Bluetongue virus in Culicoides spp. in Manabí province, Ecuador
Author:
Centeno Mariella1ORCID, Chliliquinga Denisse1, Velázquez José2, De La Torre Euclides3ORCID, Jarrín David4, Maldonado Alex5ORCID, Alava Jimmy1, Barrera Maritza1ORCID
Affiliation:
1. Veterinary Department. Faculty of Veterinary Sciences, Universidad Técnica de Manabí, Portoviejo 130105, Manabí, Ecuador 2. Rapid Diagnostic Laboratotaory. Agencia Ecuatoriana para el Control Fito y Zoosanitario (AGROCALIDAD), 130802 Manta, Manabí, Ecuador 3. Animal Diagnostic Laboratory. Agencia Ecuatoriana para el Control Fito y Zoosanitario (AGROCALIDAD), 170184 Quito, Pichincha, Ecuador 4. Molecular Biology Laboratory. Agencia Ecuatoriana para el control Fito y Zoosanitario (AGROCALIDAD), 170184 Quito, Pichincha, Ecuador 5. Animal Diagnostic Laboratory. Agencia Ecuatoriana para el Control Fito y Zoosanitario (AGROCALIDAD), 170184 Quito, Pichincha, Ecuador, Facultad de Ciencias de la Salud, Universidad Internacional SEK, Ecuador
Abstract
Bluetongue is a viral disease that affects sheep, cattle and other domestic or wild ruminants. Different species
of Culicoides transmit the virus (BTV). High BTV seroprevalence was found in farms of Manabí and other
two provinces of Ecuador, but the presence of the virus in the Culicoides spp. vector has not been reported. In
the current study, the main goal was to demonstrate the presence of BTV in Culicoides in Ecuador for the first
time and characterize the species of Culicoides collected in farms located in the central-east area of Manabí
province. Six farms were selected to be monitored by BTV c-ELISA. All the 100 tested animals were
positive. Using a CDC trap with ultraviolet light placed in three BTV-positive farms for three nights, 2240
specimens of Culicoides were collected. Six different Culicoides species have been identi-fied, which were
presented in different abundance percent: 62% C.insignis; 7% C. batesi; 1.8% C.foxi; 1.8% C.diabolicus;
15.48% C.crepuscularis; 12% C.antunesis. These last two species have been identified for the first time in
Ecuador. Q-PCR detected BTV RNA in the homogenates of female midges collected in each farm, so it was
demonstrated that the epidemiological cycle of the virus is completed; since female midges infected with
BTV were found, it is too a novel result for Ecuador.
Keywords: Bluetongue, BTV, Culicoides, cattle, real-time PCR, competitive ELISA, Ecuador, Manabi
Publisher
Clinical Biotec
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