Many viruses induce a strong T cell response that contributes to the elimin
ation of infected cells presenting viral peptides by MHC molecules. The str
ucture and expression of genes encoding molecules homologous to mammalian a
lpha beta TCRs have been recently characterized in rainbow trout and in sev
eral teleost species, but the alpha beta T cell response against pathogens
has not been directly demonstrated. To study the modifications of the T cel
l repertoire during an acute viral infection in rainbow trout, we adapted t
he immunoscope methodology, which consists of spectratyping the complementa
rity-determining region 3 length of the TCR beta chain. We showed that the
naive T cell repertoire is polyclonal and highly diverse in the naive rainb
ow trout. Using viral hemorrhagic septicemia virus (VHSV), which provokes a
n acute infection in rainbow trout, we identified skewed complementarity-de
termining region 3 size profiles for several V betaJ beta combinations, cor
responding to T cell clonal expansions during primary and secondary respons
e to VHSV. Both public and private T cell expansions were shown by immunosc
ope analysis of spleen cells from several infected individuals of a rainbow
trout clone sharing the same genetic background. The public response to VH
SV consisted of expansion of V beta 4J beta1 T cell, which appeared early d
uring the primary response and was strongly boosted during the secondary re
sponse.