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Fungal inoculation of balloon flower stems. (A) Inoculation schemes and disease evaluation procedures based on upward mycelial growth on the stem segments from the base. (B) Disease symptom development on the balloon flower stem rots caused by Rhizoctonia solani and Sclerotinia sclerotiorum. Pictures were taken 4 and 10 days after inoculation. Arrows indicate sclerotinia formed on the infected stem tissues by S. sclerotiorum.  

Fungal inoculation of balloon flower stems. (A) Inoculation schemes and disease evaluation procedures based on upward mycelial growth on the stem segments from the base. (B) Disease symptom development on the balloon flower stem rots caused by Rhizoctonia solani and Sclerotinia sclerotiorum. Pictures were taken 4 and 10 days after inoculation. Arrows indicate sclerotinia formed on the infected stem tissues by S. sclerotiorum.  

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Stem rots caused by Rhizoctonia solani and Sclerotinia sclerotiorum have been known as devastating diseases in balloon flower plants. Antifungal activities of four fungicides, azoxystrobin, polyoxin B, trifloxystrobin and validamycin A were evaluated in vitro, showing effective suppression with mycelial growth of the fungal isolates on PDA media. E...

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... This bacteria was proved to be an e cient control agent for rose powdery mildew and to improve the yield and quality of rose-cut owers (Wang et al. 2018a). In addition, this biological agent can act as antagonistic bacteria for suppression of balloon ower stem diseases caused by R. solani (Lee et al. 2012). There is a lack of research on the effectiveness of adding this bene cial bacterium to the soil to protect sugar beet against damping-off caused by R. solani. ...
... The commercially available B. subtilis strain Y1336 showed great potential to control rose powdery mildew (Wang et al. 2018a), and to signi cantly reduce the incidence of re blight on apple and pear blossoms caused by Erwinia amylovora (Bahadou et al. 2017). B. subtilis Y1336, also, reduces signi cantly the incidence of Balloon ower stem rots caused by R. solani and Sclerotium rolfsii (Lee et al. 2012). ...
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... Iminoctadine tris (albesilate) doses from 0.00625 to 0.1 µg/ml has no antibacterial effect on B. siamensis H30-3. Bacillus spp. as biological control agents were suggested to be integrated into disease management with chemical fungicides (Jacobsen et al., 2004;Korsten et al., 1997;Lee et al., 2012). B. siamensis H30-3 can be considered for strawberry disease control with the two fungicides. ...
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... Various In-vitro and In-vivo researches has been conducted across the globe to overcome the adverse effect of fungal plant diseases, i.e., Botrytis rots (Jijakli and Lepoivre, 1993), Downy mildews (Hindumathy, 2012), Fusarium rots (Schisler et al., 1995), Powdery mildews (Ng et al., 1997), Rusts, Rhizoctonia rots, Sclerotinia rots, Gray mold etc. (Lee et al., 2012;Jedryczka et al., 2002) by using yeast as biocontrol agent. It has been found that yeast having multiple bio-controlling mechanisms or produce various natural antagonistic compounds, i.e., mycoparasitism and induction of resistance in plants, diffusible metabolites, secretion of hydrolytic enzymes, toxin production, releasing volatile compounds, those have antifungal activity for the molds (Jijakli and Lepoivre, 1993;Lee et al., 2012;Jedryczka et al., 2002). ...
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Sclerotinia sclerotiorum is a filamentous fungal pathogen that can infect many economically important crops and vegetables. Alternative oxidase is the terminal oxidase of the alternative respiratory pathway in fungal mitochondria. The function of alternative oxidase was investigated in the regulation of sensitivity of S. sclerotiorum to two commercial fungicides, azoxystrobin and procymidone which have different fungitoxic mechanisms. Two isolates of S. sclerotiorum were sensitive to both fungicides. Application of salicylhydroxamic acid, a specific inhibitor of alternative oxidase, significantly increased the values of effective concentration causing 50% mycelial growth inhibition (EC50) of azoxystrobin to both S. sclerotiorum isolates, whereas notably decreased the EC50 values of procymidone. In mycelial respiration assay azoxystrobin displayed immediate inhibitory effect on cytochrome pathway capacity, but had no immediate effect on alternative pathway capacity. In contrast, procymidone showed no immediate impact on capacities of both cytochrome and alternative pathways in the mycelia. However, alternative oxidase encoding gene (aox) transcript and protein levels, alternative respiration pathway capacity of the mycelia were obviously increased by pre-treatment for 24 h with both azoxystrobin and procymidone. These results indicate that alternative oxidase was involved in the regulation of sensitivity of S. sclerotiorum to the fungicides azoxystrobin and procymidone, and that both fungicides could affect aox gene expression and the alternative respiration pathway capacity development in mycelia of this fungal pathogen.