Two groups of pigs were infected with a recent Italian isolate of swin
e vesicular disease virus (SVDV). Blood, nasal swabs and faeces were c
ollected for up to 6 months after exposure to infection and animals we
re killed at regular intervals to obtain tissues post-mortem. These sa
mples were examined for virus by conventional means and for viral RNA
(vRNA) by reverse transcription-nested polymerase chain reaction (RT-n
PCR). Virus was identified intermittently from both clinically and sub
clinically infected animals in nasal swabs, faeces and tonsillar tissu
e by either virus isolation or RT-nPCR up to 63 days post infection (d
pi). Between 63 and 119 dpi virus was not detected in the secretions,
excretions or tissues of any pigs. Following mixing of the two groups
of animals at 119 dpi, SVDV was again identified in faeces for up to 7
days suggesting that the stress of mixing reactivated the excretion o
f virus in pigs from which the agent could no longer be identified. Mi
nor antigenic changes were identified between the parental virus and i
solates recovered late in the course of infection. Altered antigenicit
y corresponded with deduced amino acid substitutions identified from d
ifferences in nucleotide sequence between early and late isolates. Thi
s investigation demonstrates that SVDV and vRNA can be present in pigs
for considerably longer after exposure to infection than has previous
ly been recognized and provides preliminary evidence for a carrier sta
te in swine vesicular disease.