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
Background: The application of polycyclic aromatic hydrocarbons (PAHs) will affect the bacterial community structure as some groups will be favoured and others not. An alkaline saline soil with electrolytic conductivity (EC) 56 dS m-1 was spiked with anthracene and acetone while their effect on bacterial community structure was investigated. Results: The percentages of Acidobacteria and Actinobacteria decreased over time, while the percentage of Proteobacteria, mostly Xanthomonadales, increased. The percentage of the phylotypes belonging to the Nocardioides, Rhodococcus and Streptomyces, known degraders of PAHs, was larger in the anthracene-amended soil than in the acetone-amended and unamended soil at day 14. The phylotypes belonging to the genera Sphingomonas, also a known degrader of PAHs, however, was lower. Weighted and unweighted PCoA with UniFrac indicated that phylotypes were similar in the different treatments at day 0, but changed at day 1. After 14 days, phylotypes in the unamended and acetone-amended soil were similar, but different from those in the anthracene-spiked soil. Conclusions: It was found that incubating the soil and contaminating it with anthracene changed the bacterial community structure, but spiking the soil with acetone had little or no effect on the bacterial community structure compared to the unamended soil.