INRA, UMR 1345 Institut de Recherche en Horticulture et Semences (IRHS), INRA, Agrocampus-Ouest, Université d’Angers, Beaucouzé, France.
Appl Environ Microbiol. 2012 May;78(9):3266-79. doi: 10.1128/AEM.06655-11. Epub 2012 Mar 2.
Pseudomonas syringae pv. maculicola causes bacterial spot on Brassicaceae worldwide, and for the last 10 years severe outbreaks have been reported in the Loire Valley, France. P. syringae pv. maculicola resembles P. syringae pv. tomato in that it is also pathogenic for tomato and causes the same types of symptoms. We used a collection of 106 strains of P. syringae to characterize the relationships between P. syringae pv. maculicola and related pathovars, paying special attention to P. syringae pv. tomato. Phylogenetic analysis of gyrB and rpoD gene sequences showed that P. syringae pv. maculicola, which causes diseases in Brassicaceae, forms six genetic lineages within genomospecies 3 of P. syringae strains as defined by L. Gardan et al. (Int. J. Syst. Bacteriol. 49[Pt 2]:469-478, 1999), whereas P. syringae pv. tomato forms two distinct genetic lineages. A multilocus variable-number tandem-repeat (VNTR) analysis (MLVA) conducted with eight minisatellite loci confirmed the genetic structure obtained with rpoD and gyrB sequence analyses. These results provide promising tools for fine-scale epidemiological studies on diseases caused by P. syringae pv. maculicola and P. syringae pv. tomato. The two pathovars had distinct host ranges; only P. syringae pv. maculicola strains were pathogenic for Brassicaceae. A subpopulation of P. syringae pv. maculicola strains that are pathogenic for Pto-expressing tomato plants were shown to lack avrPto1 and avrPtoB or to contain a disrupted avrPtoB homolog. Taking phylogenetic and pathological features into account, our data suggest that the DC3000 strain belongs to P. syringae pv. maculicola. This study shows that P. syringae pv. maculicola and P. syringae pv. tomato appear multiclonal, as they did not diverge from a single common ancestral group within the ancestral P. syringae genomospecies 3, and suggests that pathovar specificity within P. syringae may be due to independent genetic events.
丁香假单胞菌 pv. 斑点病在世界各地引起十字花科植物的细菌性斑点病,在过去的 10 年中,法国卢瓦尔河谷报告了严重的疫情。丁香假单胞菌 pv. 斑点病与丁香假单胞菌 pv. 番茄在病原性方面相似,也会感染番茄并引起相同类型的症状。我们使用了 106 株丁香假单胞菌菌株的集合来描述丁香假单胞菌 pv. 斑点病和相关致病变种之间的关系,特别关注丁香假单胞菌 pv. 番茄。gyrB 和 rpoD 基因序列的系统发育分析表明,引起十字花科植物疾病的丁香假单胞菌 pv. 斑点病在 L. Gardan 等人定义的丁香假单胞菌基因组种 3 的菌株中形成了六个遗传谱系(国际系统细菌学杂志。49[Pt 2]:469-478,1999 年),而丁香假单胞菌 pv. 番茄形成了两个不同的遗传谱系。用 8 个微卫星位点进行的多位点可变数量串联重复(VNTR)分析(MLVA)证实了 rpoD 和 gyrB 序列分析获得的遗传结构。这些结果为丁香假单胞菌 pv. 斑点病和丁香假单胞菌 pv. 番茄引起的疾病的精细流行病学研究提供了有希望的工具。这两个致病变种具有不同的宿主范围;只有丁香假单胞菌 pv. 斑点病菌株对十字花科植物具有致病性。研究表明,对 Pto 表达的番茄植物具有致病性的丁香假单胞菌 pv. 斑点病菌株亚群缺乏 avrPto1 和 avrPtoB,或含有功能失调的 avrPtoB 同源物。考虑到系统发育和病理学特征,我们的数据表明 DC3000 菌株属于丁香假单胞菌 pv. 斑点病。本研究表明,丁香假单胞菌 pv. 斑点病和丁香假单胞菌 pv. 番茄似乎是多克隆的,因为它们没有从祖先的丁香假单胞菌基因组种 3 中的单个共同祖先群体中分化出来,并表明丁香假单胞菌中的致病变种特异性可能是由于独立的遗传事件。