IIB   20738
INSTITUTO DE INVESTIGACIONES BIOLOGICAS
Unidad Ejecutora - UE
artículos
Título:
Potassium phosphite primes defense responses in potato against Phytophthora infestans
Autor/es:
MACHINANDIARENA MF; LOBATO, M. C.; FELDMAN ML; DALEO G.R.; ANDREU A. B
Revista:
JOURNAL OF PLANT PHYSIOLOGY
Editorial:
ELSEVIER GMBH
Referencias:
Lugar: Netherland; Año: 2012 vol. 15 p. 1417 - 1424
ISSN:
0176-1617
Resumen:
Article Number: 51493. IN PRESS. Although phosphite is widely used to protect plants from pathogenic oomycetes on a wide range of horticultural crops, the molecular mechanisms behind phosphite induced resistance are poorly understood. The aim of this work was to assess the effects of KPhi on potato plant defense responses to infection with Phytophtora infestans. Pathogen development was severely restricted and there was also an important decrease in lesion size in infected KPhi-treated leaves. We demonstrated that KPhi primed hydrogen peroxide and superoxide anion production in potato leaves at 12 h postinoculation with P. infestans. Moreover, the KPhi-treated leaves showed an increased and earlier callose deposition witH respect to water-treated plants, beginning 48 h after inoculation. In contrast, callose deposition was not detected in water-treated leaves until 72 h after inoculation. In addition, we carried out RNA gel blot analysis of genes implicated in the responses mediated by salicylic (SA) and  jasmonic acid (JA). To this end, we examined the temporal expression pattern of StNPR1 and StWRKY1,two transcription factors related to SA pathway, and StPR1 and StIPII, marker genes related with SA and JA pathways, respectively. The expression of StNPR1 and StWRKY1 was enhanced in response to KPhi treatment. In contrast, StIPII was down regulated in both KPhi-treated and water-treated leaves, 24 h after infection with P. infestans, suggesting that the regulation of this gene could be independent of the KPhi treatment. Our results indicate that KPhi primes the plant for an earlier and more intense response to infection and that SA would mediate this response.