COMPOSITION COMPRISING NUCLEIC ACIDS OF PARASITIC, PATHOGENIC OR INFESTING BIOLOGICAL SYSTEMS FOR INHIBITING AND/OR CONTROLLING THE GROWTH OF SAID SYSTEMS AND PROCESS FOR THE PREPARATION THEREOF

Abstract

The present disclosure describes a DNA fragment mixture for the prevention or for the treatment of at least one pathogenic, parasitic or infesting species of plants or of the environment, wherein the DNA mixture consists of random fragments of total DNA of at least one pathogenic, parasitic, or infesting species, and/or at least one phylogenetically similar species, against which the prevention and treatment are directed. Further, the disclosure describes a process and related system for improvement of the production/growth of microorganisms at high yield in bioreactors or photobioreactors, or of plants in different culture systems, where the nucleic acids of the organisms produced/grown by such a process are removed from the culture medium and the culture medium, deprived of these nucleic acid, is used again in the process.

Claims

1. Use of a composition comprising or consisting of a mixture of DNA fragments for the prevention and the treatment against at least one pathogenic, parasitic or infesting species of the plants or environment, wherein said DNA is the total DNA of said at least one pathogenic, parasitic or infesting species, and/or at least one phylogenetically similar species, against which said prevention and treatment are directed.

2. Use according to claim 1, wherein said DNA fragments are obtained by random fragmentation.

3. Use according to claim 1, wherein said total DNA is extracted from said at least one pathogenic, parasitic or infesting species or artificially synthesized.

4. Use according to claim 1, wherein said total DNA is amplified and/or fragmented by physical chemical procedures and obtained fragments are possibly amplified.

5. Use according to claim 1, wherein said composition is used as biocide, herbicide, fungicide, insecticide, acaricide, nematocide, antiprotozoic, algaecide, bactericide.

6. Use according to claim 1, wherein said composition is administered to said at least one pathogenic, parasitic or infesting species by surface contact, cytotropic administration, systemic administration.

7. Use according to claim 6, wherein the systemic administration is carried out by injection, ingestion or inhalation.

8. Use according to claim 1, wherein said composition is formulated in a form selected from the group consisting of dispersion, suspension, wettable or soluble powders, emulsions in water or other solvents, dispersible granules, suspensions of microcapsules, emulsifiable concentrates, fluid pastes, macro emulsions, oil dispersions, baits.

9. Use according to claim 1, wherein said total DNA fragments are engineered in vectors.

10. Use according to claim 1, wherein said composition further comprises pesticide compounds selected from the group consisting of fungicides, insecticides, nematocides, miticides, artropocides, bactericidal, algaecides.

11. Method for the prevention or the treatment against at least one pathogenic, parasitic or infesting species of the plants or environment, said method comprising or consisting of the following steps of: a) extraction of the total DNA of at least one of said pathogenic, parasitic or infesting species against which said prevention and treatment are directed; b) fragmentation of said total DNA in order to obtain a mixture of DNA random fragments of nucleic acids; and c) contacting said mixture of fragments with said pathogenic, parasitic or infesting species.

12. Composition comprising or consisting of a mixture of DNA fragments for the use in the prevention or treatment against at least one pathogenic, parasitic or infesting species of human or animal, wherein said DNA is the total DNA of said at least one pathogenic, parasitic or infesting species, and/or at least one phylogenetically similar species, against which said prevention and treatment are directed.

13. Composition comprising or consisting of a mixture of DNA fragments according to claim 12, wherein said DNA fragments are obtained by random fragmentation.

14. Composition comprising or consisting of a mixture of DNA fragments according to claim 12, wherein said pathogenic species is a virus.

15. Process for the production of microorganisms in bioreactors or photobioreactors or systems for hydroponic culture characterized in that the nucleic acids of the same microorganisms produced by said process are removed from culture medium and the culture medium deprived of said nucleic acid is used again in said process.

16. Process according to claim 15, wherein nucleic acids of the same microorganisms produced by said process are removed from culture medium using separation techniques selected from the group consisting of: external removal unit, preferably consisting of an external container and a system of generation of electric, or magnetic, or electromagnetic fields and at least one duct and at least one displacement means for the extraction of concentrated nucleic acids from the preceding system; integrated removal unit, preferably consisting of a system of generation of electric, or magnetic, or electromagnetic fields and at least one duct and at least one displacement means for the extraction of concentrated nucleic acids from the preceding system, the whole integrated within the same bioreactor; techniques applicable in situ and outside units, preferably centrifugation techniques; filtration techniques; treatments with DNAse and other degrading enzymes for nucleic acids; heat treatments; acidifying treatments.

17. Process according to claim 15, wherein said nucleic acids are removed from the culture medium by means of at least one external or bioreactor or photobioreactor integrated removal unit or systems for hydroponic culture using techniques selected from the group consisting of application of static electric fields, application of static magnetic fields, application of dynamic magnetic and/or electric fields, centrifugation, filtration, treatment with DNAse, heat treatment, acidifying treatment.

18. Process according to claim 15, wherein said nucleic acids isolated from culture medium are collected and optionally fragmented.

19. Process according to claim 15 wherein, when for the separation of nucleic acids an external separating unit is used, the culture medium deprived of said nucleic acids is used again in said process.

20. Process according to claim 15, wherein said nucleic acids are DNA.

21. Process according to claim 15, wherein said microorganisms are selected from pathogenic, parasitic or infesting microorganisms.

22. System for production of microorganisms comprising at least one bioreactor or photobioreactor or system for hydroponic culture, at least one unit for nucleic acid removal external to said at least one bioreactor or photobioreactor or system for hydroponic culture, said unit for nucleic acid removal being connected to said at least one bioreactor or photobioreactor or system for hydroponic culture by at least one first duct and at least one first displacement means for the withdrawal of culture medium containing nucleic acids, and at least one second duct and at least one second displacement means for the re-introduction in said at least one bioreactor or photobioreactor or system for hydroponic culture of culture medium from which nucleic acids are removed; said system comprising further at least one third duct and at least one third displacement means for the withdrawal of separated nucleic acid.

Description

[0069] The present invention now will be described, illustrative, by an illustrative but not limitative way, with particular reference to embodying examples and enclosed drawings, wherein:

[0070] FIG. 1 shows a conceptual view of the object of the invention.

[0071] FIG. 2 shows the inhibition of the germination of seeds of Lepidium and Acanthus by exposure to self DNA at optimal concentration of 200 ppm.

[0072] FIG. 3 shows the inhibition of Quercus ilex, Quercus pubescens, Hedera elix, Ampelodesma mauritanica, Festuca drimeja, Coronilla emerus, Medicago marina, Alnus cordata, Robinia pseudoacacia, Pinus halepensis plants by exposure to self DNA.

[0073] FIG. 4 shows the inhibition of Arabidopsis thaliana plants by exposure to self and Lycopersicon esculentum DNA.

[0074] FIG. 5 shows the inhibiting effect on the spore germination and hyphal growth of Aspergillus niger when said fungus is exposed to self or other fungus species DNAs (Trichoderma hartianum).

[0075] FIG. 6 shows the inhibition of Sarcophaga carnaria insect by exposure to self DNA.

[0076] FIG. 7 shows the completed metamorphoses, in percentage compared to not exposed control, in larvae of Sarcophaga carnaria dipter exposed for 4 weeks to homologous DNA at three different concentrations, or fungus (Penicillium chrysogenum) or bacterium (Bacillus subtilis) extracted heterologous DNA.

[0077] FIG. 8 shows the viable cell counts in Bacillus subtilis bacterium in cultures exposed for 24 hours to homologous DNA at three different concentrations and in not exposed control.

[0078] FIG. 9 shows the germination of the spores in the Trichoderma harzianum fungus, in percentage compared to not exposed control, in cultures exposed to homologous DNA at three different concentrations, or to heterologous DNA extracted from other fungus (Aspergillus niger), insect (Sarcophaga carnaria) or bacterium (Bacillus subtilis).

[0079] FIG. 10 shows growth dynamics of Scenedesmus obliquus microalga in two cultures exposed to homologous DNA at different concentration, and not exposed control.

[0080] FIG. 11 shows the accumulation of extracellular DNA in the liquid substrate of two different bioreactors. Panel A of FIG. 11 shows fluorescence of supernatant from Bacillus subtilis culture on 1% agarose gel+SYBR safe. Panel B shows fluorescence of supernatant from Saccharomyces cerevisiae culture on 1% agarose gel+SYBR safe. Panel C shows Saccharomyces cerevisiae cell density in a bioreactor, wherein removal of the DNA from the culture medium is suitable to remove the inhibiting effect allowing the growth stage to be restored and higher cell densities.

[0081] FIG. 12 shows: (a) the diagram of system for production of microorganisms in bioreactor characterized from an external unit for DNA removal; (b) the diagram of system for production of microorganisms in bioreactor wherein the removal of DNA from culture medium occurs by bioreactor integrated removal unit.

[0082] FIG. 13 shows: (a) a tank for hydroponic culture characterized from the presence of an external removal DNA unit and recirculation of culture medium within the hydroponic system; (b) a tank for hydroponic culture wherein the removal of the DNA from culture medium occurs by means of removal unit integrated to the same tank.

[0083] FIG. 14 shows a specific diagram of the external removal unit for the system represented in FIG. 12, wherein the separation of nucleic acid occurs by application of an electric field.

[0084] FIG. 15 shows a further diagram of the removal unit for the system showed in FIG. 12, wherein the separation of nucleic acid occurs by application of a magnetic field.

[0085] FIG. 16 shows an diagram of plant culture wherein the substrate is treated with nuclease by integration with fertirrigation system.

[0086] In all the examples of reported experiments, the nucleic acid composition used in the different treatments was prepared according to the procedure outlined in FIG. 1. In particular, the total DNA extracted with standard procedures from organic material (leaves, fungus mycelium, microbial biomass) was treated by sonication for at least three cycles lasting three minutes at maximum power with dipping sonicator until to obtain the production of composition of random fragments falling in 50 and 1000 bp size range. The verification of the fragmentation level is carried out by standard procedures using agarose or polyacrylamide gel electrophoresis and staining techniques, Sybr safe type and UV visualization.

EXAMPLE 1

Inhibition of Acanthus mollis and Lepidium sativum Plants by Exposure to Self DNAs

[0087] A first experiment was carried out on Acanthus mollis and Lepidium sativum plants, the latter species was selected because it is particularly sensitive to toxins. DNAs of acanthus, Acanthus mollis, and watercress, Lepidium sativum, were obtained by direct extraction from leaves of the two species and stored in distilled H.sub.2O. Successively 10 previously sterilized seeds of A. mollis or L. sativum, in Petri plates (9 cm diameter) are placed on a sheet of sterile filter paper. The seeds of each species are treated separately with the DNA of the two species at concentrations of 2, 20 and 200 ppm whereas sterile H.sub.2O was added to the control. The germination of the two species and the total root length were quantified after 7 days of incubation at 24 C. by observation and measurement of the roots. Each treatment was repeated thrice.

[0088] The treatment of the seeds of the two species with DNA extracted from plants of the two species, applied separately, allowed to estimate the effect of the DNA on the root growth and the optimal activity concentration. The results of the experimentation, reported in FIG. 2, show that both seeds of Lepidium and seeds of Acanthus are inhibited in the germination by the exposure to self DNA at optimal concentration of 200 ppm. On the contrary, the exposure of seeds to DNA from other species does not show noticeable effects on the seed germination.

EXAMPLE 2

Inhibition of Quercus ilex, Quercus pubescens, Hedera elix, Ampelodesma mauritanica, Festuca drimeja, Coronilla emerus, Medicago marina, Alnus cordata, Robinia pseudoacacia, Pinus halepensis Plants by Exposure to Self DNAs

[0089] A second experiment concerned the analysis of the germination and root growth of 10 species of natural environment plants. Surface sterilized seeds of Quercus ilex, Quercus pubescens, Hedera elix, Ampelodesma mauritanica, Festuca drimeja, Coronilla emerus, Medicago marina, Alnus cordata, Robinia pseudoacacia, Pinus halepensis plants, were separately treated with DNAs of all the species applied at the concentration of 500 ppm. Shortly, in Petri plates (9 cm diameter) are placed 10 seeds of each species on a sheet of sterile filter paper. The different DNAs at concentration of 500 ppm were added to the plates whereas only sterile H.sub.2O was added to the control. The germination of the species seeds and the total root length were quantified after 7 days of incubation at 24 C. by observation and measurement of the roots. Each treatment was repeated thrice. The results, reported in FIG. 3 (average of the tests carried out on the above reported different species), shows the inhibition of the germination resulting from the exposure to self DNA and the absence of inhibition in the presence of heterologous DNA.

EXAMPLE 3

Inhibition of Arabidopsis thaliana, Lycopersicon esculentum, Lepidium sativum and Lens esculentum Plants by Exposure to Self DNAs

[0090] A third experiment concerned the evaluation, again by germination and root growth tests, of the toxicity on various plant species by nucleic acid extracted from same species. DNAs of Arabidopsis thaliana, Lycopersicon esculentum, Lepidium sativum and Lens esculentum were obtained by direct extraction from the respective plants and stored in distilled H.sub.2O. Successively 10 previously sterilized seeds of each species are placed in Petri plates (9 cm diameter) on a sheet from sterile filter paper. The seeds of each plant are treated separately with the DNAs of the four species at concentrations of 2, 20 and 200 ppm whereas sterile H.sub.2O was added to the control. The experiments were carried out in growth rooms under controlled conditions and complete sterility. The germination of the four species and the total radical length were quantified after 7 days of incubation at 24 C. by observation and measurement of the roots. Each treatment was repeated thrice. The four species shown an analogous behaviour, with a remarkable inhibiting effect in the presence of self DNA and the absence of effects in the presence of DNAs of the other species. The inhibiting effect proved to be positively correlated to the DNA concentration. For exemplary purpose Arabidopsis thaliana in the presence of self and Lycopersicon esculentum DNAs, respectively, are reported. Similar inhibition results in Arabidopsis thaliana, when seeds of this species are exposed to DNA of the same species obtained by amplification of fragments of the same DNA using PCR techniques, are observed.

EXAMPLE 4

Inhibition of Aspergillus niger and Trichoderma harzianum Fungi by Exposure to Self DNAs

[0091] A fourth experiment was carried out on the Aspergillus niger fungus in order to estimate the effect of self DNA and DNA isolated from another fungus, i.e. Trichoderma harzianum, on the cellular growth. Spores of Aspergillus niger are obtained by pure cultures in laboratory on agar treated substrate (PDA, potato dextrose agar). The spores were withdrawn under sterility conditions and diluted at concentration of 110.sup.6 spores/ml. The experiment of germination was carried out in liquid substrate (PDB 10%) in 96 well ELISA plates. The comparative treatment was carried out with DNA of Trichoderma harzianum, used as heterologous, whereas the control was not treated. DNAs extracted from both the species were applied at concentrations of 100 and 1000 ppm. Shortly, in each well, with a total volume of 100 l, said two DNAs separately at different concentrations, together with 10 l of liquid nutritive substrate (PDB, potato dextrose broth), sterile water and A. niger spores were added. The germination of the spores and the length of the germinative tube were quantified by spectrophotometric readings and optical microscope after 20 hours of incubation at 24 C. The results, reported in FIG. 5, show a remarkable inhibiting effect on the germination of the spores and the hyphal growth of A. niger only when such fungus was exposed to self DNA.

EXAMPLE 5

Inhibition of Sarcophaga carnaria Insect by Exposure to Self DNA

[0092] A fifth experiment was carried out on Sarcophaga carnaria insect in order to estimate the effect of self DNA on the life-cycle. Larvae of Sarcophaga carnaria dipter were grown in laboratory pure culture at the temperature of 10 C. and fed with minced meat. The experiment of DNA toxicity was carried out in square plastic plates (size 1212 cm, height 2 cm). The comparative treatments were carried out with DNAs of Bacillus subtilis and Lepidium sativum, used as heterologous DNA. As control only minced meat without addition of other treatments was used. Dipter and other two species extracted DNAs were added to the minced meat at concentrations of 2, 20 and 200 ppm, under mixer stirring. Shortly, in each plate DNA was added at the various concentrations, stirred with 1 g of minced meat. The plates were incubated at 10 C. in the dark for 21 days. The development, the survival and the time required for the formation of the pupae are monitored every 3 days for the 21 days of incubation. The larvae under control conditions, as well as those treated with heterologous DNA, displayed a regular life-cycle. On the contrary, the exposure to self DNA inhibited the life-cycle causing the death of the larvae proportionally to the treatment concentration. FIGS. 6 and 7 report the above described results.

EXAMPLE 6

Inhibition of the Bacillus subtilis Microorganism by Exposure to Self DNA

[0093] In order to demonstrate the possible use of nucleic acid as antibiotics an evaluation of toxicity on Bacillus subtilis treated with self DNA at various concentrations was carried out. The experiment was performed using as growth substrate 4 ml of LB (Luria Broth) inoculated with 10 l of Bacillus subtilis preculture. The treatment consisted in the preparation of the cultures in the presence of Bacillus subtilis DNA at final concentrations of 4, 40, and 400 ppm. The cultures were incubated under stirring at 35 C. for 24 h with three repeats of treatment. After 24 hours of incubation, from each test tube 0.5 ml was withdrawn and serially diluted in LB medium, from which 100 microliters of agar treated LB medium in Petri plates were plated. The plates were incubated at 28 C. until the appearance of colonies (CFUcolonies forming units). The results reported in FIG. 8 show a remarkable concentration-dependent decrease of CFUs, as response to the treatment.

EXAMPLE 7

Inhibition of Trichoderma harzianum Fungus by Exposure to Self DNA

[0094] In order to demonstrate the possible use of nucleic acids as fungicide and action specificity thereof an experiment on the germination of the spores in the Trichoderma harzianum fungus was carried out. Spores of Trichoderma harzianum were obtained by pure laboratory cultures on agar treated substrate (PDA, potato dextrose agar). The spores were withdrawn under sterility conditions and diluted at concentration of 110.sup.6 spores/ml. The experiment of germination was carried out in liquid substrate (PDB 10%) in 96 well ELISA plates. The treatment was carried out with homologous or heterologous DNA, that is extracted from the same species of Trichoderma, or from a different species of fungus (Aspergillus niger), from an insect (Sarcophaga carnaria) or from a bacterium (Bacillus subtilis). The DNA extracted from the different species was applied at concentrations of 8, 80 and 800 ppm. Shortly, in each well, with a total volume of 100 l, DNA separately at different concentrations, together with 10 l of liquid nutritive substrate (PDB, potato dextrose broth), sterile water and Trichoderma spores were added. The germination of the spores and the length of the germinative tube were quantified by spectrophotometric readings and optical microscope after 20 hours of incubation at 24 C.

[0095] FIG. 9 indicates the results of the experiment showing a remarkable concentration-dependent inhibiting effect, on the germination of the Trichoderma spores only by DNA of the same fungus species. On the contrary, the treatment with various species DNAs display stimulating effects on the germination (percentage values compared to not exposed control higher than 100%).

EXAMPLE 8

Inhibition of the Scenedesmus obliquus Microalga by Exposure to Self DNA

[0096] In order to demonstrate the possible DNA use as algicide product a growth test of Scenedesmus obliquus green alga under optimal control conditions and self DNA presence was carried out in the culture substrate (CHU #10). The treatments were carried out at two different concentrations (50 and 500 ppm) with two repeats. FIG. 10 shows the growth dynamics of the alga and shows a remarkable concentration-dependent inhibiting effect of the homologous DNA compared to not exposed control.

EXAMPLE 9

Inhibition of the Physarium polycephalum Protozoan by Exposure to Self DNA

[0097] In order to demonstrate the possible DNA use as antiprotozoic product an experiment was carried out on Physarium polycephalum protozoan. As experimental material the culture kit produced from Carolina Biological Supply was used. The cultures started on Petri plates with water-agar in order to favour the movement of the organism. As nutriment oat flakes were used. A first bulk culture was carried out on 20 plates and protozoic biomass produced after 15 days was collected and used for DNA extraction using Quiagen kit. The successive experiment consisted of the preparation of three Petri plates filled up with water agar to which two small portions of oats flakes were added, one for control wetted with 5 ml of distilled water and the other with addition of 5 ml of water with DNA of the protozoan at concentration of 200 ppm. The experiment was repeated other two times, with the variation that the added DNA was from bacterium (Bacillus subtilis) and insect (Sarcophaga carnaria). The results of the experiments shown the absence of growth of Physarium polycephalum on the substrate treated with DNA of the same protozoan whereas the organism did not shown growth differences under control conditions or heterologous DNA presence.

EXAMPLE 10

Study of Production Process of Yeasts, Bacteria and Algae in Bioreactors and Photobioreactors

[0098] Considering the above reported demonstrations about the inhibiting effect on different species when exposed to self DNAs, check analyses were carried out on the extracellular DNA presence in the growth substrate in bioreactors and photobioreactors with cellular cultures at high density when conditions of growth slowing down, even if under optimal nutritive substrate presence, occur. The study involved the sampling of liquid supernatant of different cultures in bioreactors in exponential growth, slowing down and steady-state stages. The analysis concerned cultures of Saccharomyces cerevisiae yeast, Bacillus subtilis bacterium and Phaeodactylum tricornutum and Scenedesmus obliquus microalgae. Samples of the cellular culture supernatants obtained by two cycles of centrifugation at 3000 rpm for 15 minutes were analyzed in order to separate possible cell residues and then subjected to gel electrophoresis after treatment with Syber-Safe and fluorescence evaluation. FIG. 11 shows the results of some of these analyses from which it is apparent the accumulation of extracellular DNA in the liquid substrate of the bioreactors. This accumulation is clearly associated to the slowing down of the growth of the different cellular cultures and to the attainment of the steady-state stage (FIGS. 11A and 11B). FIG. 11C shows clearly as the removal of the extracellular DNA from culture medium by chemical-physical procedures and the following introduction of regenerated substrate into the reactor results in the elimination of the inhibiting effect and a consequent restoring of the cellular culture growth.