Next generation sequencing technologies have revolutionized microbial ecology, revealing the extensive diversity of bacteria and archaea in our planet (Bates et al., 2011;Thompson et al., 2017), and providing insights into their ecology (Fierer & Jackson, 2006;Martiny et al., 2006). The popularity of amplicon sequencing, where a section of a universal marker gene is amplified and sequenced, has soared over the past decade. In soil, amplicon sequencing of the 16S rRNA gene has been especially useful, as soil prokaryotes remain largely uncultured but are extremely diverse, and perform key ecosystem functions (Steen et al., 2019).Soil eukaryotes, including protists, worms, arthropods, fungi, plant roots, and others, have received comparatively less attention. This is due to technological difficulties associated with sampling, including the complexity and heterogeneity of the soil matrix (Orgiazzi et al., 2016). Consequently, data on the diversity and distributions of soil meso-and macrofauna are limited (Cameron et al., 2019), largely because the identification of these organisms is body size-specific, labour-intensive, and requires a deep knowledge of organisms' morphologies or specific biochemistry (Orgiazzi et al., 2016). Nevertheless, soil eukaryotes are essential to soil functions, as both consumers and ecosystem engineers (Thakur et al., 2019). Amplicon sequencing has become an increasingly attractive alternative for the identification of soil eukaryotes (Pawlowski et al., 2020).Universal marker genes including the ITS region, as well as the 18S rRNA, mitochondrial 16S rRNA, and COI genes, have been used to assess the global diversity of fungi (