Literature DB >> 26679582

Complete Genome Sequence of Xanthomonas campestris pv. campestris Strain 17 from Taiwan.

Yi-Chung Liu1, Shiuh-Chaun Wang2, Yu-Jen Yu3, Kit-Man Fung4, Ming-Te Yang4, Yi-Hsiung Tseng4, Shih-Feng Tsai5, H Sunny Sun6, Ping-Chiang Lyu7, Shan-Ho Chou8.   

Abstract

Xanthomonas campestris pv. campestris 17 is a Gram-negative bacterium that is phytopathogenic to cruciferous plants in Taiwan. The 4,994,426-bp-long genome consists of 24 contigs with 4,050 protein-coding genes, 1 noncoding RNA (ncRNA) gene, 6 rRNA genes, and 55 tRNA genes.
Copyright © 2015 Liu et al.

Entities:  

Year:  2015        PMID: 26679582      PMCID: PMC4683227          DOI: 10.1128/genomeA.01466-15

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Xanthomonas campestris pv. campestris is phytopathogenic to cruciferous plants and results in worldwide agricultural losses. It causes black rot, which is one of the most serious plant diseases in Taiwan (1). The warm and wet local climate is suitable for plant infection by X. campestris pv. campestris and the development of disease. The cultivation of black rot-resistant cultivars has long been recognized as an important control strategy. Meanwhile, an investigation of the genome sequence from the local strain can be used to discover its genetic and gene expression profiles to prevent black rot disease. X. campestris pv. campestris 17 was isolated from the leaves of the infected plants in Taiwan. Its genome sequencing was initially carried out using the Sanger sequencing method in 2002. After data assembly, 575 contigs consisting of 5,228,421 bp with approximately 10-fold coverage were obtained. The draft sequences were found to contain either 6,327 or 3,811 genes, as predicted by the Glimmer 2.0 (2) or ORPHEUS (3) program, respectively, using X. campestris pv. campestris ATCC 33913 as a reference. To improve the previous sequencing result, the genome of X. campestris pv. campestris 17 was resequenced on a GAIIx Illumina platform in 2012. Genome assembly was conducted using the SSAKE software (4) and Velvet assembler (5). However, some gaps were still present, which were further completed by PCR and cloning, followed by Sanger sequencing. A total length of 4,994,426 bp, comprising 24 contigs, with a contig N50 of 722,084 bp and 506.7-fold coverage, were obtained. The genome was found to be enriched with G+C content (65.1%). The sequence was annotated using the RAST server (6) and the NCBI Prokaryotic Genome Automatic Annotation Pipeline (PGAAP) (http://www.ncbi.nlm.nih.gov/genome/annotation_prok), which predicted 4,215 genes, 4,050 coding sequences (CDSs), 1 noncoding RNA (ncRNA) gene, 6 rRNA genes, and 55 tRNA genes. The genome information presented here will help discover the mechanism of X. campestris pv. campestris-plant interactions and allow for further investigation of the X. campestris pv. campestris functional and structural genomics.

Nucleotide sequence accession numbers.

The whole-genome sequence has been deposited in GenBank under the accession number CP011946. The version described in this paper is version CP011946.1.
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4.  Assembling millions of short DNA sequences using SSAKE.

Authors:  René L Warren; Granger G Sutton; Steven J M Jones; Robert A Holt
Journal:  Bioinformatics       Date:  2006-12-08       Impact factor: 6.937

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Journal:  BMC Genomics       Date:  2008-02-08       Impact factor: 3.969

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