No abstract

The complete nucleotide sequence of the genomic RNA of cymbidium mosaic potexvirus (CymMV) was determined to be 6227 nucleotides in length, excluding the poly (A) tail at the 3' terminus. Similar to other potexviruses, its genome organisation is comprised of five major open reading frames (ORFs 1 to 5), encoding a Mr 160 KDa putative RNA-dependent RNA polymerase (RdRp); a Mr 26KDa/13KDa/10KDa triple-gene-block (TGB) and a Mr 24 KDa coat protein. The CymMV encoded proteins shared a high degree of homology to their corresponding proteins of other members of the potexvirus group. The nucleotide sequence of the 5' noncoding region (NCR) of CymMV and all other potexviruses initiates with GAAAA. CymMV possesses the shortest 5' NCR among all potexviruses. Based on phylogenetic comparisons of RdRp and coat protein, CymMV shares a close relationship to PAMV, NMV, WClMV and SMYEaV. This is believed to be the first record of the complete nucleotide sequence of CymMV.

No abstract

Zucchini yellow mosaic virus (ZYMV) was first found in eucumber in Singapore in 1989. This virus was propagated m Cacurhita pepo cv. First Taste and mechanically transmitted to 12 speeies of six famtiies. It induced milder symptoms than the Connecticut and Florida strains of ZYMV in infected leaves of C. pepo ev. Zucchini Elite. ZYMV-S is neither seed nor aphid transmissible. Immunoelectron microscopy revealed that ZYMV-S is distantly related to WMV-2, Moroccan "WMV, and TelMV, but not related to PRSV or ZYFV. Cytopiasmie pinwheels and scrolls were observed in ultrathin sections of infected leaf cells hy light, eonfocal laser scanning, and transmission electron microscopy. The molecular weights of the viral coat protein and eytoplasmic inclusion protein, RNA and dsRNA were estimated to he 3.2 x 10-' , 6.

The cymbidium mosaic potexvirus (CyMV) banded inclusions and the odontoglossum ringspot tobamovirus (ORSV) paracrystalline inclusions were studied in flowers and leaves of nine orchid cultivars using the confocal laser scanning microscope. The inclusions varied in length and width and were mostly located adjacent to the cell walls. Some ORSV inclusions fully extended across entire infected cells. We propose that the CyMV banded inclusion was formed from virus aggregates which aligned as periodical stacked layers, appearing as cross bands. The virus aggregates were folded into flexible inclusions, giving rise to various shapes and forms. The ORSV paracrystalline inclusions were observed as needle-like crystals. The confocal laser scanning microscope is an effective tool for the study of the three-dimensional structures of plant virus induced inclusions.