Sesma Ane, Sundin George W, Murillo Jesús
Instituto de Agrobiotecnologı́a y Recursos Naturales, CSIC-UPNA, and Laboratorio de Patologı́a Vegetal, Departamento de Producción Agraria, Universidad Pública de Navarra, 31006 Pamplona, Spain1.
Department of Plant Pathology and Microbiology, Texas A&M University, College Station, TX 77843-2132, USA2.
Microbiology (Reading). 2000 Oct;146 ( Pt 10):2375-2384. doi: 10.1099/00221287-146-10-2375.
It was previously shown that most Pseudomonas syringae strains contain one or more plasmids with cross-hybridizing replication regions and other areas of homology, and these plasmids were designated the pPT23A-like family. The majority of these plasmids encode genes conferring epiphytic fitness or resistance to antibacterial compounds and those investigated in this study are essential for pathogenicity or increased virulence. The phylogeny of 14 pPT23A-like plasmids from five P. syringae pathovars was studied by comparing a fragment of the sequence of their repA genes (encoding a replicase essential for replication). In the phylogenetic tree obtained, four groups (< or =88.8% identity between their members) could be identified. The first group contained the plasmids from three P. syringae pv. tomato strains, a P. syringae pv. apii strain and five out of the seven P. syringae pv. syringae strains, with identity ranging between 88.8 and 100%. The clustering of the pv. syringae strains did not reflect host specialization or previously reported phylogenetic relationships. The second group contained the plasmids from two strains of pv. glycinea and pv. tomato (95.5% identity), and it also included the previously sequenced replicon of a pathogenicity plasmid from P. syringae pv. phaseolicola. The plasmids from the remaining two pv. syringae strains were distantly related to the other plasmid sequences. Hybridization experiments using different genes or transposable elements previously described as plasmid-borne in P. syringae, showed that the gene content of highly related plasmids could be dissimilar, suggesting the occurrence of major plasmid reorganizations. Additionally, the phylogeny of the different native plasmids did not always correlate with the phylogeny of their harbouring strains, as determined by the analysis of extragenic repetitive consensus (ERIC) and arbitrarily primed PCR (AP-PCR) products. Collectively, these results suggest that pPT23A-like plasmids were, in most cases, acquired early during evolution.
先前的研究表明,大多数丁香假单胞菌菌株含有一个或多个具有交叉杂交复制区域和其他同源区域的质粒,这些质粒被归为pPT23A样家族。这些质粒中的大多数编码赋予附生适应性或对抗菌化合物抗性的基因,本研究中所研究的这些基因对于致病性或增强的毒力至关重要。通过比较来自五个丁香假单胞菌致病型的14个pPT23A样质粒的repA基因(编码复制所必需的复制酶)序列片段,对其系统发育进行了研究。在得到的系统发育树中,可以识别出四个组(其成员之间的同一性≤88.8%)。第一组包含来自三个丁香假单胞菌番茄致病型菌株、一个芹菜致病型菌株以及七个丁香假单胞菌丁香致病型菌株中的五个菌株的质粒,同一性在88.8%至100%之间。丁香致病型菌株的聚类并未反映宿主特异性或先前报道的系统发育关系。第二组包含来自大豆致病型和番茄致病型的两个菌株的质粒(同一性为95.5%),并且还包括先前测序的来自菜豆致病型丁香假单胞菌的致病性质粒的复制子。其余两个丁香致病型菌株的质粒与其他质粒序列的关系较远。使用先前描述为丁香假单胞菌中质粒携带的不同基因或转座元件进行的杂交实验表明,高度相关质粒的基因内容可能不同,这表明发生了主要的质粒重组。此外,通过对基因外重复一致序列(ERIC)和任意引物PCR(AP-PCR)产物的分析确定,不同天然质粒的系统发育并不总是与其宿主菌株的系统发育相关。总体而言,这些结果表明,在大多数情况下,pPT23A样质粒是在进化早期获得的。