scholarly journals First Report of Phytophthora Blight of Lily Caused by Phytophthora nicotianae in China

Plant Disease ◽  
2010 ◽  
Vol 94 (6) ◽  
pp. 782-782 ◽  
Author(s):  
X. M. Yang ◽  
J. H. Wang ◽  
S. P. Qu ◽  
L. H. Wang ◽  
L. C. Peng

Lily (Lilium spp.) is an economically important cut flower in China. In August 2009, 30 to 40% of plants of lily cv. Siberia in a greenhouse for cut flower production in Yunnan, China were severely diseased. Infected plants developed water-soaked lesions and soft rot on the base of stems and leaves near the soil surface. As the disease progressed, stems bent and plants collapsed. Soft rot symptoms were observed on some bulbs and roots of severely diseased plants. Small, diseased tissue fragments (approximately 3 mm) were surface disinfected with 0.5% NaOCl and then plated to Phytophthora selective medium (10% V8 juice agar) (4). Inoculated dishes were incubated at 25°C in the dark. After 5 days, white colonies with abundant aerial mycelia developed from all plated tissue samples. The fungus had aseptate hyphae. Sporangia were papillate, both caducous and noncaducous, and the shape ranged from ovoid to spherical. The dimensions of sporangia were 30 to 62 × 21 to 46 μm. On the basis of morphological features, isolates were identified as Phytophthora nicotianae Breda de Haan. The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS1/ITS4 and sequenced. BLAST analysis of the 835-bp fragment showed a 99% homology with the sequence of P. nicotianae AY833527. The nucleotide sequence has been assigned GenBank No. GU299778. PCR amplification of genomic DNAs using the P. nicotianae-specific primer pair ITS3-PNIC1 generated a 455-bp sequence (3). The result further confirmed the identity of P. nicotianae. Pathogenicity tests were conducted in the greenhouse on lily cv. Siberia grown in pots. Ten 3-month-old plantlets were inoculated by watering the wounded stem bases and soil surface with 30 ml of zoospore suspensions (105 spores per ml). Five uninoculated plantlets were used as controls. All plantlets were covered with plastic bags and incubated at room temperature (22 to 26°C) for 48 h. Inoculated plants developed initial symptoms of slight chlorosis and wilting of lower leaves. Within a 3-week period, all plants died due to soft rot of stem bases and leaves. The pathogen was reisolated from inoculated plants but not from control plants that were symptomless. P. nicotianae has been reported as the causal agent of Phytophthora blight on lily in Korea, Japan, and Hungary (1,2). To our knowledge, this is the first report of Phytophthora blight of lily in China. References: (1) J. Bakonyi et al. Plant Pathol. 50:795, 2001. (2) H. J. Jee and W. G. Kim. Plant Pathol. J. 14:452, 1998. (3) P. W. Tooley et al. Appl. Environ. Microbiol. 63:1467, 1997. (4) X. B. Zheng. Phytophthora and Its Research Technology. Beijing. China Agriculture Press, Beijing, 1997.

Plant Disease ◽  
2005 ◽  
Vol 89 (11) ◽  
pp. 1241-1241 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Several species of Diplotaxis (D. tenuifolia, D. erucoides, and D. muralis), known as wild or sand rocket, are widely cultivated in Italy. Rocket is used in Mediterranean cuisine as salad, a component of packaged salad products, and as a garnish for food. In winter 2003, a severe disease was observed on D. tenuifolia grown in unheated glasshouses on commercial farms near Albenga in northern Italy. Initial symptoms included stem necrosis at the soil level and darkening of leaves. As stem necrosis progressed, infected plants wilted and died. Wilt, characterized by the presence of soft and watery tissues, occurred within a few days on young plants. The disease was extremely severe in the presence of high relative humidity and mild temperature (15°C). Necrotic tissues became covered with white mycelium that produced dark sclerotia. Diseased stem tissue was disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm streptomycin sulfate. Sclerotinia sclerotiorum (1) was consistently recovered from infected stem pieces. Sclerotia observed on infected plants measured 1.23 to 3.00 × 1.40 to 5.38 mm (average 2.10 × 2.85 mm). Sclerotia produced on PDA measured 1.00 to 4.28 × 1.00 to 6.01 mm (average 2.38 × 3.23 mm). Pathogenicity of three isolates obtained from infected plants was confirmed by inoculating 30-day-old plants of D. tenuifolia grown in 18-cm-diameter pots in a glasshouse. Inoculum, 2 g per pot of wheat kernels infested with mycelium and sclerotia of each isolate, was placed on the soil surface around the base of each plant. Three replicates of five pots each were used per isolate. Noninoculated plants served as controls. The inoculation trial was repeated once. All plants were kept at temperatures ranging between 10 and 26°C (average 15°C) with an average relative humidity of 80% and were watered as needed. Inoculated plants developed symptoms of leaf yellowing within 12 days, soon followed by the appearance of white mycelium and sclerotia, and eventually wilted. Control plants remained symptomless. S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of infection of D. tenuifolia by S. sclerotiorum in Italy as well as worldwide. The disease currently has been observed in the Liguria Region but not yet in other areas where sand rocket is cultivated. The economic importance of this disease for the crop can be considered medium at the moment, but is expected to increase in the future. Reference: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift, 75, 1949.


Plant Disease ◽  
2001 ◽  
Vol 85 (11) ◽  
pp. 1207-1207
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
G. Gilardi ◽  
M. L. Gullino

Gazania sp. hybrid is produced in pots in the Albenga Region of northern Italy for export to central and northern Europe. During fall 2000 to spring 2001, sudden wilt was observed in commercial plantings of this ornamental. Initial symptoms included stem necrosis at the soil level and yellowing and tan discoloration of leaves. As stem necrosis progressed, infected plants wilted and died. Wilt followed by soft rot occurred within a few days on young plants after the first leaf symptoms. Necrotic tissues became covered with white mycelia that produced dark, spherical (2 to 6 mm diameter) sclerotia. Sclerotinia sclerotiorum was consistently recovered from infected stem pieces of Gazania disinfested for 1 min in 1% NaOCl, plated on potato dextrose agar amended with streptomycin sulfate at 100 mg/liter. Pathogenicity of three fungal isolates was confirmed by inoculating 45- to 60-day-old plants grown in containers (14 cm diameter). Inoculum that consisted of wheat kernels infested with mycelium and sclerotia of each isolate was placed on the soil surface around the base of each plant. Noninoculated plants served as controls. All plants were maintained outdoors where temperatures ranged between 8 and 15°C. Inoculated plants developed symptoms of leaf yellowing, followed by wilt, within 7 to 10 days, while control plants remained symptomless. White mycelia and sclerotia developed on infected tissues, and S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of wilt of Gazania sp. hybrid caused by S. sclerotiorum in Italy. A crown rot of Gazania caused by S. sclerotiorum has been reported from California in the United States(1). Reference: (1) V. M. Muir and A. H. McCain. Calif. Plant Pathol. 16:1, 1973.


Plant Disease ◽  
2013 ◽  
Vol 97 (4) ◽  
pp. 560-560 ◽  
Author(s):  
H. F. Shen ◽  
B. R. Lin ◽  
J. X. Zhan ◽  
X. M. Pu

Pineapple (Ananas comosus) is an economically important tropical fruit in Hainan Province, China. During September to November 2011, heart rot disese of pineapple was found in Ledong and Wangning of Hainan Province. A survey of 150 ha producing areas of pineapple revealed that the fields were affected at an incidence ranging from 25% to 30%. Infected plants showed water-soaked lesions and soft rot on the base of heart leaves near the soil surface. Heart leaves of infected plants were easily pulled out. As the disease progressed, plants collapsed and died. Diseased tissue fragments (2 × 2 mm) were surface-disinfected for 10 min with 0.3% NaClO, then rinsed three times in sterile water, and plated to 10% V8 juice agar (4). Inoculated dishes were incubated at 26°C in the dark. After 5 days, Phytophthora (identified by the presence of coenocytic hyphae and papillate sporangia) were isolated from the tissue cultures, which has aseptate hyphae. Sporangia were papillate, noncaducous, oval or spherical, and 34.5 to 58.2 μm. Clamydospores, both terminal and intercalary, were also spherical, and were 23.4 to 34.0 μm (2). The ITS region of rDNA was amplified using primers ITS4/ITS5, and the 927-bp product of the ITS showed 99% sequence identity to Phytophthora nicotianae (GenBank Accession No. JF792540), and the sequence was accessed to NCBI (JX978446). Pathogenicity tests were confirmed by irrigating the wounded stem bases of 10 2-month-old pineapple plants with 50 ml of P. nicotionae zoospore solution (15,000 zoospores/ml), and another 10 plants of the same cultivar inoculated with sterile water served as controls. Plants were placed in pots in a greenhouse at 28°C and 90% relative humidity. After 9 days, soft rot was observed clearly on the base of heart leaves of all 10 inoculated plants, while the control plants appeared normal. P. nicotianae was reisolated from the infected pineapple plants, and confirmed to be the same as the inoculated pathogen by conducting a ITS rDNA sequence comparison and morphological characteristics. P. nicotianae was previously reported as the causal agent of heart rot of pineapple in Hawaii, U.S.A. (3) and Guangdong Province of China (1). To our knowledge, this is the first report of P. nicotianae on pineapple in Hainan Province, China. References: (1) J. Z. Chen et al. J. Yunnan Agric. Univ. 8:134, 2003. (2) H. H. Ho. Mycologia 73:705, 1981.(3) K. W. Howard et al. Plant Dis. Rep. 48:848, 1964. (4) X. B. Zheng. Page 81 in: Phytophthora and its Research Technology. China Agricultural Press, Beijing, 1997.


Plant Disease ◽  
2002 ◽  
Vol 86 (1) ◽  
pp. 71-71
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

The production of potted ornamental plants is very important in the Albenga Region of northern Italy, where plants are grown for export to central and northern Europe. During fall 2000 and spring 2001, sudden wilt of tussock bellflower (Campanula carpatica Jacq.) and butterfly flower (Schizanthus × wisetonensis Hort.) was observed on potted plants in a commercial greenhouse. Initial symptoms included stem necrosis at the soil line and yellowing and tan discoloration of the lower leaves. As stem necrosis progressed, infected plants growing in a peat, bark compost, and clay mixture (70-20-10) wilted and died. Necrotic tissues were covered with whitish mycelia that produced dark, spherical (2 to 6 mm diameter) sclerotia. Sclerotinia sclerotiorum was consistently recovered from symptomatic stem pieces of both plants disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar amended with streptomycin sulphate at 100 ppm. Pathogenicity of three isolates obtained from each crop was confirmed by inoculating 45- to 60-day-old C. carpatica and Schizanthus × wisetonensis plants grown in containers (14 cm diameter). Inoculum that consisted of wheat kernels infested with mycelia and sclerotia of each isolate was placed on the soil surface around the base of previously artificially wounded or nonwounded plants. Noninoculated plants served as controls. All plants were maintained outdoors where temperatures ranged between 8 and 15°C. Inoculated plants developed symptoms of leaf yellowing, followed by wilt, within 7 to 10 days, while control plants remained symptomless. White mycelia and sclerotia developed on infected tissues and S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of stem blight of C. carpatica and Schizanthus × wisetonensis caused by S. sclerotiorum in Italy. The disease was previously observed on C. carpatica in Great Britain (2) and on Schizanthus sp. in the United States (1). 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) J. Rees. Welsh J. Agric. 1:188, 1925.


Plant Disease ◽  
2004 ◽  
Vol 88 (9) ◽  
pp. 1044-1044
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Thymus × citriodorus is well known for the citrus aroma released by its leaves and is grown as a potted plant in northern Italy. This species is widely used in gardens and landscapes and for culinary purposes. In the Liguria Region alone, 1.5 million plants are grown. In the winter of 2002, extensive chlorosis was observed on potted plants of Thymus × citriodorus cv. Silver Queen grown outdoors on commercial farms near Albenga. Initial symptoms included stem necrosis at the soil level and darkening of leaves. As stem necrosis progressed, infected plants wilted and died. Wilt, characterized by the presence of soft and watery tissues, occurred within a few days on young plants. Necrotic tissues became covered with whitish mycelium that produced dark sclerotia. Sclerotinia sclerotiorum (Lib.) de Bary (1) was consistently recovered from infected stem pieces of Thymus × citriodorus. The diseased stem tissue was disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm of streptomycin sulfate. Sclerotia produced on PDA were ellipsoid and measured 5.2 to 4.4 × 2.1 to 1.5 mm (average 3.5 × 3.0 mm). Pathogenicity of three isolates obtained from infected plants was confirmed by inoculating 30-day-old plants grown in 14-cm-diameter pots in a screenhouse. Inoculum that consisted of wheat kernels infested with mycelium and sclerotia of each isolate was placed on the soil surface around the base of each of 10 plants. Noninoculated plants served as controls. The inoculation trial was repeated once. All plants were kept at temperatures ranging between 5 and 26°C and watered as needed. Inoculated plants developed symptoms of leaf yellowing within 13 days, soon followed by the appearance of white mycelium, and eventually wilted. Control plants remained symptomless. White mycelium and sclerotia developed on infected tissues and S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of white mold of Thymus × citriodorus caused by S. sclerotiorum. The economic importance of this disease for the crop can be considered low. Reference: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift, 1949.


Plant Disease ◽  
2000 ◽  
Vol 84 (8) ◽  
pp. 923-923
Author(s):  
G. J. Holmes

In 1999, during an evaluation of pumpkin (Cucurbita pepo) fruit for susceptibility to naturally occurring postharvest diseases, a soft rot of unknown etiology was noted. No fungal growth or sporulation was seen on the fruit surface and no root or crown rot was observed in the field. When fruit were cross-sectioned, masses of white, floccose mycelium covering large sections of the seed cavity were observed. Rot was observed in 21 fruit (6.4% of the total). The fungus was isolated from symptomatic fruit on a modified P10ARPH agar medium, semi-selective for Phytophthora spp. (2). Isolates from eight fruit formed papillate, ovoid sporangia, abundant chlamydospores, and colonies characteristic of P. nicotianae (1). No oospores were produced. Four sound pumpkin fruit (cv. Early Autumn) were inoculated with four isolates (one isolate per fruit). Each isolate was recovered from a different fruit. Pumpkins were surface sterilized at the point of inoculation by wetting with 70% ethanol. Inoculation was done by removing a small amount of mycelium from pure culture using a sterile, wooden toothpick and inserting it 2 cm deep into opposite sides of the mid section of sound fruit (two inoculations per fruit). Control fruit were punctured with sterile toothpicks (once per fruit). First symptoms appeared 4 days after inoculation at room temperature (22 to 24°C). Symptoms consisted of circular, water-soaked areas originating from the point of inoculation. Average diameter (based on four measurements on two fruit) of the water-soaked lesions were 3 cm at first appearance (i.e., 4 days) and 11 cm 10 days after inoculation. No symptoms developed on controls. When symptomatic fruit were cross-sectioned, masses of white, floccose mycelium were noted. Reisolation of this mycelium onto selective medium yielded P. nicotianae, thus fulfilling Koch's postulates. This is the first report of P. nicotianae causing fruit rot of pumpkins. References: (1) D. C. Erwin and O. K. Ribeiro. 1996. Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN. (2) H. D. Shew. Phytopathology 77:1090, 1987.


Plant Disease ◽  
2000 ◽  
Vol 84 (11) ◽  
pp. 1250-1250 ◽  
Author(s):  
M. E. Matheron ◽  
M. Porchas

In March 2000, plants began to die within two garbanzo (Cicer arietinum L.) fields about 48 km apart in southwestern Arizona. Initial symptoms included wilting of leaves and stem necrosis on individual branches, followed by entire plant necrosis and death. White mycelium was present on plant stems near the soil surface. In one field, small black irregularly shaped sclerotia (1 mm in diameter) were present on the infected stem surface along with the white mycelia, whereas in the other field the associated sclerotia were of similar shape but larger (5 to 6 mm in diameter). Isolation from diseased garbanzo stem tissue from the respective fields yielded Sclerotinia minor, which produced small sclerotia when cultured on potato-dextrose agar and S. sclerotiorum, which produced the typical larger sclerotia of this species. To fulfill Koch's postulates, healthy plants and associated soil from a garbanzo field with no evidence of infection by Sclerotinia were removed with a shovel and transferred into a series of 8-liter plastic pots. After transporting back to the laboratory, some of the plants were inoculated by wounding stems with a 5-mm-diameter cork borer, placing an agar disk containing either S. minor or S. sclerotiorum onto each wound, securing the agar disk to the stem with plastic tape, then incubating the plants at 25°C for 7 days. Control plants were treated similarly except that agar disks did not contain Sclerotinia. Stems inoculated with S. minor or S. sclerotiorum developed symptoms of wilt and necrosis, including the appearance of white mycelium and sclerotia on the stem surface, whereas control plants remained healthy. S. minor or S. sclerotiorum were recovered from garbanzo stems inoculated with the respective species of the pathogen. Sclerotinia leaf drop, which can be caused by S. minor or S. sclerotiorum on lettuce in Arizona, had been observed in both fields previously. Garbanzo fields in Arizona usually are watered by furrow irrigation. Disease was most severe in areas of the garbanzo fields that were heavily irrigated with resultant wetting of tops of plant beds. Proper management of irrigation water and avoidance of establishing a garbanzo planting in fields following lettuce could help reduce future losses from these pathogens. S. minor previously had been reported as a pathogen on Cicer arietinum from the island of Sardinia (2); however, this is apparently the first report of the pathogen on garbanzo other than in Sardinia. S. sclerotiorum has been reported as a pathogen on this host in several countries including the United States (California) (1) but not previously in the state of Arizona. References: (1) I. W. Buddenhagen, F. Workneh, and N. A. Bosque-Perez. Int. Chickpea Newsl. 19:9–10, 1988. (2) F. Marras. Rev. Appl. Mycol. 43:112, 1964.


Plant Disease ◽  
2014 ◽  
Vol 98 (7) ◽  
pp. 1011-1011 ◽  
Author(s):  
Y. Li ◽  
L. G. Mao ◽  
D. D. Yan ◽  
X. M. Liu ◽  
T. T. Ma ◽  
...  

Ginger (Zingiber officinale Roscoe) is an important commercial crop planted on more than 13,000 ha annually in Anqiu city, Shandong Province, China. From 2010 to 2011, the incidence of Pythium soft rot disease on cv. Laiwu Big Ginger reached 40 to 75% in Anqiu and yield losses of up to 60% were observed. The disease symptoms included brown spots on ginger rhizomes followed by soft rot, stems and leaves above ground becoming withered and yellow, and water soaking on the collar region. The soft rot did not produce offensive odors, which is different from bacterial rots (2). Forty symptomatic rhizomes were sampled from eight farms. Martin's method (1) was used to isolate the pathogen. Ten pieces from each rhizome were washed with sterile distilled water for 30 s and plated on Martin's selective medium at 26°C in a chamber without light. Colonies grew with cottony aerial mycelium. Main hyphae were 5.7 to 9.6 μm wide. Globose sporangia consisting of terminal complexes of swollen hyphal branches were 11.4 to 18.3 μm wide. The average diameter of zoospores was 9.2 μm. The oogonia were globose and smooth, with a diameter of 21 to 33 μm. The sequences of the rRNA gene internal transcribed spacer (ITS) regions 1 and 2 and the 5.8S gene of five isolates were amplified using primers ITS1 and ITS4 (4), and the nucleotide sequence was the same as isolate No. 2, which was deposited in GenBank (Accession No. KC594034). A BLAST search showed 99% identity with Pythium aphanidermatum strain 11-R-8 (Accession No. JQ898455.1). Pathogenicity tests of five isolates were carried out in a greenhouse. Sixty plants (cv. Laiwu Big Ginger) were grown for 30 days in plastic pots (diameter 20 cm) in sandy soil (pH 5.48) and inoculated. Ten plants were used as untreated controls. Five isolates were grown on Martin's liquid medium for 72 h and the spores were harvested in sterile distilled water. Aqueous spore suspensions of the five isolates were adjusted with deionized water to 1 × 108 CFU/ml and injected with a syringe into the soil around the rhizome of the plants. Plants were then placed in the greenhouse at 24 to 26°C and assessed for rhizome rot on the 14th day after inoculation. The inoculated isolates were recovered from the diseased rhizomes, confirming their pathogenicity. To our knowledge, this is the first report of ginger Pythium soft rot caused by P. aphanidermatum in China. Ginger Pythium soft rot caused by P. myriotylum is reported in Taiwan (3). References: (1) F. N. Martin. Page 39 in: The Genus Pythium. American Phytopathological Society, St. Paul, MN, 1992. (2) E. E. Trujillo. Diseases of Ginger (Zingiber officinale) in Hawaii, Circular 62, Hawaii Agricultural Experiment Station, University of Hawaii, December 1964. (3) P. H. Wang. Lett. Appl. Microbiol. 36:116, 2003. (4) T. J. White. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, CA, 1990.


Plant Disease ◽  
2005 ◽  
Vol 89 (4) ◽  
pp. 430-430 ◽  
Author(s):  
C. X. Hong ◽  
P. A. Richardson ◽  
P. Kong

A severe blighting of shoots on Forsythia × intermedia cv. Lynwood Gold plants was observed at several commercial nurseries in Virginia from 2001 to 2004. Crop losses ranged from 10 to 35%. Symptoms first occurred at the tips of shoots, including those that were trimmed and not trimmed, and then progressed downward. Diseased shoots wilted quickly and usually turned black, and foliage on these shoots withered and became necrotic. With PARP-V8 selective medium (2), a species of Phytophthora was isolated consistently from symptomatic shoots (including tissues from shoot tips, leaves, and stems) as well as from apparently healthy roots. These isolates produced arachnoid mycelia and numerous noncaducous, papillate sporangia but did not produce sexual structures on isolation plates; these morphological characters are consistent with those of Phytophthora nicotianae. All isolates produced a single-strand conformation polymorphism pattern typical of P. nicotianae (3). To test pathogenicity, 1-year-old, healthy-appearing cv. Lynwood Gold forsythia plants (canopy size = 100 cm × 60 cm) in four 12-liter containers were sheared. Two plants were inoculated by spraying each plant with 200 ml of a zoospore suspension (1.6 × 104 spores per ml, prepared from one isolate), and the other two plants were not treated and served as controls. Plants were covered with plastic bags overnight to encourage infection and then were grown in a field (temperature range = 20 to 33°C). Severe blight developed on trimmed shoots and new shoot tips of inoculated plants within 1 week after inoculation. The same pathogen was isolated from all blighted leaf and stem pieces assayed. Blight symptoms were not observed on control plants during a 1-month observation period. Phytophthora nicotianae has been reported to attack F. viridissima in Italy (1) causing root and collar rot but not shoot blight. To our knowledge, this is the first report of shoot blight on Forsythia spp. caused by P. nicotianae and the first report of P. nicotianae on Forsythia spp. in the United States. References: (1) S. O. Cacciola et al. Plant Dis. 78:525, 1994. (2) A. J. Ferguson and S. N. Jeffers. Plant Dis. 83:1129, 1999. (3) P. Kong et al. Fun. Gen. Biol. 39:238, 2003.


Plant Disease ◽  
2010 ◽  
Vol 94 (1) ◽  
pp. 134-134 ◽  
Author(s):  
L. Luongo ◽  
M. Galli ◽  
L. Riccioni ◽  
A. Belisario

Bird of paradise, also known as crane flower (Strelitzia reginae Aiton), is a monocotyledonous flowering plant indigenous to South Africa. It is commonly grown and commercialized as an ornamental plant and it is appreciated for its beautiful flowers. In October of 2008, dark leaf spots and leaf blight associated with a severe root and foot rot were observed on several plants of S. reginae grown in a private garden located in Fiumicino, Italy. Small fragments of tissues (approximately 3 mm) collected from the base of leaves and roots and the margins of brown lesions, previously surface disinfected with 0.5% NaOCl, were plated onto potato dextrose agar (PDA) and incubated at 22°C in the dark. White, web-like, slow-growing colonies with coenocytic mycelium and hyphal swellings consistently developed from all plated tissue samples. Sporangia were ovoid or ellipsoid with prominent papillae (including some bipapillate) and frequently caducous with a short stalk. The dimensions of sporangia were 27 to 64 × 23 to 45 μm (average 43 × 35 μm). Chlamydospores were terminal or intercalary and approximately 30 μm in diameter. Isolates were considered heterothallic because they did not produce gametangia in vitro or in planta. On the basis of morphological features, isolates were identified as Phytophthora nicotianae (Breda de Haan). The identity was confirmed by internal transcribed spacer (ITS) sequence comparison in NCBI database with 99% identity with sequences available in GenBank (e.g., EU331089) and with cytochrome c oxidase subunit I (Cox I) with 99% identity with AY564196 by Kroon et al. (2). The sequences of one isolate, AB177, were deposited in GenBank (Accession Nos. FN430681 and FN552051 for ITS and Cox I, respectively). Pathogenicity tests were conducted in the greenhouse on leaves of a 1-year-old potted S. reginae plant by placing 5-mm-diameter mycelial plugs, cut from the margins of 10-day-old actively growing cultures, with mycelium in contact with plant tissues gently wounded with a needle. Controls were treated as described above, except that PDA sterile plugs were used. Plants were misted with water and placed in sealed plastic bags for 48 h. After 10 days, artificially wounded strelitzia leaves showed lesions (approximately 1 cm long). Controls remained symptomless. All inoculated leaves showed the same leaf symptoms as observed on naturally diseased plants. The pathogen was consistently reisolated from lesions. P. nicotianae has been reported as the causal agent of leaf blight and stem, collar, and root rot on several plants (1). It has been reported as an agent of Phytophthora blight on strelitzia in Japan (3). To our knowledge, this is the first report of P. nicotianae on strelitzia in Italy. References: (1) D. C. Erwin and O. K. Ribeiro. Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN, 1996. (2) L. P. N. M. Kroon et al. Fungal Genet. Biol. 41:766, 2004. (3) S. Uematsu et al. Ann. Phytopathol. Soc. Jpn. 60:746, 1994.


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