CHARACTERIZATION OF A HYPOVIRULENT INSERTIONAL MUTANT OF PYRENOPHORA-GRAMINEA AND ANALYSIS OF THE BARLEY DEFENSE RESPONSE AFTER INOCULATION

Citation
G. Vale et al., CHARACTERIZATION OF A HYPOVIRULENT INSERTIONAL MUTANT OF PYRENOPHORA-GRAMINEA AND ANALYSIS OF THE BARLEY DEFENSE RESPONSE AFTER INOCULATION, Plant Pathology, 47(5), 1998, pp. 657-664
Citations number
34
Categorie Soggetti
Plant Sciences",Agriculture
Journal title
ISSN journal
00320862
Volume
47
Issue
5
Year of publication
1998
Pages
657 - 664
Database
ISI
SICI code
0032-0862(1998)47:5<657:COAHIM>2.0.ZU;2-J
Abstract
Pyrenophora graminea is the causal agent of barley leaf strife. A muta nt of the fungus (T2) was obtained by insertional mutagenesis from the highly virulent isolate I2 by random insertion of a plasmid that has no homology with the fungal genome. A marked reduction of disease inci dence was observed in two barley cultivars susceptible to leaf stripe, Nudinka and Mirco, when inoculated with the isogenic insertional muta nt T2 in comparison with P. graminea isolate I2. Southern blot and RAP D analysis were performed to confirm that the insertion had affected o nly a single locus and that consequently the loss of the corresponding genetic function had led to a consistent reduction of virulence. A RA PD amplification product was found to be associated with the genomic r egion tagged by the plasmid, perhaps therefore representing a part of the inactivated gene. The accumulation of four defence-related transcr ipts was monitored in the root tips of cv. Nudinka challenged with bot h the virulent isolate and the isogenic hypovirulent T2. Two kinds of response were observed in rootlets inoculated with T2 when compared wi th the wild type: a delay in the accumulation of the mRNAs homologous to thaumatin-like protein, thionin and peroxidase genes and, 24 h afte r inoculation, a higher accumulation of mRNAs homologous to beta-(1,3) -glucanases and thionins. The relationships between the plant defence response and the virulent and hypovirulent effects, as well as the pot ential use of this insertional mutant in the isolation and characteriz ation of the inactivated virulence gene are discussed.