RESUMEN
Asunto(s)
Arabidopsis/microbiología , Proteínas de la Membrana Bacteriana Externa/genética , Brassica/microbiología , Enfermedades de las Plantas/microbiología , Pseudomonas syringae/genética , Pseudomonas syringae/patogenicidad , Secuencia de Bases , Medios de Cultivo , Elementos Transponibles de ADN/genética , Genes Bacterianos , Mutación/genética , Hojas de la Planta/microbiología , Regiones Promotoras Genéticas/genéticaRESUMEN
Pseudomonas syringae pv. maculicola is a natural pathogen of members of the Brassicaceae plant family. Using a transposon-based mutagenesis strategy in Pseudomonas syringaepv. maculicola M2 (PsmM2), we conducted a genetic screen to identify mutants that were capable of growing in M9 medium supplemented with a crude extract from the leaves of Arabidopsis thaliana. A mutant containing a transposon insertion in the hrpZ gene (PsmMut8) was unable to infect adult plants from Arabidopsis thaliana or Brassica oleracea, suggesting a loss of pathogenicity. The promotorless cat reporter present in the gene trap was expressed if PsmMut8 was grown in minimal medium (M9) supplemented with the leaf extract but not if grown in normal rich medium (KB). We conducted phylogenetic analysis using hrpAZB genes, showing the classical 5-clade distribution, and nucleotide diversity analysis, showing the putative position for selective pressure in this operon. Our results indicate that the hrpAZB operon from Pseudomonas syringaepv. maculicola M2 is necessary for its pathogenicity and that its diversity would be under host-mediated diversifying selection.
Asunto(s)
Arabidopsis/microbiología , Brassica/microbiología , Enfermedades de las Plantas/microbiología , Proteínas de la Membrana Bacteriana Externa/genética , Pseudomonas syringae/genética , Pseudomonas syringae/patogenicidad , Elementos Transponibles de ADN/genética , Hojas de la Planta/microbiología , Genes Bacterianos , Medios de Cultivo , Mutación/genética , Regiones Promotoras Genéticas/genética , Secuencia de BasesRESUMEN
The phyllosphere, i.e., the aerial parts of the plant, provides one of the most important niches for microbial colonization. This niche supports the survival and, often, proliferation of microbes such as fungi and bacteria with diverse lifestyles including epiphytes, saprophytes, and pathogens. Although most microbes may complete the life cycle on the leaf surface, pathogens must enter the leaf and multiply aggressively in the leaf interior. Natural surface openings, such as stomata, are important entry sites for bacteria. Stomata are known for their vital role in water transpiration and gas exchange between the plant and the environment that is essential for plant growth. Recent studies have shown that stomata can also play an active role in limiting bacterial invasion of both human and plant pathogenic bacteria as part of the plant innate immune system. As counter-defense, plant pathogens such as Pseudomonas syringae pv tomato (Pst) DC3000 use the virulence factor coronatine to suppress stomate-based defense. A novel and crucial early battleground in host-pathogen interaction in the phyllosphere has been discovered with broad implications in the study of bacterial pathogenesis, host immunity, and molecular ecology of bacterial diseases.
Asunto(s)
Aminoácidos/metabolismo , Indenos/metabolismo , Solanum lycopersicum/fisiología , Hojas de la Planta/fisiología , Estomas de Plantas/fisiología , Pseudomonas syringae/patogenicidad , Factores de Virulencia/fisiología , Aminoácidos/genética , Solanum lycopersicum/genética , Solanum lycopersicum/microbiología , Hojas de la Planta/microbiología , Estomas de Plantas/microbiología , Pseudomonas syringae/genética , Factores de Virulencia/genéticaRESUMEN
GbERF belongs to the ERF (ethylene responsive factor) family of transcription factors and regulates the GCC-box containing pathogen-related (PR) genes in the ethylene signal transduction pathway. To study the function of GbERF in the process of biotic stress, transgenic tobacco plants expressing GbERF were generated. Overexpression of GbERF did not change transgenic plant's phenotype and endogenous ethylene level. However, the expression profile of some ethylene-inducible GCC-box and non-GCC-box containing genes was altered, such as PR1b, PR2, PR3, PR4, Osmotin, CHN50, ACC oxidase and ACC synthase genes. These data indicate that the cotton GbERF could act as a transcriptional activator or repressor to regulate the differential expression of ethylene-inducible genes via GCC and non-GCC cis-elements. Moreover, the constitutive expression of GbERF in transgenic tobacco enhanced the plant's resistance to Pseudomonas syringae pv tabaci infection. In conclusion, GbERF mediates the expression of a wide array of PR and ethylene-responsive genes and plays an important role in the plant's response to biotic stress.