Abstract:
Heuchera hybrida, also called "coral bells," is a versatile perennial with attractive
foliage and bell-shaped flowers. To meet the increasing demand for commercial scale
cultivation, tissue culture protocols have been developed. There is a necessity to
suppress the growth of fungal contaminants that were present in the original explant
or introduced as laboratory contaminants without causing an adverse effect on tissuecultured
plantlets. The goal of this study was to identify fungal contamination in in
vitro propagated H. hybrida and control those using fungicides. Complete
Randomized Design (CRD) was used to conduct the experiment. One-way, two-way
(Analysis of Variance) ANOVA, and linear regression analysis methods were used.
The contaminated fungi were isolated from tissue culture media and cultured on
Potato Dextrose Agar and incubated at 25°C for one week. The identification of
fungus were carried out by using macroscopic and microscopic examinations
depending on the colony color, shape, hyphae, conidia, conidiophores and
arrangement of spores. For the molecular identification of the contaminated fungus,
the extracted fungal DNA was amplified by PCR using a specific internal transcribed
spacer primer (ITS1 / ITS4). Six fungicides (Carbendazim®, Topsin M 70®,
Chlorothalonil®, Mancozeb®, Antracol®, and Homai®) were tested. The effectiveness
of fungicides was evaluated using the inhibition zones produced by fungicides against
fungal contaminants. Four different types of fungicides were chosen for in vitro
screening and incorporated into the MS medium at rates of 75%, 50%, 25%, and 10%
of its recommended dosage. Three fungal contaminants were identified as Penicillium
spp., Phlebia acerina, and Cladosporium spp based on both microscopic and
macroscopic features and molecular confirmation. Topsin M 70® showed strong
fungicidal effects on Penicillium spp and Cladosporium spp., while having a
fungistatic effect on Phlebia acerina. All the fungicide-treated samples did not have
any fungal contamination during the multiplication period of H. hybrida. Topsin M
70® in tissue culture medium stimulated H. hybrida growth without causing visual
toxicities in plantlets. The results of the experiment revealed that a 100 ppm
concentration of Topsin M 70® effectively controlled the identified fungal
contamination in H. hybrida, avoiding annual production losses due to fungal
contamination.
