DNA polymorphisms were evaluated for the eight strains representing Tilletia controversa Kuhn, T. laevis Kuhn and T. tritici (Bjerk.) Winter using polymorase chain reaction and restriction fragment length polymorphism (PCR-RFLP) analysis. DNA regions coding for the internal traiscribed spacers (ITS) were amplified and digested with five four-base restriction enzymes (Msp I,Hinf I, Taq I, Hha I and Hae III). No differences were shown in the PCR-RFLP patterns among the strains tested. This indicated T, controversa, T. Iaevis and T. tritici are very closely related.
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