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Host range, purification and some properties of rubus Chinese seed‐borne virus
Author(s) -
BARBARA D. J.,
ASHBY S. C.,
MCNAMARA D. G.
Publication year - 1985
Publication title -
annals of applied biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 80
eISSN - 1744-7348
pISSN - 0003-4746
DOI - 10.1111/j.1744-7348.1985.tb01546.x
Subject(s) - biology , rubus , virus , chenopodium quinoa , chenopodium , plant virus , nepovirus , botany , nucleic acid , host (biology) , staining , virology , biochemistry , ecology , weed , genetics
SUMMARY A previously undescribed virus, for which the name rubus Chinese seed‐borne virus (RCSV) is proposed, was isolated from a single, symptomless plant of an unidentified Rubus species grown from seed collected in the wild in the People's Republic of China, Experimentally RCSV infected 23 out of 39 spp. in six out of eight families. The virus was seed‐transmitted in Chenopodium quinoa (100%) and Nicotiana bigelowii (27%). RCSV was not transmitted by the nematodes Xiphinema diversicaudatum or X. index . The particles of RCSV were isometric, c . 30 nm in diameter with some penetrated by negative stains. In thin sections particles were found in double walled tubular structures with an outer membrane enclosing one or more tubules. In crude extracts some particles were found within single‐walled tubules. Two virus‐associated bands were seen in sucrose density gradients of purified preparations. The upper band was not infective and consisted of penetrated particles apparently devoid of nucleic acid. The lower, infective band was resolved into two components, of density 1.452 and 1.461 g/ml, in caesium chloride isopycnic gradients. There were two polypeptides (mol. wts c . 47 000 and 25 200 daltons) and two nucleic acid species (one of mol. wt c . 1.4 × 10 6 daltons; the second was poorly defined by the methods used but was of higher molecular weight). RCSV was distantly related serologically (6–7 SDI) to the type isolate of strawberry latent ringspot virus (SLRV) and also reacted with antisera to serologicaly distinct grape and olive isolates of SLRV. It did not react with antisera to 10 other isometric viruses.