Dermacentor species (Acari: Ixodidae) in western Canada, with detection of Dermacentor similis

• Published in: Journal of medical entomology 2025-01, Vol.62 (1), p.123-129
• Main Authors: Nichol, Grace K, Lado, Paula, Snyman, Louwrens P, Dergousoff, Shaun J, Weese, J Scott, Greer, Amy L, Clow, Katie M
• Format: Article
• Language: English
• Subjects: Alberta; Animal Distribution; Animals; British Columbia; Dermacentor - classification; Dermacentor - genetics; Female; Male; Sampling, Distribution, Dispersal; Saskatchewan
• ISSN: 0022-2585; 1938-2928; 1938-2928
• DOI: 10.1093/jme/tjae133

Numerous tick species are undergoing significant range expansion in Canada, including several Dermacentor spp Koch (Acari: Ixodidae). With the recent description of Dermacentor similis Lado in the western United States, additional research is required to determine the current range of this species. Five hundred ninety-eight Dermacentor spp. were collected from companion animals in the western Canadian provinces of British Columbia, Alberta, and Saskatchewan. Ticks were morphologically identified to species, followed by PCR and gel electrophoresis of the ITS-2 partial gene target (n = 595). Ninety-seven percent (n = 579/595) generated valid banding patterns. The banding pattern for the majority (74%, n = 206/278) of Dermacentor spp. from southern British Columbia was consistent with D. variabilis (Say), while 26% (n = 72/278) was consistent with D. andersoni Stiles. For samples from Alberta, 38% (n = 3/8) had banding patterns consistent with D. variabilis and 63% (n = 5/8) with D. andersoni. All (n = 293) ticks from Saskatchewan had banding patterns consistent with D. variabilis. After the description of D. similis was published, DNA sequencing of mitochondrial (16S rDNA gene, COI gene) and nuclear (ITS-2) markers was used to confirm the identity of 40 samples. Twenty-seven samples that had banding patterns consistent with D. variabilis from British Columbia were confirmed to be D. similis. One sample from Alberta and five from Saskatchewan were confirmed to be D. variabilis and seven samples from British Columbia were D. andersoni. The ITS-2 amplicons were not useful for differentiating between D. variabilis and D. similis. These results provide evidence of D. similis in western Canada and highlight that sequences of the mitochondrial genes are effective for distinguishing D. andersoni, D. variabilis, and D. similis.