scholarly journals First Report of Phytophthora cryptogea Causing Root Rot on Cherry Laurel Plants in Central Italy

Plant Disease ◽  
2016 ◽  
Vol 100 (5) ◽  
pp. 1025-1025 ◽  
Author(s):  
A. M. Vettraino ◽  
A. Tomassini ◽  
M. Dalla Valle ◽  
D. Liberati ◽  
P. De Angelis ◽  
...  
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 ◽  
2004 ◽  
Vol 88 (4) ◽  
pp. 425-425 ◽  
Author(s):  
C. Cappelli ◽  
V. M. Stravato ◽  
G. Carannante ◽  
R. Parisella

During April 2002 to September 2003 in unheated plastic greenhouses located in Fondi and Sperlonga (Latium Region of central Italy), in which more than 100 ha of cucumber (Cucumis sativus L.) were cultivated, an unusual disease causing decay of roots and plant wilting was observed. Many of the most common cultivars showed susceptibility, and in some farms, severe economic losses occurred. Disease symptoms observed on young plants included stunting, wilting, black root rot, and marked reduction of root development where pseudosclerotial structures were produced. The degree of root symptoms was proportional to the wilting. During periods of high evapotranspiration, wilting was severe in plants at the early stages of disease development, and even lightly infected plants wilted rapidly. Symptoms resembled those caused by vascular wilt fungi and were generally more severe in greenhouses with poorly drained soils. Samples from each of four greenhouses were collected during different periods of the growing season. Each sampling unit consisted of five to eight root pieces that were surface disinfected in 0.1% HgCl2 for 30 s, rinsed in sterile water, placed on petri dishes containing potato dextrose agar (pH 5.5), and incubated for 7 days at 25°C. Phomopsis sclerotioides van Kesteren (1,2) (identification confirmed by R. A. Samson, Centraalbureau voor Schimmelcultures of Utrecht, the Netherlands) was consistently recovered from affected tissues. Subcultures of three isolates were prepared and evaluated for pathogenicity. The experiments were conducted in a greenhouse with a 12-h photoperiod at 25 to 32°C. Seven-week-old seedlings (20 representatives per isolate) of a susceptible hybrid were dipped for 2 min in an agar slurry suspension of the pathogen and then returned to pots. Within 4 to 5 weeks after inoculation, all plants inoculated with each P. sclerotioides isolate showed the same symptoms observed in the field and caused wilting and death of approximately 80% of the inoculated plants. P. sclerotioides was consistently reisolated from the symptomatic test plant, whereas the fungus was never isolated from control plants. Another experiment using naturally infested soil in comparison with sterilized soil confirmed the soilborne nature of the fungus and its pathogenicity. To our knowledge, this is the first report of P. sclerotioides on cucumber in Italy. According to the experience of farmers and agricultural consultants, the disease was first observed in the last 3 to 4 years in unheated plastic greenhouses. However, we cannot exclude the possibility that the disease may have been present in central Italy prior to our observations, since it can be misdiagnosed and the symptoms can be masked by symptoms of other diseases. For these reasons, an accurate monitoring of the pathogen is necessary to determine the magnitude of the problem and its impact on the industry. Management practices that include long-term crop rotation with nonsusceptible hosts, removal and destruction of infected crop debris, and steam soil sterilization are suggested to reduce the economic losses. References: (1) E. Punithalingam et al. No. 461 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, U.K., 1975. (2) H. A. Van Kesteren. Neth. J. Plant Pathol. 73:112, 1967.


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 ◽  
2010 ◽  
Vol 94 (12) ◽  
pp. 1504-1504 ◽  
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
M. L. Gullino

Witloof chicory (Cichorium intybus L.) is an important crop in Italy where most of the crop is still produced in soil. In September 2009, chicory plants (cv. Pan di Zucchero) grown on a commercial farm in Tarquinia (central Italy) showed symptoms of a previously unknown disease. Symptoms, observed 20 days after transplanting, consisted of stunting, yellowing of leaves, and a crown and root rot. Affected plants turned brown, wilted, and eventually died. At the soil level, dark brown-to-black water-soaked lesions coalesced and often girdled the stem. All of the crown and root system was affected. At this location, the disease was severe and widespread, with 60% of observed plants being affected. A Phytophthora-like organism was consistently isolated on a medium selective for oomycetes (4) after disinfestation of lower stem and root pieces of C. intybus for 1 min in a solution containing 1% NaOCl. Tissue fragments of 1 mm2 were excised from the margins of the root and crown lesions. The pathogen genus was identified as Phytophthora based on morphological and physiological features. Sporangia were produced for identification by growing a pure culture for 15 days on modified V8 juice agar medium (Campbell V8 juice [200 ml], agar [15 g], CaCo3 [0.5 g], and sterile water [800 ml]) under alternating light and dark (12/12 h). Sporangia were pyriform to ovoid, papillate, and measured 33.3 to 59.2 × 18.9 to 30.2 μm (average 39.9 × 25.8 μm). Chlamydospores developed in 28-day-old cultures and measured 21.3 to 30.2 × 19.5 to 29.7 μm (average 24.4 × 23.6 μm). Oogonia were globose and measured 26 to 41 μm (average 32.5 μm). Eighty percent of antheridia were paragynous. Amphyginous antheridia (15 to 20%) were also observed. Oospores were scarcely produced and measured 24 to 32 μm in diameter. The internal transcribed spacer (ITS) region of rDNA of a single isolate was amplified using the primers ITS4/ITS6 and sequenced. BLAST analysis (1) of the 851-bp segment showed 100% homology with the sequence of Phytophthora tentaculata. The nucleotide sequence has been assigned GenBank Accession No. GU949536. Pathogenicity of this isolate was confirmed by inoculating C. intybus cv. Pan di Zucchero plants 20 days after transplant. The same isolate was grown for 15 days on a mixture of 70:30 wheat/hemp kernels and then 5 g/liter of the inoculum was mixed into a substrate containing a mixture of blond and black peat (15:85 vol/vol), pH 5.5. Five plants per 2-liter pot were transplanted and four replicates were carried out. Twenty noninoculated plants represented the control treatment. The trial was repeated. Plants were kept in two growth chambers at two temperatures (20 and 25°C). Symptoms similar to those observed in the field developed 7 days after inoculation. Twenty days later, 100 and 40% of the plants were dead at 25 and 20°C, respectively. Control plants remained symptomless. P. tentaculata was consistently reisolated from symptomatic plants. To our knowledge, this is the first report of P. tentaculata on C. intybus in the world ( http://nt.ars-grin.gov/fungaldatabases/index.cfm ). P. tentaculata was recently reported on lavender in Spain (2) and oregano in Italy (3). The economic importance of this disease is relatively low on most commercial farms. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) L. Alvarez et al. Plant Dis. 90:523, 2006. (3) P. Martini et al. Plant Dis. 93:843, 2009. (4) H. Masago et al. Phytopathology 67:425, 1977.


Plant Disease ◽  
2010 ◽  
Vol 94 (1) ◽  
pp. 131-131 ◽  
Author(s):  
S. T. Koike ◽  
Frank N. Martin

In 2006 and 2007, commercially grown spinach (Spinacia oleracea) in California's coastal Salinas Valley (Monterey County) was affected by an unreported root rot disease. Disease was limited to patches along the edges of fields. Affected plants were stunted with chlorotic older leaves. As disease progressed, most of the older foliage first wilted and then turned tan and dry; youngest leaves remained green but were stunted and leathery in texture. Plants most severely affected died. Symptoms on roots were mostly restricted to the distal portion of the root system, where feeder roots and the main taproot turned black. Isolations from root lesions consistently resulted in the recovery of a Phytophthora sp. The isolates were heterothallic, and on the basis of morphological and cytochrome oxidase 2 gene sequence data (GenBank Accession No. GQ984233), the pathogen was identified as Phytophthora cryptogea. To evaluate pathogenicity, individual inocula of four isolates were prepared by incubating colonized 6-mm-diameter V8 agar plugs in filtered soil extract for 2 days at 20°C to induce sporangia production. These cultures were then chilled at 4°C for 20 min and returned to room temperature for 1 h to induce zoospore release (4). Four-week-old spinach plants (cv. Bolero) were uprooted, soaked in suspensions of 1.0 × 105 zoospores/ml for 10 min, and repotted. After treatment, pots were placed in shallow trays of water for 24 h to saturate the root zone, then were removed from trays and incubated in a greenhouse. After 9 days, inoculated plants showed foliar wilting and chlorosis similar to that observed in the field; after 13 days, roots were examined and found to show the black necrosis as seen in the field. P. cryptogea was isolated from all inoculated plants. Control spinach plants, treated with soil extract only, did not develop disease. This experiment was completed two times and the results were similar. To our knowledge, this is the first report of Phytophthora root rot of spinach caused by P. cryptogea in California. This finding is significant because spinach in California is subject to root rots caused by three other pathogens (Fusarium oxysporum, Pythium spp., and Rhizoctonia solani) (1); symptoms from these root rots are very similar to those caused by P. cryptogea, thereby complicating diagnosis. This pathogen has been documented on spinach in Germany and Sweden (2,3). References: (1) S. T. Koike et al. Vegetable Diseases: A Color Handbook. Manson Publishing LtD. London, 2007. (2) H. Krober and E.-O. Beckmann. Phytopathol. Z. 78:160, 1973. (3) M. Larsson and J. Olofsson. Plant Pathol. 43:251, 1994. (4) S. A. Tjosvold et al. Plant Dis. 93:371, 2009.


Plant Disease ◽  
2020 ◽  
Vol 104 (4) ◽  
pp. 1254
Author(s):  
B. H. Lu ◽  
Z. Wang ◽  
G. J. Yi ◽  
G. W. Tan ◽  
F. Zeng ◽  
...  

Author(s):  
Jefferson Bertin Vélez-Olmedo ◽  
Sergio Vélez-Zambrano ◽  
Bianca Samay Angelino Bonfim ◽  
Edisson Cuenca Cuenca ◽  
Susana García ◽  
...  

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