Symptoms associated with infection by Ornithogalum mosaic virus (OMV) were
documented among horticulturally important Ornithogallum spp. grown in comm
ercial greenhouses and open fields in Israel. OMV was mechanically transmit
ted to Chenopodium quinoa and C. amaranticolor. The virus was purified from
infected C. quinoa using CsCl step gradient centrifugation. Virus yield of
18-24 mg kg(-1) were obtained. Antiserum produced to the purified virus wa
s highly specific in immunoblots and immunosorbent electron microscopy. Rev
erse transcription - polymerase chain reaction (RT-PCR) utilising potyvirus
-specific primers and the viral RNA resulted in the amplification of a DNA
product of 1275 nucleotides. This PCR product was cloned and sequenced; it
encoded an open reading frame of 333 codons and a 3' non-coding region of 2
75 nucleotides. Analysis of the amino acid sequences of the putative CP of
the Israeli isolate of OMV showed 95% similarities to the South African iso
late.