scholarly journals Field Efficacy of Thiophanate Methyl 44.8% + Kasugamycin 2.6% Sc against Major Foliar Diseases of Tomato

Author(s):  
H. Narayanaswamy ◽  
Balanagouda Patil ◽  
. Pruthviraj

Tomato (Solanum lycopersicum L.) is the important edible solanaceous plant originated from western South and Central America. Despite botanically being a fruit, it’s generally eaten and preferred like a vegetable. Tomatoes are the major dietary source of the antioxidant lycopene,   which has been linked to many health benefits, including reduced risk of heart disease                  and cancer. Early blight caused by Alternaria solani and powdery mildew caused by Erysiphe    orontii and bacterial leaf spot caused by Xanthomonas campestris has become a serious       problem for successful cultivation of tomato. Therefore, a field experiment was carried out to      know the efficacy of Thiophanate methyl 44.8% + Kasugamycin 2.6% Sc on tomato diseases   during 2017-18 and 2018-19, at College of Agriculture, Shivamogga. Experimental results     revealed that all the treatments significantly reduced the early blight, bacterial leaf spot and powdery mildew disease severity over untreated control. Among all the treatments Thiophanate methyl 44.8% + Kasugamycin 2.6% SC @ 1250 ml/ha recorded significantly less Per cent Disease Index (PDI) of Early blight (Alternaria solani) (7.78 % and 10.19 %), Bacterial leaf spot (Xanthomonas campestris) ( 3.96 and 1.39 %) and Powdery mildew (Erysiphe orontii) ( 1.67 and 2.50 %) with yield of 340.33 and 333.33 q/ha followed by Thiophanate methyl 44.8% + Kasugamycin 2.6% SC @ 1000 ml/ha.

Plant Disease ◽  
2012 ◽  
Vol 96 (7) ◽  
pp. 1064-1064 ◽  
Author(s):  
I.-S. Myung ◽  
J. Y. Lee ◽  
H. L. Yoo ◽  
J. M. Wu ◽  
H.-S. Shim

In September 2011, bacterial leaf spot was observed on zinnia plants (Zinnia elegans L.) grown in a garden in Suwon, Korea. Leaf symptoms included angular lesions that were yellow or brown-to-reddish brown in the center. Bacterial isolates (BC3293 to BC3299) were recovered on trypticase soy agar from lesions surface-sterilized in 70% ethyl alcohol for 1 min. Pathogenicity of the isolates was confirmed by spray inoculation with a bacterial suspension (106 CFU/ml) prepared in sterile distilled water and applied to zinnia plants at the four- to five-leaf growth stage (two plants per isolate). Sterile distilled water was used as the negative control. The inoculated plants were incubated in a greenhouse at 26 to 30°C and 95% relative humidity. Characteristic leaf spot symptoms developed on inoculated zinnia plants 5 days after inoculation. No symptoms were observed on the negative control plants. The bacterium reisolated from the inoculated leaves was confirmed through gyrB gene sequence analysis (3). All isolates were gram-negative, aerobic rods, each with a single flagellum. Isolates were positive for catalase and negative for oxidase. The biochemical and physiological tests for differentiation of Xanthomonas were performed using methods described by Shaad et al. (2). The isolates were positive for mucoid growth on yeast extract-dextrose-calcium carbonate agar, growth at 35°C, hydrolysis of starch and esculin, protein digestion, acid production from arabitol, and utilization of glycerol and melibiose. Colonies were negative for ice nucleation, and alkaline in litmus milk. The gyrB gene (870 bp) and the 16S-23S rRNA internal transcribed spacer (ITS) regions (884 bp) were sequenced to aid in identification of the original field isolates using published PCR primer sets Xgyr1BF/Xgyr1BR (3) and A1/B1 (1), respectively. Sequence of the gyrB gene (GenBank Accession Nos. JQ665732 to JQ665738) from the zinnia field isolates shared 100% sequence identity with the reference strain of Xanthomonas campestris pv. zinniae (GenBank Accession No. EU285210), and the ITS sequences (GenBank Accession Nos. JQ665725 to JQ665731) had 99.9% sequence identity with X. campestris pv. zinnia XCZ-1 (GenBank Accession No. EF514223). On the basis of the pathogenicity assays, biochemical and physiological tests, and sequence analyses, the isolates were identified as X. campestris pv. zinniae. To our knowledge, this is the first report of bacterial leaf spot of zinnia caused by X. campestris pv. zinniae in Korea. The disease is expected to result in economic and aesthetic losses to plants in Korean landscapes. Thus, seed treatment with bactericides will be required to control the bacterial leaf spot of zinnia before planting. References: (1) T. Barry et al. The PCR Methods Appl. 1:51, 1991. (2) N. W. Schaad et al. Page 189 in: Laboratory Guide for Identification of Plant Pathogenic Bacteria. 3rd ed. N. W. Schaad et al., eds. The American Phytopathological Society, St. Paul, MN, 2001. (3) J. M. Young et al. Syst. Appl. Microbiol. 31:366, 2008.


2013 ◽  
Vol 80 (2) ◽  
pp. 164-168 ◽  
Author(s):  
Osamu Netsu ◽  
Toshio Kijima ◽  
Yuichi Takikawa

Plant Disease ◽  
2002 ◽  
Vol 86 (2) ◽  
pp. 186-186 ◽  
Author(s):  
M. L. Lewis Ivey ◽  
S. Wright ◽  
S. A. Miller

In 2000, circular water-soaked lesions typical of bacterial leaf spot were observed on leaves of collards (Brassica oleracea L. var. viridis) throughout commercial fields in northwest Ohio. Light brown, rectangular, water-soaked lesions were observed on turnip leaves (Brassica rapa L.). Bacterial streaming from lesions on both crops was observed microscopically. Cream colored, fluorescent colonies were isolated from diseased tissues on Pseudomonas F medium, and eight representative colonies (four from collards and four from turnip) were selected and purified. Fatty acid methyl ester analysis was performed on all of the isolates. Two from collards and two from turnip were identified as Pseudomonas syringae pv. maculicola (mean similarity index = 0.82 [MIDI Inc., Newark, DE]). DNA extracts from pure cultures of the P. syringae pv. maculicola strains were used as template in a polymerase chain reaction (PCR) assay with primers derived from the region of the coronatine gene cluster controlling synthesis of the coronafacic acid moiety found in P. syringae pv. tomato and P. syringae pv. maculicola (CorR and CorF2) (D. Cuppels, personal communication). DNA from P. syringae pv. tomato strain DC3000 and P. syringae pv. maculicola strain 88–10 (2) served as positive controls, while water and DNA from Xanthomonas campestris pv. vesicatoria strain Xcv 767 were used as negative controls. The expected 0.65-kb PCR product was amplified from three of four strains (two from turnip and one from collards) and the positive control DNA, but not from the negative controls. Pathogenicity tests were performed twice on 6-week-old turnip (‘Forage Star’, ‘Turnip Topper’, ‘Turnip Alamo’, ‘Turnip 7’), collard (‘Champion’) and mustard (Brassica juncea L. ‘Southern Giant Curl’) seedlings using the three PCR-positive strains. Premisted seedlings were spray-inoculated separately with each of the three strains (2 × 108 CFU/ml, 5 ml per plant) and a water control. Greenhouse temperatures were maintained at 20 ± 1°C. For both tests, all strains caused characteristic lesions on all of the crucifer cultivars within 5 days after inoculation; the control plants did not develop symptoms. To satisfy Koch's postulates, one of the turnip strains was reisolated from ‘Turnip Topper’ plants, and the collard strain was reisolated from ‘Champion’ plants. The three original and two reisolated strains induced a hypersensitive response in Mirabilis jalapa L. and Nicotiana tabacum L. var. xanthia plants 24 h after inoculation with a bacterial suspension (1 × 108 CFU/ml). The original and reisolated strains were compared using rep-PCR with the primer BOXA1R (1). The DNA fingerprints of the reisolated strains were identical to those of the original strains. To our knowledge, this is the first report of bacterial leaf spot on commercially grown collards and turnip greens in Ohio. References: (1) B. Martin et al. Nucleic Acids Res. 20:3479, 1992. (2) R. A. Moore et al. Can. J. Microbiol. 35:910, 1989.


HortScience ◽  
1996 ◽  
Vol 31 (5) ◽  
pp. 745e-745
Author(s):  
Brent Rowell ◽  
Terry Jones ◽  
William Nesmith

Kentucky growers currently produce about 1300 acres of bell peppers worth $2 million for both fresh market and processing. Bacterial leaf spot (BLS) caused by Xanthomonas campestris pv. vesicatoria has been the scourge which continues to limit expansion of pepper production in the state. Fourteen new BLS-resistant varieties and experimental lines were evaluated together with two standard (susceptible) varieties in 1995 at two locations. All entries were exposed to an induced BLS epidemic at one location but were kept disease-free at the second location. Field resistance to four races of BLS was high for all but one of the lines tested, which claimed resistance to races 1, 2, and 3. Cultivars with resistance to only race 2 or races 1 and 2 of the pathogen were no different from susceptible checks in terms of yields and disease resistance. Six entries performed well at both locations; these will be included in further trials in 1996.


Plant Disease ◽  
2013 ◽  
Vol 97 (2) ◽  
pp. 282-282 ◽  
Author(s):  
L. H. Zhou ◽  
G. H. Ji

Rieger begonia are collectively referred to as a begonia hybrid group. Its global annual sales is 90,000,000 cutting seedlings. It is one of the top ten potted plants. In the summer of 2011, serious outbreaks of a suspected bacterial leaf spot disease were observed on five Rieger begonia cultivars (Dark Britt, Rebecca, Blitz, Barkos, and Borias). These plants were grown for potted cutting seedling production in commercial nurseries located in Shilin county of Yunnan Province, China. The initial symptoms of the disease were small circular or polygonal water-soaked needle spots on leaf margin that later these spots expanded and joined together, forming bigger inverted V-shaped necrotic specks (4). Yellow-pigmented bacterial colonies were consistently isolated from diseased leaves and stems on NA agar medium and incubated at 28°C. Twelve bacterial strains were isolated and used for further studies. All the isolates were Gram-negative, rod-shaped, motile, aerobic, and non-sporing. All of the bacterial strains isolated in the present study were identified as Xanthomonas campestris pv. begoniae (Xcb) based on biochemical and physiological identification (Biolog carbon source utilization analysis) and 16S rDNA sequences analysis and further pathogenicity determination (1). The results show that the sequence homology rate of HT1-1 (GenBank Accession No. JN648097) and X. euvesicatoria (syn. X. campestris pv vesicatoria) (GeneBank Accession No. AM039952) is 99%. This strongly suggests that the Rieger begonia isolates belong to X. campestris pv. begoniae (2). For Koch's postulates, 10 surface-disinfected young leaves from five susceptible Rieger begonia plants (cv. Dark Britt) were inoculated by spraying a phosphate-buffered saline suspension of each bacterial isolate (3.0 × 108 CFU/ml) onto the leaves (3). Controls were inoculated similarly with phosphate-buffered saline solution. All inoculated plants were covered with polyethylene bags for 24 h at 25°C and then put in the greenhouse. After inoculation, water-soaked and necrotic symptoms were observed on inoculated Rieger begonia leaves within 7 to 9 days. No symptoms were observed on controls. Bacteria were reisolated and confirmed to be identical to the original isolates by the methods described above. To our knowledge, this is the first report of Xcb causing leaf spot on Rieger begonia plants in China. The infection process of Xcb on Rieger begonia plants and rapid detection of this pathogen are underway. References: (1) M. R. Gillings et al. PNAS 12:102, 2005. (2) C. L. Oliver et al. Plant Dis. 4:96, 2012. (3) H. Ornek et al. New Dis. Rep. 13:40, 2006. (4) O. Pruvost et al. Plant Dis. 4:96, 2012.


Plant Disease ◽  
1997 ◽  
Vol 81 (11) ◽  
pp. 1334-1334 ◽  
Author(s):  
F. Sahin ◽  
S. A. Miller

A previously undescribed pathotype of Xanthomonas campestris pv. armoraciae was found in 1995 on radish plants grown on organic soil in north central Ohio. Radish foliage developed numerous small, circular, water-soaked black spots, eventually with yellow halos, on the underside of the leaves, giving the foliage a yellowish, ragged appearance. Spots were also visible on the upper surface of leaves and on petioles. Yellow xanthomonad-like bacteria were consistently isolated from the lesions and confirmed as the causal agent of the disease by fulfilling Koch's postulates. All five strains purified were gram negative, rod shaped, motile, aerobic, oxidase negative, catalase positive, amylolytic, and pectolytic. They were identified as X. campestris pv. armoraciae by fatty acid methyl ester (FAME) analysis (similarity indices [SI] range = 0.21 to 0.39), the Biolog 95 GN reaction (SI range = 0.31 to 0.36), and serological reactions with X. campestris pv. campestris/X. campestris pv. armoraciae-specific monoclonal antibodies X9, X11, X21, A11, and B35 (1). All strains caused bacterial leaf spot on collard, kale, radish, horseradish, and cabbage but not on tomato or pepper. These strains were different from X. campestris pv. raphani, which is pathogenic on kale, radish, cabbage, tomato, and pepper, but not on horseradish. These strains also differed from other previously reported strains of X. campestris pv. armoraciae that do not cause infection on kale and radish (1,2). This is the first report on the existence of a different pathogenic group within X. campestris pv. armoraciae that can cause bacterial spot on kale and radish. References: (1) A. M. Alvarez et al. Phytopathology 84:1449, 1994; (2) H. E. White. Phytopathology 20:653, 1930.


2018 ◽  
Vol 40 (3) ◽  
pp. 399-407 ◽  
Author(s):  
Olbert Nicolas ◽  
Marie Thérèse Charles ◽  
Sylvie Jenni ◽  
Vicky Toussaint ◽  
Carole Beaulieu

Plant Disease ◽  
2005 ◽  
Vol 89 (6) ◽  
pp. 683-683 ◽  
Author(s):  
S. Gaetán ◽  
N. López

Canola (Brassica napus) is an alternative crop to wheat in Argentina and ~16,000 ha are grown commercially in southern Buenos Aires Province. During 2003, experimental field plots of canola plants located at Agronomy Faculty, University of Buenos Aires, in Buenos Aires were severely damaged by a bacterial leaf spot. Average disease incidence across 25 2- to 5-month-old canola cultivars was 58% (range = 27 to 89%). During 2004, identical infection associated with blackened veins (8 to 12% of plants) were found in two commercial fields and experimental crops (rosette and flowering stages) in Tres Arroyos in southern Buenos Aires Province. Symptoms observed on adaxial surfaces consisted of v-shaped necrotic lesions on leaf margin surrounded by yellow halos. Yellow bacterial ooze was found on young lesions. The advanced phases of the disease included lesion enlargement, foliar chlorosis, and death of leaves. The disease developed from the lower leaves to the apex, resulting in complete leaf necrosis and defoliation. Ten samples (five plants per sample) with lesions were arbitrarily collected from 2003 to 2004 from commercial and experimental canola crops. Diseased leaf tissue was surface sterilized in 0.50% sodium hypochlorite for 30 s and rinsed in sterile distilled water (SDW). Leaf sections were macerated in SDW, and the extract was streaked onto nutrient agar. Plates were incubated at 28°C for 3 days. Resultant colonies were yellow, mucoid, and convex. Gram-negative, aerobic, and rod-shaped bacteria were obtained. Eight strains were biochemically characterized using API 20NE (BioMerieux, Marcy l'Etoile, France) and identified as Xanthomonas campestris (1). Strains hydrolyzed starch, gelatine, and aesculin and were positive for catalase and negative for oxidase, nitrate reduction, ureasa, and triptophanase. Strains were capable of utilizing D-glucose, D-mannose, D-maltose, malic acid, and N-acetyl-glucosamine. X. campestris. pv. campestris 8004 was used as a reference strain (2). Pathogenicity and host range for three isolates were completed by injecting a bacterial suspension (107 CFU/ml) into leaves of 2-week-old canola plants (cvs. Eclipse, Impulse, Master, and Mistral), cabbage (B. oleracea var. capitata), and cauliflower (B. oleracea var. botrytis) seedlings (two-leaf stage). The experiment (four inoculated and two control plants for each cultivar and each strain) was conducted in a greenhouse at 24°C and 75% relative humidity. Inoculated and control plants were enclosed in a plastic bag for 48 h after inoculation. Chlorotic patches on the leaves followed by a dry, brown necrosis spread beyond the initial injected area were observed in inoculated plants 8 days after inoculation. Enlarged spots caused death of leaves. The pathogen was successfully reisolated. Control plants, inoculated only with SDW, remained symptomless. The results suggest that the bacterium represents a potential threat to canola production in Argentina and indicate the need for further study to identify the pathovar involved in canola leaf spots. To our knowledge, this is the first report of an outbreak of X. campestris causing leaf spot of canola and in which the bacteria affecting canola commercial crops was biochemically characterized and host range was carried out in Argentina. References: (1) N. W. Schaad et al. Laboratory Guide for Identification of Plant Pathogenic Bacteria. 3rd ed. The American Phytopathological Society, St. Paul. MN, 2001. (2) P. Turner et al. Mol. Gen. Genet. 195:101, 1984.


2004 ◽  
Vol 22 (2) ◽  
pp. 58-62 ◽  
Author(s):  
A. K. Hagan ◽  
J. W. Olive ◽  
J. Stephenson ◽  
M. E. Rivas-Davila

Abstract Efficacy of azoxystrobin (Heritage 50W™) was assessed over a range of application rates and intervals for the control of powdery mildew (Erysiphe polygoni) and Cercospora leaf spot (Cercospora hydrangea) on bigleaf hydrangea (Hydrangea macrophylla) ‘Nikko Blue’. Rooted hydrangea cuttings were transplanted in a pine bark/peat mixture. In 1998 and 1999, azoxystrobin at 0.16 g ai/liter and 0.32 g ai/liter, as well as 0.24 g ai/liter myclobutanil (Eagle 40W™) and 0.84 g ai/liter thiophanate methyl (3336 4.5F™), greatly reduced the incidence of powdery mildew compared with the untreated control where 75% of the leaves of were infected by the causal fungus. When applied at 1-, 2-, and 3-week intervals, both rates of azoxystrobin were equally effective in both years in preventing the development of powdery mildew on bigleaf hydrangea. In 1998, all fungicides except for thiophanate methyl protected bigleaf hydrangea from Cercospora leaf spot. In the last two trials, the incidence of powdery mildew increased significantly as the application rate for azoxystrobin decreased from 0.16 to 0.04 g ai/liter and the application interval was lengthened from 1 to 3 weeks. In general, all rates of azoxystrobin applied on a 3-week schedule failed to provide the level of powdery mildew control needed to produce quality bigleaf hydrangea for the florist and landscape market. When applied at 2-week intervals, myclobutanil was equally or more effective in controlling powdery mildew than any rate of azoxystrobin applied on the same schedule. When compared to the untreated controls, significant reductions in the incidence of powdery mildew on bigleaf hydrangea were obtained with weekly applications of paraffinic oil. No symptoms of phytotoxicity were associated with the use of any of the fungicides screened.


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