strains. Glasshouse pathogenicity experiments showed that P. vinacea significantly reduced belowground and total biomass of pyrethrum plants 2 months after inoculation. Dull-tan to reddish-brown discoloration of the cortical and subcortical crown tissue was observed in 100% of the infected plants. P. vinacea infected 75% of the plants inoculated with root dip and soil drench inoculation techniques in an inoculation optimization experiment. P. vinacea, the causal agent of Paraphoma crown rot disease, represents an important pathogen that will negatively impact the commercial cultivation of pyrethrum in Tasmania.

Plant Disease ◽  
2008 ◽  
Vol 92 (8) ◽  
pp. 1253-1253 ◽  
Author(s):  
S. T. Koike

In 2006 and 2007, severely diseased strawberry (Fragaria × ananassa) plants were observed in five commercial fields in southern California (Orange County). Disease generally occurred in discrete patches. Within such patches, disease incidence ranged from 10 to 75%. Symptoms consisted of wilting of foliage, drying and death of older leaves, plant stunting, and eventual collapse and death of plants. When plant crowns were dissected, internal vascular and cortex tissues were dark brown to orange brown. Fruiting bodies or other fungal structures were not observed. A fungus was consistently isolated from symptomatic crown tissue that had been surface sterilized and placed on acidified corn meal agar (LA-CMA). All isolates produced numerous, dark, irregularly shaped sclerotia that were 67 to 170 μm long and 44 to 133 μm wide. When isolates were grown on 1.5% water agar with dried and sterilized wheat straw, dark, ostiolate pycnidia and hyaline, single-celled, cylindrical conidia were produced. On the basis of these characters, all isolates were identified as Macrophomina phaseolina (1). The symptomatic plants tested negative for Colletotrichum spp., Phytophthora spp., Verticillium dahliae, and other pathogens. Inoculum for pathogenicity tests was produced by growing six isolates on CMA on which sterilized wood toothpicks were placed on the agar surface. After 1 week, toothpicks were removed and inserted 4 to 5 mm deep into the basal crown tissue of potted strawberry plants (cv. Camarosa) grown in soilless, peatmoss-based rooting medium. Ten plants were inoculated per isolate and one toothpick was inserted per plant. Ten control strawberry plants were treated by inserting one sterile toothpick into each crown. All plants were then grown in a shadehouse. After 2 weeks, all inoculated plants began to show wilting and decline of foliage. By 4 weeks, all inoculated plants had collapsed. Internal crown tissue was discolored and similar in appearance to the original field plants. M. phaseolina was isolated from all inoculated plants. Control plants did not exhibit any disease symptoms, and crown tissue was symptomless. The test was repeated and the results were similar. While M. phaseolina has been periodically associated with strawberry in California (3), to my knowledge, this is the first report of charcoal rot disease on commercial strawberry in California. Charcoal rot of strawberry has been reported in Egypt, France, India, Israel, and the United States (Florida and Illinois) (2,4). Similar to previous reports (2,4), many of the affected California fields were not preplant fumigated with methyl bromide + chloropicrin fumigants, and it is possible that under these changing production practices this pathogen may increase in importance in California. References: (1) P. Holliday and E. Punithalingam. No. 275 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1970. (2) J. Mertely et al. Plant Dis.89:434, 2005. (3) S. Wilhelm. Plant Dis. Rep. 41:941, 1957. (4) A. Zveibil and S. Freeman. Plant Dis. 89:1014, 2005.


Plant Disease ◽  
1999 ◽  
Vol 83 (6) ◽  
pp. 589-589 ◽  
Author(s):  
S. T. Koike ◽  
D. M. Henderson ◽  
P. W. Crous ◽  
C. L. Schoch ◽  
S. A. Tjosvold

Heath (Erica capensis Salter) is a woody, evergreen plant used in Cali-fornia as a landscape shrub or ground cover. In 1997, a new root and crown disease was found in commercial nursery plantings of potted heath. A similar disease was found in 1998 on heath transplants being grown as liners. In both situations, roots were necrotic and crown tissue turned brown. Affected plants became gray-green in color, withered, and died. A Cylindrocladium species was consistently isolated from roots, crowns, and lower stems of symptomatic plants. Isolates were characterized by having penicillate conidiophores terminating in obpyriform to broadly ellipsoidal vesicles. Conidia were hyaline, 1-septate, straight with rounded ends, (30-) 45 to 55 (-60) × (3.5-) 4 to 5 μm, placing it in the Cylindrocladium candelabrum Viégas species complex. Ten single-conidial isolates produced perithecia with viable progeny of Calonectria pauciramosa C.L. Schoch & Crous when mated on carnation leaf agar with tester strains of Cylindrocladium pauciramosum C.L. Schoch & Crous (1). Matings with tester strains of all other species in this complex proved unsuccessful. Pathogenicity of 8 representative isolates was confirmed by applying 3 ml of a conidial suspension (3.0 × 105 conidia per ml) to the crowns of potted, 6-month-old, rooted heath cuttings that were subsequently maintained in a greenhouse (23 to 25°C). After 2 weeks, plant crowns and roots developed symptoms similar to those observed in the field, and plants later wilted and died. C. pauciramosum was reiso-lated from all plants. Control plants, which were treated with water, did not develop any symptoms. The tests were repeated and the results were similar. This is the first report of C. pauciramosum as a pathogen of heath, and the first record of this pathogen from North America. Reference: (1) C. L. Schoch et al. Mycologia 91:286, 1999.


Plant Disease ◽  
2005 ◽  
Vol 89 (9) ◽  
pp. 1012-1012
Author(s):  
S. T. Koike

Areca palm (Chrysalidocarpus lutescens) is a popular ornamental palm that can be grown outdoors in mild climates and is commonly used as an indoor ornamental plant. During 2005, commercial palm producers lost significant numbers of areca palm seedlings grown in transplant trays to a crown rot disease. Initial symptoms consisted of a light brown discoloration of stems near the soil line. As disease progressed, the brown discoloration extended up the stem and down into the crown, foliage became gray green, and the entire plant then dried up and died. Extensive, white, cottony mycelium and numerous sclerotia developed externally on the lower stem, crown, attached palm seed, and surrounding peat moss medium. Mycelial growth was so extensive that the fungus often grew from one transplant tray cell, bridged across the plastic cell border, and into an adjacent transplant cell. Tan, spherical sclerotia measured approximately 1 mm in diameter. Isolations from diseased plants resulted in the recovery of the same white fungus that produced sclerotia. On the basis of sclerotia morphology and the presence of clamp connections at hyphal septa, the fungus was identified as Sclerotium rolfsii. Pathogenicity was tested by growing isolates on potato dextrose agar, drying the resulting sclerotia for 48 h, and then depositing 8 to 10 sclerotia at the base of healthy areca palm seedlings. Five isolates were tested using 40 plants per isolate. Non-inoculated controls were also included. All plants were incubated in a greenhouse at 22 to 25°C. After 2 weeks, inoculated plants began to show brown necrosis at the base of the stems; by the third week, plants began to dry up, and mycelium and sclerotia developed on the crowns. S. rolfsii was reisolated from all necrotic crown and stem tissues. Noninoculated controls did not develop any disease symptoms. To my knowledge, this is the first report of southern blight of C. lutescens in California. This disease has been reported on areca palms and other foliage plants in the southern United States and Central and South America (1). Circumstantial evidence (the disease occurred on palm seedlings that were planted in previously unused transplant trays and new peat moss rooting medium) suggests that the pathogen may have been brought in on palm seed. In the nursery, other foliage plants that are susceptible to S. rolfsii were planted in the same rooting medium but were unaffected by southern blight. Reference: (1) A. R. Chase. Compendium of Ornamental Foliage Plant Diseases. The American Phytopathological Society. St. Paul, MN, 1987.


Plant Disease ◽  
2001 ◽  
Vol 85 (4) ◽  
pp. 448-448 ◽  
Author(s):  
S. T. Koike ◽  
P. W. Crous

Myrtle (Myrtus communis) is a woody, evergreen plant used in California as a landscape shrub or potted plant. In 2000, a new root and crown disease was found in commercial nursery myrtle being grown as potted plants. Roots were necrotic and crown tissue was brown. Affected plants became gray-green in color, withered, and died. A Cylindrocladium sp. was consistently isolated from roots, crowns, and lower stems of symptomatic plants. Isolates were characterized by having penicillate conidiophores terminating in obpyriform to broadly ellipsoidal vesicles. Conidia were hyaline, 1-septate, straight with rounded ends, (50-) 53 to 56 (-58) × (3.5-) 4 to 6 μm, placing it in the Cylindrocladium candelabrum Viégas species complex. Single-conidial isolates (STE-U 4012 to 4018) produced perithecia with viable progeny of Calonectria pauciramosa C.L. Schoch & Crous when mated on carnation leaf agar with tester strains of Cylindrocladium pauciramosum C.L. Schoch & Crous (2). Matings with tester strains of all other species in this complex proved unsuccessful. Only one mating type of C. pauciramosum has thus far been found in the United States. Pathogenicity of representative isolates was confirmed by applying 5 ml of a conidial suspension (1.0 × 106 conidia/ml) to the crowns of potted, 5-month-old, rooted mytle cuttings that were subsequently maintained in a greenhouse (23 to 25°C). After 4 weeks, plant crowns and roots developed symptoms similar to those observed in the nursery, and plants later wilted and died. C. pauciramosum was re-isolated from all plants. Control plants, which were treated with water, did not develop any symptoms. The tests were repeated and the results were similar. This is the first report of C. pauciramosum as a pathogen of myrtle in California. The disease has been reported on myrtle in Europe (1). References: (1) G. Polizzi and P. W. Crous. Eur. J. Plant Pathol. 105:407, 1999. (2) C. L. Schoch et al. Mycologia 91:286, 1999.


Author(s):  
Fanny B. Iriarte ◽  
Mathews L. Paret ◽  
Susannah Da Silva

On April 2017, four out of 10,000 Double Knock Out Red roses were observed presenting partially wilted and chlorotic foliage in a commercial nursery in Gadsden Co., Florida. Closer examination of the plant crown revealed brown discoloration of the woody tissue. Under high temperature (85°F) and humidity (70%), shoots progressively turned chlorotic and necrotic, leading to plant death in 4 months. A rapid-growing fungus presenting orange-brown mycelium and abundant cylindrical spores was isolated from infected woody crown tissue. BLAST analysis of the resulting sequence (GenBank no. MT019606) of this pathogen had 100% identity to Calonectria cylindrospora β-tubulin gene (GenBank no. FJ918509.1). Koch’s postulates were conducted on healthy Double Knock Out roses. Two weeks after inoculation, shoots of inoculated plants turned progressively chlorotic and then necrotic, leading to plant death in 2 months. The same pathogen was reisolated from infected plant parts, which sequence also had 100% identity to C. cylindrospora β-tubulin gene (GenBank no. FJ918509.1). This pathogen is the same as one of three isolated from crown rot of roses back in 1994 and identified as Cylindrocladium scoparium (teleomorph: C. cylindrospora [Ellis & Everh.]). In this new occurrence, all infected plants were removed from the nursery, and no further infections were detected. This finding is important for commercial growers to be aware of the potential presence of this pathogen in their nurseries. Knowing the symptoms will help them recognize the disease and take action to prevent spread of the disease.


Plant Disease ◽  
2002 ◽  
Vol 86 (9) ◽  
pp. 1051-1051 ◽  
Author(s):  
B. de los Santos ◽  
M. Porras ◽  
C. Blanco ◽  
C. Barrau ◽  
F. Romero

Crown rot of strawberry (Fragaria × ananassa Duch. cv. Camarosa) was observed in three and two production fields in 2000 and 2001, respectively, in Huelva, southwestern Andalucia, Spain. Affected plants did not exhibit typical symptoms of red stele. Instead, there was an internal red-brown discoloration of the upper crown, a bluish discoloration of leaves, and the plants were wilted. Eventually, plants collapsed and died. Fungi were isolated from surface-disinfested necrotic crown tissue on P5ARPH medium (1). Plates were placed at 21°C for 5 to 10 days. One species was isolated consistently from symptomatic tissue. Microscopic observations revealed spherical oogonia with thin walls. Antheridia were paragynous and were attached to the oogonium near the oogonial stalk. Single oospores were spherical and had double-layered, yellow-brown walls (20 to 25 μm in diameter). Sporangia were usually borne terminally and were colorless and papillate (22 to 30 μm in diameter). Based on these characteristics, the causal agent was identified as Phytophthora cactorum (Lebert & Cohn) J. Schröt. (2). The fungus was transferred to V8 juice agar and maintained at 21°C in the dark. Disks (9-mm diameter) were removed from 7-day-old cultures of P. cactoru and used to inoculate five 2-month-old ‘Camarosa’ strawberry plants grown in sterilized peat in the greenhouse. Three disks were placed in the crown of each plant at soil level. Five noninoculated plants were similarly treated with sterile V8 juice agar disks only. After 2 weeks, the pathogen was reisolated from red-brown lesions visible on crowns of all inoculated plants. Noninoculated plants did not show any symptoms. To our knowledge, this is the first report of P. cactorum attacking strawberry plants in Spain. References: (1) S. N. Jeffers and S. B. Martin. Plant Dis. 70:1038, 1986. (2) G. M. Waterhouse and J. M. Waterston. No. 111 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, UK, 1996.


2003 ◽  
pp. 427-433 ◽  
Author(s):  
R.E.M. Hernandéz-Valencia ◽  
R. López-Franco ◽  
J. Ruíz-Ordoñez ◽  
H. Ramirez-Rodriguez ◽  
A. Benavides-Mendoza

Agrikultura ◽  
2016 ◽  
Vol 27 (2) ◽  
Author(s):  
Luciana Djaya ◽  
Ineu Sulastrini ◽  
Iin Rusita

ABSTRACT Inoculation Techniques of Clavibacter michiganensis subsp. sepedonicus, the Cause of Bacterial Ring Rot Disease, on Potato (Solanum tuberosum L.). Clavibacter michiganensis subsp. sepedonicus, the cause of bacterial ring rot disease on potatoes, has been detected in potato fields in Pangalengan. To anticipate the spread of the pathogen, researches on the desease epidemiology are urgent to be carried out. Artificial inoculation techniques will be useful in the epidemiological studies. The objective of this reasearch was to evaluate some inoculation techniques, which are simple, cheap and fast in causing disease symptoms. The experiment was carried out at the laboratory and glasshouse of Balai Penelitian Tanaman Sayuran (Balitsa), Lembang. The experiment was arranged in the randomized block design with five treatments of inoculation technique and five replications. The treatments were (a) soaking wounded seed tubers in pathogen suspension, (b) soaking not wounded seed tubers in pathogen suspension, (c) pathogen suspension was injected into leaf axil, (d) pathogen suspension was injected into seed tubers, and (e) pathogen suspension was poured into the planting holes. The results showed that stabbing and soaking tubers in pathogen suspension caused the shortest incubation period (17 days after inoculation) and the highest disease incidence (60%). Keywords : Clavibacter michiganensis subsp. sepedonicus, Bacterial ring rot, Potatoes, Inoculation techniquesABSTRAKClavibacter michiganensis subsp. sepedonicus (Cms), penyebab penyakit busuk cincin bakteri pada tanaman kentang, telah terdeteksi keberadaannya pada pertanaman kentang di Pangalengan. Dalam upaya mencegah penyebaran penyakit busuk cincin bakteri di Indonesia, perlu adanya studi epidemiologi patogen tersebut. Pada penelitian epidemiologi akan diperlukan cara menginokulasi tanaman secara buatan. Tujuan dari penelitian ini adalah untuk mendapatkan teknik inokulasi buatan yang dapat menyebabkan periode inkubasi yang lebih singkat dan persentase kejadian penyakit busuk cincin bakteri paling tinggi pada tanaman kentang. Percobaan dilaksanakan di rumah kaca dan laboratorium penyakit Balai Penelitian Tanaman Sayuran (Balitsa), Lembang. Percobaan dirancang secara rancangan acak kelompok dengan lima perlakuan teknik inokulasi Cms dan lima ulangan, yaitu inokulasi dengan (a) merendam ubi benih yang telah dilukai dalam suspensi bakteri, (b) merendam ubi benih tanpa dilukai dalam suspensi bakteri, (c) suspensi bakteri ditusukkan pada ketiak daun tanaman kentang, (d) suspensi bakteri ditusukkan pada ubi benih, dan (e) suspensi bakteri disiramkan pada lubang tanam. Masing-masing ulangan terdiri dari lima tanaman. Hasil penelitian menunjukkan bahwa dari lima teknik inokulasi buatan yang dilakukan, inokulasi dengan melukai ubi benih dan merendamnya dalam suspensi patogen menghasilkanJurnal Agrikultura 2016, 27 (2): 66-71ISSN 0853-2885Teknik Inokulasi Buatan Clavibacter….67periode inkubasi tersingkat, yaitu 17 hari setelah inokulasi, dan persentase kejadian penyakit tertinggi yaitu sebesar 60%.Kata Kunci : Clavibacter michiganensis subsp. sepedonicus, Busuk cincin bakteri, Kentang, Inokulasi buatan


2021 ◽  
Vol 13 (1) ◽  
pp. 69-80
Author(s):  
Majida Hadi Mahdi Alsaady ◽  
Hussein Ali Salim ◽  
Rakib A. Al-ani ◽  
Hadi M. Aboud ◽  
Jamal Talib M Al Roubaie

In this study, the antagonistic effect of five bacteria genera namely Bacillus, Pseudomonas, Azotobacter, Azospirillum, and Streptomyces isolated from rhizosphere of wheat were evaluated against Fusarium graminearum as potential biocontrol agents in vitro. F. graminearum was molecularly diagnosed using the Polymerase chain reaction (PCR) technique. Each bacteria were tested for the production of catalase enzyme, oxidase enzyme, analysis of starch, analyze of gelatin, and the motility, where Azotobacter, Azospirillum, and Bacillus subtilis were positive for all tested. Fungal inhibition tests were performed by using the dual culture method and agar well diffusion technique. Among them, Streptomyces and Azospirillum exhibited potent inhibition to the growth of F. graminearum (72.14% and 66.42%) respectively, followed by B.pumillus, P.fluorescens, B. subtilis and Azotobacter ( 58.28%, 43.23%, 39.71% and 35.71%) respectively as compared with the control treatment (0.0%).The dry weight of the fungus biomass was decreased with bacteria P. fluorescens, Streptomyces sp, Azotobacter sp, Azospirillum sp, B. subtilis, and B. pumillus which reached (0.114, 0.103, 0.147, 0.101, 0.143, and 0.107 g) respectively compared to the control treatment that was 0. 665 g.


2020 ◽  
Author(s):  
N. L. Knight ◽  
B. Macdonald ◽  
C. Percy ◽  
M. W. Sutherland

AbstractHexaploid spring wheat (Triticum aestivum) may exhibit significant crown rot disease responses to infection by Fusarium pseudograminearum, with a range of susceptibility levels available in commercial cultivars. Dry conditions during grain-fill may lead to the expression of prematurely senescing culms, which typically fail to set grain. Assessment of hexaploid spring wheat plants exhibiting both non-senescent and prematurely senescent culms was performed using visual discolouration, Fusarium pseudograminearum biomass, vascular colonisation and quantification of wheat DNA in culm sections sampled at three different heights above the crown and at the peduncle. A comparison of these parameters at four time points from milk development, when senescent culms are first observed, to maturity was conducted. Samples from six commercial cultivars were collected in 2014 from Narrabri and Tamworth, New South Wales and Wellcamp, Queensland. Prematurely senescent culms exhibited greater visual discolouration, Fusarium pseudograminearum biomass and vascular colonisation than non-senescent culms in each cultivar. Colonisation of xylem and phloem tissue was extensive in the basal portions of prematurely senescent culms (36 to 99%), and suggests significant impacts on water and nutrient movement during crown rot disease. Maturation coincided with significant changes in Fusarium pseudograminearum biomass and vascular colonisation. Wheat DNA content varied among cultivars, culm conditions, culm sections and sampling times. The variation in the severity of disease states between culms of the same plant suggests that the timing of initiation of infection in individual culms may vary.


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