ABSTRACT
The genome sequence of Rhizobium sophoriradicis H4, a nitrogen-fixing bacterium isolated from the common bean (Phaseolus vulgaris) in Peru, is reported here. The genome assembly revealed a 6.44-Mbp genome which was distributed into 95 contigs, with N50 and L50 values of 293 kbp and 9, respectively. The genome contained 6,312 coding sequence (CDS) genes and 52 RNA genes (49 tRNAs and 3 rRNAs).
GENOME ANNOUNCEMENT
Rhizobium sophoriradicis is an alphaproteobacterial species first isolated in China as a root-nodule symbiont of the leguminous plant Sophora flavescens (1). This rhizobium was later found to be associated with the common bean (Phaseolus vulgaris) in Iran (2) and South Africa (3). During a study of the rhizobial diversity of common bean symbionts on the coast of Peru, we found that R. sophoriradicis is present in some areas where this leguminous plant is cultivated. Here, we report the genome sequence of a Peruvian strain of this species.
Sequencing was performed using the Illumina MiSeq platform with 300-bp paired-end reads. Reads were quality trimmed with Trimmomatic (4) and assembled with SPAdes (5). Genome completeness was evaluated using the program BUSCO (6). The sequences were sent to the Rapid Annotations using Subsystems Technology (RAST) server (7) for functional annotation. The genome assembly of R. sophoriradicis H4 consisted of 95 contigs ranging in size from 237 bp to 539,995 bp, with a mean coverage of 122×. The N50 and L50 values were 293 kbp and 9, respectively. A completeness score of 100% was obtained for the assembly, indicating that all of the genome of strain H4 was recovered. The genome size was estimated at 6.44 Mbp, and the GC content was 61.4%. The number of predicted CDS genes was 6,312, while the RNA genes included 49 tRNAs and 3 rRNAs.
Functions could be assigned to 74% of the CDS genes of R. sophoriradicis H4. An abundance of genes involved in the metabolism of carbon and nitrogen sources revealed that strain H4 is a metabolically versatile bacterium. The traits related to plant root colonization encoded in its genome included flagellar motility, chemotaxis, surface adhesion via a type IV pilus, siderophore production and uptake, type VI secretion, and exopolysaccharide biosynthesis.
When aligned against symbiotic plasmids of other rhizobia, R. sophoriradicis H4 contigs showed high homology to symbiovar phaseoli plasmids. Within these contigs, we found all the nodulation and nitrogen fixation genes required to establish a successful symbiotic relationship with legumes. Among nodulation genes, we found nodZ, noeI, and nolL, whose presence indicates that nodulation factors produced by strain H4 bear methylated and acetylated fucose residues at the reducing end, while genes nolO, nodS, and nodU indicate methyl and carbamoyl decorations at the nonreducing end (8). Also, putative symbiotic plasmid contigs included genes for a type III secretion system, which may be required for an optimal association (9), a type IV secretion system probably for conjugal transfer of the symbiotic plasmid (10), an uptake ABC transporter for nopaline, which may confer competitive ability (11), the genes teuBAC1C2, required for utilization of root exudates (12), and genes for the biosynthesis of gibberellins.
This study reports the first genome sequence of a rhizobial symbiont of the common bean isolated in Peru, which is also the first genome sequence of a strain of the R. sophoriradicis species.
Accession number(s).
The nucleotide sequence for strain H4 has been deposited in GenBank under the accession number PSOW00000000.
ACKNOWLEDGMENTS
This work was funded in whole or part by Fondecyt under project 238-2015.
The funders had no role in the study design, data collection and interpretation, or the decision to submit the work for publication.
Footnotes
Citation Ormeño-Orrillo E, Aguilar-Cuba Y, Zúñiga-Dávila D. 2018. Draft genome sequence of Rhizobium sophoriradicis H4, a nitrogen-fixing bacterium associated with the leguminous plant Phaseolus vulgaris on the coast of Peru. Genome Announc 6:e00241-18. https://doi.org/10.1128/genomeA.00241-18.
REFERENCES
- 1.Jiao YS, Yan H, Ji ZJ, Liu YH, Sui XH, Wang ET, Guo BL, Chen WX, Chen WF. 2015. Rhizobium sophorae sp. nov. and Rhizobium sophoriradicis sp. nov., nitrogen-fixing rhizobial symbionts of the medicinal legume Sophora flavescens. Int J Syst Evol Microbiol 65:497–503. doi: 10.1099/ijs.0.068916-0. [DOI] [PubMed] [Google Scholar]
- 2.Rouhrazi K, Khodakaramian G, Velázquez E. 2016. Phylogenetic diversity of rhizobial species and symbiovars nodulating Phaseolus vulgaris in Iran. FEMS Microbiol Lett 363:fnw024. doi: 10.1093/femsle/fnw024. [DOI] [PubMed] [Google Scholar]
- 3.Zinga MK, Jaiswal SK, Dakora FD. 2017. Presence of diverse rhizobial communities responsible for nodulation of common bean (Phaseolus vulgaris) in South African and Mozambican soils. FEMS Microbiol Ecol 93:fiw236. doi: 10.1093/femsec/fiw236. [DOI] [PubMed] [Google Scholar]
- 4.Bolger AM, Lohse M, Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30:2114–2120. doi: 10.1093/bioinformatics/btu170. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, Pyshkin AV, Sirotkin AV, Vyahhi N, Tesler G, Alekseyev MA, Pevzner PA. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. doi: 10.1089/cmb.2012.0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Simão FA, Waterhouse RM, Ioannidis P, Kriventseva EV, Zdobnov EM. 2015. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics 31:3210–3212. doi: 10.1093/bioinformatics/btv351. [DOI] [PubMed] [Google Scholar]
- 7.Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: Rapid Annotations using Subsystems Technology. BMC Genomics 9:75. doi: 10.1186/1471-2164-9-75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Perret X, Staehelin C, Broughton WJ. 2000. Molecular basis of symbiotic promiscuity. Microbiol Mol Biol Rev 64:180–201. doi: 10.1128/MMBR.64.1.180-201.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Fauvart M, Michiels J. 2008. Rhizobial secreted proteins as determinants of host specificity in the rhizobium-legume symbiosis. FEMS Microbiol Lett 285:1–9. doi: 10.1111/j.1574-6968.2008.01254.x. [DOI] [PubMed] [Google Scholar]
- 10.Pérez-Mendoza D, Domínguez-Ferreras A, Muñoz S, Soto MJ, Olivares J, Brom S, Girard L, Herrera-Cervera JA, Sanjuán J. 2004. Identification of functional mob regions in Rhizobium etli: evidence for self-transmissibility of the symbiotic plasmid pRetCFN42d. J Bacteriol 186:5753–5761. doi: 10.1128/JB.186.17.5753-5761.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Oger P, Petit A, Dessaux Y. 1997. Genetically engineered plants producing opines alter their biological environment. Nat Biotechnol 15:369. doi: 10.1038/nbt0497-369. [DOI] [PubMed] [Google Scholar]
- 12.Rosenblueth M, Hynes MF, Martínez-Romero E. 1998. Rhizobium tropici teu genes involved in specific uptake of Phaseolus vulgaris bean-exudate compounds. Mol Gen Genet 258:587–598. doi: 10.1007/s004380050772. [DOI] [PubMed] [Google Scholar]