Anthracnose is a serious problem of both Andean lupine and tamarillo in Ecuador. Morphological features, internal transcribed spacer (ITS) sequences, and host specificity were used to characterize Colletotrichum isolates from lupine and tamarillo. Based on phenotypic and molecular characterization, the causal agent of anthracnose on both hosts was Colletotrichum acutatum. All isolates were identified in a C. acutatum-specific polymerase chain reaction assay. Colony diameter, conidia shape, and insensitivity to benomyl also placed isolates from both hosts in the C. acutatum group. However, a detailed analysis of the ITS sequences placed the lupine and tamarillo isolates from the Ecuadorian Andean zone in two clades, with both lupine and tamarillo isolates in each clade. C. acutatum isolates from Andean lupine were distinct from other C. acutatum isolates on lupine around the world. In cross-infection studies, the diameter of lesions produced by isolates from each host was compared on the main stem of two tamarillo and three lupine cultivars. Some isolates produced larger lesions on the host from which they were isolated but others showed similar aggressiveness on their alternate host. Isolates from both hosts were biotrophic on lupine stems, producing little necrosis and abundant sporulation whereas, on tamarillo stems, they produced dark lesions with few conidia. The collection of C. acutatum isolates from lupine and tamarillo provides interesting material for the study quantitative host adaptation.
Anthracnose, caused by Colletotrichum acutatum, is the most destructive fungal disease of Andean lupin (Lupinus mutabilis Sweet) in Ecuador and of other lupin species around the world. Symptoms of necrotic spots occur throughout the main stem, and infection progresses to cause bending of the main stem and lateral branches, resulting in yield loss. Although there is no known anthracnose resistance, this study aims to assess tolerance of Andean lupin and investigate lupin–C. acutatum interactions. Two Andean lupin genotypes, I-450 Andino and I-451 Guaranguito, were inoculated on the meristematic section of the main stem, either by spraying or by pipetting C. acutatum spores on to an artificial wound. Although the two methods gave similar results, spraying is the preferred method because it mimics natural pathogen infection. Plant-pathogen interactions were assessed at five different phenological stages (leaf stages 2–3, 4–5, 6–7, 8–9, and 10–11) with three C. acutatum isolates by using a 0–5 scale to assess disease symptoms. In both genotypes, anthracnose symptoms were greater at early seedling stage (2–3-leaf stage), decreasing significantly in early vegetative phase (6–7-leaf stage) and increasing again when the flower stage began (10–11-leaf stage). However, the tolerance of these two Andean lupin genotypes to anthracnose was not equally expressed at all developmental stages. We recommend, in a breeding program, that screening for anthracnose first occurs at the 6–7-leaf stage (6 weeks old) and again when flowering starts at the 10–11-leaf stage (10 weeks old) so that the overall tolerance can be determined. This method could be used in lupin breeding programs for improving resistance to anthracnose.
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