“…Antigenic variants can be selected for in immune or partially immune hosts (Gebauer, De la Torre, Gomes, Maten, Barahona, Tiraboshi, Bergman, De Mello & Domingo 1988), although Diez, Mateu & Domingo (1989) reported that antigenic variants may accumulate over time even in the absence of antibody selection. Studies have shown that cattle and buffalo carriers (subclinically infected animals) may be a significant source of genetic variation (Salt, Samuel & Kitching 1996;Vosloo, Bastos, Kirkbride, Esterhuysen, Janse van Rensburg, Bengis, Keet & Thomson 1996;Vosloo, De Klerk, Boshoff, Botha, Dwarka, Keet & Haydon 2007). In particular, capsid protein VP1, encoded by the 1D gene, greatly contributes to the antigenicity of FMDV Mateu, Camarero, Giralt, Andreu & Domingo 1995) due to the existence of an immuno-dominant site, located between beta-strands G and H (the G-H loop) of VP1 which also acts as the cell receptor recognition site (Kitson, McCahon & Belsham 1990).…”