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Histological Quantification to Determine Lung Fungal Burden in Experimental Aspergillosis
Published on: March 9, 2018
Telomere-to-telomere genome sequence of the model mould pathogen Aspergillus fumigatus
Paul Bowyer1, Andrew Currin2, Daniela Delneri3
1Manchester Fungal Infection Group, Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK. paul.bowyer@manchester.ac.uk.
Abstract:
The pathogenic fungus Aspergillus fumigatus is a major etiological agent of fungal invasive and chronic diseases affecting tens of millions of individuals worldwide. Draft genome sequences of two clinical isolates (Af293 and A1163) are commonly used as reference genomes for analyses of clinical and environmental strains. However, the reference sequences lack coverage of centromeres, an accurate sequence for ribosomal repeats, and a comprehensive annotation of chromosomal rearrangements such as translocations and inversions. Here, we used PacBio Single Molecule Real-Time (SMRT), Oxford Nanopore and Illumina HiSeq sequencing for de novo genome assembly and polishing of two laboratory reference strains of A. fumigatus, CEA10 (parental isolate of A1163) and its descendant A1160. We generated full length chromosome assemblies and a comprehensive telomere-to-telomere coverage for CEA10 and near complete assembly of A1160 including ribosomal repeats and the sequences of centromeres, which we discovered to be composed of long transposon elements. We envision these high-quality reference genomes will become fundamental resources to study A. fumigatus biology, pathogenicity and virulence, and to discover more effective treatments against diseases caused by this fungus.
Insights
High-quality genome assemblies for Aspergillus fumigatus were generated, improving our understanding of this pathogenic fungus. These enhanced reference genomes will aid in studying fungal diseases and developing new treatments.
Area of Science:
- Mycology
- Genomics
- Infectious Diseases
Background:
- Aspergillus fumigatus is a pathogenic fungus causing significant global health issues.
- Existing reference genomes have limitations in centromere, ribosomal repeat, and chromosomal rearrangement coverage.
- Accurate genomic data is crucial for understanding fungal pathogens.
Purpose of the Study:
- To generate high-quality, de novo genome assemblies for Aspergillus fumigatus reference strains.
- To improve the accuracy of centromere and ribosomal repeat sequences.
- To provide comprehensive annotation of chromosomal rearrangements.
Main Methods:
- Utilized PacBio SMRT, Oxford Nanopore, and Illumina HiSeq sequencing technologies.
- Performed de novo genome assembly and polishing for strains CEA10 and A1160.
- Achieved telomere-to-telomere chromosome coverage and characterized centromeric regions.
Main Results:
- Generated full-length chromosome assemblies for CEA10 with complete telomere-to-telomere coverage.
- Obtained near-complete assembly for A1160, including ribosomal repeats and centromere sequences.
- Discovered centromeres are composed of long transposon elements.
Conclusions:
- The new high-quality reference genomes provide a fundamental resource for Aspergillus fumigatus research.
- These assemblies will advance studies on fungal biology, pathogenicity, and virulence.
- Improved genomic data will facilitate the discovery of more effective antifungal treatments.
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