Disease Of Watermelon Research Articles

Efficacy of two organic amendments and a nematicide for management of root-knot nematode (Meloidogyne incognita) of watermelon

A field experiment was conducted during two consecutive years for the management of root- knot nematode(Meloidogyne incognita) of watermelon with two organic soil amendments poultry refuse (3 and 5 t/ha), mustard oilcake (0.3 and 0.6 t/ha) and a nematicide Furadan 5G 40 kg/ha. Organic amendments were incorporated in the soil 3 weeks before and Furadan 5G on the day of seedling transplanting. PR 3 t/ha and MOC 0.3 t/ha were used alone and integrated with Furadan 5G 20 kg/ha. The soil was inoculated with galled roots of tomato at the time of treatment application. Two organic soil amendments alone or integration with Furadan 5G gave satisfactory reduction of root-knot and increase plant growth in both years. The most effective treatment was PR 5 t/ha followed by PR 3 t/ha + Furadan 5G 20 kg/ha. Efficacy of PR 3 t/ha and MOC 0.6 t/ha were also appreciable. In first and second years, gall index values were 8.13 and 5.67 under control, respectively. The severity was reduced from 3.13 to 5.80 in first year and 2.34 to 3.94 in the second year due to treatments. Based on findings of the study, PR alone 5 t/ha and PR 3 t/ha + Furadan 5G 20 kg/ha were noted as effective treatment to manage root-knot disease of watermelon. Key words: Poultry refuse, mustard oilcake, furadan, Meloidogyne incognita.

First Report of Bacterial Black Spot Disease in Watermelon Caused by Acidovorax valerianellae in Korea.

Watermelon (Citrullus lanatus (Thunb.) Matsum. & Nakai), an important member of the Cucurbitaceae family, is cultivated on 21,000 ha that produces 850,000 t in Korea. In April 2011, we received grafted watermelon with necrotic leaf spots from a commercial watermelon grower in Andong, Korea. Black spots were observed on cotyledons of the plants in seedbeds, and approximately 9% of watermelon plants were infected with the disease. Initial symptoms on the seedling were black, greasy spots sometimes surrounded by a halo of discoloration. Younger leaves usually showed symptoms later than cotyledons. Bacteria isolated from the infected plants were gram-negative, motile, straight rods with a single flagellum and 0.84 to 0.89 μm wide and 1.54 to 1.69 μm long. They formed rough colonies with a white-cream color after 48 h of incubation on Luria-Bertani (LB) agar at 28°C. Colonies of isolates were nonfluorescent, smooth, and white on King's medium B. On YBGA (7 g of yeast extract, 7 g of bactopeptone, 7 g of glucose, 15 g of agar, 1,000 ml of distilled water; pH 7.2) colonies are circular, raised with an entire margin, and white to cream. Pathogenicity tests were conducted with potted, greenhouse-grown watermelon plants. Bacterial colonies grown on LB medium for 48 h at 28°C were suspended in sterile distilled water, and the suspension (1.0 × 108 CFU/ml) was infiltrated into mesophyll of watermelon leaves with a syringe as previously described (2). Inoculated plants were maintained at 28°C and 90% relative humidity in a growth chamber with a daily 12-h photoperiod of fluorescent light. Five plants were used for inoculation. Sterilized distilled water was used as a control. The bacterial isolates induced necrosis in the infiltrated area within 3 to 5 days. Typical water-soaked spots appeared after 3 days of incubation and became gray to black after 6 days. The bacterium was successfully reisolated from the diseased lesions, thus completing Koch's postulates. A cell suspension (50 μl of 1 × 106 CFU/ml) was infiltrated with a syringe into the intercellular spaces of tobacco leaves to determine the hypersensitive reaction (HR). A typical HR developed 20 h after leaf infiltration. The 16S rDNA region of the isolates, amplified by using universal PCR primers, shared 99% sequence identity with an Acidovorax valerianellae strain (GenBank Accession No. AJ431731) (1). The resulting sequences of 1,424 bp were deposited in GenBank (Accession No. JN983471). The isolates we obtained in this study clustered with A. valerianellae on a phylogenetic tree generated by the neighbor-joining method implemented in MEGA Version 4.1. In the Biolog Microbial Identification System, Version 4.2 (Biolog Inc., Hayward, CA), all isolates were 63 to 77% similar with a match probability of 100% to A. konjaci. Fatty acid composition analysis of isolates based on the MIDI Library version TSBA 5.0 and Library Generation system software version 5.0 showed that the isolates were 52 and 72% similar to an Acidovorax sp., respectively. To our knowledge, this is the first report of bacterial black spot disease in watermelon caused by A. valerianellae in Korea. A. valerianellae is a causal agent of bacterial black spot in corn salad and is transmitted by inoculated seeds (3). Further studies are required to determine whether it is seed transmitted in watermelon.

Identification of Resistance to Fusarium oxysporum f. sp. niveum Race 2 in Citrullus lanatus var. citroides Plant Introductions

Fusarium wilt (FW) is a major disease of watermelon in North America and around the world. Control of this disease is difficult because the soilborne causal agent Fusarium oxysporum f. sp. niveum (Fon) produces chlamydospores that remain infectious in the soil for many years. Although various levels of resistance to Fon Races 0 and 1 exist in watermelon cultivars, no resistance to Race 2 or 3 has been reported. In this study, we used seed and seedling inoculation procedures to screen 110 U.S. PIs of wild watermelon (Citrullus lanatus var. citroides) for resistance to Race 2 FW. Of these 110 accessions, 15 showed significantly higher resistance to Fon Race 2 than that found in the watermelon cultivars Sugar Baby or Charleston Grey as well as in the C. lanatus var. citroides PI 296341 that was reported to contain resistance to FW. PI 271769, another C. lanatus var. citroides that was previously reported as containing resistance to FW, is among the 15 resistant accessions described here. These 15 accessions are potential sources for resistance to Race 2 FW in watermelon breeding.

Rhizosphere soil microorganism populations and community structures of different watermelon cultivars with differing resistance to Fusarium oxysporum f. sp. niveum

Fusarium wilt is an increasingly serious disease of watermelon that reduces crop productivity. Changes in microorganism populations and bacterial and fungal community structures in rhizosphere soil of watermelon cultivars resistant or susceptible to Fusarium oxysporum f. sp. niveum were investigated using a plate culture method and PCR-DGGE analysis. Plate culture showed that populations of culturable bacteria and actinomycetes were more abundant in the rhizosphere of the resistant watermelon cultivar than the susceptible cultivar, but the fungi population had the opposite pattern. Populations of Penicillium , Fusarium , and Aspergillus were significantly lower in the resistant cultivar than the susceptible cultivar at the fruiting and uprooting stages (p< 0.05). Pattern matching analysis generated the dendrogram of the DGGE results indicating the relatedness of the different resistant watermelon cultivars and their corresponding rhizosphere microbial communities. Further sequencing analysis of specific bands from DGGE profiles indicated that different groups of bacteria and fungi occurred in the rhizosphere of different watermelon cultivars. Our results demonstrated that plant genotype had a significant impact on soil microbial community structure, and the differences in the rhizosphere microbial community may contribute to the differences in resistance to F. oxysporum f. sp. niveum.

Detection of fungi associated with watermelon roots and their effects in seed germination and seedlings

This experiment involved a survey of damping - off and root rot disease of watermelon in Anbar , Baghdad and Babylon provinces. Determination of pathogens and testing their pathogenesity were also investigated. Results of the field survey showed the existence of the disease in all the surveyed provinces with 13%-27% root rot and post emergence damping off disease and decrease the percentage of germination to 40%-57% in all the surveyed regions. Results of isolation and identification showed the presence of 12 genera and 10 species associated with the infected seedlings. The fungus Fusarium solani was found to be present in all surveyed areas in mean percentage of occurrence of 27.03%. The, F. oxysporum , Phoma spp., Rhizoctonia solani and Cylindrocarpon spp. waer found to be present in percentage of 7.1%, 11.2%, 14.0% and 16.6% respectively. Results of pathogenicity tests of some fungal isolates which were associated with watermelon roots showed that the isolates gave a significant reduction in percentage of seeds germination of watermelon and increased the percentage of disease severity , R. solani isolate (O) had the maximum effect where the germination percent was 6.6% and the disease severity was 93% followed by F. oxysporum isolate (B) where the percentage of seeds germination and disease severity were 10% and 90% respectively , ther isolates showed variable significant reduction in percentage of seeds germination of watermelon ranging betwee 16.6% - 50%. The isolates also increased the percentage of disease severity which were ranging between 50% - 83.3% compared with control treatment in which the germination percentage and disease severity were 90% and 0.0% respectively. Results of the interaction between some of pathogenic fungi isolates showed a reduction in percentage of seeds germination and increase in disease severity . The combination between R. solani (O) isolate + F. oxysporum (B) isolate and R. solani (O) isolate + F. oxysporum (B) isolates + Cylindocarpon sp. The (A) isolate reduced percentage of seeds germination to zero and increased disease severity to 100%. Other combination O+A and B+A reduced percentage of seed germination to 3.3% and 6.6% respectively and increased the disease severity to 96.6% and 93%, respectively.

Development of a mode of application of bioorganic fertilizer for improving the biocontrol efficacy to Fusarium wilt

More effective ways of applying biocontrol products should be developed based both on the characteristics of the biocontrol agents and the normal practices of the agricultural producer. A new system was developed to improve the biocontrol efficacy of Fusarium wilt for watermelon production, and this system was tested in pot and field experiments. Biocontrol was achieved by applying a novel bioorganic fertilizer product (BIO) to Fusarium-infested soil. The best biocontrol was obtained by application of a bioorganic fertilizer, BIO, into soil during the nursery phase of watermelon seedling followed by a second application to Fusarium-infested soil when watermelon seedlings were transplanted. In comparison with the controls, the incidence of the disease was reduced by 60–100% in the pot experiment and by 59–73% in the field experiment when the BIO was applied during the nursery stage. After application of BIO during the nursery stage, the number of colony-forming units of Fusarium oxysporum in rhizospheric soil was significantly (P < 0.05) inhibited compared to the controls. An in vitro experiment showed that the antagonist Paenibacillus polymyxa in the BIO could effectively colonize the rhizosphere of watermelon and proliferate along the extending plant roots. This inhibited growth of Fusarium oxysporum in the rhizosphere of watermelon and protected the watermelon roots from attack by the pathogens. The method used for biocontrol Fusarium wilt disease in watermelon should be a useful strategy to improve field efficacy of other biocontrol agents.

Identifying Resistance to Powdery Mildew Race 2W in the USDA‐ARS Watermelon Germplasm Collection

Powdery mildew caused by Podosphaera xanthii has recently become an important disease of watermelon [Citrullus lanatus (Thunb.) Matsum. &amp; Nakai] in the United States. The disease can be controlled with fungicides, but it would be more economical and environmentally safe to use genetic resistance. Here, we report sources of resistance to powdery mildew race 2W identified in the evaluation of the entire U.S. watermelon Plant Introduction collection made of four Citrullus Schrad. ex. Eckl. &amp; Zeyh. species and Praecitrullus fistulosus (Stocks) Pangalo species. A total of 1654 PI accessions, cultivars, and breeding lines (hereafter collectively referred to as cultigens) were tested in the greenhouse using at least seven replications. From that, 54 cultigens including the 44 most resistant and 10 susceptible checks were retested in greenhouse and field experiments. All cultigens showed symptoms of powdery mildew. Resistance was identified in wild PI accessions. Eight cultigens had high resistance and 21 had intermediate resistance. Leaf and stem disease severity ratings were positively correlated (r = 0.86, P &lt; 0.0001). Data were summarized from the screening and retest studies, and the most resistant cultigens were PI 632755, PI 386015, PI 189225, PI 346082, PI 525082, PI 432337, PI 386024, and PI 269365. The most susceptible cultigens were PI 222775 and PI 269677. Many of the resistant cultigens originated from Nigeria and Zimbabwe.

Effect of nitrogen doses on disease severity and watermelon yield

Nitrogen fertilization is an important step for watermelon (Citrullus lanatus) production due to its influence over yield, fruit quality, and disease severity. Currently, the gummy stem blight (Didymella bryoniae) and the downy mildew (Pseudoperonospora cubensis) can be taken as the most important watermelon diseases, since they impose severe impairment to the crop. Furthermore, studies focusing on plant responses to nitrogen fertilization regarding fruit yield and quality, and disease resistance are rare. Hence, the present study aimed at evaluating the effect of nitrogen doses on fruit yield and quality, and on disease prevalence in watermelon. Two experiments were carried out at the Universidade Federal de Tocantins, employing sprinkler irrigation, in an area previously used to grow watermelon. The experimental design was blocks at random, with five treatments (N doses, applied twice as side-dressing, in kg ha-1, as follows: T1= control treatment without N, T2= 20, T3= 40, T4= 80, and T5= 120), and four replications. Urea (45% N) was used as the N source. In the first assay, the highest fruit yield and average weight were observed when 40 kg ha-1 of N were applied. The highest severity of the gummy stem blight was observed when the highest nitrogen doses were applied (80 and 120 kg ha-1). In the second assay, the highest severity levels of the gummy stem blight, as well as of mildew, were observed again when N doses were the highest (80 and 120 kg ha-1). The lowest severity levels for both diseases were observed in the control treatment.

Type IV Pili Are Required for Virulence, Twitching Motility, and Biofilm Formation of Acidovorax avenae subsp. citrulli

Acidovorax avenae subsp. citrulli is the causal agent of bacterial fruit blotch (BFB), a threatening disease of watermelon, melon, and other cucurbits. Despite the economic importance of BFB, relatively little is known about basic aspects of the pathogen's biology and the molecular basis of its interaction with host plants. To identify A. avenae subsp. citrulli genes associated with pathogenicity, we generated a transposon (Tn5) mutant library on the background of strain M6, a group I strain of A. avenae subsp. citrulli, and screened it for reduced virulence by seed-transmission assays with melon. Here, we report the identification of a Tn5 mutant with reduced virulence that is impaired in pilM, which encodes a protein involved in assembly of type IV pili (TFP). Further characterization of this mutant revealed that A. avenae subsp. citrulli requires TFP for twitching motility and wild-type levels of biofilm formation. Significant reductions in virulence and biofilm formation as well as abolishment of twitching were also observed in insertional mutants affected in other TFP genes. We also provide the first evidence that group I strains of A. avenae subsp. citrulli can colonize and move through host xylem vessels.

Isolation and characterisation of fusaricidin-type compound-producing strain of Paenibacillus polymyxa SQR-21 active against Fusarium oxysporum f.sp. nevium

A bacterial strain was isolated from the rhizosphere of healthy watermelon plants in a heavily wilt-diseased field. This isolate was tentatively identified as Paenibacillus polymyxa (SQR-21) based on biochemical tests and partial 16S rRNA sequence similarity. The purified antifungal compounds were members of the fusaricidin group of cyclic depsipeptides having molecular masses of 883, 897, 947, and 961 Da with an unusual 15-guanidino-3-hydroxypentadecanoic acid moiety, bound to a free amino group. The strain SQR-21 was not able to produce antifungal volatile compounds but was able to produce cellulase, mannase, pectinase, protease, β-1,3-glucanase and lipase enzymes. However, the strain did not show any chitinase activity. Biocontrol potential of this strain was evaluated against Fusarium oxysporum cause of Fusarium wilt disease of watermelon in a greenhouse experiment. This strain combined with organic fertiliser decreased the disease incidence by 70% and increased the dry plant weight by 113% over the control.

First Report of Fusarium Wilt Caused by Fusarium oxysporum f. sp. niveum Race 2 in Georgia Watermelons.

Watermelon (Citrullus lanatus (Thunb.) Matsum. & Nakai) is the number one specialty crop grown in Georgia, a state that ranks fourth nationally in watermelon production. In the last 5 years, Fusarium wilt caused by Fusarium oxysporum f. sp. niveum (Fon) has been the greatest yield-limiting disease of watermelon in Georgia. In 2004, a seedless-watermelon field of 'Regency' and 'Tri-X 313' in Berrien County, GA exhibited approximately 40% of wilted plants. Affected plants also exhibited strong discoloration in the crown xylem. Plant samples (cultivars unknown) from a similarly affected field were also tested from Crisp County, GA. Xylem tissue was excised from the main stem of eight diseased plants in the area between the second and third internode, surface sterilized for 1 min in 1% NaOCl, rinsed with 80% ethanol, and plated onto water agar amended with 100 μg/liter of streptomycin sulfate. Fungi with the morphological characteristics of Fusarium oxysporum (4) were consistently recovered from the diseased tissue of all eight plants. The isolates were hyphal tipped and maintained in vials of sterile artificial potting mix until ready for use (1). Isolates were grown on Esposito and Fletcher medium (2) for 10 days, filtered through cheesecloth, and adjusted to 1 × 106 spores/ml. Reference isolates of race 1 and 2 were used as comparisons for race determination of the unknowns. In each of four studies, plants at the two-leaf stage were removed from potting mix, washed gently, and their roots were uniformly trimmed to 2.5 cm. Before repotting, the seedlings were subjected to a 2-min root-dip in the respective spore-containing media. In each study, approximately 40 plants of each watermelon differential were inoculated with the respective isolates. In disease scoring, each plant was considered a rep. 'Black Diamond' is susceptible to races 0, 1, and 2; 'Charleston Gray' is resistant to race 0; 'Calhoun Gray' is resistant to races 0 and 1, and PI-296341-FR (3) is resistant to races 0, 1, and 2 of Fon. Four plants were planted per 15-cm plastic pot, maintained in an air-conditioned headhouse for 24 h, and then placed in the greenhouse in a randomized complete block design. After 30 days, all plants were rated as to healthy, wilted, or dead plants. From eight isolates tested, one isolate from each county was determined to be Fon race 2 on the basis of its ability to wilt/kill a high percentage of the race 1 resistant differential, i.e., 'Calhoun Gray'. Mean disease percentages for the isolates from each of the two counties on the watermelon differentials were 95 and 100% on 'Black Diamond', 68 and 80% on 'Charleston Gray', and 70 and 86% on 'Calhoun Gray.' Because of apparent genetic drift within our PI-296341-FR population, we determined that these data were not useful for identifying race 2. In fact, we observed a range of 17 to 80% wilt/death in the PI-296341-FR over a total of four studies that included a known race 2 isolate (Calg 13(15); E. Vivoda). To our knowledge, this is the first report of race 2 in Georgia and it increases the number of states to seven in which race 2 has been identified. Five of the top 10 watermelon-producing states have now reported race 2 of Fon for which there is no genetic resistance within commercial cultivars.

Effect of fusaric acid on biomass and photosynthesis of watermelon seedlings leaves

Wilt disease of watermelon caused by Fusarium oxysporum f. sp. niveum in long-term monoculture system has been much often found particularly in protected land cultivation system worldwide. Fusaric acid (FA), a fungal phytotoxin, was extracted from F. oxysporum f. sp. niveum isolated from diseased watermelon plant. The influence of FA on the biomass and leaves photosynthesis of watermelon seedlings was investigated in a labora- tory study. Results obtained are listed as follows. Plant height, fresh weight, main root length and lateral roots of watermelon seedling exposed to FA (400 mg·L -1 ) for 12 hours and then grown in ordinary condition for nine days were decreased by 23.0%, 23.1%, 23.6% and 33.6% compared with control respectively. Cotyledons were wilted to death completely and necroses occurred on the first true leaf and the upper leaves had become crinkled and chlorosis, which was a typical symptom of wilting disease of watermelon. And thus physiological functions were inhibited and damaged strongly. Net photosynthesis rate, stomatal conductance, intercellular CO2 concentration, and chlorophyll (SPAD reading) of the seedlings decreased with the increasing of concentrations of FA and dura- tion of exposure to FA. Compared with control, stomatal conductances of leaves treated with FA were declined by 87.4-98.4% and net photosynthesis rates of leaves were decreased by 51.8-92.1%. Intercellular CO2 concentration of the seedlings treated with FA was reduced by 66.6 -94.8%. Chlorophyll content in the leaves of the seedlings was decreased by 42.7-72.3%. Transpiration rate fell down to 86.8-96.3%. It was concluded that FA strongly reduced the chlorophyll content of watermelon seedlings leaves resulting to heavy suppression of leaf photosynthesis, which therefore affected seedlings growth finally leading to leaf wilting and necrosis.

Histopathology comparison and phenylalanine ammonia lyase (PAL) gene expressions in Fusarium wilt infected watermelons

Fusarium wilt disease of watermelon (Citrullus lanatus (Thunb.) Matsum &amp; Nakai), caused by Fusarium oxysporum f. sp. niveum (FON), is one of the limiting factors of worldwide watermelon production. In this study, a Fusarium wilt resistant watermelon JSB, which was derived from a spontaneous mutation of the susceptible Sugar Baby (SB), was used to investigate histopathology. The number and diameter of xylem vessels in the root (10 mm below the shoot base) of resistant JSB plants were significantly higher than those in susceptible SB plants. At 9 days post inoculation (dpi), using the plate assay on Nash-PCNB media, FON could be recovered from 86% of the roots in the symptomless plants of both watermelon lines, and from 55% and 64% of the stem segments (5 mm above the shoot base) in resistant and susceptible plants, respectively. In paraffin and free-hand tissue sections, at 8, 13, and 35 dpi, the xylem of roots and stems close to the soil surface in resistant watermelon JSB plants was also colonised by FON, but to a much lower percentage than the susceptible SB ones. No colonisation below the middle of stems was observed in the resistant JSB plants. The susceptible plants grown in infested soil were all dead by 35 dpi, while the resistant plants remained healthy. These observations suggest that reducing FON colonisation in the vascular systems of the host may contribute to the resistance in JSB. Furthermore, the higher expression of the phenylalanine ammonia lyase (PAL) gene in JSB induced by FON and the effects of PAL inhibitor on the resistance of JSB suggested that PAL is involved in resistance of watermelon to Fusarium wilt pathogen.

Series on Diseases in the Florida Vegetable Garden: Watermelon

PP 241, an 8-page illustrated fact sheet by Pamela Roberts, Rosa Muchovej, Tom Kucharek, Ken Pernezny, and Timur Momol, describes microorganisms that cause plant diseases, including fungi, bacteria and viruses, plus specific watermelon diseases. Includes tips for disease prevention. Published by the UF Department of Plant Pathology, October 2007.

Resistência de Didymella bryoniae a fungicidas no Brasil

O crestamento gomoso do caule (Didymella bryoniae) é uma das mais importantes doenças da melancia (Citrullus lanatus) no mundo. O controle químico, embora amplamente adotado, nem sempre pode impedir o progresso da doença no campo. A resistência do agente causal a alguns ingredientes ativos foi relatada na Europa, Japão e nos Estados Unidos, porém nenhum estudo foi feito no Brasil. Este trabalho descreve os resultados de três ensaios in vitro para resistência a fungicidas, medida pela taxa de crescimento micelial. No primeiro ensaio, sete isolados foram submetidos a nove fungicidas na metade da dose comercial recomendada. Evidência de resistência a Tiofanato metílico (TM), Carbendazim (CARB) (benzimidazóis) bem como a mistura Tiofanato metílico + Clorotalonil (TM + CHLO) foi detectada. Nenhuma resistência foi detectada contra Mancozebe, Difenoconazole, Tebuconazole e as misturas Mancozebe + Difenoconazole ou Trifloxistrobina + Propiconazole. O teste foi repetido com os mesmos sete isolados de D. bryoniae contra TM, CARB, TM + CHLO e Oxicloreto de Cobre a ¼, ½, 1 e 2 vezes a dose recomendada. Apenas Oxicloreto de cobre diminuiu consistentemente a taxa de crescimento micelial com o aumento da dose. TM não teve efeito na taxa de crescimento micelial em nenhuma concentração testada, e CARB e TM + CHLO mostraram mínimo efeito com o aumento da concentração do produto. Finalmente, 31 isolados de sete estados brasileiros foram testados para resistência a Tiofanato metílico na dose recomendada (490 ppm). Oitenta e um porcento dos isolados mostraram-se altamente resistentes. Isolados resistentes e sensíveis foram encontrados em uma mesma região geográfica. Considerando a prevalência de isolados resistentes a ambos TM e CARB, uma evidência de resistência cruzada, o uso de benzimidazoles não deve ser recomendado no controle do crestamento gomoso do caule.

Reação de genótipos de melancia ao crestamento gomoso do caule

Face à importância do crestamento gomoso do caule e à escassez de relatos da reação de genótipos de melancia na literatura nacional e internacional, este trabalho teve por objetivo avaliar a resposta de genótipos comerciais de melancia ao crestamento gomoso. No campo, estudou-se o nível de infecção nas folhas em delineamento de blocos ao acaso com nove cultivares de melancia e quatro repetições, com inoculação de duas plantas por parcela aos 43 dias após o plantio (DAP). Foram avaliadas as cultivares Crimson Sweet, Onix, Rubi, Safira, Eureka, Georgia, Sheila, Savana e Riviera. Em casa de vegetação, estudou-se a infecção no caule em vasos, com delineamento inteiramente casualizado, com três repetições, em esquema fatorial de 9 x 3, sendo o fator "a" = cultivares e o fator "b" = isolados. Foram avaliadas as mesmas cultivares do ensaio de campo, com inoculação artificial com disco de micélio aos 15 dias após a semeadura, quando do surgimento da primeira folha definitiva. Os isolados de D. bryoniae utilizados na inoculação das plântulas foram: UnB 76 (Melão-DF), UnB 75 (Melancia-PE) e UnB 81 (Abóbora-DF). Dentre as cultivares avaliadas no campo, Riviera mostrou-se mais resistente e apresentou menores (P&lt;0,05) índices de infecção foliar aos 74 e 79 dias após plantio (DAP), e também menor valor da área abaixo da curva de progresso de doença (AACPD). Foram altamente suscetíveis Crimson Sweet, Rubi, Onix e Safira, que apresentaram os mais altos níveis de infecção nas folhas aos 74 DAP e também altos valores de AACPD. Na avaliação da doença no caule, em casa de vegetação, Riviera também apresentou a menor AACPD (P&lt;0,05). Foi significativa a correlação (r=0,77) entre a resposta das cultivares em campo (resistência das folhas) e em casa de vegetação (resistência no caule).

Lifestyles of Colletotrichum acutatum.

Lifestyles of Colletotrichum acutatum.

New Sources of Resistance to Gummy Stem Blight in Watermelon

Gummy stem blight, caused by Didymella bryoniae (Auersw.) Rehm, is a major disease of watermelon [Citrullus lanatus (Thunb.) Matsum. &amp; Nakai]. Plant breeders need sources of resistance that can be incorporated into adapted breeding lines to help control the disease. We tested all the available accessions from the USDA‐ARS watermelon germplasm collection, including C. lanatus var citroides (L.H. Bailey) Mansf., for resistance to gummy stem blight. The experiment was a randomized complete block with 1332 cultigens, two sites (field and greenhouse), two or four replications, and two to six plants per plot. The resistant check was PI 189225 and the susceptible check was ‘Charleston Gray’. PI 279461, PI 482379, PI 254744, PI 526233, PI 482276, PI 271771, PI 164248, PI 244019, PI 296332, and PI 490383 were selected as the most resistant cultigens to be used in future breeding efforts. The most susceptible cultigens were PI 183398, PI 169286, PI 223764, PI 226445, PI 525084, PI 534597, and PI 278041.

Resistance to Azoxystrobin in the Gummy Stem Blight Pathogen Documented in Georgia

Gummy stem blight, caused by the fungus Didymella bryoniae, is the most destructive disease of watermelon in Georgia and in many other watermelon producing areas of the U.S. The QoI fungicide azoxystrobin has been used for gummy stem blight control in Georgia since 1998. As early as 1999, reduced control of gummy stem blight with azoxystrobin was noted in several research sites and commercial fields of cucumber and watermelon in Georgia. Isolates from several of these fields were later confirmed to be resistant to azoxystrobin. To determine how widespread the resistance problem was in Georgia, extensive surveys of watermelon and muskmelon fields and transplant houses were conducted in 2001 and 2002 to determine the frequency of azoxystrobin-resistant isolates in populations of D. bryoniae. Of the 272 isolates collected in 2001, 247 (91%) were resistant to azoxystrobin. In 2002, 82% of the 170 isolates collected were resistant to azoxystrobin, and of the 40 isolates collected from watermelon transplants, all but one were resistant to azoxystrobin, suggesting that resistant isolates in the field may have originated from seed or transplants. Georgia melon growers are now advised to use alternative fungicides that are chemically unrelated to the QoIs for gummy stem blight control. Accepted for publication 2 November 2004. Published 7 December 2004.

Wet Seed Treatment with Peroxyacetic Acid for the Control of Bacterial Fruit Blotch and Other Seedborne Diseases of Watermelon.

Prevention of seed transmission of Acidovorax avenae subsp. citrulli into the transplant house or field is the most effective control of bacterial fruit blotch of watermelon currently available. Peroxyacetic acid was evaluated as a disinfectant that might efficaciously eradicate A. avenae subsp. citrulli from contaminated seed and also be efficacious against other seed-transmitted diseases of watermelon. Peroxyacetic acid at low concentrations eliminated A. avenae subsp. citrulli, Fusarium oxysporum, and Didymella bryoniae from microbial suspensions. Treatments of seed contaminated with A. avenae subsp. citrulli and D. bryoniae with peroxyacetic acid at 1,600 μg/ml and higher for 30 min were effective in preventing seed transmission of bacterial fruit blotch and gummy stem blight. Hydrochloric acid treatments at 10,000 μg/ml, while effective in eliminating seed transmission to watermelon seedlings, can adversely affect seed germination, especially with triploid seed. Efficacious dosages of peroxyacetic acid can be applied safely to freshly harvested triploid watermelon seed without concerns for reduction in seed quality. A most effective wet seed treatment protocol involved a 30-min treatment with peroxyacetic acid at 1,600 μg/ml followed by seed drying at low humidity in a 40°C drying oven for 48 h.