Abstract
Lysobacter capsici strain X2-3 was isolated from the wheat rhizosphere in China and exhibits a remarkable capacity to inhibit the growth of multiple pathogens. Here, we report the draft genome sequence of L. capsici strain X2-3 in China.
GENOME ANNOUNCEMENT
The genus Lysobacter is composed of 16 species that are typically found in soil and water habitats (1). A striking feature of Lysobacter is its lytic activity against other microorganisms, including fungi, bacteria, and nematodes (2). Lysobacter capsici is a novel species established in 2008, which was first isolated from the rhizosphere of pepper (3). A few strains of this species that serve as sources of potential biocontrol agents have shown antimicrobial activity against several plant pathogens (4–6). Strain X2-3 was isolated from the wheat rhizosphere and identified as L. capsici by 16S rRNA gene sequence analysis (accession no. KP978015). Strain X2-3 showed antimicrobial activities against several plant pathogenic fungi and oomycetes in vitro, such as Rhizoctonia cerealis, Rhizoctonia solani, Bipolaris sorokiniana, Fusarium oxysporum f. sp. cucumerinum, Verticillium dahliae, Colletotrichum gloeosporioides, Pythium myriotylum, Botrytis cinerea, Botryosphaeria ribis, Valsa mali, and Phytophthora parasitica var. nicotianae. Because of its potential as a biocontrol agent, we describe the draft genome sequence of strain X2-3 to better understand its genetic background.
Genomic DNA was extracted with the cetyltrimethylammonium bromide (CTAB) protocol (7). The genome of L. capsici X2-3 was sequenced with massively parallel sequencing (MPS) Illumina technology. A paired-end library with an insert size of 500 bp and a mate pair library with an insert size of 5 kb were constructed. The two libraries were sequenced using an Illumina MiSeq by PE300 strategy and an Illumina HiSeq 2500 by PE100 strategy, respectively. A total of 5,931,492 filtered reads were assembled into 13 contigs (N50 length, 699,639 bp), with a combined length of 6,126,365 bp. The largest contig was 1,781,518 bp, while the shortest contig was 6,232 bp. Gene prediction of the X2-3 genome assembly was performed with an integrated model, which combined the results generated with GeneMarkS and Heuristic model parameters. A total of 5,117 genes were predicted from the X2-3 genome, in which 4,880 coding sequences were annotated based on BLASTx analysis against the nonredundant protein database. Only 1,861 genes were assigned functions, while 2,019 were considered to code for hypothetical proteins. The G+C content of X2-3 is 66.79%, which is similar to that of L. capsici YC5194T (65.4%), L. capsici AZ78 (66.43%), and Lysobacter antibioticus 13-6 (67.14%) (3, 8, 9).
BLASTn alignments revealed that the L. capsici X2-3 genome harbors gene clusters putatively involved in the degradation of chloroalkane, chloroalkene, ethylbenzene, toluene, bisphenol, and polycyclic aromatic hydrocarbon. A number of the genes associated with drug resistance were also identified in the genome.
As expected, the L. capsici genome contains a number of genes involved in the biosynthesis of nonribosomal peptide siderophores and antibiotics, such as penicillin, cephalosporin, streptomycin, butirosin, neomycin, tetracycline, novobiocin, vancomycin, and ansamycins, which may play important roles in the suppression of plant pathogens. Additionally, the genes coding for lytic enzymes, such as lytic protease, chitinases, glucanases, lipases, and xylanase, were identified in the X2-3 genome. The genetic information of L. capsici strain X2-3 provides deep insights into understanding its antimicrobial activity, which is critical for the development of a biological control agent for plant disease management.
Nucleotide sequence accession numbers.
This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession no. LBMI00000000. The version described in this paper is version LBMI01000000.
ACKNOWLEDGMENTS
This research was supported by the Shandong Science and Technology Development Planning in China (2013GNC11015) and the Modern Agricultural Technology Support project (SDAIT-04-022-06).
Footnotes
Citation Yi J-L, Wang J, Li Q, Liu Z-X, Zhang L, Liu A-X, Yu J-F. 2015. Draft genome sequence of the bacterium Lysobacter capsici X2-3, with a broad spectrum of antimicrobial activity against multiple plant-pathogenic microbes. Genome Announc 3(3):e00589-15. doi:10.1128/genomeA.00589-15.
REFERENCES
- 1.Zhang W, Li Y, Qian G, Wang Y, Chen H, Li YZ, Liu F, Shen Y, Du L. 2011. Identification and characterization of the anti-methicillin-resistant Staphylococcus aureus WAP-8294A2 biosynthetic gene cluster from Lysobacter enzymogenes OH11. Antimicrob Agents Chemother 55:5581–5589. doi: 10.1128/AAC.05370-11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Christensen P, Cook FD. 1978. Lysobacter, a new genus of nonfruiting, gliding bacteria with a high base ratio. Int J Syst Bacteriol 28:367–393. doi: 10.1099/00207713-28-3-367. [DOI] [Google Scholar]
- 3.Park JH, Kim R, Aslam Z, Jeon CO, Chung YR. 2008. Lysobacter capsici sp. nov., with antimicrobial activity, isolated from the rhizosphere of pepper, and emended description of the genus Lysobacter. Int J Syst Evol Microbiol 58:387–392. doi: 10.1099/ijs.0.65290-0. [DOI] [PubMed] [Google Scholar]
- 4.Jochum CC, Osborne LE, Yuen GY. 2006. Fusarium head blight biological control with Lysobacter enzymogenes strain C3. Biol Control 39:336–344. doi: 10.1016/j.biocontrol.2006.05.004. [DOI] [Google Scholar]
- 5.Lee YS, Park YS, Anees M, Kim YC, Kim YH, Kim KY. 2013. Nematicidal activity of Lysobacter capsici YS1215 and the role of gelatinolytic proteins against root-knot nematodes. Biocontrol Sci Technol 23:1427–1441. doi: 10.1080/09583157.2013.840359. [DOI] [Google Scholar]
- 6.Tofazzal Islam M. 2010. Mode of antagonism of a biocontrol bacterium Lysobacter sp. SB-K88 toward a damping-off pathogen Aphanomyces cochlioides. World J Microbiol Biotechnol 26:629–637. doi: 10.1007/s11274-009-0216-y. [DOI] [Google Scholar]
- 7.Del Sal G, Manfioletti G, Schneider C. 1989. The CTAB-DNA precipitation method: a common mini-scale preparation of template DNA from phagemids, phages or plasmids suitable for sequencing. Biotechniques 7:514–520. [PubMed] [Google Scholar]
- 8.Puopolo G, Sonego P, Engelen K, Pertot I. 2014. Draft genome sequence of Lysobacter capsici AZ78, a bacterium antagonistic to plant-pathogenic oomycetes. Genome Announc 2(2):e00325-14. doi: 10.1128/genomeA.00325-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Zhou L, Li M, Yang J, Wei L, Ji G. 2014. Draft genome sequence of antagonistic agent Lysobacter antibioticus 13-6. Genome Announc 2(5):e00566-14. doi: 10.1128/genomeA.00566-14. [DOI] [PMC free article] [PubMed] [Google Scholar]