We present a new method, CIDER-Seq (Circular DNA Enrichment sequencing) for the unbiased enrichment and long-read sequencing of viral-sized circular DNA molecules. We used CIDER-Seq to produce single-read full-length virus genomes for the first time. CIDER-Seq combines PCR-free virus enrichment with Single Molecule Real Time sequencing and a new sequence de-concatenation algorithm. We apply our technique to produce >1200 full-length, highly accurate geminivirus genomes from RNAi-transgenic and control plants in a field trial in Kenya. Using CIDER-Seq we can demonstrate for the first time that the expression of antiviral double-stranded RNA (dsRNA) in transgenic plants causes a consistent shift in virus populations towards species sharing low homology to the transgene derived dsRNA. Our method and its application in an economically important crop plant opens new possibilities in periodic virus sequence surveillance and accurate profiling of diverse circular DNA elements.
Deep-sequencing of virus isolates using short-read sequencing technologies is problematic since viruses are often present in complexes sharing a high-degree of sequence identity. The full-length genomes of such highly-similar viruses cannot be assembled accurately from short sequencing reads. We present a new method, CIDER-Seq (Circular DNA Enrichment Sequencing) which successfully generates accurate full-length virus genomes from individual sequencing reads with no sequence assembly required. CIDER-Seq operates by combining a PCR-free, circular DNA enrichment protocol with Single Molecule Real Time sequencing and a new sequence deconcatenation algorithm. We apply our technique to produce more than 1,200 full-length, highly accurate geminivirus genomes from RNAi-transgenic and control plants in a field trial in Kenya. Using CIDER-Seq we can demonstrate for the first time that the expression of antiviral doublestranded RNA (dsRNA) in transgenic plants causes a consistent shift in virus populations towards species sharing low homology to the transgene derived dsRNA. Our results show that CIDER-seq is a powerful, cost-effective tool for accurately sequencing circular DNA viruses, with future applications in deep-sequencing other forms of circular DNA such as transposons and plasmids.
Synergism among the groundnut rosette disease (GRD) pathogens of Groundnut rosette assistor virus (GRAV, Luteovirus) and Groundnut rosette virus (GRV, Umbravirus) associated with a satellite-ribonucleic acid (sat-RNA), have declined groundnut (Peanut, Arachis hypogaea L.) production in Kenya. The polyphagous groundnut aphid (Aphis craccivora Koch; Homoptera: Aphididae) efficiently transmits GRD in sub-Saharan Africa. Inadequate information available on the pathosystem, epiphytology and genomic characterization of GRAV, GRV and sat-RNA pathogens in Kenya, have hampered control and management technologies due to their intimate complex etiology, the bottleneck which this study unravels. A survey of GRD was conducted in western Kenya among the four counties of Bungoma, Busia, Kisumu and Kisii during the short rains season of 2019. A total of 10 symptomatic leaf samples were selected from the collected samples and preserved until use. Total RNA was extracted from the symptomatic leaf samples using GeneJET Plant RNA Purification Mini Kit according to the manufacturers' protocol. RT-PCR detection of GRD pathogens was done using specific primers of GRAV, GRV and sat-RNA. DNA libraries were prepared and sequenced using the Sanger sequencing platform. Phylogenetic analyses and comparisons were performed using MEGA X software. The sequence quality were checked based on the peak of the electrophoregram and trimmed using CLC main work bench v20. The sequences were assembled with final consensus exported as FASTA file format and BLAST searched against NCBI database using BLASTn. The BLAST hit with nucleotide identity of at least 97% identity were considered, downloaded, uploaded to MEGA X and multiple alignment done with Gap Opening Penalty of 15 and Gap Extension Penalty of 5.5. Phylogenetic trees were constructed with best DNA/Protein model based on automatic Neighbor Joining Tree and Maximum Likelihood method of nucleotides substitution by Kimura 2 Parameter with Invariant Plus Gamma. The two GRAV isolates from Kenya (Ken_G10 and Ken_G2) clustered together in group II while the rest clustered in group I. The Kenyan novel GRAV isolates are more similar to each other than with any other sequences implying common ancestry than with the other African isolates. The Kenyan sat-RNA isolates formed two distinct groups with sub-groups within the clusters. Isolates Ken_G11 and Ken_G6 clustered together in group II while Ken_G10 and Ken_G7 clustered together in group I. Ken_G6 clustered with other Kenyan sat-RNA isolates implying a possible identity by descent (IBD), suggesting a possible impact of a genetic bottleneck whose cause should be investigated further to infer any conclusions.
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