Sawada H, Suzuki F, Matsuda I, Saitou N
National Institute of Agro-Environmental Sciences, 3-1-1 Kannondai, Tsukuba, Ibaraki 305-8604, Japan.
J Mol Evol. 1999 Nov;49(5):627-44. doi: 10.1007/pl00006584.
Pseudomonas syringae are differentiated into approximately 50 pathovars with different plant pathogenicities and host specificities. To understand its pathogenicity differentiation and the evolutionary mechanisms of pathogenicity-related genes, phylogenetic analyses were conducted using 56 strains belonging to 19 pathovars. gyrB and rpoD were adopted as the index genes to determine the course of bacterial genome evolution, and hrpL and hrpS were selected as the representatives of the pathogenicity-related genes located on the genome (chromosome). Based on these data, NJ, MP, and ML phylogenetic trees were constructed, and thus 3 trees for each gene and 12 gene trees in total were obtained, all of which showed three distinct monophyletic groups: Groups 1, 2 and 3. The observation that the same set of OTUs constitute each group in all four genes suggests that these genes had not experienced any intergroup horizontal gene transfer within P. syringae but have been stable on and evolved along with the P. syringae genome. These four index genes were then compared with another pathogenicity-related gene, argK (the phaseolotoxin-resistant ornithine carbamoyltransferase gene, which exists within the argK-tox gene cluster). All 13 strains of pv. phaseolicola and pv. actinidiae used had been confirmed to produce phaseolotoxin and to have argK, whose sequences were completely identical, without a single synonymous substitution among the strains used (Sawada et al. 1997a). On the other hand, argK were not present on the genomes of the other 43 strains used other than pv. actinidiae and pv. phaseolicola. Thus, the productivity of phaseolotoxin and the possession of the argK gene were shown at only two points on the phylogenetic tree: Group 1 (pv. actinidiae) and Group 3 (pv. phaseolicola). A t test between these two pathovars for the synonymous distances of argK and the tandemly combined sequence of the four index genes showed a high significance, suggesting that the argK gene (or argK-tox gene cluster) experienced horizontal gene transfer and expanded its distribution over two pathovars after the pathovars had separated, thus showing a base substitution pattern extremely different from that of the noncluster region of the genome.
丁香假单胞菌可分为约50个致病型,具有不同的植物致病性和宿主特异性。为了解其致病性分化及致病相关基因的进化机制,对属于19个致病型的56株菌株进行了系统发育分析。采用gyrB和rpoD作为指标基因来确定细菌基因组的进化过程,并选择hrpL和hrpS作为基因组(染色体)上致病相关基因的代表。基于这些数据,构建了NJ、MP和ML系统发育树,每个基因得到3棵树,共12棵基因树,所有这些树都显示出三个不同的单系类群:第1组、第2组和第3组。在所有四个基因中同一组OTU构成每个类群的观察结果表明,这些基因在丁香假单胞菌内未经历任何类群间水平基因转移,而是在丁香假单胞菌基因组上保持稳定并随其进化。然后将这四个指标基因与另一个致病相关基因argK(抗菜豆毒素鸟氨酸氨甲酰基转移酶基因,存在于argK - tox基因簇中)进行比较。所有13株菜豆致病变种和猕猴桃致病变种菌株均已证实能产生菜豆毒素并具有argK,其序列完全相同,所用菌株之间无单个同义替换(泽田等人, 1997a)。另一方面,除了猕猴桃致病变种和菜豆致病变种外,所用的其他43株菌株的基因组上均不存在argK。因此,菜豆毒素的产生能力和argK基因的拥有情况仅在系统发育树上的两个点显示:第1组(猕猴桃致病变种)和第3组(菜豆致病变种)。对这两个致病型之间argK的同义距离和四个指标基因的串联组合序列进行t检验显示出高度显著性,表明argK基因(或argK - tox基因簇)经历了水平基因转移,并在致病型分离后在两个致病型中扩展了其分布,从而显示出与基因组非簇区域截然不同的碱基替换模式。