Determining the Geographic Distribution of Filarioid Nematodes in Caribou in Canada

• Main Author: Mariyam Thomas, Aparna
• Other Authors: Kutz, Susan J., Melin, Amanda Dawn, Soghigian, John Steven, Verocai, Guilherme Gomes, Buret, Andre G.
• Format: Master Thesis
• Language: English
• Published: Graduate Studies 2023
• Subjects: Filarioid; Nematode; Rangifer tarandus; Setaria yehi; Onchocerca cervipedis; ddPCR; Canadian Arctic; Caribou; Vectorborne parasites; Climate change; Parasitology; Veterinary Science; Arctic; Newfoundland; Nunavut; Northwest Territories; Canada; Fennoscandia
• Online Access: https://hdl.handle.net/1880/117569

The caribou (Rangifer tarandus sspp.) is a keystone wildlife species in northern ecosystems that plays a central role in the lives of the Indigenous People as a cultural and spiritual icon. The Arctic is currently experiencing unpredictable changes due to various factors, including climate change, and warming temperatures and change in precipitation in the Arctic facilitate the transmission of arthropod-borne parasites. Caribou are hosts to several vector-borne parasites, which includes protozoans such as Babesia odocoilei and Besnoitia tarandi, and filarioid nematodes of the genus Setaria, Onchocerca, and Rumenfilaria. Some caribou populations are declining as a result of rapidly changing climate and multiple stressors, including these vector-borne parasites. Filarioids are an important cause of morbidity, and occasional mortality in Rangifer in Fennoscandia. However, the ecology and epidemiology of these parasites in caribou in North America, including Canada is unknown. The objective of this study was to determine the parasitic diversity and geographic distribution of filarioid nematodes in three Canadian designatable units (DU) of caribou, representing Barrenground, Boreal Woodland and Dolphin & Union Caribou from Northwest Territories, Nunavut, and Newfoundland & Labrador. Genomic DNA extracted from 768 blood samples was screened using real-time PCR. The positive samples were Sanger sequenced to identify the parasite present. Based on the sequencing results, we identified Setaria yehi and Onchocerca cervipedis s.l. I then standardized a TaqMan probe based duplex droplet digital PCR (ddPCR) protocol for the simultaneous detection of S. yehi and O. cervipedis s.l. I adopted a conservative approach for ddPCR to make the technique time- and cost-effective. Out of 768 samples, 136 samples were screened using ddPCR. Based on real-time PCR results, 8/768 samples were positive. Setaria yehi and O. cervipedis s.l. were present in 4 separate samples (0.5%) each. Using ddPCR, 60/136 samples were positive ...