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United States Department of Agriculture

Agricultural Research Service

Research Project: BIOLOGICAL APPROACHES FOR MANAGING DISEASES OF TEMPERATE FRUIT CROPS Title: Differential gene expression during the pathogenic interaction between Pichia fermentans and peach fruit

item Fiori, Stefano -
item Scherm, Barbara -
item Migheli, Quirico -
item Farrell, Robert -
item Wisniewski, Michael
item Budroni, Marilena -

Submitted to: Acta Horticulturae
Publication Type: Proceedings
Publication Acceptance Date: July 15, 2011
Publication Date: August 31, 2011
Citation: Fiori, S., Scherm, B., Migheli, Q., Farrell, R., Wisniewski, M.E., Budroni, M. 2011. Differential gene expression during the pathogenic interaction between Pichia fermentans and peach fruit. Acta Horticulturae. 905:103-105.

Technical Abstract: A biofilm-forming strain of Pichia fermentans was found to be a very strong antagonist against brown rot and grey mold in artificially wounded apple fruit when co-inoculated with either Monilinia fructicola or Botrytis cinerea, respectively. The same strain of yeast; however, was an aggressive pathogen when inoculated on peach fruit, causing rot of fruit tissues even in the absence of other pathogens. Optical and scanning electron microscopy showed that P. fermentans produces only yeast-like shaped cells during colonization of apple tissue while exhibiting pseudohyphal growth on peach tissue. A rapid subtractive hybridization approach (RaSH) was used to identify differentially expressed genes in the pathogenic form of P. fermentans by comparing the cDNA of P. fermentans sampled after 24 hours growth on apple with the cDNA of the same strain grown 24 hours on peach fruit. A total of 450 clones were analysed by a reverse Northern Blotting technique yielding some fragments which were significantly expressed on peach but less on apple tissue. These sequences were compared to the available genome sequences of another dimorphic yeast, Candida albicans, and homologous genes were identified. The relationship between these genes, dimorphism, and pathogenicity will be discussed.

Last Modified: 8/26/2016
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