Sesma A, Sundin GW, Murillo J
Laboratorio de Patologia Vegetal, Escuela Tecnica Superior de Ingenieros Agronomos, Universidad Publica de Navarra, 31006 Pamplona, Spain.
Appl Environ Microbiol. 1998 Oct;64(10):3948-53. doi: 10.1128/AEM.64.10.3948-3953.1998.
Many Pseudomonas syringae strains contain native plasmids that are important for host-pathogen interactions, and most of them contain several coexisting plasmids (pPT23A-like plasmids) that cross-hybridize to replication sequences from pPT23A, which also carries a gene cluster coding for the phytotoxin coronatine in P. syringae pv. tomato PT23. In this study, three functional pPT23A-like replicons were cloned from P. syringae pv. glycinea race 6, suggesting that the compatibility of highly related replicons is a common feature of P. syringae strains. Hybridization experiments using three separate incompatibility determinants previously identified from pPT23A and the rulAB (UV radiation tolerance) genes showed that the organization of the replication region among pPT23A-like plasmids from several P. syringae pathovars is poorly conserved. The putative repA gene from four pPT23A-like replicons from P. syringae pv. glycinea race 6 was amplified by using specific primers. The restriction profiles of the resulting PCR products for the race 6 plasmids were more similar to each other than they were to that of pPT23A. These data, together with the existence of other cross-hybridizing DNA regions around the replicon among the race 6 pPT23A-like plasmids, suggest that some of these plasmids may have originated from duplication events. Our results also imply that modifications of the repA sequences and the poor conservation of putative maintenance determinants contribute to the suppression of incompatibility among members of the pPT23A-like family, thus enhancing the genomic plasticity of P. syringae.
许多丁香假单胞菌菌株含有对宿主 - 病原体相互作用很重要的天然质粒,并且其中大多数含有几个共存的质粒(pPT23A样质粒),这些质粒与来自pPT23A的复制序列交叉杂交,pPT23A在丁香假单胞菌番茄致病变种PT23中还携带一个编码植物毒素冠菌素的基因簇。在本研究中,从丁香假单胞菌大豆致病变种6号小种中克隆了三个功能性pPT23A样复制子,这表明高度相关复制子的兼容性是丁香假单胞菌菌株的一个共同特征。使用先前从pPT23A鉴定出的三个单独的不相容性决定簇和rulAB(耐紫外线辐射)基因进行的杂交实验表明,来自几种丁香假单胞菌致病型的pPT23A样质粒之间复制区域的组织保守性很差。通过使用特异性引物扩增了来自丁香假单胞菌大豆致病变种6号小种的四个pPT23A样复制子的假定repA基因。所得6号小种质粒PCR产物的限制性图谱彼此之间比与pPT23A的限制性图谱更相似。这些数据,连同6号小种pPT23A样质粒之间复制子周围其他交叉杂交DNA区域的存在,表明其中一些质粒可能起源于重复事件。我们的结果还表明,repA序列的修饰和假定的维持决定簇的保守性差有助于抑制pPT23A样家族成员之间的不相容性,从而增强了丁香假单胞菌的基因组可塑性。