Sources of resistance to Fusarium spp. are needed to develop maize hybrids resistant to the accumulation of fungal mycotoxins in the grain. In a search for resistant germplasm in 1999 and 2000, a set of Argentinian maize populations was evaluated in Ottawa, Canada, for resistance to ear rots after inoculation with local isolates of Fusarium verticillioides and F. graminearum. Sixteen of these populations, varying in observed resistance levels, were re-evaluated in 2003 and 2004 in Pergamino, Argentina, using local isolates of the same fungi. Conidial suspensions of each fungal species were inoculated into the silk channel of primary ears. Disease severity was assessed after physiological maturity using a scale based on the percentage of visibly infected kernels. Genotype effect was more important than genotype-by-fungal species or genotype-by-fungal species-by-environment interaction effects. In addition, disease severity levels associated with each fungal species were positively correlated (P < 0.05) (r = 0.90, r = 0.81, r = 0.87 and r = 0. 53, in Ottawa 1999and 2000, and Pergamino 2003and 2004. Populations ARZM 01107, ARZM 07138, ARZM 10041, ARZM 13031, ARZM 16002 and Pora INTA exhibited the highest and most stable resistance to both species. Considering that disease resistance exhibited low specificity to the environment and to the fungal species in evaluations conducted in a wide range of environments and with fungal isolates collected from different hemispheres, the most resistant populations are potential sources of genes for stable resistance to these Fusarium spp.
Fusarium solani f.sp. eumartii Carp. Snyder and Hansen (Fusarium eumartii) is a soil inhabitant that induces the so-called Potato Wilt and Stem End Rot disease. Prior to wilting, the pathogen induces peculiar small bronze spots on the leaflets. Failure to isolate E eumartii from infected leaflets suggests the involvement of a toxin in the disease. The fungus was grown in liquid Richard's medium and thereafter a filtrate was obtained dialyzing (MW cutoff 12,000-14,000) and sterilizing the culture by filtration (0.22 #m). Potato leaves treated with both the pathogen or the filtrate showed symptoms of bronze spots and significantly higher electrolyte leakage when compared to controls. Tomato leaves showed neither bronze spots nor electrolyte leakage after plant inoculation with the pathogen or with the filtrate treatment. Both, the absence of visible symptoms and the lack of electrolyte leakage in tomato could be associated to a certain degree of host specificity of the F. eumartii filtrate towards potato. The filtrate also induced symptoms similar to infections by E eumartii in adult plants and in vitro plantlets of cultivars Huinkul MAG and Kennebec. Callus responses to the filtrate were related to responses of the cultivars to the pathogen in greenhouse. These results show the potential of the culture filtrate of E eumartii for use in screening for wilting resistance.
Asian soybean rust (ASR), caused by Phakopsora pachyrhizi Syd. & P. Syd., has been reported in Argentina on soybean (Glycine max) and kudzu (Pueraria lobata and Pueraria javanica) since the 2002 growing season (1–4). On 29 May 2006, plants of Phaseolus spp. were found to have tan ASR-like rust lesions on leaves at eight different field plots located in the northwestern province of Salta, Argentina. Growth stages of infected bean plants within plots were between pod setting and physiological maturity. Diagnosis of ASR on bean leaves was performed with a stereoscopic microscope to view rust pustules, and suspected uredinia of P. pachyrhizi were observed, furthermore, typical ASR urediniospores also were also observed at ×400. ELISA and PCR methods gave positive results for ASR. Rust spores from these plants were used to inoculate soybean plants at the V3 growth stage with rust spores from field bean plants produced under greenhouse conditions. Typical ASR tan pustules developed within 21 days of inoculation. Bean rust caused by Uromyces phaseoli also was seen in some of the bean plots but was easily differentiated from ASR because the uredinia were much darker and affected the upper leaves, while the ASR uredinia were lighter and spread from the lower leaves to the upper leaves. This finding is of significance in Argentina because bean is an important crop grown in the northwestern region of the country and is planted approximately 2 months after soybean planting. Given this planting time difference, bean may provide an overwintering host for the survival of ASR spores, thereby providing a green bridge for infection of soybean plants during the following growing season. References: (1) A. J. Ivancovich. Soybean rust situation in Argentina. Oral presentation. Symposium: Soybean Rust: Too Close for Comfort. Annual Meeting of the American Phytopathological Society. 2003. (2) A. J. Ivancovich. Plant Dis. 89:667, 2005. (3) A. J. Ivancovich and G. Botta. Rev. Tecnología Agropecuaria 7(21):16, 2002. (4) A. J. Ivancovich et al. Phytopathology (Abstr.) 94(suppl.):S44, 2004.
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