ABSTRACT
We present here the draft genome sequences of bacterial pathogens of the Araceae family, Xanthomonas axonopodis pv. dieffenbachiae LMG 695 and Xanthomonas campestris pv. syngonii LMG 9055, differing in host range. A comparison between genome sequences will help understand the mechanisms involved in tissue specificity and adaptation to host plants.
GENOME ANNOUNCEMENT
Among the different members of the aroids, the tropical flower anthurium (Anthurium andreanum Linden ex André) is an economically important crop cultivated in tropical and temperate areas. Production of anthurium in the world is threatened by Anthurium bacterial blight (ABB), which is caused by Xanthomonas axonopodis pv. dieffenbachiae (1). Strains of X. axonopodis pv. dieffenbachiae isolated from anthurium can infect other aroids, and particularly different ornemental species of Dieffenbachia, Caladium, Philodendron, Syngonium, or edible aroids, such as Colocasia species. Other Xanthomonas strains, first classified as Xanthomonas campestris pv. syngonii (2), have a narrower host range and infect Syngonium plants causing the bacterial leaf blight of Syngonium. Based on rep-PCR and multilocus sequence analysis (MLSA), the two strains LMG 695 and LMG 9055 grouped in the X. axonopodis 9.4 cluster (3, 4). Hybridization values (<70%) between LMG 695 or LMG 9055 and the type strain of X. axonopodis LMG 982 did not support their inclusion in X. axonopodis (5). A polyphasic taxonomic approach based on MLSA, DNA/DNA hybridization, average nucleotide identity (ANI) values, and phenotypic analyses confirmed these results and proposed to reclassify this cluster as Xanthomonas phaseoli (6). In addition to differences in pathogenicity, these data also supported the separation of the two categories of strains represented by LMG 695 and LMG 9055 in distinct pathovars named dieffenbachiae and syngonii, respectively.
The genomes of both strains were sequenced using the Illumina HiSeq 2000 platform (GATC Biotech, Germany). Shotgun sequencing yielded 25,320,564 read pairs (12,846,409 100-bp paired-end reads with an insert size of 250 bp, and 12,474,156 50-bp mate-pair reads with an insert size of 3 kb) and 30,521,960 read pairs (17,529,832 100-bp paired-end reads with an insert size of 250 bp and 12,992,128 50-bp mate-pair reads with an insert size of 3 kb) for LMG 695 and LMG 9055, respectively.
A combination of Velvet (7), SOAPdenovo, and SOAP GapCloser (8) yielded 10 contigs >500 bp (N50, 1,343,781 bp), with the largest contig being 1,543,007 bp, for a total assembly size of 5,035,943 bp for strain LMG 695, and 33 contigs >500 bp (N50, 414,753 bp), with the largest contig being 751,399 bp, for a total assembly size of 5,000,894 bp for strain LMG 9055. Genomic contigs were annotated using the EuGene-P annotation pipeline to identify RNAs and protein-coding genes (9). The draft genomes were predicted to contain 4,423 and 4,665 coding sequences (CDSs) for strains LMG 695 and LMG 9055, respectively.
The two genomes have an average nucleotide identity (ANI) of 97.33% (10). The two genomes share >3,700 CDSs, and each contains approximately 200 CDSs, with no orthologs in other Xanthomonas species (11). Nineteen and 22 predicted type 3 effector (T3E) genes are present in the LMG 695 and LMG 9055 genomes, respectively. At least 13 of these T3E genes are shared by the two strains.
Accession number(s).These whole-genome shotgun projects have been deposited in GenBank under the accession no. CP014347 for strain LMG 695 and LSLD00000000 for strain LMG 9055. The versions described in this paper are the first versions.
ACKNOWLEDGMENTS
This research was funded by the French Agence Nationale de la Recherche, the European Regional Development Fund 2007–2014 (grant 2007FR161PO004), the Conseil Régional de la Réunion, and CIRAD.
FOOTNOTES
- Received 12 July 2016.
- Accepted 18 July 2016.
- Published 1 September 2016.
- Copyright © 2016 Robène et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
