The development of the torus in the wood of Osmanthus americanus was investigated using transmission and scanning electron microscopy. Torus formation on either side of the pit membrane did not begin until after the development of the associated pit border was well underway. No plasmodesmata were encountered in the torus at any time during its ontogeny. Synthesis of torus material was correlated with a mass of randomly oriented microtubules and dictyosome vesicles. The two halves of the torus did not develop synchronously; deposits of torus material were evident first in the older of two adjacent cells. Selective hydrolysis of the matrix material of the margo also began fIrst on that side of the pit membrane associated with a mature tracheary element. Evidence is presented for a fibrillar as weIl as a matrix component in the torus.
Bordered pit pairs connecting tracheary elements in the wood of Osmanthus americanus (L.) Benth. ' Hook. ex Gray contained a torus in the pit membrane. This structure is approximately 2.5 μm in diameter, and is located at or near the centre of the pit membrane. The encrusting material of the torus could be removed by treatment with sodium chlorite. Thin seetions through theJorus showed it to consist of a pad of wall material appressed to either side of the compound middle lamella. The membrane surrounding the torus (the margo) consisted of fibrils and a variable amount of enc10sing matrix. The fibrils were generally c1oseIy packed and randomly oriented, although occasionally a radial component was also present. Aspiration of the pit membrane in air-dried material caused the torus to seal off one of the pit apertures. During this process the torus probably prevented rupture of the pit membrane at that site.
Tomato golden mosaic virus (TGMV), a member of the geminivirus group, has a genome consisting of two DNA molecules designated the A and B components. Both are required for infectivity in healthy plants, although the former has been shown to replicate independently in transgenic plants containing tandem direct repeats of the A genome component. In the studies presented here, petunia plants transgenic for either both components (A×B hybrids) or the A component alone were examined for the presence of virus particles and encapsidated, single stranded viral DNA. The results of DNase protection experiments and direct observation of extracts from transgenic plants by electron microscopy indicate that single stranded TGMV DNA is in both cases packaged into paired particles identical to those obtained from virus-infected plants. DNase-treated virions isolated from A×B hybrid petunia are infectious when inoculated onto healthy Nicotiana benthamiana. Likewise, virions obtained from transgenic A petunia are infectious for plants transgenic for the B component.Our observations of TGMV replication in transgenic plants indicate that TGMV A DNA encodes all viral functions necessary for the replication and encapsidation of viral DNA. The possible role of the B component in TGMV replication is discussed.
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