Passage of foot-and-mouth disease virus under selection by neutralizing antibodies repeatedly led to critical amino acid replacements at one position in site A, which were never observed without it.
Critical amino acid replacements leading to important changes in antigenic specificity of FMDV occur only as a result of selection by neutralizing antibodies.
Antigenic variants of foot-and-mouth disease virus (FMDV) were generated and frequently became dominant in clonal populations of FMDV (clone C-S8c1) grown in the absence of anti-FMDV antibodies. We have now passaged eight samples of the same FMDV clone in the presence of a limited amount of neutralizing polyclonal antibodies directed to the major antigenic site A of capsid protein VP1. Complex populations of variants showing increased resistance to polyclonal sera and to site A-specific monoclonal antibodies were selected. Some populations exhibited marked decreases in viral fitness. Multiple amino acid replacements within site A--and also elsewhere in VP1--accumulated upon passage of the virus in either the absence or the presence of neutralizing antibodies. However, antigenically critical replacements at one position in site A occurred repeatedly in FMDV passaged under antibody selection, but they were never observed in many passages carried out either in the absence of antiviral antibodies or in the presence of an irrelevant antiviral serum. Thus, even though antigenic variation of FMDV can occur in the absence or presence of immune selection, critical replacements which lead to important changes in antigenic specificity were observed only as a result of selection by neutralizing antibodies.
Borrego et al. (Fri,) conducted a other in Foot-and-mouth disease virus (FMDV). Neutralizing polyclonal antibodies directed to the major antigenic site A of capsid protein VP1 vs. Absence of antiviral antibodies or presence of an irrelevant antiviral serum was evaluated on Antigenic variation and amino acid replacements. Passage of foot-and-mouth disease virus under selection by neutralizing antibodies repeatedly led to critical amino acid replacements at one position in site A, which were never observed without it.