scholarly journals First Report of Phytophthora capsici on Cucumber and Melon in Southeastern Spain

Plant Disease ◽  
2002 ◽  
Vol 86 (5) ◽  
pp. 558-558 ◽  
Author(s):  
M. L. Herrero ◽  
R. Blanco ◽  
M. Santos ◽  
J. C. Tello

In autumn 1999, crown and root rot along with wilting of cucumber (Cucumis sativus L.) were observed in greenhouses in southeastern Spain (Granada). Symptoms appeared again during the 2000 to 2001 growing season. In spring 2001, root and crown symptoms were observed also on melon (Cucumis melo L.) in greenhouses in another area of southeastern Spain (Almeria). Isolates from diseased plants from both locations were identified as Phytophthora capsici (Leonian). Isolates produced papillate sporangia of variable shape, some of them with two or three papilla. Sporangia were caducous with pedicels of variable lengths that could be longer than the sporangia. Three isolates were crossed with P. capsici strains of known mating type. All isolates produced amphigynous antheridia and were mating type A1. Isolates grew well at 35°C and did not produce chlamydospores. Pathogenicity was examined for one isolate from cucumber and one from melon. Cucumber and melon plants at the four-leaf stage and pumpkin (Cucurbita maxima × C. moschata) plants at the five-leaf stage were inoculated with a mycelium suspension. Both isolates caused wilting and death of plants on the three host species tested. The pathogen was reisolated from roots and stems of diseased plants. To our knowledge, this is the first time P. capsici has been found on cucumber in Spain. It is also the first time P. capsici has been found on melon in the greenhouses of southeastern Spain, and the first time it has been reported to cause root and crown rot of melon. Previously, P. capsici has been reported to cause disease of field-grown melon (2) and greenhouse-grown pepper (Capsicum annum) (1) in eastern and southeastern Spain, respectively. References: (1) J. C Tello. Comun. INIA 22, 1984. (2) J. J. Tuset Barrachina. An. INIA 7:11, 1977.

Plant Disease ◽  
2008 ◽  
Vol 92 (7) ◽  
pp. 1138-1138 ◽  
Author(s):  
M. L. Herrero ◽  
M. B. Brurberg ◽  
A. Hermansen

In December 2004, symptoms of root and crown rot were observed on cucumbers (Cucumis sativus L.) in a greenhouse in Norway. Cucumbers were the only crop of the greenhouse that used rockwool as a growing substrate in a hydroponical system. The first symptoms were detected in propagation material. One week after planting, symptoms of root and crown rot were observed and approximately 10% of the plants died. Later, losses of 50% in some greenhouses were observed. A yield reduction as much as 65% was estimated in the winter period (January and February). The two main cucumber cultivars planted were Armada and Lopez. In February 2005, Phytophthora capsici (Leonian) (1) was isolated on potato dextrose agar from a sample of cv. Lopez. The isolate produced deciduous, papillate sporangia (occasionally with two or three papilla) and pedicels that were sometimes longer than the sporangia. Sequencing of amplicons of the internal transcribed spacer region (ITS) rDNA and of the mitochondrial cytochrome c oxidase subunit 1 (Cox1) gene (2) confirmed the identification. Three isolates collected through 2005 from the same greenhouse were crossed with tester strains of P. cryptogea. Formation of oogonia and amphigynous antheridia was always observed in crosses with mating type A2; thus, all isolates were the A1 mating type. All three isolates grew well at 35°C and did not produce chlamydospores. A pathogenicity test was performed with one isolate of P. capsici. Four plants of cucumber cvs. Indira and Jessica were grown in a growth chamber at 24°C. Plants at the two-leaf stage were drenched with 20 ml of a zoospore suspension of 106 zoospores per ml per plant. After 18 days, all plants of both cultivars developed symptoms of crown rot or wilted and died. P. capsici was reisolated from inoculated plants of both cultivars. The pathogenicity test was repeated in the same way, but in a greenhouse with temperatures that ranged between 18 and 29°C. In addition, four plants of both cultivars at the four-leaf stage were inoculated with a suspension of 105 zoospores per ml. After 1 week, all plants developed crown rot or were irreversibly wilted, independently of the plant age or the zoospore concentration. To our knowledge, this is the first report of P. capsici in Norway. 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. Phytopathology 94:613, 2004.


Plant Disease ◽  
1998 ◽  
Vol 82 (11) ◽  
pp. 1283-1283 ◽  
Author(s):  
A. M. Pennisi ◽  
G. E. Agosteo ◽  
S. O. Cacciola ◽  
A. Pane ◽  
R. Faedda

Pepper (Capsicum annuum L.) has become an economically important crop in the coastal provinces of Catanzaro and Vibo Valentia, in Calabria (southern Italy). An old local selection Riggitano, very susceptible to root and crown rot caused by Phytophthora capsici Leonian, is the prevalent cultivar in this area. Although repeated applications of metalaxyl are used as a soil drench, severe outbreaks occur each year on greenhouse crops. To examine metalaxyl resistance in P. capsici, 60 single-hypha isolates of P. capsici were tested in vitro for their level of sensitivity to metalaxyl. The isolates were collected from 1992 to 1997, during epidemic outbreaks of root and crown rot, from two commercial greenhouse pepper crops, near Vibo Valentia and Lametia Terme (Catanzaro). Fungicide sensitivity was determined by plating mycelial plugs onto potato dextrose agar (PDA) amended with metalaxyl. The fungicide was added to PDA after autoclaving, at final concentrations of 0.1, 1, 5, 10, 50, 100, and 200 μg/ml a.i. The percentage of inhibition of radial growth on metalaxyl-amended medium compared with the growth on unamended medium was determined after 6 days of incubation in the dark at 25°C. Three replicate petri dishes were used per treatment and each test was performed twice. The isolates were paired in culture on V8 agar with isolates of P. capsici of known mating type and all proved to be A2 mating type. Significant variation was observed among the isolates tested in responce to metalaxyl. The ED50 values for in vitro inhibition of mycelial growth by metalaxyl ranged from 1 to 11 μg/ml, whereas an ED 50 value of 0.1 μg/ml had been reported for a wild-type isolate of P. capsici obtained from pepper in northern Italy (3). The variation observed among the isolates from Calabria appeared unrelated to both the geographical origin and the year of isolation. The isolates from Calabria were inhibited by between 1 and 12% at 0.1 μg/ml and by between 7 and 27% at 1 μg/ml, proving to be less sensitive to metalaxyl than isolates from Capsicum spp. originating from Central America, tested by other authors (1). According to the criterion used in a recent screening for sensitivity to metalaxyl (2), 19% of the isolates from Calabria should be considered sensitive, as they were inhibited by more than 60% at 5 μg/ml, while all the others were intermediate, as they were inhibited less than 60% at 5 μg/ml but more than 60% at 100 μg/ml. On the basis of this preliminary screening, we report the presence of insensitivity to metalaxyl in field isolates of P. capsici in southern Italy. Although no isolate tested appeared highly resistant to metalaxyl, the presence of a high proportion of isolates with an intermediate level of resistance should be a reason for the growers to use metalaxyl more cautiously to control root and collar rot. References: (1) M. D. Coffey and L. A. Bower. Phytopathology 74:502, 1984. (2) G. Parra and J. Ristaino. Plant Dis. 82:711, 1998. (3) M. L. Romano and A. Garibaldi. La difesa delle piante 3:153, 1984.


Plant Disease ◽  
2019 ◽  
Vol 103 (3) ◽  
pp. 448-455 ◽  
Author(s):  
S. Rooney-Latham ◽  
C. L. Blomquist ◽  
K. L. Kosta ◽  
Y. Y. Gou ◽  
P. W. Woods

Phytophthora tentaculata was detected for the first time in North America in 2012 in a nursery on sticky monkeyflower plant (Diplacus aurantiacus) and again in 2014 on outplanted native plants. At that time, this species was listed as a federally actionable and reportable pathogen by the USDA. As a result of these detections, California native plant nurseries were surveyed to determine the prevalence of Phytophthora species on native plant nursery stock. A total of 402 samples were collected from 26 different native plant nurseries in California between 2014 and 2016. Sampling focused on plants with symptoms of root and crown rot. Symptomatic tissue was collected and tested by immunoassay, culture, and molecular techniques (PCR). Identifications were made using sequences from the internal transcribed spacer (ITS) rDNA region, a portion of the trnM-trnP-trnM, or the atp9-nad9 mitochondrial regions. Phytophthora was confirmed from 149 of the 402 samples (37%), and from plants in 22 different host families. P. tentaculata was the most frequently detected species in our survey, followed by P. cactorum and members of the P. cryptogea complex. Other species include P. cambivora, P. cinnamomi, P. citricola, P. hedraiandra, P. megasperma, P. multivora, P. nicotianae, P. niederhauserii, P. parvispora, P. pini, P. plurivora, and P. riparia. A few Phytophthora sequences generated from mitochondrial regions could not be assigned to a species. Although this survey was limited to a relatively small number of California native plant nurseries, Phytophthora species were detected from three quarters of them (77%). In addition to sticky monkeyflower, P. tentaculata was detected from seven other hosts, expanding the number of associated hosts. During this survey, P. parvispora was detected for the first time in North America from symptomatic crowns and roots of the nonnative Mexican orange blossom (Choisya ternata). Pathogenicity of P. parvispora and P. nicotianae was confirmed on this host. These findings document the widespread occurrence of Phytophthora spp. in native plant nurseries and highlight the potential risks associated with outplanting infested nursery-grown stock into residential gardens and wildlands.


Plant Disease ◽  
2006 ◽  
Vol 90 (9) ◽  
pp. 1135-1142 ◽  
Author(s):  
C. Silvar ◽  
F. Merino ◽  
J. Díaz

Phytophthora crown rot, caused by Phytophthora capsici, is potentially the most destructive disease of pepper in Spain. Phenotypic and genetic diversity of 16 P. capsici isolates collected from 11 farms in northwest Spain was characterized based on virulence, mating type, sensitivity to metalaxyl, and genetic analysis using random amplified polymorphic DNA (RAPD) methods. Low variability was observed among the isolates in their metalaxyl response, with 87.5% being highly sensitive. No isolates of the A2 mating type were detected. More variability was found in the virulence assay, and isolates were classified into two groups according to their pathogenicity on a set of four pepper cultivar differentials. Genetic variation examined with eight RAPD primers generated 92 polymorphic bands and revealed the existence of different patterns among isolates. Cluster analysis using the unweighted pair-group method with arithmetic averages (UPGMA) separated the Spanish isolates into three RAPD groups and established a relationship between the Spanish population and a representative worldwide group of isolates. No correlation was found between groups obtained by RAPD analysis and groups defined by virulence or metalaxyl response.


Plant Disease ◽  
2019 ◽  
Vol 103 (4) ◽  
pp. 691-696 ◽  
Author(s):  
Jeannette Guajardo ◽  
Sebastián Saa ◽  
Natalia Riquelme ◽  
Gregory Browne ◽  
Cristian Youlton ◽  
...  

English (Persian) walnut (Juglans regia) trees affected by root and crown rot were surveyed in five regions of central Chile between 2015 and 2017. In each region, nine orchards, ranging from 1 to 21 years old, were randomly selected and inspected for incidence and severity of tree decline associated with crown and root rot. Soil and symptomatic crown and root tissues were collected and cultured in P5ARP semiselective medium to isolate potential oomycete pathogens, which were identified through morphology and molecularly using ITS sequences in the rDNA gene and beta tubulin gene. The most frequently isolated species was Phytophthora cinnamomi. Pathogenicity tests were conducted with representative oomycete isolates. P. cinnamomi, P. citrophthora, and Pythium ultimum were all pathogenic in J. regia. Nevertheless, only P. cinnamomi and P. citrophthora were pathogenic to English walnut. Py. ultimum caused limited levels of root damage to English walnut seedlings. Our research indicates that as the Chilean walnut industry has expanded, so have walnut crown and root rots induced by oomycetes.


Plant Disease ◽  
2002 ◽  
Vol 86 (9) ◽  
pp. 1050-1050 ◽  
Author(s):  
R. L. Wick ◽  
M. B. Dicklow

From 1999 to 2001, a Massachusetts nursery received a number of shipments of Pothos, Epipremnum aureum (Lindl. & André) Bunting, with significant crown, petiole, and leaf rot. The plants were imported from Costa Rica. Sporangia were observed on diseased tissues, and five presumptive isolates of Phytophthora were recovered from infected petioles and stems for species identification. The five isolates were morphologically indistinguishable from each other. Sporangia were produced in water and on V8 juice agar under fluorescent light at 22°C. Mating type was determined by pairing isolates with A1 and A2 mating types of Phytophthora capsici Leonian. Sporangial measurements were taken from water cultures. Determination of caducity, and measurements of pedicels and oospores were taken from V8 agar cultures. Measurements represent an average of 50 observations a single isolate. In water culture, sporangia were borne in umbellate clusters. Sporangium length/breadth was 48.29 and 22.33 μm respectively; length/breadth ratio 2.16. On solid media, sporangia were upright and caducous. The bases of the sporangia were mostly tapered. Pedicel lengths were 22 to 49 μm (average 35 μm). Oogonia had amphigynous antheridia and developed only in the presence of an opposite mating type, and oospores measured 25.74 μm diameter. All five isolates were the A1 mating type. Chlamydospores were absent in V8 and corn meal agar (CMA) cultures. Metalaxyl sensitivity was determined at 0, 0.1, 0.5, and 5 ppm in CMA with five replications. The isolate was completely sensitive to 5 ppm metalaxyl, but grew as well as the controls at 0.1 ppm metalaxyl. Growth response to temperature was determined on V8 agar at 15, 20, 25, 30, and 35°C in five replications. After 4 days, colony diameters at 20, 25, and 30°C were not significantly different (P = 0.01) and colonies filled the 100-mm petri dishes. At 15 and 35°C, average colony diameter was 65.7 and 71.4 mm, respectively. Based on the above characteristics, the isolates were identified as P. capsici. Koch's postulates were carried out on pepper, Capsicum annuum ‘Italia’, squash, Cucurbita pepo ‘Patty Pan’ seedlings, and rooted cuttings of pothos. Pepper and squash seedlings and rooted pothos were transplanted in 4-in. (10 cm) pots containing a soilless growing medium (Metro Mix 360, W.R. Grace, Columbia, MD). Phytophthora cultures were grown on V8 juice agar for 4 days. An agar culture was added to 200 ml of sterile distilled water and briefly blended. Ten milliliters of the resulting mycelial slurry were pipetted in the soil one cm from the crown on two sides of the plant. Controls received no mycelial slurry. Petiole, leaf, and crown rot of pothos developed within 2 weeks following inoculation. Squash and pepper plants did not become diseased. In a second pathogenicity test, a 1-cm-diameter plug of mycelial growth from a V8 agar culture was placed between the stem and petiole of the lowest leaf of pothos cuttings directly after transplanting. Inoculated plants died within 3 days. The development of umbellate clusters of sporangia, sporangial shape, length/breadth ratio, and lack of pathogenicity to pepper suggest that the P. capsici isolated from pothos belong to the CAPB (tropical) subgroup of Mchau and Coffey (2). References: (1) S. S. A. Al-Hedaithy and P. H. Tsao. Mycologia 71:392, 1979. (2) G. R. Mchau. and M. D. Coffey. Mycol. Res. 99:89, 1995.


Plant Disease ◽  
2001 ◽  
Vol 85 (6) ◽  
pp. 603-606 ◽  
Author(s):  
B. A. Latorre ◽  
M. E. Rioja ◽  
W. F. Wilcox

Phytophthora cactorum, P. cryptogea, P. gonapodyides, and P. megasperma were isolated from necrotic root and crown tissues or the rhizospheres of apple trees exhibiting typical symptoms of Phytophthora root and crown rot in the Central Valley of Chile. Representative isolates of all four species were pathogenic on a variety of apple rootstocks and scions in trials conducted on excised shoots and 1-year-old MM.106 rootstock grown for 4 months in infested potting medium. P. cactorum was the most frequently isolated species and the most virulent in pot tests, although a significant Phytophthora sp.-apple genotype interaction was observed. This is the first report of any species other than P. cactorum causing root and crown rot of apple trees in Chile.


Plant Disease ◽  
1998 ◽  
Vol 82 (10) ◽  
pp. 1165-1170 ◽  
Author(s):  
H. Förster ◽  
J. E. Adaskaveg ◽  
D. H. Kim ◽  
M. E. Stanghellini

Tomato and pepper plants were grown hydroponically in a greenhouse using phosphate or technical and commercial formulations of phosphite as sources of phosphorus nutrition to determine the effects on plant development and susceptibility to Phytophthora root and crown rot. Phosphite-treated tomato and pepper plants were deficient of phosphate and developed phosphorus-deficiency symptoms. Growth of plants (leaf area and leaf, stem, and root dry weights) that were fertilized with phosphite was significantly (P < 0.05) reduced compared with phosphate-fertilized plants. In Phytophthora capsici–inoculated pepper plants, incidence of Phytophthora crown rot was significantly reduced in phosphite-treated plants compared with no phosphorus or phosphate-treated plants. Incidence of crown rot in pepper plants treated with 1 mM phosphate plus 0.3 mM phosphite was intermediate between plants treated with only phosphite (1 mM or 0.1 mM) and plants treated with phosphate (1 mM).


HortScience ◽  
2017 ◽  
Vol 52 (11) ◽  
pp. 1471-1476 ◽  
Author(s):  
Gregory T. Browne

Many species of Phytophthora de Bary are important pathogens of cultivated Prunus L. species worldwide, often invading the trees via their rootstocks. In a series of greenhouse trials, resistance to Phytophthora was tested in new and standard rootstocks for cultivated stone fruits, including almond. Successive sets of the rootstocks, propagated as hardwood cuttings or via micropropagation, were transplanted into either noninfested potting soil or potting soil infested with Phytophthora cactorum (Lebert & Cohn) J. Schöt., Phytophthora citricola Sawada, Phytophthora megasperma Drechs, or Phytophthora niederhauserii Z.G. Abad & J.A. Abad. Soil flooding was included in all trials to facilitate pathogen infection. In some trials, soil flooding treatments were varied to examine their effects on the rootstocks in both the absence and presence of Phytophthora. Two to 3 months after transplanting, resistance to the pathogens was assessed based on the severity of root and crown rot. ‘Hansen 536’ was consistently more susceptible than ‘Lovell’, ‘Nemaguard’, ‘Atlas’, ‘Viking’, ‘Citation’, and ‘Marianna 2624’ to root and/or crown rot caused by P. cactorum, P. citricola, and P. megasperma. By contrast, susceptibility to P. niederhauserii was similarly high among all eight tested genotypes of peach, four genotypes of peach × almond, two genotypes of (almond × peach) × peach, and one genotype of plum × almond. Most plum hybrids were highly and consistently resistant to crown rot caused by P. niederhauserii, but only ‘Marianna 2624’ was highly resistant to both crown and root rot caused by all of the Phytophthora species. The results indicate that there is a broad tendency for susceptibility of peach × almond rootstocks and a broad tendency for resistance of plum hybrid rootstocks to multiple species of Phytophthora.


Plant Disease ◽  
2018 ◽  
Vol 102 (10) ◽  
pp. 2044-2044
Author(s):  
M. de Cara ◽  
A. Ayala-Doñas ◽  
A. Aguilera-Lirola ◽  
E. Badillo-López ◽  
J. Gómez-Vázquez

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