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Strategies For Control

FMD Control in Europe

 

Historical Control

 

FMD outbreaks were numerous throughout Europe for most of the first half of the 20th century. However, as a result of advances in the large-scale production of vaccine it was possible to begin mass annual vaccination campaigns in the 1950s and 60s.

Some countries which had never vaccinated (e.g., United Kingdom, Ireland), or had given up vaccination a long time ago (Denmark), began to control FMD through importation control, slaughter and zoosanitary measures.

Mass annual prophylactic vaccination was very successful in totally eliminating European outbreaks by 1990. The banning of importation of bone-in beef from non-FMD-free states in 1978 assisted these FMD eradication policies.

Historically, the original source of FMDV for vaccine production was clinically derived material, such as infected cattle tongues (Vallée et al., 1926). In 1951 a new technique was described for the production of FMDV on an industrial scale in tongue explants (Frenkel, 1951). It was FMD vaccine made in this system that was used in The Netherlands in the first of the highly successful mass annual prophylactic vaccination campaigns to be carried out in Europe. The advantages of this production system were its simplicity, low cost and the fact that adaptation of the virus to the culture system was not required.

A significant development in FMDV antigen production was the transition to tissue culture methods for virus growth. Initially, small scale production in roller bottles using primary calf kidney cells was instigated in Italy (Ubertini et al., 1963). However, following the introduction in 1964 of a continuous cell line (BHK21), derived from baby hamster kidney fibroblasts, that supported the growth of FMDV (Stoker and MacPherson, 1964), this system gained wide acceptance in FMDV vaccine production. A significant scale-up in production capacity was achieved with the advent of technology which exploited the ability of BHK21 cells to grow in an anchorage independent manner in deep suspension culture (Capstick et al., 1965). Subsequently, a variety of monolayer systems was devised for anchorage-dependent cultures, to increase culture vessel surface area and thus productivity (Spier and Whiteside, 1976; Girard et al., 1980).

   


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