Differentiation of Cotton-defoliating and Nondefoliating Pathotypes of Verticillium dahliae by RAPD and Specific PCR Analyses |
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| Authors: | Encarnación Pérez-Artés María D García-Pedrajas José Bejarano-Alcázar Rafael M Jiménez-Díaz |
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| Institution: | (1) Departamento de Protección de Cultivos, Instituto de Agricultura Sostenible (IAS), Consejo Superior de Investigaciones Científicas (CSIC), Apartado 4084, 14080 Córdoba, Spain;(2) Departamento de Protección Vegetal, Centro de Investigación y Formación Agraria, Consejería de Agricultura y Pesca, Junta de Andalucía, Apartado 4240, 14080 Córdoba, Spain;(3) Departamento de Agronomía, Universidad de Córdoba, Apartado 3048, 14080 Córdoba, Spain;(4) Departamento de Protección de Cultivos, IAS-CSIC, Apartado 4084, 14080 Córdoba, Spain |
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| Abstract: | Severe Verticillium wilt of cotton in southern Spain is associated with the spread of a highly virulent, defoliating (D) pathotype of Verticillium dahliae. Eleven of the D and 15 of a mildly virulent, nondefoliating (ND) pathotype were analyzed by random amplified polymorphic DNA (RAPD) using the polymerase chain reaction (PCR). Six of 21 primers tested generated pathotype-associated RAPD bands. Another 21 V. dahliae isolates were compared in blind trials both by RAPD-PCR using the six selected primers and pathogenicity tests on cotton cultivars. There was a 100% correlation between pathotype characterization by each method. Unweighted paired group method with arithmetic averages cluster analysis was used to divide the 47 V. dahliae isolates into two clusters that correlated with the D or ND pathotypes. There was more diversity among ND isolates than among D isolates, these latter isolates being almost identical. ND- and D-associated RAPD bands of 2.0 and 1.0 kb, respectively, were cloned, sequenced, and used to design specific primers for the D and ND pathotypes. These pathotype-associated RAPD bands were present only in the genome of the pathotype from which they were amplified, as shown by Southern hybridization. The specific primers amplified only one DNA band of the expected size, and in the correct pathotype, when used for PCR with high annealing temperature. These specific primers successfully characterized V. dahliae cotton isolates from China and California as to D or ND pathotypes, thus demonstrating the validity and wide applicability of the results. |
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| Keywords: | Verticillium wilt Gossypium hirsutum molecular markers genetic diversity virulence |
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