Silva Josué J da, Iamanaka Beatriz T, Ferranti Larissa S, Massi Fernanda P, Taniwaki Marta H, Puel Olivier, Lorber Sophie, Frisvad Jens C, Fungaro Maria Helena P
Centro de Ciências Biológicas, Universidade Estadual de Londrina, Londrina, Paraná 86057-970, Brazil.
Centro de Ciência e Qualidade de Alimentos, Instituto de Tecnologia de Alimentos, Campinas, São Paulo 13070-178, Brazil.
J Fungi (Basel). 2020 Dec 17;6(4):371. doi: 10.3390/jof6040371.
Diversity of species within clade, currently represented by and , was investigated combining three-locus gene sequences, , secondary metabolites profile and morphology. Firstly, approximately 700 accessions belonging to this clade were investigated using calmodulin gene sequences. Based on these sequences, eight haplotypes were clearly identified as ( = 247) and 17 as ( = 403). However, calmodulin sequences did not provide definitive species identities for six haplotypes. To elucidate the taxonomic position of these haplotypes, two other , part of the beta-tubulin gene and part of the RNA polymerase II gene, were sequenced and used to perform an analysis of Genealogical Concordance Phylogenetic Species Recognition. This analysis enabled the recognition of two new phylogenetic species. One of the new phylogenetic species showed morphological and chemical distinguishable features in comparison to the known species and . This species is illustrated and described as sp. nov. In contrast to and , strains produced asperazine, but none of them were found to produce ochratoxin A and/or fumonisins. Sclerotium production on laboratory media, which does not occur in strains of and and strictly sclerotium-associated secondary metabolites (14-Epi-hydroxy-10,23-dihydro-24,25-dehydroaflavinine; 10,23-Dihydro-24,25-dehydroaflavinine; 10,23-Dihydro-24,25-dehydro-21-oxo-aflavinine) were found in The strain type of sp. nov. is ITAL 47,456 (T) (=IBT 35556).
结合三个基因座的基因序列、次生代谢产物谱和形态学,对进化枝内目前由[具体名称1]和[具体名称2]代表的物种多样性进行了研究。首先,使用钙调蛋白基因序列对属于该进化枝的约700份种质进行了研究。基于这些序列,明确鉴定出8个单倍型为[单倍型1名称](n = 247),17个为[单倍型2名称](n = 403)。然而,钙调蛋白序列未能为6个单倍型提供明确的物种身份。为了阐明这些单倍型的分类地位,对另外两个基因,β-微管蛋白基因的一部分和RNA聚合酶II基因的一部分进行了测序,并用于进行系统发育一致性系统发育物种识别分析。该分析识别出两个新的系统发育物种。其中一个新的系统发育物种与已知物种[已知物种1名称]和[已知物种2名称]相比,具有形态和化学上可区分的特征。该物种被图示并描述为[新物种名称] sp. nov.。与[已知物种1名称]和[已知物种2名称]不同,[新物种名称]菌株产生曲霉嗪,但未发现它们产生赭曲霉毒素A和/或伏马菌素。在实验室培养基上产生菌核,这在[已知物种1名称]和[已知物种2名称]菌株中不会发生,并且在[新物种名称]中发现了与菌核严格相关的次生代谢产物(14-表-羟基-10,23-二氢-24,25-脱氢黄曲霉宁;10,23-二氢-24,25-脱氢黄曲霉宁;10,23-二氢-24,25-脱氢-21-氧代-黄曲霉宁)。[新物种名称] sp. nov.的模式菌株是ITAL 47,456(T)(= IBT 35556)。