scholarly journals First Report of Botrytis Blight Caused by Botrytis cinerea on Purple Coneflower (Echinacea purpurea) in Italy

Plant Disease ◽  
2018 ◽  
Vol 102 (4) ◽  
pp. 821-821
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
S. Franco Ortega ◽  
M. L. Gullino
Plant Disease ◽  
2012 ◽  
Vol 96 (4) ◽  
pp. 582-582 ◽  
Author(s):  
Y.-W. Tseng ◽  
W.-L. Deng ◽  
C.-J. Chang ◽  
C.-C. Su ◽  
C.-L. Chen ◽  
...  

Purple coneflower (Echinacea purpurea), widely grown as an ornamental and medicinal plant, is a perennial flowering plant that is native to eastern North America. In July 2011, symptoms indicative of phytoplasma disease, including floral virescence, phyllody, and witches'-broom (WB), were observed to be affecting plants in coneflower fields in Wufeng, Taichung City, Taiwan. Incidence of infected plants was estimated to be greater than 90% within a single field. Phytoplasmas previously associated with purple coneflower WB disease have all been classified as aster yellows group (16SrI) strains (GenBank Accession Nos. EU333395, AY394856, EU416172, and EF546778) except for pale purple coneflower (Echinacea pallida) WB in Australia, which was identified as a subgroup 16SrII-D member (2). Three diseased plants were uprooted and transplanted in a greenhouse for further study. Transmission electron microscopy revealed clusters of phytoplasma cells ranging from 170 to 490 nm in diameter in phloem sieve elements of virescent and phylloid flowers and stems from diseased plants. Comparable tissues from symptomless plants were devoid of phytoplasma. Total DNA was extracted from plant tissue samples (50 to 100 mg each) including stems, leaves, and flowers by a modified CTAB method (1) from three symptomatic plants as well as from three asymptomatic coneflower plants seedlings. Analyses by a nested PCR using universal primer pairs P1/P7 followed by R16F2n/R16R2 were performed to detect putative phytoplasma (2). Each primer pair amplified a single PCR product of either 1.8 or 1.2 kb, respectively, from diseased plant tissues only. The nested PCR products (1.2 kb) amplified from phylloid flowers of the three diseased plants were cloned separately and sequenced (GenBank Accession Nos. JN885460, JN885461, and JN885462). Blast analysis of the sequences revealed a 99.7 to 99.8% sequence identity with those of Echinacea WB phytoplasma strain EWB5 and EWB6 (GenBank Accession Nos. JF340076 and JF340080), which reportedly belonged to the 16SrII-D subgroup (2). Moreover, iPhyClassifier software (3) was used to perform sequence comparison and generate the virtual restriction fragment length polymorphism (RFLP) profile. The 16S rDNA sequences share a 99.4 to 99.5% similarity with that of the ‘Candidatus Phytoplasma australasiae’ reference strain (Y10097) and the RFLP patterns are identical to that of the 16SrII-A subgroup. Taken together, these results indicated that the phytoplasma infecting purple coneflower in Taiwan is a ‘Ca. Phytoplasma australasiae’-related strain and belongs to the 16SrII-A subgroup. To our knowledge, this is the first report of a 16SrII-A subgroup phytoplasma causing WB disease on purple coneflower in Taiwan. The occurrence of phytoplasma on purple coneflower could have direct implication for the economically important ornamental, medicinal plant, and floral industry in Taiwan, especially to the growers and breeders that eagerly promote the purple coneflower industry. References: (1) T. M. Fulton et al. Plant Mol. Biol. Rep. 13:207, 1995. (2) T. L. Pearce et al. Plant Dis. 95:773, 2011. (3) Y. Zhao et al. Int. J. Syst. Evol. Microbiol. 59:2582, 2009.


Plant Disease ◽  
2019 ◽  
Vol 103 (7) ◽  
pp. 1786-1786
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
S. Matic ◽  
M. L. Gullino

Plant Disease ◽  
2019 ◽  
Vol 103 (9) ◽  
pp. 2474
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
G. Gilardi ◽  
S. Matic ◽  
M. L. Gullino

Plant Disease ◽  
2008 ◽  
Vol 92 (4) ◽  
pp. 654-654 ◽  
Author(s):  
I.-M. Lee ◽  
K. D. Bottner ◽  
E. L. Dally ◽  
R. E. Davis

Purple coneflower (Echinacea purpurea (L.) Moench) is a flowering perennial plant native to North America and is widely grown as an ornamental flower. It is also grown commercially to make herbal teas and extracts purported to help strengthen the immune system. Propagation is by seed or root cuttings. Aster yellows phytoplasmas (strains belonging to group 16SrI) have been reported to be associated with purple coneflower exhibiting virescence and phyllody symptoms in the northern United States and Canada. A subgroup 16SrI-A phytoplasma was identified to be associated with symptomatic purple coneflower in Wisconsin (2). During the summers of 1994 and 2007, purple coneflower plants in Maryland sporadically exhibited symptoms resembling those caused by phytoplasma infection. Symptoms included stunting, virescence, phyllody, and abnormal flower bud proliferation from the cone. Samples from four symptomatic and two asymptomatic purple coneflower plants were collected. Total nucleic acid was extracted from leaf tissue. To assess the etiology of the disease, nested PCR with universal phytoplasma primer pair P1/P7 followed by R16F2n/R16R2 was employed for the detection of phytoplasmas (1). An amplicon of approximately 1.2 kb was amplified from all four symptomatic purple coneflower plants but not from the two asymptomatic plants. Restriction fragment length polymorphism (RFLP) patterns of 16S rDNA digested singly with restriction enzymes AluI, KpnI, HpaI, MseI, HhaI, and RsaI indicated that affected purple coneflower plants were infected by a phytoplasma belonging to aster yellows group 16SrI (‘Candidatus Phytoplasma asteris’-related strains), subgroup 16SrI-B (1). Nucleotide sequence analysis of cloned 16S rDNA (GenBank Accession Nos. EU333394 and EU333395) confirmed the results from RFLP analyses. To our knowledge, this is the first report of a 16SrI-B phytoplasma infecting an Echinacea sp. in Maryland. References: (1) I.-M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998. (2) G. R. Stanosz et al. Plant Dis. 81:424, 1997.


Plant Disease ◽  
1997 ◽  
Vol 81 (12) ◽  
pp. 1461-1461 ◽  
Author(s):  
K. F. Chang ◽  
R. J. Howard ◽  
S. F. Hwang

Coneflowers (Echinacea purpurea (L.) Moench and E. pallida (Nutt.) Nutt. var. angustifolia (DC.) Cronq.) are popular medicinal herbs in North America and Europe. In May 1997, a previously undescribed disease was observed in a commercial field of 3-year-old E. pallida var. angustifolia plants in Vernon, British Columbia, Canada. Diseased plants had small to large, brown or black lesions on leaves and stems. Botrytis cinerea Pers.:Fr. (1,2) was consistently isolated from affected tissues. The pathogen appeared to infect leaves along the margins and tips, and occasionally on other parts of the blade as well. Lesions expanded rapidly under cool, humid conditions. Once the pathogen had invaded the midrib or veins, it advanced rapidly to the petiole and stem, which resulted in collapse of the leaf. The pathogen produced profuse conidia and mycelia on the surface of dead and dying leaves, stems, and blossoms, which resulted in a moldy gray appearance. Under dry conditions, the disease developed slowly or even became quiescent. Large lesions often split and formed holes in leaves. The average size of the conidia produced on naturally infected leaves ranged from 5.5 to 10.5 × 6.8 to 18.3 μm (average 8.1 × 13.0 μm), and on potato dextrose agar (1-month-old culture) ranged from 5.5 to 10.0 × 7.5 to 16.3 μm (average 7.4 × 11.3 μm) based on 100 spore measurements, respectively. Microsclerotia were round, spherical or irregular in shape, and ranged from 1.1 to 3.6 × 1.0 to 3.0 mm. Koch's postulates were verified by spraying potted, 3-month-old, narrow-leaved coneflower (E. pallida var. angustifolia) and 2-year-old purple coneflower (E. purpurea) plants with a spore suspension (4 × 105 conidia/ml). Inoculated plants were enclosed in transparent plastic bags for 7 days at 15/22°C (night/day) with a 12-h photoperiod. Typical symptoms were produced 2 to 7 days after inoculation. Some infected leaves quickly twisted and dried after removal of the plastic bags. Botrytis cinerea was reisolated from the affected tissues. This is the first report of Botrytis blight on Echinacea spp. Although B. cinerea does not usually kill coneflower plants, it often heavily infects disc flowers and young shoots. Therefore, Botrytis blight could have a significant impact on the establishment and productivity of this crop in both the field and greenhouse, especially under cool, wet, growing conditions. References: (1) J. R. Coley-Smith et al. 1980. The Biology of Botrytis. Academic Press, New York. (2) D. J. Morgan. Trans. Br. Mycol. Soc. 56:319, 1971.


Planta Medica ◽  
2013 ◽  
Vol 79 (05) ◽  
Author(s):  
MT Khosravi ◽  
A Mehrafarin ◽  
H Naghdibadi ◽  
E Khosravi

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Dahanayake Nilanthi ◽  
Yue-Sheng Yang

Echinacea purpurea (purple coneflower) is being used for the preparation of more than 240 extracts, salves, and tinctures to help cure diseases like rabies, cold, and upper respiratory infections. Hence, efforts were made to develop a culture medium for successful in vitro culturing of cornflower and to regenerate buds and induce roots to enable mass propagation of selected clones. Of the three levels of sucrose tested as a supplement to MS media (Murashige and Skoog’s medium, 1962) 3% showed better rooting of buds and appeared morphologically normal and identical as compared to those grown at higher and lower concentrations (2 and 4%). The additives hydrolyzed lactabumin (0.0, 100, 300, and 900 mgL−1), peptone (0.0, 100, 300, and 900 mgL−1), and yeast (0.0, 100, 300, and 900 mgL−1) to media containing 0.3 mgL−1 BA (6-benzyladenine) and 0.01 mgL−1 NAA (naphthaleneacetic acid-plant growth regulators) has negatively influenced proliferation of shoots. The higher concentrations of the above have delayed the development of plantlets. Shoot multiplication was enhanced by coconut water with 2% being the best among 4 and 8% tested. Shoot organogenesis was not influenced by copper sulphate (0, 1.5, 3, 6, and 12 mgL−1) and silver nitrate (0.0, 0.5, 2.5, and 12.5 mgL−1) supplements and at higher concentrations of the above inhibited plant growth.


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