Биотехнология и селекция растений (Feb 2022)
Molecular screening of the VIR strawberry varieties collection for the presence of a marker for the anthracnose black rot resistance gene <i>Rca2</i>
Abstract
Background. Anthracnose black rot caused by the phytopathogenic fungus Colletotrichum acutatum Simmonds became an extremely harmful disease of strawberries in Southern Russia. The disease is widespread throughout the world, and relatively recently it appeared in Russia. Yield losses due to the disease reach up to 80%; besides, the pathogen causes significant plant losses in mother plantations. The most reliable protection against the pathogen is the cultivation of resistant varieties. In strawberries, resistance is controlled by different genes, including Rca2. To identify this gene, molecular markers STS_Rca2_240 and STS-Rca2_417 have been developed. The purpose of this study was to use the markers for screening the VIR collection of strawberry varieties at the VIR Maikop Experiment Station (Maikop ES VIR). Material and methods. The present work studied 135 varieties of Fragaria × ananassa (Duchesne ex Weston) Duchesne ex Rozier, 83 domestic and 52 foreign ones. The domestic varieties included 17 created at the Maikop ES. Plants were evaluated for anthracnose field resistance in the Republic of Adygea from 2018 to 2021. Molecular screening was performed using STS_Rca2_240 and STS-Rca2_417, the molecular markers closely linked to the Rca2 gene. Microsatellite primers EMFv020 were used to control the PCR. The cultivar ‘Sudarushka’, in which the presence of STS_Rca2_240 marker was described in the literature, served as a positive control. Results and discussion. The marker Rca2_240 was detected in 22 cultivars from 135 studied. Among domestic varieties, the frequency of the marker was 18.1%, while among the foreign varieties it was slightly lower and amounted to 13.0%. Among the 17 varieties created at the Maykop SE, the marker was found in three: ‘Majkopskaya rannyaya’, ‘Peryt’, and ‘Shapsugskaya’. The association of the diagnostic fragment with resistance was 73.0%. The marker efficiency was not very high due to the significant number of resistant varieties which do not generate the diagnostic fragments. The resistance in such varieties can be provided by other genes, for example, FaRCa1. The STS-Rca2_417 marker was not effective during screening. Conclusion. Twenty-two varieties with the STS_Rca2_240 marker were identified in the VIR collection, maintained at the Maykop ES VIR, 16 of which were resistant to C. acutatum. These varieties represent a valuable breeding material. The STS-Rca2_240 marker can be used as an important diagnostic trait for the certification of varieties.
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