Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris

被引:345
|
作者
Qian, W
Jia, YT
Ren, SX
He, YQ
Feng, JX
Lu, LF
Sun, QH
Ying, G
Tang, DJ
Tang, H
Wu, W
Hao, P
Wang, LF
Jiang, BL
Zeng, SY
Gu, WY
Lu, G
Rong, L
Tian, YC
Yao, ZJ
Fu, G
Chen, BS
Fang, RX
Qiang, BQ
Chen, Z
Zhao, GP [1 ]
Tang, JL
He, CZ
机构
[1] Chinese Natl Human Genome Ctr Shanghai, Lab Hlth & Dis Genom, Shanghai 201203, Peoples R China
[2] Chinese Acad Sci, Inst Microbiol, Natl Key Lab Plant Genom, Beijing 100080, Peoples R China
[3] Fudan Univ, Sch Life Sci, Dept Microbiol, Natl Key Lab Genet Engn, Shanghai 200433, Peoples R China
[4] Guangxi Univ, Guangxi Key Lab Subtrop Bioresources Conservat &, Nanning 530004, Guangxi, Peoples R China
[5] Univ Chicago, Dept Ecol & Evolut, Chicago, IL 60637 USA
[6] Shanghai Ctr Bioinformat Technol, Shanghai 200235, Peoples R China
[7] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Plant Physiol, Bioinformat Ctr, Shanghai 200032, Peoples R China
[8] Chinese Natl Human Genome Ctr Beijing, Beijing 100176, Peoples R China
关键词
D O I
10.1101/gr.3378705
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:757 / 767
页数:11
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