In vitro efficiency of Trichoderma harzianum mutants in biocontrol of Fusarium oxysporum f. sp. radicis-cucumerinum | ||
| Journal of Crop Protection | ||
| Article 9, Volume 9, Issue 2, 2020, Pages 285-300 PDF (709.83 K) | ||
| Document Type: Original Research | ||
| DOI: 10.48311/jcp.2020.1478 | ||
| Authors | ||
| Leila Sahampoor1; Fatemeh Zaker Tavallaie* 1; Seyed Reza Fani2; Samira Shahbazi3 | ||
| 1Plant Biotechnology, Higher Education Complex of Shirvan, Shirvan, Iran. | ||
| 2Plant Protection Research Department, Yazd Agricultural and Natural Resources Research and Education Center, AREEO, Yazd, Iran. | ||
| 3Plant Protection Research Department, Nuclear Science and Technology Research Institute (NSTRI), Atomic Energy Organization of IRAN (AEOI), Karaj, Iran. | ||
| Abstract | ||
| Trichoderma is very important as a bio control agent and probably a good alternative for chemical fungicides. Fusarium oxysporum is a plant pathogen that causes wilt in a wide range of plants. The use of gamma irradiation can be employed to increase Trichoderma efficiency against F. oxysporum. The induced mutation provides genetic changes in Trichoderma and in some of the mutated isolates the efficiency of bio control may be improved. In this study the efficiency of mutated T. harzianum CS5 against the F. oxysporum f.sp. radicis-cucumerinum was evaluated. Among 16 wild isolates of Trichoderma, CS5 isolate was chosen based on synchronous and nonsynchronous mutual cultivation with pathogen. The spore suspensions of T. harzianum CS5 were irradiated in a cobalt- 60 γ- irradiator at a dose rate of 0.23 Gy/Sec in Nuclear Agriculture Research School, (NSTRI, AEOI). Then antagonist screening of 76 mutants was investigated in the experiments of synchronous and nonsynchronous dual culture with pathogen. The results showed that only 17 mutants were able to control the pathogen better than wild type, and YFTM80 isolate had the most prevention. Using the ERIC-PCR marker, the distinction was investigated between the wild type and the 17 selected mutants. The results showed that the gamma ray is able to improve biocontrol efficiency of Trichoderma and the ERIC-PCR marker can differentiate among derived mutants, but it does not have the ability to distinguish mutants from wild type. In terms of antagonistic superiority, mutations might have occurred in antagonistic sites, which have led to improved antagonistic efficiency. Probably the ERIC-PCR marker has failed to replicate these areas. | ||
| Keywords | ||
| Trichoderma; Gama ray; Mutation; Fusarium oxysporum f. sp. radicis-cucumerinum | ||
| References | ||
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