Sugar Beet Seed Institute in cooperation with the Crop Science Society of Iran (CSSI) Journal of Sugar Beet 1735-0670 20 2 2005 02 19 A study on genetic diversity of Iranian populations of Erysiphe betae(Vanha) Weltzien causal agent of sugar beet powdery mildew using rDNA-RFLP method A study on genetic diversity of Iranian populations of Erysiphe betae(Vanha) Weltzien causal agent of sugar beet powdery mildew using rDNA-RFLP method 159 149 6876 10.22092/jsb.2005.6876 FA M. Sheikholeslami Department of Plant Protection. College of Agriculture, University of Tehran, Iran M. Okhovvat Department of Plant Protection. College of Agriculture, University of Tehran, Iran Gh. Hejaroude Department of Plant Protection. College of Agriculture, University of Tehran, Iran A. Sharifi-Tehrani Department of Plant Protection. College of Agriculture, University of Tehran, Iran M. Seidel Phytotechnology Lab. University of Applied Sciences of Heilbronn, Weinsberg, Germany M. Javan-Nikkhah Department of Plant Protection. College of Agriculture, University of Tehran, Iran Journal Article 2004 07 15 A total of 105 isolates of Erysiphe betae from different regions of Iran were investigated. For probable polymorphism of ITS-5.8S regions using PCR-based RFLP, the mentioned fragments were amplified via PCR by ITS1 and ITS4 primers and subjected to 1.5% agarose gel electrophoresis. PCR products were digested by HaeIII, AluI, TaqI, HindIII, CfoI, EcoRI, MspI, SacI and RsaI REs and the digestion products were resolved on 7.5% polyacrylamide. PCR product of all isolates was only one 645 bp fragment. Among nine REs tested AluI, CfoI, MspI and HaeIII had recognition sequences on PCR products. Because of unstability, results for AluI were ignored.Digestion products for CfoI were 280, 185 and 180bp, for MspI, 325, 160, 120 and 40bp and those of HaeIII, 325, 180, 75, 40 and 30bp fragments for all isolates. Electrophoretic patterns of PCR products and digested products were completely similar,thus no polymorphism was discernible between 105 isolates. Based on the results,Iranian populations of E.betae seems to be highly uniform. A total of 105 isolates of Erysiphe betae from different regions of Iran were investigated. For probable polymorphism of ITS-5.8S regions using PCR-based RFLP, the mentioned fragments were amplified via PCR by ITS1 and ITS4 primers and subjected to 1.5% agarose gel electrophoresis. PCR products were digested by HaeIII, AluI, TaqI, HindIII, CfoI, EcoRI, MspI, SacI and RsaI REs and the digestion products were resolved on 7.5% polyacrylamide. PCR product of all isolates was only one 645 bp fragment. Among nine REs tested AluI, CfoI, MspI and HaeIII had recognition sequences on PCR products. Because of unstability, results for AluI were ignored.Digestion products for CfoI were 280, 185 and 180bp, for MspI, 325, 160, 120 and 40bp and those of HaeIII, 325, 180, 75, 40 and 30bp fragments for all isolates. Electrophoretic patterns of PCR products and digested products were completely similar,thus no polymorphism was discernible between 105 isolates. Based on the results,Iranian populations of E.betae seems to be highly uniform.

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