PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of genannJournal InfoAuthorsPermissionsJournals.ASM.orggenomeA ArticleGenome Announcements
 
Genome Announc. 2017 April; 5(14): e00130-17.
Published online 2017 April 6. doi:  10.1128/genomeA.00130-17
PMCID: PMC5383896

Draft Genome Sequence of the Rhizobacterium Pseudomonas chlororaphis PCL1601, Displaying Biocontrol against Soilborne Phytopathogens

ABSTRACT

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.

GENOME ANNOUNCEMENT

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.

Accession number(s).

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.

ACKNOWLEDGMENTS

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.

Footnotes

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.

REFERENCES

1. Cazorla FM, Duckett SB, Bergström ET, Noreen S, Odijk R, Lugtenberg BJJ, Thomas-Oates JE, Bloemberg GV 2006. Biocontrol of avocado dematophora root rot by antagonistic Pseudomonas fluorescens PCL1606 correlates with the production of 2-hexyl 5-propyl resorcinol. Mol Plant Microbe Interact 19:418–428. doi:.10.1094/MPMI-19-0418 [PubMed] [Cross Ref]
2. Pliego C, López-Herrera C, Ramos C, Cazorla FM 2012. Developing tools to unravel the biological secrets of Rosellinia necatrix, and emergent threat to woody crops. Mol Plant Pathol 13:226–239. doi:.10.1111/J.1364-3703.2011.00753.X [PubMed] [Cross Ref]
3. Loewen PC, Villenueva J, Fernando WG, de Kievit T 2014. Genome sequence of Pseudomonas chlororaphis strain PA23. Genome Announc 2(4):e00689-14. doi:.10.1128/genomeA.00689-14 [PMC free article] [PubMed] [Cross Ref]
4. Weber T, Blin K, Duddela S, Krug D, Kim HU, Bruccoleri R, Lee SY, Fischbach MA, Müller R, Wohlleben W, Breitling R, Takano E, Medema MH 2015. antiSMASH 3.0–a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res 43:W237–W243. doi:.10.1093/nar/gkv437 [PMC free article] [PubMed] [Cross Ref]
5. Calderón CE, Ramos C, de Vicente A, Cazorla FM 2015. Comparative genomic analysis of Pseudomonas chlororaphis PCL1606 reveals new insight into antifungal compounds involved in biocontrol. Mol Plant Microbe Interact 28:249–260. doi:.10.1094/MPMI-10-14-0326-FI [PubMed] [Cross Ref]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)