Netherlands Journal of Plant Pathology

, Volume 91, Issue 2, pp 77–92 | Cite as

Characterization of a carlavirus from dandelion (Taraxacum officinale)

  • Jeanne Dijkstra
  • Yvonne Clement
  • H. Lohuis
Article

Abstract

A carlavirus was isolated from leaves of a dandelion plant raised in the experimental garden of the Hugo de Vries Laboratory in Amsterdam. The virus was readily sap-transmissible and infected 24 out of the 52 plant species and cultivars tested, with visible symptoms in 18 of them.Myzus persicae andCuscuta subinclusa (dodder) did not transmit the virus. In addition the virus was not seed-transmitted in dandelion. Dilution end-point was 10−5, thermal inactivation occurred at between 80–85°C and longevity in vitro was approximately 24h. The virus had a sedimentation coefficient of 136 S. Polyacrylamide gel electrophoresis of the coat protein gave two bands, consisting of proteins with molecular masses ranging from 37 000 to 34 300 Da (band I) and from 34 000 to 32 800 Da (band II). The molecular mass of the RNA was 2.84 x 106 Da. The average buoyant density of the virus was 1.306 gcm−3 and the average A260/A280 ratio 1.16. The virus particles had a normal length of 668 nm. with the light microscope, large mainly vacuolate inclusions were observed in the epidermal cells of infectedNicotiana cleavelandii leaves. In ultra-thin sections of systemically infected leaves ofN. clevelandii, bundles of aggregated virus particles were detected, whereas in infected dandelion leaves there were fewer aggregates and more scattered virus particles. There was a close serological relationship to dandelion latent virus, chrysanthemum virus B and potato virus S and a more distant one to carnation latent virus, elderberry carlavirus,Helenium virus S and potato virus M. The occurrence of the virus was found to be restricted to dandelion plants in the experimental garden in Amsterdam. On the basis of large differences in host range, symptomatology and lack of transmission byM. persicae it was decided that the virus could not be considered a strain of either dandelion latent virus, chrysanthemum virus B or potato virus S. We therefore propose that it be called dandelion carlavirus.

Samenvatting

Een carlavirus werd geïsoleerd uit een paardebloemplant, die opgekweekt was in de proeftuin van het Hugo de Vries-Laboratorium in Amsterdam. Het virus kon gemakkelijk met sap worden overgebracht en was in staat 24 van de 52 getoetste plantesoorten en-cultivars te infecteren, waarbij op 18 van deze symptomen zichtbaar werden.Myzus persicae en warkruid (Cuscuta subinclusa) konden het virus niet overbrengen. Evenmin kon het virus met zaad van geïnfecteerde planten van paardebloem overgaan. De verdunningsgrens was 10−5, de inactiveringstemperatuur 80–80°C en de houdbaarheid in vitro ongeveer 24 uur. Het virus had een sedimentatiecoëfficiënt van 136 S. Polyacrylamide-gelelektroforese van het manteleiwit resulteerde in twee banden, bestaande uit eiwitten met molecuulmassa's die varieerden van 37000 tot 34 3000 Da (band I) en van 34 000 tot 32 800 Da (band II). De molecuulmassa van het RNA was 2,84×106Da. De gemiddelde zweefdichtheid van het virus bedroeg 1,306g cm−3 en de gemiddelde A260/A280 verhouding was 1,16. Het virus had een normale lengte van 668 nm. In de epidermiscellen van geïnfecteerde bladeren vanNicotiana clevelandii werden met de lichtmicroscoop insluitsels met draderige en vacuoleachtige structuren waargenomen. In ultradunne coupes van systemisch geïnfecteerde bladeren vanN. clevelandii waren bundels geaggregeerde virusdeeltjes zichtbaar. In geïnfecteerde bladeren van paardebloem werden daarentegen meer verspreid voorkomende virusdeeltjes gevonden en minder aggregaten. Het virus vertoonde een sterke serologische verwantschap met het ‘dandelion latent virus’, chrysantevirus B en aardappelvirus S; er was een geringe verwantschap met het latente anjervirus, het carlavirus van vlier, ‘Helenium virus S’ en het aardappelvirus M. Het vóórkomen van het virus bleek beperkt te zijn tot paardebloemen in de proeftuin in Amsterdam. Gezien de grote verschillen in waardplantenreeks, symptomatologie en overdracht metM. persicae hebben we gemeend, dat het virus niet slechts als een stam kon worden beschouwd van hetzij het ‘dandelion latent virus’, hetzij het chrysantevirus B en het aardappelvirus S. We stellen voor de naam carlavirus van paardebloem aan dit virus te geven.

Additional keywords

carnation latent virus chrysanthemum virus B dandelion carlavirus dandelion latent virus elderberry carlavirus Helenium virus S potato virus M potato virus S 

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References

  1. Bailey, J.M. & Davidson, N., 1976. Methylmercury as a reversible denaturing agent for gel electrophoresis. Anal. Biochem. 70: 75–85.CrossRefPubMedGoogle Scholar
  2. Boccardo, G. & Milne, R.G., 1976. Poplar mosaic virus: Electron microscopy and polyacrylamide gel analysis. Phytopath. Z. 87: 120–131.Google Scholar
  3. Bruner, R. & Vinograd, J.H., 1965. The evaluation of standard sedimentation coefficients of sodium RNA and sodium DNA from sedimentation velocity data in concentrated NaCl and CsCl solutions. Biochim. biophys. Acta 108: 18–29.PubMedGoogle Scholar
  4. Brunt, A.A. & Kenten, R.H., 1973. Cowpea mild mottle, a newly recognized virus infecting cowpeas (Vigna unguiculata) in Ghana. Ann. appl. Biol. 74: 67–74.PubMedGoogle Scholar
  5. Christie, R.G. & Edwardson, J.R., 1977. Light and electron microscopy of plant virus inclusions. Fla. agric. exp. Stn Monogr. Ser. 9.Google Scholar
  6. Clark, M.F. & Adams, A.N., 1977. Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses. J. gen. Virol. 34: 475–483.PubMedGoogle Scholar
  7. Hamilton, R.I., Edwardson, J.R., Francki, R.I.B., Hsu, H.T., Koenig, R. & Milne, R.G., 1981. Guidelines for the identification and characterization of plant viruses. J. gen. Virol. 54: 223–241.Google Scholar
  8. Hearon, S.S., 1982. A carlavirus fromKalanchoë blossfeldiana. Phytopathology 72: 838–844.Google Scholar
  9. Hurk, J. van den, Tas, P.W.L. & Peters, D., 1977. The ribonucleic acid of tomato spotted wilt virus. J. gen. Virol. 36: 81–91.Google Scholar
  10. Jayasinghe, U. & Dijkstra, J., 1979.Hippeastrum mosaic virus and another filamentous virus inEucharis grandiflora. Neth. J. Pl. Path. 85: 47–65.Google Scholar
  11. Jenniskens, M.J.P.J., 1984. Aspects of the biosystematics ofTaraxacum sectionTaraxacum. Academic Press, Amsterdam.Google Scholar
  12. Johns, L.J., 1982. Purification and partial characterization of a carlavirus fromTaraxacum officinale. Phytopathology 72: 1239–1242.Google Scholar
  13. Markham, R., 1960. A graphical method for the rapid determination of sedimentation coefficients. Biochem. J. 77: 516–519.PubMedGoogle Scholar
  14. Nijs, J.C.M. den & Sterk, A.A., 1984a. Cytogeography ofTaraxacum sectioTaraxacum and sectioAlpestria in France and adjacent parts of Italy and Switzerland, including some taxonomic remarks. Acta bot. neerl. 33: 1–24.Google Scholar
  15. Nijs, J.C.M. den & Sterk, A.A., 1984b. Cytogeography and cytotaxonomy of someTaraxacum sections in Belgium and northern France. Acta bot. neerl. 33: 431–455.Google Scholar
  16. Slogteren, D.H.M. van, 1954. VIII. Serological micro-reactions with plant viruses under paraffin oil. Proc. 2nd Conf. Pot. Vir. Dis., Lisse-Wageningen: 51–54.Google Scholar
  17. Tavantzis, S.M., 1983. Improved purification of two potato carlaviruses. Phytopathology 73: 190–194.Google Scholar
  18. Veerisetty, V. & Brakke, M.K., 1977. Differentiation of legume carlaviruses based on their biochemical properties. Virology 83: 226–231.CrossRefGoogle Scholar
  19. Veerisetty, V. & Brakke, M.K., 1978. Purification of some legume carlaviruses. Phytopathology 68: 59–64.Google Scholar
  20. Wrigley, N.G., 1968. The lattice spacing of crystalline catalase as an internal standard of length in electron microscopy. J. Ultrastruct. Res. 24: 454–464.CrossRefPubMedGoogle Scholar

Copyright information

© Koninklijke Nederlandse Planteziektenkundige Vereniging 1985

Authors and Affiliations

  • Jeanne Dijkstra
    • 1
  • Yvonne Clement
    • 1
  • H. Lohuis
    • 1
  1. 1.Laboratory of VirologyAgricultural UniversityWageningenthe Netherlands

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