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Volume 17, Number 2—February 2011


Orbiviruses in Rusa Deer, Mauritius, 2007

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EID Jori F, Roger M, Baldet T, Delécolle J, Sauzier J, Jaumally MR, et al. Orbiviruses in Rusa Deer, Mauritius, 2007. Emerg Infect Dis. 2011;17(2):312-313.
AMA Jori F, Roger M, Baldet T, et al. Orbiviruses in Rusa Deer, Mauritius, 2007. Emerging Infectious Diseases. 2011;17(2):312-313. doi:10.3201/eid1702.101293.
APA Jori, F., Roger, M., Baldet, T., Delécolle, J., Sauzier, J., Jaumally, M. R....Roger, F. (2011). Orbiviruses in Rusa Deer, Mauritius, 2007. Emerging Infectious Diseases, 17(2), 312-313.

To the Editor: Bluetongue and epizootic hemorrhagic disease are caused by orbiviruses transmitted by Culicoides spp. biting midges (Diptera: Ceratopogonidae). These diseases are restricted to regions where their vectors exist (1) and seem to be expanding to previously unaffected areas (2). Infection of wild and domestic ruminants is common. Bluetongue virus (BTV) causes severe clinical disease in certain breeds of sheep; BTV and epizootic hemorrhagic disease virus (EHDV) cause clinical disease in some species of deer (3,4).

Rusa deer (Cervus timorensis rusa), originally from Indonesia, are found in diverse countries in the Pacific region (Papua New Guinea, New Caledonia, New Zealand, and Australia). Introduced to the island of Mauritius in 1639, they are commonly raised in high numbers (≈60,000) for meat production (5). Mauritius is considered free from major livestock diseases; its animal health surveillance is based mainly on clinical monitoring and inspection of carcasses at slaughter. To our knowledge, circulation of orbiviruses in Rusa deer has not been reported in detail in any country where this deer is present.

Our study was an initial screening survey of the deer population on the island. A total of 369 deer, representing 28 private farms, were chosen from a list of 42,959 deer. Blood was collected at slaughter, and serum samples were sent to Onderstepoort Veterinary Institute, South Africa, to be tested for antibodies against orbiviruses with a homemade indirect ELISA. To distinguish between BTV and EHDV, samples positive by indirect ELISA were tested for BTV antibodies with the competitive ELISA produced by the Institute for Animal Health (Pirbright, UK). Of the samples positive by competitive ELISA, 3 were tested by serum neutralization against the 24 BTV serotypes (cutoff value >16).


Thumbnail of Location of farms where Rusa deer were sampled (open circles), herds with orbivirus-seropositive deer (closed circles), biting midge collection sites (triangles), and main cities (crosses) in Mauritius. Most (99%) Culicoides spp. midges were trapped at sites 1 and 3. Inset show location of Mauritius (in square) in relation to Africa and Madagascar.

Figure. Location of farms where Rusa deer were sampled (open circles), herds with orbivirus-seropositive deer (closed circles), biting midge collection sites (triangles), and main cities (crosses) in Mauritius. Most (99%) Culicoides spp....

Simultaneously, Culicoides spp. midges were trapped in Onderstepoort-type blacklight traps at 3 deer farms in coastal areas (Figure). Trapping was conducted 1 night at each farm, during optimal weather conditions. Midges were kept at room temperature in 95% ethanol until sent to Strasbourg University, France, for identification.

Of the 369 deer serum samples tested, 15 were positive for BTV and 5 for EHDV; seroprevalence was 4.1% for BTV (95% confidence interval 2.0%–6.1%) and 1.3% for EHDV (95% confidence interval 2.0%–6.1%). No significant differences were observed for sex (χ2 = 0.05, p = 0.82). Antibodies (indirect ELISA) against orbiviruses were more prevalent among adults (χ2 = 4.56, p = 0.03). The 3 samples tested by serum neutralization had high titers against BTV-2 (256, 256, and 128) and lower but positive titers against BTV-17 (32 in each), BTV-10 (16 in each), and BTV 21 (32 in 1). Despite reports of clinical signs in other deer species infected with both viruses (3,4), no signs of bluetongue or epizootic hemorrhagic disease were reported for the Rusa deer population in our survey. This absence of clinical disease might be the result of natural resistance of this species to orbiviruses or to the fact that the circulating serotypes are endemic to the area.

A total of 13,356 Culicoides spp. midges were obtained; 12% were identified as C. imicola (1,459 females, 138 males) and 88% as C. enderleini (8,800 females, 2,878 males). The former species has been reported in Mauritius (6). In our study, the positive serum came from deer on 4 farms located in the coastal area. This finding could indicate a higher abundance and activity of C. imicola midges in coastal areas, where climate and altitude are more favorable for the vector.

Serum neutralization results suggested that at least 4 serotypes could have been circulating in deer from Mauritius. During outbreaks of both viruses in neighboring Réunion Island, several serotypes of BTV were isolated from sheep (7,8) and of EHDV from cattle (9). However, BTV serotypes 17 and 21 have never been isolated from Indian Ocean countries, and serotype 21 has been detected only in Australia (2). Equally, diverse BTV serotypes circulate at different locations on the Indian Ocean and the east coast of Africa (2,5,6).

Our results provide serologic indication that EHDV and BTV circulate in Rusa deer in Mauritius. The large population of Rusa deer can represent a potential reservoir host for those viruses and a risk for transmission to other ruminants in Mauritius and neighboring countries. However, Rusa deer could be used as a sentinel population to regularly monitor the circulation of orbiviruses and the introduction of new serotypes to Mauritius. To detect and isolate circulating serotypes and genotypes of these viruses in ruminant species and in potential vectors in Mauritius, further research is needed. In addition, the extent of both viruses and the distribution of Culicoides midges over the island should be investigated in more detail.


We thank the Division of Veterinary Services of Mauritius for providing logistical assistance and laboratory facilities, all deer herd managers for their collaboration, and Truuske Gerdes for reviewing the manuscript and advising with regard to the analysis.

This work was supported with the funds from the French Ministry of Foreign Affairs within the project “Support to the harmonization of epidemiological surveillance networks for livestock diseases” (FSP project no. 2003–067).

Ferran JoriComments to Author , Matthieu Roger, Thierry Baldet, Jean-Claude Delécolle, Jacqueline Sauzier, Mahmad Reshad Jaumally, and François Roger

Author affiliations: Author affiliations: French Agricultural Research Center for International Development (CIRAD), Montpellier, France (F. Jori, F. Roger); University of Pretoria, Pretoria, South Africa (F. Jori); CIRAD, Sainte-Clotilde, La Réunion Island, France (M. Roger); CIRAD, Cotonou, Bénin (T. Baldet); Université de Strasbourg, Strasbourg, France (J.C. Delécolle); Mauritius Deer Farming Coopérative Society Ltd, Curepipe, Mauritius (J. Sauzier); Ministry of Agro Industry and Fisheries, Réduit, Mauritius (M.R. Jaumally)


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DOI: 10.3201/eid1702.101293

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Table of Contents – Volume 17, Number 2—February 2011


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Ferran Jori, CIRAD-UPR AGIRs, Department ES TA 30/E, Campus International de Baillarguet, Montpellier 34080, France

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