The diversity of races and prevalence of pathogenic populations ofFusarium oxysporumf. sp.dianthi(Fod) were surveyed in an area in southern Spain. From 54 farms, 132 isolates were collected from wilted carnation plants. Isolates were characterized by RAPDPCR, DNA sequence analysis of theTEF1-α gene, and race-specific molecular markers. Selected isolates from RAPD groups were phenotypically evaluated by pathogenicity tests. Data analysis showed that Fod race 2 was the most frequent and prevalent race in the study area, followed by race 1/8. Moreover, phylogenetic analyses showed similar results, which were different to those of the race-specific PCR assays. It was concluded that (i) seven isolates were not classified in groups where Fod testers were clustered; even they showed different results when race-specific markers were used, (ii) ten isolates with retarded race 1 or race 8 specific band were characterized asF. proliferatumbyTEF1-α gene sequencing and clustered into an outgroup, and (iii) six isolates failed to generate an amplification signal using race-specific markers. Furthermore, three of them were grouped close to race 2 tester according to the phylogenetic analyses, showing the same differential pathogenicity as race 2. This may indicate a Fod race 2 subgroup in this region.
Genetic diversity of Fusarium oxysporum f. sp. dianthi in Southern Spain / Castaño, Raúl; Scherm, Barbara; Avilés, Manuel. - In: JOURNAL OF MYCOLOGY. - ISSN 2356-7481. - 2014:(2014), pp. 1-14. [10.1155/2014/582672]
Genetic diversity of Fusarium oxysporum f. sp. dianthi in Southern Spain
Scherm, Barbara;
2014-01-01
Abstract
The diversity of races and prevalence of pathogenic populations ofFusarium oxysporumf. sp.dianthi(Fod) were surveyed in an area in southern Spain. From 54 farms, 132 isolates were collected from wilted carnation plants. Isolates were characterized by RAPDPCR, DNA sequence analysis of theTEF1-α gene, and race-specific molecular markers. Selected isolates from RAPD groups were phenotypically evaluated by pathogenicity tests. Data analysis showed that Fod race 2 was the most frequent and prevalent race in the study area, followed by race 1/8. Moreover, phylogenetic analyses showed similar results, which were different to those of the race-specific PCR assays. It was concluded that (i) seven isolates were not classified in groups where Fod testers were clustered; even they showed different results when race-specific markers were used, (ii) ten isolates with retarded race 1 or race 8 specific band were characterized asF. proliferatumbyTEF1-α gene sequencing and clustered into an outgroup, and (iii) six isolates failed to generate an amplification signal using race-specific markers. Furthermore, three of them were grouped close to race 2 tester according to the phylogenetic analyses, showing the same differential pathogenicity as race 2. This may indicate a Fod race 2 subgroup in this region.File | Dimensione | Formato | |
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