Here, we report a 29-Mb draft genome sequence of strain 72-15.1 of Simplicillium aogashimaense (Cordycipitaceae, Hypocreales). Strain 72-15.1 was a unique fungal isolate obtained from asymptomatic tillers of the tropical grass Brachiaria brizantha.
ABSTRACT
Here, we report a 29-Mb draft genome sequence of strain 72-15.1 of Simplicillium aogashimaense (Cordycipitaceae, Hypocreales). Strain 72-15.1 was a unique fungal isolate obtained from asymptomatic tillers of the tropical grass Brachiaria brizantha.
ANNOUNCEMENT
Simplicillium aogashimaense strain 72-15.1 is a putative fungal endophyte of Brachiaria brizantha (host accession number CIAT 16320) and was isolated from an asymptomatic leaf (1). This species was originally described from soil samples in Asia (2). Preliminary identification of S. aogashimaense strain 72-15.1 was based on morphological characteristics and a phylogenetic analysis with the internal transcribed spacer (ITS) region (1). S. aogashimaense strain 72-15.1 was isolated only once from B. brizantha and was the only species of the Simplicillium genus (as described by Zare and Gams [3]) to be isolated from nine species of Brachiaria grasses (1).
The 29-Mb draft genome of S. aogashimaense strain 72-15.1 is 1 of only 13 genomes of Simplicillium species to have been described thus far (4, 5). Simplicillium species are both ecologically and economically interesting due to their widespread distribution, diverse host specificities, varied lifestyles (4, 5), utility as biocontrol agents (6–8), and production of bioactive compounds (9–13). Previously, we showed high antifungal activity of the sequenced strain 72-15.1 against the phytopathogenic fungi Alternaria alternatum, Bipolaris sp. aff. sorokiniana, and Curvularia trifolii (1). The genome of strain 72-15.1 can therefore be mined for the discovery of these antifungal secondary metabolites, as well as for other metabolites that may be responsible for the antimicrobial properties exhibited by some members of this genus against bacterial and fungal plant pathogens as well as plant parasitic nematodes (8, 14, 15).
To obtain fungal material for DNA extraction, a pure culture was lacerated with sterile water, and the resulting solution was spread onto a sheet of cellophane on the surface of a peptone-dextrose agar (PDA) plate and then incubated at 24°C for ∼4 days. High-quality DNA was extracted from strain 72-15.1 using a Zymo Research Quick-DNA fungal/bacterial miniprep kit, following the manufacturer’s protocol, except mycelium was ground with a plastic pestle fitted to a drill under liquid nitrogen. Two libraries were constructed for whole-genome shotgun sequencing, one for paired-end reads with an insert size of 350 nucleotides (nt) and one for mate pair reads with an insert size of 7 kb, using the Illumina TruSeq DNA Nano low-throughput (LT) 350-bp and Illumina Nextera mate pair gel-plus kits. The libraries were sequenced on an Illumina HiSeq 2000 instrument using v3 chemistry. The instrument produced 30 million paired-end read pairs and 33 million mate pair read pairs with a read length of 125 nt. All paired reads were quality trimmed and filtered using Trimmomatic v0.33 (16) and assembled using Edena v3.2 (17) with default parameters. Contigs shorter than 200 nt were discarded. The contigs were further assembled into scaffolds using the program SSPACE v3.0 (18) with the parameters -k 5, -a 0.7, -x 1, -m 30, and -o 20. The pipeline produced 22 scaffolds with a final genome size of 29.247 Mb, an N50 value of 4 Mb, and a 49% GC content. A BUSCO (19) run using the Ascomycota database vodb9 (20) and Aspergillus nidulans as the gene predictor template reported a genome completeness of 99.1%, 5 duplicated benchmarking universal single-copy orthologs (BUSCOs) (0.4%), and 5 fragmented BUSCOs (0.4%).
Data availability.
This whole-genome shotgun project has been deposited at DDBJ/ENA/GenBank under the accession number JAALXG000000000. The version described in this paper is version JAALXG010000000. The raw Illumina data from BioProject PRJNA599221 were submitted to the NCBI Sequence Read Archive (SRA) under accession numbers SRX7508659 and SRX7508658.
ACKNOWLEDGMENTS
This study was supported by Grasslanz Technology Ltd. and the International Livestock Research Institute (ILRI). The latter was through a contract with the Swedish International Development Cooperation Agency (SIDA) for the program “Innovative Programmatic Approach to Climate Change in Support of Biosciences Eastern and Central Africa’s (BecA) Mission: Climate-Smart Brachiaria Grasses for Improving Livestock Production in East Africa.”
REFERENCES
- 1.Teasdale SE, Caradus JR, Johnson LJ. 2018. Fungal endophyte diversity from tropical forage grass Brachiaria. Plant Ecol Divers 11:611–624. doi: 10.1080/17550874.2019.1610913. [DOI] [Google Scholar]
- 2.Nonaka K, Kaifuchi S, Ōmura S, Masuma R. 2013. Five new Simplicillium species (Cordycipitaceae) from soils in Tokyo, Japan. Mycoscience 54:42–53. doi: 10.1016/j.myc.2012.07.002. [DOI] [Google Scholar]
- 3.Zare R, Gams W. 2001. A revision of Verticillium section Prostrata. IV. The genera Lecanicillium and Simplicillium gen. nov. Nova Hedwigia 73:1–50. [Google Scholar]
- 4.Wei D-P, Wanasinghe DN, Hyde KD, Mortimer PE, Xu J, Xiao Y-P, Bhunjun CS, To-Anun C. 2019. The genus Simplicillium. MycoKeys 60:69–92. doi: 10.3897/mycokeys.60.38040. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Chen W-H, Liu C, Han Y-F, Liang J-D, Tian W-Y, Liang Z-Q. 2019. Three novel insect-associated species of Simplicillium (Cordycipitaceae, Hypocreales) from Southwest China. MycoKeys 58:83–102. doi: 10.3897/mycokeys.58.37176. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Ward NA, Schneider RW, Aime MC. 2011. Colonization of soybean rust sori by Simplicillium lanosoniveum. Fungal Ecol 4:303–308. doi: 10.1016/j.funeco.2011.03.008. [DOI] [Google Scholar]
- 7.Ward NA, Robertson CL, Chanda AK, Schneider RW. 2012. Effects of Simplicillium lanosoniveum on Phakopsora pachyrhizi, the soybean rust pathogen, and its use as a biological control agent. Phytopathology 102:749–760. doi: 10.1094/PHYTO-01-11-0031. [DOI] [PubMed] [Google Scholar]
- 8.Zhao D, Liu B, Li LY, Zhu XF, Wang YY, Wang JQ, Duan YX, Chen LJ. 2013. Simplicillium chinense: a biological control agent against plant parasitic nematodes. Biocontrol Sci Technol 23:980–986. doi: 10.1080/09583157.2013.809514. [DOI] [Google Scholar]
- 9.Uchida R, Kondo A, Yagi A, Nonaka K, Masuma R, Kobayashi K, Tomoda H. 2019. Simpotentin, a new potentiator of amphotericin B activity against Candida albicans, produced by Simplicillium minatense FKI-4981. J Antibiot (Tokyo) 72:134–140. doi: 10.1038/s41429-018-0128-x. [DOI] [PubMed] [Google Scholar]
- 10.Dong Q, Dong R, Xing X, Li Y. 2018. A new antibiotic produced by the cyanobacterium-symbiotic fungus Simplicillium lanosoniveum. Nat Prod Res 32:1348–1352. doi: 10.1080/14786419.2017.1343320. [DOI] [PubMed] [Google Scholar]
- 11.Fukuda T, Sudoh Y, Tsuchiya Y, Okuda T, Igarashi Y. 2014. Isolation and biosynthesis of preussin B, a pyrrolidine alkaloid from Simplicillium lanosoniveum. J Nat Prod 77:813–817. doi: 10.1021/np400910r. [DOI] [PubMed] [Google Scholar]
- 12.Liang X, Zhang X-Y, Nong X-H, Wang J, Huang Z-H, Qi S-H. 2016. Eight linear peptides from the deep-sea-derived fungus Simplicillium obclavatum EIODSF 020. Tetrahedron 72:3092–3097. doi: 10.1016/j.tet.2016.04.032. [DOI] [Google Scholar]
- 13.Liang X, Nong X-H, Huang Z-H, Qi S-H. 2017. Antifungal and antiviral cyclic peptides from the deep-sea-derived fungus Simplicillium obclavatum EIODSF 020. J Agric Food Chem 65:5114–5121. doi: 10.1021/acs.jafc.7b01238. [DOI] [PubMed] [Google Scholar]
- 14.Gomes AAM, Pinho DB, Cardeal ZL, Menezes HC, De Queiroz MV, Pereira OL. 2018. Simplicillium coffeanum, a new endophytic species from Brazilian coffee plants, emitting antimicrobial volatiles. Phytotaxa 333:188–298. doi: 10.11646/phytotaxa.333.2.2. [DOI] [Google Scholar]
- 15.Le Dang Q, Shin TS, Park MS, Choi YH, Choi GJ, Jang KS, Kim IS, Kim J-C. 2014. Antimicrobial activities of novel mannosyl lipids isolated from the biocontrol fungus Simplicillium lamellicola BCP against phytopathogenic bacteria. J Agric Food Chem 62:3363–3370. doi: 10.1021/jf500361e. [DOI] [PubMed] [Google Scholar]
- 16.Bolger AM, Lohse M, Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30:2114–2120. doi: 10.1093/bioinformatics/btu170. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Hernandez D, François P, Farinelli L, Osterås M, Schrenzel J. 2008. De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer. Genome Res 18:802–809. doi: 10.1101/gr.072033.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Boetzer M, Henkel CV, Jansen HJ, Butler D, Pirovano W. 2011. Scaffolding pre-assembled contigs using SSPACE. Bioinformatics 27:578–579. doi: 10.1093/bioinformatics/btq683. [DOI] [PubMed] [Google Scholar]
- 19.Simão FA, Waterhouse RM, Ioannidis P, Kriventseva EV, Zdobnov EM. 2015. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics 31:3210–3212. doi: 10.1093/bioinformatics/btv351. [DOI] [PubMed] [Google Scholar]
- 20.Waterhouse RM, Tegenfeldt F, Li J, Zdobnov EM, Kriventseva EV. 2013. OrthoDB: a hierarchical catalog of animal, fungal and bacterial orthologs. Nucleic Acids Res 41:358–365. doi: 10.1093/nar/gks1116. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
This whole-genome shotgun project has been deposited at DDBJ/ENA/GenBank under the accession number JAALXG000000000. The version described in this paper is version JAALXG010000000. The raw Illumina data from BioProject PRJNA599221 were submitted to the NCBI Sequence Read Archive (SRA) under accession numbers SRX7508659 and SRX7508658.
