scholarly journals Evaluation of Lisianthus Cultivars for Resistance to Botrytis cinerea

Plant Disease ◽  
2007 ◽  
Vol 91 (8) ◽  
pp. 997-1001 ◽  
Author(s):  
Stephen N. Wegulo ◽  
Miguel Vilchez

Lisianthus (Eustoma grandiflorum) is a high-value cut flower. However, major yield losses often result from gray mold caused by Botrytis cinerea. Various techniques were used to evaluate 12 lisianthus cultivars for resistance B. cinerea. Disease evaluations from detached leaf, leaf disc, cut stem, and in vivo growth chamber stem (GC) assays were correlated with those from an in vivo greenhouse stem (GH) assay, in which commercial greenhouse production of lisianthus was simulated. In all assays, stems or leaves were wounded before inoculation with spores or mycelia of B. cinerea. There was a significant (P ≤ 0.03) positive correlation between stem lesion length in the GH assay and disease incidence in the same assay (R = 0.74), stem lesion length from spore spray inoculation in the GC assay (R = 0.62), and percent necrosis from spore spray inoculation of detached leaves (R = 0.71). Correlations between stem lesion length in the GH assay and disease evaluations from spore drop and mycelial inoculation of detached leaves, leaf discs, and cut stems were not significant at P = 0.05. Considering only screening methods with significant correlations, ‘Magic Champagne’ was the most resistant cultivar (mean rank [mr] = 2 of 12). ‘Echo White’ and ‘Echo Lavender’ were the least resistant cultivars (mr = 11). The other cultivars were ‘Magic White’ (mr = 4); ‘Avila Ivory’, ‘Balboa Yellow’, ‘Echo Pink’, and ‘Magic Rose’ (mr = 5); ‘Balboa Blue’ (mr = 6); ‘Avila Blue Rim’ (mr = 8); and ‘Avila Purple’ and ‘Catalina Purple’ (mr = 9). The results from this study indicate that in vivo disease incidence, in vivo stem assays, and detached leaf assays, all initiated with wounding followed by spore spray inoculation, may be more reliable in evaluating lisianthus cultivars for resistance to B. cinerea than spore drop and mycelial inoculation of detached leaves, leaf discs, and cut stems. The results also indicate that lisianthus cultivars with moderate resistance to B. cinerea are commercially available. These cultivars have potential for use as germplasm in breeding lisianthus for resistance to the pathogen.

2004 ◽  
Vol 84 (1) ◽  
pp. 311-317 ◽  
Author(s):  
H. Wang ◽  
S. F. Hwang ◽  
K. F. Chang ◽  
B. D. Gossen ◽  
G. D. Turnbull ◽  
...  

The disease reaction of alfalfa (Medicago sativa) cultivars to spring black stem was evaluated in field trials and greenhouse experiments. In field trials, differences in cultivar reaction to leaf spot (predominantly spring black stem) were observed in 9 of 16 station years. The reaction of certain cultivars was consistent across most trials, but other cultivars were quite variable. Under controlled conditions, one isolate each of Phoma sclerotioides and P. exigua produced symptoms on alfalfa leaves that were similar to those caused by P. medicaginis. These results indicate that P. medicaginis is not the only pathogen responsible for symptoms of spring black stem on alfalfa in the prairie region. In a detached-leaf study, one isolate each of P. medicaginis, P. sclerotioides and P. exigua produced leaf lesions on all 18 alfalfa cultivars assessed. Disease incidence in Absolute, Algonquin, Pickseed 3006 and Anik (M. sativa subsp. falcata) was lower than in 630 and AC Blue J. Inoculation of eight selected cultivars using a range of spore concentrations under controlled conditions showed a similar pattern; all three isolates produced leaf lesions on all eight cultivars. Ino culation with conidial suspensions of P. medicaginis resulted in a lower disease incidence on Absolute than on Beaver. Key words: Medicago sativa, Medicago sativa subsp. falcata, Phoma medicaginis, P. sclerotioides, P. exigua, detached leaves.


2014 ◽  
Vol 40 (4) ◽  
pp. 353-357 ◽  
Author(s):  
Camila Turra ◽  
Erlei M. Reis ◽  
Amarilis L. Barcellos

The method of preserving detached wheat leaves in Petri dish was used for the inoculation and development of the fungus Puccinia triticina, the causal agent of wheat leaf rust. The reaction of 26 wheat cultivars was compared by using seedlings cultivated in pots (in vivo) and detached leaves (in vitro) inoculated with four physiological races of the pathogen. After inoculation, the material was kept in a growth chamber for 15 days. The reaction was evaluated on the 15th day after inoculation. Results for each race in the evaluated genotypes confirmed the efficiency of the detached leaf method in assessing the reaction of wheat cultivars.


Plant Disease ◽  
2003 ◽  
Vol 87 (4) ◽  
pp. 402-406 ◽  
Author(s):  
J. E. Hollowell ◽  
B. B. Shew ◽  
T. G. Isleib

Sclerotinia minor is a major pathogen of peanut in North Carolina, Virginia, Oklahoma, and Texas. Partial resistance to S. minor has been reported based on field screening, but field performance is not always correlated with laboratory or greenhouse evaluations of resistance. More efficient screening methods and better understanding of the mechanisms contributing to Sclerotinia blight resistance are needed, and a detached leaf assay was developed and evaluated. Detached leaflets of 12 greenhouse-grown peanut lines were inoculated on the adaxial surface with a 4-mm-diameter mycelial plug of a single isolate of S. minor. Leaflets were incubated in the dark at 20°C in Nalgene utility boxes containing moistened sand. Lesion length 3 days after inoculation ranged from 11 to 24 mm, with a mean of 19 mm. Lengths differed significantly among the entries, with GP-NC WS 12, an advanced breeding line derived from a cross of NC 6 × (NC 3033 × GP-NC WS 1), being the most resistant. Forty-eight isolates of S. minor obtained from peanut were inoculated on leaflets of the susceptible cultivar NC 7 and aggressiveness was assessed by measuring lesion-length expansion. Three days after inoculation, lesion length differed among the isolates and ranged from 2 to 24 mm, with a mean of 15 mm. Finally, the potential for specific interactions between peanut lines and S. minor isolates was evaluated. A subset of S. minor isolates was selected to represent the observed range of aggressiveness and a subset of peanut entries was selected to represent the range of resistance or susceptibility. Nine-week-old greenhouse- or field-grown plants were compared for five peanut entries. Main effects of isolates and entries were highly significant, but isolate-entry interactions were not significant. The most resistant peanut entry (GP-NC WS 12) performed consistently with all isolates regardless of plant source.


Plant Disease ◽  
2013 ◽  
Vol 97 (6) ◽  
pp. 848-848 ◽  
Author(s):  
D. Fernández-Ortuño ◽  
P. K. Bryson ◽  
A. Grabke ◽  
G. Schnabel

Gray mold caused by Botrytis cinerea Pers.:Fr. is one of the most economically important diseases of cultivated strawberry (Fragaria × ananassa) worldwide. Control of gray mold mainly depends on fungicides, including the phenylpyrrole fludioxonil, which is currently marketed in combination with cyprodinil as Switch 62.5WG (Syngenta Crop Protection, Research Triangle Park, Raleigh, NC). In 2012, 790 strains of B. cinerea were collected from 76 strawberry fields in eight states, including Arkansas, Florida, Georgia, Kansas, Maryland, North Carolina, South Carolina, and Virginia. Strains were collected from sporulating flowers and fruit and sensitivity to fludioxonil was determined using a conidial germination assay as previously described (2). Only one isolate from a farm located in Westmoreland County, Virginia, grew on medium amended with the discriminatory dose of 0.1 μg/ml fludioxonil and was therefore considered low resistant. The isolate did not grow on 10 μg/ml. All other 789 isolates did not grow at either of the two doses. This assay was repeated twice with a single-spore culture of the same strain. In both cases, residual growth was observed on the fludioxonil-amended medium of 0.1 μg/ml. The single spore isolate was confirmed to be B. cinerea Pers. using cultural and molecular tools as described previously (1). To assess resistance in vivo, commercially grown ripe strawberry fruit were rinsed with sterile water, dried, placed into plastic boxes (eight strawberries per box for each of the three replicates per treatment), and sprayed 4 h prior to inoculation with either water or 2.5 ml/liter of fludioxonil (Scholar SC, Syngenta) to runoff using a hand mister. This dose reflects the rate recommended for gray mold control according to the Scholar label. Each fruit was stabbed at three equidistant points, each about 1 cm apart and 1 cm deep using a syringe tip. Wounds were injected with a 30-μl droplet of conidia suspension (106 spores/ml) of either 5 sensitive or the resistant isolate. Control fruit were inoculated with water. After inoculation, the fruit were kept at 22°C for 4 days. In two independent experiments, sensitive and low resistant isolates were indistinguishable in pathogenicity on detached, unsprayed fruit. The low resistant isolate developed gray mold disease on all treated and untreated fruit (100% disease incidence) as determined by the absence or presence of gray mold symptoms. The sensitive isolates only developed disease on untreated fruit. The EC50 values, determined in microtiter assays with concentrations of 0.01, 0.03, 0.1, 0.3, 1, 3, and 10 μg/ml fludioxonil, were 0.01 μg/ml for the sensitive isolates and 0.26 μg/ml for the resistant isolate. To our knowledge, this is the first report of fludioxonil resistance in B. cinerea from strawberry in North America. Our monitoring results indicate that resistance is emerging 10 years after the introduction of fludioxonil and stress the importance of chemical rotation for gray mold control. References: (1) X. P. Li et al. Plant Dis. 96:1634, 2012. (2) R. W. S. Weber and M. Hahn. J. Plant Dis. Prot. 118:17, 2011.


2020 ◽  
Vol 55 (1) ◽  
pp. 27-34
Author(s):  
G. Zadehdabagh ◽  
K. Karimi ◽  
M. Rezabaigi ◽  
F. Ajamgard

The northern of Khuzestan province in Iran is mainly considered as one of the major areas of miniature rose production. Blossom blight caused by Botrytis cinerea has recently become a serious limiting factor in rose production in pre and post-harvest. In current study, an attempt was made to evaluate the inhibitory potential of some local Trichoderma spp. strains against B. cinerea under in vitro and in vivo conditions. The in vitro results showed that all Trichoderma spp. strains were significantly able to reduce the mycelial growth of the pathogen in dual culture, volatile and non-volatile compounds tests compared with control, with superiority of T. atroviride Tsafi than others. Under in vivo condition, the selected strain of T. atroviride Tsafi had much better performance than T. harzianum IRAN 523C in reduction of disease severity compared with the untreated control. Overall, the findings of this study showed that the application of Trichoderma-based biocontrol agents such as T. atroviride Tsafi can be effective to protect cut rose flowers against blossom blight.


2019 ◽  
Vol 15 (1) ◽  
pp. 63-70
Author(s):  
Shiv Dev Singh ◽  
Arvind Kumar ◽  
Firoz Babar ◽  
Neetu Sachan ◽  
Arun Kumar Sharma

Background: Thienopyrimidines are the bioisoster of quinazoline and unlike quinazoline exist in three isomeric forms corresponding to the three possible types annulation of thiophene to the pyrimidine ring viz thieno[2,3-d] pyrimidine, thieno[3,2-d] pyrimidine and thieno[3,4-d]pyrimidine. Heterocyclic containing the thienopyrimidinone moiety exhibits various pronounced activities such as anti-hypertensive, analgesic and anti-inflammatory, antiviral, platelet aggregation inhibitory, antiprotozoal bronchodilatory, phosphodiesterase inhibitory, antihistaminic, antipsychotic and antimicrobial activity. Objective: Synthesis of novel 3(N,N-dialkylamino)alkyl/phenyl substituted thieno[2,3-d]pyrimidinones as H1-anti-histaminic and antimicrobial agents. Methods: A series of 3-[(N,N-dialkylamino)alkyl/phenyl]-2-(1H)thioxo-5,6,7,8-tetrahydrobenzo(b) thieno(2,3-d)pyrimidine-4(3H)-ones[4a-d], their oxo analogous [5a-d] and 3-[(N,N-dialkylamino)alkyl]- 2-chlorophenyl-5,6,7,8-tetrahydrobenzo(b)thieno(2,3-d)pyrimidine- 4 (3H)-ones[6a-d]derivative were synthesized from 2-amino-4,5,6,7-tetrahydrobenzo(b)thiophene-3-carboxylic acid by nucleophilic substitution of different N,N-dialkyl alkylene/phenylene diamines on activated 3-acylchloride moiety followed by cyclocondensation with carbon disulfide and ethanolic potassium hydroxide to get [4a-d] and in second reaction by condensation with 4-chlorobenzoyl chloride to get [6a-d] by single pot novel innovative route. The oxo analogous [5a-d] were prepared by treating derivatives [4a-d] with potassium permagnate in ethanolic KOH. The synthesized compound were evaluated for H1-antihistaminic and antimicrobial activities. Results: All synthesized compounds exhibited significant H1-antihistaminic activity by in vitro and in vivo screening methods and data were verified analytically and statistically. The compound 4a, 4b, 5a and 5b showed significant H1-antihistaminiic activity than the reference standard chlorpheniramine maleate. The compound 6d, 6c, 5c and 4c exhibited significant antimicrobial activity.


2021 ◽  
Vol 9 (2) ◽  
pp. 379
Author(s):  
Breanne M. Head ◽  
Christopher I. Graham ◽  
Teassa MacMartin ◽  
Yoav Keynan ◽  
Ann Karen C. Brassinga

Legionnaires’ disease incidence is on the rise, with the majority of cases attributed to the intracellular pathogen, Legionella pneumophila. Nominally a parasite of protozoa, L. pneumophila can also infect alveolar macrophages when bacteria-laden aerosols enter the lungs of immunocompromised individuals. L. pneumophila pathogenesis has been well characterized; however, little is known about the >25 different Legionella spp. that can cause disease in humans. Here, we report for the first time a study demonstrating the intracellular infection of an L. bozemanae clinical isolate using approaches previously established for L. pneumophila investigations. Specifically, we report on the modification and use of a green fluorescent protein (GFP)-expressing plasmid as a tool to monitor the L. bozemanae presence in the Acanthamoeba castellanii protozoan infection model. As comparative controls, L. pneumophila strains were also transformed with the GFP-expressing plasmid. In vitro and in vivo growth kinetics of the Legionella parental and GFP-expressing strains were conducted followed by confocal microscopy. Results suggest that the metabolic burden imposed by GFP expression did not impact cell viability, as growth kinetics were similar between the GFP-expressing Legionella spp. and their parental strains. This study demonstrates that the use of a GFP-expressing plasmid can serve as a viable approach for investigating Legionella non-pneumophila spp. in real time.


2015 ◽  
Vol 41 (4) ◽  
pp. 251-255 ◽  
Author(s):  
Daiane Cristina Martins Barros ◽  
Inês Cristina de Batista Fonseca ◽  
Maria Isabel Balbi-Peña ◽  
Sérgio Florentino Pascholati ◽  
Douglas Casaroto Peitl

ABSTRACTThe incidence and the levels of yield loss caused by the white mold of soybean (caused by the fungus Sclerotinia sclerotiorum) have increased in areas of higher altitude at Cerrado and Southern Brazil, causing yield losses of up to 60%. The aim of this study was to select saprobic fungi with the potential to control the white mold of soybean. First, in vitroantagonism screening was carried out to test eight saprobic fungi against S. sclerotiorum. Assessment of S. sclerotiorum mycelial growth was done at four and seven days after its placement on the culture medium. The isolate showing greatest antagonistic effect in all tests/assessments was Myrothecium sp. An in vivo experiment was conducted in a greenhouse and growth chamber, where plants previously treated with eight saprobic fungi were artificially inoculated with S. sclerotiorum. The fungal culture medium (potato-dextrose) and the commercial resistance inducer acibenzolar-S-methyl were used as controls. In the in vivotests, severity of the white mold was assessed at 8, 14 and 21 days after inoculation. The highest reduction percentage in the lesion length was observed for the treatment with Myrothecium sp. (70%), which has the greater potential to be used as biocontrol agent of soybean under the conditions of this experiment.


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