Abstract
Giardia duodenalis, a major cause of waterborne infection, infects a wide range of mammalian hosts and is subdivided into eight genetically well-defined assemblages named A through H. However, fragmented genomes and a lack of comparative analysis within and between the assemblages render unclear the molecular mechanisms controlling host specificity and differential disease outcomes. To address this, we generated a near-complete de novo genome of AI assemblage using the Oxford Nanopore platform by sequencing the Be-2 genome. We generated 148,144 long-reads with quality scores of > 7. The final genome assembly consists of only nine contigs with an N50 of 3,045,186 bp. This assembly agrees closely with the assembly of another strain in the AI assemblage (WB-C6). However, a critical difference is that a region previously placed in the five-prime region of Chr5 belongs to Chr4 of Be-2. We find a high degree of conservation in the ploidy, homozygosity, and the presence of cysteine-rich variant-specific surface proteins (VSPs) within the AI assemblage. Our assembly provides a nearly complete genome of a member of the AI assemblage of G. duodenalis, aiding population genomic studies capable of elucidating Giardia transmission, host range, and pathogenicity.
Original language | English (US) |
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Article number | 13582 |
Pages (from-to) | 13582 |
Journal | Scientific Reports |
Volume | 14 |
Issue number | 1 |
DOIs | |
State | Published - Jun 12 2024 |
Keywords
- Annotation
- Genome assembly
- Giardia
- Long-read sequencing
- Ploidy
- Synteny
- Genome, Protozoan
- Humans
- Phylogeny
- Genomics/methods
- Protozoan Proteins/genetics
- Giardiasis/parasitology
- Homozygote
- Animals
- Conserved Sequence
- Giardia lamblia/genetics
ASJC Scopus subject areas
- General