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1 Rlchard H. Convem USDA-ARS, Oregon State University, Corvallis Anthony N. Adams, Derek J. Barbara, and Mlchael F. Clark Institute of Horticultural Research, East Malling. United Kingdom Rudolf Carper West German Ministry of Agriculture, Braunschweig Ruprto F. Hepp Universidad de Concepcibn, Chillan, Chile Robert R. Martin Agriculture Canada, Vancouver, BC T homrs J. Morrls University of California, Berkeley Sara Splegel Volcani Centre, Bet Dagan, Israel Nobuyukl Yoshlkawa hate University, Morioka, Japan Lal:,.matory E-Lection of Viruses and Mycoplasmalike Orr -=-'---- in Stram--b-?ry u -- The cultivatcd strawbeny {Fragarirr X ananasso Duchesne), an important fresh market and processed fruit crop in many parts of the world, is infected by many viruses and myeoplasmaiike organisms (MLOs). Currently, 29 are known, and we can anticipate that more will be found. A few of these pathogens kill infected strawberry plants, but the majority reduce productivity while inducing no distinctive symptoms. Beeause vegetatively propagated cultinn are used to grow this crop, techniques other than diagnosis by visual symptoms have been necessary to dctcrminc the virus status of potential strawberry planting material. h f gmft bioassays are currently used to detect most viruses in strawberry plants (6). Recent dwelopments in plant vim serology and molecular biology have provided rapid, Cmpntive nstarch ktween the United Statm Depsnmmt of Agricultum, Agricultural Research Scrvict. and the Oregon Agricultural Expcrimcat Station. Technical paper 8496 d tt# ]attar. This aitlcle le in the publlc domnin and nnt copyrightabta. It may be freely mprtnted with cultornary crediting ol the source. The American Phytopmthologhl Society, lw. 744 Plant DlrrtlaneNol. 72 No. 9 accurate, and sensitive techniques to augment or replace thtse standard bioassays. The USDA's Agricultnral Handbook 631 (6) provides a convenient review of the literature pertinent to stmwbtrry viruses and MLOs and their laboratory detection through Our purpose in tbis article is to present developments in ibis field hat have been reported in the literature ovw the last 8 ymrs. Strawberry mottle virus (SMV). In 1968, Frazier (10) mechanicslly transmitted this semipersistent aphid-borne virus to Chmopodium quinog Wid. to produce characteristic mild vein banding, vein necrosis, and epinasty {Fig. I). This work was recently repeated (514). From both C. quinoa and F. vesca L, VS-I infected with SMV. two bands of doublestranded RNA (dsrna) were detected with rtlative molecular weights of approximately 5.4 and 4.6 million daltons (2). In other experiments (16), however, no dsrna bands could be detected in I? *sea illftcted with SMV by aphid inoculations. The virus was successfully trornsmittwl mechanically or by the aphid Chuerosfpkon fragrrfoiii (Cockerell) from C. quinw to F. v. var. sempeflorem cv. Alpine, where it produced symptoms typical of strawberry mottle disease (14). This contrasts with unsuc~sful attempts by others either to return the virus from C. qukoa and other herbaceous hosts to F. vesca by means of aphids, grafting, and dodder (2.10) or to purify the virus (2). These discrepancies may reflect differences among isolates of SMV. Partial purification of SMV from infected C. quinoa leaves by means of h~mogmization in buffer, polyethylene glycol precipitation, low- and high-speed centrifugation, and CsCl ~quilibrium density gradient centrifugation gave rise to preparations containing isometric viruslike particles having a buoyant density of 1.351cmJ, with a prticle diameter of 30 nm, as determined by electron microscopy of preparations stained with 2% neutral phwphotungstate, Such partidcs wewen aknt from uninoculated control plants (14). smwberrywfn~v~(sv8v). SVBV (Fig. 2) was previously chmw terized sufficiently to establish its group status as a plant cauhovirus (23),
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