scholarly journals First Report of Blight of Field Peppers Caused by Phytophthora capsici in Ontario

Plant Disease ◽  
2000 ◽  
Vol 84 (6) ◽  
pp. 705-705 ◽  
Author(s):  
T. R. Anderson ◽  
R. Garton

In August 1994, a disease of sweet peppers (Capsicum annuum L.) and butternut squash (Cucurbita pepo L.) was observed in a 2-ha field near Harrow, Essex County, ON, Canada. In 1995, a similar disease was noted on peppers at two locations 30 km apart in Essex County. In 1997, the disease occurred on peppers in a 20-ha field in the vicinity of the 1994 outbreak. Yield loss was estimated at 40 to 60% in pepper fields and 20% in the affected squash field. Brown, necrotic lesions were more prevalent on pepper fruits and upper stems and lateral branches than basal stems. Affected plants occurred in lower areas of fields that had been flooded by rain or irrigation. Gray, floccose masses of sporangia were evident on fruits and stems under humid conditions and on the internal surfaces of infected fruits. Symptoms were similar to those described for Phytophthora blight of pepper (1). Squash infections occurred where fruits contacted soil. Isolations were made from sections of fruit, stems, and leaves of pepper and squash plants with symptoms of disease on lima beans (Difco Laboratories, Detroit) or 20% V8 agar medium and incubated at 22°C. Phytophthora capsici was readily isolated from all plants with disease symptoms. Observations of colony morphology and growth were made on cultures on 20% V8 agar at 25°C under continuous fluorescent light. Sporangia were papillate and averaged 45 ± 5.9 × 27 ± 3.5 μm in size (range 28 to 58 × 21 × 39 μm). Oospores were spherical and 23 ± 2.9 μm in diameter (range 16 to 28 μm) and, when the external wall was included, were 28 ±2.7 μm in diameter (range 23 to 37 μm). Pedicels varied in length, averaging 63 ± 30.9 μm (range 9 to 129 μm). These observations are similar to those described for P. capsici (2). Mating type was determined by coculture with isolates obtained from A. F. Schmitthenner (OARDC, Wooster, OH) designated A1 and A2. Oospore development was determined after 10 days growth at 25°C on 20% V8 agar. Mating types A1 and A2 occurred among Ontario isolates from pepper and squash. In 1995, 13 of 15 isolates tested were A1, and in 1997, 1 of 5 was A1. Both mating types were found in the same field. Pathogenicity of pepper and squash isolates was tested by inoculating greenhouse-grown pepper cvs. Merlin and North Star at the 5-leaf stage by adding 5 ml of a spore suspension (1,000 sporangia per ml) to the crown and adjacent soil or sprayed on the foliage until run off. Plants were covered in plastic bags for 24 h. Wilting and plant death occurred at 4 and 10 days, respectively, with both cultivars. Crown-inoculated plants wilted prior to development of brown lesions on lower stems at the soil line. Symptoms on foliar-inoculated plants were first observed on young tissue at growing points and stem nodes. P. capsici was reisolated from affected tissue. This is the first report of Phytophthora blight of sweet pepper in Ontario. References: (1) L. H. Leonian. Phytopathology 12:401, 1922. (2) P. H. Tsao and A. Alizadeh. 1988. Proceedings of the 10th International Cocoa Research Conference. Santo Domingo, Dominican Republic, pp. 441–445.

2018 ◽  
Vol 7 (1) ◽  
pp. 51-51
Author(s):  
Sajjad Hyder ◽  
Muhammad Inam-ul-Haq ◽  
Raees Ahmed ◽  
Amjad S. Gondal ◽  
Nida Fatima ◽  
...  

Bell pepper (Capsicum annuum L.) is one of the extensively cultivated vegetable crop in Punjab, Pakistan. During two years of field surveys, February-November 2016-17, damping off and blight symptoms were observed. Average seedling mortality was recorded as 18.7% while yield loss due to blight was estimated 32 to 41% at mature stages. Maximum blight infection was recorded from the areas frequently flooded with canal irrigation system. At early stages, lesions were noticed on stem portions at soil line level while at crop maturity stages blight symptoms were noted. Leaves were blanched and wilted while fruits were covered with white mold. Masses of sporangia were evident on and inside the infected fruits under humid conditions. A total of twelve isolates were recovered from infected root, stem and fruit portions on rye agar media (Caten and Jinks, 1968) incubated at 25oC under fluorescent light. Papillated sporangia were averaged 42 ± 2.6 X 27 ± 1.7 μm in size (range 27 - 52 × 23 - 36 μm). Oospores were produced on 20% V8 agar and were spherical 22 ± 1.4 μm in diameter (range 14 to 27 μm) while average pedicels length was recorded as 58 ± 12.5 μm (range 13 to 120 μm). These observations were similar to those described for P. capsici (Cocoa, 1988). DNA was extracted using Cetyl Trimethylammonium Bromide (CTAB) method and the internal transcribed spacer regions (ITS1 and ITS2) were amplified by polymerase chain reaction (White et al., 1990). The amplicons were purified and sequenced in both directions (GenBank Accession No. MF322868 and MF322869). BLAST analysis revealed these isolates showed 99% identity with ITS sequences of Phytophthora capsici (KM369964 and KU518782). Pathogenicity assay was performed on healthy bell pepper seedlings with five repeats. Soil was flooded with 20ml sporangial suspension (1 x 103 sporangia/ml) in pots containing seedlings while 5ml suspension was sprayed until run off on mature plants (Hyder et al., 2018). A set of uninoculated seedlings was used as control. Pots were kept in dew chamber for 10-20 days at 25±2 oC. Seedling mortality was observed five days after inoculation while at later stage plants develop brown-to-black stem lesions with white mycelial growth on leaves. These symptoms were identical to the P. capsici infections in field. Consistent re-isolations of P. capsici confirm its association with the disease. To our knowledge, this is the first report of Phytophthora blight on bell pepper from Pakistan


Plant Disease ◽  
2009 ◽  
Vol 93 (5) ◽  
pp. 548-548 ◽  
Author(s):  
Z. M. Sheu ◽  
J. R. Chen ◽  
T. C. Wang

Phytophthora capsici Leonion was first identified on pepper (Capsicum annuum L) in Taiwan in 1976. At that time, only the A1 mating type was present (2). In 2007, the A2 mating type of P. capsici was identified on tomato and eggplant in the central part of the country (1). During an excessively rainy period in mid-2008, many chili and sweet pepper fields in Taiwan suffered severe losses due to P. capsici. Symptoms included a foliar blight and stem, root, and fruit rot. Plants eventually wilted and died. Symptomatic plants were collected from chili- and sweet pepper-production areas in central, southern, and eastern Taiwan. Fifty-three isolates from single zoospores were identified by PCR using species-specific primers CAPFW/CAPRV2 (4). Mating type was determined by co-inoculating rape seed agar plates (3) with mycelial plugs of the tester and a known isolate. Pc134, maintained by the mycology unit at The World Vegetable Center, and 27220, provided by P. J. Ann at the Taiwan Agricultural Research Institute, were used as reference isolates of A1 and A2 mating types, respectively. Plates were examined microscopically for oospores after 5 to 7 days of incubation at 24°C in the dark. Of the 53 isolates, 15 were identified as the A2 mating type and the remaining 38 isolates were identified as A1. The A2 mating type was found in the central and southern regions while the A1 mating type was widely distributed across all three regions. The sporangia of the A2 mating type were 60.4 to 73.4 × 40.9 to 51.8 μm (average 69.2 × 44.7 μm), whereas sporangia of the A1 mating type were 50.1 to 73.9 × 37.9 to 48.1 μm (average 61.4 × 44.1 μm). In general, the A2 mating type produced longer sporangia and only a few isolates produced chlamydospores in V8 broth and on agar. To our knowledge, this is the first report of the A2 mating type of P. capsici infecting peppers in Taiwan. The presence of both mating types in the same field has been observed. References: (1) P. J. Ann et al. Plant Pathol. Bull. 17:69, 2008. (2) L. S. Leu and C. W. Kao. Plant Prot. Bull. (Taiwan) 23:59, 1981. (3) M. M. Sautor. Mycologia 59:161, 1967. (4) C. Silvar et al. Eur. J. Plant Pathol. 112:43, 2005.


Plant Disease ◽  
2008 ◽  
Vol 92 (11) ◽  
pp. 1488-1492 ◽  
Author(s):  
A. R. Camp ◽  
H. R. Dillard ◽  
C. D. Smart

The efficacy of Muscodor albus, a potential soil biofumigant, to control root and stem rot by Phytophthora capsici, was examined in a greenhouse study. P. capsici-infested potting mix was treated with three rates of M. albus, mefenoxam (Ridomil Gold EC, Syngenta Crop Protection, Inc.), or nothing. Seedlings of five sweet pepper cultivars and one butternut squash cultivar were transplanted into the treated potting mix. After 7 days, the plants were rated on a scale of 0 (healthy) to 5 (dead). The experiment was conducted three times and there was a significant interaction between pepper cultivar and soil treatment. Treatment with the highest rate of M. albus resulted in a slight but significant reduction in disease severity on Alliance, Aristotle, Paladin, and Revolution pepper compared with the pathogen-only control, while no significant decreases in disease severity were observed with butternut squash or the highly susceptible pepper cv. Red Knight. Of the four less-susceptible pepper cultivars, Paladin (the most tolerant cultivar) was the only one on which M. albus, as applied in this study, reduced disease severity to commercially acceptable levels.


Plant Disease ◽  
1998 ◽  
Vol 82 (6) ◽  
pp. 711-711 ◽  
Author(s):  
Greg Parra ◽  
Jean Ristaino

Phytophthora blight caused by the pathogen Phytophthora capsici has caused economic losses in bell pepper and cucurbit fields in the U.S., and the prevalence of the disease has increased in recent years. The pathogen can be dispersed in soil, with surface water, and via splash dispersal from the soil to foliage. Management of the disease relies on modifications in cultural practices, crop rotation, and judicious use of fungicides. Disease occurred in fields that were sprayed with multiple applications of Ridomil Gold (mefenoxam) according to labeled recommendations in 1997. Mefenoxam is the active enantiomer contained in the racemic fungicide metalaxyl. Mefenoxam was widely used on bell pepper for the first time in 1997, but disease was widespread. Insensitivity to mefenoxam and metalaxyl has not been reported previously in field isolates of P. capsici. However, selection for metalaxyl insensitive isolates in the laboratory after mutagenesis has been reported. Insensitivity to metalaxyl has been reported among other Oomycete pathogens including Phytophthora infestans, Pseudoperonospora cubensis, Peronospora tabacina, Bremia lactucae, and Pythium spp. Infected plants were collected from 12 fields in North Carolina by the authors and one additional field in New Jersey (courtesy of Steve Johnston). Infected plants (10 to 30 per field) were surface disinfested in 10% bleach and plated on selective media to isolate P. capsici. Colonies of the pathogen were transferred to V8 juice agar or maintained on cornmeal agar slants. Mefenoxam-amended V8 juice agar was prepared at levels of 0, 5, and 100 ppm. Screening for sensitivity was conducted by placing agar plugs containing the pathogen onto two replicate plates of mefenoxam-amended media at each concentration. Isolates were categorized as sensitive if growth was less than 40% of the unamended control at 5 ppm. Intermediate isolates exhibited growth greater than 40% of the unamended control at 5 ppm but less than 40% of the unamended control at 100 ppm mefenoxam. Insensitive isolates exhibited growth greater than 40% of the unamended control at 100 ppm mefenoxam. Concentrations of the fungicide used to screen for insensitivity were within the range applied in the field. Thus far, 161 isolates have been screened for sensitivity. Of these, 54 isolates were classified as sensitive, 15 as intermediate, and 92 or 57% of the isolates were insensitive. Three quarters of the fields sampled contained insensitive isolates and insensitivity ranged from 11 to 80% within fields. Both A1 and A2 mating types were recovered from some fields and insensitive isolates occurred among both mating types. Isolates that were insensitive to mefenoxam were also insensitive to metalaxyl. A significant proportion of the isolates obtained from infected plants in fields where Ridomil Gold has been used recently were insensitive. The ability of insensitive isolates to cause disease on fungicide-treated plants will be studied in further experiments. Isolates collected between 1988 and 1994 were screened and all isolates were sensitive to metalaxyl (Ridomil 2E). A dramatic shift in populations of P. capsici to insensitivity to the new metalaxyl substitute mefenoxam has occurred in bell pepper fields in a 3-year period.


Plant Disease ◽  
2018 ◽  
Vol 102 (1) ◽  
pp. 253-253 ◽  
Author(s):  
M. Cara ◽  
T. Yaseen ◽  
J. Merkuri

HortScience ◽  
2016 ◽  
Vol 51 (5) ◽  
pp. 518-524 ◽  
Author(s):  
Nathan Shoaf ◽  
Lori Hoagland ◽  
Daniel S. Egel

Phytophthora blight has become one of the most serious threats to the vegetable industry. Managing this disease is challenging, because the oomycete pathogen responsible, Phytophthora capsici, can move rapidly through crop fields, has a wide host range, is resistant to many commonly used fungicides, and produces resilient spores that can survive in soil for up to 10 years. Recent studies have demonstrated that biochar amendments can suppress infection by many soil-borne pathogens—indicating that these amendments could have the potential to help control phytophthora blight. In this study, greenhouse trials were conducted to determine whether two commercially available biochar amendments could suppress P. capsici infection in sweet bell pepper (Capsicum annuum) using three naturally infested field soils. Soil biological and chemical assays were conducted to evaluate whether potential changes induced by biochar amendments were correlated with suppressive activity. Amending soil with a biochar product that included a proprietary mix of beneficial microorganisms and enriched substrates resulted in lower soil P. capsici abundance in all soils, and lower percent root infection in two of the soils tested. This product also resulted in higher soil pH, and lower soil nitrogen availability and leaf chlorophyll content. The other biochar product did not suppress P. capsici, and had few effects on soil chemical and biological properties. Results of this study indicate that some commercially available biochar amendments have the potential to help mediate phytophthora blight, but further trials are needed to confirm that suppressive effects will be observed in field trials. Additional research is also recommended to identify the mechanisms regulating biochar-mediated suppression of phytophthora blight to develop products that can reliably suppress soil-borne diseases in the field.


Plant Disease ◽  
2001 ◽  
Vol 85 (10) ◽  
pp. 1069-1075 ◽  
Author(s):  
Gregory Parra ◽  
Jean Beagle Ristaino

Incidence of Phytophthora blight in bell pepper fields that were sprayed for the first time with Ridomil Gold (mefenoxam) according to labeled recommendations was higher in North Carolina in 1997 than in previous years. Mefenoxam is the more active enantiomer contained in the racemic fungicide metalaxyl. A total of 150 isolates were obtained from 17 fields at eight grower locations. Among isolates from all locations, 30% were classified as sensitive, 10% as intermediate, and 59% were resistant to mefenoxam. Mefenoxam-resistant isolates were found in 82% of the fields sampled (14 of 17 fields). The proportion of resistant isolates in individual (fields ranged from 28 to 100%. The mean effective concentration (EC50) values for mefenoxam-sensitive isolates was 0.568 μg ml-1 (ranging from 0.12 to 1.1 μg ml-1), whereas the mean EC50 value for mefenoxam-resistant isolates was 366.5 μg ml-1 (ranging from 3 to 863 μg ml-1). The mean EC50 value for metalaxyl-sensitive isolates was 0.27 μg ml-1 (ranging from 0.00002 to 1.3 μg ml-1) and for metalaxyl-resistant isolates was 470.34 μg ml-1 (ranging from 10 to 966 μg ml-1). The greatest proportion of resistant isolates came from fields where mefenoxam was used alone rather than in combination with other fungicides. Both mating types were found among resistant isolates, suggesting that these isolates may persist in soil in subsequent years. Field isolates of Phytophthora capsici resistant to mefenoxam on pepper have not been reported previously and now pose new challenges for management of this important disease.


Plant Disease ◽  
2017 ◽  
Vol 101 (10) ◽  
pp. 1827-1827 ◽  
Author(s):  
N. Ali ◽  
A. C. Ramdass ◽  
R. K. Latchoo ◽  
S. N. Rampersad

Plant Disease ◽  
2011 ◽  
Vol 95 (8) ◽  
pp. 1028-1028
Author(s):  
M. T. McGrath ◽  
J. Strauss ◽  
H. R. Dillard

Phytophthora capsici Leonian is an important pathogen of solanaceous and cucurbit crops. Phytophthora blight was first reported on snap bean (Phaseolus vulgaris L.) in Michigan in 2003 (2) and Connecticut in 2010 (3). This report documents the discovery of P. capsici on snap bean (cv. Bronco) grown in Riverhead, NY in September 2008 and August 2010 on snap bean (cv. Valentino) in Holley, NY, more than 690 km away. Disease was favored by frequent rainfall and prolonged wet periods with air temperatures of 24 to 29°C. Both locations were commercial fields previously planted to pepper or cucurbits affected by P. capsici. In Riverhead, infected pods had characteristic yeast-like growth of P. capsici, which were predominantly sporangia. In Holley, large water-soaked lesions were observed on snap bean foliage, and as the disease progressed, leaves became necrotic and detached from the plant. Reddish brown lesions were observed on stems in advance of white areas of sporulation. Infected pods displayed white mycelial growth, were shriveled, and desiccated. P. capsici was isolated from symptomatic tissues. Stems and pods were surface disinfested for 3 min in 0.525% sodium hypochlorite solution, rinsed for 3 min in sterile distilled water, transferred to PARPH (4) media, and incubated at 22°C. After 5 days, hyphae from colony margins were excised and transferred to 15% unclarified V8 agar media. Cultures consisting of white mycelia and ovoid papillate sporangia on long pedicels were identified as P. capsici. Sporangia were 25.0 to 70.0 × 10.0 to 22.5 μm (average 42.0 × 16.25 μm). Identity was further confirmed by PCR primers specific to P. capsici (1). DNA was extracted from mycelia produced on V8 agar and amplification with the species-specific primers resulted in a PCR product of the same size as that obtained from a known isolate of P. capsici. Pathogenicity of the isolate from Holley was determined by two methods on 50-day-old snap bean plants (cv. Valentino) grown in a greenhouse. In method one, four plants were inoculated with 1-cm-diameter mycelial plugs excised from 8-day-old cultures. A single plug was placed against the stem at the soil line. Four control plants were treated similarly with noncolonized agar plugs. In method two, entire plants were atomized with 10 ml of a zoospore suspension (2.6 × 105/ml). Control plants were atomized with sterile distilled water. All plants were placed in a growth chamber with continuous mist for 24 h at 24°C. After 24 h, plants were enclosed in plastic bags and placed in a greenhouse at 27°C. Stem lesions similar to those observed in affected fields were evident on plants treated with mycelia plugs 2 days after inoculation. Plants inoculated with the zoospore suspension developed stem lesions and desiccated pods. Control plants were asymptomatic. P. capsici was successfully recovered from infected plant tissue, fulfilling Koch's postulates. The Riverhead isolate was demonstrated as pathogenic on snap bean and cucumber by placing colonized plugs on pods and fruit that were subsequently incubated in moist chambers (24°C, 90 to 100% relative humidity). P. capsici was successfully recovered from symptomatic pods and fruit. To our knowledge, this is the first report of Phytophthora blight caused by P. capsici on snap bean in New York. References: (1) A. R. Dunn et al. Plant Dis. 94:1461, 2010. (2) A. J. Gevens et al. Plant Dis. 92:201, 2008. (3) J. A. LaMondia et al. Plant Dis. 94:134, 2010. (4) G. C. Papavisas et al. Phytopathology 71:129, 1981.


2017 ◽  
Vol 142 (4) ◽  
pp. 260-264
Author(s):  
Ping Li ◽  
Dong Liu ◽  
Min Guo ◽  
Yuemin Pan ◽  
Fangxin Chen ◽  
...  

Sexual reproduction in the plant parasite Phytophthora capsici Leonian requires the interaction of two distinct mating types, A1 and A2. Co-occurrence of these mating types can enhance the genetic diversity of P. capsici and alter its virulence or resistance characteristics. Using an intersimple sequence repeat (ISSR) screen of microsatellite diversity, we identified, cloned, and sequenced a novel 1121-base pair (bp) fragment specific to the A1 mating type of P. capsici. Primers Pcap-1 and Pcap-2 were designed from this DNA fragment to specifically detect the A1 mating type. Polymerase chain reaction (PCR) using these primers amplified an expected 997-bp fragment from known A1 mating types, but yielded a 508-bp fragment from known A2 mating types. This PCR-based assay could be adapted to accurately and rapidly detect the co-occurrence of A1 and A2 P. capsici mating types from field material.


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