This viral multiplication will end up causing the metabolic modification or the destruction of the cell. The proliferation of the viruses inside vegetable fabrics can in certain cases not involve any visible Symptôme initially (phenomenon of masking) but very often the virus attacks appear by symptoms such as marblings or fasciations (Document)
The viruses have an evolutionary potential very important because their multiplication proceeds in the genetic intimacy of the host cell. Many rearrangements, changes, exchanges of Gène S are possible. Despite everything, the lines of virus evolved/moved independently from/to each other. Indeed like the majority of the Endoparasite S, the viruses multiply in isolation in their host S. the evolution in parallel of the viral strains and of the resistant hosts (Co-evolution) is at the origin of a great specialization of the viruses with respect to their host. One will find thus viruses able to tackle only one species or only one family of plants. The virus of the mosaic of the tobacco for example, is able to tackle the majority of the plants belonging only to the family of the Solanacée S (Tomate, Tabac, the Eggplant…)
The structure of the phytovirus is well defined. It is presented in the form of viral particles (or Virion S) which have isometric characteristics , rigid or filamentous sticks, as well as bacilliform forms . The organization of the phytovirus of categories, kind and family is primarily based on three criteria:
the nature of the genetic material: DNA or ARN, mono or bicaténaire (a bit or two)
the level of homology (resemblance resulting from a common ancestor) of genes. To be done, one sequence the genetic material of each virus. One compares the successions of the nitrogenized bases various viruses, one gathers in same a taxon the viruses to which the sequences are closest. According to the degree of homology one will define the kinds (for example Caulimovirus) then the families (for example Caulimoviridea).
To a lesser extent one uses as criterion the shape of the viral particles. One uses this criterion for the group of the viruses with ARN monocaténaire messenger. This family is subdivided in isometric viruses, helicoid in stick or flexuous particles.
The viroïdes are made up exclusively of a circular ARN monocaténaire which has a very compact and rigid space structure. There is no Capside and even less envelope. The Viroïde S were classified in two families: the Pospoviroïdae and the Avsunviroïdae .
The ARN polymerase of the plant ensures the synthesis new viroïdes which accumulates then in the nucleole, the remainder of the core or the membrane of the Thylakoïde S of the chloroplasts. This accumulation of viroïdes inside the cell involves a metabolic dysfunction preventing for example the cellular multiplication. The multiplication of the viroïdes is supported by an increase in the duration of day and an increase in the temperature, for this reason they are implied in tropical diseases, Mediterranean or plants of ornament raised under greenhouse. One of these attacks causes “Cadang Cadang” which leads to a deterioration slow but lethal of the coconuts and which already decimated thousands of trees.
We have just presented the organization of the smallest agents to you known and perhaps most pathogenic. We will now discover how a viral particle can starting from one only individual, to produce different thousands of them by using the vegetable Cellule like source of matter and energy.
In this part we chose not to develop all the existing modes of multiplications. Only most significant and simplest were selected. There exists indeed of other modes of multiplication whose comprehension would require a more thorough knowledge in molecular biology.
The introduction of a ARN monocaténaire (=simple bit) into the cell leads to the synthesis of many molecules of viral ARN and the synthesis of many proteins constitutive of the capsid. To be done, the virus uses the cellular machinery of its host: enzymes, reticulum, ribosomes of which itself is deprived. The viral ARN has a function messenger which leads to the formation of a foreign protein to the plant: an enzyme ARN viral Polymerase which thus will amplify creation again bit of viral ARN. The viruses with ARN, can have other pieces of ARN (satellite ARN). The satellite ARN depend on this ARN polymerase of the virus says “assisting virus”.
If the viruses are not put in the presence of cells to parasitize, they degenerate quickly. Once in contact with the cells of the plant host by the means of a mechanical agent (shears for example) or biological (a ravageur) they can be propagated in all the plant. This third stage will enable us to discover how that is possible.
The viruses transmitted by the animals can be classified in two categories, the viruses not circulating and the circulating viruses.
nonpersistent viruses: these viruses have one very short lifespan apart from the plant. The meal of acquisition is of very short duration (a few seconds) and must be inoculated very quickly to be able to be propagated.
persistent semi viruses: these viruses have one lifespans longer apart from the plant (a few hours), moreover to be able to be propagated the meal of acquisition and the meal of inoculation must be longer (a few hours also)
nematodes, vectors of wire father At a group of nematodes, Xiphinema, the transmission of a Népovirus is done according to the circulating mode but with a persistence which can go from a few weeks to a few months. If the nematode saw sufficiently a long time, it can ensure the transmission of the virus between two annual cultures.
The parameters which govern the expansion of a viral disease transmitted by vectors depends on the various factors relating to the biology of the vector itself. The knowledge of the parameters makes it possible to set up estimated systems making it possible to lead an effective fight: elimination of the sources of virus during inter culture or the interference with the behavior of the vectors.
The natural means of defense of the plants (protein synthesis of defenses, over-sensitiveness (see last sequence of the booklet) to fight against the viruses are of genetic nature. This definite aptitude concept of varietal resistance. The experiment proves that the more one plant is selected in an objective of output, and the more it is weakened. The geneticists were thus brought to create new varieties by introducing genes of resistance by the means of crossings and selection or by the means of technique of transgénèse. For example one crosses tomato seedlings Lycopersicon esculentum with wild species like Lycopersicon hirsutum or Lycopersicon peruvianum in order to improve resistance to the viruses of the Mosaïque of the tobacco, of the Marbrure of the tobacco and the Virus Y of the potato. In the same way crossing are carried out between the barley and the triticale in order to obtain varieties resistant to the virus of the yellowing mosaic.
For the nonpersistent viruses the propagation of the epidemic is made in a ray of a hundred put around the seedling virus disease.
For the viruses persisting the propagation of the viruses can be done on hundreds of km. The control of the population of phytophagous vector can sometimes be essential. In these cases there, the use of an insecticide on the foliage or in the ground can be recommended. This type of treatment intervenes in particular for the virus of the rolling up of potato or the virus of the Jaundice nanifiante of the Orge.
Thermotherapy consists in exposing the plant to a strong temperature. It is able to destroy the viruses with the image of a fever at the human ones. For that one proceeds to hot baths or one places in an environment heated the plants “to treat”. This solution is considered only for small cultures.
strawberry plants with the heat! Seedlings of strawberry plants infected by the virus of the marbling can be cleansed by a stay from 3 to 4 weeks with 37/38 ° C. In general this technique of thermotherapy is reserved for the preventive fight to produce grafts or unscathed seedlings of virus.
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