Two hosts that are susceptible to TMV (tomato and pinto bean) are inoculated with the virus. Within 5 to 7 days, symptoms will appear on bean. On tomato, a systemic host, the symptoms will not appear on inoculated leaves, but on the leaves that develop after inoculation. Symptoms will appear in 1-3 weeks, depending on the variety and concentration of virus in the inoculum. These new leaves on infected tomato plants will exhibit a mottle or green and yellow color pattern and may be distorted. The plants also may be stunted (Figure 11). The virus moves throughout tissues and multiplies in most of its cells. Thus, the presence of the virus in the leaf cells can affect color (mottling) and leaf shape (often long and pointed) of leaves that were not inoculated.
On pinto beans, the symptoms appear only on the inoculated leaves. Small (about 1 mm), reddish-brown local lesions will appear on the inoculated leaves in a number proportional to the concentration of virus particles in the plant extract. The virus is restricted to the parenchyma cells (mesophyll) of the bean's leaf tissue, and the tissue surrounding the point of entry dies, thus creating the necrotic local lesions. The differences in symptom development between tomato and bean can be attributed to plant-virus interactions.
Differences in the anatomy of healthy and TMV-infected leaves are obvious when comparing cross sections of tissue with the compound light microscope at 100X and 400X. Regions within the mesophyll areas of TMV-infected leaves are thinner and less organized than those of healthy leaves. The palisade and spongy mesophyll layers are not well differentiated, and the mesophyll cells, particularly in the palisade layer, are more round and contain fewer chloroplasts than those in healthy tissue.
An extract from TMV-infected tomato is treated at various temperatures then assayed on the local lesion host, pinto bean, to determine if the virus loses its ability to induce lesions during heating. This virus loses its ability to infect plants at temperatures above 50-60° C because of changes in the structure of the viral protein. When the protein structure is changed, it no longer protects the RNA from degradation. An ideal experiment would be to have the class test a range of temperatures (e.g., 25, 50, 75, and 100° C) to demonstrate the progressive loss of infectivity associated with increasing the temperature.
Table 1. Example of table to record data from heat treatment of virus extract.
Temperature,°C
Number of lesions/ half-leaf
Plant #
1 2 3 4
Average # of lesions/ half-leaf
25
50
75
100
An extract from TMV-infected tomato is passed through a filter (220 nm) that prevents the passage of most bacteria through the filter. Because of the virus's small size (18 nm x 300 nm), it can pass through the filter. The ability to pass through the filter is indicated by no loss of infectivity of the filtrate when tested by its ability to produce necrotic local lesions on pinto bean leaves.