Jelmer Dijkstra, Anouk C. van Westerhoven, Lucia Gomez-Gil, Carolina Aguilera-Galvez, Giuliana Nakasato-Tagami, Sebastien D. Garnier, Masaya Yamazaki, Tsutomu Arie, Takashi Kamakura, Takayuki Arazoe, Antonio Di Pietro, Michael F. Seidl, Gert H.J. Kema
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Here we determined the karyotype of F. oxysporum Tropical Race 4 (TR4), which causes the ongoing pandemic of Fusarium wilt of banana (FWB). We show that the single accessory chromosome of TR4 isolate II5 has undergone extensive intrachromosomal duplications, resulting in triplication of the chromosome size compared to other closely related TR4 strains. By obtaining mutant strains that have lost the accessory chromosome, we demonstrate that this chromosome is dispensable for vegetative growth but is required for full virulence on banana. Lastly, we found that the loss of chromosome 12 co-occurs with structural rearrangements of core chromosomes, which are generally co-linear between members of the F. oxysporum species complex. 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引用次数: 0
摘要
丝状真菌进化出了分区基因组,由保守的核心区和动态的附属区组成,有助于适应不断变化的环境,包括与宿主生物的相互作用。在氧孢镰刀菌物种群中,附属区在感染过程中发挥着重要作用,有报道称这些区域经历了大量的复制,但目前还不清楚这种复制是如何形成附属区的。此外,除了编码毒力效应因子外,附属区的功能也不完全清楚。在这里,我们测定了导致香蕉镰刀菌枯萎病(FWB)大流行的 F. oxysporum 热带第 4 种族(TR4)的核型。我们发现 TR4 分离物 II5 的单条附属染色体经历了广泛的染色体内复制,与其他近缘 TR4 株系相比,染色体大小增加了两倍。通过获得失去附属染色体的突变株,我们证明了该染色体对无性繁殖是不可或缺的,但对香蕉的完全毒力却是必需的。最后,我们发现 12 号染色体的缺失与核心染色体的结构重排同时发生,这在 F. oxysporum 物种复合体成员之间通常是共线性的。总之,我们的研究结果为我们提供了有关氧孢子菌种群中香蕉感染 TR4 系染色体动态的新见解。
Extensive intrachromosomal duplications in a virulence-associated fungal accessory chromosome
Filamentous fungi have evolved compartmentalized genomes consisting of conserved core regions and dynamic accessory regions, which aid the adaptation to changing environments including the interaction with host organisms. In the Fusarium oxysporum species complex, accessory regions play an important role during infection and it has been reported that these regions undergo extensive duplications, however, it is currently unknown how such duplications shape accessory regions. Moreover, the function of accessory regions apart from encoding virulence effectors is not completely understood. Here we determined the karyotype of F. oxysporum Tropical Race 4 (TR4), which causes the ongoing pandemic of Fusarium wilt of banana (FWB). We show that the single accessory chromosome of TR4 isolate II5 has undergone extensive intrachromosomal duplications, resulting in triplication of the chromosome size compared to other closely related TR4 strains. By obtaining mutant strains that have lost the accessory chromosome, we demonstrate that this chromosome is dispensable for vegetative growth but is required for full virulence on banana. Lastly, we found that the loss of chromosome 12 co-occurs with structural rearrangements of core chromosomes, which are generally co-linear between members of the F. oxysporum species complex. Together, our results provide new insights into the chromosome dynamics of the banana infecting TR4 lineage of the F. oxysporum species complex.