Patent Application
20200315169
The present invention relates to compositions comprising terpenes and hollow glucan particles or cell wall particles and methods for preparing such compositions. The compositions increase terpene stability and activity and provide a suitable carrier for the terpenes. The invention also relates to methods of using such compositions in the medical, veterinary and agricultural fields.
Terpenes are chemical compounds that are widespread in nature, mainly in plants as constituents of essential oils. Their building block is the hydrocarbon isoprene (C5H8)n. Examples of terpenes include citral, pinene, nerol, b-ionone, geraniol, carvacrol, eugenol, carvone, terpeniol, anethole, camphor, menthol, limonene, nerolidol, farnesol, phytol, carotene (vitamin A1), squalene, thymol, tocotrienol, perillyl alcohol, borneol, myrcene, simene, carene, terpenene, and linalool.
Terpenes are classified as Generally Recognized as Safe (GRAS) and have been used for many years in the flavouring and aroma industries. The LD50 in rats of citral is approximately 5 g/kg, which is a further indication of the relative safety of these compounds. Furthermore, terpenes have a relatively short life span of approximately 28 days once exposed to oxygen (e.g. air). Terpenes will decompose to CO2 and water. This decomposition or break down of terpenes demonstrates the safety and environmental friendliness of the compositions and methods of the invention.
Terpenes have been found to inhibit the growth of cancerous cells, decrease tumour size, decrease cholesterol levels, and have a biocidal effect on micro-organisms in vitro. Owawunmi, (Letters in Applied Microbiology, 1993, 9(3): 105-108), showed that growth media with more than 0.01% citral reduced the concentration of E. coli, and at 0.08% there was a bactericidal effect. U.S. Pat. No. 5,673,468 describes a terpene formulation, based on pine oil, used as a disinfectant or antiseptic cleaner. U.S. Pat. No. 5,849,956 teaches that a terpene found in rice has antifungal activity. U.S. Pat. No. 5,939,050 describes an oral hygiene antimicrobial product with a combination of 2 or 3 terpenes that showed a synergistic effect. Several U.S. Patents (U.S. Pat. Nos. 5,547,677, 5,549,901, 5,618,840, 5,629,021, 5,662,957, 5,700,679, 5,730,989) teach that certain types of oil-in-water emulsions have antimicrobial, adjuvant, and delivery properties.
Terpenes have been found to be effective and nontoxic dietary anti-tumor agents, which act through a variety of mechanisms of action (Crowell et al. Crit. Rev. Oncog., 1994, 5(1): 1-22; Crowell et al. Adv. Exp. Med. Biol., 1996, 401: 131-136). The terpenes geraniol, tocotrienol, perillyl alcohol, b-ionone, and d-limonene, suppress hepatic HMG-CoA reductase activity, a rate limiting step in cholesterol synthesis, and modestly lower cholesterol levels in animals (Elson et al, J. Nutr., 1994, 124: 607-614). D-limonene and geraniol reduced mammary tumors (Elegbede et al. Carcinogenesis, 1984, 5(5): 661-664; Elegbede et al., J. Natl. Cancer Inst., 1986, 76(2): 323-325; Karlson et al. Anticancer Drugs, 1996, 7(4): 422-429) and suppressed the growth of transplanted tumors (Yu et al., J. Agri. Food Chem., 1995, 43: 2144-2147).
Terpenes have also been found to inhibit the in vitro growth of bacteria and fungi (Chaumont et al.), Ann. Pharm. Fr., 1992, 50(3): 156-166; Moleyar et al., Int. J. Food Microbiol, 1992, 16(4): 337-342; and Pattnaik et al. Microbios, 1997, 89(358): 39-46) and some internal and external parasites (Hooser et al., J. Am. Vet. Med. Assoc., 1986, 189(8): 905-908). Geraniol was found to inhibit growth of Candida albicans and Saccharomyces cerevisiae strains by enhancing the rate of potassium leakage and disrupting membrane fluidity (Bard et al., Lipids, 1998, 23(6): 534-538). B-ionone has antifungal activity which was determined by inhibition of spore germination, and growth inhibition in agar (Mikhlin et al., A. Prikl. Biokhim. Mikrobiol, 1983, 19: 795-803; Salt et al., Adam. Physiol. Molec. Plant Path, 1986, 28: 287-297). Teprenone (geranylgeranylacetone) has an antibacterial effect on H. pylori (Ishii, Int. J. Med. Microbiol. Virol. Parasitol. Infect. Dis., 1993, 280(1-2): 239-243). Rosanol, a commercial product with 1% rose oil, has been shown to inhibit the growth of several bacteria (Pseudomonas, Staphylococus, E. coli, and H. pylori). Geraniol is the active component (75%) of rose oil. Rose oil and geraniol at a concentration of 2 mg/L inhibited the growth of H. pylori in vitro. Some extracts from herbal medicines have been shown to have an inhibitory effect in H. pylori, the most effective being decursinol angelate, decursin, magnolol, berberine, cinnamic acid, decursinol, and gallic acid (Bae et al., Biol. Pharm. Bull., 1998, 21(9) 990-992). Extracts from cashew apple, anacardic acid, and (E)-2-hexenal have shown bactericidal effect against H. pylori.
Diterpenes, i.e., trichorabdal A (from R. Trichocarpa), have shown a very strong antibacterial effect against H. pylori (Kadota et al., Zentralbl. Bakteriol, 1997, 287(1): 63-67).
Solutions of 11 different terpenes were effective in inhibiting the growth of pathogenic bacteria in in vitro tests; levels ranging between 100 ppm and 1000 ppm were effective. The terpenes were diluted in water with 1% polysorbate 20 (Kim et al., J. Agric. Food Chem., 1995, 43: 2839-2845).
There may be different modes of action of terpenes against microorganisms; they could (1) interfere with the phospholipid bilayer of the cell membrane, (2) impair a variety of enzyme systems (HMG-reductase), and (3) destroy or inactivate genetic material. It is believed that due to the modes of action of terpenes being so basic, e.g., blocking of cholesterol, that infective agents will not be able to build a resistance to terpenes.
There are, however, a number of drawbacks to the use of terpenes.
These include:
There are limitations to the current techniques of spray coating, extrusion, coacervation, molecular encapsulation, and spray drying/cooling to provide ingredient delivery systems.
Baker's yeast cell walls are derived from baker's yeast cells and are composed of the insoluble biopolymers β-1,3-glucan, β-1,6-glucan, mannan and chitin. They are typically 2-4 micron in diameter microspheres with a shell wall that is only 0.2-0.3 micron thick surrounding an open cavity. This material has considerable liquid holding capacity, typically absorbing 5-25 times its weight in liquid. The shell is sufficiently porous that payloads up to 150,000 Daltons in size can pass through the outer shell and be absorbed into the hollow cavity of the spherical particle. Baker's yeast cell walls have several unique properties, including heat stability (e.g. to 121° C.), shear stability, pH stability (e.g. pH 2-12), and at high concentrations they do not build significant viscosity. In addition to its physical properties this composition contains natural and healthy dietary fibres that deliver cardiovascular and immunopotentiation health benefits.
Yeast cell walls are prepared from yeast cells by the extraction and purification of the insoluble particulate fraction from the soluble components of the yeast cell. The fungal cell walls can be produced from the insoluble byproduct of yeast extract manufacture. Further, the yeast cells can be treated with an aqueous hydroxide solution, without disrupting the yeast cell walls, which digests the protein and intracellular portion of the cell, leaving the yeast cell wall component devoid of significant protein contamination, and having substantially the unaltered cell wall structure of β(1-6) and β(1-3) linked glucans. A more detailed description of whole glucan particles and the process of preparing them is described by Jamas et al. in U.S. Pat. No. 4,810,646 and in co-pending patent applications U.S. Ser. No. 166,929, U.S. Ser. No. 297,752 and U.S. Ser. No. 297,982. U.S. Pat. No. 6,242,594, assigned to Novogen Research Pty Ltd., describes a method of preparing yeast glucan particles by alkali extraction, acid extraction and then extraction with an organic solvent and finally drying. U.S. Pat. No. 5,401,727, assigned to AS Biotech-Mackzymal, discloses the methods of obtaining yeast glucan particles and methods of using them to promote resistance in aquatic animals and as an adjuvant for vaccinations. U.S. Pat. No. 5,607,677, assigned to Alpha-Beta Technology Inc., discloses the use of hollow whole glucan particles as a delivery package and adjuvant for the delivery of a variety of pharmaceutical agents. The teachings of the abovementioned patents and applications are incorporated herein by reference.
Other types of yeast and fungi cells have cell walls that do not contain glucan. The cell walls of such yeast and fungi can be isolated by similar techniques to those mentioned above to obtain cell wall particles.
Additionally, the cells of many plants, algae, bacteria and other micro-organisms also comprise a cell wall. The structure and composition of the cell wall varies between micro-organism, but in general it is a robust and relatively inert structure. It is possible to obtain cell wall particles derived from such cells through conventional techniques, such as those mentioned above in relation to yeast.
We have now found that terpenes can be taken up and stably encapsulated within hollow glucan particles or cell wall particles. Encapsulation of terpenes into such particles can be achieved by incubation of the particles with the terpene.
According to the present invention there is provided a composition comprising a hollow glucan particle or a cell wall particle encapsulating a terpene component.
The term “hollow glucan particle” as used herein includes any hollow particle comprising glucan as a structural component. Thus, in particular, the term includes yeast cell walls (in purified or crude forms) or hollow whole glucan particles. The term “cell wall particle” refers to a particle comprising the wall of a cell (in a purified or crude form), wherein glucan is not a structural component. Suitable particles include the cell walls of plant, algal, fungal or bacterial cells. Cell wall particles generally retain the shape of the cell from which they are derived, and thus, like a hollow glucan particle, provide a hollow central cavity suitable for encapsulating the terpene component.
For the present invention it is necessary that the hollow glucan particle or cell wall particle is able to stably encapsulate the terpene component. In general this means the hollow glucan particle or cell wall particle must be able to maintain its structure during incubation with the terpene component (generally the terpene component is at a relatively high concentration), and that terpene component must be able to migrate into the particle. Hollow glucan particles and cell wall particles are generally formed from relatively inert materials and are porous, and thus it can be assumed that, in general, hollow glucan particles and cell wall particles will be able to encapsulate a terpene component.
Compositions according to the present invention are effective against various infective agents including bacteria, viruses, mycoplasmas, fungi, nematodes arthropods and/or arachnids.
The compositions according to the present invention can provide the following advantages:
Particularly suitable hollow glucan particles or cell wall particles are fungal cell walls, preferably yeast cell walls. Yeast cell walls are preparations of yeast cells that retain the three-dimensional structure of the yeast cell from which they are derived. Thus they have a hollow structure which allows the terpene component to be encapsulated within the yeast cell walls. The yeast walls may suitably be derived from Baker's yeast cells (available from Sigma Chemical Corp., St. Louis, Mo.). Yeast cell wall particles with desirable properties can also be obtained from Biorigin (Sao Paolo, Brazil) under the trade name Nutricell MOS 55. These particles are a spray dried extract of S. cerevisiae.
Alternative particles are those known by the trade names SAF-Mannan (SAF Agri, Minneapolis, Minn.) and Nutrex (Sensient Technologies, Milwaukee, Wis.). These are hollow glucan particles that are the insoluble waste stream from the yeast extract manufacturing process. During the production of yeast extracts the soluble components of partially autolyzed yeast cells are removed and the insoluble residue is a suitable material for terpene loading. These hollow glucan particles comprise approximately 25-35% beta 1,3-glucan w/w. A key attribute of these materials are that they contain more than 10% lipid w/w and are very effective at absorbing terpenes. In addition, as a waste stream product they are a relatively cheap source of hollow glucan particles.
Alternative hollow glucan particles which have higher purity are those produced by Nutricepts (Nutricepts Inc., Burnsville, Minn.) and ASA Biotech. These particles have been alkali extracted, which removes additional intracellular components as well as removes the outer mannoprotein layer of the cell wall yielding a particle of 50-65% glucan w/w.
Higher purity hollow glucan particles are the WGP particles from Biopolymer Engineering. These particles are acid extracted removing additional yeast components yielding a product 75-85% glucan w/w.
Very high purity hollow glucan particles are Adjuvax™ from Alpha-beta Technology, Inc. (Worcester, Mass.) and microparticulate glucan from Novogeh (Stamford, Conn.). These particles are organic solvent extracted which removes residual lipids and so the particles comprise more than 90% glucan w/w.
In some embodiments a high purity glucan particle or cell wall particle may be required, for example where strict control over possible contaminants is required. In these instances the higher purity particles would be preferred over other less pure products. For other embodiments, the less pure particles would be preferred for economic reasons; those particles have also been found to be more effective at absorbing terpenes.
Preferably the hollow glucan particle or cell wall particle has a slight lipid content, such as 1 or 2% w/w lipid. A slight lipid content can increase the ability of the particle to encapsulate the terpene component. Preferably the lipid content of the hollow glucan particle or cell wall particle is 5% w/w or greater, more preferably 10% w/w or greater.
Optionally the terpene component of the present invention can be associated with a surfactant. The surfactant can be non-ionic, cationic, or anionic. Examples of suitable surfactants include sodium lauryl sulphate, polysorbate 20, polysorbate 80, polysorbate 40, polysorbate 60, polyglyceryl ester, polyglyceryl monooleate, decaglyceryl monocaprylate, propylene glycol dicaprilate, triglycerol monostearate, polyoxyethylenesorbitan, monooleate, Tween®, Span® 20, Span® 40, Span® 60, Span® 80, Brig 30 or mixtures thereof. The surfactant acts to hold the terpene component in an emulsion and also assists encapsulation of the terpene component into the hollow glucan particle or cell wall particle.
The terpene component of the present invention can comprise a single terpene or a mixture of terpenes. Mixtures of terpenes can result in synergistic effects.
The term “terpene” as used herein refers not only to terpenes of formula (C5H8)n, but also encompasses terpene derivatives, such as terpene aldehydes or terpene polymers. Natural and synthetic terpenes are included, for example monoterpenes, sesquiterpenes, diterpenes, triterpenes, and tetraterpenes. In addition, reference to a single name of a compound will encompass the various isomers of that compound. For example, the term citral includes the cis-isomer citral-a (or geranial) and the trans-isomer citral-b (or neral).
It should be noted that terpenes are also known by the names of the extract or essential oil which contain them, e.g. lemongrass oil (contains citral).
The terpenes which are exempted from US regulations and which are listed in EPA regulation 40 C.F.R. Part 152 (incorporated herein by reference in its entirety) are suitable for use in this invention.
Particularly suitable terpenes for use in the present invention include those selected from the group consisting of citral, pinene, nerol, b-ionone, geraniol, carvacrol, eugenol, carvone (for example L-carvone), terpeniol, anethole, camphor, menthol, thymol, limonene, nerolidol, farnesol, phytol, carotene (vitamin A1), squalene, thymol, tocotrienol, perillyl alcohol, borneol, myrcene, simene, carene, terpenene, linalool and mixtures thereof.
Preferably the terpenes used in the present invention have the general structure C10H16 as this sub-group is generally more effective against infective agents.
More preferably the terpene component comprises a terpene selected from the group consisting of geraniol, thymol, citral, carvone (for example L-carvone), eugenol and b-ionone.
The terpene component can suitably comprise thymol, as this terpene has been shown to be particularly effective in treating or preventing fungal plant infections.
Another particularly suitable terpene is citral which has demonstrated particular efficacy against a number of micro-organisms.
A combination of geraniol, thymol and eugenol has demonstrated particular efficacy in combating plant infections, and is thus a particularly suitable terpene component.
Citral alone or a combination of thymol, eugenol and citral has demonstrated particular efficacy in combating mite infestations, and are thus particularly suitable terpene components.
Other terpene formulations which have shown high efficacy in treating plant infections include (percentages are w/w):
Accordingly a terpene component comprising any of the above formulations is particularly suitable for use in the present invention.
In one embodiment the terpene component includes one or more terpenes which contain oxygen. Citral, for example citral 95, is an oxygenated C10H8 terpene, C10H16O CAS No. 5392-40-5 (3,7-dimethyl-2,6-octadien-1-al). A stable suspension of citral can be formed up to about 2500 ppm. Citral can be made into a solution at up to about 500 ppm. A stable suspension of hollow glucan particles incorporating citral of 25 ppt citral can be made.
The composition of the invention can comprise 1 to 99% by volume terpenes, 0 to 99% by volume surfactant and 1 to 99% hollow glucan particles or cell wall particles. More specifically the composition can comprise about 10% to about 67% w/w terpenes, about 0.1-10% surfactant and about 40-90% hollow glucan particles or cell wall particles.
Suitably a composition of the present invention comprises from about 500 to about 10,000 ppm hollow glucan particles or cell wall particles, where the particles contain from about 1 to about 67% terpene component. Preferably the composition comprises from about 1000 to about 2000 ppm hollow glucan particles or cell wall particles, where the particles contain from about 10 to about 50% terpene component.
Specific compositions can include e.g., for bacteria and fungi, hollow glucan particles or cell wall particles encapsulating terpenes in water or standard 0.9% saline with up to 67% L-carvone, up to 67% eugenol, up to 67% citral, up to 67% thymol and L-carvone, up to 67% geraniol, or up to 67% citral and L-carvone and eugenol, and 1% Tween® 80; for mold, hollow glucan particles or cell wall particles encapsulating terpenes in water or standard 0.9% saline with up to 67% citral and 1% Tween® 80; or for mycoplasma, hollow glucan particles or cell wall particles encapsulating terpenes in water or standard 0.9% saline with up to 67% citral, up to 67% L-carvone and eugenol, up to 67% eugenol, up to 67% geraniol, or up to 67% geraniol, thymol, and 1% Tween® 80.
Concentrations of hollow glucan particles or cell wall particles encapsulating terpenes of 1, 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 125, 130, 140, 150, 160, 175, 190, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, 500, 525, 550, 575, 600, 625, 650, 675, 700, 725, 750, 775, 800, 825, 850, 875, 900, 925, 950, 975, 1000, 1100, 1250, 1375, 1425, 1500, 1600, 1750, or 2000 ppm can be used as effective concentrations in the compositions and methods of the current invention. Even higher concentrations (up to 25 ppt, i.e. parts per thousand) can be made and may be useful in the current invention.
The composition of the present invention can comprise between about 1 ppm and about 25 ppt (25000 ppm) of the terpene component, preferably 100 to 2000 ppm of the terpene component, for example, 250, 500, 1000, 2000 ppm thereof.
The terpenes, surfactants, and other components of the invention may be readily purchased or synthesised using techniques generally known to synthetic chemists.
It is highly preferred that terpenes used in the present invention, for safety and regulatory reasons, are at least food grade terpenes (as defined by the United States FDA or equivalent national regulatory body outside the USA).
Optionally the composition can comprise other food-grade active compounds in addition to the terpene component, for example other antimicrobial agents, enzymes, or the like.
Optionally the composition can comprise a further active agent in addition to the terpene component, for example an antimicrobial agent, an anti-fungal agent, an insecticidal agent, an anti-inflammatory agent, an anaesthetic or the like. Suitable agents include:
The composition can comprise an antioxidant to reduce oxidation of the terpene. An example of such an anti-oxidant might be rosemary oil, vitamin C or vitamin E.
The composition of the present invention can be in the form of a dry powder. The composition can be provided in combination with an agriculturally, food or pharmaceutically acceptable carrier or excipient in a liquid, solid or gel-like form.
For solid compositions, suitable carriers include pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharin, talc, cellulose, glucose, sucrose, magnesium carbonate, and the like. Suitably the formulation is in tablet or pellet form. As suitable carrier could also be a human or animal food material. Additionally, conventional agricultural carriers could also be used.
A pellet, tablet or other solid form of the composition can preferably also contain a dispersal agent which promotes dispersal of the composition when placed into a liquid, e.g. water. Suitable dispersal agents include xanthan gum, maltodextrin, alginates, or the like.
Liquid compositions can, for example, be prepared by dispersing the composition in water, saline, aqueous dextrose, glycerol, ethanol, or the like, to form a solution or suspension. If desired, these compositions can contain minor amounts of non-toxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents (for example, sodium acetate, sorbitan monolaurate, triethanolamine sodium acetate or triethanolamine oleate). The methods of preparing such liquid compositions are known, or will be apparent, to those skilled in this art; for example see Remington: The Science and Practice of Pharmacy; Lippincott, Williams & Wilkins; (Dec. 15, 2000)—which is incorporated herein by reference. Again a liquid composition could be prepared by dispersing the composition in a liquid human or animal food or drink material. Additionally a suitable liquid agricultural excipient could be used.
For oral administration tablets and granules are generally preferred. Tablets may contain binders and lubricants. Fine powders or granules may contain diluting, dispersing and/or surface active agents and can be presented in water or in a syrup. Capsules or sachets can conveniently contain the composition in a dry state. Non-aqueous solutions or suspensions of the composition are also suitable and may contain suspending agents. Where desirable or necessary, flavouring, preserving, suspending, thickening, or emulsifying agents can be included. Of course, it would be suitable to use a food or drink material as an oral delivery method.
Parental administration is generally characterised by injection. For injectables it will be appreciated that, in general, all materials used in the composition and any excipient used must be of pharmaceutical grade. Injectables can be prepared in conventional forms, either as liquid solutions, emulsions or suspensions, solid forms suitable for dissolution, suspension in liquid prior to injection, or as emulsions. An alternative approach for parental administration involves use of a slow release or sustained release system, such that a constant level of dosage is maintained. See, for example, U.S. Pat. No. 3,710,795, which is incorporated by reference herein. Preparations for parenteral can also contain buffers, diluents and other suitable additives. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils (such as olive oil), and injectable organic esters (such as ethyl oleate). Aqueous carriers include water, alcoholic/aqueous solutions, emulsions, or suspensions, including saline and buffered media. Other parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's, or fixed oils. Vehicles for intravenous use include fluid and nutrient replenishers, electrolyte replenishers (such as those based on Ringer's dextrose) and the like. Preservatives and other additives can also be present such as, for example, antimicrobials, anti-oxidants, chelating agents, inert gases, and the like.
For topical administration liquids, suspension, lotions, creams, gels, ointments, drops, suppositories, sprays and powders may be used. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners, and the like can be used as necessary or desirable.
The present invention further provides a method of preparing a hollow glucan particle or cell wall particle encapsulating a terpene component, said method comprising the steps of;
Optionally the above method can further comprise the step of drying the particles encapsulating the terpene component. Drying may be achieved in a number of ways and mention may be made of freeze drying, fluidised bed drying, drum drying or spray drying, all of which are well known processes.
In step a) of the above method, the terpene component is suitably provided as a suspension in an aqueous solvent, and optionally in the presence of a surfactant. Suitably the solvent is water. A suitable surfactant is Tween-80 (polyoxyethylenesorbitan monooleate), and preferably the surfactant is present at a concentration of about 0.1 to 10% by volume of the total reaction mixture, more preferably about 1%. Alternatively the terpene component may be provided as a true solution in a solvent, e.g. water. A true solution of terpene in water can be obtained by mixing the terpene in water at high shear until a true solution is obtained. Publication No WO 03/020024 provides further details of forming true solutions of terpenes in water.
In step b) of the above method, the hollow glucan particle or cell wall particle is suitably provided as a suspension in water or other suitable liquid. Suitably the suspension comprises approximately 1 to 1000 mg particles per ml, preferably 200 to 400 mg/ml. Alternatively the particles may be provided as a dry powder and added to the terpene-surfactant suspension.
Alternatively the particles are provided in sufficient liquid to minimally hydrate the particles, but not in significant excess. The term “hydrodynamic volume” (HV) is used to describe the volume of liquid required to minimally hydrate the particles. Thus suitably the particles are provided with a volume ranging from the HV and a volume of 1.5 times the HV (1.5 HV). This makes the subsequent drying step more efficient. Also, where a low volume of liquid is used (i.e. around HV to 1.5 HV), it is also possible to extrude the finished product into pellet or noodle form, which is convenient for fluidised bed drying.
It has been found that the terpene component can become encapsulated by the hollow glucan particle or cell wall particle at room temperature. The rate of encapsulation is, however, increased at 37° C. but the temperature should be kept below the boiling point or denaturing temperature of any component of the composition. Suitable conditions for step c) of the above method are therefore atmospheric pressure at a temperature of 20 to 37° C. Optimisation of the conditions for a particular encapsulation reaction will be a matter of routine experimentation.
The present invention further provides a method of killing a microorganism, said method comprising the step of;
Suitable compositions are those defined in more detail above.
The present invention further provides a method of preventing or treating an infection in a patient, said method comprising the step of;
Suitable compositions are those defined in more detail above.
The infection of the patient may be caused by any infectious agent. Examples of these infectious agents include, but are not restricted to Staphylococcus aureus, Aspergiffius fumigatus, Mycoplasma iowae, Penicillium sp., and Mycoplasma pneumoniae.
For internal administration the composition may be administered orally, vaginally, rectally, by inhalation, or by parenteral routes, e.g. by intradermal, subcutaneous, intramuscular, intraperitoneal, intrarectal, intraarterial, intralymphatic, intravenous, intrathecal and intratracheal routes. Suitable formulations of the composition for these routes are discussed above.
For external treatment, the composition may be applied topically, for example as a cream or ointment or as a dry powder for treatment of a wound.
The amount of terpene administered in the above method should clearly be sufficient to achieve the desired result, i.e. prevention and/or treatment of the infection, but should not be at a level which will induce serious toxic effects in the patient.
The amount of composition administered will, of course, be dependent on the manner of administration, on the patient being treated, i.e. their weight, their age, condition, sex and extent of the disease in the subject and on the judgement of the prescribing physician. The dose, schedule of doses, and route of administration can be varied. One of skill in the art would readily be able to determine an anti-infective amount for a given application based on the general knowledge in the art and the procedures in the Examples given below. It should be noted that the term “patient” as used herein refers to any individual, either human or animal, to which the treatment is applied. Thus, the patient can be a domesticated animal (e.g., cat, dog, etc.), livestock (e.g., cattle, horse, pig, sheep, goat, etc.), laboratory animal (e.g., mouse, rabbit, rat, guinea pig, etc.), birds and fish. Suitably the subject is a mammal and especially a primate, for example a human.
In a further aspect the present invention provides a method of killing an insect or arachnid, said method comprising the step of;
Insects which may be killed according to the present invention include, for example, ants, termites, lice, aphids, fleas, lice, locusts, grasshoppers, thrips.
Arachnids which may be killed according to the present invention include, for example, mites, spiders and ticks.
In one embodiment the present invention provides a method of killing mites which infest plants, for example two-spotted spider mites. Compositions including citral alone or a combination of eugenol, thymol and citral are particularly suitable for killing two-spotted spider mites.
Administration may suitably be by spraying or otherwise spreading the composition onto the insect or arachnid or by spraying onto a plant leaf which may then be ingested by the insect or arachnid. Alternatively, an object infested with the insect or arachnid may be immersed in the composition.
Where a human, animal is infested with the insect or arachnid the composition may be administered, for example, in the form of a shampoo or the like.
Where fabric, e.g. clothing is infested with the insect or arachnid the composition may be administered during washing of the clothes. For example the composition could be administered as part of a fabric detergent or softener composition.
In a further embodiment the present invention provides a method of treating or preventing infection or infestation of a plant, said method comprising the step of;
Suitable compositions are those defined in more detail above.
Terpenes have been shown to eliminate a number of plant pathogens (see WO 03/020024) and, as described in co-pending application U.S. 60/538,627 also effectively kill nematodes which are significant plant parasites. Terpenes alone in suspension or solution, however, are somewhat unstable and degrade rapidly in the soil environment, thus losing efficacy.
Incorporation of a terpene component in a hollow glucan particle or cell wall particle can reduce the rate of terpene release and degradation, thus increasing the duration of action of the terpene in the soil.
Suitably the infection of a plant which is to be treated or prevented in the above method is infection by nematodes.
Other plant infections that may be treated or prevented include fungal plant infections, especially those affecting the surface of a plant. Such infections include downy mildew, powdery mildew or botrytis bunch rot; these infections particularly affect grape vines.
In one embodiment, the plant infection may be caused by one or more of the following: Aspergillius fumigatus, Sderotinia homeocarpa, Rhizoctonia solani, Colletotrichum graminicola, phytophtora infestans or Penicillium sp.
Plant infestations that can be prevented or treated include infestations by insects or arachnids. Examples of insect infestations which can be treated include those by flies, aphids, ants, locusts, grasshoppers and thrips. Examples of arachnid infestations that can be prevented or treated include herbivorous mites (including two-spotted spider mites).
Compositions according to the present invention have been shown to be especially effective in treating plant infestations with mites, in particular two-spotted spider mites. Compositions including citral alone or a combination of eugenol, thymol and citral are particularly suitable for killing two-spotted spider mites.
An advantage of a terpene based treatment of plants is that it can be applied shortly before harvest.
Many conventional treatments require an extended period before re-entry to the treated area (generally 3 weeks). This means that an outbreak of a plant disease shortly before harvest cannot be treated with conventional treatments as it would then not be possible to harvest the crop at the desired time. The compositions of the present invention can suitably be applied at any time up until harvest, for example 21 days prior to harvest, 14 days prior to harvest, 7 days prior to harvest, or even 3 days or less before harvest.
Encapsulated terpenes have shown particular efficacy in treating downy mildew, powdery mildew and botrytis bunch rot in grapes, and thus the present invention provides a method of treating or preventing these diseases. Additionally, encapsulated terpenes have been shown to be particularly effective in treating two-spotted spider mite infestation, and thus the present invention also provides a method of treating or preventing such infestations.
Prevention of plant infections can be achieved by treating plants which the encapsulated terpenes regularly as a prophylactic measure.
Suitably the composition of the present invention is applied by spraying. This is particularly suitable for treating a plant disease which affects the surface of a plant. For spraying, a preparation comprising 2 g/l of the composition in water may be used. Concentrations of from 2 to 4 g/l are particularly effective, and concentrations of greater than 4 g/l can be used as required. Obviously it is important that the concentration of the composition used is sufficient to kill or inhibit the disease causing agent, but not so high as to harm the plant being treated.
When spraying plants a rate of 500 UHa or greater is suitable to cover the plants. Preferably a rate of 900 UHa or greater, more preferably 1200 UHa or greater is used to ensure good coverage. Where grape vines are being treated, a rate of 1200 UHa has proven suitably effective.
The composition of the present invention may alternatively be applied via irrigation. This is particularly suitable for treating nematodes or other soil borne pathogens or parasites.
In another embodiment the invention provides the use of a composition comprising a hollow glucan particle or cell wall particle encapsulating a terpene component as an insecticide or as an arachnicide (i.e. a composition capable of killing arachnids), in particular as an acaricide.
In a further embodiment the invention provides the use of a composition comprising a hollow glucan particle or cell wall particle encapsulating a terpene component for the preparation of an insecticide or an arachnicide, in particular an acaricide.
In a further embodiment the present invention also provides a composition comprising a hollow glucan particle or cell wall particle encapsulating a terpene component for use in the prevention or treatment of an infection in a patient or a plant. Suitable compositions are those defined in more detail above.
In a further embodiment the present invention provides the use of a composition comprising a hollow glucan particle or cell wall particle encapsulating a terpene component in the manufacture of a medicament for the treatment of infection caused by a micro-organism. Suitable compositions are those defined in more detail above.
The present invention will now by further described with reference to the following, non-limiting, examples and figures in which:
The following examples are provided to further enable those of ordinary skill in the art to make or perform the present invention. They are purely exemplary and are not intended to limit the scope of the invention. Unless indicated otherwise, parts are parts by volume or parts by weight, as indicated, temperature is in degrees Celsius (° C.) or is at ambient temperature, and pressure is at or near atmospheric. There are numerous variations and combinations of the compositions and conditions for making or using them, e.g., component concentrations, desired solvents, solvent mixtures, temperatures, pressures, and other ranges and conditions that can be used to optimise the results obtained from the described compositions and methods. Only reasonable and routine experimentation will be required to optimise these.
The following protocol was performed to demonstrate that terpenes would load into yeast cell walls and other hollow glucan particles.
Emulsions of citral and L-carvone were prepared by mixing 150 μl of the terpene with 100 μl of 10% Tween 80 in water and 250 μl of water.
Baker's yeast particles (YP) or Levacan™ yeast glucan particles (YGP), available from Savory Systems International, Inc., Branchburg, N.J., were mixed with water to form a 250 mg/ml suspension.
500 μl of the YP or YGP suspension and 250 μl of the terpene emulsion were mixed together and incubated overnight under constant agitation., 500 μl YP or YGP suspension and 500 μl of water were used as a control. The particles were then washed with water until free from external emulsion. The particle preparations were then frozen and lyophilised until dry.
The particles were then rehydrated and examined under light microscope. The results are shown in
The following protocol was performed to determine the maximal amounts of terpenes that would load into YP.
Citral or L-carvone-water emulsion was mixed with YP and Tween 80 surfactant overnight at room temperature. Samples were centrifuged at 14,000×g for 10 minutes and the appearance of free terpene floating on the aqueous layer was scored. The results are shown in the right hand column labelled free terpene of Table 1.
The expression “free terpene” refers to the visible presence of terpene in the centrifuged reaction mixture. The absence of free terpene indicates complete absorption of the terpene by the particles. The highest volume of terpene absorbed by the particles, as evidenced by the absence of free terpene, was recorded as the maximal volume of absorbed terpene emulsion.
As can be seen from the results, YP is capable of absorbing and encapsulating at least 16.5 μl of L-carvone terpene emulsion or at least 5 μl of citral emulsion per 10 mg of YP.
The following protocol was performed to demonstrate that the presence of surfactant improves terpene loading and to determine the minimum level of Tween-80 surfactant required for the YP terpene loading reaction.
Loading reactions were set up as shown in Table 2 below.
Citral or L-carvone-water emulsion was mixed with YP with 0-10% v/v Tween 80 surfactant overnight at room temperature. Samples were centrifuged at 14,000×g for 10 minutes and the appearance of free terpene floating on the aqueous layer was scored. The results are shown in the right hand column labelled free terpene of Table 2.
The expression “free terpene” refers to the visible presence of terpene in the centrifuged reaction mixture. The absence of free terpene indicates complete absorption and encapsulation of the terpene by the YP. The highest volume of terpene absorbed by the YP, as evidenced by the absence of free terpene, was recorded as the maximal volume of absorbed terpene emulsion.
As can be seen from the results a Tween-80 concentration of 1% (i.e. 100 μl of 10% Tween-80 in 1000 μl of reaction mixture) is sufficient to allow complete uptake of the terpene in the above reaction. A 2% Tween-80 causes no improvement in results, whereas with a 0.33% concentration free terpene was observed. This indicates that:
Terpenes are absorbed into YP particles in the absence of a surfactant, but the presence of surfactant significantly increases terpene absorption.
A Tween-80 concentration of around 1% is optimum for YP loading as it ensures proper loading whilst maximising the terpene payload of the YP particles.
The following protocol was performed to determine the maximal amounts of terpenes that would load into YP at high YP levels.
Citral or L-carvone-water emulsion was mixed with YP and Tween 80 surfactant overnight at room temperature. Samples were centrifuged at 14,000×g for 10 minutes and the appearance of free terpene floating on the aqueous layer was scored. The results are shown in the right hand column labelled free terpene of Table 3.
The expression “free terpene” refers to the visible presence of terpene in the centrifuged reaction mixture. The absence of free terpene indicates complete absorption of the terpene by the YP. The highest volume of terpene absorbed by the YP, as evidenced by the absence of free terpene, was recorded as the maximal volume of absorbed terpene emulsion.
As can be seen from the results in Table 3, YP is capable of absorbing and encapsulating terpenes at high YP concentration. YP absorbed and encapsulated at least 112.5 μl of L-carvone terpene emulsion or at least 75 μl of citral emulsion per 125 mg of YR This demonstrates that the terpene encapsulation reaction is independent of YP concentration within the ranges tested.
The following protocol was performed to analyse the loading properties of different types of particles. The particles studied were Baker's Yeast Cell Wall Particles (Sigma Chemical Corp., St. Louis, Mo.), Nutrex™ Walls (Sensient Technologies, Milwaukee, Wis.), SAF-Mannan™ (SAF Agri, Minneapolis, Minn.), Nutricept Walls™ (Nutricepts Inc., Burnsville, Minn.), Levacan™ (Savory Systems International, Inc., Branchburg, N.J.) and WGP™ (Alpha-beta Technology, Inc. Worcester, Mass.).
L-carvone and citral emulsions were prepared by sonicating 7 g terpene+3 ml 3.3% Tween-80.
Table 4 below compares the purity with the number of yeast particles per mg and the packed solids weight/volume ratio.
4 × 107
1 × 108
From Table 4 it can be concluded that the number of particles per mg is inversely proportional to purity. Thus the number of particles per mg of WGP is almost 10-fold higher than Baker's YP.
The YP suspensions were prepared as follows:
The packed volume of the above particles is identical which means that equal numbers of particles were assayed.
Loading reactions were set up as shown in Table 5 and left to incubate overnight. Samples were centrifuged at 14,000×g for 10 minutes and the appearance of free terpene floating on the aqueous layer and the color of the encapsulated terpenes in the pellet was scored. The results are shown in the two right hand columns of Table 5. The highest volume of terpene absorbed by particles as evidenced by the absence of free terpene was recorded as the volume of absorbed terpene emulsion.
From the results the following conclusions were reached:
The following protocol was adopted to compare the loading kinetics of various types of yeast particles.
L-carvone and citral emulsions were prepared by sonicating 7 g terpene with 3 ml 3.3% Tween-80. 1% Tween-80 solution was prepared by sonicating 1 ml 10% Tween-80 in 10 ml water.
Loading reactions were set up as shown in Table 6.
The reactions were incubated for 1, 3, 6, 9 and 24 hours at room temperature or 37° C. After incubation samples were centrifuged at 14,000×g for 10 minutes and the appearance of free terpene floating on the aqueous layer was scored. The results are shown in the two right hand columns of Table 6. The highest volume of terpene absorbed by the particles as evidenced by the absence of free terpene was recorded as the volume of absorbed terpene emulsion. Colour of the encapsulated pellet was scored at 24 hours.
From the results shown in Table 6 and other observations the following conclusions can be made:
The following protocol was adopted to compare the loading efficiency of Baker's YP versus SAF Mannan™.
Terpene emulsions were prepared as follows:
Emulsions composed of terpene:water:surfactant ratio of 0.75:0.3:0.05 were used for these experiments.
Increasing volumes of terpene emulsion were mixed with 250 mg/ml Baker's YP or 250 mg/ml SAF Mannan™ overnight at room temperature as shown in Tables 7 and 8. Samples were centrifuged at 14,000×g for 10 minutes and the appearance of free terpene floating on the aqueous layer was scored. The highest volume of terpene emulsion absorbed by Baker's YP or SAF Mannan™ as evidenced by the absence of free terpene was recorded as the volume of absorbed terpene emulsion. Colour of encapsulated terpenes in the pellet was recorded. The results in Tables 7 and 8 show that all single and terpene combinations were efficiently loaded into both Baker's YP or SAF Mannan particles.
From the results the following observations were made:
The approximate maximal loading for each particle type was determined and is shown in Tables 9 and 10 below. Percentage loaded represents a ratio of the amount of terpene loaded to the amount of particle present (weight for weight).
Terpene stability was assessed by the observation of citral formulations for the formation of a yellow colored oxidation product. As noted in the right hand column in Tables 5-8 citral emulsions and citral encapsulated Bakers YP turned a progressively increasing yellow color over time. However, citral encapsulation in SAF Mannan™ increased citral stability as evidenced by a reduction or absence of yellow color over time.
The following protocol was carried out to evaluate the possibility that terpene loading and encapsulation into YP could be carried out at a very high Yeast Particles (YP) solids level to allow for direct extrusion of the loaded formulation into a fluidised bed drier. The minimal amount of water to completely hydrate the SAF Mannan™ particles was determined to be 3.53 g water per g solids. This defines the hydrodynamic volume (HV) or water absorptive capacity of the particles. At this level of water the hydrated particles have a consistency of a stiff dough which is thixotropic, i.e. shear thinning like mayonnaise. Addition of water up to 40% above the HV results in a thick flowable paste. The standard reaction that has been used in the above examples was carried out at 3×HV water.
A series of terpene (L-carvone) loading reactions were carried out keeping the ratio of particle:terpene:Tween (1:0.44:0.04) constant and varying the amount of water in the system from the HV (3.53 g) to HV+40% water (4.92 g). Controls were the standard loading system which uses 3×HV water, particles only and terpene only reactions. Following overnight incubation samples of the mixtures were evaluated microscopically for free terpene and evidence of terpene uptake into the particles and for material flow characteristics by assessing flow in inverted tubes over 15 minutes. In addition, the presence of free oil was assessed by hydrating the reaction mixture with 5×HV, vortexing to obtain a complete dispersion of particles and centrifugation to sediment the particle encapsulated terpene. The results are shown in Table 11 and
The results shown in Table 11 and
These results extend our understanding of the conditions to load terpenes into hollow glucan particles. The flexibility to use a minimal volume of water to hydrate the particles during the loading process will allow loading of the terpenes under conditions where the reaction mixture is a malleable dough-like consistency using standard food-grade swept surface dough mixers. The consistency of the final high solids terpene loaded mixture is suitable for direct extrusion to form noodles and pellets for fluidised bed drying.
Suitable facilities to scale up production in this manner would require:
The following protocol was adopted to evaluate the effect of an interstitial hydrocolloid to increase dried hollow glucan particle encapsulated terpene formulations to disperse when hydrated.
The effect of increasing xanthan gum levels on dry hollow glucan particle encapsulated L-carvone dispersion in water was assessed by loading L-carvone into SAF Mannan by incubating 1.1 g of an L-carvone emulsion (L-carvone:water:surfactant ratio of 0.75:0.3:0.05) with 1 g SAF Mannan and 4.4 g 0.1% Tween 80 containing 0-1% xanthan gum as shown in Table 12.
The results in Table 12 and
It may also be worthwhile to include a pellet coating to increase the stability of the loaded terpenes, and to provide a sustained release of terpene.
The results of a protocol performed to compare the MIC of fresh versus freeze dried hollow glucan particle encapsulated terpene formulations are shown below in Table 13. A simple terpene emulsion was also tested and the results are shown for comparison.
The conclusions taken from the above results were:
Anti-microbial assays were carried out with encapsulated terpenes and mixtures produced at the pilot plant scales against S. aureus. Both the fresh and freeze dried encapsulated terpene samples containing materials demonstrated strong anti-microbial activities. The results are summarised in Table 14 below.
Terpenes were encapsulated in SAF-Mannan™ at a 2.5 Kg scale. A mixture of three terpenes (Geraniol, 275 g; Eugenol, 385 g; and thymol, 440 gram was dissolved and homogenized with 100 g Tween-80 and 8 L of water. SAF-Mannan™ (2.5 Kg) was added to form a homogenous suspension. The suspension was passed through a Gaulin homogenizer to reduce particle size and the homogenate was incubated overnight at room temperature. A sample of the encapsulated terpene was removed and stored at room temperature. The remaining encapsulated terpene was then frozen in trays and freeze dried. The freeze dried encapsulated terpene powder was ground and stored at room temperature.
Staphylococcus aureus assays
At the pilot plant scale both the fresh and freeze dried samples were equally potent on a w/w terpene basis.
Based on the large scale preparation results, the predicted effective dose of the freeze dried formulation against S. aureus is 200 ppm (the formulation contains ˜50% terpene w/w) or 0.2 g/L water.
Terpene emulsions were prepared as follows:
SAF-Mannan™ (2.5 g) was mixed with 3 ml of each emulsion and 7 ml of 1% Tween 80 and incubated overnight to encapsulate the terpenes and terpene mixtures. The encapsulated terpene formulations were frozen and freeze dried and the powders ground to a fine powder. Suspensions of encapsulated terpenes (25 mg/ml) and unencapsulated terpene emulsions were assayed for antibacterial activity against Mycobacterium. The results are set out in Table 15
Preparations of yeast cell walls encapsulating citral were prepared according to the procedures described above. The hollow glucan particles contained 17.5% citral, and the particles were present at in the test preparations at a concentration of 1000 ppm. This means that terpenes were effectively present at a concentration of 175 ppm.
1.0 ml of the test preparations was added to 0.1 to 0.15 ml of water containing root-knot nematodes. 1.0 water was added to the nematodes as the control.
Observations were made as previously described and the kill rate assessed (i.e. percentage dead) after 24 and 48 hrs. The results shown below in Table 16 are an average of 2 sets of results.
The results demonstrate that hollow glucan particles encapsulating terpenes are effective at killing root-knot nematodes at a particle concentration of 1000 ppm, which corresponds to a citral concentration of only 175 ppm.
Thus hollow glucan particles encapsulating terpenes appear to be as effective as terpenes in solution or with surfactant as nematicides. The nematicidal activity is retained despite the terpene being encapsulated within the particle. It can be expected that higher concentrations of terpenes within the hollow glucan particles, or higher concentrations of the particles would result in an even higher kill rate, as is the case for terpenes in solution or with surfactant.
The following protocols were carried out to assess the fungicidal properties of various terpene combinations, and to compare the efficacy of encapsulated and non-encapsulated compositions.
A microtitre plate assay was used to assess the minimum inhibitory concentration (MIC) of a range of terpene compounds against different pathogenic organisms. The assay used for each organism is described in detail later but important general features are as follows.
The assay uses two incubation periods to distinguish between static (growth inhibition) and cidal (killing) activities. The first incubation period allows assessment of growth inhibition, but cannot distinguish between merely prevention of growth and killing of the cells. The purpose of the second incubation period is to allow sufficient time and nutrients for any dormant or inhibited cells that survive terpene exposure to proliferate. Any cells that were inhibited by fungistatic effects should respond and grow during the second incubation period, whereas cells that were killed by exposure to terpenes will not grow in the fresh medium.
Initial screening experiments were carried out using a total of 31 different terpene formulations (Table 17). These experiments were repeated using a subset of strongly active terpene formulations (Table 18).
A combination of the terpenes geraniol, eugenol and thymol in a ratio of 2:1:2 encapsulated within glucan particles was also tested; this sample is referred to as YP-GET. A non-encapsulated geraniol, eugenol and thymol combination in the same ratio was also tested for comparison with the encapsulated form.
MIC Assay Using Saccharomyces cerevisiae
S. cerevisiae (5×105 cells/mL in YPD growth medium) were added to each well of a 96-well microtitre plate in 100 μL aliquots. At least one column per plate was designated as a cell-only control and no terpene was added to these wells. Aliquots (100 μL) of different terpene formulations were added to the first row of the remaining columns, and serial 2-fold dilutions were performed by transferring 100 μL from one row to the next a total of 7 times. Finally, 100 μL was discarded from the last row in order to ensure that all wells contained the same volume. Microtitre plates were incubated statically overnight at 30° C.
Following incubation, plates were scored for inhibition of growth (evidenced by a lack of turbidity). Growth inhibition (≥75%) was visually confirmed by microscopy.
Once the MIC had been determined for each formulation, the microtitre plates were centrifuged and the spent medium was removed from non-turbid wells. The cells were resuspended in fresh medium (100 μL) and the plates were re-incubated overnight at 30° C. Assessment of growth inhibition was performed as before.
The different terpene formulations were serially diluted in the 96-well microtitre plate as described for S. cerevisiae. Molten YPD agar was then added to the wells, together with 5 μL mixed inoculum (prepared from mouldy grape leaves to a concentration of 5×104 cells/mL). The plates were incubated statically for 24 hours at room temperature and spore growth was visually assessed by microscopy.
Due to the use of solid medium, the second incubation period in fresh media could not be performed.
MIC Assay Using Colletotrichum graminicola
The different terpene formulations were serially diluted in the 96-well microtitre plate as described for S. cerevisiae. C. graminicola (300 spores/well) were added to the diluted terpenes and the plates were incubated statically for 48 hours at room temperature. Spore germination and growth were visually assessed by microscopy.
Once the MIC had been determined for each formulation, the microtitre plates were centrifuged and the spent medium was removed from growth-inhibited wells. The spores were resuspended in fresh medium (100 μL) and the plates were re-incubated overnight at room temperature. Assessment of growth inhibition was performed as before.
Saccharomyces
Colletotrichum
cerevisiae
graminicola
a Terpene combinations were mixed in a 1:1 (w/w) ratio unless otherwise indicated.
b MICs calculated by terpene content.
Saccharomyces
Colletotrichum
cerevisiae
graminicola
a Terpene combinations were mixed in a 1:1 (w/w) ratio unless otherwise indicated.
b 1 × 104 cells/mL stock suspension.
c MICs calculated by terpene content.
Using a mixed inoculum presents a number of problems. The variability in spore content between preparations results in poor interassay reproducibility, and growth of contaminating organisms impedes the scoring of spore germination. Unicellular yeast species are particularly problematic in masking spore growth. Although precise data could not be obtained from this assay, an inhibitory effect of terpenes was observed.
Identification of spores was easier during scoring of the repeat assay than during the initial screening assay as a larger number of spores were used (approximately 50/well versus approximately 10/well). Therefore, data obtained during the repeat assay may provide a more reliable estimate of MIC.
Colletotrichum graminicola
The generally higher MIC values obtained from the repeat assay compared to the initial screening assay may be due to:
YPD growth medium (100 μL) was added to each well of a 96-well microtitre plate and aliquots of different terpene formulations were added to the first row, giving a total volume of 200 μL in this row. One column was designated as a cell-only control and no terpene was added to these wells. Serial 2-fold dilutions were performed by transferring 100 μL from one row to the next a total of 7 times. Finally, 100 μL was discarded from the last row in order to ensure that all wells contained the same volume. S. cerevisiae (5×105 cells/mL in YPD growth medium) were then added to each well in 100 μL aliquots, and the absorbance at 620 nm (A620) was measured for each well using a microtitre plate reader. Microtitre plates were incubated statically overnight at 30° C.
Following incubation, the A620 was measured again and plates were scored for inhibition of growth (≥75%). Growth inhibition was visually confirmed by microscopy.
For the free terpene emulsions, once the MIC had been determined for each formulation, the microtitre plates were centrifuged and the spent medium was removed from the growth-inhibited wells. The cells were resuspended in fresh medium (100 μL) and the plates were re-incubated overnight at 30° C. Assessment of growth inhibition was performed as before.
MIC and fungicidal MIC results are summarised in Table 19.
a Terpene combinations were mixed in a 1:1 (w/w) ratio unless otherwise indicated.
b Yeast-encapsulated formulations unless otherwise indicated.
c MIC calculated by terpene content.
d Non-encapsulated emulsion formulation.
For both the terpene emulsions and yeast-encapsulated terpenes, MICs were typically 5125 ppm, with the most active formulations inhibiting growth at ˜60 ppm. MIC values obtained for the terpene emulsions were similar to those obtained for their respective yeast-encapsulated formulations. When different values were obtained, they only differed by approximately one 2-fold dilution.
Many of the free terpene emulsions were fungicidal at the growth inhibitory MIC, with the majority showing fungicidal activity at a 2-fold higher concentration.
These results demonstrate that terpenes encapsulated in glucan particles are at least as effective at killing fungus as non-encapsulated forms. Additionally the encapsulated compositions used may have had reduced potency due to having been stored for 45 days at 4° C. and having a sub-optimal terpene content of ˜4% w/w.
The assay to determine fungicidal activity involves a centrifugation step, which attempts to separate the microbial cells from any residual terpene in the growth medium by producing a pellet of cells at the bottom of the well. This pellet is then resuspended in fresh media and incubated for a second time in the absence of terpene. However, the centrifugation step cannot discriminate between microbial cells and yeast particles, therefore when yeast-encapsulated terpenes are used, the cell pellet will also contain terpene-loaded yeast particles. As a result, both the yeast particles and the microbial cells are then resuspended in the fresh medium.
This methodology issue is not considered to affect the results obtained in the experiments described above for the following reasons.
In previous experiments, terpene emulsions have been used instead of terpene-loaded yeast particles and fungicidal activity has been clearly shown.
Encapsulated terpenes are released by diffusion, and an equilibrium between the concentration of encapsulated terpenes and the concentration of released terpenes in the surrounding medium is quickly reached. Thus, following centrifugation and resuspension in fresh medium, the concentration of released terpene in the growth medium is likely to be well below that required for growth inhibitory activity.
There was no growth when the contents of the fungicidal MIC well were plated onto solid agar growth medium. When plated onto solid growth medium, diffusion of any residual terpene throughout the large volume of the agar plate results in a local terpene concentration that is too low to cause growth inhibition. The lack of growth from the contents of the fungicidal MIC well must therefore be due to initial fungicidal activity. In contrast, when an MIC was obtained that was lower than the fungicidal MIC and the contents of the MIC well were plated onto solid agar growth medium, growth was observed, indicating a fungistatic effect.
The purpose of the following protocol was to encapsulate a terpene composition into hollow glucan particles for subsequent field trials.
The yeast cell wall particles were obtained from Biorigin (Sao Paolo, Brazil) under the trade name Nutricell MOS 55, and were manufactured by Agucareira Quatá S. A, Usina Quatá, Quatá—Sao Paolo—Brazil—Zip Code 19780 000. The particles are a spray dried cell wall extract of S. cerevisiae and are a free flowing powder of light beige to tan colour.
Protocol:
The following protocol was suitable for a 1 Kg of particles, but can simply be scaled up for larger production.
Results:
Encapsulated geranoil, eugenol and thymol in hollow glucan particles was obtained as a paste. The paste was easily converted to a dry powder by conventional spray drying techniques. The paste is the “liquid” composition referred to in the following protocols, and the “powder” is the spray dried form.
In grapes, downy mildew is caused by the fungus Plasmopara viticola, which infects vineyards worldwide and can cause devastating losses for grape-growers in terms of crop yield and wine quality. The fungus attacks the fruits and all green parts of the vine, causing the leaves to wither and the flowers and berries to rot. The disease manifests as irregular pale yellow or yellow—green spots on the upper surface of leaves, with dense, white—grey, cotton-like fungal growth covering the underside of the leaf lesions. Berries may also be covered with the downy growth and, depending on the time of infection, may turn brown and soft or may not soften at all. Downy mildew is spread through the dispersal of spores by the wind and rain, and requires wet conditions for infection. It is particularly problematic in environments with high humidity. Preventative measures are recommended for management of the disease, with early applications of fungicides followed by repeat applications at appropriate intervals. Resistance has arisen to some treatments, and although the development of resistance can be minimised by rotating the use of different fungicides, it remains a problem.
The purpose of this trial was to investigate the efficacy of the encapsulated terpene formulation of Example 16 (YGP-GET) supplied as a liquid or powder (spray dried) formulation, for the prevention of downy mildew in grapes.
Four adjacent blocks, each covering 0.1 ha, were identified on site 20 in the Kir-Yianni vineyard.
Kir-Yianni is a 35 ha vineyard at an elevation of 300 m. It is bordered by a mixed oak forest on the north and west, and overlooks orchards and vineyards to the south and east.
All four blocks had been treated with multiple products prior to application of the terpene formulation. On 26 Jun. 2004, two of the four blocks were sprayed with the terpene powder formulation at a dose of either 0.5 g/L or 2 g/L (see schematic illustration in
Four further adjacent blocks, each covering 0.1 ha, were identified on site 18 in the Kir-Yianni vineyard. All four blocks had been treated with multiple products prior to application of the terpene formulation. On 26 June 2004, two of the four blocks were sprayed with the terpene liquid formulation at a dose of either 1 g/L or 4 g/L (
For both sites, the terpene product was applied at a rate of 1200 L/ha.
The following growth stages of the grapes were recorded:
The study applications took place pre-veraison.
The 2004 growing season was exceptionally late and was wet throughout. Disease pressure from downy mildew was extremely high, botrytis levels were elevated, and powdery mildew pressure was moderate.
Both the powder and liquid YGP-GET formulations were stored at room temperature. No special storage conditions were used.
Powder formulation trial: Bordeaux mix, manufactured by Manica Spa, Italy, packed in Greece by Moscholios Chemicals SA; wettable sulphur.
Liquid formulation trial: Mikal® (fosetyl-al 50%, folpet 25%), manufactured by Bayer CropScience, distributed in Greece by Bayer Hellas SA.
The comparator products were applied as follows:
One application before bud-break at a dosage of 15 g/L followed by two more applications per year at a dosage of 6.5 g/L. A spraying rate of 1000 Uha was used for all three applications.
Powder formulation trial: Bordeaux mix (2 g/L) and wettable sulphur (2.2 g/L) were applied on 26 Jun. 2004.
Liquid formulation trial: Mikal (3.2 g/L) was applied on 28 Jun. 2004.
Vines were visually examined for symptoms of downy mildew. Onset of the disease was marked by an average of two oily spots per leaf. Treatments that prevented the appearance of further spots were considered to provide effective protection against downy mildew.
The conventional treatment of Bordeaux mixture provided good protection against downy mildew. Mild symptoms of downy mildew were observed in the control vines. The 0.5 g/L terpene product concentration did not provide protection, and the 2 g/L terpene product concentration provided only slightly better protection than the control. Note: the disease pressure at this site was very low because of the recent pesticide treatment.
Difficulties were encountered in dissolving the powder formulation as it was very fine, resulting in dispersion in the air. This may have adversely affected the efficacy of the product.
When administered at a dose of 4 g/L, the terpene product provided excellent protection against downy mildew on exposed canopy. No protection was provided by the 1 g/L dosage. Serious symptoms of downy mildew were observed in the control block.
The liquid formulation was easy to use and had a pleasant odour.
Downy mildew can cause devastating losses for grape-growers because of its effects on crop yield and wine quality. Management of the disease focuses on prevention because, once established, the infection can quickly spread. At the site sprayed with the powder formulation, YGP-GET did not exhibit efficacy at the lower dosage (0.5 g/L), and the dose of 2 g/L was less effective than the conventional treatment. At this site, the recent pesticide applications resulted in low disease pressure, which may have limited the apparent efficacy of the terpene treatment. However, it was considered that a dosage of less than 2 g/L of the terpene product was inadequate.
At the site sprayed with the liquid formulation, excellent protection of exposed canopy was provided by the higher dose level of 4 g/L. Excessive vegetative growth at this site resulted in more effective treatment of the outer, younger branches compared with the older growth in the inner canopy. Complete foliar coverage by the terpene product is useful, as the treatment is not systemic. It is estimated that an approximately 30% increase over the volume used for conventional systemic treatments would achieve good coverage using the terpene treatment.
Foliar application of YGP-GET liquid formulation was highly effective at controlling downy mildew at a concentration of 4 g/L. The lower concentrations of 0.5 g/L powder and 1 g/L liquid were not effective.
Powdery mildew of grapes is caused by the fungus Uncinula necator, and causes reductions in vine growth, fruit quality and winter hardiness of vines. In wine grapes, an infection level of only 3% of berries can affect wine quality. The disease is characterised by small white-grey patches of fungal growth that enlarge into a powdery, white coating on the leaves. The fungal growth can also occur on the berries, which may split. In contrast to downy mildew, which requires warm wet conditions, powdery mildew can be a problem in drier growing seasons, as it favours shaded areas with humid but not rainy weather conditions. Preventative measures are recommended for management of powdery mildew, with early applications of fungicides followed by repeat applications at appropriate intervals.
This study aimed to investigate the efficacy of application of the YGP-GET composition for the prevention of powdery mildew in grapes.
Three adjacent blocks, each covering 0.1 ha, were identified on site 18 in the Kir-Yianni vineyard. On 19 Jul. 2004, one of the three blocks was sprayed with the YGP-GET liquid formulation at a dose of 2 ml/L and one was left untreated. The remaining block was sprayed with the conventional treatment of Equesion (2.5 g/L), Alliete (0.9 g/L) and Punch (0.075 mL/L) (see
Three further adjacent blocks, each covering 0.1 ha, were identified on site 20 in the Kir-Yianni vineyard. On 20 Jul. 2004, one of the three blocks was sprayed with the YGP-GET liquid formulation at a dose of 2 mL/L and the two remaining blocks were left untreated (see
At both sites, the blocks had previously been treated with multiple products, including a prior application of terpene product.
All terpene treatments were applied at a rate of 1200 Uha to ensure complete coverage.
The following growth stages of the grapes were recorded
The study applications took place pre-veraison.
The 2004 growing season was exceptionally late and was wet throughout. Disease pressure from downy mildew was extremely high, botrytis levels were elevated, and powdery mildew pressure was moderate.
No comparator product was used at site 20. The comparator treatment used at site 18 is detailed below.
Punch® (flusilazole 40%), DuPont.
On 19 Jul. 2004, Punch was applied at a dose of 0.075 ml/L as a preventative treatment for powdery mildew according to the manufacturer's instructions.
No additional products were used at site 20. The additional products used at site 18 are detailed below.
Equesion system (famoxadone 22.5% plus cymoxanil 30%)
Alliete (fosetyl-al 80%)
On 19 Jul. 2004, Equesion (2.5 g/L) and Alliete (0.9 g/L) were applied as preventative treatments for downy mildew. The dose was determined according to the manufacturer's instructions.
The comparator and additional products represent conventional treatments in the integrated pest management schedule.
Vines were visually examined for symptoms of powdery mildew.
Approximately 20% of the peduncles and stems in the control block were black, indicating moderate infection from powdery mildew. In both the conventional treatment block and the terpene-treated block, all stems and bunches were green, indicating that adequate protection had been provided.
No evidence of powdery mildew infection was observed in any of the blocks.
At the end of the growing season, the blocks at sites 18 and 20 generally showed less stress due to disease than the rest of the vineyard.
Powdery mildew infections cause considerable losses to growers through reductions in vine growth, fruit quality and winter hardiness of vines. Furthermore, wine quality can be affected by an infection level of as little as 3% of berries. Management of the disease focuses on prevention because, once established, the infection can quickly spread. In this study, the application of terpene product YGP-GET at site 18 effectively prevented powdery mildew infection, and the level of control exhibited by the terpene product was comparable to that provided by the conventional treatment. The results from site 20 are inconclusive, however, due to the lack of powdery mildew infection. This lack of infection is likely to be due to the extensive application of pesticides prior to the study, which resulted in low disease pressure.
The lower level of stress due to disease at sites 18 and 20 suggests that the earlier terpene treatment applied at these sites may have been beneficial in control of infection in the long term.
YGP-GET effectively prevented powdery mildew infection, with a comparable level of control to that provided by the conventional treatment.
The study aimed to further investigate the efficacy of YGP-GET for the treatment of powdery mildew in Grimson Seedless table grapes.
A 0.1 ha plot on the Tsigaras vineyard (approximately 80 km south of the Kir-Yianni vineyard) was inadvertently left untreated during an application of Cisteine on 1 Jul. 2004. The vines in this plot subsequently showed severe symptoms of powdery mildew on the leaves, stems and grapes. On 12 Jul. 2004, the untreated plot was sprayed with 3 ml/L liquid YGP-GET formulation at a rate of 1200 l/ha, and the rest of the vineyard was sprayed with the comparator product Rogana. The vines were assessed for symptoms of powdery mildew after 24 hours.
Vines were trained in a high lyre trellis system.
Rogana (fenbuconazol 5%, binocap 16%), manufactured by BASF (BASF Agro Hellas S. A., Athens, Greece)
On 12 Jul. 2004, Rogana was applied to the Tsigaras vineyard as a treatment for powdery mildew. The dose was determined according to the manufacturer's instructions.
Vines were visually examined for symptoms of powdery mildew.
Severe symptoms of powdery mildew were evident prior to application of YGP-GET. Only 24 hours after YGP-GET application, the white bloom of the powdery mildew turned black, indicating effective antifungal activity. As the disease was effectively halted at this time, no further treatments were applied. YGP-GET showed comparable efficacy to the conventional treatment.
In this study, an established powdery mildew infection was treated quickly and effectively using YGP-GET. Only 24 hours after application, the previously severe powdery mildew infection was halted by application of the terpene product, with comparable efficacy to the conventional treatment.
The preliminary data obtained from this study suggest that YGP-GET may be efficacious in treating established fungal infections in addition to showing preventative ability.
In the current trial, the use of YGP-GET was investigated as part of a Tasmanian vineyard's (Frogmore Creek Vineyard, Hathaway Trading Pty Ltd, Box 187, Richmond TAS 7025, Australia) experimental programme to control powdery mildew using organic products. The aim of this study was to investigate the short-term efficacy of the application of YGP-GET in the organic control of powdery mildew in Chardonnay grapevines.
In this trial grapevines (Chardonnay variety) were either treated with the terpene product YGP-GET or left untreated (control) on 7 Feb. 2005. Although suppressed by previous organic treatments, the pre-trial severity of powdery mildew was at a level considered unacceptable commercially and was equivalent in the 6 active-treatment plots and 6 control plots. The crop stage was approximately E-L 33-34 (pre-veraison).
YGP-GET (4 mL/L) (liquid formulation) was sprayed onto 6 Chardonnay plots, which had been treated previously with milk. Six Chardonnay plots served as untreated controls, but they had been treated previously with oil/whey. The number of vines per plot was typically 7.
Details of the composition of the YGP-GET used in this protocol are given in Table 20.
The severity of powdery mildew was assessed 3 days before terpene treatment and again 3 days post-treatment. In each plot, 20 grape bunches were selected at random (10 bunches per panel side), and disease severity was estimated as the percentage area of the bunches covered with active mildew colonies. No further assessment was possible because the grower subsequently sprayed the entire trial area with sulphur and a vegetable oil-based spraying adjuvant (Synertrol Horti Oil).
Test product: YGP-GET (4 mL/L) to be applied to 6 Chardonnay plots (total of approximately 42 vines), which had been treated previously with milk.
Control: No treatment was applied to 6 Chardonnay plots (total of approximately 42 vines) to be used as controls, but they had been treated previously with oil/whey.
Vitis vinifera (Chardonnay) vines in Block B2: vertical shoot positioning with arched canes.
Spacing: Distance of 2.5 m between rows and 1.25 m between vines (within row), with 3,200 vines per hectare. Row orientation was north to south.
The point-quadrat method was used to characterise the pre-trial canopy density of the Chardonnay vines (Table 21). Measurements were taken on 13 Jan. 2005 by selecting representative sections of the canopy within the Chardonnay plots that previously had been either treated with sulphur or left untreated. Ten measurements were taken in each of the 6 plots of each prior treatment (i.e. a total of 60 measurements for the sulphur-treated plots and 60 measurements for the untreated control plots). In addition, the length and number of nodes on 3 upright shoots (per plot) were measured.
Previous treatment of these plots with experimental materials suppressed powdery mildew in comparison to the untreated control. However, the level of powdery mildew was considered commercially unacceptable, although equivalent in both the milk- and oil/whey-treated plots.
YGP-GET treatment (4 mL/L) was applied on 7 Feb. 2005 with a hand gun connected to a hose reel and pump mounted on the flat tray of a utility vehicle. The spray was propelled with a pump pressure of 1500-1600 kPa (200-230 psi), delivering approximately 63 mL/second. The standard spray volume for conventional treatments (approximately 900 L/ha) was used.
The severity of powdery mildew, estimated as the area (%) of the grape bunches covered with active mildew colonies, was assessed for 20 bunches selected at random within each plot (10 bunches per panel side). Disease severity was assessed on 4 Feb. 2005, 3 days before application of the YGP-GET treatment, and again on 10 Feb. 2005, 3 days after terpene application.
Data were transformed using arcsin transformation to obtain mean separations.
Prior to treatment, the mean severity of powdery mildew on Chardonnay grape bunches in the 6 plots to be treated with terpene (20.4%) was similar to that in the 6 control plots (23.2%; Table 22). Statistical analysis based on arcsin transformation of these data found that there was no significant difference in disease severity before treatment (Table 23).
Three days after treatment, however, the mean severity of powdery mildew was 23.8% on the YGP-GET-treated bunches versus 37.8% on the controls (Table 22). Arcsin transformation of these data showed a statistically significant difference in favour of the terpene-treated grape bunches, which had a smaller area covered with active mildew colonies (p=0.058; Table 23).
Infection of grapevines with powdery mildew can cause considerable losses to growers through detrimental effects on vine growth and hardiness, as well as on the quality of the fruit and wine. In organically managed vineyards, growers are searching for alternatives to treatments such as elemental sulphur.
This study investigated the efficacy of encapsulated terpene formulations (4 mL/L) as a liquid formulation in controlling powdery mildew in an organic vineyard in Tasmania, Australia. While other experimental treatments had been used as little as 3 weeks before terpene application, the level of powdery mildew infection was still considered commercially unacceptable. Three days after treatment of Chardonnay vines with YGP-GET, the severity of powdery mildew on treated grapes was significantly less than that on untreated controls. While the severity of infection in untreated controls worsened during the 6 days between pre- and post-treatment assessments, it remained steady in treated vines. Therefore, YGP-GET appeared to have slowed the rate of disease increase on grape bunches that had well-established colonies of sporulating powdery mildew before treatment. Presumably, colony expansion was inhibited, although existing colonies continued to sporulate to some degree. More long-term assessment of efficacy was not possible because the grower subsequently sprayed the entire trial area with sulphur.
These encouraging results demonstrate the efficacy of YGP-GET in controlling powdery mildew in grapevines.
Botrytis bunch rot of grapes is caused by Botrytis cinerea, a common fungus that can cause serious losses in fruit yield. Berries are the predominant site of infection, although the disease can also affect blossom and leaves. Initially, infected berries appear soft and watery, and may become covered with grey fungal growth in conditions of high humidity and moisture. Over time, infected berries shrivel and drop. Botrytis favours humid conditions with poor air circulation, and split or damaged berries are particularly susceptible to the spread of infection. Management strategies for botrytis include promotion of good air circulation, prevention of wounding and application of fungicides at appropriate times during the growing season.
The aim of this study was to investigate the efficacy of YGP-GET in the treatment of botrytis infection in grapes.
The emergence of botrytis in the Kir-Yianni vineyard in mid October 2004 (3 weeks after an application of Teldor® could not be treated with conventional agrochemicals because the associated re-entry time restrictions would prevent the planned harvest. Two adjacent 0.1 ha plots were therefore identified on site 7 of the vineyard, and, on 12 Oct. 2004, one of these plots was treated with 4 mL/L YGP-GET liquid formulation and the other was left untreated (see
Site 7 had been treated with multiple products prior to the application of the terpene formulation but still showed botrytis infection.
Vines were given a single application of 4 ml/L YGP-GET liquid formulation at a rate of 1200 l/ha.
The following growth stages of the grapes were recorded:
The study applications took place 3 days before harvest.
The 2004 growing season was exceptionally late and was wet throughout. Disease pressure from downy mildew was extremely high, powdery mildew pressure was moderate and botrytis levels were elevated.
YGP-GET was applied at this time to assess its potential efficacy against a botrytis infection that could not otherwise have been treated because of pesticide time restrictions prior to harvest.
Visual assessment of the site prior to terpene product application revealed evidence of botrytis infection. After harvest, the berries were displayed on a conveyor belt and infected berries were manually separated from uninfected berries prior to crushing. The proportion of infected berries was calculated as a percentage of the total yield (by weight) for each plot.
Visual assessment of the site prior to YGP-GET application revealed evidence of botrytis infection. Following harvest (3 days after YGP-GET application), the proportions of infected berries were 13% and 23% in the treated and untreated plots, respectively. The tested areas were not sufficient to assess statistical significance; however, YGP-GET treatment clearly slowed the progression of the disease.
Fermentation was not affected by the mixing of uninfected berries from the untreated and terpene-treated plots.
Conventional treatments for botrytis must be halted 3 weeks before harvest, leaving time for considerable damage to crop yield and quality to occur. The development of a treatment that could be used until harvest, or that could be continued closer to harvest than the existing products, could result in significant improvements in crop yield and wine quality, and would be of considerable benefit to growers. In this study, treatment with the terpene product YGP-GET visibly slowed progression of an established botrytis infection only 3 days prior to harvest, resulting in a lower proportion of infected berries in the terpene-treated plot than in the untreated plot. Furthermore, despite the use of YGP-GET close to harvest, fermentation was unaffected by the combination of treated and untreated grapes.
These results suggest that YGP-GET is efficacious in reducing the impact of established botrytis infections and can be used near to harvest without detrimental effects on subsequent fermentation.
A trial of YGP-GET was carried out on 25/08/04 applying the composition at a rate of 1000 g per 250 liters.
A vineyard of Cabernet Sauvignon which was 100% infected and suffering substantial leaf loss due to Downy Mildew was sprayed. Any remaining leaves were infected with spots of Downy Mildew as evidenced by the yellow spot on top of the leaf and the fuzzy growth on the leaf bottom; the classical indication of Downy Mildew. Many of the leaves were almost entirely yellow indicating substantial infection. This leaf loss and the infection in general delays the maturity of the grapes and in many cases the grapes never fully ripen for winemaking purposes.
Observation of totally unripened (i.e. hard dark green berries ˜1 cm diameter and oval in shape) bunches occasionally in the vines indicated that the vines were likely infected before veraison, and likely at bloom or before. No early copper (Bordeaux or basic Copper sulfate) application has been used. This vineyard was heavily infected in the previous harvest to the point that no crop was produced from the Cabernet Sauvignon. Leaf loss last year was 100% despite Potassium Bi-carbonate treatment in an attempt to contact kill the Downy Mildew, followed by Stilbourin application for longer term systemic protection.
On 19 Sep. 2004 the grapes treated in this trial were picked and crushed and the following observations were made on the must (Table 24):
These results indicate the grapes from the treated vines are riper than those of the untreated vines. Observation of the grapes themselves indicated that the untreated grapes were, on average, lighter in color, some with a transparent pinkish/purple/green tint, indicative of grapes just past veraison, whereas the treated grapes were dark purple on average and opaque, typical of fully or nearly fully ripened grapes.
Tasting of these grapes revealed the treated grapes to have a fuller fruitier taste typical of ripe Cabernet Sauvignon, whereas the untreated grapes did not have the full fruity taste. The untreated grapes had a green apple sour taste indicating probable a high malic/tartaric ratio unsuitable for good winemaking.
These grapes were crushed and destemmed in preparation for producing a wine from these grapes to demonstrate the difference in these grapes and to demonstrate the suitability of the treated grapes for winemaking. The grape grower was concerned that this treatment would affect the flavor of the wine, although at my suggestion he tasted treated grapes the day after application of YGP-GET and found no lingering taste or aroma.
The difference in the treated and untreated grapes is further demonstrated in the color of the must. The juice of the untreated grapes was light greenish/uncolored (somewhat like a white wine must) whereas the must from the treated grapes was a pinkish color typical of ripe Cabernet Sauvignon grapes immediately after crushing.
These results indicate that YGP-GET is efficacious in late summer vineyard treatment by killing and stopping Downy Mildew re-infection, in at least the short term.
Further research into the long term efficacy of the YGP-GET in controlling downy mildew would be useful, but the results presented show that YGP-GET is a useful treatment.
Late onset Downy Mildew can completely ruin a crop and there are currently no effective treatments which can be applied shortly before harvest and that retain their ability to provide protection. The great strength of YGP-GET is the ability to provide a quick kill and maintain this efficacy over a longer time than other contact fungicides.
There are a number of anti-fungals in this market which have an established track record against Downy Mildew, but all need some time after application before the crop can be harvested. Some treatments (like sulfur containing products) cannot be used if the temperature rises above 85° F. Phytotoxicity of copper containing fungicides is also significant depending on the variety of grape. Contact fungicides do not have a long term effect so a second application of a longer active fungicide is often needed, but may be restricted by relevant regulation (e.g. PHI or REI).
Many conventional treatments for Downy Mildew have a restricted reentry (REI and or PHI) which means the grower cannot apply the treatment in fear that he will apply something like Mancozeb, which has a PHI of 66 days; the grower would then be unable to harvest his grapes at peak maturity.
Downy Mildew is implicated as the primary cause of the many poor wines being produced east of the Mississippi. YGP-GET could allow affected grapes to ripen properly and be picked at peak maturity in this rapidly growing industry.
Advantageously YGP-GET should be eligible for approval by the various “organic” committees (many self-appointed) that this product is suitable for use on grapes grown under “organic” guidelines. This opens another niche in a rapidly growing market segment in the US and worldwide.
Further tests were conducted to assess the 31 non-encapsulated terpene preparations set out in Example 15 and preparations 16 and 22 encapsulated in glucan particles.
To conduct these assays, 20,000 spores were placed in ⅓ strength potato dextrose broth (PDB) and sufficient quantities of selected terpene formulations were added to give concentrations ranging from 10 to 1000 ppm. These test materials were placed in separate sterile capped Eppendorf tubes with Botrytis cinerea (B.c.) spores, incubated for 24 hr, then the spores were recovered by centrifugation, and the terpene solutions were discarded. The spores/biomass were rinsed with sterile water, centrifuged again and then taken back up in 300 μl of ⅓ strength PDB and transferred to 96 well plates. The optical density of the surviving spores growing into mycelia was measured over time. Fungicidal activity is defined as total killing of 20,000 spores after 24 hours terpene exposure, as evidence by the absence of mycelial growth.
The results suggest that certain formulations were not fungicidal at a statistically significant level under the present test conditions (results not shown). These were:
1, 2, 4, 5, 6, 8, 9, 11, 12, 14, 15, 17, 18, 19, 20, 21, 23, 24, 25, 27, 28, 29, 30. Refer to Example 15 (Table 17) for details of the compositions.
The minimum inhibitory concentration for the most effective compounds is set out in Table 26.
Samples of formulations 16 (geraniol, eugenol and thymol) and 22 (eugenol, thymol and citral) encapsulated in hollow glucan particles were prepared in accordance with techniques previously described. The fungicidal properties were then assessed for encapsulated and non-encapsulated formulations using the protocol previously described for the non-encapsulated formulations.
The results were quite different with encapsulated terpene formulations as compared with the terpenes suspended in water, as shown in
The minimum effective concentration is shown below in Table 26.
Thus, the results with materials 16 and 22 are quite different when in aqueous suspension and when tested encapsulated in glucan particles. (Note: as mentioned later, there was some variability in the results with terpenes suspended in water, the experiment noted above is an example of this). The MIC values are composites from several trials. Importantly, the results with encapsulated terpene formulations do not suffer from the problems of variability associated with aqueous terpene suspensions. There have been five separate tests of terpenes suspended in water and three with the YPs.
Encapsulated terpene formulations are readily miscible with water and provide a slow release terpene formulation into the aqueous medium. This results in a longer exposure time of the spores to the terpenes.
Problems monitoring the non-encapsulated terpene formulations in suspension in the test media were encountered which may have affected the results in this regard.
Two-spotted spider mites, which feed on a variety of plants including tomatoes were used in this study. The purpose of the present study was to conduct preliminary in planta experiments in a commercial greenhouse to determine the efficacy of two YP-terpene mixtures against two-spotted spider mites (TSSM, Tetranychus urticae) and foliar diseases (Botrytis) of tomato. Naturally occurring populations of two-spotted spider mites were used.
YP-4 (citral) and YP-22 (thymol, eugenol and citral) (16% terpene formulations) were used.
On 28 March, a double row of 68 tomato plants (Lycopersicon esculentum var. Trust) were transplanted at the 6 true-leaf stage onto black plastic mulch covering native soil; the trial was conducted using ‘Trust’ as the tomato variety—this variety is more susceptible to TSSM than other varieties such as ‘Boa’. Plant spacing was 12-inch in-row, offset. The cooperating grower pruned and trellised the plants vertically to a single growing point. Blocks of two plants per treatment were flagged and randomized in the double row with 4 replicates. Two untreated plants separated all blocks. Terpene formulations YP-4 and YP-22 were applied at a rate of 4 ml/L to leaf wetness on the following days: May 11 (Note: all dates in this example are in 2005), June 2 and 15, and July 1 and 18. Control treatments were treated with water until leaf wetness on the same dates.
Yield data (fruit numbers and weights), disease incidence and percent foliage damage by TSSM were recorded every 1-2 weeks beginning on 27 May until the trial conclusion on 29 July.
Numbers of mites per square centimetre were also measured on July 25. Leaf samples were taken from each plant ca. 1.5 meters from the ground (lower) and ca. 2.5 meters from the ground (upper). Leaves were placed in moist paper bags to avoid drying. The underside of each leaf was examined microscopically and counts were made. Total numbers of living mites (actively moving and quiescent) were determined. Mites in a quiescent phase strike a characteristic pose that is easily distinguishable from dead mites. No distinction was made between females and males or between adults and juveniles.
This trial was in some respects was complicated by, two factors. First, in most tomato greenhouse production older senescing leaves are removed as plants grow. This reduces mite populations since a substantial amount of the mites are removed along with these older leaves. These older leaves were intentionally left on the plant as a measure to increase the severity of the test.
Second, one plant in the trial, which was one of the plants treated with YP-22 in the fourth replicate, became infected with a virus that caused severe malformation of the plant. It also had the surprising result of being extremely attractive to mites and conducive to mite replication. This led to a tremendous population boom of mites that surrounded this plant. The plant was removed from the trial about June 25 but the very high level of mites that derived from this virus infected plant spread to adjacent plots over time and skewed the results.
This very high mite population could not have been controlled by any product. Mite populations, even if knocked back, rebound very quickly. For this reason, the data reported here shows results over time on a rep-by-rep basis.
Early in the trials, there appeared to be a low level of fungal diseases that occurred, probably Botrytis cinerea. This disease was rated until the damage by mites became so overwhelming that no further ratings were possible. The results are shown below in
Given the virus plant issues, this discussion will focus on results by individual replicates, with a summary to follow. The results of the mite damage assessment are shown in
Mites were enumerated microscopically from the undersides of leaves taken from each plant ca. 1.5 meters (lower) from the ground and ca. 2.5 meters (upper) from the ground. The results are shown in Table 27.
These data indicate good mite control. There is great variation in the numbers of mites/leaf on the control plants, as would be expected for this pest. However, the maximum numbers with both treatments, especially the YP-22, treatment is substantially lower than the control.
Mites were controlled in this study especially by YP-22. However, where very high mite pressures occurred, YP-22 was insufficient in providing adequate control. It is likely that no acaricide would provide good control due to the very high mite populations in part of this study. It also is worthy of note that we applied the materials every two weeks and since mites have good rebound abilities, the YP test materials had residual activity; this was almost certainly provided as a result of encapsulation.
The results are extremely encouraging since the formulations to be used, the rate of application and the frequency of application were not optimised. It would no doubt be possible to improve efficacy by optimizing terpene mixtures, rates of application and frequency of application. Such optimisation would be a matter of trial and error to achieve.
Additionally, there are at least two types of adjuvants that can be used to increase efficacy. Silwet is an organosilicone surfactant that is added to pesticides as a tank mix. Good data indicate that this material increases activity of acaricides (reference available upon request). It can be used with all plants and is ready available. We have data also indicating that similar materials enhance efficacy of fungal disease control with biocontrol agents. Alternatively, Stirrup is a pheromone product that attracts mites to deposits of pesticides and enhances uptake of the material.
The present study was conducted to determine the most effective terpene mixtures and the levels at which they are active in relation to powdery mildew.
31 terpenes or terpene mixtures encapsulated in yeast cell walls (YP-terpenes) were assessed; the codes used in relation to the particular compositions are set out in Table 17 of Example 15.
Protocol development was driven by the basic biology of the organism. The fungus is an obligate pathogen and so cannot be cultured other than on the leaves of grapes. We therefore inoculated plants (‘Riesling’ seedlings) and harvested conidia by washing infected leaves with copious sporulation.
A variation on the method used by Reuveni (2001; Can. J. Plant Pathol. 23:52-59) was employed. One to two leaves infected with Uncinula necator were placed in a sterile 50 mL plastic tube. Tween-20 (7.5 mL, 0.0005%) was added to the tube and the leaves were vigorously vortexed for 30 seconds. Conidia were counted using a Petroff-Hauser counting chamber and adjusted to 1-2×105 conidia/mL.
YP-terpenes were diluted to working solutions of 4000 ppm. Reactions took place in 600 μL siliconized eppendorf tubes and the final reaction volume was 60 μL. YP terpenes were diluted in the tube to give final concentrations of 100, 250, 500, 750 or 1000 ppm terpene. 40 μL of the conidia suspension was added to each tube and each tube was briefly vortexed. Water and test material 32 (particles only, no terpene) were included as controls. The test materials and conidia were incubated for 1-1.5 hr to provide sufficient contact time for inhibition of the spores without adversely affecting spore germination in the absence of the terpenes. This brief immersion was essential in order to permit adequate contact time with the terpenes since the terpene mixtures on the agar surface rapidly volatilized or were absorbed into the water.
Glass microscope slides were coated with 750 μL of 1.5% water agar. The glass slides were placed in germination boxes each containing a moist blotter. When attempts were made to directly place conidia and terpene mixtures directly on the agar, there were few effects of the terpenes, probably because of inadequate contact time. Lids were placed on each box and the materials were allowed to incubate for 48 h at room temperature on the benchtop. In some experiments, slides with different levels of terpenes were contained within the same box. This technique was found to permit erroneous results since the volatiles from slides with high levels of terpenes inhibited conidia on slides with lower levels of the materials. Therefore final data was taken from slides in boxes containing only one or two levels of the same test material.
After 48 h the slides were examined using a light microscope. Various settings of phase-contrast were used to obtain a sharp outline of each conidium. The YPs are many times smaller than the conidia and the two were easy to differentiate. At least 100 spores were assessed for germination per spot; if the number of observable spores was less than 100, every spore found was counted. Germ tube lengths of at least 10 germinated conidia were measured as well although this data was later not found to be very useful.
We also found that a small percentage of conidia are already germinated when they are washed off of the leaves. This is expected since powdery mildew conidia do not need free water to germinate and therefore can germinate at any time. We therefore set a maximum of 4% germination as our cutoff for fungicidal activity since this was the level frequently observed in the 0 time water controls. The age of the powdery mildew infection also resulted in some variability. Infections older than 3 weeks provided a lower level of overall germination in the controls (36% in water controls on agar slides) while younger infections gave much higher germination levels (around 70%). We observed all test materials several times, with data being collected at levels where inhibition occurred. 3 replicates per test were used.
Concentrations of materials ranged from 100 to 1000 ppm of terpene. Every test material was fungicidal at least at the highest concentration tested. Four classes of fungicidal efficacy were established for the 31 formulations. The terpene formulations and their grouping, based on minimal inhibitory dose (fungicidal), are provided below.
The fungicidal dose was calculated based upon germination of powdery mildew conidia 48 hr after reaction as determined by microscopic observation. Since powdery mildew conidia germinate within 24 hr in the control, if germination did not occur with 48 hr, we considered that the spores were killed. In a few cases, we continued to observe for 72 hr or more, but no additional information was obtained.
The present study was conducted to determine the most effective terpene mixtures and the levels at which they are active in relation to downy mildew.
Plasmopara viticola, the causal agent of downy mildew of grape, in vitro, was used in all studies. This was a wild type pathogenic strain obtained from colleagues at Cornell. The organism was maintained on leaves of seedlings obtained from ‘Reisling’ seeds.
Protocol development was driven by the basic biology of the organism. The fungus is an obligate pathogen and so cannot be cultured other than on the leaves of grapes. We therefore inoculated plants (‘Riesling’ seedlings) and harvested sporangia by gently washing infected leaves with water. We originally attempted to conduct assays by observing sporangia on glass slides with cover slips. However, we wanted to look at the slides over time and this method simply did not allow for this. The volumes used were too small for adequate assessment, the sporangia often would disintegrate from the pressure of the cover slip and the zoospores would encyst very quickly after release. A variation on the method used by Reuveni (2001; Can. J. Plant Pathol. 23:52-59) using depression slides was used. These slides do not require cover slips, the zoospores remain motile for many hours and the volumes used allowed for multiple assessments over time.
For all experiments, sporangia from 1-3 leaves infected with Plasmopara viticola were gently washed with sterile water into a beaker and counted using a Petroff-Hauser counting chamber. The concentration of sporangia was at least 1×105/ml.
YP-terpenes were diluted to working solutions of 4000 ppm. Reactions took place in 600 μL siliconized eppendorf tubes and the final reaction volume was 100 μL. YP-terpenes were diluted in the tube to give final concentrations of 10, 50, 100, 250 and 500 ppm terpene. Seventy-five μL of the sporangia suspension was added to each tube and gently mixed by pipetting the suspension up and down. Water and test material 32 (YP only, no terpene) were included as controls.
A preliminary assessment was done for all 31 test materials at 10, 50 and 100 ppm terpene to estimate the correct range of efficacy (i.e., no motile zoospores observed during the subsequent 8 hours). Once sporangia were observed to germinate and zoospores were observed in the controls (0.5-1 hour later), 15 μL were transferred to a glass depression slide from the tube one at a time and immediately observed using a light microscope. If motile zoospores were seen this concentration was not observed further. The slide was wiped clean. Every 2-3 hours, the process was repeated with new test material from the tube. At the end of 8 hours, the percent germination of the first 100 sporangia was determined. Samples were left at room temperature and observed again the next day. The criteria for cidal activity were (a) no greater sporangial germination than in 0 time controls (no more than 10%) and (b) no motile zoospores. The percentages of sporangial germination in the effective doses ranged from 1.8% to 6.7% compared to the controls of water (87%) and YP-32 (76%).
In this assay, the sporangia were in constant contact with the test materials in a sealed container.
The assay system described above may not provide accurate data on cidal (i.e. lethal) concentrations since the absence of sporangial germination and motile zoospores are in the presence of the materials in closed tubes and the test materials are continually immersed in the test solutions. We cannot remove the cells from materials in solution because centrifugation is lethal to the sporangia and zoospores. Therefore, after 1 hr incubation in enclosed Eppendorf tubes, the test mixtures (40 μl) were transferred to depression slides. In this thin layer, the terpenes are expected to volatilize into the air and therefore cidal concentrations more accurately determined.
The slides were stored in germination boxes each containing a moist blotter. Every 2 hours the slides were inspected for motile zoospores. The concentration at which no motile zoospores were observed after 24 hours was considered the MIC in this assay.
aConcentrations of test materials differed between assays but overall ranged from 10 to 500 ppm of terpene. Every test material was effective at least at the highest concentration tested in both assays. Three classes of Minimum Effective Concentrations (MICs) were established for the 31 terpenes for each test. The MIC for each test material is the concentration at which motile zoospores are absent.
The groups listed using the test numbers are as follows:
Thirty-one YP-terpene test materials were assessed for their abilities to inhibit the release of motile zoospores from sporangia of Plasmopara viticola. Two assays were conducted. In the first test we examined both sporangial germination and zoospore motility from materials incubated in closed tubes; in the second test we assessed only zoospore motility in depression slides after incubation in the closed tubes for only one hour.
The absence of motile zoospores is the clearest way to determine efficacy of the test materials and therefore was used as the definitive criterion. Zoospore motility is critical to infection by this pathogen. Inhibition of sporangial germination is the first step toward controlling downy mildew disease: if the sporangia remain intact, then the zoospores will not be released. Our data on sporangial germination supports the above MICs even though germination was never 0%. Some sporangia were already germinated when they were harvested from the leaves. The percent germination at 0 h (no zoospores observed) ranged from 6% to 16%.
In the first assay, the terpenes controlled the release of zoospores under ideal test conditions. Unmistakably, the test materials have a cidal effect on the downy mildew pathogen. However, Assay #2 provides a better test of lethality in situations, which also will occur on plant leaves, where the terpenes dissipate by volatility. Taken together, the two assays provide a complete assessment of the in vitro abilities of the YP-terpene materials to control the grape downy mildew pathogen.
15 terpenes or terpene mixtures encapsulated in yeast cell walls were assessed. The formulations tested did not contain L-carvone.
Botrytis cinerea was used in all studies. The strain identification is B36 and was obtained from Cornell University. The organism was maintained on V8 agar at 25° C.
The protocol for this study combines aspects of a resazurin (Alamar Blue) assay with another protocol previously used with B. cinerea. The presence of the resazurin allows us to measure cidal levels of the terpenes in the presence of the yeast particles.
Spores of Botrytis cinerea were harvested in water and adjusted to a concentration of 1×105 spores/mL. YP terpenes were diluted to final concentrations of 100, 250 or 500 ppm in sterile 1.5 mL eppendorf tubes. 50 μL of the spore suspension and 375 μL of ⅓ strength PDB were added to the tubes. The suspensions were vortexed briefly and incubated at room temperature for 24 h. The inside of each tube was then scraped using a sterile toothpick to release hyphae from the walls.
After 24 hr, two separate samples of 50 μl of the test suspensions were removed and placed in microtiter plate wells together with 30 μl of ⅓ strength PDB and 20 μL of 250 ppm resazurin. These mixtures were incubated overnight for 16-20 hours. Visual observations were then made. Those concentrations of YP and spore suspensions where the test mixtures remained purple were considered to be fungistatic. Resazurin suspensions are purple, but if reduced by biological activity the solutions become pink and then clear.
After the two samples of the test suspensions were removed, the tubes were centrifuged at 3000 rpm for 10 min and the supernatant was discarded. The precipitate, which contained YPs, Botrytis spores and any germinated hyphae, was washed with 400 μL of water. The tubes were centrifuged again and the pellet was resuspended in 400 μl of sterile ⅓ PDB. To each tube, 150 μL of 250 ppm resazurin were added. The tubes were vortexed and incubated at room temperature overnight for 16-20 hours. Visual assessments were made and those concentrations of YP and spore suspensions where the test mixtures remained purple were considered to be fungicidal.
After 72 hours, visual assessments of the tubes were made again and purple samples were considered to be fungicidal.
Each well or tube was assigned a colour rating. No change in colour was rated 4; clear wells were rated 0. A rating of 3 or higher was considered static (little or no colour change) and only a rating of 4 (no change at all) was considered cidal.
Three replicates of each test material at each concentration were used for each experiment and each experiment was done twice.
Fungistatic Tests—Every test material was fungistatic at least at the highest concentration tested. The criterion for efficacy was at least 75% growth inhibition relative to the control. Ranges of efficacy were established for the 15 terpenes and are provided below.
Fungicidal Tests—Visual assessment of colour change for fungicidal tests was measured twice: once after 16-20 h and once again after 72 h. After 20 h, all test materials were fungistatic at least at the highest concentration tested. However, after 72 h only a few of the samples were still considered fungicidal. The ranges of efficacy for each terpene at each time point are provided below.
Each range of efficacy was assigned a rating (Group A=1, B=2 and C=3). The following tables (Tables 28 to 30) show the ratings for each test and the overall ratings for each YP terpene. The lower the number, the better the efficacy.
The 8 most effective test materials have thymol (T) either alone or as a mixture component.
In previous in vitro studies, YP terpene test materials that contained L-carvone provided minimal effectiveness in controlling important plant pathogens. The 16 test materials that contained this component were therefore excluded.
Resazurin was included as an indicator dye. As Botrytis degrades resazurin a colour change from purple to pink to clear occurs. For the fungistatic assays, samples were transferred to 96-well microtiter plates and reacted with resazurin for 16-20 h before visual assessment of colour change. After centrifugation and washing, the remaining material in the tubes was reacted with resazurin to provide fungicidal assessments.
Test material YP-7 was the most effective sample in each test. YP-7 is the most effective material at controlling powdery mildew, in vitro, as well.
All YP test materials were fungistatic against Botrytis cinerea at least at 500 ppm. After 16-20 h, all materials were considered to be fungicidal at least at 500 ppm. However, after 72 h, only 10 test materials were still considered to be fungicidal.
The most effective ones were fungicidal between 250 and 500 ppm.
All three of the bacteria tested are Proteobacteria and are Gram-negative. They have an outer membrane mainly composed of lipopolysaccharides. Erwinia amylovora is in the family Enterobacteriaceae. Other bacteria in this family include Salmonella spp., Escherichia coli, and Serratia marcescens. Pseudomonas syringae is in the family Pseudomonadaceae. Other important members of this family include Pseudomonas aeruginosa (an opportunistic pathogen). Closely related to Xanthomonas campestris pv. phaseoli are several important pathovars including those that infect rice and carrot. Pseudomonas and Xanthomonas are very closely related.
During the 20th century, introductions of infested plant material served to establish E. amylovora in Europe, the Middle East, and New Zealand. E. amylovora causes fire blight in apple and in pear. In 1995, fire blight was first observed in the Po River Valley of northern Italy, which is the largest pear production area in the world. Since 1995, the Italian government has destroyed 500,000 pear trees in an attempt to eradicate E. amylovora (http://www.apsnetorg/education/LessonsPlantPath/FireBlight/HISTORY, HTM).
Common bean and halo blights are one of the most economically important and widespread diseases of dry and snap beans. The US, Canada and Colombia are some of the largest growers of these beans. Most management strategies involve planting only certified pathogen-free seed, rotating crops and making weekly chemical sprays (http://www.ipgenetics.com/commonbean.asp).
Erwinia amylovora (strain Ea273; fire blight of apple), Pseudomonas syringae pv. phaseolicola (strain Pph MF; halo blight of bean) and Xanthomonas campestris pv. phaseoli (strain Xph XPW; common blight of bean) were used in this study. These strains were obtained from Cornell University.
Cultures—All three bacteria were cultured on LB (Luria-Bertani) plates (Sambrook et al., 1989) at 28 C. Starter cultures (50 mL LB broth) were inoculated from plates and grown overnight (170 rpm, 28 C). One mL of starter culture was transferred to a new 50 mL LB broth flask and grown under the same conditions until the stationary phase was reached. Cultures were read at 620 nm for optical density (OD) and then diluted with LB broth to give 105-106 cells/mL. This diluted material was used to inoculate the wells in the microtiter plate assays.
The plate assays were conducted using LB broth as the growth medium. YP-Terpene test materials were diluted in the plate to give a range of 7.8 to 1000 ppm (Al terpene). Diluted bacteria were added to each well to give a final well volume of 200 uL. Control wells did not contain any YP-terpenes. Plates were read at 620 nm for initial measurements (initial OD) and incubated at 28° C. for two days.
After two days, the plates were read again at 620 nm (final OD). Final OD minus initial OD (delta OD) gives the change in growth over time. The criterion for efficacy was at least 75% inhibition of growth relative to the control. Therefore, the delta OD in test wells had to be less than 25% of the growth in the control wells in order to be considered effective at controlling the bacteria.
After the bacteriostatic assays were completed, the plates were centrifuged at 2000 rpm for 10 minutes. The supernatant was removed and 100 μL of fresh LB broth were added to each well. The plates were read at 620 nm (initial OD), incubated at 28° C. for 3-4 days and read again at 620 nm (final OD). Effective concentrations provided at least 75% growth inhibition relative to the control.
Two replicates were used for each YP-terpene and both assays (static and cidal) were conducted three times for each bacterium.
Bacteriostatic Assay— For all three bacteria, every test material was bacteriostatic at least at the highest concentration tested. The assay ran for 48 hours. The criterion for efficacy was at least 75% growth inhibition relative to the control. Ranges of efficacy were established for the 31 terpenes and are provided below.
Erwinia amylovora
Pseudomonas
syringae
Xanthomonas
campestris
Bactericidal Assay— A large number of terpene formulations were not effective at killing the bacteria at the highest concentration tested. Ranges of efficacy were established for the 31 terpenes and are provided below in Table 32.
Erwinia amylovora
Pseudomonas
syringae
Xanthomonas
campestris
In each test, Erwinia was the pathogen most sensitive to the YP-terpene formulations followed by Xanthomonas and then Pseudomonas.
Ratings were assigned to each YP-terpene for each assay for each bacterium. The lower the rating number, the better the efficacy of the test material. The static and cidal ratings were multiplied to give a combination score. This number indicates how well the YP-terpene controlled each bacterium. The three combination scores (one for each bacterium) were added to give a composite score, which indicates YP-terpene efficacy across all three bacteria. Table 33 lists the YP-terpenes in order of efficacy based on the composite (overall) score along with the composition of each test material.
The 8 best YP-terpene formulations for controlling these bacteria each contain thymol. Most combinations that contain L-carvone are very poor at controlling these bacteria.
Certain combinations of encapsulated terpenes showed particular efficacy against certain types of plant pathogens. These combinations were observed to be:
These results indicate that four terpenes citral, eugenol, geraniol and thymol alone or in combination, especially when encapsulated in yeast glucan particles exhibit strong anti-bacterial and antifungal activity. In most cases is the presence of thymol is significant.
Tables 34 to 36 summarise the rankings of the performance of the various formulations.
| Number | Date | Country | |
|---|---|---|---|
| 60741129 | Nov 2005 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12095584 | Aug 2009 | US |
| Child | 16856693 | US |
