AI Article Synopsis

  • Fungal complexes feature closely related species that are hard to distinguish morphologically but can have different pathogenic traits and mycotoxin production.
  • Identifying these cryptic species is crucial for better disease management and understanding pathogen spread.
  • The study showed that mitochondrial DNA (mtDNA) analysis, particularly through homing endonucleases (HEGs) and SNP analysis, effectively identifies important cereal pathogen species with a high success rate of 96%.

Article Abstract

Fungal complexes are often composed of morphologically nearly indistinguishable species with high genetic similarity. However, despite their close relationship, they can exhibit distinct phenotypic differences in pathogenicity and production of mycotoxins. Many plant pathogenic and toxigenic fungi have been shown to consist of such cryptic species. Identification of cryptic species in economically important pathogens has added value in epidemiologic studies and provides opportunities for better control. Analysis of mitochondrial genomes or opens up dimensions for improved diagnostics of fungi, especially when efficient recovery of DNA is problematic. In comparison to nuclear DNA, mitochondrial DNA (mtDNA) can be amplified with improved efficacy due to its multi-copy nature. However, to date, only a few studies have demonstrated the usefulness of mtDNA for identification of cryptic species within fungal complexes. In this study, we explored the value of mtDNA for identification of one of the most important cereal pathogens (). We found that homing endonucleases (HEGs), which are widely distributed in mitogenomes of fungi, display small indel polymorphism, proven to be potentially species specific. The resulting small differences in their lengths may facilitate further differentiation of from the other cryptic species belonging to species complex. We also explored the value of SNP analysis of the mitogenome for typing The success in identifying strains was estimated at 96%, making this tool an attractive complement to other techniques for identification of

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439580PMC
http://dx.doi.org/10.3389/fmicb.2021.714651DOI Listing

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