ABSTRACT
Endophytic Klebsiella variicola KvMx2 and Klebsiella pneumoniae KpMx1 isolates obtained from the same sugarcane stem were used for whole-genome sequencing. The genomes revealed clear differences in essential genes for plant growth, development, and detoxification, as well as nitrogen fixation, catalases, cellulases, and shared virulence factors described in the K. pneumoniae pathogen.
GENOME ANNOUNCEMENT
Klebsiella variicola has been described as an endophyte and has been identified in different plants (1). However, Klebsiella pneumoniae is considered a pathogen in humans and equally as an endophytic bacterium; nevertheless, few data and scarce genomes have been described for isolates obtained from plants. In the case of K. pneumoniae 342, obtained from maize (2), the isolate actually corresponds to K. variicola (3). A clear difference between these species is the capacity of K. variicola to fix atmospheric nitrogen and promote plant growth (1, 3–6). For this study, Klebsiella species colonies were obtained from the root of a sugarcane plant (ATMEX 96-40) grown in Cuautla, Morelos, Mexico. A multiplex PCR (M-PCR-1) (7) was used for the proper identification and differentiation of K. variicola and K. pneumoniae isolates. Colonies of both the K. variicola KvMx2 and K. pneumoniae KpMx1 isolates were identified and then used for whole-genome sequencing.
Total genomic DNA was extracted and purified using the DNeasy kit (Qiagen, Germany). Whole-genome sequences were generated using an Illumina (MiSeq) platform, and a total of 4,706,652 paired-end reads in K. variicola KvMx2 and 2,562,748 paired-end reads in K. pneumoniae KpMx1 with a length of 150 bp were obtained. Quality-based trimming was performed with the SolexaQA software, and de novo assembly was done with SPAdes version 3.1.1. The contigs were subjected to a scaffolding process with SSPACE version 2.0. For K. variicola KvMx2 and K. pneumoniae KpMx1, respectively, a total of 37 contigs (N50, 397,617 bp) and 50 contigs (N50, 377,295 bp) and estimated genome sizes of 5,528,301 bp (128× coverage) and 5,371,602 bp (72× coverage) were determined. Gene prediction and annotation were carried out using the bioinformatic MicroScope platform (8). In the K. variicola KvMx2 genome, a total of 5,431 coding DNA sequences (CDSs), 75 tRNA genes, and 6 rRNAs were found. In the K. pneumoniae KpMx1 genome, a total of 5,324 CDSs, 82 tRNA genes, and 9 rRNAs were found. The average G+C contents were similar in the two genomes, at 57.39% for K. variicola KvMx2 and 57.46% for K. pneumoniae KpMx1. An average nucleotide identity (ANI) >95% (9) confirmed the bacterial species.
A genomic comparison between K. variicola KvMx2 and K. pneumoniae KpMx1 showed a pangenome of 6,306 families of proteins, with a core genome of 4,306 families and a variable genome of 1,078 families of proteins for K. variicola KvMx2 and 922 families of proteins for K. pneumoniae KpMx1. The K. variicola KvMx2 genome revealed genes essential for the biosynthesis of indole-3-acetic acid (IAA), acetoin and 2,3-butanediol, and rhodanase, which are involved in plant growth, development, and detoxification of cyanide compounds (10), respectively. Likewise, the K. variicola genome contains the nifJ-NifQ nitrogen fixation gene cluster and is a clear difference between the two bacterial species. Otherwise, the catalase genes bglX and katGE are contained in both bacterial species; however, the cellulase bglH gene is contained only in K. variicola KvMx2.
With respect to virulence factors, the entB, mrkABCDFHJL, ureA, uge, and wabG genes are contained in both the K. variicola KvMx2 and K. pneumoniae KpMx1 genomes. Only in the K. variicola KvMx2 genome was the kfuABC operon identified. Finally, K. pneumoniae KpMx1 contained the copper resistance pcoABCDER operon.
Accession number(s).
The annotated genome sequences are available at the European Nucleotide Archive under accession numbers FLLH01000001 to FLLH01000037 (K. variicola KvMx2) and FLLB01000001 to FLLB01000050 (K. pneumoniae KpMx1).
ACKNOWLEDGMENTS
This work was funded by the Consejo Nacional de Ciencia y Tecnología (CONACYT), grants SEP-CONACYT grant 256988 and CONACYT grant PDCPN 0247780.
Footnotes
Citation Reyna-Flores F, Barrios-Camacho H, Dantán-González E, Ramírez-Trujillo JA, Lozano Aguirre Beltrán LF, Rodríguez-Medina N, Garza-Ramos U, Suárez-Rodríguez R. 2018. Draft genome sequences of endophytic isolates of Klebsiella variicola and Klebsiella pneumoniae obtained from the same sugarcane plant. Genome Announc 6:e00147-18. https://doi.org/10.1128/genomeA.00147-18.
REFERENCES
- 1.Rosenblueth M, Martínez L, Silva J, Martínez-Romero E. 2004. Klebsiella variicola, a novel species with clinical and plant-associated isolates. Syst Appl Microbiol 27:27–35. doi: 10.1078/0723-2020-00261. [DOI] [PubMed] [Google Scholar]
- 2.Fouts DE, Tyler HL, DeBoy RT, Daugherty S, Ren Q, Badger JH, Durkin AS, Huot H, Shrivastava S, Kothari S, Dodson RJ, Mohamoud Y, Khouri H, Roesch LFW, Krogfelt KA, Struve C, Triplett EW, Methé BA. 2008. Complete genome sequence of the N2-fixing broad host range endophyte Klebsiella pneumoniae 342 and virulence predictions verified in mice. PLoS Genet 4:e1000141. doi: 10.1371/journal.pgen.1000141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Martínez-Romero E, Rodriguez-Medina N, Beltrán-Rojel M, Silva-Sanchez J, Barrios-Camacho H, Perez-Rueda E, Garza-Ramos U. 2017. Genome misclassification of Klebsiella variicola and Klebsiella quasipneumoniae isolated from plants, animals and humans. Salud Publica Mex 60:56–62. doi: 10.21149/8149. [DOI] [PubMed] [Google Scholar]
- 4.Pinto-Tomás AA, Anderson MA, Suen G, Stevenson DM, Chu FST, Cleland WW, Weimer PJ, Currie CR. 2009. Symbiotic nitrogen fixation in the fungus gardens of leaf-cutter ants. Science 326:1120–1123. doi: 10.1126/science.1173036. [DOI] [PubMed] [Google Scholar]
- 5.Wei C-Y, Lin L, Luo L-J, Xing Y-X, Hu C-J, Yang L-T, Li Y-R, An Q. 2013. Endophytic nitrogen-fixing Klebsiella variicola strain DX120E promotes sugarcane growth. Biol Fertil Soils 50:657–666. doi: 10.1007/s00374-013-0878-3. [DOI] [Google Scholar]
- 6.Martínez-Romero E, Rodriguez-Medina N, Beltrán-Rojel M, Toribio-Jimenez J, Garza-Ramos U. 2018. Klebsiella variicola and Klebsiella quasipneumoniae genomic analysis provides insights into their capacity to adapt to clinical and plant settings. Salud Publica Mex 60:29–40. [DOI] [PubMed] [Google Scholar]
- 7.Garza-Ramos U, Silva-Sánchez J, Martínez-Romero E, Tinoco P, Pina-Gonzales M, Barrios H, Martínez-Barnetche J, Gomez-Barreto RE, Tellez J. 2015. Development of a multiplex-PCR probe system for proper identification of Klebsiella variicola. BMC Microbiol 15:64. doi: 10.1186/s12866-015-0396-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Vallenet D, Belda E, Calteau A, Cruveiller S, Engelen S, Lajus A, Le Fèvre F, Longin C, Mornico D, Roche D, Rouy Z, Salvignol G, Scarpelli C, Thil Smith AA, Weiman M, Médigue C. 2013. MicroScope–an integrated microbial resource for the curation and comparative analysis of genomic and metabolic data. Nucleic Acids Res 41:D636–D647. doi: 10.1093/nar/gks1194. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P, Tiedje JM. 2007. DNA-DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol 57:81–91. doi: 10.1099/ijs.0.64483-0. [DOI] [PubMed] [Google Scholar]
- 10.Liu W, Wang Q, Hou J, Tu C, Luo Y, Christie P. 2016. Whole genome analysis of halotolerant and alkalotolerant plant growth-promoting rhizobacterium Klebsiella sp. D5A. Sci Rep 6:26710. doi: 10.1038/srep26710. [DOI] [PMC free article] [PubMed] [Google Scholar]