| Autor: |
Paquette SJ; Centre for Vector-Borne Diseases, National Centre for Animal Diseases, Canadian Food Inspection Agency, Lethbridge, AB T1J 3Z4, Canada., Czekay D; Centre for Vector-Borne Diseases, National Centre for Animal Diseases, Canadian Food Inspection Agency, Lethbridge, AB T1J 3Z4, Canada., Manalaysay J; Centre for Vector-Borne Diseases, National Centre for Animal Diseases, Canadian Food Inspection Agency, Lethbridge, AB T1J 3Z4, Canada.; Departments of Chemistry & Biochemistry, University of Lethbridge, Lethbridge, AB T1K 3M4, Canada., Furukawa-Stoffer T; Centre for Vector-Borne Diseases, National Centre for Animal Diseases, Canadian Food Inspection Agency, Lethbridge, AB T1J 3Z4, Canada., Ambagala A; National Centre for Foreign Animal Diseases, Canadian Food Inspection Agency, Winnipeg, MB R3E 3M4, Canada., Vigil S; Southeastern Cooperative Wildlife Disease Study, University of Georgia, Athens, GA 30602, USA., Shahhosseini N; Centre for Vector-Borne Diseases, National Centre for Animal Diseases, Canadian Food Inspection Agency, Lethbridge, AB T1J 3Z4, Canada.; Department of Biological Sciences, University of Lethbridge, Lethbridge, AB T1K 3M4, Canada. |
| Abstrakt: |
Species delimitation of Culicoides complex species can be challenging. Among species within the Culicoides variipennis complex, C. sonorensis is considered the primary vector of bluetongue virus (BTV) and epizootic hemorrhagic disease virus (EHDV) in North America. Morphological identification of C. sonorensis within the C . variipennis complex is laborious, time-consuming, and requires entomology expertise. Therefore, in this study we developed and validated a multiplex real-time PCR for rapid detection and differentiation of C. sonorensis from the two other main cryptic species ( C. variipennis and C. occidentalis ) within the C. variipennis complex. The assay targets the EF1α gene and has a built-in internal control targeting 18 S. The specificity and the sensitivity of the multiplex real-time PCR were evaluated using morphologically identified reference and field-collected specimens. The multiplex PCR was 100% specific when nucleic acid extracted from C. variipennis , sonorensis , and occidentalis specimens was tested. When nucleic acid extracted from pools of midges was tested, the multiplex PCR was able to detect all three Culicoides species with comparable sensitivity. The multiplex assay, however, failed to detect eight morphologically identified C. sonorensis specimens collected from Alberta in 2014. The EF1α gene sequences of these specimens formed a distinct phylogenetic cluster, amongst those from C. variipennis , sonorensis , and occidentalis , suggesting that they belong to a different species. We hypothesize that those specimens might be C. albertensis , the only other species remaining in the C. variipennis complex with known geographical distribution in North America. We believe that this highly sensitive and specific multiplex real-time PCR assay could be an effective tool for rapid detection and differentiation of C. sonorensis , the known vector of BTV and EHDV, in trap collections in future vector surveillance programs. |
