Isolation of Arabidopsis mutants with enhanced disease susceptibility by direct screening.

To discover which components of plant defense responses make significant contributions to limiting pathogen attack, we screened a mutagenized population of Arabidopsis thaliana for individuals that exhibit increased susceptibility to the moderately virulent bacterial pathogen Pseudomonas syringae pv. maculicola ES4326 (Psm ES4326). The 12 enhanced disease susceptibility (eds) mutants isolated included alleles of two genes involved in phytoalexin biosynthesis (pad2, which had been identified previously, and pad4, which had not been identified previously), two alleles of the previously identified npr1 gene, which affects expression of other defense genes, and alleles of seven previously unidentified genes of unknown function. The npr1 mutations caused greatly reduced expression of the PR1 gene in response to PsmES4326 infection, but had little effect on expression of two other defense genes, BGL2 and PR5, suggesting that PR1 expression may be important for limiting growth of PsmES4326. While direct screens for mutants with quantitative pathogen-susceptibility phenotypes have not been reported previously, our finding that mutants isolated in this way include those affected in known defense responses supports the notion that this type of screening strategy allows genetic dissection of the roles of various plant defense responses in disease resistance.

[1]  B. Kunkel,et al.  A useful weed put to work: genetic analysis of disease resistance in Arabidopsis thaliana. , 1996, Trends in genetics : TIG.

[2]  D. Shah,et al.  Disease resistance conferred by expression of a gene encoding H2O2-generating glucose oxidase in transgenic potato plants. , 1995, The Plant cell.

[3]  J. Ryals,et al.  Arabidopsis signal transduction mutant defective in chemically and biologically induced disease resistance. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[4]  R. Leah,et al.  Enhanced quantitative resistance against fungal disease by combinatorial expression of different barley antifungal proteins in transgenic tobacco. , 1995, The Plant journal : for cell and molecular biology.

[5]  N V Raikhel,et al.  Small cysteine-rich antifungal proteins from radish: their role in host defense. , 1995, The Plant cell.

[6]  Xinnian Dong,et al.  Characterization of an Arabidopsis Mutant That Is Nonresponsive to Inducers of Systemic Acquired Resistance. , 1994, The Plant cell.

[7]  F. Ausubel,et al.  Isolation of phytoalexin-deficient mutants of Arabidopsis thaliana and characterization of their interactions with bacterial pathogens. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[8]  R. Dixon,et al.  Enhanced Protection Against Fungal Attack by Constitutive Co–expression of Chitinase and Glucanase Genes in Transgenic Tobacco , 1994, Bio/Technology.

[9]  A. Sattler,et al.  A disease resistance gene in Arabidopsis with specificity for two different pathogen avirulence genes. , 1994, The Plant cell.

[10]  P. Hasegawa,et al.  Osmotin overexpression in potato delays development of disease symptoms. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[11]  M. Sela-Buurlage,et al.  A Novel Pathogen- and Wound-Inducible Tobacco (Nicotiana tabacum) Protein with Antifungal Activity , 1994, Plant physiology.

[12]  M. Sela-Buurlage,et al.  A new class of tobacco chitinases homologous to bacterial exo-chitinases displays antifungal activity. , 1994, The Plant journal : for cell and molecular biology.

[13]  Leslie Friedrich,et al.  Requirement of Salicylic Acid for the Induction of Systemic Acquired Resistance , 1993, Science.

[14]  E. Ward,et al.  Increased tolerance to two oomycete pathogens in transgenic tobacco expressing pathogenesis-related protein 1a. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[15]  A. Bent,et al.  RPS2, an Arabidopsis disease resistance locus specifying recognition of Pseudomonas syringae strains expressing the avirulence gene avrRpt2. , 1993, The Plant Cell.

[16]  M. Sela-Buurlage,et al.  Only Specific Tobacco (Nicotiana tabacum) Chitinases and [beta]-1,3-Glucanases Exhibit Antifungal Activity , 1993, Plant physiology.

[17]  H. Kindl,et al.  Disease resistance results from foreign phytoalexin expression in a novel plant , 1993, Nature.

[18]  C. Chapple,et al.  An Arabidopsis mutant defective in the general phenylpropanoid pathway. , 1992, The Plant cell.

[19]  I. Raskin,et al.  Signal molecules in systemic plant resistance to pathogens and pests , 1992, Cell.

[20]  D. Klessig,et al.  Salicylic acid and plant disease resistance , 1992 .

[21]  Franky R. G. Terras,et al.  Analysis of two novel classes of plant antifungal proteins from radish (Raphanus sativus L.) seeds. , 1992, The Journal of biological chemistry.

[22]  S. Potter,et al.  Acquired resistance in Arabidopsis. , 1992, The Plant cell.

[23]  S. Somerville,et al.  Phytoalexin Accumulation in Arabidopsis thaliana during the Hypersensitive Reaction to Pseudomonas syringae pv syringae. , 1992, Plant physiology.

[24]  R. Cressman,et al.  Transgenic Plants with Enhanced Resistance to the Fungal Pathogen Rhizoctonia solani , 1991, Science.

[25]  C. Woloshuk,et al.  Pathogen-induced proteins with inhibitory activity toward Phytophthora infestans. , 1991, The Plant cell.

[26]  F. Ausubel,et al.  Induction of Arabidopsis defense genes by virulent and avirulent Pseudomonas syringae strains and by a cloned avirulence gene. , 1991, The Plant cell.

[27]  R. Dixon,et al.  Molecular Communication in Interactions Between Plants and Microbial Pathogens , 1990 .

[28]  R. Dixon,et al.  Signals and transduction mechanisms for activation of plant defenses against microbial attack , 1989, Cell.

[29]  T. Boller,et al.  Antifungal Hydrolases in Pea Tissue : II. Inhibition of Fungal Growth by Combinations of Chitinase and beta-1,3-Glucanase. , 1988, Plant physiology.

[30]  M. Legrand,et al.  Biological function of ‘pathogenesis‐related’ proteins: four PR proteins of tobacco have 1,3‐β‐glucanase activity , 1987, The EMBO journal.

[31]  M. Legrand,et al.  Biological function of pathogenesis-related proteins: Four tobacco pathogenesis-related proteins are chitinases. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[32]  T. Boller,et al.  Plant chitinases are potent inhibitors of fungal growth , 1986, Nature.

[33]  J. Paxton Phytoalexins — A Working Redefinition , 1981 .