Screening of promising olive cultivars and local genotypes for resistance to Verticillium dahliae in Iranian collection | ||
| آفات و بیماری های گیاهی | ||
| Article 4, Volume 88, Issue 1 - Serial Number 110, September 2020, Pages 39-51 PDF (622.98 K) | ||
| Document Type: Plant Pathology | ||
| DOI: 10.22092/jaep.2020.127330.1300 | ||
| Authors | ||
| Hossein Jafary* 1; Neda Zand2; Mahdi Taheri3; Aliasghar Zeinanloo4; Shamsollah Najafi2 | ||
| 1Associate Professor of Plant Protection Research Department, Zanjan Agricultural and Natural Resources Research and Education Center, AREEO, Zanjan, Iran. | ||
| 2Researcher, Plant Protection Research Department, Zanjan Agricultural and Natural Resources Research and Education Center, AREEO, Zanjan, Iran. | ||
| 3Associate Professor, Soil and Water Research Department, , Zanjan Agricultural and Natural Resources Research and Education Center, AREEO, Zanjan, Iran. | ||
| 4Horticultural Sciences Research Institute, AREEO, Karaj, Iran. | ||
| Abstract | ||
| Verticilliumwilt of olive (VWO) caused by fungus Verticillium dahliae, is one of the most important diseases of olive worldwide. The response of 15 promising olive cultivars and 15 local varieties was evaluated to the fungus. The olive saplings of each genotype were inoculated with suspension of the fungus using root dip method. The degree of susceptibility/resistance of each genotype was evaluated based on both morphological feature and quantification of fungus in the root system of different genotypes. Total DNA was extracted from root of saplings at different sampling intervals: 0, 2, 12, 45 and 80 days post inoculation. The gradual increase for DNA of fungus in saplings was quantified by Real-time PCR technique and utilizing of SYBR Green system with specific primer pairs for ß-tubulin2 gene. Based on both morphological and quantitative Real-time PCR assays: QG-11, DD2-1, treeNo2, PS-5 and Manzanilla were highly susceptible and KH-13, TTS-1, DS-5 code 5 Lorestan and DS-5 were evaluated as resistant genotypes to the VWO. Moreover, we found parallel results for conventional method of screening (based on disease symptoms) and quantification of DNA in root system of olive by Real-time PCR technique. Olive genotypes evaluated as highly susceptible or resistant to the disease in conventional method showed the similar reaction to the fungus in Q-PCR method. This may suggest that conventional method of evaluation for resistance could be replaced by Q-PCR molecular method in high thropout screening of olive germplasm. | ||
| Keywords | ||
| Olive cultivars; Quantitative assessment; Real time PCR; Resistance | ||
| References | ||
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