This report details the development of an RT-PCR assay for the specific det
ection of US isolates of avian pneumovirus (APV). Of the several primer pai
rs tested, two sets of primers derived from the matrix gene of APV were abl
e to specifically detect the viral RNA of APV. The nucleotide sequence comp
arison of the PCR products of APV isolates from Minnesota suggested that th
ese viruses were closely related to the Colorado strain of APV, but were di
stinct from subtypes A and B European isolates of turkey APV (turkey rhinot
racheitis: TRT). This M gene-based PCR was found to be very specific and se
nsitive. APV as low as 8 x 10(-5) TCID50 (0.0323 mu g/ml) could be detected
using this assay. In addition, the two primers were able to differentiate
isolates from turkeys in Minnesota.