scholarly journals Occurrence of Stem Rot of Chrysanthemum Caused by Sclerotinia sclerotiorum in Argentina

Plant Disease ◽  
2003 ◽  
Vol 87 (1) ◽  
pp. 98-98 ◽  
Author(s):  
E. R. Wright ◽  
H. E. Palmucci

Chrysanthemum (Dendranthema × grandiflorum (Ramat.) Kitam.) is one of the most popular flowering plants in Argentina. A previously undescribed stem rot disease was observed in cvs. Alba and Palisade in greenhouses near Buenos Aires and La Plata, an area of intensive floriculture production. The stem was killed within 10 to 15 days causing the plant to wilt and die. Necrotic tissues were covered with whitish mycelium that produced black, irregular shaped (3 to 7 mm diameter) sclerotia. The pathogen was isolated from symptomatic stem sections, surface disinfested for 1 min in 2% NaOCl, and plated on potato dextrose agar (PDA) (1, slightly modified). The organism isolated produced white aerial mycelia and large number of sclerotia characteristic of Sclerotinia sclerotiorum (Lib.) de Bary. Symptoms were reproduced in the greenhouse by inoculating stems of 10 3-month-old plants with five mycelial plugs per plant from 7-day-old PDA cultures. Inoculated plants were enclosed in transparent plastic bags for 6 days with near saturation humidity and incubated in a growth chamber at 22 to 24°C with a 12-h photoperiod. Control plants were treated similarly except agar disks did not contain the fungus. After 6 to 9 days, symptoms were similar to those previously observed, and infected plants died 3 weeks after inoculation. No disease symptoms were observed on uninoculated plants. Koch's postulates were satisfied after reisolating the fungus. To our knowledge, this is the first report of the occurrence of white mold caused by S. sclerotiorum on chrysanthemum in Argentina. The disease has been previously observed in Argentina on lisianthus (Eustoma grandiflora (Raf.) Shinn.) in 1988 (2) and on carnation (Dianthus caryophyllus L.) in 1991, among other floriculture crops of economic importance. References: (1) A. Garibaldi et al. Plant Dis. 85:446, 2001. (2) S. Wolcan et al. Plant Dis. 80:223, 1996.

Plant Disease ◽  
2005 ◽  
Vol 89 (5) ◽  
pp. 530-530 ◽  
Author(s):  
S. Gaetán ◽  
M. Madia

Canola (Brassica napus) was introduced as an alternative crop for wheat in Argentina. During 2003, typical symptoms of stem rot disease were observed on canola plants in two commercial fields located at Bragado, in northern Buenos Aires Province in Argentina. Average disease incidence across four canola cultivars was 21% (range = 13 to 29%). Symptoms included chlorosis and wilting of foliage and necrosis of basal stems. The disease appeared singly or in patches consisting of 4- to 5-month-old plants. The first visible symptom noticed was chlorosis and wilting of the foliage beginning from the basal leaves. Infection of the main stem at ground level typically was followed by a grayish white discoloration that progressed above the soil line to the apex. In advanced stages of the disease, stems and branches became bleached and eventually died. Black and irregularly shaped sclerotia (average size 5.5 × 2.8 mm) inside necrotic stem tissue were the typical signs of the pathogen. From September to October 2003, four samples consisting of six affected plants per sample were arbitrarily collected from two commercial fields located at Bragado. Sclerotia were taken from diseased stems, dipped in 70% ethanol, surface sterilized with 1% sodium hypochlorite for 1 min, and rinsed in sterile water. Each sclerotium was blotted dry on sterile Whatman's filter paper and placed on potato dextrose agar. Plates were incubated in the dark at 25°C for 2 to 3 days, followed by incubation under 12-h NUV light/12-h dark for 6 to 8 days. Six resulting colonies were identified as Sclerotinia sclerotiorum (Lib.) de Bary on the basis of taxonomic characteristics of the plant pathogenic species of Sclerotinia (3). Koch's postulates for three fungal isolates from infected plants were carried out on 6-week-old canola plants (cvs. Eclipse, Impulse, Master, and Mistral) by placing a colonized agar disk into wounds made in the basal stem region with a sterile scalpel. Pathogenicity tests, which included five inoculated and three control plants potted in a sterilized soil mix (soil/sand, 3:1), were conducted in a greenhouse at 23 to 26°C and 75% relative humidity with no supplemental light. Characteristic symptoms identical to the original observations developed within 12 days after inoculation on 100% of the inoculated plants for three isolates. Symptoms included wilted foliage, collapsed plants, and plant death. White mycelium and sclerotia developed on infected tissues, and the pathogen was successfully reisolated from symptomatic plants in all instances. Control plants, which were treated similarly except that the agar disk did not contain fungal growth, remained healthy. The experiment was repeated, and the results were identical to the first inoculations. Canola stem rot disease incited by S. sclerotiorum was first reported in Argentina during 1995 at experimental field plots in Buenos Aires. S. sclerotiorum, which has been reported to cause disease in canola in Canada (2) and the United States (1,4), currently represents a serious problem to the main canola cultivars grown in Argentina. To our knowledge, this is the first report of the occurrence of S. sclerotiorum causing a high incidence of stem rot in commercial crops of canola in Argentina. References: (1) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St. Paul, MN, 1989. (2) L. B. Jamaux et al. Plant Pathol. 44:22, 1995. (3) L. M. Kohn. Phytopathology 69:881, 1979. (4) D. V. Phillips et al. Phytopathology 92:785, 2002.


Plant Disease ◽  
1997 ◽  
Vol 81 (9) ◽  
pp. 1093-1093 ◽  
Author(s):  
K. F. Chang ◽  
R. J. Howard ◽  
R. G. Gaudiel ◽  
S. F. Hwang

Purple coneflower (Echinacea purpurea (L.) Moench; Asteraceae), a perennial herb originating from North America, is used as a garden ornamental and is grown commercially for use in medicinal preparations as an immunostimulant. In October 1996, a previously undescribed stem rot disease was observed in a research plot of 6-month-old echinacea plants at Brooks. Seedlings had been raised in small rockwool cubes (2 × 2 × 5 cm3) in a greenhouse, then transplanted into the field in early June. By late August, dead and dying plants were observed throughout the stand. They had dark brown to black stem lesions above and at the soil level and dead leaves with bleached petiole lesions that extended ca. 15 cm above the axil. Diseased stems and petioles often disintegrated, leaving only fibrous tissues intact. Roots were rotted and black. Superficial white mycelium developed over the basal part of affected stems. Black, oblong to irregular-shaped sclerotia, 5.1 to 17.6 mm in size, formed externally on the crown areas after plant death. Sclerotinia sclerotiorum (Lib.) de Bary (1) was isolated from the diseased plants. Five isolates were selected to fulfill Koch's postulates with 3-month-old echinacea seedlings grown in 12-cm pots of soilless mix. Sclerotia from wilted, field-grown echinacea plants were transferred onto potato dextrose agar medium for 2 days at 20°C. Agar disks were cut with a 1-cm cork borer and two plugs containing sclerotial and mycelial tissues were inserted into the soilless mix 0.5 cm deep and 0.5 cm from the opposite sides of stems of test plants. Inoculated plants were enclosed in transparent plastic bags for 5 days and incubated in a growth chamber at 15/18°C (night/day) with a 12-h photoperiod. One to four lower leaves per plant wilted within 1 week after inoculation and aerial mycelia appeared on the petioles. Infected leaves quickly withered, dried, and dropped off the plant after the bags were removed. Plants often died 3 weeks after inoculation and S. sclerotiorum was reisolated from infected crown tissues. This disease was also found on 3-year-old plants of E. pallida (Nutt.) Nutt. var. angustifolia (DC.) Cronq. in Vernon, British Columbia, Canada, in May 1997. This is the first report of sclerotinia stem rot on Echinacea spp., a disease that could have a significant impact on the longevity and productivity of this crop in the field and greenhouse. Reference: (1) L. H. Purdy. Phytopathology 69:875, 1979.


Plant Disease ◽  
2008 ◽  
Vol 92 (12) ◽  
pp. 1708-1708
Author(s):  
D. Aiello ◽  
G. Parlavecchio ◽  
A. Vitale ◽  
G. Polizzi

Common jasmine (Jasminum officinalis L.) is an evergreen shrub that is native to the Middle and Far East. It is widely grown in Europe as an ornamental plant and in southeastern France for fragrance for the perfume industry. In March of 2008, a previously undescribed disease was observed on potted (6-month- to 3-year-old) common jasmine plants growing in open fields in a nursery of eastern Sicily, Italy. More than 20% of the plants showed disease symptoms. Diseased plants had small to large, brown or black lesions on stem. The lesions expanded rapidly, girdled the stem and caused blight of entire branches, and occasionally killed the plant. Abundant conidia and mycelia were detected on the surface of dead and dying stems under cool and humid conditions, which resulted in a moldy gray appearance. Botrytis cinerea Pers.:Fr. (1) was consistently isolated from affected tissues disinfected for 1 min in 1% NaOCl, rinsed in sterile water, and plated on potato dextrose agar (PDA). Colonies were at first white then became gray after 6 to 7 days when spores differentiated. White sclerotia developed after 8 to 9 days and turned black with age. Size of the conidia produced on 1-month-old culture ranged from 5.0 to 9.5 × 6.5 to 12.5 μm on the basis of 50 spore measurements. Sclerotia were spherical or irregular and ranged from 1.0 to 2.5 × 0.9 to 2.9 mm (average 1.7 × 1.8 mm). Stems of eight 6-month-old common jasmine plants were lightly wounded with a sterile razor and inoculated with 3-mm-diameter plugs of PDA from 10-day-old mycelial cultures, eight similar plants were inoculated with mycelium without wounding, and an equal number of noninoculated plants inoculated with only PDA plugs served as control. After inoculation, plants were enclosed in transparent plastic bags at 20 ± 2°C for 5 days. Stem lesions identical to the ones observed in the nursery were detected on all wounded and on two nonwounded fungus-inoculated plants within 5 to 7 days. Control plants remained healthy. B. cinerea was reisolated from typical lesions. The unusually cool and humid weather conditions recorded in Sicily are supposed to be highly conducive of disease outbreak. Although B. cinerea does not usually kill the plants, under these environmental conditions this disease can cause significant economic loss to ornamental nurseries. To our knowledge, this is the first report of B. cinerea causing stem blight on J. officinalis. Reference: (1) M. B. Ellis. Dematiaceous Hyphomycetes. CAB, Kew, Surrey, England, 1971.


2017 ◽  
Vol 12 (1) ◽  
Author(s):  
Şener Kurt ◽  
Aysun Uysal ◽  
Merve Kara ◽  
Soner Soylu ◽  
Emine Mine Soylu

Plant Disease ◽  
1997 ◽  
Vol 81 (3) ◽  
pp. 311-311 ◽  
Author(s):  
K. F. Chang ◽  
R. J. Howard ◽  
R. G. Gaudiel ◽  
S. F. Hwang

Stevia (Stevia rebaudiana Bertoni; Asteraceae), an annual plant originating from Paraguay, contains glucosides of a diterpenoid (2), which is used as a low-caloric sweetener in some South American and southeast Asian countries. The main active ingredient, stevioside, is 100 to 300 times as sweet as sucrose. Stevia has been experimentally grown under field conditions in central and western Canada and has the potential to become a commercially viable alternative crop. In August 1996, a previously undescribed stem rot disease was observed on stevia plants at the Crop Diversification Centre South, Brooks, Alberta. The disease was found in research plots where 4-month-old plants were growing in loam soil. Diseased stems showed dark brown lesions above and at soil level when plant height reached approximately 30 cm. Under dry conditions, mild stem lesions caused plant stunting with lower leaves turning black and curling downward. Wilted leaf symptoms gradually spread upward in affected plants. Partial wilting symptoms appeared when girdling was restricted to branches. The entire plant collapsed when girdling of the crown and roots occurred. Superficial white mycelium developed over the basal part of affected stems under moist conditions, especially after rainy periods. Black, round to oblong sclerotia, 3.5 to 10.1 mm in size, formed externally on the crown areas after plant death. Sclerotinia sclerotiorum (Lib.) de Bary (1) was consistently isolated from the diseased plants. To confirm pathogenicity, 4-week-old stevia seedlings were obtained from shoot cuttings and grown in 12-cm pots of soilless mix. Sclerotia produced on potato dextrose agar were inserted into the mix 0.5 cm deep and 0.5 cm from the stems of test plants. Plants were placed in a growth chamber at 22°C with a 12-h photoperiod and 95% relative humidity. Two weeks after soil infestation, plants wilted and S. sclerotiorum was reisolated from the diseased crown tissues. This is the first report on stevia of sclerotinia stem rot, a disease that could significantly reduce foliar growth and stevioside production in field plantings. References: (1) L. H. Purdy. Phytopathology 69:875, 1979. (2) T. Robinson. 1991. The Organic Constituents of Higher Plants: Their Chemistry and Interrelationships. 6th ed. Cordus Press, North Amherst, MA.


Plant Disease ◽  
2005 ◽  
Vol 89 (8) ◽  
pp. 913-913
Author(s):  
C. Eken ◽  
S. Ercişli ◽  
A. Eşitken ◽  
E. Demirci ◽  
G. Y. Yuen

Orchis palustris Jacq. is a wild orchid native to wetlands in eastern Anatolia. During June of 2003, near Erzurum, Turkey, a decline of this orchid was observed in several meadows that had been irrigated for forage production. Stems were chlorotic, wilted, and collapsed. There was a soft, watery rot at the crowns and lower stems. White mycelium and black sclerotia formed on necrotic stem and crown tissues. The fungus was isolated from sclerotia on potato dextrose agar (PDA) and identified as Sclerotinia minor Jagger on the basis of small sclerotia (0.5 to 2.5 mm long) scattered throughout the colonies (2). Pathogenicity was confirmed by inoculating stems of 8-week-old plants with mycelial plugs from 5-day-old PDA cultures and enclosing inoculated plants in transparent plastic bags for 3 days. After 2 weeks, symptoms similar to those in the field were observed, and S. minor was reisolated from inoculated plants. Noninoculated control plants remained asymptomatic. The disease was previously observed on O. laxiflora Lam. in Turkey (1), but to our knowledge, this is the first report of S. minor infecting O. palustris References: (1) C. Eken et al. Plant Pathol. 52:802, 2003. (2) L.M. Kohn. Phytopathology 69:881, 1979.


Plant Disease ◽  
2005 ◽  
Vol 89 (9) ◽  
pp. 1014-1014
Author(s):  
E. R. Wright ◽  
M. C. Rivera ◽  
G. Chiesa ◽  
D. Morisigue

Three ornamental species, Osteospermum sp. (L.), Felicia amelloides (L.) Voss, and Ranunculus asiaticus L., cultivated in greenhouses on the outskirts of Buenos Aires, showed sudden wilt and death during October 2002. These species are new ornamentals in Argentina. The diseased plants were cultivated in plastic containers filled with commercial potting mix. Soft rot was observed at the base of the plants. Stem lesions became covered with whitish mycelium that produced large, black sclerotia (5 to 7 mm in diameter) characteristic of Sclerotinia sclerotiorum (Lib.) de Bary (1). The fungus was consistently recovered from infected stem pieces that were disinfested for 1 min in 0.2% NaOCl and plated on potato dextrose agar (PDA), pH 7. Pathogenicity of the three isolates obtained from infected plants was confirmed by inoculating 10 3-month-old healthy plants of each species in 14-cm-diameter plastic pots. Each isolate was inoculated on the host from which it had been isolated. Inoculum consisted of three mycelial plugs from 7-day-old PDA cultures that were placed on the substrate at the base of the plants. Control plants were treated with sterile agar plugs. Inoculated and noninoculated plants were covered with transparent plastic bags for 2 days and incubated in a growth chamber at 20 to 24°C with a 12-h photoperiod. All inoculated plants developed symptoms of leaf yellowing and wilt. Soft and watery tissues were observed at the base of the plants, soon followed by the appearance of white mycelium. Disease symptoms were similar to those observed on the original infected plants and appeared 6, 5, and 3 days after inoculation on Osteospermum sp., F. amelloides, and R. asiaticus, respectively. All inoculated plants died within 3 weeks, and control plants remained healthy. S. sclerotiorum was reisolated from inoculated plants of each species, fulfilling Koch's postulates. To our knowledge, this is the first report of the occurrence of Sclerotinia stem rot on these three plant species in Argentina. Reference: (1) J. E. M. Mordue and P. Holliday. No. 513 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK. 1976.


Plant Disease ◽  
2002 ◽  
Vol 86 (4) ◽  
pp. 440-440
Author(s):  
L. Swart ◽  
S. Coertze

Geraldton waxflower (Chamelaucium uncinatum Schauer, family Myrtaceae), indigenous to western Australia, is cultivated commercially in South Africa as a cut-flower crop and exported to markets in the Northern Hemisphere. In September 2000, disease symptoms were observed on 4-year-old plants in a commercial orchard of C. uncinatum cv. Ofir in Philippe, in the Western Cape Province. The base of the petals and the calyxes of the waxflowers showed brown necrotic lesions. Eventually the calyx and all the petals turned brown, and the flowers shriveled and abscised. B. cinerea Pers.:Fr was consistently isolated from affected petal and calyx tissues. When placed in a moist chamber, conidia and mycelia formed on the surface of dead and infected tissue. Koch's postulates were confirmed by spraying flower stems of C. uncinatum cv. Ofir with a spore suspension (1 × 106 conidia per ml). Inoculated flower stems were placed in a bottle filled with water and enclosed in transparent plastic bags for 24 h at 21°C. Typical symptoms developed on the petals and calyx within 3 days after inoculation. B. cinerea was reisolated from affected tissues. Botrytis flower blight or gray mold, causing a flower petal disease, has been recorded on C. uncinatum in Australia (1), but this is the first record of Botrytis flower blight of C. uncinatum in South Africa. Because Geraldton waxflower is a major cut-flower crop grown for export, this disease can cause significant losses to the industry, especially under cool, wet growing conditions. Reference: (1) A. Tomas et al. Aust. Plant Pathol. 24:26, 1995.


Plant Disease ◽  
2021 ◽  
Author(s):  
Chang-Gi Back ◽  
Walftor Dumin ◽  
You-Kyoung Han ◽  
Yeong-Seok Bae ◽  
Jong-Han Park

Botryosphaeria dothidea (B. dothidea) is a fungal pathogen commonly associated with stem canker, dieback, and rot disease in a variety of woody plants worldwide (Dong and Guo, 2020). In Korea, B. dothidea was reported to cause a disease problem to serval crops such as apple and blueberry (Kim, 1995; Choi, 2011). In early 2020, a typical symptom resembling the stem rot disease was spotted to occur at a plumcot cultivation area around Wanju (35.827870, 127.030380) province, Korea. At the early stage of infection, a small blister appeared on the plumcot branch and stem. However, as the blister extended, a light brown canker was observed appeared on the infected area and in some cases a sticky sap oozed from the branch bark crack. If not managed or treated properly, all leaves beyond the infection site will turn brown, wilt, and the whole plumcot tree eventually dies. A survey in the affected area showed that approximately 5% of the plumcot trees were infected which cause up to 10% reduction in total production. To identify the causal agent, symptomatic tissues were excised and surface sterilized with 70% ethanol for 30 sec followed by 1% NaClO for 30 sec before rinsing with sterile water, thrice. The samples were then dried with a piece of filter paper and later air-dried before being placed on a potato dextrose agar (PDA). The PDA plates were then incubated at 25°C for 5 days with 12 hours light/dark cycles period. Among several fungal isolates obtained, four were selected for further analyses. Morphological identification revealed that the fungal conidia were hyaline, ovoid, fusiform (type that rarely form a septum) and unicellular with an average size of 18 - 20 μm × 4.5 -5.5 μm (n = 50). These morphological characters have a strong resemblance to B. dothidea that described by Slipper et al., (2004). For molecular identification, Internal transcribed spacer (ITS), beta-tubulin (β-tubulin) and elongation factor 1 alpha (EF-1α) were amplified and sequenced using universal primer pairs ITS1/ITS4 (White et al., 1990), Bt2a/Bt2b (Glass and Donaldson, 1995) and EF1/EF2 (O’Donnell et al. 1998) respectively. Alignment analysis showed that ITS (LC602817), β-tubulin (LC602820) and EF-1α (LC602821) sequences were 99-100% identical to the orthologous genes identified in B. dothidea infecting soybean in China [MW130133 (identity 537/536 bp), MW147482 (identity 394/394 bp) and MW147481 (identify 250/250 bp) respectively] (Chen et al. 2021). However, phylogenetic analysis of concatenated ITS, β-tubulin and EF-1α genes sequence established the identity of these isolate as B. dothidea. Due to the 100% identical at the molecular level, isolate NIHHS 20-262 was selected as a representative for further analysis. For the pathogenicity test, fungal mycelium (via PDA plug) was used as a source of inoculum for both intact and detached plumcot stems trials. For the intact trial, mycelium was inoculated on the wounded spots of ten plumcot stems that grew at the NIHHS trial farm. Ten days post-inoculation (dpi), disease symptoms i.e. stem colour turn from greenish to dark brown was observed at the inoculated sites. For the detached trial, mycelium was inoculated on the wounded spots of ten detached plumcot stems. The inoculated stems were kept in a closed container to maintain 90% humidity before incubated at 25ºC in the dark. Interestingly, on the detached stems, disease symptoms (greenish colour turn to dark brown) were observed to appear seven days early compare to intact stems. A sterile PDA plug replacing fungal mycelium served as a negative control and the result shows no symptoms were observed on either intact or detached control stems. For consistency purposes, pathogenicity tests on intact stems were performed on three different plumcot trees, whereas three biological replicates for detached stems. Isolation and re-identification of two colonies from the infected sites (intact and detached stems) were attempted and the results obtained were identical to the original isolate, thus fulfilling Koch’s postulates. Local farmers described this disease as a “certain death disease” in plumcot. Therefore, accurate identification of B. dothidea as the causal agent is critical for effective disease management to minimise qualitative and quantitative losses in the plumcot industry. Although has been reported to cause dieback disease in blueberry in Korea (Choi, 2011), to our knowledge, this is the first study to report B. dothidea causing stem rot diseases on the plumcot trees in Korea.


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