Abstract
Cladobotryum mycophilum is the causal agent of cobweb disease in many important mushroom crops. In this study, we report the complete mitochondrial genome of C. mycophilum for the first time. The genome is 78,729 bp long and comprises 52 protein-coding genes (PCGs), 2 ribosomal RNA genes (rRNA), and 26 transfer RNA (tRNA) genes. The nucleotide composition of C. mycophilum mitochondrial genome is as follows: A (38.06%), T (34.68%), C (12.19%), and G (15.07%). Phylogenetic analysis revealed that C. mycophilum had a close relationship with Cladobotryum varium from Hypocreaceae. This study provided a basis for studies of the mitochondrial evolution of Hypocreaceae.
Cobweb disease is one of the most serious diseases in mushroom cultivation, which causes important economic losses in mushroom farms (McKay et al. Citation1999). The causal agents of cobweb disease are several species of the genus Cladobotryum, including Cladobotryum mycophilum, Cladobotryum varium, Cladobotryum dendroides, Cladobotryum protrusum, and Cladobotryum cubitense (Wang et al. Citation2018; Sossah et al. Citation2019). Cladobotryum mycophilum has been reported to cause Cobweb disease in many important mushroom crops, such as Agaricus bisporus, Pleurotus eryngii, Flammulina velutipes, and Ganoderma lucidum (Sossah et al. Citation2019). At present, the complete mitochondrial genome of C. varium (teleomorph name Hypomyces aurantius) has been sequenced and published (Deng et al. Citation2016), but other species of the genus Cladobotryum were not involved. The mitogenome of C. mycophilum reported here would provide supplementary information on the evolution and taxonomy of Cladobotryum.
The specimen was isolated from a G. lucidum fruiting body with cobweb disease in Sichuan Province, China (105.98 E; 32.20 N). The strain was identified as C. mycophilum and was stored in the Sichuan Academy of Agricultural Sciences (No. Cmy1). We extracted the whole genomic DNA from the mycelia by a fungal DNA Kit D3390-00 (Omega Bio-Tek, Norcross, GA). The complete mitochondrial genome of C. mycophilum was sequenced using an Illumina HiSeq 2500 Platform (Illumina, San Diego, CA). Genes were assembled by MITObim v1.9 (Hahn et al. Citation2013). We annotated the C. mycophilum mitogenome with the MFannot tool, combined with manual corrections. tRNAs were predicted with the tRNAscan-SE 2.0 (Lowe and Chan Citation2016).
The mitogenome of C. mycophilum was assembled as circular DNA molecules with 78,529 bp in length, with the GC content of 27.26% and the following base composition: A (38.06%), T (34.68%), G (15.07%), and C (12.19%). The mitogenome comprised 80 genes, including 52 protein-coding genes (PCGs), 26 tRNA genes and 2 ribosomal RNA genes (rnl and rns). The 52 PCGs include 14 typical genes and 38 ORFs. Among these ORFs, we found 30 ORFs located in introns and the remaining 8 ORFs were regarded as free-standing genes. The mitogenome of C. mycophilum was submitted to GenBank database under accession No. MT108299.
The Bayesian inference method was used for phylogenetic analysis based on the combined gene dataset (14 typical genes) using MrBayes 3.2.6 (Ronquist et al. Citation2012). We established the phylogenetic relationships of C. mycophilum and 13 species within Sordariomycetes, using Cairneyella variabilis of Leotiomycetes as an outgroup. We obtained a stable evolutionary tree topology () with all of the recovered clades well supported (BPP ≥ 0.97). The phylogenetic analysis revealed that C. mycophilum had a close relationship with C. varium and they were clustered in a sister group. The clade (C. mycophilum + C. varium) was closely related to the genus Trichoderma of Hypocereaceae.
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No potential conflict of interest was reported by the author(s).
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References
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