Gabriel Dean W, Allen Caitilyn, Schell Mark, Denny Timothy P, Greenberg Jean T, Duan Yong Ping, Flores-Cruz Zomary, Huang Qi, Clifford Jennifer M, Presting Gernot, González Enid T, Reddy Joseph, Elphinstone John, Swanson Jill, Yao Jian, Mulholland Vincent, Liu Li, Farmerie William, Patnaikuni Manjeera, Balogh Botond, Norman David, Alvarez Anne, Castillo Jose A, Jones Jeffrey, Saddler Gerry, Walunas Theresa, Zhukov Aleksey, Mikhailova Natalia
Plant Pathology Department, University of Florida, Gainesville, USA.
Mol Plant Microbe Interact. 2006 Jan;19(1):69-79. doi: 10.1094/MPMI-19-0069.
An 8x draft genome was obtained and annotated for Ralstonia solanacearum race 3 biovar 2 (R3B2) strain UW551, a United States Department of Agriculture Select Agent isolated from geranium. The draft UW551 genome consisted of 80,169 reads resulting in 582 contigs containing 5,925,491 base pairs, with an average 64.5% GC content. Annotation revealed a predicted 4,454 protein coding open reading frames (ORFs), 43 tRNAs, and 5 rRNAs; 2,793 (or 62%) of the ORFs had a functional assignment. The UW551 genome was compared with the published genome of R. solanacearum race 1 biovar 3 tropical tomato strain GMI1000. The two phylogenetically distinct strains were at least 71% syntenic in gene organization. Most genes encoding known pathogenicity determinants, including predicted type III secreted effectors, appeared to be common to both strains. A total of 402 unique UW551 ORFs were identified, none of which had a best hit or >45% amino acid sequence identity with any R. solanacearum predicted protein; 16 had strong (E < 10(-13)) best hits to ORFs found in other bacterial plant pathogens. Many of the 402 unique genes were clustered, including 5 found in the hrp region and 38 contiguous, potential prophage genes. Conservation of some UW551 unique genes among R3B2 strains was examined by polymerase chain reaction among a group of 58 strains from different races and biovars, resulting in the identification of genes that may be potentially useful for diagnostic detection and identification of R3B2 strains. One 22-kb region that appears to be present in GMI1000 as a result of horizontal gene transfer is absent from UW551 and encodes enzymes that likely are essential for utilization of the three sugar alcohols that distinguish biovars 3 and 4 from biovars 1 and 2.
获得了青枯雷尔氏菌3号小种2型(R3B2)菌株UW551的8倍基因组草图,并进行了注释。UW551菌株是从天竺葵中分离出的一种美国农业部选择生物制剂。UW551基因组草图由80,169条 reads 组成,产生582个 contig,包含5,925,491个碱基对,平均GC含量为64.5%。注释显示预测有4,454个蛋白质编码开放阅读框(ORF)、43个tRNA和5个rRNA;其中2,793个(或62%)ORF有功能注释。将UW551基因组与已发表的青枯雷尔氏菌1号小种3型热带番茄菌株GMI1000的基因组进行比较。这两个系统发育上不同的菌株在基因组织上至少71%是同线的。大多数编码已知致病决定因素的基因,包括预测的III型分泌效应子,在两个菌株中似乎是共同的。共鉴定出402个独特的UW551 ORF,其中没有一个与任何青枯雷尔氏菌预测蛋白有最佳匹配或>45%的氨基酸序列同一性;16个与其他细菌植物病原体中发现的ORF有强(E < 10(-13))最佳匹配。402个独特基因中的许多基因是成簇的,包括在hrp区域发现的5个基因和38个连续的潜在前噬菌体基因。通过聚合酶链反应在一组来自不同小种和生化变种的58个菌株中检测了一些UW551独特基因在R3B2菌株中的保守性,从而鉴定出可能对R3B2菌株的诊断检测和鉴定有用的基因。UW551中不存在一个22-kb的区域,该区域因水平基因转移而存在于GMI1000中,它编码的酶可能是利用区分生化变种3和4与生化变种1和2的三种糖醇所必需的。