scholarly journals First report of Phytophthora capsici in the Lao PDR

2016 ◽  
Vol 11 (1) ◽  
Author(s):  
S. E. Callaghan ◽  
A. P. Williams ◽  
T. Burgess ◽  
D. White ◽  
T. Keovorlajak ◽  
...  
Plant Disease ◽  
2017 ◽  
Vol 101 (6) ◽  
pp. 1059 ◽  
Author(s):  
R. Petry ◽  
M. E. N. Fonseca ◽  
L. S. Boiteux ◽  
A. Reis

2016 ◽  
Vol 11 (1) ◽  
Author(s):  
K. B. Ireland ◽  
B. S. Weir ◽  
E. J. Cother ◽  
S. Phantavong ◽  
P. Phitsanoukane ◽  
...  

1994 ◽  
Vol 60 (5) ◽  
pp. 257-260 ◽  
Author(s):  
A.H. Thompson ◽  
M.D.R. Uys ◽  
W.J. Botha

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.


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

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

Plant Disease ◽  
2016 ◽  
Vol 100 (6) ◽  
pp. 1247 ◽  
Author(s):  
C. A. Sánchez-Borges ◽  
R. A. Souza-Perera ◽  
J. J. Zúñiga-Aguilar ◽  
S. Shrestha ◽  
K. Lamour ◽  
...  

Plant Disease ◽  
2008 ◽  
Vol 92 (6) ◽  
pp. 982-982 ◽  
Author(s):  
L. M. Aragon-Caballero ◽  
O. P. Hurtado-Gonzales ◽  
J. G. Flores-Torres ◽  
W. Apaza-Tapia ◽  
K. H. Lamour

During 2006, spears, roots, and crowns of asparagus (Asparagus officinalis) exhibiting brown necrotic lesions with water soaking were collected from several sites across Peru (Ica, Lima, and Trujillo). Small infected tissue sections were washed thoroughly with tap and sterile distilled water and transferred to corn meal agar plates (CMA) amended with PARP (100 ppm of pimaricin, 100 ppm of ampicillin, 30 ppm of rifampicin, and 100 ppm of pentachloronitrobenzene) and incubated for five days at 25°C. Hyphal tips were subcultured from actively expanding mycelium. Sporangia produced on CMA were papillate and averaged 38 μm long × 29 μm wide. Chlamydospores were terminal or intercalary and averaged 35 μm in diameter. Isolates incubated in the dark for more than 3 weeks did not produce oospores in single culture. Mating with Phytophthora capsici tester isolates CBS 121656 = A1 and CBS 121657 = A2 indicate that all five isolates were A2. For pathogenicity tests, inoculum was generated by incubating 300 g of autoclaved wheat seeds with four agar plugs (7 mm) of expanding mycelium in polyethylene bags for 1 month at 25°C. Nine-week-old asparagus plants (UC151 F1) were transferred into pots containing autoclaved substrate (1 part sand, 1 part potting soil, and 1 part peat). Inoculum was added as 1 g of inoculum per kilogram of substrate. Plants were maintained in the greenhouse at 23°C and watered daily. Decline symptoms as well as root and spear rot were observed after 7 days and a Phytophthora sp. was reisolated from infected tissue. No symptoms were observed on asparagus plants inoculated with sterile inoculum. DNA was isolated from two representative isolates, and the nuclear ribosomal internal transcribed spacer (ITS) region was amplified with ITS4 and ITS6 primers and sequenced. ITS sequence was submitted for a BLAST search in the NCBI database, showing Phytophthora nicotianae strain UQ848 Accession No AF266776 as the closest match with 99% sequence similarity (1). The consensus ITS sequence was deposited in NCBI (Accession No. EU433396). These results, together with the morphological characteristics, indicate that the Phytophthora sp. isolated from asparagus in Peru is P. nicotianae (Breda de Haan) (2). To our knowledge, this is the first report of P. nicotianae infecting asparagus and represents a new threat for asparagus growers in Peru. Control methods such as moderate watering and metalaxyl application are being applied to reduce Phytophthora outbreaks. References: (1) D. E. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (2) D. C. Erwin and O. K. Ribeiro. Phytophthora Diseases Worldwide. The American Phytopathological Society. St Paul, MN, 1996.


Plant Disease ◽  
2018 ◽  
Vol 102 (2) ◽  
pp. 455-455
Author(s):  
J. F. Cao ◽  
C. Huo ◽  
M. Y. Yang ◽  
N. A. Rajput ◽  
Z. J. Zhao

2016 ◽  
Vol 11 (1) ◽  
Author(s):  
S. E. Callaghan ◽  
V. I. Puno ◽  
A. P. Williams ◽  
B. S. Weir ◽  
V. Balmas ◽  
...  

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