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. 2013 Feb 7;1(1):e00032-12. doi: 10.1128/genomeA.00032-12

Genome Sequence of Xanthomonas campestris pv. campestris Strain Xca5

Stéphanie Bolot a,b, Endrick Guy a,b, Sébastien Carrere a,b, Valérie Barbe c, Matthieu Arlat a,b,d, Laurent D Noël a,b,
PMCID: PMC3569304  PMID: 23405315

Abstract

An annotated high-quality draft genome sequence for Xanthomonas campestris pv. campestris race 1 strain Xca5 (originally described as X. campestris pv. armoraciae), the causal agent of black rot on Brassicaceae plants, has been determined. This genome sequence is a valuable resource for comparative genomics within the campestris pathovar.

GENOME ANNOUNCEMENT

Xanthomonas campestris pv. campestris is the causal agent of black rot on a wide range of Brassicaceae plants, including vegetable crops, such as cabbages, ornamental crucifers, and weeds, as well as the model plant Arabidopsis thaliana. The bacteria are seed transmitted and enter the plant vascular system by the hydathodes, causing V-shaped lesions, vein blackening, and leaf tissue necrosis. X. campestris pv. campestris strains have been sorted into 9 physiological races based on their interactions with diverse Brassicaceae plants. X. campestris pv. campestris genome sequences for races 3 and 9 are available (1, 2). Yet, no strains from X. campestris pv. campestris race 1 have had their genome sequences determined, despite belonging to probably the most represented X. campestris pv. campestris race worldwide (3).

Xca5 is an American race 1 X. campestris pv. campestris strain originally classified as pathovar armoraciae by M. Daniels (Sainsbury Laboratory, Norwich, United Kingdom). Yet, pathogenicity tests (3), as well as multilocus sequence analyses (data not shown), clearly identified this strain as a bona fide X. campestris pv. campestris strain. Xca5 genome shotgun sequencing was performed on a GAIIx Illumina platform. A total of 28,569,308 76-bp paired-end reads corresponding to 4,342,534,816 bp and 868-fold coverage were obtained. Genome assembly was performed using a combination of Short Oligonucleotide Analysis Package (SOAP) de novo (4) and Velvet (5) assemblers and yielded 130 contigs that were >500 bp and had an N50 of 121,265 bp. The average contig size was 38,385 bp, and the largest was 447,475 bp long, for a total genome size of 4,990,056 bp. One hundred twenty of those contigs were further organized into 4 pseudomolecules. The largest one corresponds to the chromosome (4,905,337 bp; 65.2% G+C content) based on X. campestris pv. campestris 8004 chromosomal organization. The remaining pseudomolecules match known Xanthomonas plasmid sequences. Due to the highly repetitive nature of the structures of known transcriptional activator-like (TAL) protein-encoding loci hax2 (plasmid borne), hax3, and hax4, their sequences (accession no. AY993937, AY993938, and AY993939, respectively) could not be assembled automatically (6) and were manually added to the final submission. In total, the genome is composed of 17 pseudomolecules/contigs totaling 5,001,025 bp. Annotation transfer was performed using the Rapid Annotation Transfer Tool (RATT) (7) with X. campestris pv. campestris B100, 8004, and ATCC 33913 as references. De novo annotation was performed on remaining areas using FrameD (8) and was inspected manually. We identified 4,592 coding sequences (CDSs), 51 tRNA genes, and 2 rRNA genes.

Phylogenetic analyses based on the core genome sequence shared with the 3 available X. campestris pv. campestris reference genome sequences and the genome sequence of X. campestris pv. raphani strain 756C were performed using Unus (9). These analyses showed that, indeed, Xca5 is most closely related to X. campestris pv. campestris strains 8004 and ATCC 33913. Using OrthoMCL (percent match cutoff, 80; blast parameter, F = false) (10), Xca5 was found to share 3,711 CDSs with the 3 X. campestris pv. campestris reference strains. Despite the availability of the 3 X. campestris pv. campestris reference genome sequences, this genome sequence represents the first X. campestris pv. campestris strain with TAL protein genes and plasmids, suggesting that much more genomic diversity might be expected at the intraspecific level than is anticipated from the available X. campestris pv. campestris genome sequences (1, 2, 11).

Nucleotide sequence accession numbers.

The Whole Genome Shotgun project has been deposited at EMBL under the accession no. CAOR01000001 to CAOR01000130.

ACKNOWLEDGMENTS

This study was funded by the Laboratoire d’Excellence (LABEX) TULIP (ANR-10-LABX-41), Genoscope grant, AP10/11-N° 28_Rott, a Ph.D. grant from the French Ministry of National Education and Research and French Guiana to E.G., and an Agence Nationale de la Recherche–Jeunes Chercheurs grant (Xopaque ANR-10-JCJC-1703-01) to L.D.N.

Footnotes

Citation Bolot S, Guy E, Carrere S, Barbe V, Arlat M, Noël LD. 2013. Genome sequence of Xanthomonas campestris pv. campestris strain Xca5. Genome Announc. 1(1):e00032-12. doi:10.1128/genomeA.00032-12.

REFERENCES

  • 1. da Silva AC, Ferro JA, Reinach FC, Farah CS, Furlan LR, Quaggio RB, Monteiro-Vitorello CB, Van Sluys MA, Almeida NF, Alves LM, do Amaral AM, Bertolini MC, Camargo LE, Camarotte G, Cannavan F, Cardozo J, Chambergo F, Ciapina LP, Cicarelli RM, Coutinho LL, Cursino-Santos JR, El-Dorry H, Faria JB, Ferreira AJ, Ferreira RC, Ferro MI, Formighieri EF, Franco MC, Greggio CC, Gruber A, Katsuyama AM, Kishi LT, Leite RP, Lemos EG, Lemos MV, Locali EC, Machado MA, Madeira AM, Martinez-Rossi NM, Martins EC, Meidanis J, Menck CF, Miyaki CY, Moon DH, Moreira LM, Novo MT, Okura VK, Oliveira MC, Oliveira VR, Pereira HA, Rossi A, Sena JA, Silva C, de Souza RF, Spinola LA, Takita MA, Tamura RE, Teixeira EC, Tezza RI, Trindade dos Santos M, Truffi D, Tsai SM, White FF, Setubal JC, Kitajima JP. 2002. Comparison of the genomes of two Xanthomonas pathogens with differing host specificities. Nature 417:459–463 [DOI] [PubMed] [Google Scholar]
  • 2. Qian W, Jia Y, Ren SX, He YQ, Feng JX, Lu LF, Sun Q, Ying G, Tang DJ, Tang H, Wu W, Hao P, Wang L, Jiang BL, Zeng S, Gu WY, Lu G, Rong L, Tian Y, Yao Z, Fu G, Chen B, Fang R, Qiang B, Chen Z, Zhao GP, Tang JL, He C. 2005. Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris. Genome Res. 15:757–767 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Vicente JG, Conway J, Roberts SJ, Taylor JD. 2001. Identification and origin of Xanthomonas campestris pv. campestris races and related pathovars. Phytopathology 91:492–499 [DOI] [PubMed] [Google Scholar]
  • 4. Li R, Zhu H, Ruan J, Qian W, Fang X, Shi Z, Li Y, Li S, Shan G, Kristiansen K, Li S, Yang H, Wang J, Wang J. 2010. De novo assembly of human genomes with massively parallel short read sequencing. Genome Res. 20:265–272 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 18:821–829 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Kay S, Boch J, Bonas U. 2005. Characterization of AvrBs3-like effectors from a Brassicaceae pathogen reveals virulence and avirulence activities and a protein with a novel repeat architecture. Mol. Plant Microbe Interact. 18:838–848 [DOI] [PubMed] [Google Scholar]
  • 7. Otto TD, Dillon GP, Degrave WS, Berriman M. 2011. RATT: rapid annotation transfer tool. Nucleic Acids Res. 39:e57 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Schiex T, Gouzy J, Moisan A, de Oliveira Y. 2003. FrameD: a flexible program for quality check and gene prediction in prokaryotic genomes and noisy matured eukaryotic sequences. Nucleic Acids Res. 31:3738–3741 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Rodriguez-R LM, Grajales A, Arrieta-Ortiz ML, Salazar C, Restrepo S, Bernal A. 2012. Genomes-based phylogeny of the genus Xanthomonas. BMC Microbiol. 12:43 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Li L, Stoeckert CJ, Jr, Roos DS. 2003. OrthoMCL: identification of ortholog groups for eukaryotic genomes. Genome Res. 13:2178–2189 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Vorholter FJ, Schneiker S, Goesmann A, Krause L, Bekel T, Kaiser O, Linke B, Patschkowski T, Ruckert C, Schmid J, Sidhu VK, Sieber V, Tauch A, Watt SA, Weisshaar B, Becker A, Niehaus K, Puhler A. 2008. The genome of Xanthomonas campestris pv. campestris B100 and its use for the reconstruction of metabolic pathways involved in xanthan biosynthesis. J. Biotechnol. 134:33–45 [DOI] [PubMed] [Google Scholar]

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