2021
DOI: 10.1264/jsme2.me20152
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RNA Viral Metagenome Analysis of Subnanogram dsRNA Using Fragmented and Primer Ligated dsRNA Sequencing (FLDS)

Abstract: Fragmented and primer ligated dsRNA sequencing (FLDS) is a sequencing method applicable to long double-stranded RNA (dsRNA) that enables the complete genome sequencing of both double- and single-stranded RNA viruses. However, the application of this method on a low amount of dsRNA has been hindered by adaptor dimer formation during cDNA amplification and sequence library preparation. We herein developed FLDS ver. 3 by optimizing the terminal modification of an oligonucleotide adaptor and the conditions of adap… Show more

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Cited by 21 publications
(28 citation statements)
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“…Nucleic acid contamination from DNA viruses, hosts, and environments may occur when analyzing RNA viromes. To overcome this issue, techniques to selectively extract and sequence RNA virus-derived nucleic acids, such as the FLDS method ( Urayama et al , 2016 ; Hirai et al , 2021 ), have been developed. However, it is still challenging to eliminate all contamination from sequencing data.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Nucleic acid contamination from DNA viruses, hosts, and environments may occur when analyzing RNA viromes. To overcome this issue, techniques to selectively extract and sequence RNA virus-derived nucleic acids, such as the FLDS method ( Urayama et al , 2016 ; Hirai et al , 2021 ), have been developed. However, it is still challenging to eliminate all contamination from sequencing data.…”
Section: Discussionmentioning
confidence: 99%
“…However, identifying RNA virus-derived sequences from metatranscriptome data is challenging because of the low abundance of viral RNA in sequencing reads and high nucleotide diversity among RNA viruses ( Cobbin et al , 2021 ). Therefore, we developed a method of double-stranded RNA (dsRNA) sequencing named “fragmented and primer-ligated dsRNA sequencing” (FLDS) to enrich RNA virus sequences in the cellular transcriptome ( Urayama et al , 2016 , 2018 ; Hirai et al , 2021 ). Long dsRNAs are rare in eukaryotic cells; therefore, they are mainly derived from the genomes of dsRNA viruses or replicative intermediates of single-strand RNA (ssRNA) viruses ( Kumar and Carmichael, 1998 ).…”
mentioning
confidence: 99%
“…Nucleic acid contamination from DNA viruses, hosts, and environments is an issue when analyzing RNA viromes. To overcome this issue, techniques to selectively extract and sequence RNA virus-derived nucleic acids, such as the FLDS method (Urayama et al, 2016; Hirai et al, 2021), have been developed. However, it is still challenging to eliminate all contamination from the sequencing data.…”
Section: Discussionmentioning
confidence: 99%
“…However, identifying RNA virus-derived sequences from metatranscriptome data is challenging because of the low abundance of viral RNA in sequencing reads and the high nucleotide diversity among RNA viruses (Cobbin et al, 2021). Thus, we have developed a method of double-stranded RNA (dsRNA) sequencing named “fragmented and primer ligated dsRNA sequencing” (FLDS) to enrich the RNA virus sequences in the cellular transcriptome (Urayama et al, 2016, 2018; Hirai et al, 2021). Long dsRNAs are rare in eukaryotic cells; therefore, they are mainly derived from the genomes of dsRNA viruses or replicative intermediates of single-strand RNA (ssRNA) viruses (Kumar and Carmichael, 1998).…”
Section: Introductionmentioning
confidence: 99%
“…Quality filtering of raw sequence data, including removal of the Illumina adaptor, cDNA amplification adaptors, and low-quality, low-complexity, and experimentally contaminated sequences, was performed as previously described ( Urayama et al , 2018 ; Hirai et al , 2021 ). rRNA sequences were removed using SortMeRNA 2.0 ( Kopylova et al , 2012 ).…”
Section: Methodsmentioning
confidence: 99%