scholarly journals First Report of Strawberry Anthracnose (Colletotrichum acutatum) in Strawberry Fields in New York

Plant Disease ◽  
2002 ◽  
Vol 86 (8) ◽  
pp. 922-922 ◽  
Author(s):  
W. W. Turechek ◽  
C. Heidenreich ◽  
M. P. Pritts

Strawberry plants with red to black, sunken, fusoid lesions on runners and leaf petioles were found in several first-year plantings in grower's fields in western New York in 2000. Affected cultivars included Honeoye, Jewel, and Primetime. Sections of petiole were excised from lesion margins and plated on potato dextrose agar (PDA) amended with chloramphenicol, streptomycin sulfate, and tetracycline hydrochloride at 100 μg/ml. The fungus, Colletotrichum acutatum (J.H. Simmonds), was consistently isolated and identified based on conidia morphology and its growth rate in culture relative to reference cultures of C. acutatum, C. gloeosporoides, and C. fragariae (1,2). The average size of conidia produced on PDA was 15.2 × 5 μm. For each of six isolates, three plants each of six-week-old Honeoye and Kent were spray inoculated with a conidial suspension (106 conidia per ml), and petioles, leaves, and crowns were stabbed with a sterile pin following inoculation. After 14 days at 20 to 25°C, petioles and leaves on all inoculated plants developed lesions consistent with those seen in the field. The fungus was readily reisolated from leaf and petiole lesions. Subsequent inoculations on detached fruit under the same conditions yielded circular, sunken, dry lesions that produced a salmon-colored, slimy, spore mass typical of C. acutatum. This is the second report of strawberry anthracnose in the northeastern United States (3) and to our knowledge, the first report in New York. References: (1) J. A. García Muñoz et al. Mycologia 92:288, 2000. (2) P. S. Gunnel and W. D. Gubler. Mycologia 84:157, 1992. (3) J. A. LaMondia. Plant Dis. 75:1286, 1991.

Plant Disease ◽  
2000 ◽  
Vol 84 (6) ◽  
pp. 706-706 ◽  
Author(s):  
C. J. Ramallo ◽  
L. D. Ploper ◽  
M. Ontivero ◽  
M. P. Filippone ◽  
A. Castagnaro ◽  
...  

Isolates were obtained from strawberry tissue with anthracnose symptoms from several locations near Tucumán, Argentina. Isolates were characterized using several criteria. Isolates produced fusiform conidia, tapered to a point at both ends, and averaged 13.5 × 4.9 μm. On potato dextrose agar, colonies produced a white cottony mycelial colony that turned orange in older cultures. Compared with Colletotrichum fragariae, the new isolates produced fewer appressoria. Pathogenicity tests were conducted on detached leaves and plants in the greenhouse and field. Detached immature leaves of cvs. Chandler, Fern, and Sweet Charlie were inoculated with a 20-μl droplet of an aqueous conidial suspension (106 conidia per ml) placed on the adaxial surface. Control leaves were inoculated with sterile distilled water. Leaves were maintained under white light (2,000 lux, 12 h/day) at 26°C, and 100% relative humidity. Necrotic spots were visible 4 days after inoculation. Greenhouse and field plants were spray-inoculated and covered for 48 h. Disease symptoms were mainly observed on petioles and runners 9 days after inoculation. No lesions were observed on control detached leaves or plants. Koch's postulates were confirmed in all cases. Based on morphological and cultural characteristics, isolates were identified as C. acutatum Simmonds (1). This is the first report of C. acutatum causing strawberry anthracnose in northwestern Argentina. Reference: (1) B. Smith and L. L. Black. Plant Dis. 74:69, 1990.


Plant Disease ◽  
2008 ◽  
Vol 92 (8) ◽  
pp. 1247-1247 ◽  
Author(s):  
M. H. Nam ◽  
T. I. Kim ◽  
M. L. Gleason ◽  
J. Y. Song ◽  
H. G. Kim

Symptoms typical of anthracnose fruit rot; sunken, dark brown lesions on maturing fruits, were found in a commercial field of strawberry (Fragaria × ananassa) cv. Cal Giant in Yangyang County, Korea in May 2007. Masses of conidia were produced in acervuli in the center of lesions. The fungus was isolated on potato dextrose agar (PDA). Colonies grown on PDA were pale to mouse gray and became dark green to black in reverse. Conidia were formed in orange-to-salmon pink masses in the center of the culture. The average size of conidia on PDA was 15.2 × 4.6 μm, and they were hyaline, straight, cylindrical, with pointed ends, and aseptate (1). The fungus did not form an ascigerous stage in culture. Mycelial growth rate was 7.5 mm per day at 25°C on PDA. The identity of two isolates was confirmed as Colletotrichum acutatum J.H. Simmonds by PCR amplification using species-specific primers TBCA and TB5 (2), resulting in a characteristic 330-bp band on agarose gel. Morphological characters were in accordance with previous reports on C. acutatum. A pathogenicity test was conducted with five healthy plants of cvs. Cal Giant, Maehyang, Seolhyang, Kumhyang, Akihime, and Redpearl. After fruits and flowers were sprayed with a conidia suspension (105 conidia per ml), the plants were maintained at 10 to 25°C and 100% relative humidity in a greenhouse. As a control, five healthy plants were sprayed with sterile distilled water and incubated under the same conditions. Dark brown, water-soaked spots appeared on mature fruits of all cultivars after 5 days, and lesions on green fruits appeared on individual achenes. Flowers developed dark lesions, dried out, and died. No symptoms were found on the control plants. After the pathogen was reisolated from fruits and flowers lesions, the morphological characters developed in culture as described above. To our knowledge, this is the first report of C. acutatum causing strawberry anthracnose in Korea. References: (1) B. J. Smith and L. L. Black. Plant Dis. 74:69, 1990. (2) P. Talhinhas et al. Appl. Environ. Microbiol. 71:2987, 2005.


Plant Disease ◽  
2001 ◽  
Vol 85 (5) ◽  
pp. 558-558 ◽  
Author(s):  
A. Stensvand ◽  
G. M. Strømeng ◽  
R. Langnes ◽  
L. G. Hjeljord ◽  
A. Tronsmo

Anthracnose caused by Colletotrichum acutatum J. H. Simmonds was detected in strawberry (Fragaria × ananassa Duch.) for the first time in Norway in 1999. Symptoms were found in greenhouse grown strawberries in the cultivar Korona. Symptoms were typical of strawberry anthracnose: sunken, brown, and firm lesions appeared on maturing fruits. Masses of conidia were produced in acervuli in the center of lesions. The fungus was isolated on acidified potato dextrose agar. Colonies grown on potato dextrose agar (PDA) were pale to mouse gray and became dark greenish to blackish in reverse. Conidia were formed in orange to salmon pink masses in the center of the culture. Conidia in cultures were 16.5 (13.8 to 18.8) × 4.5 (3.8 to 5) μm, and were hyaline, cylindrical, with pointed ends, and aseptate. Setae were never observed in culture or on fruits. The fungus did not form an ascigerous stage in culture. Mycelial growth rate at 25 to 26°C on PDA was 8.1 to 8.4 mm per day. Morphological characters and growth rate were in accordance with previous reports on C. acutatum (1,2). The isolated fungus was confirmed to be C. acutatum by both the International Mycological Institute, Egham, England, and Centraalbureau voor Schimmelcultures, Baarn, the Netherlands. Koch's postulates were fulfilled by inoculating ripe and unripe fruits on strawberry plants with the isolated fungus. Fruits were either sprayed with a conidial suspension (106 conidia per ml) or slightly wounded with a needle that had been dipped in a conidial mass from a pure culture of C. acutatum. Symptoms appeared after 4 days at 20°C, and after 5 days, brown, sunken, circular lesions reached a size of 1 cm in diameter on wounded, ripe fruits. In unripe fruits the lesions developed more slowly, and in unwounded fruits sprayed with a conidial suspension, large, irregular spots developed. Leaves were inoculated by placing a small block of agar at the base of petioles on intact strawberry plants. The tissue underneath the agar was either unwounded or slightly wounded with a needle. After 20 days (at 20 to 25°C) some necrosis developed on both unwounded and wounded petioles. No symptoms were observed in the crown tissue where the inoculated petioles were attached. The fungus was readily reisolated from both fruits and petioles, after which typical morphological characters developed in culture as described above. References: (1) P. S. Gunnell and W. D. Gubler. Mycologia 84:157, 1992. (2) B. J. Smith and L. L. Black. Plant Dis. 74:69, 1990.


Plant Disease ◽  
2011 ◽  
Vol 95 (8) ◽  
pp. 1029-1029 ◽  
Author(s):  
J. Debode ◽  
W. Van Hemelrijck ◽  
K. Heungens ◽  
M. Maes ◽  
P. Creemers

In April 2010, pink-orange spore masses that later turned brown were observed on 7 to 50% of the transplant lots during a routine screening of Belgian strawberry (Fragaria × ananassa, cv. Elsanta) for the latent presence of Colletotrichum acutatum using the petiole freeze method (4). These spore masses contained hyaline, canoe-shaped to allantoid conidia (mean size 7.5 × 1.8 μm), which is not consistent with C. acutatum spore morphology. Subsequently, a spore mass was transferred onto potato dextrose agar (PDA) and a gray-to-brown colony with whitish, aerial mycelium was produced, which is also not consistent with C. acutatum isolates. To identify the fungus, the ITS1-5.8S-ITS2 rDNA region was amplified by PCR and sequenced. The 485-bp region was 100% identical to that of Pilidium concavum specimen voucher BPI 1107275 (GenBank Accession No. AY487094). P. concavum (Desm.) Höhn. (synanamorph Hainesia lythri; teleomorph Discohainesia oenotherae) is a pathogen of strawberry causing tan-brown rot of fruit and is a common secondary invader of roots and dead strawberry plant parts (3). A recent strain of P. concavum from strawberry, isolate UPL 50, obtained from Brazil (L. Zambolim, Univ. Fed. de Viçosa, personal communication) showed similar colony, microscopic (mean spore size of 6.8 × 1.8 μm), and molecular (ITS sequence 98% identical to that of P. concavum specimen voucher BPI 1107275) features as the Belgian isolate. Pathogenicity tests were conducted on mature strawberry fruits by submerging 15 fruits per isolate for 3 min in a conidial suspension (2 × 106 conidia ml–1 of water) obtained from a 2-week-old colony on PDA. Controls were submerged in sterile distilled water. The inoculated fruits were incubated in a moist chamber at 25°C. Sunken, yellowish brown lesions with pink and later orange-brown spore masses were observed starting 3 days after inoculation on 88 and 94% of the fruit for the Brazilian and Belgian isolate, respectively. The control fruits remained healthy. The fungal isolates were reisolated from symptomatic fruits and their identity was confirmed based on morphological features. During a strawberry field survey in July 2010 in Sint-Truiden (Belgium), lesions typical of those described above were observed on eight strawberry fruits (cv. Elsanta). The fungus was isolated from the symptomatic tissue of two fruits and characterized as described above. Since P. concavum was latently present on strawberry transplants and caused disease on the fruits in the field, we conclude that P. concavum is a potential threat for Belgian strawberry production. Moreover, no strawberry cultivars with resistance to the pathogen have been reported. The disease has previously been reported on strawberry in South America and Poland (1,2), but to our knowledge, this is the first report of P. concavum on strawberry in Belgium. Although the spore and colony morphology of P. concavum is different from C. acutatum, the spore masses of P. concavum can easily be confused with the spore masses of C. acutatum when using the freeze method. This suggests the need for microscopic analysis of these spore masses during routine analyses. References: (1) L. Cedeno et al. Interciencia 26:113, 2001. (2) U. P. Lopes et al. New Dis. Rep. 21:7, 2010. (3) J. L. Maas. Compendium of Strawberry Diseases. The American Phytopathological Society St. Paul, MN, 1998. (4) J. C. Mertely and D. E. Legard. Plant Dis. 88:407, 2004.


Plant Disease ◽  
2000 ◽  
Vol 84 (12) ◽  
pp. 1345-1345 ◽  
Author(s):  
M. C. Rivera ◽  
E. R. Wright ◽  
S. Carballo

Chinese rose (Hibiscus rosa-sinensis L.) is a shrub frequently planted in Argentina. In November 1999, dieback and anthracnose symptoms were detected on stems and leaves of plants cv. Hawaii cultivated in Buenos Aires. Disease prevalence was 50%. Pieces of infected tissues were surface-sterilized for 1 min in 2% NaOCl, plated on potato-dextrose agar and incubated at 24 ± 2°C. The isolate that was consistently recovered from diseased tissues was identified as Colletotrichum gloeosporioides (Penz.) Penz. and Sacc., based on morphological characteristics (1,2). Teleomorph stage was not observed. Inoculation for pathogenicity testing was carried out by spraying a conidial suspension (6.5 × 106 conidia per ml) on plants with previously punctured leaves and pruned stems. Inoculated plants with unwounded tissues, as well as noninoculated controls, were included. Five replications of each treatment were done. Plants were incubated in moist chambers at 24°C. Whitish areas of 0.3 to 0.5 cm diameter surrounded by a purple halo developed on all punctured leaves within 10 days. Stem blight and leaf drop were observed. The center of the lesions was covered by black acervuli 14 days after inoculation. Unwounded and noninoculated controls remained symptomless. The pathogen was reisolated from inoculated leaves, completing Koch's postulates. This is the first report of C. gloeosporioides causing disease on Chinese rose in Argentina. References: (1) J. A. Bailey and M. J. Jeger, eds. 1992. Colletotrichum. CAB International, Surrey, England. (2) B. C. Sutton. 1980. The Coelomycetes. CMI, Kew.


Plant Disease ◽  
2001 ◽  
Vol 85 (12) ◽  
pp. 1285-1285 ◽  
Author(s):  
C. Barrau ◽  
B. de los Santos ◽  
F. Romero

An anthracnose disease was observed affecting leaves of high-bush blueberry plants (Vaccinium corymbosum L. ‘Sharpblue’) in small areas within two production fields in Huelva Province of Andalucía, in southwestern Spain. The first symptoms observed in late spring were circular, necrotic lesions, red to salmon in color, and ranging from 3 to 20 mm in diameter. Later, lesions became salmon colored in the center with a brilliant red halo. Fungal isolations were made from the lesions. Infected tissues were surface-disinfected in 1% sodium hypochlorite for 1 min, blotted dry on sterile filter paper, and plated on 2% water agar. The plates were incubated at 25°C for 5 to 10 days. Fungal colonies isolated from the tissues were transferred to potato dextrose yeast agar (PDYA). Only one fungal species was consistently isolated from affected leaf tissues and was identified as Colletotrichum acutatum J.H. Simmonds based on morphological characteristics (2) and enzyme-linked immunosorbent assay (1). Colonies of the fungus on PDYA showed a white-to-gray dense mycelium covered with salmon-colored spore masses. The reverse of the plates was a pink-salmon color. Colony diameter on PDYA averaged 50 mm after 7 days at 25°C. Conidia were hyaline, aseptate, fusiform to cylindrical, and 12.5 × 3.2 μm. Inoculation of leaves and fruits of blueberry cv. Misty with a conidial suspension (106 conidia per ml) of C. acutatum produced lesions on the leaves and fruits similar to those observed on diseased plants in the field. The pathogen was isolated from lesions on inoculated plants. To our knowledge, this is the first report of C. acutatum in high-bush blueberry plants in Spain. References: (1) T. A. Cooke et al. EPPO Bull. 25:57, 1995. (2) B. C. Sutton. The Coelomycetes. CMI, Kew, England, 1980.


Plant Disease ◽  
2009 ◽  
Vol 93 (3) ◽  
pp. 323-323 ◽  
Author(s):  
F. T. Arroyo ◽  
Y. Llergo ◽  
A. Aguado ◽  
F. Romero

In the spring of 2007, wilted and dead strawberry plants (Fragaria × ananassa Duch. cvs. Camarosa and Ventana) were observed in a soilless culture system in Huelva, southwestern Spain. Approximately 8% of the plants in the field died. Isolations from necrotic crowns and roots and necrotic flowers were made on potato dextrose agar after disinfestation in 0.6% NaOCl for 30 s. Colonies with light purple mycelia and beige or orange reverse colony colors developed after 9 days of incubation at 25°C. Colonies produced abundant microconidia, macroconidia, and chlamydospores. Microconidia were hyaline and oval-ellipsoid to cylindrical (5.9 to 9.2 × 2.1 to 3.4 μm). Macroconidia were 3 to 5 septate and fusoid-subulate with a pedicellate base (28.8 to 37.3 × 3.2 to 4.3 μm). Morphology and growth matched descriptions of Fusarium oxysporum Schlechtend emend. Snyder & Hansen (2). A PCR assay for amplification of r-DNA using primers PFO2 and PFO3 established the identity of the isolate as F. oxysporum (1). To confirm the pathogenicity of the fungus, roots of 30-day-old strawberry cvs. Camarosa and Ventana (20 plants each) were inoculated by dipping the roots into a conidial suspension (107 conidia per ml) for 15 min. The inoculated plants were transplanted into plastic pots containing sterilized peat and maintained at 25°C and 100% relative humidity in a growth chamber with a daily 12-h photoperiod of fluorescent light. The pathogenicity test was conducted twice. Within 30 days, all inoculated plants developed wilt symptoms similar to that observed in the field and eventually 75% of the plants died. No symptoms were observed on plants dipped in distilled water. The fungus was successfully reisolated from crowns, roots, and necrotic flowers, fulfilling Koch's postulates. To our knowledge, this is the first report of the occurrence of Fusarium wilt caused by F. oxysporum on strawberry plants in Spain. References: (1) V. Edel et al. Mycol. Res. 104:518, 2000. (2) W. C. Snyder and H. N. Hansen. Am. J. Bot. 27:64, 1940.


Plant Disease ◽  
2010 ◽  
Vol 94 (11) ◽  
pp. 1378-1378 ◽  
Author(s):  
U. P. Lopes ◽  
L. Zambolim ◽  
H. S. S. Duarte ◽  
P. G. C. Cabral ◽  
O. L. Pereira ◽  
...  

There are more than 300 blackberry (Rubus) species worldwide. Rubus brasiliensis Mart. is a native Brazilian species found in tropical forests. In January 2009, samples of R. brasiliensis with severe leaf blight were collected from an area of rain forest in the city of São Miguel do Anta, State of Minas Gerais, Brazil. Dark spots began developing in the young leaves and progressed to necrotic spots with occasional twig dieback. From the spots, a fungus was isolated with the following morphology: acervuli that were 20 to 50.0 × 50 to 125.0 μm and hyaline amerospores that were ellipsoid and fusiform and 7.5 to 23.75 × 2.5 to 5.0 μm. On the basis of these morphological characteristics, the fungus was identified as Colletotrichum acutatum. In Brazil, C. acutatum is reported in apple, citrus, strawberry, peach, plum, nectarine, olive, medlar, and yerba-mate, but it was not reported as the causal agent of leaf blight in R. brasiliensis. A sample was deposited in the herbarium at the Universidade Federal de Viçosa, Minas Gerais, Brazil (VIC 31210). One representative isolate, OLP 571, was used for pathogenicity testing and molecular studies. Identity was confirmed by amplifying the internal transcribed spacer (ITS) regions of the ribosomal RNA with primers ITS4 (3), CaInt2 (a specific primer for C. acutatum [2]) and CgInt (a specific primer for C. gloeosporioides [1]). Isolates of C. acutatum (DAR78874 and DAR78876) and C. gloeosporioides (DAR78875) obtained from Australian olive trees were used as positive controls. The primers ITS4 and CaInt2 amplified a single DNA product of 500 bp expected for C. acutatum. OLP 571 was grown for 7 days on potato dextrose agar. Young leaves of R. brasiliensis were inoculated with a conidial suspension (106 conidia/ml) on young leaves. Inoculated plants were maintained in a moist chamber for 2 days and subsequently in a greenhouse at 25°C. Necrotic spots similar to those described were detected on young leaves 3 days after the inoculation. Control leaves, on which only water was sprayed, remained healthy. The same fungus was reisolated from the inoculated symptomatic tissues. To our knowledge, this is the first report of C. acutatum causing leaf blight in the native species of R. brasiliensis in Brazil. References: (1) P. R. Mills et al. FEMS Microbiol. Lett. 98:137, 1999. (2) S. Sreenivasaprasad et al. Plant Pathol. 45:650, 1996. (3) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990.


Plant Disease ◽  
2003 ◽  
Vol 87 (1) ◽  
pp. 99-99 ◽  
Author(s):  
S. Kurt

During December 2001 to March 2002, Septoria blight of parsley was observed in approximately 500 ha of commercial parsley crops in Arsuz County, Hatay, in the Mediterranean Region of Turkey. Incidence of disease ranged from 42 to 80%. Symptoms included irregularly shaped, grayish brown spots (average 3 to 8 mm diameter) with a slightly darker brown margin of necrotic tissue that developed into tan-to-brown lesions surrounded by chlorotic halo on the leaves. Oval-shaped lesions were observed occasionally on petioles. Lesions contained erumpent, dark brown, flask-shaped pycnidia with the ostiole on the upper surface of the foliage. Thirty samples, consisting of diseased leaves and petioles of parsley, were collected from each field. Infected tissues were surface-sterilized in 1% NaOCl for 2 min, rinsed in sterile distilled water, placed on petri dishes containing potato dextrose agar (PDA), and incubated for 10 to 14 days at 25°C. The fungus formed long, multiseptate (0 to 4), hyaline, filiform conidia (14 to 29 μm × 0.5 to 1.9 μm), and short conidiophores within the pycnidia. Based on the morphological characteristics of the fungus, the pathogen was identified as Septoria petroselini Desm. (1). Monoconidial cultures of 18 isolates were prepared. Pathogenicity was confirmed by brush-inoculating slightly wounded foliage of 5- to 7- week-old parsley plants (cv. Kereviz yapragi) with a conidial suspension (106 conidia per ml of sterile water) of each isolate of S. petroselini. Control plants that were brush-inoculated with distilled water and inoculated plants were placed in clear polyethylene bags that were closed and incubated at 20°C for 48 h. The bags were removed, and plants were maintained in a dew chamber for 21 days at 65 to 70% relative humidity. Foliar symptoms developed 15 days after inoculation and appeared similar to lesions observed in the field. Yellowing and necrosis of leaves was also observed on >60% of inoculated plants. No lesions developed on the control plants. The pathogen was readily reisolated on PDA from inoculated plants. To our knowledge, this is the first report of Septoria blight of parsley in the Mediterranean Region of Turkey. Reference: (1) R. F. Cerkauskas and J. Uyenaka. Plant Dis. 74:1037, 1990.


Plant Disease ◽  
1999 ◽  
Vol 83 (3) ◽  
pp. 301-301 ◽  
Author(s):  
B. de los Santos G de Paredes ◽  
F. Romero Muñoz

A wilting disease of strawberry (Fragaria × ananassa Duchesne ‘Oso Grande’) was observed in production fields in Huelva, southwestern Andalucía, Spain. Crowns of wilted plants developed a reddish brown, firm rot. Longitudinal sections of roots of diseased plants showed a black coloration of the cortex. Symptons also included blighting of flowers due to floral infection and rotting of green and ripening fruits. On the fruit, the round, firm sunken lesions were covered with masses of salmon-colored spores. Lesions on the leaves were round, ranged in diameter from 5 to 10 mm, and were light brown with purple edges. Infected tissues were surface disinfected in 20% sodium hypoclorite, blotted dry, and plated on water agar. Dishes were incubated at 25°C; hyphal tips made of fungi growing from lesions were transferred to potato dextrose agar (PDA) and incubated under cool-white fluorescent light at 25°C. One fungus was isolated consistently from lesions on different tissues. It was identified as Colletotrichum acutatum by morphological characteristics (2) and enzyme-linked immunosorbent assay (1). On PDA, the mycelium of the fungus was white to gray and covered with salmon spore masses. Colony diameters on PDA averaged 45 mm after 7 days at 25°C. Hyaline, aseptate conidia were cylindrical, fusiform, and intermediate in shape and averaged 12.8 × 4.2 μm in size. The fungus produced setae on infected fruit. Inoculations of strawberry cvs. Oso Grande and Chandler with conidial suspensions (106 conidia per ml) of C. acutatum produced lesions on the fruit, petioles, and crowns, and caused wilt. The pathogen was reisolated from lesions on the inoculated plants. This is the first report of C. acutatum causing strawberry anthracnose in Huelva. References: (1) T. A. Cooke et al. EPPO Bulletin 25:57, 1995. (2) B. C. Sutton. The Coelomycetes. CMI, Kew, England, 1980.


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