Pionnat S, Keller H, Héricher D, Bettachini A, Dessaux Y, Nesme X, Poncet C
Institut National de la Recherche Agronomique (INRA), Phytopathologie et Botanique, Unité Santé Végétale et Environnement, 06606 Antibes Cedex, France.
Appl Environ Microbiol. 1999 Sep;65(9):4197-206. doi: 10.1128/AEM.65.9.4197-4206.1999.
Crown gall caused by Agrobacterium is one of the predominant diseases encountered in rose cultures. However, our current knowledge of the bacterial strains that invade rose plants and the way in which they spread is limited. Here, we describe the integrated physiological and molecular analyses of 30 Agrobacterium isolates obtained from crown gall tumors and of several reference strains. Characterization was based on the determination of the biovar, analysis of 16S ribosomal DNA restriction fragment length polymorphisms by PCR (PCR-RFLP), elucidation of the opine type, and PCR-RFLP analysis of genes involved in virulence and oncogenesis. This study led to the classification of rose isolates into seven groups with common chromosome characteristics and seven groups with common Ti plasmid characteristics. Altogether, the rose isolates formed 14 independent groups, with no specific association of plasmid- and chromosome-encoded traits. The predominant Ti plasmid characteristic was that 16 of the isolates induced the production of the uncommon opine succinamopine, while the other 14 were nopaline-producing isolates. With the exception of one, all succinamopine Ti plasmids belonged to the same plasmid group. Conversely, the nopaline Ti plasmids belonged to five groups, one of these containing seven isolates. We showed that outbreaks of disease provoked by the succinamopine-producing isolates in different countries and nurseries concurred with a common origin of specific rootstock clones. Similarly, groups of nopaline-producing isolates were associated with particular rootstock clones. These results strongly suggest that the causal agent of crown gall disease in rose plants is transmitted via rootstock material.
由土壤杆菌引起的冠瘿病是玫瑰栽培中常见的主要病害之一。然而,我们目前对侵入玫瑰植株的细菌菌株及其传播方式的了解有限。在此,我们描述了从冠瘿瘤中获得的30株土壤杆菌分离株以及几种参考菌株的综合生理和分子分析。鉴定基于生物型的测定、通过聚合酶链反应(PCR-RFLP)分析16S核糖体DNA限制性片段长度多态性、确定冠瘿碱类型以及对参与毒力和肿瘤发生的基因进行PCR-RFLP分析。这项研究导致将玫瑰分离株分为具有共同染色体特征的七组和具有共同Ti质粒特征的七组。总的来说,玫瑰分离株形成了14个独立的组,质粒和染色体编码性状之间没有特定关联。主要的Ti质粒特征是,16株分离株诱导产生不常见的冠瘿碱琥珀酰冠瘿碱,而其他14株是产生胭脂碱的分离株。除了一株外,所有琥珀酰冠瘿碱Ti质粒都属于同一质粒组。相反,胭脂碱Ti质粒属于五组,其中一组包含七株分离株。我们表明,在不同国家和苗圃中由产生琥珀酰冠瘿碱的分离株引发的疾病爆发与特定砧木克隆的共同起源一致。同样,产生胭脂碱的分离株组与特定的砧木克隆相关。这些结果强烈表明,玫瑰植株冠瘿病的病原体是通过砧木材料传播的。