SEROLOGICAL AND PHYSICAL PROPERTIES OF SOME STONE-FRUIT VIRUSES: NON-VIRUS PARTICLES ASSOCIATED WITH INFECTION

1961 ◽  
Vol 39 (6) ◽  
pp. 1447-1452 ◽  
Author(s):  
R. S. Willison ◽  
J. H. Tremaine ◽  
M. Weintraub

Cherry yellow virus, isolates Y.2 and Y.4, and necrotic ring spot virus, isolates N.4 and N.5, purified either from cucumber leaves or from sour cherry petals, were characterized by antigenically related particles that sedimented at approximately 72 S. Some preparations of each virus derived from either host also contained either a 35 S or a 22 S component usually having a low nucleic acid content. Such preparations were shown by the agar gel double-diffusion technique to contain two antigens, V and Q, that were only distantly, if at all, related. The 72 S component is associated with the V antigen, whereas the 22 S and 35 S components are tentatively considered to be two forms of the Q antigen. The Q antigen could also be detected in clarified expressed sap of infected cucumber tissue, but not in that of healthy cucumber nor in extracts prepared from healthy sources by methods used to purify the viruses. The Q antigen is thus associated with infection, but its origin has not yet been satisfactorily determined.

1962 ◽  
Vol 40 (2) ◽  
pp. 361-373 ◽  
Author(s):  
J. H. Tremaine ◽  
R. S. Willison

Concentrated extracts of petals from trees infected with stone-fruit virus diseases, and of cucumber plants inoculated with viruses isolated from these trees, were tested serologically by the gel-diffusion technique with antisera prepared by injection of petal and cucumber plant preparations into rabbits. An antigen, antigen Q, was detected in two yellows, latent and recurrent necrotic ring spot, two green ring mottle isolates from sour cherry, a prune dwarf isolate, two tatter leaf of sweet cherry isolates, and isolates from latent infections of plum and peach. Another antigen, the V antigen, was detected in all the isolates with the exception of a latent necrotic ring spot isolate. A third antigen, antigen P, was detected only in the two yellows, recurrent necrotic ring spot, two green ring mottle isolates from sour cherry, a prune dwarf isolate, and two tatter leaf isolates from sweet cherry. Some differences between the Q antigens in certain isolates were demonstrated, but the V antigens differed little from isolate to isolate. The recurrent necrotic ring spot isolate was shown to contain at least two distinct viruses and the P antigen was associated with one of these viruses.


1965 ◽  
Vol 45 (6) ◽  
pp. 525-535 ◽  
Author(s):  
T. R. Davidson ◽  
J. A. George

In a randomized block experiment sour cherry trees were infected at 1, 2, 4, or 6 years of age with either the necrotic ring spot virus (NRSV) or the sour cherry yellows virus (SCYV) or with both. Tree growth was retarded by both viruses but the effects of SCYV were most severe. A marked retardation of the growth rate following SCYV infection persisted for two to five years depending on the age of the tree when infected. The growth rate of trees infected with both viruses was very similar to that for trees with SCYV only and indicates the predominance of this virus in these combinations. NRSV alone caused a slight reduction in growth rate but there was never an abrupt effect.Because the effects of SCYV on growth and tree form were severe, yields were very low. NRSV caused only a 10 to 30% reduction in growth but the reduction in yield varied from 36 to 56%. Hence the effects of NRS may be of more economic importance than the relatively minor reductions in growth have indicated.


1962 ◽  
Vol 40 (8) ◽  
pp. 1041-1049 ◽  
Author(s):  
R. S. Willison

One-year-old virus-free sour cherry trees of the variety Montmorency were inoculated singly with buds from different source trees infected with sour cherry yellows, necrotic ring spot, prune dwarf, and tatter leaf respectively. The infections thus established in the test trees were later challenged by inoculation with isolates from different sources. Conspicuous recurrent symptoms occurred when infection from a tatter leaf isolate was challenged by either of two necrotic ring spot virus strains, but not when the order of challenge was reversed. These symptoms are interpreted as a synergistic response to infection by two viruses, one from each source, within a limited range of interaction. Trees previously infected with necrotic ring spot when reinoculated with cherry yellows isolates showed symptoms of cherry yellows, usually preceded by secondary shock. The reciprocal challenges, on the other hand, induced no symptoms of necrotic ring spot, probably because each of the cherry yellows sources carried a strain of the necrotic ring spot virus. There were indications, however, of interference between the two viruses. Infection with the prune dwarf virus did not protect against subsequent infection with the cherry yellows virus. Mixed infections with the necrotic ring spot and prune dwarf viruses did not cause cherry yellows.


1959 ◽  
Vol 39 (4) ◽  
pp. 431-436 ◽  
Author(s):  
T. R. Davidson ◽  
J. A. George

Each month throughout the growing seasons of 1954 and 1955 two pairs of virus-free Montmorency sour cherry trees were inoculated by budding or patch grafting, one pair with cherry yellows and the other with necrotic ring spot virus. Shock symptoms induced by the two viruses were indistinguishable except that growth was retarded more severely and longer with yellows than with ring spot. However, the type and distribution of initial symptoms varied with the time of inoculation. Four symptom patterns were distinguished, and each was associated with an inoculation period. Seasonal symptom variations also revealed that the rate of movement of the yellows virus differed from that of the ring spot virus.


1964 ◽  
Vol 44 (5) ◽  
pp. 471-484 ◽  
Author(s):  
T. R. Davidson ◽  
J. A. George

In the Niagara Peninsula of Ontario necrotic ring spot (NRS) and sour cherry yellows (SCY) are the two principal virus diseases of sour cherry. Since 1951 most trees grown in this area have been propagated from virus-free budwood but about 4% of the rootstock used carries virus.A combination of symptoms known as ’shock’ is the usual reaction to infection with either virus. However, in some trees the first sign of infection is only an etch, which is usually considered to be a secondary symptom of NRS. In a few trees the primary symptoms are very mild trace reactions strongly suggestive of trees that have been infected for a long time. Indexing on peach seedlings is generally not a good indicator of current season infection. It is however very accurate in detecting virus in trees that have been infected for more than 1 year.The rate of virus spread in young orchards is dependent upon the age of the orchard, the proximity of older diseased trees, and the amount of disease within the orchard. Necrotic ring spot virus (NRSV) spreads very slowly in orchards under 4 years old but can spread very rapidly in orchards over 4 years old. Most rapid spread of NRS occurs after 20% of the trees in an orchard are infected. Sour cherry yellows virus on the other hand does not spread rapidly until after the 10th year. Both viruses can spread over a considerable distance, NRSV at least 800 yd and SCYV about 100 yd, but most infections of both occur within 50 ft of a known source. There is no indication that any plant other than sour cherry serves as a source of inoculum.


Plant Disease ◽  
2004 ◽  
Vol 88 (2) ◽  
pp. 221-221 ◽  
Author(s):  
R. K. Jain ◽  
K. M. Nasiruddin ◽  
Jyoti Sharma ◽  
R. P. Pant ◽  
A. Varma

Papaya (Carica papaya L.) is an important fruit crop in Bangladesh. During surveys conducted in Dhaka and Mymensingh regions from April to June 2003, >50% of papaya plants were observed to have leaf mottling, mosaic and mild distortion, and water-soaked streaks on petioles and stem, which are typical symptoms of Papaya ring spot virus (PRSV) infection. Electron-microscopic examination of negatively stained leaf-dip preparations from 10 symptomatic samples revealed the association of flexuous virus particles that were decorated with polyclonal antibodies raised to an isolate from India (PRSV-D). The identity of PRSV associated with the papaya disease in Bangladesh was further confirmed by reverse transcription polymerase chain reaction and sequence analysis (2). By using PRSV specific primers (2), the 3′-terminal region comprising a part of the nuclear inclusion b gene, the coat protein (CP) gene, and the untranslated region were amplified and sequenced (GenBank Accession No. AY423557). The CP gene consisted of 286 amino acids and the conserved regions common to the genus Potyvirus, such as WCIEN and QMKAA, were present. Like all known PRSV sequences (1), a stretch of glutamic acid and lysine repeats (EK region) after the aphid transmission motif (DAG) also was present. Comparative CP amino acid sequence analyses revealed that the virus infecting papaya in Bangladesh, designated as PRSV-Bd, shared 89 to 92% identity with PRSV isolates from India and 88 to 93% identity with isolates from other parts of the world. To our knowledge, this is the first report of occurrence of PRSV infecting papaya in Bangladesh. References: (1) M. F. Bateson et al. J. Gen. Virol. 83:2575, 2002. (2) R. K. Jain et al. Ann Appl. Biol. 132:413, 1998.


1963 ◽  
Vol 43 (3) ◽  
pp. 276-288 ◽  
Author(s):  
J. A. George ◽  
T. R. Davidson

Montmorency sour cherry trees, 3 years of age and older, became infected more often with necrotic ring spot virus when exposed during May than when caged individually under 32-mesh screen during May. In screened compartments, necrotic ring spot spread only when bees were present during blossoming. Though necrotic ring spot spread to all but 1 untreated tree in a bearing orchard, it did not spread to neighbouring trees from which blossom buds were removed. Finally, necrotic ring spot virus was transferred to at least 4, and sour cherry yellows virus to at least 1 and possibly a second, of 14 trees that were emasculated and then pollinated with pollen from diseased trees. It is concluded that the viruses causing these diseases are transmitted from one cherry tree to another through pollination.


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