Encapsidation and spread of African cassava mosaic virus DNA A in the absence of DNA B when agroinoculated to Nicotiana benthamiana
- 1 June 1990
- journal article
- research article
- Published by Microbiology Society in Journal of General Virology
- Vol. 71 (6) , 1409-1412
- https://doi.org/10.1099/0022-1317-71-6-1409
Abstract
Agroinoculation of African cassava mosaic virus DNA A alone into Nicotiana benthamiana resulted in the occasional spread of viral DNA throughout the stem, leaves and root. The amount of DNA A reached 5% of that associated with full infection following agroinoculation of both DNAs A and B, although the plants remained asymptomatic. Detection of virus particles in the upper leaves indicates that DNA B is not essential for virus assembly. The predominant form of the virus-specific DNA was single-stranded, which is possibly encapsidated within the virus particles. Double-stranded DNA forms could also be detected in the upper leaves.This publication has 17 references indexed in Scilit:
- “Agroinfection,” an alternative route for viral infection of plants by using the Ti plasmidProceedings of the National Academy of Sciences, 1986
- Pseudorecombinants between Cloned DNAs of Two Isolates of Cassava Latent VirusJournal of General Virology, 1985
- Major polyadenylated transcripts of cassava latent virus and location of the gene encoding coat proteinThe EMBO Journal, 1985
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Isolation ofAgrobacterium tumefaciensBiovar 3 from Grapevine Galls and Sap, and from Vineyard SoilPhytopathology®, 1983
- Serological studies on cassava latent virusAnnals of Applied Biology, 1982
- Transcription of cauliflower mosaic virus DNA. Detection of transcripts, properties, and location of the gene encoding the virus inclusion body proteinVirology, 1981
- Detection of potato leafroll and potato mop‐top viruses by immunosorbent electron microscopyAnnals of Applied Biology, 1979
- Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate.Proceedings of the National Academy of Sciences, 1979
- A Biochemical Test for Crown Gall BacteriaNature, 1963