Takamatsu Susumu, Ito Arakawa Hanako, Shiroya Yoshiaki, Kiss Levente, Heluta Vasyl
Department of Bioresources, Graduate School, Mie University, 1577 Kurima-Machiya, Tsu 514-8507, Japan
Department of Bioresources, Graduate School, Mie University, 1577 Kurima-Machiya, Tsu 514-8507, Japan.
Mycologia. 2015 Sep-Oct;107(5):903-14. doi: 10.3852/15-062. Epub 2015 Aug 3.
Phylogenetic relationships of the Uncinula lineage, which is the basal group in the genus Erysiphe, were investigated with 167 sequences of nuc ITS1-5. 8S-ITS2 and the 28S rDNA regions. Backbone tree analyses with six datasets and two tree-constructing methods revealed that the Uncinula lineage is divided into seven distinct clades. Clades 1-5 each contained a representative powdery mildew species, namely E. australiana in Clade 1, E. liquidambaris in Clade 2, E. adunca in Clade 3, E. fraxinicola in Clade 4 and E. actinidiae in Clade 5. Clade 6 comprises 71 sequences including the Microsphaera lineage and 17 species of the Uncinula lineage, such as E. carpinicola, E. carpinilaxiflorae, E. miyabei, E. glycines and E. necator. Topology tests supported the Microsphaera lineage forming a monophyletic clade in Clade 6, suggesting that Microsphaera-type appendages appeared only once in this clade to diverge into the Microsphaera lineage. Clade 7 consists of 72 sequences containing 30 species, including species of sects. Californiomyces and Typhulochaeta, four species from Nothofagus, species of sect. Erysiphe parasitising herbaceous plants belonging to the Asteraceae, Rosaceae and Saxifragaceae. Molecular clock analysis suggests that the major seven clades appeared 50-30 million years ago (Ma) in the Paleogene Period. The Microsphaera lineage may have split from the Uncinula lineage at the boundary of the Paleogene and Neogene, when appendages with dichotomously branched tips appeared. The clade of the species on Nothofagus split from the northern hemisphere species about 20-10 million years ago (Ma) in the Miocene Epoch, and host-shift from trees to herbs also might have occurred in this period.
利用核内转录间隔区1(ITS1)-5.8S-ITS2和28S核糖体DNA(rDNA)区域的167个序列,对白粉菌属基部类群钩丝壳谱系的系统发育关系进行了研究。采用六个数据集和两种建树方法进行的主干树分析表明,钩丝壳谱系分为七个不同的分支。分支1-5各包含一种代表性白粉菌物种,即分支1中的澳洲白粉菌、分支2中的枫香白粉菌、分支3中的弯丝白粉菌、分支4中的梣生白粉菌和分支5中的猕猴桃白粉菌。分支6包含71个序列,包括小钩丝壳谱系以及钩丝壳谱系的17个物种,如麻栎白粉菌、麻栎长花白粉菌、宫部白粉菌、大豆白粉菌和烟草白粉菌。拓扑结构检验支持小钩丝壳谱系在分支6中形成一个单系分支,这表明小钩丝壳型附属丝在该分支中仅出现一次并分化形成小钩丝壳谱系。分支7由72个序列组成,包含30个物种,包括加州白粉菌组和拟丝钩白粉菌组的物种、来自假山毛榉属的四个物种、寄生在菊科、蔷薇科和虎耳草科草本植物上的白粉菌组物种。分子钟分析表明,这七个主要分支在古近纪时期距今5000万至3000万年前(Ma)出现。小钩丝壳谱系可能在古近纪和新近纪的边界处从钩丝壳谱系中分化出来,当时出现了具二叉分枝顶端的附属丝。假山毛榉属上的物种分支在中新世距今约2000万至1000万年前(Ma)从北半球物种中分化出来,并且在这一时期也可能发生了从树木到草本植物的寄主转移。