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In this study, we present the draft genome sequence of the bacterial strain Pseudomonas chlororaphis PCL1601. This bacterium was isolated from the rhizosphere of healthy avocado trees and displayed antagonistic and biological control activities against different soilborne phytopathogenic fungi and oomycetes.
Pseudomonas chlororaphis PCL1601 is a Gram-negative aerobic bacterium isolated from the rhizosphere of a healthy avocado tree allocated in an area affected by avocado white root rot (1), a fungal disease caused by the soilborne phytopathogen Rosellinia necatrix (2). The bacterial isolation was carried out from avocado root samples, with further isolation of different nutrient media with cycloheximide (100 µg/ml) to avoid fungal growth interference. P. chlororaphis PCL1601 formed opaque and light-yellow colonies when grown on solid nutrient medium, and the colonies were fluorescent when grown in King’s B (KB) medium. Furthermore, PCL1601 presented antagonistic activity against several soilborne pathogens, such as Fusarium oxysporum and Rhizoctonia solani, but especially to the avocado soilborne pathogens R. necatrix and Phytophthora cinnamomi (1). Additionally, P. chlororaphis PCL1601 showed biological control activity against R. necatrix on avocado and to F. oxysporum f. sp. radicis-lycopersici on tomato (1). This strain is able to produce some antimicrobial compounds, such as hydrogen cyanide (HCN), phenazine-1-carboxylic acid (PCA), and phenazine-1-carboxamide (PCN) (1).
Here, we report the draft genome sequence of P. chlororaphis PCL1601. Genomic DNA of P. chlororaphis PCL1601 was extracted with the PowerSoil DNA isolation kit (Mo Bio Laboratories, Inc., Carlsbad, CA, USA) after overnight growth in liquid KB medium at 25°C. Genome sequencing was performed at ChunLab, Inc. (Seoul, South Korea) using the Pacific Biosciences 20 K method. Sequencing depth was 223.26× coverage of the genome, which was assembled de novo into 25 contigs with the PacBio SMRT Analysis pipeline version 2.3.0 (ChunLab, Inc.). The resulting draft genome sequence was ordered using the genome sequence of P. chororaphis PA23 as the template (3). The resulting draft genome sequence was annotated with the NCBI Prokaryotic Genome Annotation Pipeline. Additionally, the secondary metabolite- and antibiotic-encoding gene clusters were predicted with antiSMASH (4).
The draft genome of PCL1601 is 6,755,444 bp in length, containing a G+C content of 64% and 5,897 predicted coding sequences, 17 rRNAs, and 68 tRNAs, features similar to those previously described for the biocontrol strain P. chlororaphis PCL1606, also isolated from avocado rhizosphere (5). However, genome annotation displayed a wider range of putative genes involved in general metabolism (carbohydrates, amino acids, lipids, etc.) and transport (such as inorganic ion transport and metabolism, intracellular trafficking, secretion, and vesicular transport). Using antiSMASH, we found 13 potential biosynthetic gene clusters potentially involved in secondary metabolite production, highlighting the phenazine biosynthetic gene cluster, but also bacteriocins (n = 4), siderophores (n = 2), and nonribosomal peptide synthetases (NRPS; n = 2), most of them displaying architecture (higher than 90%) similar to other biosynthetic operons also described in other P. chlororaphis strains. The remaining clusters have lower homologies and need further characterization.
This whole-genome shotgun project has been deposited in GenBank under the accession no. MSCT00000000 (from MSCT01000001 to MSCT01000025). The version described in this paper is the first version.
This work was supported by Plan Nacional I+D+I from Ministerio de Economía (MINECO) (grants AGL11-30354-C02-01 and AGL14-52518-C2-I-R), cofinanced by FEDER funds (EU). C. Vida was supported by a Ph.D. fellowship from the FPI program of MINECO.
Citation Vida C, de Vicente A, Cazorla FM. 2017. Draft genome sequence of the rhizobacterium Pseudomonas chlororaphis PCL1601, displaying biocontrol against soilborne phytopathogens. Genome Announc 5:e00130-17. https://doi.org/10.1128/genomeA.00130-17.