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Subterranean clover red leaf virus (SCRL V) was purified from infected peas using cellulase to assist in virus extraction. Yields of 0.5–3.0 mg/kg tissue were obtained. The virions were isometric with a diam. of 27 nm and sedimented as a single component of 114 S. The mean A260/A280 of purified preparations was 1.85. Apterae of Aulaeorthum solani (Kltb.) when fed on purified preparations through parafilm membranes were able to acquire and transmit virus. Purified virus had a dilution end point of 1.36 µg/ml, a thermal inactivation point between 55 and 60°C, and longevity in vitro of greater than 14 days. Gel electrophoresis of disrupted virions revealed that the coat protein was a single polypeptide with a molecular weight of 22 600. An antiserum with a homologous titre of 11256 in gel diffusion tests was prepared. SCRL V was shown to be serologically very closely related to soybean dwarf virus and less closely to bean leafroll, legume yellows, potato leaf roll, and tomato yellow top viruses. A more distant relationship was shown with beet western yellows virus. All the properties of SCRL V are consistent with it being a member of the luteovirus group and suggest that it is probably identical with soybean dwarf virus.
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Ashby et al. (1982) studied this question.
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