Hairpin loop to hairpin loop: a full-length assembly of the ASFV genome using Oxford Nanopore long-read sequencing

Short-read assembly of the African swine fever virus (ASFV) genome is challenging due to the presence of inverted terminal repeat (ITR) and hairpin loop sequences, which often cause ambiguity in contig reconstruction. In this study, we employed Oxford Nanopore long-read sequencing to assemble a full-length ASFV genome from passage 50 of an ASFV strain adapted to MA-104 cells. We identified duplicated reverse complementary reads from the ITR and hairpin loop regions, which, if not properly analyzed, could lead to an inaccurate assembly that falsely represents these complex regions. Our findings highlight the power of long-read sequencing for resolving complex viral genomes and reveal potential challenges for other viruses with similar terminal structures.

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Publication Details

Journal
Frontiers in Microbiology
Published
2025-08-08
DOI
https://doi.org/10.3389/fmicb.2025.1615977
Citations
1
Primary Topic
Animal Disease Management and Epidemiology
Type
article
Field-Weighted Citation Impact
1.90

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article

Hairpin loop to hairpin loop: a full-length assembly of the ASFV genome using Oxford Nanopore long-read sequencing

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1 citations
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article

Hairpin loop to hairpin loop: a full-length assembly of the ASFV genome using Oxford Nanopore long-read sequencing

Asawin Wanitchang, Theeradej Thaweerattanasinp, Chutima Sonthirod, Anan Jongkaewwattana, Jeremy R. Shearman, Sonicha U‐thoomporn, Sithichoke Tangphatsornruang, Wirulda Pootakham, Poompat Phadphon, Janya Saenboonrueng
article en
1 citations

Abstract

Short-read assembly of the African swine fever virus (ASFV) genome is challenging due to the presence of inverted terminal repeat (ITR) and hairpin loop sequences, which often cause ambiguity in contig reconstruction. In this study, we employed Oxford Nanopore long-read sequencing to assemble a full-length ASFV genome from passage 50 of an ASFV strain adapted to MA-104 cells. We identified duplicated reverse complementary reads from the ITR and hairpin loop regions, which, if not properly analyzed, could lead to an inaccurate assembly that falsely represents these complex regions. Our findings highlight the power of long-read sequencing for resolving complex viral genomes and reveal potential challenges for other viruses with similar terminal structures.

Frontiers in MicrobiologyVol. 16
National Science and Technology Development Agency (TH)
National Science and Technology Development Agency, Thailand Science Research and Innovation
Good health and well-being
Openalex Percentile: Top 13%
Animal Disease Management and Epidemiology
1.90
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Hairpin loop to hairpin loop: a full-length assembly of the ASFV genome using Oxford Nanopore long-read sequencing — Asawin Wanitchang, Theeradej Thaweerattanasinp, et al. · Frontiers in Microbiology (2025) | TGRS Research Map | TGRS