Abstract
BackgroundLong-read sequencing is increasingly being used to determine eukaryotic genomes. We used nanopore technology to generate chromosome-level assemblies for 3 different strains of Drechmeria coniospora, a nematophagous fungus used extensively in the study of innate immunity in Caenorhabditis elegans.ResultsOne natural geographical isolate demonstrated high stability over decades, whereas a second isolate not only had a profoundly altered genome structure but exhibited extensive instability. We conducted an in-depth analysis of sequence errors within the 3 genomes and established that even with state-of-the-art tools, nanopore methods alone are insufficient to generate eukaryotic genome sequences of sufficient accuracy to merit inclusion in public databases.ConclusionsAlthough nanopore long-read sequencing is not accurate enough to produce publishable eukaryotic genomes, in our case, it has revealed new information about genome plasticity in D. coniospora and provided a backbone that will permit future detailed study to characterize gene evolution in this important model fungal pathogen.
Highlights
Long-read sequencing is increasingly being used to determine eukaryotic genomes
We used nanopore technology to generate chromosome-level assemblies for 3 different strains of Drechmeria coniospora, a nematophagous fungus used extensively in the study of innate immunity in Caenorhabditis elegans
We adopted D. coniospora strain American Type Culture Collection (ATCC) 96-282, derived from a strain isolated in Sweden, as a model pathogen for Caenorhabditis elegans 20 years ago [2]
Summary
We used nanopore technology to generate chromosome-level assemblies for 3 different strains of Drechmeria coniospora, a nematophagous fungus used extensively in the study of innate immunity in Caenorhabditis elegans. Conclusions: nanopore long-read sequencing is not accurate enough to produce publishable eukaryotic genomes, in our case, it has revealed new information about genome plasticity in D. coniospora and provided a backbone that will permit future detailed study to characterize gene evolution in this important model fungal pathogen. We adopted D. coniospora strain ATCC 96-282, derived from a strain isolated in Sweden, as a model pathogen for Caenorhabditis elegans 20 years ago [2] We have cultured this strain, referred to here as Swe, continuously since using it to understand innate immune mechanisms in its nematode host [3, 4].
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