3 research outputs found

    Cot filtration approach for advancing genome sequencing of the cattle tick, Rhipicephalus (Boophilus) microplus

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    The size and repetitive nature of the Rhipicephalus microplus genome makes obtaining a full genome sequence fiscally and technically difficult with current technologies. To bridge the gap in sequence information between traditional ESTs and whole genome sequence, we used Cot filtration to selectively obtain gene-enriched regions of this tick's genome. This Cot-filtered DNA was sequenced via 454 pyrosequencing. The sequenced Cot-filtered genomic DNA was assembled with an EST-based gene index of 14,586 unique entries (http://compbio.dfci.harvard.edu/tgi/cgi-bin/tgi/gimain.pl?gudb=b_microplus) where each EST served as a potential 1Cseed 1D for assembly and scaffold formation. Comparison of the BAC and Cot filtration data indicates that Cot filtration was highly successful in filtering repetitive DNA out of the genomic DNA used in 454 sequencing. Cot filtration is a very useful strategy to incorporate into genome sequencing projects on organisms with large genome sizes and which contain high percentages of repetitive, difficult to assemble, genomic DNA. Current sequence database for R. microplus includes, 175Mb of assembled contigs sequences from Cot-based sequencing for gene enriched regions, three transcriptome library assemblies (21Mb) representing over 33,000 transcripts, BAC-end sequences (7.2Mb), and targeted whole BAC sequence (1.5Mb)

    Genomic insights into the Ixodes scapularis tick vector of Lyme disease

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    Ticks transmit more pathogens to humans and animals than any other arthropod. We describe the 2.1 Gbp nuclear genome of the tick, Ixodes scapularis (Say), which vectors pathogens that cause Lyme disease, human granulocytic anaplasmosis, babesiosis and other diseases. The large genome reflects accumulation of repetitive DNA, new lineages of retro-transposons, and gene architecture patterns resembling ancient metazoans rather than pancrustaceans. Annotation of scaffolds representing ∼57% of the genome, reveals 20,486 protein-coding genes and expansions of gene families associated with tick-host interactions. We report insights from genome analyses into parasitic processes unique to ticks, including host 'questing', prolonged feeding, cuticle synthesis, blood meal concentration, novel methods of haemoglobin digestion, haem detoxification, vitellogenesis and prolonged off-host survival. We identify proteins associated with the agent of human granulocytic anaplasmosis, an emerging disease, and the encephalitis-causing Langat virus, and a population structure correlated to life-history traits and transmission of the Lyme disease agent
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