ABSTRACT
We report here the complete genome sequence of Rhizobium sp. strain ACO-34A, isolated from Agave americana L. rhizosphere. No common nod genes were found, but there were nif genes for nitrogen fixing. A low average nucleotide identity to reported species supports its designation as a novel Rhizobium species that has a complete ribosomal operon in a plasmid.
GENOME ANNOUNCEMENT
Nitrogen-fixing microorganisms and plant growth-promoting bacteria are useful alternatives for replacing chemical fertilizers in nonlegume plants (1). Rhizobium sp. strain ACO-34A was isolated from Agave americana L. rhizosphere and promotes plant growth due to phosphate solubilization and indole-3-acetic acid biosynthesis (2). We found that ACO-34A does not form nodules in Phaseolus vulgaris, which is a promiscuous plant for nodulation.
The ACO-34A genome was sequenced using the Pacific Biosciences (PacBio RSII) single-molecule real-time (SMRT) platform. Three SMRT cells of a 15- to 20-kb insert library were sequenced; 271,302 reads, with an average read length of 11,950 bp, were used for the de novo genome assembly using RS_HGAP_Assembly.3 for SMRT Portal Analysis version 2.3.0 (3), and a 347× coverage was obtained. Genome annotation was performed using the NCBI Prokaryotic Genome Annotation Pipeline (http://www.ncbi.nlm.nih.gov/genome/annotation_prok). Clusters of orthologous groups (4) were allocated using BLASTx searches, and hits with an E value cutoff of 1e−10 were considered. rRNA operons and prophages were identified with RNAmmer (5) and PHAST (6), respectively. Average nucleotide identity (ANI) (7) was calculated with the pyani module of Python (8). Relative synonymous codon usage and principal component analysis were applied to identify chromids and plasmids (9).
The 6,284,736-bp (61% GC content) ACO-34A genome sequence comprises one chromosome (4.75 Mb) and four extrachromosomal replicons that correspond to two plasmids (516 and 213 kb) and two chromids (494 and 305 kb) according to reported standards (9). The 516-kb plasmid contains one complete operon of ribosomal genes identical to the three chromosomal homologs. Ribosomal genes located on a plasmid may be the result of a transposition-integration event since they are contiguous to an integrase gene. In addition, repA and repB phylogenies group each of the extrachromosomal replicons with respective chromids or plasmids. In other rhizobia, genes for nodulation and biological nitrogen fixation are located in symbiotic plasmids (pSym) with sizes from 370 to 600 kb (10, 11). The 213-kb plasmid from strain ACO-34A might be a deleted pSym because it lacks nod genes, although it contains the nifHDK operon that encodes nitrogenase structural genes and other nif and fix genes; this plasmid is smaller than other pSyms and could be conjugative because it contains tra and trb genes. Host specificity genes, such as the nodL, nodT, and nodN, were found in the chromosome (as in R. etli CFN42 and R. gallicum R602). A 57.7-kb chromosomal region represents a complete prophage with 80 open reading frames, 34 of which resembled Rhizobium phage RR1-A (NCBI reference sequence NC_021560), a temperate phage found in deep subseafloor sediments (12). The ANI values in comparison to 221 Rhizobium genomes showed 85% identity to R. selenitireducens ATCC BAA-1503 (a nonnodulating environmental isolate) (13), but the ANI values were lower in comparison to other species, suggesting that ACO-34A corresponds to a new species, which could be named R. agavense. The genomic information for Rhizobium sp. ACO-34A may be used to further explore the role of nonnodulating rhizobia in promoting growth in nonlegume plants.
Accession number(s).
The whole-genome nucleotide sequence of Rhizobium sp. ACO-34A was deposited in GenBank under the accession numbers CP021371, CP021372, CP021373, CP021374, and CP021375.
ACKNOWLEDGMENTS
This study was supported by project CB-2015-253281 from the Consejo Nacional de Ciencia y Tecnología (CONACyT) (México) to Tecnológico Nacional de México (TNM) (México) (5665.15-P and 5663.15-P) and by grants CONACyT 253116 and PAPIIT UNAM IN207615. We thank CONACyT for its grant-aided support to A.L.-L.
Footnotes
Citation Ruíz-Valdiviezo VM, Rogel-Hernandez MA, Guerrero G, Rincón-Molina CI, García-Perez LG, Gutiérrez-Miceli FA, Villalobos-Maldonado JJ, López-López A, Martinez-Romero E, Rincón-Rosales R. 2017. Complete genome sequence of a novel nonnodulating Rhizobium species isolated from Agave americana L. rhizosphere. Genome Announc 5:e01280-17. https://doi.org/10.1128/genomeA.01280-17.
REFERENCES
- 1.de Souza Rd, Ambrosini A, Passaglia LMP. 2015. Plant growth-promoting bacteria as inoculants in agricultural soils. Genet Mol Biol 38:401–419. doi: 10.1590/S1415-475738420150053. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.De La Torre-Ruiz N, Ruiz-Valdiviezo VM, Rincón-Molina CI, Rodríguez-Mendiola M, Arias-Castro C, Gutiérrez-Miceli FA, Palomeque-Domínguez H, Rincón-Rosales R. 2016. Effect of plant growth-promoting bacteria on the growth and fructan production of Agave americana L. Braz J Microbiol 47:587–596. doi: 10.1016/j.bjm.2016.04.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Chin CS, Alexander DH, Marks P, Klammer AA, Drake J, Heiner C, Clum A, Copeland A, Huddleston J, Eichler EE, Turner SW, Korlach J. 2013. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data. Nat Methods 10:563–569. doi: 10.1038/nmeth.2474. [DOI] [PubMed] [Google Scholar]
- 4.Tatusov RL, Koonin EV, Lipman DJ. 1997. A genomic perspective on protein families. Science 278:631–637. doi: 10.1126/science.278.5338.631. [DOI] [PubMed] [Google Scholar]
- 5.Lagesen K, Hallin P, Rødland EA, Staerfeldt HH, Rognes T, Ussery DW. 2007. RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res 35:3100–3108. doi: 10.1093/nar/gkm160. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Zhou Y, Liang Y, Lynch KH, Dennis JJ, Wishart DS. 2011. PHAST: a fast phage search tool. Nucleic Acids Res 39:W347–W352. doi: 10.1093/nar/gkr485. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Richter M, Rosselló-Móra R. 2009. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci U S A 106:19126–19131. doi: 10.1073/pnas.0906412106. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Pritchard L, Glover RH, Humphris S, Elphinstone JG, Toth IK. 2016. Genomics and taxonomy in diagnostics for food security: soft-rotting enterobacterial plant pathogens. Anal Methods 8:12–24. doi: 10.1039/C5AY02550H. [DOI] [Google Scholar]
- 9.Harrison PW, Lower RPJ, Kim NKD, Young JPW. 2010. Introducing the bacterial “chromid”: not a chromosome, not a plasmid. Trends Microbiol 18:141–148. doi: 10.1016/j.tim.2009.12.010. [DOI] [PubMed] [Google Scholar]
- 10.González V, Santamaría RI, Bustos P, Hernández-González I, Medrano-Soto A, Moreno-Hagelsieb G, Janga SC, Ramírez MA, Jiménez-Jacinto V, Collado-Vides J, Dávila G. 2006. The partitioned Rhizobium etli genome: genetic and metabolic redundancy in seven interacting replicons. Proc Natl Acad Sci U S A 103:3834–3839. doi: 10.1073/pnas.0508502103. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Rogel MA, Bustos P, Santamaría RI, González V, Romero D, Cevallos MÁ, Lozano L, Castro-Mondragón J, Martínez-Romero J, Ormeño-Orrillo E, Martínez-Romero E. 2014. Genomic basis of symbiovar mimosae in Rhizobium etli. BMC Genomics 15:575. doi: 10.1186/1471-2164-15-575. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Engelhardt T, Sahlberg M, Cypionka H, Engelen B. 2013. Biogeography of Rhizobium radiobacter and distribution of associated temperate phages in deep subseafloor sediments. ISME J 7:199–209. doi: 10.1038/ismej.2012.92. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hunter WJ, Kuykendall LD, Manter DK. 2007. Rhizobium selenireducens sp. nov.: a selenite-reducing alpha-proteobacteria isolated from a bioreactor. Curr Microbiol 55:455–460. doi: 10.1007/s00284-007-9020-9. [DOI] [PubMed] [Google Scholar]
