Link to home

Differential Gene Expression in Individual Papilla-Resistant and Powdery Mildew-Infected Barley Epidermal Cells

July 2004 , Volume 17 , Number  7
Pages  729 - 738

Torben Gjetting , 1 Timothy L. W. Carver , 2 Leif Skøt , 2 and Michael F. Lyngkjær 1

1Plant Research Department, Risø National Laboratory, DK-4000 Roskilde, Denmark; 2Institute of Grassland and Environmental Research, Aberystwyth, Ceredigion SY23 3EB, U.K.

Go to article:
Accepted 1 March 2004.

Resistance and susceptibility in barley to the powdery mildew fungus (Blumeria graminis f. sp. hordei) is determined at the single-cell level. Even in genetically compatible interactions, attacked plant epidermal cells defend themselves against attempted fungal penetration by localized responses leading to papilla deposition and reinforcement of their cell wall. This conveys a race-nonspecific form of resistance. However, this defense is not complete, and a proportion of penetration attempts succeed in infection. The resultant mixture of infected and uninfected leaf cells makes it impossible to relate powdery mildew-induced gene expression in whole leaves or even dissected epidermal tissues to resistance or susceptibility. A method for generating transcript profiles from individual barley epidermal cells was established and proven useful for analyzing resistant and successfully infected cells separately. Contents of single epidermal cells (resistant, infected, and unattacked controls) were collected, and after cDNA synthesis and PCR amplification, the resulting sample was hybridized to dot-blots spotted with genes, including some previously reported to be induced upon pathogen attack. Transcripts of several genes, (e.g., PR1a, encoding a pathogenesis related protein, and GLP4, encoding a germin-like protein) accumulated specifically in resistant cells, while GRP94, encoding a molecular chaperone, accumulated in infected cells. Thus, the single-cell method allows discrimination of transcript profiles from resistant and infected cells. The method will be useful for microarray expression profiling for simultaneous analysis of many genes.

Additional keywords: single-cell analysis

© 2004 The American Phytopathological Society