scholarly journals First Report of Pre- and Postemergence Damping-off of Cowpea Caused by Pythium ultimum in South Africa

Plant Disease ◽  
2000 ◽  
Vol 84 (8) ◽  
pp. 922-922 ◽  
Author(s):  
T. A. S. Aveling ◽  
A. Adandonon

During a disease survey of cowpea (Vigna unguiculata (L.) Walp.) in Southern Africa in 1999, a major problem recorded by small-holder rural farmers in areas with wet soil types was reduced seedling emergence. Nongerminated, diseased seeds in these fields were either a brown blotchy color or had a soft rot and disintegrated upon touch. Germinated seedlings failing to emerge above the soil line were characterized by water-soaked lesions girdling the hypocotyl. Emerged seedlings had necrotic taproots and few lateral roots. Infected hypocotyls above the soil line had light brown lesions, and seedlings showed symptoms of wilting. Diseased seeds and seedlings were collected, surface-sterilized, plated on 2% water agar, and Pythium ultimum was isolated. Identification was based on characteristics given in van der Plaats-Niterink (1). Sterile soilbased compost, infested by mixing with P. ultimum mycelia (10 CFU/g of compost), was used to fill 104-cell plastic seedling trays (40 × 28 × 3.5 cm). A single cowpea seed was planted at a depth of 2 cm in each cell, and trays were maintained in a greenhouse at approximately 20°C. Seeds and seedlings showed symptoms identical to those in the field 10 days after planting, and the pathogen was successfully reisolated. Seedlings in noninoculated compost remained symptomless. This is the first report of P. ultimum on cowpea in South Africa. Reference: (1) A. J. van der Plaats-Niterink. Monograph of the Genus Pythium. Centraalbureau voor Schimmelcultures, Baarn, 1981.

Plant Disease ◽  
1999 ◽  
Vol 83 (7) ◽  
pp. 696-696 ◽  
Author(s):  
S. J. Raffel ◽  
E. R. Kazmar ◽  
R. Winberg ◽  
E. S. Oplinger ◽  
J. Handelsman ◽  
...  

Corynespora cassiicola (Berk. & M. A. Curtis) C. T. Wei was isolated from diseased soybean plants (Glycine max) collected in two fields near Racine and Arlington, WI. Plants sampled at seedling emergence (VC), late vegetative (V5), and mid-reproductive (R5) stages exhibited reddish to dark brown longitudinal lesions on the exterior of the tap root extending vertically on the hypocotyl to the soil line, and extensive necrosis of lateral roots. Sample size at each growth stage was 144 plants per site. Roots were surface sterilized in 0.5% sodium hypochlorite for 2 min and sections of symptomatic tissue placed on water agar (12 g/liter) containing 100 μg of streptomycin per ml. Sporulation occurred on lesions and on mycelium that had grown out from the plant tissue onto the water agar following a 2-week incubation at 24°C under fluorescent light (280 μmol s-1 m-2). Incidence of isolation of C. cassiicola at both sites was 40% of plants sampled at growth stage VC, 67% at V5, and 78% at R5. Conidia characteristic of C. cassiicola were particularly abundant on the surface of necrotic lateral root tissue. Elongated conidia produced on water agar were 151 ± 5 μm × 15 ± 0.5 μm with an average of 13 ± 0.4 cells separated by hyaline pseudosepta (1). To confirm pathogenicity, a 1-cm lateral slice into each of four 5-day-old soybean seedling roots was made and a plug of agar taken from the margin of a colony of C. cassiicola grown on potato dextrose agar was placed in each wound and incubated for 14 days at 24°C in a growth chamber. Symptoms similar to those of diseased field plants were observed and C. cassiicola was reisolated from all plants inoculated with C. cassiicola; all controls treated with agar alone had no symptoms and C. cassiicola was recovered from none of the noninoculated controls. This is the first report of root rot caused by C. cassiicola on soybean in Wisconsin. Reference: (1) W. L. Seaman and R. A. Shoemaker. Can. J. Bot. 43:1461, 1965.


Plant Disease ◽  
2003 ◽  
Vol 87 (11) ◽  
pp. 1399-1399 ◽  
Author(s):  
S.-C. Yun ◽  
J.-W. Kim

Soybean (Glycine max Merr.) sprouts have been a traditional Korean food for at least 1,000 years. During the summers of 2000 and 2001, severe hypocotyl and root rot occurred on fully grown soybean sprouts, especially in commercial recirculating mass production systems. Brown rot on water-soaked hypocotyls and roots of soybean sprouts caused a 10 to 20% loss in production yield. To investigate the cause, 180 sections of tissue were surface sterilized for 30 s in 75% ethanol and plated on potato dextrose agar (PDA). A fungus with white, aerial mycelia and cultural characteristics of Pythium sp. was isolated consistently. The fungal isolates were identified as Pythium deliense Meurs based on various mycological characteristics (2) on corn meal agar (CMA) and sucrose-asparagine bentgrass leaf culture medium (1). P. deliense oogonia were spherical, smooth, 19 to 23 μm in diameter, and their stalks bent toward the antheridia. The antheridia were the shape of a straw hat, curved club-shaped, terminal or intercalary, monoclinous, occasionally diclinous, 12 to 15 × 8 to 11 μm, and 1 per oogonium (2). In pathogenicity tests, soybean sprouts and the fungus were cultured simultaneously in containers (30 × 30 × 50 cm [W × L × H]) with a daily 3-h showering period at 25°C. There were 8,000 to 10,000 seeds per container inoculated with four plugs of agar inoculum (2 × 2 cm). Inoculum was prepared from 5-day-old fungal cultures grown on PDA. After 6 days, the inoculated soybean sprouts showed the same symptoms as described above, whereas the noninoculated sprouts remained healthy. The fungal pathogen was reisolated from all the inoculated sprouts. P. deliense has never been reported as a pathogen of soybean sprouts. To our knowledge, this is the first report of hypocotyl and root rot disease caused by Pythium deliense on soybean sprout in Korea. References: (1) J.-W. Kim and E.-W. Park. Kor. J. Mycology 25:276, 1997. (2) A. J. Van der Plaatis-Niterink. Monograph of the genus Pythium. Vol. 21, Studies in Mycology. Centraalbureau voor Schimmelcultures, Inst. R. Neth. Acad. Sci. Lett. The Netherlands, 1981.


Plant Disease ◽  
2021 ◽  
Author(s):  
Hao Zhang ◽  
Yang Xu ◽  
Dan Zhao ◽  
Yuwen Yang ◽  
Tingchang Zhao ◽  
...  

Aconitum carmichaelii Debx. is a Chinese traditional medicine herb, and is widely planted in China. The processed lateral roots of A. carmichaelii is known as Fuzi, and is used for the treatment of pain and inflammation in the joints (Zhou et al., 2015). In July 2019, a high incidence (approximately 50-100%) of soft rot of A. carmichaelii was observed in several commercial fields in Jiangyou County of Szechuan Province of China. Soft rot brownish lesions developed on infected stems, leading to collapse and wilting of entire plants. From symptomatic plants, the margins between the diseased and healthy areas were cut into pieces (5 × 5 mm), which were surface sterilized using 75% ethanol for 30 s and 2% NaOCl for 1 min, followed by three rinses with sterile water. The sterilized sections were macerated in drops of sterile water, and the extract was streaked onto King’s B (KB) agar medium and incubated for 48 h at 30°C. Single colonies that are round, convex and creamy on the plates after 2 days were streaked on KB agar plates. Ten bacterial strains were isolated, and the strain Fuzi915 was chosen for further analyses. The 16S rDNA gene sequence (GenBank accession MZ881946) amplified by primer pair 27F/1492R (Monciardini et al., 2002) showed 99.85% identity to the sequence of Pectobacterium brasiliense (syn. Pectobacterium carotovorum subsp. brasiliense, Pcb) strain HNP201736 (MN393938.1) and P. carotovorum subsp. carotovorum strain PJP201706 (MN394020.1), respectively, and also showed 99.78% identity to P. brasiliense strain SX309 (CP020350.1). To further identify the Fuzi915 strain, the PCR assay was carried out using primer pairs Y1/Y2, EXPCCF/EXPCCR and BR1f/L1r (De Boer and Ward, 1995; kang et al., 2003; Duarte et al., 2004), specific to P. carotovorum, P. carotovorum subsp. carotovorum and P. carotovorum subsp. brasiliense (Pcb), respectively. Specific fragments of 434 bp and 322 bp were amplified by the Y1/Y2 and BR1f/L1r primer sets, receptively, but there was no amplification by the EXPCCF/EXPCCR primer set, indicating that the Fuzi915 strain belongs to Pcb (Onkendi and Moleleki, 2014). Additional phylogenetic trees based on two housekeeping genes mdh (MZ892962) and gapA (MZ892963) were constructed using Maximum-likelihood method with 1000 bootstraps. The Fuzi915 strain clustered with all P. brasiliense strains including type strain P. brasiliense BC1. Further, a pathogenicity test was conducted on healthy A. carmichaelii roots and seedlings maintained in a growth chamber at 25°C and 95% humidity. Root inoculation was followed by drenching 107 CFU/ml of the cell suspension of Fuzi915 strain in soil surrounding the A. carmichaelii roots. Ten roots were inoculated with cell suspension while 10 roots were drenching inoculated with sterile water as negative control. Stem inoculation was followed by injecting 103 CFU/ml of the cell suspension in the stem of 10 A. carmichaelii seedlings, while 10 were injected with sterile water as negative control. After 5 days, Pcb-inoculated roots became brown and soft, and Pcb-inoculated seedlings became wilted and water soaked and started to collapse, similar to symptoms observed in the field. No symptoms were observed on the control plants inoculated with sterile water. The strain was re-isolated successfully from symptomatic A. carmichaelii and was identified as P. brasiliense by using PCR with the same primers to complete Koch’s postulates. To our knowledge, this is the first report of the soft rot of A. carmichaelii caused by P. brasiliense in China.


Plant Disease ◽  
2019 ◽  
Vol 103 (10) ◽  
pp. 2667-2667 ◽  
Author(s):  
N. Zlatković ◽  
A. Prokić ◽  
K. Gašić ◽  
N. Kuzmanović ◽  
M. Ivanović ◽  
...  

Plant Disease ◽  
2017 ◽  
Vol 101 (6) ◽  
pp. 1048-1048 ◽  
Author(s):  
M. Han ◽  
M. N. Choi ◽  
H. R. Lee ◽  
E. J. Park

2015 ◽  
Vol 30 (1) ◽  
pp. 34-35 ◽  
Author(s):  
Kwanele Gqunta ◽  
Johan van Wyk ◽  
Pieter Ekermans ◽  
Colleen Bamford ◽  
Clinton Moodley ◽  
...  
Keyword(s):  

Plant Disease ◽  
2018 ◽  
Vol 102 (2) ◽  
pp. 437-437
Author(s):  
A. H. Zhang ◽  
X. X. Zhang ◽  
F. J. Lei ◽  
L. X. Zhang

Author(s):  
H. Heyne ◽  
E.A. Ueckermann ◽  
L. Coetzee

Leptotrombidium subquadratum larvae were collected for the first time in 1994 from dogs in Bloemfontein. The larvae have been collected annually, during the summer months, over a period of 6-7 years. Previously the only known hosts were scrub hare (Lepus saxatilis) (locality unknown) and short-snouted elephant shrew (Elephantulus brachyrhynchus) (Kruger National Park). These mites cause severe itching and dermatitis in humans and dogs.


Plant Disease ◽  
2019 ◽  
Vol 103 (7) ◽  
pp. 1774 ◽  
Author(s):  
N. van den Berg ◽  
M. du Toit ◽  
S. W. Morgan ◽  
G. Fourie ◽  
Z. W. de Beer

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