COMPOSITIONS CONTAINING FORMALDEHYDE AND ORGANIC ACID FOR PREVENTION OF AFRICAN SWINE FEVER

Abstract

The present invention relates to compositions and methods to prevent the incidence of African Swine Fever (ASF) in swine. Another aspect of the present invention relates to the administration of formaldehyde and at least one organic acid, preferably in the animal's feed or drinking water. The invention is unexpectedly effective in controlling the spread of the ASP virus but also keeping the animal feed virus-free for up to 7 days.

Claims

1. A composition for preventing and/or treating African Swine Fever (ASF) in swine comprising: at least one formaldehyde and; at least one organic acid.

2. The composition of claim 1, whereby the at least one organic acid is selected from the group consisting of acetic acid, propionic acid, butyric acid, citric acid, malic acid, tartaric acid, oxalic acid, lactic acid, formic acid, and benzoic acid.

3. The composition of claim 2 whereby the at least one organic acid is propionic acid and/or formic acid.

4. The composition of claim 1 further including an emulsifier.

5. The composition of claim 1, further including a pharmaceutically acceptable carrier.

6. The composition of claim 1, further including animal feed.

7. The composition of claim 6, whereby the composition is added to animal feed and includes at least 40 kg of the formaldehyde/metric ton of the animal feed, and at least 10 kg of the at least one organic acid/metric ton of the animal feed.

8. The composition of claim 7 whereby the composition includes at least 6 kg of an emulsifier/metric ton of the animal feed.

9. A method of preventing or treating African Swine Fever (ASF) in swine comprising: administering to swine a composition comprising a formaldehyde; and at least one organic acid.

10. The method of claim 9 whereby the composition whereby the at least one organic acid is selected from the group consisting of acetic acid, propionic acid, butyric acid, citric acid, malic acid, tartaric acid, oxalic acid, lactic acid, formic acid, and benzoic acid.

11. The method of claim 10 whereby the at least one organic acid is propionic acid and/or formic acid.

12. The method of claim 10, whereby the composition is administered to the swine by providing the composition in animal feed.

13. The method of claim 10, whereby the swine is a pig.

14. The method of claim 10, whereby the composition includes at least 40 kg of the formaldehyde/metric ton of the animal feed, and at least 10 kg of the at least one organic acid/metric ton of the animal feed.

15. The method of claim 14, whereby the composition further includes between about 6 kg of an emulsifier/metric ton of the animal feed.

16. The method of claim 10 whereby the composition is administered to the swine with a pharmaceutically acceptable carrier.

17. The method of claim 10 whereby the composition is administered to the swine through the swine's water source.

18. A method of manufacturing a composition for preventing and/or treating African Swine Fever (ASF) in swine comprising: combining a formaldehyde; and at least one organic acid to form a composition.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0008] FIG. 1 is a graph illustrating OIE Realtime PCR method confirming positive HADs as set forth in Example 1.

[0009] FIG. 2 is a sequencing analysis demonstrating that Nam Dinh and Ha Nam belong to genotype II as set forth in Example 1.

[0010] FIG. 3 is a graph illustrating Realtime PCR based on OIE protocol as set forth in Example 1.

[0011] FIG. 4 is a graph illustrating HAD50 data as set forth in Example 1.

[0012] FIG. 5A-5F are graphs illustrating the mean of Cq value following doses of ASFV exposure at 30 min (5A), 1 h (5B), 2 h (5C), 3 h (5D), 12 h (5E), and 24 h (5F).

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0013] The invention relates to the use of formaldehyde in combination with an organic acid for treatment of animal feed to lower the incidence and/or prevent African swine fever (ASF) via feed and water as vectors. When used on animal feed and or drinking water, the unique combination of formaldehyde and organic acid results in both viral hemolysis as well as a decrease of ASF viral load. When only a combination of organic acids is used, only a decrease of ASF viral load is observed.

[0014] The present invention may be used to reduce any type or form of African swine fever (ASF) disease in swine caused by the African swine fever virus (ASFV), a large double stranded DNA virus in the Asfarviridae family, via feed and water as vectors

[0015] According to at least one embodiment of the invention, pigs or other swine are provided through their food or water source a composition containing one or more forms of formaldehyde and organic acid. As used herein, the term “formaldehyde” is intended to include any form of formaldehyde including, but not limited to, the hydrate methanediol that is formed when formaldehyde is dissolved in water, as well as derivatives thereof, such as the linear polymer paraformaldehyde and the cyclic trimer metaformaldehyde (1,3,5-trioxane), as well as urea formaldehyde

[0016] The formaldehyde is combined with at least one organic acid which acts as an antimicrobial and enables the reduction of virus by the formaldehyde and other ingredients. Any organic acid will work for this purpose so long as it is safe for ingestion and compatible with the formaldehyde and other ingredients used in the formulation. Suitable organic acids for this purpose include small to medium chain organic acids that include fatty, volatile fatty, lipophilic, weak, or carboxylic acids, as well as derivatives thereof. These include, but are not limited to, acetic acid, propionic acid, butyric acid, citric acid, malic acid, tartaric acid, oxalic acid, lactic acid, formic acid, and benzoic acid. According to at least one embodiment of the present invention, propionic acid and or formic are preferred organic acids.

[0017] In addition to formaldehyde and at least one organic acid, one or more emulsifiers/surfactants may also be applied to the feed. Suitable emulsifiers for this purpose include, but are not limited to, soya lecithin, glycerin monostearate, potassium stearate, calcium stearoyl lactylate (CSL), DATEM, glyceryl monostearate, mono propylene glycol, SPAN 80, sodium stearoyl lactylate (SSL), Tween, sodium stearate, glycerol triacetate, sugar esters, non-dairy creamer, calcium stearate, polyglycerol polyricinoleate (PGPR), lecithin, mono and diglycerides, monoglyceride derivatives, polyglycerol esters (PGE), propylene glycol esters (PGMS), sucrose esters, and sorbitan esters and polysorbates. Preferred emulsifiers for this purpose include Tween 80 and propylene glycol. If included, the emulsifier(s) should be added to the feed in an amount of from about 0.001-10.0% by weight.

[0018] The feed compositions of the invention should preferably include at least about 40 kgs of formaldehyde/metric ton of feed, at least about 10 kgs of organic acid/metric ton of feed and, if included, at least about 6 kgs of emulsifier/metric ton of feed.

[0019] In one embodiment of the invention, the composition includes the commercial formulation Sal CURB® RM E Liquid which contains about 33% formaldehyde and 10% propionic acid in a solution of coloring agents, with a pH of 4.6-5.6, and having a typical application of 2.0-2.5 kg/T of feed. In another embodiment, the composition includes the commercial formulation Sal CURB® F2 Dry, which contains about 4% formaldehyde, about 53% formic, 12% propionic acid, 4% Tween 80, 3% propylene glycol, and pinene alpha (0.35%) and thymol (0.15%) as flavors. In another embodiment, the composition includes the commercial formulation Sal CURB® K2 Liquid, which contains about 55% formic, 15% anhydrous ammonia, 10% propionic acid, 10 lactic acid, 1% Tween 80, and 1% BHA.

[0020] The compositions of the invention may optionally include other ingredients, such as antioxidants, so long as the other ingredients are compatible with the formaldehyde and organic acid. Antioxidants are well known in the art and include, but are not limited to, vitamin A, vitamin C, vitamin E, beta-carotene, lycopene, lutein, selenium, manganese, zeaxanthin, flavonoids, flavones, catechins, polyphenols, and phytoestrogens. In one embodiment, the composition includes butylated hydroxyanisole to prevent oil oxidation.

[0021] The compositions of the invention can further include other ingredients or compounds that may be beneficial for pigs including, but not limited to, carbohydrate, protein, fat and oil, vitamins, minerals, probiotics, medicines, flavors, colors, etc. The compositions may also be combined with a pharmaceutically acceptable carrier that may include one or more carriers or excipients, such as fillers, diluents, binders, lubricants, and disintegrants. Such ingredients and their relative amounts to be included are well known to persons skilled in the art.

[0022] While the compositions of the invention are described in particular for administration in the animal's feed, the compositions may likewise be administered in the animal's water source.

[0023] According to at least one embodiment, the ingredients of the formulation may be combined by simply mixing at room temperature (25-30° C.) with or without agitation. The ingredients of the invention can either be mixed sequentially or can be added all at once to achieve the unique composition of the invention. In preferred embodiments the ingredients are mixed with agitation to improve miscibility. The composition can in turn be simply combined with the animal feed prior to administration to the animals. Animal feed formulations may be provided to the animals through any convention means well known to persons skilled in the art, include but not limited to top-dress, mixed in by hand, pelleted, mixed with crumbles, etc.

[0024] Once combined with the animal feed, the composition of the invention is preferably provided to the animals ad libitum, and preferably for a time period of 7 days or more and optimally through the various feeding periods (nursery, grower, finisher, gestation, lactation, farrowing) of the swine.

[0025] The following examples are offered to illustrate but not limit the invention. Thus, it is presented with the understanding that various formulation modifications as well as method of delivery modifications may be made and still are within the spirit of the invention.

EXAMPLE 1

Viricidal Activity of Sal Curb® Products

[0026] I. Information of ASF Strain Used in this Study [0027] ASFVs isolated from died pigs in Ha Nam and Nam Dinh provinces in 2019

[0028] 1.1. HAD test: Positive

[0029] 1.2. Real-time PCR: Positive (FIG. 1)

[0030] 1.3. Sequencing analysis (Based on genotyping primer p72 U/D—OIE protocol): Positive. Nam Dinh and Ha Nam belong to genotype II (FIG. 2)

[0031] 1.4. HAD50:

TABLE-US-00001 TABLE 1 HAD50/ml ASF Isolates First Second Third Ha Nam 10.sup.5.9 10.sup.6  10.sup.6  Nam Dinh 10.sup.5.7 10.sup.5.9 10.sup.5.7

Conclusion:

[0032] Ha Nam isolate was selected for Examination of Kemin (Sal Curb) Products inhibiting viricidal activity. This isolate is genotype II.

II. Experiment Design

[0033] Feed model: complete swine feed, negative for ASFV. [0034] Treatment of the feed with Kemin products before contamination with ASFV [0035] To ensure a homogeneous spread of the product on the feed, 200 g of complete feed will be treated with Sal CURB RM E Liquid, Sal CURB K2 Liquid and Sal CURB F2 Dry (3.0 kg/T). [0036] Number of samples: 3 sampling time points*3 samples/time point*5 treatments [0037] (a) Sampling timepoint 1: 1 day post contamination (DPC) [0038] (b) Sampling timepoint 2: 3 DPC [0039] (c)Sampling timepoint 3: 7 DPC (end of experiment) [0040] Negative control (No ASFV added) [0041] Positive control (complete feed containing 1×10.sup.5 (HAD50) of ASFV) [0042] Treatment 1: positive control treated with Sal CURB RM E Liquid [0043] Treatment 2: positive control treated with Sal CURB F2 Dry [0044] Treatment 3: positive control treated with Sal CURB K2 liquid

Virus/Feed Contamination Methods:

[0045] Use 5 g of feed in 50 mL mini bioreactor tubes (Corning Inc., Corning, N.Y.); with vented caps to allow exchange of temperature and humidity between the interior and exterior of the tube [0046] Spike the feed with 100 μL of MEM (minimum essential media, Gibco, ThermoFisher Scientific, Waltham, Mass., US) containing 1×10.sup.5 (HAD50) of ASFV. [0047] Negative control: 5 g of feed with 100 μl sterile MEM medium/sterile PBS [0048] Vortex the samples for 10 seconds following the addition of the virus inoculum [0049] Incubation of the samples at 20° C. and ˜60% RH (as per lab conditions) for 7days

Processing of Samples:

[0050] At the different sampling time points (i.e. DPC), process the samples for virus isolation. [0051] Resuspend each sample in 15 ml sterile PBS [0052] Vortex for 10 seconds and centrifuge (only to remove feed particles) [0053] Collect supernatant and centrifuge for 10 000 g for 10 minutes. [0054] Use supernatant for virus isolation according to SOP and for virus titration.

References:

[0055] Dee et al. (2018), Survival of viral pathogens in animal feed ingredients under transboundary shipping models. PLoS ONE 13(3): e0194509.

III. Methods

[0056] 1. Virus isolation and HAD test: OIE protocol [0057] 2. Conventional PCR and real-time PCR: OIE protocol

IV. Results

4.1 Conventional PCR Using PPA1 and PPA2

Note:

[0058] No 1. positive control treated with Sal CURB RM E Liquid

[0059] No 2. positive control treated with Sal CURB F2 Dry

[0060] No3. positive control treated with Sal CURB K2 liquid

[0061] No 4. Negative control (No ASFV added, only feed)

[0062] No 5. Positive control: complete feed containing 1×10.sup.5 (HAD50) of ASFV

4.2. Realtime PCR Based on OIE Protocol

[0063] For detail, please see HAD and Cq values files (FIG. 3).

4.3. HAD50 Data

[0064] For detail, please see HAD and Cq values files (FIG. 4).

V. Conclusion

[0065] Sal CURB RM E Liquid shown a strong inhibition of viricidal activity of ASFV isolated in Vietnam (realtime PCR from DPC1 to 7, HAD from DPC 3 to 7) [0066] Sal CURB F2 Dry shown a significant inhibition of viricidal activity of ASFV from DPC3 to 7 based on realtime PCR and only DPC7 by HAD [0067] Sal CURB K2 liquid shown only significant effect on DPC7 by realtime PCR. No effect was observed by HAD [0068] ASFV can survive in feed up to 7days based on conventional PCR and realtime PCR

EXAMPLE 2

Examination of Kemin Sal Curb RME Liquid Inhibiting Viricidal Activity in Water

[0069] I. Information of ASF Strain Used in this Study [0070] ASFVs isolated from died pigs in Ha Nam and Nam Dinh provinces in 2019

II. Experiment Design

[0071] Water model: Fresh water, negative for ASFV. [0072] Treatment of fresh water with Sal CURB RME Liquid before contamination with ASFV
a. Control Groups [0073] Positive control: fresh water treated with ASFV isolated in Vietnam at different doses: 10{circumflex over ( )}1HAD50 and 10{circumflex over ( )}3HAD50 [0074] Negative control: Fresh water (ASFV negative by real-time PCR)
b. Experiment Groups [0075] Fresh water treated with Sal CURB RME Liquid different doses at 3 kg, 1 kg, 0.75 kg, 0.5 kg/1000 litter (3 g, 1 g, 0.75 g and 0.5 g/1000 ml). Shaking the mix for 10 mins [0076] The Sal Curb RME Liquid-treated water were exposed to ASFV at different doses of 10{circumflex over ( )}1HAD50 and 10{circumflex over ( )}3HAD50, respectively

III. Sample Collection

[0077] Samples were collected at 30 min, 1 h, 2 h, 3 h, 12 h and 24 h after ASFV exposure and DNA extraction were performed immediately. DNA were stored at −20 for evaluation by real-time PCR.

TABLE-US-00002 TABLE 2 Sampling schedule for treatment and collection (10{circumflex over ( )}1HAD50) Time 3 kg/1000 1 kg/1000 0.75 kg/1000 0.5 kg/1000 Positive Negative Order points litter litter litter litter Control Control 1 30 min 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 2 1 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 3 2 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 4 3 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 5 12 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 6 24 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples

TABLE-US-00003 TABLE 3 Sampling schedule for treatment and collection (10{circumflex over ( )}3HAD50) Time 3 kg/1000 1 kg/1000 0.75 kg/1000 0.5 kg/1000 Positive Negative Order points litter litter litter litter Control Control 1 30 min 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 2 1 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 3 2 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 4 3 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 5 12 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples 6 24 h 3 samples 3 samples 3 samples 3 samples 3 samples 3 samples

IV. Methods

[0078] Real-time PCR using OIE protocol

V. Results (FIG. 5)

VI. Conclusion

[0079] No effect of Sal CURB were observed at 30 min, 1 h, 2 h and 3 h after ASFV exposure when compared to control group [0080] A significant effects was noted at 3 kg-treated group at 12 h after exposure to ASFV at both of doses of 10{circumflex over ( )}1HAD50 and 10{circumflex over ( )}3HAD50 when compared to control group (p<0.05); a modest enhance of Cq value was recognized in 1 kg-treated group at 12 h at both of 10{circumflex over ( )}1HAD50 and 10{circumflex over ( )}3HAD50 [0081] Sal CURB shown a strong antiviral effect after 24 h exposure in which at the dose of 3 kg, 1 kg and 0.75 kg/1000 litter, no Cq were noted in group spiked to 10{circumflex over ( )}1HAD50 of ASFV, a statistic effects were observed in the group exposed to 10{circumflex over ( )}3HAD50 at doses of 3 kg and 1 kg/1000 L of Sal CURB RME Liquid (p<0.05)

[0082] It should be appreciated that minor dosage and formulation modifications of the composition and the ranges expressed herein may be made and still come within the scope and spirit of the present invention.

[0083] Having described the invention with reference to particular compositions, theories of effectiveness, and the like, it will be apparent to those of skill in the art that it is not intended that the invention be limited by such illustrative embodiments or mechanisms, and that modifications can be made without departing from the scope or spirit of the invention, as defined by the appended claims. It is intended that all such obvious modifications and variations be included within the scope of the present invention as defined in the appended claims. The claims are meant to cover the claimed components and steps in any sequence which is effective to meet the objectives there intended, unless the context specifically indicates to the contrary.

[0084] The foregoing description has been presented for the purposes of illustration and description. It is not intended to be an exhaustive list or limit the invention to the precise forms disclosed. It is contemplated that other alternative processes and methods obvious to those skilled in the art are considered included in the invention. The description is merely examples of embodiments. It is understood that any other modifications, substitutions, and/or additions may be made, which are within the intended spirit and scope of the disclosure. From the foregoing, it can be seen that the exemplary aspects of the disclosure accomplishes at least all of the intended objectives.