de Beer Z W, Procter M, Wingfield M J, Marincowitz S, Duong T A
Department of Biochemistry, Genetics & Microbiology; Forestry and Agricultural Research Institute (FABI), University of Pretoria, Pretoria 0002, South Africa.
Stud Mycol. 2022 Jul;101:57-120. doi: 10.3114/sim.2022.101.02. Epub 2022 Mar 30.
The was erected in 1980. Since that time, several of the genera have been redefined and others have been described. There are currently 14 accepted genera in the Order. They include species that are the causal agents of plant and human diseases and common associates of insects such as bark beetles. Well known examples include the Dutch elm disease fungi and the causal agents of sporotrichosis in humans and animals. The taxonomy of the was confused for many years, mainly due to the convergent evolution of morphological characters used to delimit unrelated fungal taxa. The emergence of DNA-based methods has resolved much of this confusion. However, the delineation of some genera and the placement of various species and smaller lineages remains inconclusive. In this study we reconsidered the generic boundaries within the . A phylogenomic framework constructed from genome-wide sequence data for 31 species representing the major genera in the Order was used as a guide to delineate genera. This framework also informed our choice of the best markers from the currently most commonly used gene regions for taxonomic studies of these fungi. DNA was amplified and sequenced for more than 200 species, representing all lineages in the Order. We constructed phylogenetic trees based on the different gene regions and assembled a concatenated data set utilising a suite of phylogenetic analyses. The results supported and confirmed the delineation of nine of the 14 currently accepted genera, and . The two most recently described genera, and , were not included in the multi-locus analyses. This was due to their high sequence divergence, which was shown to result in ambiguous taxonomic placement, even though the results of phylogenomic analysis supported their inclusion in the . In addition to the currently accepted genera in the , well-supported lineages emerged that were distinct from those genera. These are described as novel genera. Two lineages included the type species of and and these genera are thus reinstated and their circumscriptions redefined. The descriptions of all genera in the were standardised and refined where this was required and 39 new combinations have been provided for species in the newly emerging genera and one new combination has been provided for . The placement of could not be confirmed using the available data and the genus has been treated as in the . was not included in this study, due to the absence of living material available for this monotypic fossil genus. Overall, this study has provided the most comprehensive and robust phylogenies currently possible for the . It has also clarified several unresolved One Fungus-One Name nomenclatural issues relevant to the Order. Z.W. de Beer & M. Procter, Z.W. de Beer & M. Procter, Z.W. de Beer & M. Procter, Z.W. de Beer & M. Procter. M. Procter & Z.W. de Beer. (M. Morelet) M. Procter & Z.W. de Beer, (Kubono & Shin. Ito) M. Procter & Z.W. de Beer, (K.H. Kim ) M. Procter & Z.W. de Beer, (L.R. Batra) M. Procter & Z.W. de Beer, (Masuya) M. Procter & Z.W. de Beer, (K. Jacobs & M.J. Wingf.) M. Procter & Z.W. de Beer, (Paciura .) M. Procter & Z.W. de Beer, (Jankowiak .) M. Procter & Z.W. de Beer, (Paciura .) M. Procter & Z.W. de Beer, (K. Jacobs & M.J. Wingf.) M. Procter & Z.W. de Beer, (R. Chang .) M. Procter & Z.W. de Beer, (de Errasti & Z.W. de Beer) M. Procter & Z.W. de Beer, (X.W. Liu ) M. Procter & Z.W. de Beer, (Paciura ) M. Procter & Z.W. de Beer, (Masuya & M.J. Wingf.) M. Procter & Z.W. de Beer, (Linnak. .) M. Procter & Z.W. de Beer, (Jankowiak ) M. Procter & Z.W. de Beer, (D.R. Simmons ) M. Procter & Z.W. de Beer, (L.R. Batra) M. Procter & Z.W. de Beer, (T.C. Harr. ) Z.W. de Beer & M. Procter, (Kowalski & Butin) Z.W. de Beer & M. Procter, (Arx) M. Procter & Z.W. de Beer, (B. Strzałka & Jankowiak) Z.W. de Beer & M. Procter, (Olchow. & J. Reid) M. Procter & Z.W. de Beer, (R.W. Davidson) M. Procter & Z.W. de Beer, (R.W. Davidson & Eslyn) M. Procter & Z.W. de Beer, (R.W. Davidson) Z.W. de Beer & M. Procter, (Olchow. & J. Reid) M. Procter & Z.W. de Beer, (E.F. Wright & Cain) M. Procter & Z.W. de Beer, (B.K. Bakshi) M. Procter & Z.W. de Beer, (Olchow. & J. Reid) M. Procter & Z.W. de Beer, (J.J. Kim ) M. Procter & Z.W. de Beer, (R. Chang & Z.W. de Beer) M. Procter & Z.W. de Beer, (B.K. Bakshi) M. Procter & Z.W. de Beer, (Masuya) Z.W. de Beer & M. Procter, (R. Chang ) M. Procter & Z.W. de Beer, (Z. Wang & Q. Lu) M. Procter & Z.W. de Beer, (Linnak. ) M. Procter & Z.W. de Beer, (Linnak. ) M. Procter & Z.W. de Beer, (Massee & E.S. Salmon) M. Procter & Z.W. de Beer. de Beer W, Procter M, Wingfield MJ, Marincowitz S, Duong TA (2022). Generic boundaries in the reconsidered and revised. : 57-120. doi: 10.3114/sim.2022.101.02.
该类群于1980年确立。自那时起,其中一些属被重新定义,还有一些属被描述。目前该目有14个公认的属。它们包括导致植物和人类疾病的物种以及诸如树皮甲虫等昆虫的常见共生菌。著名的例子包括荷兰榆树病真菌以及人和动物孢子丝菌病的病原体。多年来,该类群的分类一直很混乱,主要是由于用于界定不相关真菌类群的形态特征存在趋同进化。基于DNA的方法的出现解决了许多此类混乱问题。然而,一些属的划分以及各种物种和较小谱系的定位仍无定论。在本研究中,我们重新考虑了该类群内的属界。利用代表该目中主要属的31个物种的全基因组序列数据构建的系统发育基因组框架作为划分属的指南。该框架也为我们从目前最常用的基因区域中选择用于这些真菌分类研究的最佳标记提供了参考。对代表该目所有谱系的200多个物种进行了DNA扩增和测序。我们基于不同的基因区域构建了系统发育树,并利用一系列系统发育分析组装了一个串联数据集。结果支持并确认了目前14个公认属中的9个属的划分。最近描述的两个属未包含在多位点分析中。这是由于它们的序列分歧很大,这导致分类定位不明确,尽管系统发育基因组分析的结果支持将它们纳入该类群。除了该类群中目前公认的属之外,还出现了一些得到充分支持的谱系,它们与那些属不同。这些被描述为新属。两个谱系包括某属和另一属的模式种,因此这两个属被恢复,其范围也重新定义。对该类群中所有属的描述进行了标准化,并在需要的地方进行了完善,为新出现的属中的物种提供了39个新组合,为某属提供了1个新组合。利用现有数据无法确认某属的定位,在该类群中已将其视为另一属。由于缺乏可用于这个单型化石属的活材料,某属未包含在本研究中。总体而言,本研究为该类群提供了目前可能的最全面和最可靠的系统发育关系。它还澄清了与该目相关的几个未解决的“一个真菌一个名称”的命名问题。Z.W. 德比尔 & M. 普罗克特,Z.W. 德比尔 & M. 普罗克特,Z.W. 德比尔 & M. 普罗克特,Z.W. 德比尔 & M. 普罗克特。M. 普罗克特 & Z.W. 德比尔。(M. 莫雷莱) M. 普罗克特 & Z.W. 德比尔,(久保野 & 伊藤信) M. 普罗克特 & Z.W. 德比尔,(金基勋) M. 普罗克特 & Z.W. 德比尔,(L.R. 巴特拉) M. 普罗克特 & Z.W. 德比尔,(益屋) M. 普罗克特 & Z.W. 德比尔,(K. 雅各布斯 & M.J. 温菲尔德) M. 普罗克特 & Z.W. 德比尔,(帕丘拉) M. 普罗克特 & Z.W. 德比尔,(扬科维亚克) M. 普罗克特 & Z.W. 德比尔,(帕丘拉) M. 普罗克特 & Z.W. 德比尔,(K. 雅各布斯 & M.J. 温菲尔德) M. 普罗克特 & Z.W. 德比尔,(张润) M. 普罗克特 & Z.W. 德比尔,(德埃拉斯蒂 & Z.W. 德比尔) M. 普罗克特 & Z.W. 德比尔,(刘学武) M. 普罗克特 & Z.W. 德比尔,(帕丘拉) M. 普罗克特 & Z.W. 德比尔,(益屋 & M.J. 温菲尔德) M. 普罗克特 & Z.W. 德比尔,(林纳克) M. 普罗克特 & Z.W. 德比尔,(扬科维亚克) M. 普罗克特 & Z.W. 德比尔,(D.R. 西蒙斯) M. 普罗克特 & Z.W. 德比尔,(L.R. 巴特拉) M. 普罗克特 & Z.W. 德比尔,(T.C. 哈尔) Z.W. 德比尔 & M. 普罗克特,(科瓦尔斯基 & 布丁) Z.W. 德比尔 & M. 普罗克特,(阿尔克斯) M. 普罗克特 & Z.W. 德比尔,(B. 斯特尔扎尔卡 & 扬科维亚克) Z.W. 德比尔 & M. 普罗克特,(奥尔乔 & J. 里德) M. 普罗克特 & Z.W. 德比尔,(R.W. 戴维森) M. 普罗克特 & Z.W. 德比尔,(R.W. 戴维森 & 埃斯林) M. 普罗克特 & Z.W. 德比尔,(R.W. 戴维森) Z.W. 德比尔 & M. 普罗克特,(奥尔乔 & J. 里德) M. 普罗克特 & Z.W. 德比尔,(E.F. 赖特 & 凯恩) M. 普罗克特 & Z.W. 德比尔,(B.K. 巴克希) M. 普罗克特 & Z.W. 德比尔,(奥尔乔 & J. 里德) M. 普罗克特 & Z.W. 德比尔,(J.J. 金) M. 普罗克特 & Z.W. 德比尔,(张润 & Z.W. 德比尔) M. 普罗克特 & Z.W. 德比尔,(B.K. 巴克希) M. 普罗克特 & Z.W. 德比尔,(益屋) Z.W. 德比尔 & M. 普罗克特,(张润) M. 普罗克特 & Z.W. 德比尔,(王泽 & 卢强) M. 普罗克特 & Z.W. 德比尔,(林纳克) M. 普罗克特 & Z.W. 德比尔,(林纳克) M. 普罗克特 & Z.W. 德比尔,(马斯 & E.S. 萨蒙) M. 普罗克特 & Z.W. 德比尔。德比尔W、普罗克特M、温菲尔德MJ、马林科维茨S、杜昂TA (2022年)。重新考虑和修订了该类群的属界。《真菌学研究》:57 - 120页。doi: 10.3114/sim.2022.101.02 。