Draft Genome Sequence of the Reference Strain of the Korean Medicinal Mushroom Wolfiporia cocos KMCC03342

Abstract

Wolfiporia cocos is a wood-decay brown rot fungus belonging to the family Polyporaceae. While the fungus grows, the sclerotium body of the strain, dubbed Bokryeong in Korean, is formed around the roots of conifer trees. The dried sclerotium has been widely used as a key component of many medicinal recipes in East Asia. Wolfiporia cocos strain KMCC03342 is the reference strain registered and maintained by the Korea Seed and Variety Service for commercial uses. Here, we present the first draft genome sequence of W. cocos KMCC03342 using a hybrid assembly technique combining both short- and long-read sequences. The genome has a total length of 55.5 Mb comprised of 343 contigs with N50 of 332 kb and 95.8% BUSCO completeness. The GC ratio was 52.2%. We predicted 14,296 protein-coding gene models based on ab initio gene prediction and evidence-based annotation procedure using RNAseq data. The annotated genome was predicted to have 19 terpene biosynthesis gene clusters, which was the same number as the previously sequenced W. cocos strain MD-104 genome but higher than Chinese W. cocos strains. The genome sequence and the predicted gene clusters allow us to study biosynthetic pathways for the active ingredients of W. cocos.

Keywords:

• Wolfiporia cocos
• secondary metabolite biosynthesis gene cluster
• whole genome sequence

1. Introduction

Wolfiporia cocos is a medicinal basidiomycete fungus decaying wood and has a subterranean growth habit in association with pine trees [1]. The fungus is known to develop a hard endurable underground sclerotium body during its life cycle [2]. The sclerotium of W. cocos has been widely used as a key component of traditional medicine in East Asia because of its pharmacological properties including diuretic and sedative effects [2]. Various polysaccharides and triterpenoids are thought to be the major bioactive component of W. cocos but their biosynthetic pathways are not fully understood yet [3]. Among many active components isolated from W. cocos, pachymic acid is one of the well-known triterpenoids that display antitumor and anti-inflammatory activities [4]. Comprehensive genomic analysis of W. cocos is required to understand the genetic basis of various biosynthetic pathways, which can guide scientists to breed commercial strains and use W. cocos as a potent medicine to treat a variety of human diseases. The genome sequence of the W. cocos strain MD-104 isolated in Florida, United States, had been first revealed by the U.S. Department of Energy Joint Genome Institute (JGI) as a part of the 1000 Fungal Genomes Project [5]. Several W. cocos strains sampled in China have been reported but only two of those Chinese W. cocos strain genome sequences were publicly available [6,7]. W. cocos strain KMCC03342 (Cultivar name: Bokryeong1ho) is the reference dikaryotic strain of the W. cocos in South Korea and is maintained by the Korea Seed and Variety Service. Here, we report the high-quality genome sequence of the reference strain, W. cocos KMCC03342, for the scientific community.

2. Methods and materials

2.1. DNA/RNA extraction and sequencing

Total DNA was extracted with a modified protocol based on DNeasy^® Plant Mini Kit (Qiagen, Hilden, Germany), described in the previous fungal genome project [8]. RNA was extracted with the Qiagen RNeasy^® Mini Kit (Qiagen) following the manufacturer’s protocol. The short read sequencing library for DNA and RNA sequencing was prepared with Illumina^® DNA Prep kit (Illumina, CA, USA) and NEBNext^® Ultra™ II RNA Library Prep Kit (New England Biolabs, USA), respectively. Sequencing was carried out on the Illumina MiSeq platform (Illumina) using Illumina MiSeq reagent kit V3 (300 bp paired-end). The long-read sequencing library was prepared using Oxford Nanopore Ligation Sequencing Kit (Oxford Nanopore, Oxford, UK). Sequencing was carried out on a MinION sequencing device (Oxford Nanopore) equipped with a MinION flow cell (R9.4.1) (Oxford Nanopore). PacBio single-molecule real-time (SMRT) sequencing was performed by Macrogen (Seoul, South Korea) on four SMRT cells using the PacBio RS II system.

2.2. Genome assembly and gene prediction

The initial assembly was assembled using the FALCON assembler (v0.4.0) with default options [9]. Draft de novo assembly was assembled using Canu assembler (v2.0) with default options [10]. Duplicated contigs from the draft genome were removed using the purge_dups (v1.2.5) program with default options [11]. Adapter sequences of short reads were removed using TrimGalore (v0.6.7) [12] with the ‘–paired’ option. Errors in the draft genome sequence were corrected with Racon (v1.4.11) [13] and Pilon (v1.24) [14] with default options. The mitochondrial genome sequence was removed from the assembly by BLAST+ (v.2.12.0+) [15] alignment of W. cocos strain BL16 mitochondrial genome sequence (GenBank accession: NC_050681.1) to the W. cocos strain KMCC03342 assembly. Genome completeness analyses were performed using BUSCO (v5.2.2) [16] with the OrthoDB fungi v10 (fungi_odb10) database.

Gene prediction was performed with FunGAP (v1.1.0) [17] using Laccaria bicolor for the AUGUSTUS species model and 20,875,982 reads from RNA-seq results as evidence for the gene models. Transposable element-related genes were removed with the detect_te_genes.py script from FunGAP.

2.3. Functional annotation

Functional annotation of predicted protein-coding genes was carried out with InterProScan (v.5.51-85) [18] for protein domain annotation. Secondary metabolite biosynthesis gene cluster analysis was performed by antiSMASH (v6.0.1) [19] with a ‘strict’ strictness option.

2.4. Genome tree building using single copy ortholog concatenation

A total of 34 fungi genomes of the order Polyporales were retrieved from the NCBI database for comparative analysis. The species tree was built using FastTree (v2.1) [20] from the single copy ortholog genes identified by OrthoFinder (v2.5.4) using diamond for sequence alignment [21]. Mafft (v7.490) [22] and ClipKIT (v1.3.0) [23] were used to align multiple sequences to extract the conserved sequences with ‘-m gappy’ for ClipKIT parameters.

3. Results and discussion

A total of 5.5 billion bases from 430,844 reads with an average read length of 12,702 bases were retrieved from long-read sequencing by the PacBio platform. The initial assembly assembled with PacBio reads only was comprised of 442 contigs and had a total length of 46.4 Mb but BUSCO revealed the genome completeness of 90.3%. To improve the quality of the reference genome, we added more sequencing data and employed a hybrid assembly technique using both short- and long-reads obtained from Illumina and Oxford Nanopore sequencing platforms, respectively. First, we obtained a total of 1.1 billion bases from 156,279 reads by sequencing with the Oxford Nanopore MinION platform. Reads from PacBio and Oxford Nanopore sequencing were combined for de novo assembly. Overlapping contigs from the diploid W. cocos KMCC03342 genome assembly was purged to a single contig. The assembly was polished with a total of 2.2 billion bases from 3,665,972 reads obtained from the Illumina MiSeq platform. The final polished assembly resulted in 343 contigs with the longest contig length of 1,489,262 bp and an N50 value of 332,393 bp. We found that genome completeness was also increased after polishing with short reads from 90.3 to 95.8% by the BUSCO analysis. The total length of the W. cocos KMCC03342 genome was 55,457,880 bp and the GC ratio was 52.2%. When compared to JGI W. cocos MD-104 genome assembly, the assembly of W. cocos KMCC03342 was considerably improved, showing a larger contig N50 value (332,393 bp) than that of the MD-104 (109,659 bp) with a smaller number (343) of contigs than that of the MD-104 (2,228) (Table 1). The genome of W. cocos KMCC03342 was missing 24 BUSCOs (3.1%) while the JGI MD-104 assembly was missing 22 BUSCOs (2.9%). The quality of genome assembly was acceptable to proceed with the genome annotation using RNA-seq data. To make reliable gene model predictions based on the transcriptomic data, we additionally conducted RNAseq of W. cocos KMCC03342, resulting in a total of 12.5 billion bases from 20,875,982 reads. Using RNAseq as the gene model prediction evidence data, we predicted 14,296 protein-coding genes from the FunGAP annotation pipeline. The genome data (gene models) was used to build the maximum likelihood phylogenetic tree based on single copy ortholog genes, reassuring the taxonomic rank of W. cocos KMCC03342 by placing KMCC03342 strain next to W. cocos MD-104 among other Polyporales genomes (Figure 1).

Figure 1. Maximum likelihood (ML) tree generated using single copy ortholog genes from 34 NCBI GenBank Polyporales genomes and Wolfiporia cocos KMCC03342. Serpula lacrymans var. lacrymans S7.9 genome (GenBank: GCA_000218685.1) was used as an outgroup.

Table 1. Summary of the genome assembly and gene prediction of Wolfiporia cocos KMCC03342 in comparison to W. cocos MD-104 (JGI).

Statistics	W. cocos KMCC03342	W. cocos MD-104
Total assembly length (bp)	55,457,880	50,483,556
Number of contigs	343	2,228
Largest contig length (bp)	1,489,262	547,220
Contig N50 (bp)	332,393	109,659
Contig L50	38	129
GC content (%)	52.15	49.85
BUSCO completeness (%)	95.8	96.6
Protein coding genes	14,296	12,746

Functional annotation of W. cocos KMCC03342 revealed that 7,564 gene models contain at least one Pfam domain and 30.7% of gene models were multiple domain proteins (≥2 Pfam domains). The secondary metabolite biosynthesis gene cluster prediction program, antiSMASH [19], identified 27 gene clusters in the strain KMCC03342 and annotated 19 of the predicted clusters as potential terpene biosynthesis gene clusters. The number of predicted terpene biosynthetic gene clusters in the strain KMCC03342 (19) was the same as W. cocos strain MD-104 (19) and higher than public Chinese W. cocos strains, 2018LT001 and CGMCC5.78 (18 and 15, respectively) [6,7]. In addition, 13 terpene synthase genes were found in the W. cocos strain KMCC03342 assembly, while only 11 terpene synthase genes were identified in the W. cocos strain MD-104 genome. These observations indicate that the capability of W. cocos KMCC03342 for the terpene biosynthesis might be higher than other known W. cocos strains.

Draft genome sequence of W. cocos KMCC03342 will provide a genetic reference to breed better commercial strains and allow us to study the genes related to pachymic acid biosynthesis and other functional compounds found in W. cocos. The genome of W. cocos KMCC03342 was deposited in GenBank under the accession number JAKOOS000000000, BioProject number PRJNA801446, and BioSample number SAMN25349909.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This study was funded by the Cooperative Research Program for the National Agricultural Genome Program, Rural Development Administration, Republic of Korea (project no. PJ01337602) and a National Research Foundation of Korea (NRF) grant funded by the government of the Republic of Korea (MEST) (grant NRF-2019R1A2C1089704). The authors were supported by Korea University grant.