scholarly journals FIRST NOTICE OF PHYTOPHTHORA CROWN AND ROOT ROT OF EUPHORBIA PULCHERRIMA IN POLISH GREENHOUSES

2013 ◽  
Vol 53 (4) ◽  
pp. 307-311 ◽  
Author(s):  
Leszek B. Orlikowski ◽  
Magdalena Ptaszek

Abstract The plant pathogen, Phytophthora cryptogea, was recovered from 4/5 of the 75 poinsettias collected from two greenhouse farms. The poinsettias showed stunting and wilting as well as stem base and root rot symptoms. Representative isolates of the species from two poinsettia cultivars, colonized stem parts, leaf petioles, leaf blades and root parts. Stem parts of 6 cultivars were colonized at a slower rate than other poinsettia organs. Isolate from Euphorbia pulcherrima also colonized stem parts and leaf blades of E. amygdaloides, E. cyparissias, and E. polychroma. Isolates of P. cryptogea from the other 6 plant hosts, colonized the overground parts of poinsettia cv. Allegro. This is the first report describing symptoms and colonization of poinsettia cultivars by P. cryptogea in Poland.

Plant Disease ◽  
2017 ◽  
Vol 101 (6) ◽  
pp. 1038 ◽  
Author(s):  
J. Beckerman ◽  
H. Nisonson ◽  
N. Albright ◽  
T. Creswell

Plant Disease ◽  
2021 ◽  
Author(s):  
Yaxing Li ◽  
Yangfan Feng ◽  
Cuiping Wu ◽  
Junxin Xue ◽  
Binbin Jiao ◽  
...  

During a survey of pathogenic oomycetes in Nanjing, China from June 2019 to October 2020, at least ten adjacent Rhododendron pulchrum plants at a Jiangjun Mountain scenic spot showed symptoms of blight, and crown and root discoloration . Symptomatic root tissues collected from three 6-year-old plants were rinsed with water, cut into 10-mm pieces, surface sterilized with 70% ethanol for 1 min, and plated onto 10% clarified V8 PARP agar (cV8A-PARP) containing pimaricin (20 mg/liter), ampicillin (125 mg/liter), rifampicin (10 mg/liter), and pentachloronitrobenzene (20 mg/liter). Four Pythium-like isolates were recovered after three days of incubation at 26°C, and purified using hyphal-tipping. Ten agar plugs (2×2 mm2) of each isolate were grown in 10 mL of 10% clarified V8 juice (cV8) in a 10 cm plate at 26°C for 3 days to produce mycelial mats, and then the cV8 was replaced with sterile water. To stimulate sporangial production, three to five drops of soil extract solution were added to each plate. Sporangia were terminal, ovoid to globose, and the size is 24 to 45.6 (mean 34.7) (n=10.8) in length x 23.6 to 36.0 (mean 29.8) (n=6.2) in width. Gametangia were not observed in cV8A or liquid media after 30 days. For colony morphology, the isolates were sub-cultured onto three solid microbial media (cV8A-PARP, potato dextrose agar, corn meal agar) . All isolates had identical morphological features in the three media. Complete ITS and partial LSU and cox2 gene regions were amplified using primer pairs ITS1/ITS4, NL1/NL4, and FM58/FM66 , respectively. The ITS, LSU, and cox2 sequences of isolate PC-dj1 (GenBank Acc. No. MW205746, MW208002, MW208003) were 100.00% (936/936 nt), 100.00% (772/772 nt), and 99.64% (554/556 nt) identical to those of JX985743, MT042003, and GU133521, respectively. We built a maximum-likelihood tree of Phytopythium species using the concatenated dataset (ITS, LSU, cox2) to observe interspecific differences. Based on the morphological characters and sequences, isolate PC-djl was identified as Phytopythium litorale . As the four isolates (PC-dj1, PC-dj2, PC-dj3 and PC-dj4) tested had identical morphological characters and molecular marker sequences, the pathogenicity of the representative isolate, PC-dj1, was tested using two inoculation methods on ten one-year-old R. pulchrum plants. For the first inoculation method, plants were removed from the pot, and their roots were rinsed with tap water to remove the soil. Each of these plants was placed in a glass flask containing 250 mL of sterile water and 10 blocks (10 x 10 mm2) of mycelial mats harvested from a three-day-old culture of P. litorale, while the other plant was placed in sterile water as a control, and incubated at 26°C. After three days, symptoms including crown rot, root rot and blight was observed on the inoculated plants whereas the control remained asymptomatic. For the second inoculation method, ten plants were dug up to expose the root ball. Ten three-day-old cV8A plugs (5×5 mm2) from a PC-dj1 culture or sterile cV8A plugs were evenly insert into the root ball of a plant before it was planted back into the original pots. Both plants were maintained in a growth chamber set at 26°C with a 12/12 h light/dark cycle and irrigated as needed. After 14 to 21 days, the inoculated plant had symptoms resembling those in the field , while the control plant remained asymptomatic. Each inoculation method was repeated at triplicate and the outcomes were identical. Phytopythium isolates with morphological features and sequences identical to those of PC-dj1 were recovered from rotted crown and root tissues of all inoculated plants. Previously, P. litorale was found causing diseases of apple and Platanus orientalis in Turkey, fruit rot and seedling damping-off of yellow squash in southern Georgia, USA. This is the first report of this species causing crown and root rot on R. pulchrum, an important ornamental plant species in China. Additional surveys are ongoing to determine the distribution of P. litorale in the city of Nanjing.


2020 ◽  
Vol 102 (4) ◽  
pp. 1353-1353
Author(s):  
Dalia Aiello ◽  
Alberto Fiorenza ◽  
Giorgio Gusella ◽  
Giancarlo Polizzi

Plant Disease ◽  
2009 ◽  
Vol 93 (2) ◽  
pp. 204-204 ◽  
Author(s):  
D. Aiello ◽  
A. Vitale ◽  
E. Lahoz ◽  
R. Nicoletti ◽  
G. Polizzi

Murraya paniculata (L.) Jack, commonly called orange jessamine or orange jasmine (Rutaceae), is a small tropical tree that is native to Asia. This species, closely related to Citrus, is grown as an ornamental tree or hedge. During October of 2007, crown and root rot was observed on approximately 12,000 pot-grown, 4-month-old plants in a nursery in eastern Sicily, Italy. Basal leaves turned yellow and gradually became necrotic, and infected plants often died. Disease symptoms were observed on 1,800 (15%) plants. Isolations from affected tissues on potato dextrose agar (PDA) amended with streptomycin sulfate at 100 mg/liter recovered a fungus with mycelial and morphological characteristics consistent with Rhizoctonia solani Kühn. Fungal colonies were initially white, turned brown with age, and produced irregularly shaped, brown sclerotia. Microscopic examination revealed that hyphae had a right-angle branching pattern, were constricted at the base of the branch near the union with main hyphae, and were septate near the constriction. The nuclear condition of hyphal cells was determined on cultures grown at 25°C on 2% water agar (WA) when stained with 3% safranin O solution and examined at ×400. Anastomosis groups were determined by pairing isolates on 2% WA in petri plates (4). Pairings were made with tester strains AG-1 IA, AG-2-2-1, AG-2-2IIIB, AG-2-2IV, AG-3, AG-4, AG-5, AG-6, and AG-11. Anastomosis was observed only with tester isolates of AG-4 producing both C2 and C3 reactions. The hyphal diameter at the point of anastomosis was reduced, the anastomosis point was obvious, and cell death of adjacent cells was observed. These results were consistent with other reports on anastomosis reactions (1). The identification of group AG-4 within R. solani has been confirmed by electrophoretic patterns of pectic enzymes (polygalacturonases) in vertical pectin-acrylamide gel stained with ruthenium red (2). Pathogenicity tests were conducted on potted, healthy, 6-month-old seedlings of orange jessamine. Twenty-five plants were inoculated by placing 1-cm2 PDA plugs from 5-day-old mycelial cultures near the base of the stem. The same number of plants inoculated with PDA plugs served as controls. Plants were maintained at 25°C and 95% relative humidity on a 12-h fluorescent light/dark regimen. Wilt symptoms, identical to ones observed in the nursery, developed 3 months after inoculation because of crown and root rot. Control plants remained disease free. The pathogen was reisolated from symptomatic tissues, completing Koch's postulates. Collar rot due to R. solani was previously detected on M. koenigii (3). To our knowledge, this is the first report of R. solani causing disease on M. paniculata. References: (1) D. E. Carling. Page 37 in: Grouping in Rhizoctonia solani by Hyphal Anastomosis Reactions. Kluwer Academic Publishers, the Netherlands, 1996. (2) R. H. Cruickshank and G. C. Wade. Anal. Biochem. 107:177, 1980. (3) A. C. Jain and K. A. Mahmud. Rev. Appl. Mycol. 32:460, 1953. (4) C. C. Tu and J. W. Kimbrough. Mycologia 65:941, 1973.


Plant Disease ◽  
2018 ◽  
Vol 102 (10) ◽  
pp. 2045-2045 ◽  
Author(s):  
J. Beckerman ◽  
J. Stone ◽  
G. Ruhl ◽  
T. Creswell

Plant Disease ◽  
2000 ◽  
Vol 84 (5) ◽  
pp. 593-593 ◽  
Author(s):  
G. S. Karaoglanidis ◽  
D. A. Karadimos ◽  
K. Klonari

A severe rot of sugar beet roots was observed in the Amyndeon area of Greece during summer 1998. Infected plants initially showed a temporary wilt, which became permanent, and finally died. Slightly diseased roots showed necrotic spots toward the base, whereas more heavily diseased roots showed a more extensive wet rot that extended upward. Feeder roots also were infected and reduced in number because of decay. Rotted tissue was brown with a distinguishing black margin. In most of the isolations, carried out on potato dextrose agar (PDA), the pathogen obtained was identified as Phytophthora cryptogea Pethybr. & Lafferty Mycelium consisted of fairly uniform, fine hyphae that showed a slightly floral growth pattern. In autoclaved soil-extract medium, chains or clusters of hyphal swellings (average 12 µm diameter) formed. Sporangia were not produced on solid media but were abundant in soil-extract medium. Sporangia were oval to obpyriform in shape, nonpapillate with rounded bases, and varied in size (39 to 80 × 24 to 40 µm). Oospores were plerotic, thick-walled, and averaged 25 µm in diameter. The isolated pathogen, cultured on PDA, could not grow at all at 36°C. The closely related species P. drechsleri Tucker has been reported to cause similar root rot symptoms on sugar beet (3). However, P. drechsleri grows well at 36°C, while P. cryptogea cannot grow at this temperature; this is the major distinguishing feature that separates the two species (1). To test the pathogenicity of the organism, surface-sterilized sugar beet roots (cv. Rizor) were inoculated with 5-mm-diameter PDA plugs containing actively growing mycelium. Sterile PDA plugs were used to inoculate control sugar beet roots. Inoculated roots were kept at 27°C in the dark for 10 days. Extensive decay of inoculated roots developed, similar to decay observed in the field, whereas control roots showed no decay. P. cryptogea was reisolated from rotted tissues. This pathogen has been recognized previously as a cause of root rot of sugar beet in Japan (1) and Wyoming (2). This is the first report of Phytophthora root rot of sugar beet in Greece. References: (1) D. C. Erwin and O. K. Ribeiro. 1996. Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN. (2) P. C. Vincelli et. al. Plant Dis. 74:614, 1990. (3) E. D. Whitnew and J. E. Duffus, eds. 1986. Compendium of Beet Diseases and Insects. The American Phytopathological Society, St. Paul, MN.


Plant Disease ◽  
2002 ◽  
Vol 86 (6) ◽  
pp. 697-697
Author(s):  
M. L. Molinero-Ruiz ◽  
J. M. Melero-Vara

In 2001, sunflower (Helianthus annuus L.) plants with symptoms of stem and root rot and wilt were observed in Soria, Spain. Light brown, water-soaked lesions developed on the collar of infected plants and extended along the stem, affecting the pith and causing early and sudden wilt. White mycelium and sclerotia (0.5 to 2 mm long) formed in the pith of stems. The sclerotia were disinfested in NaClO (10% vol/vol) for 1 min, transferred to potato dextrose agar (PDA), and incubated at 20°C. The fungus consistently obtained was identified as Sclerotinia minor Jagger (1). Pathogenicity was confirmed in a greenhouse experiment (15 to 25°C, 13 h light). Seven-week-old plants of six genotypes of sunflower (‘Peredovik’, HA89, HA821, HA61, RHA274, and HA337) were inoculated by placing one PDA disk with active mycelial growth adjacent to each basal stem just below the soil line and covering it with peat/sand/silt (2:2:1, vol/vol). Six plants of each genotype were inoculated without wounding, and another six were inoculated immediately after stem base wounding with a scalpel; six wounded and uninoculated plants were used as controls. First symptoms (wilting) appeared 4 days after inoculation in all genotypes. Two weeks after inoculation, the percentage of dead plants ranged from 33 to 92% (depending on cultivar), white mycelium was observed at the base of affected plants, and sclerotia were present in the pith of diseased plants. There was no effect of plant wounding on disease incidence or severity, and the fungus was reisolated from inoculated plants. To our knowledge, this is the first report of S. minor in Spain. Reference: (1) L. M. Kohn. Mycotaxon IX 2:365, 1979.


Plant Disease ◽  
2015 ◽  
Vol 99 (12) ◽  
pp. 1864 ◽  
Author(s):  
S. T. Koike ◽  
O. Daugovish ◽  
S. C. Kirkpatrick ◽  
P. M. Henry ◽  
T. R. Gordon

2019 ◽  
Vol 101 (4) ◽  
pp. 1249-1249
Author(s):  
Wassim Yezli ◽  
Nisserine Hamini-Kadar ◽  
Nebia Zebboudj ◽  
Laurence Blondin ◽  
Didier Tharreau ◽  
...  

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