Laboratory of Phytopathology, Wageningen University & Research, Wageningen 6700 AA, The Netherlands.
Theoretical Biology and Bioinformatics, Department of Biology, Utrecht University, Utrecht 3584 CS, The Netherlands.
G3 (Bethesda). 2024 Mar 6;14(3). doi: 10.1093/g3journal/jkad262.
Accurate taxonomic classification of samples from infected host material is essential for disease diagnostics and genome analyses. Despite the importance, diagnosis of fungal pathogens causing banana leaf diseases remains challenging. Foliar diseases of bananas are mainly caused by 3 Pseudocercospora species, of which the most predominant causal agent is Pseudocercospora fijiensis. Here, we sequenced and assembled four fungal isolates obtained from necrotic banana leaves in Bohol (Philippines) and obtained a high-quality genome assembly for one of these isolates. The samples were initially identified as P. fijiensis using PCR diagnostics; however, the assembly size was consistently 30 Mb smaller than expected. Based on the internal transcribed spacer (ITS) sequences, we identified the samples as Zasmidium syzygii (98.7% identity). The high-quality Zasmidium syzygii assembly is 42.5 Mb in size, comprising 16 contigs, of which 11 are most likely complete chromosomes. The genome contains 98.6% of the expected single-copy BUSCO genes and contains 14,789 genes and 10.3% repeats. The 3 short-read assemblies are less continuous but have similar genome sizes (40.4-42.4 Mb) and contain between 96.5 and 98.4% BUSCO genes. All 4 isolates have identical ITS sequences and are distinct from Zasmidium isolates that were previously sampled from banana leaves. We thus report the first continuous genome assembly of a member of the Zasmidium genus, forming an essential resource for further analysis to enhance our understanding of the diversity of pathogenic fungal isolates as well as fungal diversity.
准确的分类学鉴定对于感染宿主材料的样本至关重要,这对于疾病诊断和基因组分析至关重要。尽管意义重大,但引起香蕉叶病害的真菌病原体的诊断仍然具有挑战性。香蕉叶片病害主要由 3 种假尾孢菌引起,其中最主要的病原体是斐济假尾孢菌。在这里,我们对从菲律宾薄荷岛坏死的香蕉叶片中获得的四个真菌分离物进行了测序和组装,并获得了其中一个分离物的高质量基因组组装。这些样本最初使用 PCR 诊断方法鉴定为 P. fijiensis;然而,组装大小始终比预期小 30Mb。基于内部转录间隔区(ITS)序列,我们将这些样本鉴定为 Zasmidium syzygii(98.7%的同源性)。高质量的 Zasmidium syzygii 组装大小为 42.5Mb,包含 16 个 contigs,其中 11 个很可能是完整的染色体。基因组包含 98.6%预期的单拷贝 BUSCO 基因,包含 14789 个基因和 10.3%的重复序列。这 3 个短读长组装的连续性较差,但基因组大小相似(40.4-42.4Mb),并且包含 96.5-98.4%的 BUSCO 基因。所有 4 个分离物的 ITS 序列完全相同,与之前从香蕉叶片中采样的 Zasmidium 分离物不同。因此,我们报告了 Zasmidium 属成员的第一个连续基因组组装,为进一步分析提供了重要资源,以增强我们对致病真菌分离物多样性以及真菌多样性的理解。