scholarly journals Tobacco mosaic virus and the virescence of biotechnology

1999 ◽  
Vol 354 (1383) ◽  
pp. 665-673 ◽  
Author(s):  
Thomas H. Turpen

There is a growing realization that a modern combination of molecular biology and agriculture will provide a photosynthetic basis for the biosynthesis of an increasing variety of complex and valuable molecules. This ‘greening’ of biotechnology may impact on the global environment in many beneficial ways, but will perhaps have its most significant impact on human health. In the past decade, the capacity to use plants as an expanded source of therapeutics has grown through the accelerated development of effective viral transfection vectors for gene transfer to cultivated crops. Recombinant vectors based on tobacco mosaic virus (TMV) and other members of the Tobamovirus genus are now used to transfect commercially meaningful quantities of plant biomass cultivated in enclosed greenhouses and multiacre fields. Viral RNA promoters are effectively manipulated for the synthesis of recombinant messenger RNAs in whole plants. Chimeric plant virus and virus–like particles are designed for peptide production and display from recombinant structural protein–gene fusions. Gene functions are assessed and modified by either virus–mediated expression or cytosolic inhibition of expression at the RNA level. Recombinant virus populations, propagated by inoculating plants with infectious RNA transcripts or recombinant virions, have proved to be genetically stable over product–manufacturing cycles. Large volumes of highly purified protein products isolated from transfected foliage conform reproducibly to the specifications required for well–characterized biologics. In some cases, they exceed the specific activities of molecules purified from alternative recombinant and native sources. The resulting products are then formulated according to the developing national regulatory guidelines appropriate for agriculture–based manufacturing. Each of these innovations was first realized by researchers using clones of tobamovirus genes and recombinant genomes. This progress is founded on the heritage of a century of fundamental TMV research.

2001 ◽  
Vol 82 (6) ◽  
pp. 1503-1508 ◽  
Author(s):  
O. I. Kiselyova ◽  
I. V. Yaminsky ◽  
E. M. Karger ◽  
O. Yu. Frolova ◽  
Y. L. Dorokhov ◽  
...  

The structure of complexes formed in vitro by tobacco mosaic virus (TMV)-coded movement protein (MP) with TMV RNA and short (890 nt) synthetic RNA transcripts was visualized by atomic force microscopy on a mica surface. MP molecules were found to be distributed along the chain of RNA and the structure of MP–RNA complexes depended on the molar MP:RNA ratios at which the complexes were formed. A rise in the molar MP:TMV RNA ratio from 20:1 to 60–100:1 resulted in an increase in the density of the MP packaging on TMV RNA and structural conversion of complexes from RNase-sensitive ‘beads-on-a-string’ into a ‘thick string’ form that was partly resistant to RNase. The ‘thick string’-type RNase-resistant complexes were also produced by short synthetic RNA transcripts at different MP:RNA ratios. The ‘thick string’ complexes are suggested to represent clusters of MP molecules cooperatively bound to discrete regions of TMV RNA and separated by protein-free RNA segments.


1989 ◽  
Vol 67 (1) ◽  
pp. 88-94 ◽  
Author(s):  
Iqrar A. Khan ◽  
Gary E. Jones

In an isolate of tobacco mosaic virus, TMV U1, a small subpopulation of virus that invokes the hypersensitive reaction on Nicotiana sylvestris Spegaz. & Comes exists and is strongly selected for during replication in plants that are undergoing development of shoot axes during bolting. Virus of this phenotype (NL) can infect and move systemically in rapidly developing parts of N. sylvestris plants and is strongly selected for in upper tissues of the plants only during the development of the shoot axis. This selection results in a dramatic change in the genetic composition of the virus population in the upper part of the plant. No accumulation of NL-type virus occurred when N. sylvestris plants were inoculated with TMV204, a clonal population derived from RNA transcripts of a plasmid carrying a cDNA copy of the TMV genome.


2013 ◽  
Vol 41 (2) ◽  
pp. 427 ◽  
Author(s):  
Sercan PAZARLAR ◽  
Mustafa GÜMÜŞ ◽  
Gölgen Bahar ÖZTEKİN

Changes in some growth (plant leaf number and area, plant biomass, plant height, root length, and plant stem diameter) and physiological (photosynthetic pigments, relative water content (RWC) and proline content) parameters of pepper (Capsicum annuum L.) varieties were studied as they were affected by Tobacco mosaic virus (TMV) infection. The greenhouse pepper cvs ‘Ergenekon F1’, ‘Kumsal F1’, and one candidate variety (‘497 F1’) were used as material to compare infected versus non-infected control plants. Infected plants showed various degrees of stunting; necrosis on stems, leaves and fruits; mosaic symptoms on leaves; deformations, defoliation of leaves, and reduction in fruit size. Besides these, TMV infection resulted in reduction of vegetative growth parameters, RWC, chlorophyll a and b, plant fresh and dry production in different parts of the plants, but increase of proline content in leaves. The level of response differed depending on varieties.


1999 ◽  
Vol 354 (1383) ◽  
pp. 587-591 ◽  
Author(s):  
Milton Zaitlin

Proteins unique to tobacco mosaic virus (TMV)–infected plants were detected in the 1970s by electrophoretic analyses of extracts of virus–infected tissues, comparing their proteins to those generated in extracts of uninfected tissues. The genome organization of TMV was deduced principally from studies involving in vitro translation of proteins from the genomic and subgenomic messenger RNAs. The ultimate analysis of the TMV genome came in 1982 when P. Goelet and colleagues sequenced the entire genome. Studies leading to the elucidation of the TMV genome organization are described.


1989 ◽  
Vol 67 (4) ◽  
pp. 984-989 ◽  
Author(s):  
Iqrar A. Khan ◽  
Gary E. Jones

In an isolate of tobacco mosaic virus strain U1 there exists a small subpopulation containing a variant strain of the virus that induces the hypersensitive response on Nicotiana sylvestris Spegazzini & Comes. This type of variant is strongly selected for during the regeneration of plantlets from mature leaf tissue of plants infected with tobacco mosaic virus U1. When whole plants derived from disks were transferred into a glasshouse, those containing this type of variant were severely stunted, showed mosaic symptoms, and most of them died. Some that had originally contained lower titers of variant-type virus survived to flower but produced only a few seeds. Plants that initially contained only wild-type virus had high titers of tobacco mosaic virus, survived and grew well, exhibited mosaic symtoms, and flowered and set seed normally. Repeated assays of virus in these plants revealed no detectable variant-type virus. Apparently, during callus development and organogenesis in culture, partial segregation of the mixed U1 population occurred, and variants preferentially infected the developing tissues. This represents a situation in which dramatic change in the genetic structure of an RNA virus population occurs during development of the host plant.


Virology ◽  
1990 ◽  
Vol 179 (1) ◽  
pp. 395-402 ◽  
Author(s):  
T.E. Mirkovs ◽  
G. Kurath ◽  
D.M. Mathews ◽  
K. Elliott ◽  
J.A. Dodds ◽  
...  

1993 ◽  
Vol 42 (2-3) ◽  
pp. 227-239 ◽  
Author(s):  
Thomas H. Turpen ◽  
Ann M. Turpen ◽  
Nicole Weinzettl ◽  
Monto H. Kumagai ◽  
William O. Dawson

Author(s):  
Irwin Bendet ◽  
Nabil Rizk

Preliminary results reported last year on the ion etching of tobacco mosaic virus indicated that the diameter of the virus decreased more rapidly at 10KV than at 5KV, perhaps reaching a constant value before disappearing completely.In order to follow the effects of ion etching on TMV more quantitatively we have designed and built a second apparatus (Fig. 1), which incorporates monitoring devices for measuring ion current and vacuum as well as accelerating voltage. In addition, the beam diameter has been increased to approximately 1 cm., so that ten electron microscope grids can be exposed to the beam simultaneously.


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