Zhao Youfu, Ma Zhonghua, Sundin George W
Department of Plant Pathology, Michigan State University, East Lansing, MI 48824, USA.
J Bacteriol. 2005 Mar;187(6):2113-26. doi: 10.1128/JB.187.6.2113-2126.2005.
Members of the pPT23A plasmid family of Pseudomonas syringae play an important role in the interaction of this bacterial pathogen with host plants. Complete sequence analysis of several pPT23A family plasmids (PFPs) has provided a glimpse of the gene content and virulence function of these plasmids. We constructed a macroarray containing 161 genes to estimate and compare the gene contents of 23 newly analyzed and eight known PFPs from 12 pathovars of P. syringae, which belong to four genomospecies. Hybridization results revealed that PFPs could be distinguished by the type IV secretion system (T4SS) encoded and separated into four groups. Twelve PFPs along with pPSR1 from P. syringae pv. syringae, pPh1448B from P. syringae pv. phaseolicola, and pPMA4326A from P. syringae pv. maculicola encoded a type IVA T4SS (VirB-VirD4 conjugative system), whereas 10 PFPs along with pDC3000A and pDC3000B from P. syringae pv. tomato encoded a type IVB T4SS (tra system). Two plasmids encoded both T4SSs, whereas six other plasmids carried none or only a few genes of either the type IVA or type IVB secretion system. Most PFPs hybridized to more than one putative type III secretion system effector gene and to a variety of additional genes encoding known P. syringae virulence factors. The overall gene contents of individual PFPs were more similar among plasmids within each of the four groups based on T4SS genes; however, a number of genes, encoding plasmid-specific functions or hypothetical proteins, were shared among plasmids from different T4SS groups. The only gene shared by all PFPs in this study was the repA gene, which encoded sequences with 87 to 99% amino acid identityamong 25 sequences examined. We proposed a model to illustrate the evolution and gene acquisition of the pPT23A plasmid family. To our knowledge, this is the first such attempt to conduct a global genetic analysis of this important plasmid family.
丁香假单胞菌的pPT23A质粒家族成员在这种细菌病原体与宿主植物的相互作用中发挥着重要作用。对几个pPT23A家族质粒(PFPs)进行的全序列分析,让我们得以初步了解这些质粒的基因组成和毒力功能。我们构建了一个包含161个基因的宏阵列,以评估和比较来自丁香假单胞菌12个致病变种(属于四个基因组种)的23个新分析的PFPs和8个已知PFPs的基因组成。杂交结果显示,PFPs可根据所编码的IV型分泌系统(T4SS)进行区分,并分为四组。12个PFPs以及来自丁香假单胞菌丁香致病变种的pPSR1、来自菜豆致病变种的pPh1448B和来自番茄斑疹致病变种的pPMA4326A编码IVA型T4SS(VirB-VirD4接合系统),而10个PFPs以及来自丁香假单胞菌番茄致病变种的pDC3000A和pDC3000B编码IVB型T4SS(tra系统)。两个质粒编码了两种T4SS,而其他六个质粒要么没有携带IVA型或IVB型分泌系统的任何基因,要么只携带了少数几个该系统的基因。大多数PFPs与不止一个假定的III型分泌系统效应子基因以及各种编码已知丁香假单胞菌毒力因子的其他基因杂交。基于T4SS基因,四个组中每个组内各个PFPs的总体基因组成彼此更为相似;然而,一些编码质粒特异性功能或假定蛋白的基因在来自不同T4SS组的质粒之间是共享的。本研究中所有PFPs共有的唯一基因是repA基因,在所检测的25个序列中,该基因编码的序列氨基酸同一性为87%至99%。我们提出了一个模型来说明pPT23A质粒家族的进化和基因获得情况。据我们所知,这是首次对这个重要质粒家族进行全面的遗传分析。