TY - UNPB
T1 - The Genome of the American Dog Tick (
Dermacentor variabilis).
AU - Cassens, Jacob
AU - Villalta, Matt
AU - Aguirre, Saul
AU - Ecklund, Lauren
AU - Stenger, Trek
AU - Abdi, Idil
AU - Venigalla, Sree
AU - Shiffman, Elizabeth
AU - Bastug, Kristen
AU - Thielen, Beth K
AU - Faulk, Christopher
PY - 2025/3/14
Y1 - 2025/3/14
N2 - The American dog tick (
Dermacentor variabilis) is a vector of zoonotic pathogens in North America that poses emerging threats to public health. Despite its medical importance, genomic resources for
D. variabilis remain scarce. Leveraging long-read nanopore sequencing, we generated a high-quality genome assembly for
D. variabilis with a final size of 2.15 Gb, an N50 of 445 kb, and a BUSCO completeness score of 95.2%. Comparative BUSCO analyses revealed fewer duplicate genes in our assembly than in other
Dermacentor genomes, indicating improved haplotype resolution. The mitochondrial genome, assembled as a single circular contig, clustered monophyletically with
D. variabilis isolates from the Upper Midwest, corroborating regional phylogenetic relationships. Repetitive element analysis identified 61% of the genome as repetitive, dominated by LINEs and LTR elements, with 24% remaining unclassified, underscoring the need for further exploration of transposable elements in tick genomes. Gene annotation predicted 21,722 putative genes, achieving a protein BUSCO completeness of 80.88%. Additionally, genome-wide methylation analysis revealed 9.9% global 5mC methylation, providing the first insights into epigenetic modifications in
D. variabilis. Further, nanopore sequencing detected
Rickettsia montanensis and a non-pathogenic
Francisella-like endosymbiont. These findings expand our understanding of tick genomics and epigenetics, offering valuable resources for comparative studies and evolutionary analyses.
AB - The American dog tick (
Dermacentor variabilis) is a vector of zoonotic pathogens in North America that poses emerging threats to public health. Despite its medical importance, genomic resources for
D. variabilis remain scarce. Leveraging long-read nanopore sequencing, we generated a high-quality genome assembly for
D. variabilis with a final size of 2.15 Gb, an N50 of 445 kb, and a BUSCO completeness score of 95.2%. Comparative BUSCO analyses revealed fewer duplicate genes in our assembly than in other
Dermacentor genomes, indicating improved haplotype resolution. The mitochondrial genome, assembled as a single circular contig, clustered monophyletically with
D. variabilis isolates from the Upper Midwest, corroborating regional phylogenetic relationships. Repetitive element analysis identified 61% of the genome as repetitive, dominated by LINEs and LTR elements, with 24% remaining unclassified, underscoring the need for further exploration of transposable elements in tick genomes. Gene annotation predicted 21,722 putative genes, achieving a protein BUSCO completeness of 80.88%. Additionally, genome-wide methylation analysis revealed 9.9% global 5mC methylation, providing the first insights into epigenetic modifications in
D. variabilis. Further, nanopore sequencing detected
Rickettsia montanensis and a non-pathogenic
Francisella-like endosymbiont. These findings expand our understanding of tick genomics and epigenetics, offering valuable resources for comparative studies and evolutionary analyses.
U2 - 10.1101/2025.03.12.642860
DO - 10.1101/2025.03.12.642860
M3 - Preprint
C2 - 40161633
T3 - bioRxiv : the preprint server for biology
BT - The Genome of the American Dog Tick (
Dermacentor variabilis).
ER -