Comparative and functional genomic analyses of the pathogenicity of phytopathogen<i>Xanthomonas campestris</i>pv.<i>campestris</i>

Wei Qian(Chinese Academy of Sciences), Yantao Jia(Chinese Academy of Sciences), Shuangxi Ren(Fudan University), Yong-Qiang He(Guangxi University), Jia‐Xun Feng(Guangxi University), Ling-Feng Lu(Chinese National Human Genome Center), Qi‐Hong Sun(Chinese Academy of Sciences), Ying Ge(Chinese Academy of Sciences), Dong‐Jie Tang(Guangxi University), Hua Tang(University of Chicago), Wei Wu(Chinese Academy of Sciences), Pei Hao(Chinese Academy of Sciences), Lifeng Wang(Chinese Academy of Sciences), Bo‐Le Jiang(Guangxi University), Shen-yan Zeng(Chinese Academy of Sciences), Wenyi Gu(Chinese National Human Genome Center), Gang Lü(Chinese National Human Genome Center), Rong Li(Chinese National Human Genome Center), Yingchuan Tian(Chinese Academy of Sciences), Zhijian Yao(Chinese National Human Genome Center), Gang Fu(Chinese National Human Genome Center), Baoshan Chen(Guangxi University), Rongxiang Fang(Chinese Academy of Sciences), Boqin Qiang(Chinese National Human Genome Center), Zhu Chen(Chinese National Human Genome Center), Guoping Zhao(Chinese Academy of Sciences), Ji‐Liang Tang(Guangxi University), Chaozu He(Chinese Academy of Sciences)
Genome Research
May 17, 2005
Cited by 409Open Access
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Abstract

Xanthomonas campestris pathovar campestris (Xcc) is the causative agent of crucifer black rot disease, which causes severe losses in agricultural yield world-wide. This bacterium is a model organism for studying plant-bacteria interactions. We sequenced the complete genome of Xcc 8004 (5,148,708 bp), which is highly conserved relative to that of Xcc ATCC 33913. Comparative genomics analysis indicated that, in addition to a significant genomic-scale rearrangement cross the replication axis between two IS1478 elements, loss and acquisition of blocks of genes, rather than point mutations, constitute the main genetic variation between the two Xcc strains. Screening of a high-density transposon insertional mutant library (16,512 clones) of Xcc 8004 against a host plant (Brassica oleraceae) identified 75 nonredundant, single-copy insertions in protein-coding sequences (CDSs) and intergenic regions. In addition to known virulence factors, full virulence was found to require several additional metabolic pathways and regulatory systems, such as fatty acid degradation, type IV secretion system, cell signaling, and amino acids and nucleotide metabolism. Among the identified pathogenicity-related genes, three of unknown function were found in Xcc 8004-specific chromosomal segments, revealing a direct correlation between genomic dynamics and Xcc virulence. The present combination of comparative and functional genomic analyses provides valuable information about the genetic basis of Xcc pathogenicity, which may offer novel insight toward the development of efficient methods for prevention of this important plant disease.


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