4.7 Article

Long-read PacBio genome sequencing of four environmental saprophytic Sporothrix species spanning the pathogenic clade

Journal

BMC GENOMICS
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12864-022-08736-w

Keywords

Sporothrix phasma; Sporothrix curviconia; Sporothrix protearum; Sporothrix variecibatus; Sporotrichosis; SMRT PacBio sequencing; Long-read sequencing; De novo assembly; Comparative genomics

Funding

  1. National Science Foundation of China [81371746, 81974300]
  2. China Postdoctoral Science Foundation [2020T130151ZX]
  3. Science and Technology Planning Project of Guangdong [2016A020215066]
  4. Special Project of Supercomputer Application of Sun Yat-sen University, Guangzhou, China [20190507269]
  5. University of Messina, Italy [36036]

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This study presents the annotated genome assemblies of four environmental Sporothrix species generated using PacBio SMRT sequencing data. The results show differences in genome size and gene content among these Sporothrix species, as well as differences in transposable elements and orthologous genes. Carbohydrate-active enzyme analysis reveals no significant differences between pathogenic and environmental species. The assembly of mitochondrial genomes is also reported. These findings provide a starting point for future studies on the diversification, ecological/host adaptation, and origin of pathogenic lineages within the genus Sporothrix.
Background: The genus Sporothrix belongs to the order Ophiostomatales and contains mainly saprobic soil and plant fungi, although pathogenic species capable of causing human infections are also present. The whole-genomes of disease-causing species have already been sequenced and annotated but no comprehensive genomic resources for environmental Sporothrix species are available, thus limiting our understanding of the evolutionary origin of virulence-related genes and pathogenicity. Result: The genome assembly of four environmental Sporothrix species resulted in genome size of similar to 30.9 Mbp in Sporothrix phasma, similar to 35 Mbp in S. curviconia, similar to 38.7 Mbp in S. protearum, and similar to 39 Mbp in S. variecibatus, with a variable gene content, ranging from 8142 (S. phasma) to 9502 (S. variecibatus). The analysis of mobile genetic elements showed significant differences in the content of transposable elements within the sequenced genomes, with the genome of S. phasma lacking several class I and class II transposons, compared to the other Sporothrix genomes investigated. Moreover, the comparative analysis of orthologous genes shared by clinical and environmental Sporothrix genomes revealed the presence of 3622 orthogroups shared by all species, whereas over 4200 genes were species-specific single-copy gene products. Carbohydrate-active enzyme analysis revealed a total of 2608 protein-coding genes containing single and/or multiple CAZy domains, resulting in no statistically significant differences among pathogenic and environmental species. Nevertheless, some families were not found in clinical species. Furthermore, for each sequenced Sporothrix species, the mitochondrial genomes was assembled in a single circular DNA molecule, ranging from 25,765 bp (S. variecibatus) to 58,395 bp (S. phasma). Conclusion: In this study, we present four annotated genome assemblies generated using PacBio SMRT sequencing data from four environmental species: S. curviconia, S. phasma, S. protearum and S. variecibatus with the aim to provide a starting point for future comparative genome evolution studies addressing species diversification, ecological/host adaptation and origin of pathogenic lineages within the genus Sporothrix.

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