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Effect of temperature on survival and rate of virogenesis of African horse sickness virus in Culicoides variipennis sonorensis (Diptera: Ceratopogonidae) and its significance in relation to the epidemiology of the disease

Published online by Cambridge University Press:  10 July 2009

Martin P. Wellby
Affiliation:
Institute for Animal Health, Pirbright, Surrey, UK
Matthew Baylis
Affiliation:
Institute for Animal Health, Pirbright, Surrey, UK
Peter Rawlings
Affiliation:
Institute for Animal Health, Pirbright, Surrey, UK
Philip S. Mellor*
Affiliation:
Institute for Animal Health, Pirbright, Surrey, UK
*
Institute for Animal Health, Ash Road, Pirbright, Woking, Surrey GU24 ONF, UK.

Abstract

Culicoides variipennis sonorensis Wirth & Jones and C. nubeculosus (Meigen) were orally infected with African horse sickness virus (AHSV) type 9 and subsequently incubated at 10, 15, 20 and 25°C (R.H. 80%±10%). A time course of infection rates and virus titres was recorded by assaying flies individually or in pools, and survival rates of flies were also estimated. Survival rates at 10, 15 and 20°C were very similar and 80–90% of flies remained alive after 14 days; at 25°C after the same period survival was reduced to 40%. None of the C. nubeculosus became persistently infected with AHSV, but the virus took longer to clear as the incubation temperature dropped. At temperatures of 10, 15, 20 and 25°C virus was undetectable on days 12, 8, 5, and 4 days post infection (dpi), respectively. In C. v. sonorensis both the infection rate and rate of virogenesis were related to temperature. At 25°C a maximum mean titre of 104.3 TCID50/fly was reached by 9 dpi and the infection rate remained between 60 and 80%. At 20°C virogenesis was slower and a maximum mean titre of 104.3 TCID50/fly was reached only after 23 days; the infection rate was also reduced to 50–70%. At 15°C there was an overall decline in virus titre with time, although between 12 and 15 dpi some pools of flies contained 103.0–104.0 TCID50/fly, demonstrating that virogenesis can occur. The infection rate at this temperature decreased dramatically to 0–15% after 9 dpi. At 10°C there was no detectable virogenesis and all pools tested at 13 dpi were negative. The apparent infection rate dropped to 0–5% between 13 and 35 days post infection. However, when surviving flies were then returned to 25 °C for 3 days the infection rate increased to 15.5%. It therefore appears that at low temperatures the virus does not replicate but infectious virus may persist at a level below that detectable by the usual assay systems. The implications of these findings for the epidemiology of AHS are discussed.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 1996

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