Open Access

Complete genome of Pseudomonas chlororaphis strain UFB2, a soil bacterium with antibacterial activity against bacterial canker pathogen of tomato

Standards in Genomic Sciences201510:117

DOI: 10.1186/s40793-015-0106-x

Received: 19 June 2015

Accepted: 29 September 2015

Published: 1 December 2015

Abstract

Strain UFB2 was isolated from a soybean field soil in Mississippi and identified as a member of Pseudomonas chlororaphis. Strain UFB2 has a broad-spectrum antimicrobial activity against common soil-borne pathogens. Plate assays showed that strain UFB2 was especially efficient in inhibiting the growth of Clavibacter michiganensis 1–07, the causal agent of the devastating bacterial canker of tomato. Here, the complete genome sequence of P. chlororaphis strain UFB2 is reported and described. The strain UFB2 genome consists of a circular chromosome of 6,360,256 bp of which 87.86 % are protein-coding bases. Genome analysis revealed multiple gene islands encoding various secondary metabolites such as 2,4-diacetylphloroglucinol. Further genome analysis will provide more details about strain UFB2 antibacterial activities mechanisms and the use of this strain as a potential biocontrol agent.

Keywords

Pseudomonas chlororaphis strain UFB2 Complete genome Biocontrol Bacterial canker of tomato Secondary metabolites

Introduction

Bacterial strains of Pseudomonas chlororaphis are aerobic Gram-positive bacteria and many of the strains possess a wide-spectrum antifungal activity against soil-borne plant pathogens [15]. P. chlororaphis strains have been reported to be efficient plant-growth-promoting bacteria, which can be used as inoculants for biofertilization, phytostimulation and biocontrol [6]. The use of P. chlororaphis strains as biocontrol agents is promising because they are capable of producing a variety of antimicrobial secondary metabolites including phenazine-1-carboxamide, 2-hydroxyphenazine, pyrrolnitrin, hydrogen cyanide, chitinases and proteases [68]. Moreover, P. chlororaphis is considered to be nonpathogenic to humans, wildlife, or the environment according to U.S. environmental protection agency (EPA) [9]. Antimicrobial activities and low risks to animals and the environments have made the bacterium P. chlororaphis highly potential biocontrol agents in agriculture [8, 10]. A genome-wide research and analysis could provide useful information about the mechanisms of how P. chlororaphis protects plants against soil-borne phytopathogens. Currently, the whole genomes of a few P. chlororaphis strains that exhibit antifungal activity have been sequenced. These include P. chlororaphis strain PA23 that can protect canola from stem rot disease caused by the fungal pathogen Sclerotinia sclerotiorum [2, 11], and P. chlororaphis PCL1606 that was isolated from avocado rhizosphere and exhibited biocontrol activity against soil-borne phytopathogenic fungi [1]. In addition, another functionally-uncharacterized strain, P. chlororaphis subsp. aurantiaca JD37, was recently sequenced (NCBI reference sequence: NZ_CP009290.1). Genome sequences of P. chlororaphis strains with significant antibacterial activity have not been reported previously.

Strain UFB2 was isolated from a soybean field soil in Mississippi. Preliminary analysis of the 16S rRNA gene indicated that it is a member of P. chlororaphis . Plate assays indicated P. chlororaphis strain UFB2 has a broad spectrum of antimicrobial activities, especially against bacterial canker pathogen of tomato: Clavibacter michiganensis [12, 13]. Greenhouse trials demonstrated both living cells and culture extract of strain UFB2 can be used for disease management of bacterial canker of tomato. In this study, the P. chlororaphis strain UFB2 complete genome sequence and annotation are reported. The gene islands within strain UFB2 genome that encode various secondary metabolites, including antimicrobial compounds, are also described. The detailed description of the strain UFB2 genome will shed light into further studies of biocontrol effectiveness and applications of Pseudomonas species.

Organism information

Classification and features

Strain UFB2 was isolated from rhizosphere soil sample collected from soybean field near Cleveland, Mississippi, USA, where healthy soybean plants were found growing in charcoal rot disease patch. Phylogenetic analyses based on multilocus sequence typing [14] (gyrB, rpoB, rpoD and 16 s rRNA) revealed that strain UFB2 belongs to Pseudomonas chlororaphis (Fig. 2). Strain UFB2 is rod-shaped, motile, non-spore-forming Gram-negative bacterium in the order Pseudomonadales of the class Gammaproteobacteria . UFB2 cells are approximately 3.0 ± 0.8 μm in width and 0.9 ± 0.3 μm in length (Fig. 1). The strain is relatively fast-growing, forming approximately 1 mm opaque yellowish colonies after overnight incubation at 28 °C on nutrient-broth yeast extract agar [15]. Strain UFB2 can also be grown on rich media such as LB [16] and PDA, as well as M9 minimal medium [17]. Phenotypic characterization of strain UFB2 was carried out using the API 50CH system as recommended by manufacturer. According to the result, strain UFB2 could utilize almost all carbon sources in API 50CH tests, including D-glucose, D-galactose, L-rhamnose, D-mannitol, D-raffinose, D-fructose, D-arabinose, D-ribose, L-arabinose, L-xylose and D-xylose, but not potassium gluconate.
Fig. 1

Image of P. chlororaphis UFB2 cells and plate assay of UFB2 antibacterial activity against Clavibacter michiganensis 107. The plate bioassay was conducted as described by Scholz-Schroeder and colleagues [44]

Plate bioassays demonstrated that strain UFB2 possesses significant antibacterial activity against a broad array of plant bacterial pathogens. Other than Clavibacter michiganensis 1–07, the tested bacteria sensitive to strain UFB2 also include Erwinia amylovora [18, 19], Burkholderia glumae [20], Ralstonia solanacearum Rso [21, 22] and Erwinia carotovora WSCH1 [19, 23]. Of the tested plant pathogenic bacteria, the Gram-positive bacterium Clavibacter michiganensis 1–07, the pathogen causing bacterial canker of tomato [24], is most sensitive to strain UFB2 with a radius of 28 ± 1 mm clear inhibitory zone (Fig. 1). In addition, the growth of fungal pathogen Geotrichum candidum Km, which causes sour rot of citrus fruits, tomatoes, carrot and some vegetables [25], can also be inhibited by strain UFB2. To test the field biocontrol efficacy of strain UFB2, greenhouse experiments were set up according to the method described by Lu and Ingram [26]. Preliminary data showed the control efficacies of both strain UFB2 culture extract and living cells on bacterial canker of tomato are equivalent to that of streptomycin at the recommended rate for plant disease management. The genome of strain UFB2 was sequenced with the aim to identify the genes associated with the antimicrobial characters. The information about the genome sequence of strain UFB2 is summarized in Table 1, and its phylogenetic position is shown in Fig. 2.
Table 1

Classification and general features of Pseudomonas chlororaphis UFB2 according to the MIGS recommendations [55]

MIGS ID

Property

Term

Evidence codea

 

Classification

Domain Bacteria

TAS [56]

  

Phylum Proteobacteria

TAS [57]

  

Class Gammaproteobacteria

TAS [58, 59]

  

Order Pseudomonadales

TAS [19, 60]

  

Family Pseudomonadaceae

TAS [19, 61]

  

Genus Pseudomonas

TAS [19, 6163]

  

Species Pseudomonas chlororaphis

TAS [19, 64, 65]

  

strain: UFB2

NAS

 

Gram stain

negative

TAS [66]

 

Cell shape

Rod

TAS [66]

 

Motility

Motile

TAS [66]

 

Sporulation

None

NAS

 

Temperature range

Mesophilic

IDA

 

Optimum temperature

33 °C

IDA

 

pH range; Optimum

not determined

IDA

 

Carbon source

D-glucose, D-galactose, L-rhamnose, D-mannitol, D-raffinose, D-fructose, D-arabinose, 2D-ribose, L-arabinose, L-xylose, D-xylose.

TAS [66]

MIGS-6

Habitat

Soil

NAS

MIGS-6.3

Salinity

not determined

IDA

MIGS-22

Oxygen requirement

Aerobic

NAS

MIGS-15

Biotic relationship

free-living/Rhizospheric

NAS

MIGS-14

Pathogenicity

non-pathogen

IDA

MIGS-4

Geographic location

Mississippi, USA

IDA

MIGS-5

Sample collection

2011

IDA

MIGS-4.1

Latitude

34.1 N

IDA

MIGS-4.2

Longitude

90.6 W

IDA

MIGS-4.4

Altitude

40 M

IDA

aEvidence codes - IDA Inferred from Direct Assay, TAS Traceable Author Statement (i.e., a direct report exists in the literature), NAS Non-traceable Author Statement (i.e., not directly observed for the living, isolated sample, but based on a generally accepted property for the species, or anecdotal evidence). These evidence codes are from the Gene Ontology project [67]

Fig. 2

Phylogenetic analysis of concatenated four multilocus sequence typing loci of P. chlororaphis UFB2 and related species. Phylogenetic tree based on the concatenated sequence (3775 bp) of four housekeeping gene fragments [gyrB (729 bp), rpoB (885 bp), rpoD (711 bp) and 16 s rRNA (1450 bp)]. Phylogenetic analyses were performed using MEGA, version 6.06 [51]. The tree was built using the Neighbor-Joining method [52]. Bootstrap analysis with 1000 replicates was performed to assess the support of the clusters

Chemotaxonomic data

Fatty acid analysis was performed by gas chromatography (gas chromatograph, model 6890 N, Agilent Technologies) and analyzed by the Microbial Identification System (MIDI, Sherlock Version 6.1; database, TSBA40). The analysis of total cells showed the major fatty acids are C 16:1 ω7c (32 %), C 16:0 (28 %), C 18:1 ω7c (19 %). Fatty acid 3-hydroxy C 12:0 (5 %), C 12:0 (4 %), 2-hydroxy C 12:0 (4 %) and 3-hydroxy C 10:0 (3 %) were found in minor amount.

Genome sequencing information

Genome project history

P. chlororaphis strain UFB2 was selected for sequencing because of its significant antimicrobial activities and its potential as a biocontrol agent for agricultural use. Genomes of three P chlororaphis strains have been sequenced as of May 2015. Sequencing of the whole genome of strain UFB2 makes more data available for genome comparison and analysis within P. chlororaphis species.

The genome project is deposited in the Genomes OnLine Database [27] and the NCBI BioProject database [28]. The annotated genome is publicly available from the Intergrated Microbial Genomes Database [29] under the accession number Gp0111981 and GenBank under accession number CP011020. A summary of the project information is provided in Table 2.
Table 2

Project information

MIGS ID

Property

Term

MIGS 31

Finishing quality

Finished

MIGS-28

Libraries used

libraries of 400 bp, mate pair library of 2,000, 5,000 and 8,000 bp

MIGS 29

Sequencing platforms

Illumina

MIGS 31.2

Fold coverage

600 ×

MIGS 30

Assemblers

DNAStar Seqman NGen v12

MIGS 32

Gene calling method

NCBI Prokaryotic Genome Annotation Pipeline

 

Locus Tag

VM99

 

Genbank ID

CP011020

 

GenBank Date of Release

Jun 9th, 2015

 

GOLD ID

Gp0111981

 

BIOPROJECT

PRJNA277727

MIGS13

Source Material Identifier

UFB2

 

Project relevance

Biocontrol

Growth conditions and genomic DNA preparation

P. chlororaphis strain UFB2 was cultured in liquid NBY medium overnight at 28 °C in a shaker at 220 rpm. The genomic DNA was extracted from 50 mL of the culture using the Wizard Genomic DNA Purification Kit (Promega Corporation, Madison, WI, USA). Totally approximately 900 μg of DNA were obtained with an OD260/280 of 1.9. The DNA sample was used for library construction with Illumina Genomic DNA Sample Preparation Kit (Illumina, CA, USA).

Genome sequencing and assembly

One standard library with an average insert size of 400 bp and three mate pair libraries with an average insert size of 2,000 bp, 5,000 bp and 8,000 bp were prepared and sequenced on the Illumina MiSeq instrument according to the manufacturer’s instructions. The genome was de novo assembled using a method as described by Durfee et al. [30] using DNAStar Seqman NGen (Version 12, DNASTAR, Inc. Madison, WI U.S.). The standard library and 2,000 bp mate pair library were selected for the de novo assembly. A total of 30 million short reads were scanned and extracted from the raw data files as input data. The short reads were preprocessed by Seqman NGen to trim adaptors and filter low-quality reads. Automatic Mer size and a minimum match percentage of 98 % were selected. 29 million short reads were assembled into 29 contigs and SeqMan Pro (Version 12, DNASTAR, Inc. Madison, WI U.S.) was used to order the contigs in one scaffold according to the mate pair data. The first round assembled sequence was then used as a template for a complete reassembly. The 2,000 bp and 8,000 bp mate pair data were incorporated to proofread the first assembly and to maximize coverage and quality. Adjacent contigs, if possible, were merged. Remaining gaps were filled by PCR and Sanger sequencing. No contigs that might correspond to plasmids remained unassembled. IslandViewer [31] was used to predict and identify genomic islands.

Genome annotation

Automatic annotation was performed using the NCBI Prokaryotic Genome Annotation Pipeline [32], which combines gene calling algorithm with similarity-based gene detection approach to predict protein-coding genes, structural RNAs (5S, 16S, 23S), tRNAs and small non-coding RNAs. Additional gene prediction analysis and functional annotation were performed by the Integrated Microbial Genomes platform [29].

Genome properties

The complete genome of P. chlororaphis strain UFB2 consists of one circular chromosome of 6,360,256 bp with a GC content of 62.03 %. 5,556 genes were identified from the genome, of which 5,473 are protein coding genes. 90 of the 5,556 genes were predicted to be pseudogenes or partial genes. The genome encodes 1 noncoding RNA, 5 rRNA operons and 65 tRNAs. Seventy genomic islands ranging from 4 kbp to 43.5 kbp were also identified throughout the strain UFB2 genome, among which majority of the islands encode hypothetical proteins. The genome features of P. chlororaphis strain UFB2 are summarized in Tables 3 and 4, and the circular chromosome of strain UFB2 is shown in Fig. 3.
Table 3

Genome statistics

Attribute

Value

% of Total

Genome size (bp)

6,360,256

100.00

DNA coding (bp)

5,588,126

87.86

DNA G + C (bp)

3,945,558

62.03

DNA scaffolds

1

100.00

Total genes

5,556

100.00

Protein coding genes

5,473

98.51

RNA genes

83

1.49

Pseudo genes

90

1.62

Genes in internal clusters

5,473

98.51

Genes with function prediction

4,886

87.94

Genes assigned to COGs

4,092

73.65

Genes with Pfam domains

4,748

85.46

Genes with signal peptides

577

10.39

Genes with transmembrane helices

1,228

22.10

CRISPR repeats

0

0

Table 4

Number of genes associated with general COG functional categories

Code

Value

% age

Description

J

231

4.89

Translation, ribosomal structure and biogenesis

A

1

0.02

RNA processing and modification

K

418

8.85

Transcription

L

123

2.60

Replication, recombination and repair

B

3

0.06

Chromatin structure and dynamics

D

39

0.83

Cell cycle control, Cell division, chromosome partitioning

V

101

2.14

Defense mechanisms

T

316

6.69

Signal transduction mechanisms

M

262

5.55

Cell wall/membrane biogenesis

N

166

3.52

Cell motility

W

44

0.93

Extracellular structures

U

137

2.90

Intracellular trafficking and secretion

O

166

3.52

Posttranslational modification, protein turnover, chaperones

C

304

6.44

Energy production and conversion

G

227

4.81

Carbohydrate transport and metabolism

E

483

10.23

Amino acid transport and metabolism

F

92

1.95

Nucleotide transport and metabolism

H

242

5.12

Coenzyme transport and metabolism

I

234

4.96

Lipid transport and metabolism

P

257

5.44

Inorganic ion transport and metabolism

Q

142

3.01

Secondary metabolites biosynthesis, transport and catabolism

R

430

9.11

General function prediction only

S

260

5.51

Function unknown

-

1464

26.35

Not in COGs

The total is based on the total number of protein coding genes in the genome

Fig. 3

Circular representation of the P. chlororaphis UFB2 genome compared with six sequenced Pseudomonas whole genomes. Rings from inside to outside: (1) Scale, (2) GC content (navy), (3) GC skew (purple), (4) BLAST comparison with P. syringae pv. syringae B728a (deep pink), (5) BLAST comparison with P. putida KT2440 (pink), (6) BLAST comparison with P. chlororaphis strain PA23 (cyan), (7) BLAST comparison with P. aeruginosa PAO1 (violet), (8) BLAST comparison with P. fluorescens Pf0-1 (skyblue), (9) BLAST comparison with P. sp. UW4 (yellow), (10) Coding sequences of P. chlororaphis UFB2 genome (dark cyan), (11) Gene islands (medium purple), (12) rRNA genes (orange), tRNA genes (dark green) and ncRNA (red). BLASTn comparison of genomes was visualized by BRIG [53] and UFB2 genome the image was generated with Circos [54]

Insights from the genome sequence

Blast research of P. chlororaphis strain UFB2 genome against P. syringae pv. syringae B728a (NC_007005), P. putida KT2440 (NC_002947), P. chlororaphis strain PA23 (NZ_CP008696), P. aeruginosa PAO1 (NC_002516), P. fluorescens Pf0-1 (NC_007492) and P. sp. UW4 (NC_019670) genome revealed multiple unique gene regions which were only found in the strain UFB2 genome (Fig. 3). The BLASTn atlas showed noticeable genome diversity of strain UFB2 when compared to other Pseudomonas species. Seventy genomic islands ranging from 4 kbp to 30 kbp were also identified throughout the strain UFB2 genome, indicating significant horizontal gene transfers occurred during the evolution of strain UFB2 to better adapt the environment it inhabited.

P. chlororaphis strain UFB2 harbors an intact phl gene cluster (VM99_23970-23995), which is responsible for biosynthesis of the antimicrobial compound 2,4-diacetylphloroglucinol [33, 34]. 2,4-diacetylphloroglucinol is an especially efficient agent against soil borne fungal plant pathogens [35]. The phl gene cluster is involved in the Pseudomonas antifungal activity against Clavibacter michiganensis 1–07 [36]. Hydrogen cyanide [37, 38] biosynthesis gene homologs were also identified in strain UFB2 genome. The production of hydrogen cyanide by Pseudomonas species helps protect plants from soil-borne fungal pathogens [39, 40]. Biosynthetic gene clusters of common Pseudomonas species-produced antibiotics such as phenazine [41], pyrrolnitrin [42] and pyoluteorin [43] were not identified in strain UFB2 genome. Biosynthetic gene clusters of common toxins that contribute to plant and animal pathogenicity and/or virulence of Pseudomonas species were also searched for within strain UFB2 genome. The toxin biosynthetic gene cluster that were not identified in strain UFB2 genome include the phytotoxin lipopeptide syringomycin [44], tobacco wildfire spotting causal agent tabtoxin [45], bacterial canker of kiwifruit causal agent phaseolotoxin [46], plant-hormone-mimic toxin coronatine [47], and cytotoxic agent pederin [48]. Strain UFB2 genome harbors homolog genes to those in the bacterial apical necrosis causal agent mangotoxin [49] biosynthesis gene cluster. However, mboC gene homolog that is required for mangotoxin production [50] was not identified in strain UFB2 genome. Overall, the lack of the key pathogenicity/virulence genes in strain UFB2 further indicates that strain UFB2 has a great potential as a biocontrol agent.

Conclusions

The complete genome sequence of P. chlororaphis strain UFB2 is described in this report. The strain UFB2 was originally isolated from the rhizosphere of a healthy soybean plant growing in a group of plants exhibiting charcoal rot disease in Mississippi. This strain possesses significant antimicrobial activities against a wide range of plant pathogenic bacteria and fungi. It is evident that the genome of P. chlororaphis strain UFB2 harbors the complete gene set for production of the antimicrobial compounds 2,4-DAPG and HCN, which may largely contribute to its antimicrobial activities. However, gene homologs required for biosynthesis of all the known toxins to plants, such as syringomycin, tabtoxin, phaseolotoxin, tolaasin, coronatine, or pederin, were absent from the strain UFB2 genome. The genome sequence of P. chlororaphis strain UFB2 will help in understanding genetic mechanisms of the antimicrobial activity studies that are useful for development of biologically-based disease management in agriculture.

Declarations

Acknowledgements

We thank Chuan-Yu Hsu and Kurt C. Showmaker for sequencing services and Richard Baird, Sead Sabanadzovic and Justin Thornton for helpful discussion. This research was funded by USDA NIFA to SL (MIS-401170).

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Biochemistry, Molecular Biology, Entomology and Plant Pathology, Mississippi State University
(2)
Department of Plant Pathology, Shandong Agricultural University

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