Macrophomina phaseolina (Tassi) Goid remains the prevailing causal agent of charcoal rot disease that significantly suppresses the yield of a variety of oilseed crops. Its wide host range and ability to survive under arid conditions, coupled with the ineffective use of fungicides against it, have spurred scientific endeavours for alternative avenues to control this phytopathogen. Hence, the present study aimed to provide empirical evidence of the efficacy of three fungal isolates (T2, T10 and T12) of Trichoderma harzianum as biological control agents against charcoal rot in soybean (Glycine max L.). The results of the in vitro studies revealed that all three fungal isolates significantly inhibited the growth of M. phaseolina phytopathogen, with T12 showing considerably higher inhibition effect than T2 and T10 isolates. T12 inhibited the growth of M. phaseolina in the dual culture (72.31%) and volatile production (63.36%) assays, and the hyperparasitism test indicated cell lysis following the interactions with T12 mycelia. T12 isolate was mostly effective in field experiments, observable in the attained minimum plant disease indices both in the soil incorporation (11.98%) and seed inoculation (5.55%) treatments, in comparison to isolates T2 and T10. Moreover, the stem and root lengths, as well as the seed weight, were considerably increased, as compared to the control. Hence, the findings reported in the present study supported the applicability of T12 isolate as possible alternative to fungicides for the control of charcoal rot in soybean.
Genomic DNA of the mutant lines of the three potato cultivars, Cardinal, Diamant and Desiree, with respect to controls were isolated and analyzed for polymorphisms by using random amplified polymorphic DNA (RAPD) markers. Four 10 bp random fragment primers, S-13, S-18, S-19 and R-17 were studied and all of them gave the amplification of genomic DNA. All of the mutant lines gave different banding pattern against different primers with respect to control plants of the three varieties, and bands are present at 50 bp to 1500 bp. All these primers with specific banding pattern were unique in their polymorphic behavior. Different banding pattern of total protein contents were also observed by PAGE analysis of all the mutant lines as compared with the control plants. It is therefore suggested that RAPD and protein analyses would be important tools to detect the polymorphism in mutated lines of potato.
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