Annotation and analysis of the mitochondrial genome of Coniothyrium glycines, causal agent of red leaf blotch of soybean, reveals an abundance of homing endonucleases

PLoS One. 2018 Nov 7;13(11):e0207062. doi: 10.1371/journal.pone.0207062. eCollection 2018.

Abstract

Coniothyrium glycines, the causal agent of soybean red leaf blotch, is a USDA APHIS-listed Plant Pathogen Select Agent and potential threat to US agriculture. Sequencing of the C. glycines mt genome revealed a circular 98,533-bp molecule with a mean GC content of 29.01%. It contains twelve of the mitochondrial genes typically involved in oxidative phosphorylation (atp6, cob, cox1-3, nad1-6, and nad4L), one for a ribosomal protein (rps3), four for hypothetical proteins, one for each of the small and large subunit ribosomal RNAs (rns and rnl) and a set of 30 tRNAs. Genes were encoded on both DNA strands with cox1 and cox2 occurring as adjacent genes having no intergenic spacers. Likewise, nad2 and nad3 are adjacent with no intergenic spacers and nad5 is immediately followed by nad4L with an overlap of one base. Thirty-two introns, comprising 54.1% of the total mt genome, were identified within eight protein-coding genes and the rnl. Eighteen of the introns contained putative intronic ORFs with either LAGLIDADG or GIY-YIG homing endonuclease motifs, and an additional eleven introns showed evidence of truncated or degenerate endonuclease motifs. One intron possessed a degenerate N-acetyl-transferase domain. C. glycines shares some conservation of gene order with other members of the Pleosporales, most notably nad6-rnl-atp6 and associated conserved tRNA clusters. Phylogenetic analysis of the twelve shared protein coding genes agrees with commonly accepted fungal taxonomy. C. glycines represents the second largest mt genome from a member of the Pleosporales sequenced to date. This research provides the first genomic information on C. glycines, which may provide targets for rapid diagnostic assays and population studies.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Ascomycota / genetics*
  • Ascomycota / physiology*
  • Codon / genetics
  • Endonucleases / genetics
  • Endonucleases / metabolism*
  • Genome, Mitochondrial / genetics*
  • Genomics
  • Glycine max / microbiology*
  • Introns / genetics
  • Molecular Sequence Annotation*
  • Plant Diseases / microbiology*
  • RNA, Transfer / genetics

Substances

  • Codon
  • RNA, Transfer
  • Endonucleases

Grants and funding

The genome referenced in this publication was sequenced at MRIGlobal through funding provided by U.S. Department of Homeland Security, Science & Technology Directorate through Contract No. HSHQDC-13-C-B0009 "Capturing Global Biodiversity of Pathogens by Whole Genome Sequencing". The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. MRIGlobal provided support in the form of salaries for authors (BC and RAW), but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the "author contributions" section.