Short Communication

Seroprevalence of Bluetongue and Associated Risk Factors in Costa Rican Sheep Flocks

Rodolfo Villagra-Blanco1*, Gaby Dolz1, Danilo Montero-Caballero2, Juan José Romero-Zúñiga2

1Programa de Investigación en Medicina Poblacional, Escuela de Medicina Veterinaria, Universidad Nacional (UNA), P.O. Box 86-3000, Heredia, Costa Rica; 2 Cátedra de Salud de Hato y Control de la Producción, Escuela de Medicina Veterinaria, UNA, P.O. Box 86-3000, Heredia, Costa Rica.

Editor | Muhammad Munir, The Pirbright Institute, UK.

Received | August 24, 2015; Accepted | October 28, 2015; Published | November 22, 2015

*Correspondence | Rodolfo Villagra-Blanco, Programa de Investigación en Medicina Poblacional, Escuela de Medicina Veterinaria, Universidad Nacional (UNA), P.O. Box 86-3000, Heredia, Costa Rica; E-mail: [email protected]

DOI | http://dx.doi.org/10.17582/journal.bjv/2015.2.5.74.79

Citation | Villagra-Blanco, R., G. Dolz, D. Montero-Caballero and J. J. Romero-Zúñiga. 2015. Seroprevalence of bluetongue and associated risk factors in Costa Rican sheep flocks. British Journal of Virology, 2(5): 74-79.

Introduction

Bluetongue (BT) is a non-contagious viral disease affecting domestic and wild ruminants that is transmitted by insects, particularly biting midges of the Culicoides species (OIE, 2011). It is caused by a double stranded RNA orbivirus of the family Reoviridae, with more than 25 distinct serotypes distributed worldwide (Boden et al., 1971). The clinical signs of the disease range from a mild febrile illness to edema of lips and face, crusts on lips and muzzle, nasal discharge, conjunctivitis and extensive erosions of the oral mucosa, which can be mistaken for vesicular stomatitis virus, an endemic occurring disease in our country (Rodríguez et al., 1996), and for foot and mouth disease (Buxton & Frazer, 1977), not present in Costa Rica. Various techniques have been used to detect antibodies against bluetongue virus (BTV), however only agar gel immunodiffusion test (AGIDT), and enzyme-linked immunosorbent assay (ELISA) are accepted for international trade according the OIE Manual of Standards for Diagnostic Tests and Vaccines (Breard et al., 2004).

The incidence and geographical distribution of BTV depend on seasonal conditions, the presence of vectors, and the availability of susceptible animals. The midges prefer warm, moist conditions and are in their greatest numbers and most active after rain periods (Animal Health Australia, 2008). More than 40 species of Culicoides have been identified as vectors for BTV in the country (Greiner et al., 1990; Tanya et al., 1992), however Culicoides insignis was identified as the primary vector, since it was detected in more than 90.0% of the collections (Greiner et al., 1993; Sáenz and Greiner, 1994).

Prevalence of antibodies against BTV among sheep, goat and cattle had been reported in many tropical and subtropical areas, considered endemic zones, including Central America (Homan et al., 1985a,b; Mo et al., 1994; Mertens et al., 2009; Legisa et al., 2014). In Costa Rica, presence of BTV has been studied in cattle 30 years ago using AGIDT (Homan et al., 1985a,b), and serotypes 1, 3 and 6 were identified (Thompson et al., 1992), indicating the importance of Central America as a possible source of BTV for the rest of the continent (Mertens et al., 2009). However, the serologic evidence of this agent in sheep flocks, an emerging industry in Costa Rica, had not been studied to date. The aim of this study was to determine if antibodies against BTV were present in Costa Rican sheep blood samples, using a commercial competitive ELISA, and to identify risk factors associated to this viral infection.

Materials and Methods

Studied population

Sheep flocks registered at the Costa Rican Association of Sheep Producers were sampled, most of them were used commercially (87.0%), to produce tropical hair breed lambs (100.0%), and these animals were maintained mainly in intensive systems (93.0%). The sampled sheep breeds were Dorper, Pellybuey, Kathadin, Blackbelly, Texel, Suffolk, Santa Ines and their crosses.

Sample size

The sample size was calculated with an estimated population of 25,000 animals distributed in 138 sheep herds in Costa Rica (20.0% overall expected prevalence, 95.0% confidence level and 5.0% expected error), yielding a total of 244 samples to analyze; however, to enhance the power of the study, a total of 359 sheep were sampled. Within each herd, the number of animals to be sampled was calculated to determine presence or absence of antibodies against BTV, with 95.0% confidence, assuming a sensitivity and specificity of the ELISA of 99.0% (Vandenbussche et al., 2008; Niedbalski, 2011) using the formula described by Cannon and Roe (1982). Since most of the sheep farms presented similar management conditions and the distribution of the agent was unknown, the same chance of infection on each farm was assumed, thus, all animals within each farm had an equal chance of being infected. A random selection of farms within regions was performed in order to get a representative sample population in each region and inside each flock. The study was conducted in 15 Costa Rican sheep herds. According proportional allocation, the farms were distributed as follows: seven in the Central region (46.0%), two in the Chorotega region (13.5%), two in the Central Pacific region (13.5%), two in the North Huetar region (13.5%) and two in the Atlantic Huetar region (13.5%). The Brunca region was not analyzed, since it was not possible to find farms willing to participate in this study. However, less than 10.0% of animals were registered in this region.

Sample collection and survey

Blood was collected between August 2012 and February 2013. Tubes were transported using coolers for keeping a temperature between 4°C to 7°C. Afterwards in the laboratory the samples were centrifuged for 5 minutes at 10,000 g, sera was separated, and frozen at -20°C until processed by ELISA. A questionnaire applied during a Maedi Visna research (Villagra-Blanco et al., 2015) was analyzed again to obtain information in order to determine risk factors associated with BT disease such as housing, animal movement between herds, lamb husbandry, reproductive management and presence of compatible clinical signs of BT in each farm.

Enzyme-linked immunosorbent assay (ELISA)

The IDScreen® Bluetongue Competition Multispecies ELISA (Montpellier, France) was used. This assay reported a sensitivity and specificity of 99.0% (Vandenbussche et al., 2008). The methodology recommended by the manufacturer was used.

Statistical analysis

Frequencies of the general characteristics and management practices of the sheep flocks were calculated. To assess the relationship between BTV and the management practices, the odds ratio (OR) was calculated using a mixed effects logistic regression, being the sheep flock the random variable. The data was analyzed using SAS/STAT ver. 9.2 (SAS Institute Inc.).

Results and Discussion

Seropositive animals were detected in 14 (93.3%)

Table 1: Number and percentage of animals tested in15 sheep flocks and distribution of seropositive individuals according to flocks and regions

D: Dorper; K: Katahdin; P: Pelibuey; S: Suffolk; T: Texel; B: Blackbelly; Om: Other mixed breeds

Table 2: Risk factors associated with BTV seropositivity in sheep flocks in Costa Rica

OR: Odds Ratio; UL: Upper limit; LL: Lower limit; CI: Confidence Interval

flocks; however, in the seronegative flock only four animals were tested. From a total of 359 serum samples analysed, 290 sheep (80.8%) showed antibodies against BTV, the seropositivity in the regions analysed ranged between 63.5% and 100.0%. Meanwhile, the flock seropositivities determined ranged between 0% and 100.0% (Table 1). This study was the first attempt to detect BTV antibodies in sheep flocks in Costa Rica, an emerging and fast growing industry in the country. Previously, higher seroprevalences (from 15.0% to 75.0%) were reported in cattle by Homan et al. (1985 a, b, 1990, 1992).

Flocks with the highest seropositivity were found in low altitude regions close to the Atlantic and Pacific coast. Furthermore, only one small flock localized in a mountainous area (over 1,500 meters) with just four animals, all born inside this flock, was seronegative (Figure 1). According to Homan et al. (1985a, b) Costa Rica presented an inverse association between antibody prevalence of cattle and altitude of the farm, observation that coincides with the results obtained in our research.

Two management practices were determined as risk factors for BTV seropositivity: buying animals from other farms without any sanitary control (59.1% of the participating farms, OR= 2.54; IC= 1.49 to 4.35), and the lack of quarantine areas or separated boxes for sick animals in each flock (70.47% of the studied flocks, OR= 6.47; IC= 3.68 to 11.40). These risk factors have been described in the literature as factors facilitating the infection of sheep and goat flocks with different virus, bacteria and parasites (Vasileiou et al., 2015), including BTV (Mozaffari et al., 2014), especially if the animals are moved into high-humid

Figure 1: Location of the participating flocks with Bluetongue virus (BTV) seropositive sheep (black dots) and seronegative animals (white dots) within the five analysed regions of Costa Rica

endemic coast areas (Homan et al., 1990). Lack of sanitary control and lack of quarantine areas are not considered risk factors for BTV (Bosnić et al., 2015), the only risk factor would be exposure to Culicoides (Sáenz and Greiner, 1994), which was not analyzed in the present study.

On the other hand, all seronegative individuals (19.2%) belonged to flocks with partial stabling, indicating this management practice as a protective factor for BTV infection (OR= 1.10; IC= 1.06 to 1.14) (Table 2), since stabled animals are likely exposed to fewer Culicoides (Meiswinkel et al., 2000). However, BT disease occurs, when seronegative animals are bitten by Culicoides, typically as adults, and controlling exposure to these mosquitoes in Costa Rica might actually lead to clinical disease if infection is delayed (Holbrook, 1996).

Finally, no clinical signs of disease were observed in the analyzed sheep, findings that are in accordance with Mo et al. (1994). Sheep in endemic areas are naturally resistant to BT, and clinical disease is only observed when non-native ruminants, particularly European breeds, are introduced into these areas (OIE, 2011).

Measures for preventing and controlling the disease in endemic areas are based mainly on sentinel monitoring programs, in combination with surveillance programs of insect vectors (OIE, 2011).

The positive results obtained in this study confirmed the presence of antibodies against BTV in Costa Rican sheep flocks. Risk and protective factors determined in the present study were not in accordance with this insect borne disease, probably due to the type of study (cross-sectional). We recommend carrying out further studies, to determine the presence of BTV in goats and wild ruminants, and to identify serotypes present in the country.

Acknowledgements

Thanks to all farmers that participated in this research. We wish to thank Roberto Leiva and Jose Segura for their help.

Conflict of interest

There is no conflict of interest in this study.

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