Screening and identification of resistance related proteins from apple leaves inoculated with Marssonina coronaria (EII. & J. J. Davis)

Background: apple,an invaluable fruit crop worldwide,is often prone to infection by pathogenic fungi. identification of potentially resistance-conferring apple proteins is one of the most important aims for studying apple resistance mechanisms and promoting the development of disease-resistant apple strains. in order to find proteins which promote resistance to marssonina coronaria,a deadly pathogen which has been related to premature apple maturation,proteomes from apple leaves inoculated with m. coronaria were characterized at 3 and 6 days post-inoculation by two dimensional electrophoresis (2-de).results: overall,59 differentially accumulated protein spots between inoculation and non-inoculation were successfully identified and aligned as 35 different proteins or protein families which involved in photosynthesis,amino acid metabolism,transport,energy metabolism,carbohydrate metabolism,binding,antioxidant,defense and stress. quantitative real-time pcr (qrt-pcr) was also used to examine the change of some defense and stress related genes abundance under inoculated conditions.conclusions: in a conclusion,different proteins in response to marssonina coronaria were identified by proteomic analysis. among of these proteins,there are some pr proteins,for example class iii endo-chitinase,beta-1,3-glucanase and thaumatine-like protein,and some antioxidant related proteins including aldo/keto reductase akr,ascorbate peroxidase and phi class glutathione s-transferase protein that were associated with disease resistance. the transcription levels of class iii endo-chitinase (l13) and beta-1,3-glucanase (l17) have a good relation with the abundance of the encoded protein's accumulation,however,the mrna abundance of thaumatine-like protein (l22) and ascorbate peroxidase (l28) are not correlated with their protein abundance of encoded protein. to elucidate the resistant mechanism,the data in the present study will promote us to investigate further the expression regulation of these target proteins. © 2014 li et al.; licensee biomed central ltd.