In 1994, potato samples for certification from Idaho seed fields react
ed in enzyme-linked immunosorbent assay (ELISA) tests to a polyclonal
potato carlavirus M (PVM) antiserum. Sample affinity to the antiserum
was lower than control samples. Furthermore, ELISA-positive samples we
re obtained from both symptomatic as well as asymptomatic plants. A co
mplementary DNA library was prepared using both reverse transcription-
polymerase chain reaction and primers based on published PVM sequences
, or oligo d(T) primed reverse transcribed sequences. The nucleotide s
equence was determined for the 3'-terminus of the genome. Putative coa
t protein amino acid sequence was compared to published PVM and potato
virus S coat protein sequences. While this new isolate is likely a st
rain of PVM, it is significantly different from known PVM coat protein
sequences in the amino terminus region. These differences may explain
the poor reactivity to other PVM antisera and suggest that it is a ne
w strain of PVM, which we have designated PVM-ID.