First report of Eutypella species associated with dying cotton (Gossypium hirsutum L.)

Author(s):  
Linda Smith ◽  
Paul Greenfield ◽  
Dinesh Kafle ◽  
Joy Conroy ◽  
Linda Scheikowski ◽  
...  
Plant Disease ◽  
1997 ◽  
Vol 81 (7) ◽  
pp. 832-832 ◽  
Author(s):  
R. E. Baird ◽  
D. E. Carling

During a study to determine the pathogenic fungi overwintering on dead cotton (Gossypium hirsutum L.) roots, two isolates of Rhizoctonia solani Kühn anastomosis group 7 (AG-7) were identified. Isolate #213 was obtained from dead roots near Tifton, GA, and isolate #219 was cultured from cotton roots near Midville, GA. Rhizoctonia solani AG-7 was previously reported in Arkansas, Indiana, and Asia (1). Isolates #213 and #219 were tested in the greenhouse for pathogenicity by mixing 25 ml of 2-week-old cornmeal sand inoculum (3 g of cornmeal, 100 g of sand, and 20 ml of distilled water) into 20 × 100 cm pots containing 2.25 liters of sterile soil (Tifton loamy sand, pH 6.1) per pot. Pots with noninfested soil were included as a control. Eight seeds of cotton (Delta and Pineland 90 DPL 90) were sown per pot. Each pot was a replicate and each treatment was replicated five times. At 20 days after planting, plant stands in soil infested with isolate #213 or #219 averaged 2 to 3 or 4 to 5 plants per pot, respectively, while stands in noninfested soil averaged 7 to 8 plants per pot. Brownish colored, sunken lesions were observed on roots, hypocotyles, and cotyledons of plants from pots infested with R. solani AG-7. Isolates #213 and #219 were reisolated from plants grown in their respective treatments. This is the first report of R. solani AG-7 in Georgia. Reference: (1) R. E. Baird et al. Plant Dis. 80:1421, 1996.


Plant Disease ◽  
1999 ◽  
Vol 83 (5) ◽  
pp. 487-487 ◽  
Author(s):  
R. E. Baird ◽  
J. H. Brock

In a field study evaluating the diversity and density of the soilborne mycobiota in a cotton (Gossypium hirsutum L.) production system, Macrophomina phaseolina (Tassi) Goidanich was isolated on potato dextrose agar from dark brown to black lesions on feeder and secondary roots. Multiple proliferations of feeder and secondary roots were also observed. Isolate RB 656 obtained from these lesions was tested for pathogenicity in the greenhouse by mixing 25 ml of 2-week-old cornmeal sand inoculum (3 g of cornmeal, 100 g of sand, and 20 ml of distilled water) with 5 liters of autoclaved soil (Leefield loamy sand, pH 6.2) per pot (40 × 200 cm). Control pots containing autoclaved soil alone were included for comparison. On 17 September, 10 cotton seeds of DPL 90 were sown per pot. Each treatment had five replications. Forty days after planting, plant heights from pots containing M. phaseolina were lower (14.8 cm) than those in the control pots (19.6 cm), but stand counts were similiar. On this date, four plants were left in each pot to allow the remaining seedlings to reach full maturity. On 9 December, the four plants per replicate pot were removed and roots evaluated for damage. Lesions similiar to those seen originally were observed on the secondary and feeder roots of the infested pots, and the characteristic proliferation of feeder and secondary roots was noted. Tap roots in pots containing M. phaseolina were smaller (11.6 cm) than in the control pots (18.6 cm). Isolate RB 656 was reisolated from the damaged roots in the treated pots. This is the first report of M. phaseolina on cotton in Georgia.


Plant Disease ◽  
2000 ◽  
Vol 84 (10) ◽  
pp. 1156-1156
Author(s):  
R. Baird ◽  
W. Batson ◽  
D. Carling ◽  
M. Scruggs

During a field study of the soilborne mycobiota on cotton (Gossypium hirsutum L.) roots, Rhizoctonia solani Kühn AG-7 was isolated from dark brown lesions present on the tap, feeder, and secondary roots onto potato-dextrose agar (PDA) (34 g of medium per liter of distilled water). Isolate identification was confirmed using tester R. solani AG-7 isolates (Carling, University of Alaska) for comparison during anastomosis pairing. To confirm pathogenicity, six AG-7 isolates (65, 66, 67, 68, 69, 70) obtained from cotton roots were tested in a plant growth incubator (18–24°C) by mixing 2.5 ml of 2-week-old cornmeal sand inoculum (3 g cornmeal, 100 g sand, and 20 ml distilled water) with 500 ml of autoclaved soil into each of five replicate polystyrene pots (15 cm wide × 20 cm long) per isolate. Five control pots containing noninfested soil were added for comparison. Five seed of cv. Deltapine 50 were sown into each pot. For all six isolates, mean stand counts (ranging from 0 and 1.3 plants per pot) were significantly lower (P ≤ 0.05) compared with those of plants in noninfested pots (3.8 plants per pot) at 21 days after planting. Furthermore, when the roots of surviving seedlings were evaluated for disease severity, brown, discolored lesions were observed at the base of stems and on roots in infested pots for all six isolates. Six AG-7 cultures of the pathogen were reisolated from symptomatic tissues onto PDA. The experiment was repeated with similar results. This is the first report of AG-7 occurring in Mississippi.


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