Abstract
We report here the draft genome sequence of Burkholderia gladioli strain NGJ1. The strain was isolated from healthy rice seeds and exhibits broad-spectrum antifungal activity against several agriculturally important pathogens, including Rhizoctonia solani, Magnaporthe oryzae, Venturia inaequalis, and Fusarium oxysporum.
GENOME ANNOUNCEMENT
Burkholderia spp. are rod-shaped Gram-negative bacteria found in diverse habitats. Some of them are reported to be pathogenic to plants and humans; however, a few plant growth-promoting, endophytic, and antifungal strains with potential biocontrol activity have also been reported (1–5). We have isolated a yellow-pigmented bacterium from surface-sterilized healthy IR64 rice seeds, which demonstrated broad-spectrum antifungal activity against Rhizoctonia solani (the causal of sheath blight disease of rice), Magnaporthe oryzae (the rice blast pathogen), Venturia inaequalis (the apple scab pathogen), Fusarium oxysporum (vascular wilt pathogen), and several other fungal pathogens. 16S rRNA gene sequencing, deep phylogeny, and segregation rooting analyses identified the bacterium to be B. gladioli, and henceforth, the strain was named B. gladioli NGJ1.
The draft genome sequence of the bacterium was determined using the Illumina NextSeq 500 sequencing system with a paired-end library. A total of 36,488,466 paired-end reads were produced, and after quality trimming and error correction, 33,951,148 (93.05%) high-quality reads were retained. Sequence processing and assembly were performed using the A5 assembly pipeline (version A5-miseq 20150522), according to the workflow described by Tritt et al. (6). The assembly resulted in 155 contigs (minimum, 503 bp; maximum, 573,482 bp; N50, 283,251 bp). The final assembly contained 8,020,595 bp, with a G+C content of 68.07% and a median coverage of 650×. Genome completeness was assessed using the AMPHORA software version 2 (7, 8), which reflected the presence of 31 highly conserved phylogenetic marker genes in the draft genome of the bacterium. Interestingly, some of these marker genes had less-confident assignment scores to B. gladioli, suggesting divergence of the NGJ1 strain from other sequenced strains of B. gladioli. Annotation using Prokka version 1.11 (9) predicted 6,865 protein-coding sequences, 68 tRNAs, and 1 transfer-messenger RNA (tmRNA) in B. gladioli NGJ1. The genome is enriched in genes encoding secondary metabolites, microbial metabolism in diverse environments, biosynthesis of antibiotics, etc. This correlates with its antifungal ability and indicates its adaptability in diverse habitats. The detailed comparative and functional genomic analyses of this bacterium will help identify novel antifungal compounds and reveal their potential utilization in managing plant diseases.
Nucleotide sequence accession numbers.
This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession no. LEKY00000000. The version described in this paper is version LEKY01000000.
ACKNOWLEDGMENTS
I.T. and S.G. were supported by fellowships from Council of Scientific and Industrial Research (Government of India). This work was financially supported by a core research grant from the National Institute of Plant Genome Research, India.
We acknowledge Praveen Raj S. and Shantanu Kumar, CromDx Solutions Pvt. Ltd. for assistance in genome sequencing and computational analysis.
Footnotes
Citation Jha G, Tyagi I, Kumar R, Ghosh S. 2015. Draft genome sequence of broad-spectrum antifungal bacterium Burkholderia gladioli strain NGJ1, isolated from healthy rice seeds. Genome Announc 3(4):e00803-15. doi:10.1128/genomeA.00803-15.
REFERENCES
- 1.Seo Y-S, Lim JY, Park J, Kim S, Lee H-H, Cheong H, Kim S-M, Moon JS, Hwang I. 2015. Comparative genome analysis of rice-pathogenic Burkholderia provides insight into capacity to adapt to different environments and hosts. BMC Genomics 16:349. doi: 10.1186/s12864-015-1558-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Song JY, Kwak MJ, Lee KY, Kong HG, Kim BK, Kwon SK, Lee SW, Kim JF. 2012. Draft genome sequence of the antifungal-producing plant-benefiting bacterium Burkholderia pyrrocinia CH-67. J Bacteriol 194:6649–6650. doi: 10.1128/JB.01779-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Estrada-De Los Santos P, Vinuesa P, Martínez-Aguilar L, Hirsch AM, Caballero-Mellado J. 2013. Phylogenetic analysis of Burkholderia species by multilocus sequence analysis. Curr Microbiol 67:51–60. doi: 10.1007/s00284-013-0330-9. [DOI] [PubMed] [Google Scholar]
- 4.Coenye T, Vandamme P. 2003. Diversity and significance of Burkholderia species occupying diverse ecological niches. Environ Microbiol 5:719–729. doi: 10.1046/j.1462-2920.2003.00471.x. [DOI] [PubMed] [Google Scholar]
- 5.Elshafie HS, Camele I, Racioppi R, Scrano L, Iacobellis NS, Bufo SA. 2012. In vitro antifungal activity of Burkholderia gladioli pv. agaricicola against some phytopathogenic fungi. Int J Mol Sci 13:16291–16302. doi: 10.3390/ijms131216291. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Tritt A, Eisen JA, Facciotti MT, Darling AE. 2012. An integrated pipeline for de novo assembly of microbial genomes. PLoS One 7:e42304. doi: 10.1371/journal.pone.0042304. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Wu M, Scott AJ. 2012. Phylogenomic analysis of bacterial and archaeal sequences with AMPHORA2. Bioinformatics 28:1033–1034. doi: 10.1093/bioinformatics/bts079. [DOI] [PubMed] [Google Scholar]
- 8.Wu D, Jospin G, Eisen JA. 2013. Systematic identification of gene families for use as “markers” for phylogenetic and phylogeny-driven ecological studies of bacteria and archaea and their major subgroups. PLoS One 8:e77033. doi: 10.1371/journal.pone.0077033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Seemann T. 2014. Prokka: rapid prokaryotic genome annotation. Bioinformatics 30:2068–2069. doi: 10.1093/bioinformatics/btu153. [DOI] [PubMed] [Google Scholar]