Nucleotide sequences of mouse parvovirus (MPV) isolate, named MPV/UT, and mouse minute virus (MMV) were analyzed and used for expressing
recombinant proteins in E. coli. ELISA tests using recombinant major
capsid protein (rVP2) and recombinant major non-structural
protein (rNS1) as
antigens were developed and their performance in serologic detection of rodent
parvovirus infection was assessed. MPV-rVP2 and MMV-rVP2 ELISAs reacted specifically with anti-MPV and anti-MMV mouse sera, respectively. MMV-rNS1
antigen had a wide reaction range with
antisera to rodent parvoviruses including MPV, MMV, Kilham rat virus (KRV) and H-1 virus. All mice oronasally infected with MPV were seropositive at 4 weeks post-
infection in screening by ELISAs using MPV-rVP2 and MMV-rNS1
antigens, but were negative by conventional ELISA using whole MMV
antigen. A contact transmission experiment revealed that transmission of MPV occurred up to 4 weeks post-
infection, and all cage mates were seropositive in screening with MPV-rVP2 and MMV-rNS1 ELISAs. These results indicate that MPV-rVP2 and MMV-rVP2 are specific ELISA
antigens which distinguish between MPV and MVM
infection, while MMV-rNS1
antigen can be used in generic ELISA for a variety of rodent parvoviruses. The higher sensitivity of MPV-rVP2 ELISA than conventional ELISA for detecting seroconversion to MPV in oronasally infected mice as well as in cage mates suggests the usefulness of MPV-rVP2 ELISA in quarantine and microbiological monitoring of MPV
infection in laboratory mice.