The application relates to a primer and a
locked nucleic acid probe group for real-time fluorescent quantitative PCR detection of two strong and weak strains of
goose parvovirus, wherein the strong and weak strains of
goose parvovirus include MDGPV strong and weak viruses and SBDSV strong and weak viruses, and the sequences of the primer and the
locked nucleic acid probe group are shown in SEQ ID NO. 1-8. The LNA-
TaqMan real-time fluorescent quantitative PCR detection method established by using the primer and the LNA-
TaqMan probe group can simultaneously detect, differentially diagnose and accurately quantify the strong and weak strains of
goose parvovirus (duck small goose plague
virus and / or duck short-
beak dwarf syndrome
virus strong and weak viruses), and is high in sensitivity, strong in specificity and good in
repeatability.