Rotaviruses, members of the Reoviridae family, are major etiologic age
nts of acute nonbacterial gastroenteritis of the young in a wide varie
ty of mammalian and avian species, including humans. The need for effe
ctive immunoprophylaxis against rotaviral gastroenteritis has stimulat
ed interest in the biochemical, molecular, genetic, and clinical aspec
ts of these agents with the aim of developing safe and effective vacci
nes. Because neutralizing antibodies appear to play an important role
in protection against many viral diseases, rotavirus antigens that ind
uce neutralizing antibodies have played a central role in research and
development of a rotavirus vaccine. The VP7 glycoprotein and VP4 spik
e protein that constitute the outer capsid of a complete rotavirus par
ticle have been shown to be independent neutralization antigens. Since
type specificity of the outer capsid proteins of a rotavirus appears
to play an important role in protection against disease in experimenta
l animal models, continued efforts have been made for classification a
nd typing of neutralization specificities on the VP7 or VP4 capsid pro
tein. Based on a criterion of >20-fold differences between the homolog
ous and heterologous reciprocal neutralizing antibody titers, fourteen
VP7 (G) serotypes have been established. Studies are underway to char
acterize and classify the VP4 (P) serotypes among the strains that exh
ibit the fourteen different G serotypes. Attempts to classify the VP4
serotypes based on the same criterion (i.e., >20-fold antibody differe
nces) that is applied to classification of VP7 serotypes are in progre
ss. This standard of >20-fold antibody differences can be applied with
hyperimmune serum raised to a reassortant possessing the VP4 encoding
gene (and an unrelated VP7 encoding gene). Genotypes can provide lead
s towards classification but the serotype of a strain should be based
on neutralization.