Patent Grant
10568917
This application is a U.S. National Phase Application of International Application No. PCT/KR2016/012906, filed Nov. 10, 2016, which claims priority to Korean Application No. 10-2015-0182593, filed Dec. 21, 2015, each of which are hereby incorporated by reference in their entirety.
The Sequence Listing submitted Jul. 5, 2018 as a text file named “08162_0044U1_Revised_Sequence_Listing.txt,” created on Jun. 28, 2018, and having a size of 52,260 bytes is hereby incorporated by reference pursuant to 37 C.F.R. § 1.52(e)(5).
1. Field of the Invention
The present invention relates to a bacteriophage isolated from the nature that infects and kills Pasteurella multocida cells, and a method for preventing and treating the infections of Pasteurella multocida using a composition comprising the bacteriophage as an active ingredient. More particularly, the present invention relates to a Myoviridae bacteriophage Pas-MUP-1 (Accession NO: KCTC 12706BP) that is isolated from the nature and can kill Pasteurella multocida cells specifically, which has a genome represented by the nucleotide sequence of SEQ. ID. NO: 1, and a method for preventing the infections of Pasteurella multocida and thereafter treating them using the composition comprising said bacteriophage as an active ingredient.
2. Description of the Related Art
Pasteurella multocida is a Gram-negative, non-motile bacillus, which is classified according to capsular polysaccharides into 5 types: A, B, D, E and F. In detail, Pasteurella multocida type A is associated with pulmonary diseases in cattle, sheep, pigs, Pasteurella multocida type B provokes hemorrhagic sepsis in cattle and buffalo, and Pasteurella multocida type D triggers atrophic rhinitis in pigs. As such, Pasteurella multocida gives rise to various diseases in livestock animals, thus leading to economical damages seriously in the livestock farming industry. Therefore, it is required to develop a novel procedure for preventing diseases and conditions caused by Pasteurella multocida in animals, and further treating the infections of Pasteurella multocida.
In the livestock farming industry, antibiotics are utilized a lot in order to prevent and treat the infections of Pasteurella multocida. However, antibiotic-resistant bacterial strains are emerging so as to continuously reduce the effectiveness of antibiotics. Moreover, such an abuse of antibiotics for animals is being prohibited under national regulations fortified. Therefore, it is currently requested to develop a novel effective procedure rather than antibiotics. Especially, environmental-friendly methods may be preferred.
Recently, the use of bacteriophages has drawn our attention as a new way of treating bacterial infections. Particularly, the reason of our high interest in bacteriophages is because bacteriophage-based treatment is a nature-friendly method. Bacteriophages are an extremely small microorganism that infects bacteria, which are called phage in short. Once bacteriophage infects bacteria, the bacteriophage is proliferated in the inside of the bacterial cell. After proliferation, the progenies destroy the bacterial cell wall to escape from the host, suggesting that the bacteriophage has the killing ability of bacteria. The bacteriophage infection is characterized by its high specificity, so that a certain bacteriophage infects only a specific bacterium. That is, the bacterium that can be infected by certain bacteriophage is limited, suggesting that bacteriophage can kill only a specific bacterium and cannot harm other bacteria. Due to this cell specificity, the bacteriophage confers antibacterial effects upon target bacteria and excludes commensal bacteria in environmental or internal conditions of animal. Conventionally, universal antibiotics for therapeutic use of bacteria affect various kinds of bacteria coincidently, which results in a lot of problems polluting environment, disturbing normal microflora in animals or the like. Fortunately, the use of bacteriophages does not affect normal microflora and the like, because of killing the target bacteria selectively. Hence, the bacteriophage may be safe and thus lessen the probability of adverse actions, compared to any other antibiotics.
Bacteriophage was first found out by an English bacteriologist Twort in 1915 when he noticed that Micrococcus colonies melted and became transparent by something unknown. In 1917, a French bacteriologist d'Herelle found out that Shigella dysenteriae in the filtrate of dysentery patient feces melted by something, and further studied about this phenomenon. As a result, he identified bacteriophage independently, and named it as bacteriophage which means a bacteria killer. Since then, bacteriophages specifically acting against such pathogenic bacteria as Shigella, Salmonella Typhi and Vibrio cholerae have been continuously identified.
Owing to the unique capability of bacteriophage to kill bacteria, bacteriophages have been studied and anticipated as a better method to treat bacterial infections. However, after penicillin was found by Fleming, studies on bacteriophages had been only continued in some of Eastern European countries and the former Soviet Union because of the universalization of antibiotics. After the year of 2000, the merit of the conventional antibiotics faded because of the increase of antibiotic-resistant bacteria. So, bacteriophages are once again spotlighted as a new antibacterial agent that can replace the conventional antibiotics. Furthermore, the recent regulation of using antibiotics is fortified by the government world-widely. The interest on bacteriophages is increasing more and also industrial applications are increasingly achieved.
As demonstrated above, bacteriophages tend to be highly specific for bacteria. The specificity often makes bacteriophages effective upon a part of bacteria, even though belonging to the same kinds. In addition, the effectiveness of bacteriophage is different, depending upon target bacterial strains. Therefore, it is necessary to collect many kinds of bacteriophages that are useful to control specified bacteria efficiently. Hence, in order to develop a use of bacteriophages for coping with Pasteurella multocida, a lot of bacteriophages (many kinds of bacteriophages that give an antibacterial action against Pasteurella multocida) should be acquired. Furthermore, the resulting bacteriophages need to be screened whether or not superior to others in respects of antibacterial strength and spectrum.
Therefore, the present inventors tried to develop a composition applicable for the prevention or treatment of Pasteurella multocida infections by using a bacteriophage that is isolated from the nature and can kill Pasteurella multocida cells selectively, and further to establish a method for preventing or treating the infections of Pasteurella multocida using the composition. As a result, the present inventors isolated bacteriophages suitable for this purpose and secured the nucleotide sequence of the genome that distinguishes the bacteriophage of the present invention from other bacteriophages. Then, we have developed a composition comprising the isolated bacteriophage as an active ingredient, and confirmed that this composition could be efficiently used to prevent and treat the infections of Pasteurella multocida, leading to the completion of the present invention.
It is an object of the present invention to provide a Myoviridae bacteriophage Pas-MUP-1 (Accession NO: KCTC 12706BP, deposited under the Budapest Treaty on the International Procedure at the Korean Collection for Type Cultures, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daijeon 305-806, Republic of Korea; the deposit was made on Nov. 7, 2014.) that is isolated from the nature and can kill Pasteurella multocida cells specifically, which has the genome represented by the nucleotide sequence of SEQ. ID. NO: 1.
It is another object of the present invention to provide a composition applicable for the prevention of Pasteurella multocida infections, which comprises the bacteriophage Pas-MUP-1 that can infect and kill Pasteurella multocida cells, as an active ingredient and a method for preventing the infections of Pasteurella multocida using said composition.
It is another object of the present invention to provide a composition applicable for the treatment of Pasteurella multocida infections, which comprises the bacteriophage Pas-MUP-1 that can infect and kill Pasteurella multocida cells, as an active ingredient and a method for treating the infections of Pasteurella multocida using said composition.
It is another object of the present invention to provide a disinfectant for preventing and treating the infections of Pasteurella multocida using said composition.
It is also an object of the present invention to provide a feed additive effective upon farming by preventing and treating the infections of Pasteurella multocida using said composition.
To achieve the above objects, the present invention provides a Myoviridae bacteriophage Pas-MUP-1 (Accession NO: KCTC 12706BP) that is isolated from the nature and can kill specifically Pasteurella multocida cells, which has the genome represented by the nucleotide sequence of SEQ. ID. NO: 1, and a method for preventing and treating the infections of Pasteurella multocida using a composition comprising the bacteriophage as an active ingredient.
The bacteriophage Pas-MUP-1 has been isolated by the present inventors and then deposited at Korean Collection for Type Cultures, Korea Research Institute of Bioscience and Biotechnology in Nov. 7, 2014 (Accession NO: KCTC 12706BP).
In addition, the present invention also provides a disinfectant and a feed additive applicable for the prevention or treatment of Pasteurella multocida infections, which comprises the bacteriophage Pas-MUP-1 as an active ingredient.
Since the bacteriophage Pas-MUP-1 included in the composition of the present invention kills Pasteurella multocida cells efficiently, it is regarded effective to prevent or treat diseases (infections) caused by Pasteurella multocida. Therefore, the composition of the present invention can be utilized for the prevention and treatment of diseases caused by Pasteurella multocida.
In this description, the term “prevention” or “prevent” indicates (i) to block the infections of Pasteurella multocida; and (ii) to block the development of diseases caused by Pasteurella multocida.
In this description, the term “treatment” or “treat” indicates (i) to suppress the diseases caused by Pasteurella multocida; and (ii) to relieve the condition of diseases caused by Pasteurella multocida.
In this description, the term “isolation” or “isolated” indicates all the actions to separate the bacteriophage by means of experimental techniques and to secure the characteristics that can distinguish this bacteriophage from others, and further includes the action of proliferating the bacteriophage by means of bioengineering techniques so as to make it useful.
The pharmaceutically acceptable carrier included in the composition of the present invention is the one that is generally used for the preparation of a pharmaceutical formulation, which is exemplified by lactose, dextrose, sucrose, sorbitol, mannitol, starch, acacia rubber, calcium phosphate, alginate, gelatin, calcium silicate, microcrystalline cellulose, polyvinyl pyrrolidone, cellulose, water, syrup, methylcellulose, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate, and mineral oil, but not always limited thereto. The composition of the present invention can additionally include lubricants, wetting agents, sweeteners, flavors, emulsifiers, suspending agents, and preservatives, in addition to the above ingredients.
In the composition of the present invention, the bacteriophage Pas-MUP-1 is included as an active ingredient. At this time, the bacteriophage Pas-MUP-1 is included at the concentration of 1×101 pfu/ml˜1×1030 pfu/ml or 1×101 pfu/g˜1×1030 pfu/g, and preferably at the concentration of 1×104 pfu/ml˜1×1015 pfu/ml or 1×104 pfu/g˜1×1015 pfu/g.
The composition of the present invention can be formulated by conventional methods that are conducted by those in the art with pharmaceutically acceptable carriers and/or excipients in the form of unit dose or in a multi-dose container. The formulation can be in the form of solution, suspension or emulsion in oil or water-soluble medium, extract, powder, granule, tablet or capsule and additionally, a dispersing agent or stabilizer can be included.
The composition of the present invention can be prepared as a disinfectant or a feed additive according to the purpose of use, but not always limited thereto.
For this purpose, other bacteriophages that can confer an antibacterial activity against other bacterial species can be further comprised in the composition of the present invention in order to improve its effectiveness. In addition, other kinds of bacteriophages that have an antibacterial activity against Pasteurella multocida can be further comprised in the composition of the present invention. Besides, these bacteriophages can be combined properly so as to maximize antibacterial effects, because their antibacterial activities against Pasteurella multocida can be differential in respects of antibacterial strength and spectrum.
The method for preventing and treating the infections of Pasteurella multocida using this composition comprising the bacteriophage Pas-MUP-1 as an active ingredient, has the advantage of high specificity for Pasteurella multocida, compared with the conventional methods based on the chemical materials including the conventional antibiotics. That means, the composition of the present invention can be used for preventing or treating the infections of Pasteurella multocida specifically without affecting normal microflora, and accordingly has fewer side effects. In general, when chemical materials such as antibiotics are used, commensal bacteria are also damaged so as to weaken immunity in animals with carrying various side effects. In the meantime, the composition of the present invention uses the bacteriophage isolated from the nature as an active ingredient, so that it is very nature-friendly. Besides, the antibacterial activity of bacteriophages against target bacteria is different, even if belonging to the same species, in respects of antibacterial strength and spectrum (within several strains of Pasteurella multocida, the antibacterial range of bacteriophages contributing to every strain. Typically, bacteriophages are usually effective upon a part of bacterial strains even in the same species. That is to say, the antibacterial activity of bacteriophage is different depending on bacterial strain in spite of belonging to the same species). Then, the bacteriophage of the present invention can provide antibiotic activity against Pasteurella multocida different to that provided by other bacteriophages acting on Pasteurella multocida. Therefore, the bacteriophage of the present invention can provide different applicability for livestock industry.
The application of the preferred embodiments of the present invention is best understood with reference to the accompanying drawings, wherein:
Practical and presently preferred embodiments of the present invention are illustrative as shown in the following Examples.
However, it will be appreciated that those skilled in the art, on consideration of this disclosure, may make modifications and improvements within the spirit and scope of the present invention.
Samples were collected from the nature to isolate the bacteriophage capable of killing Pasteurella multocida. The Pasteurella multocida strains used for the bacteriophage isolation herein were the strains that had been isolated by the present inventors and identified as Pasteurella multocida previously.
The isolation procedure of the bacteriophage is described in detail hereinafter. The collected sample was added to the TSB (Tryptic Soy Broth) medium (pancreatic digest of casein, 17 g/L; papaic digest of soybean, 3 g/L; dextrose, 2.5 g/L; sodium chloride, 5 g/L; dipotassium phosphate, 2.5 g/L) inoculated with Pasteurella multocida at the ratio of 1/1000, followed by shaking culture at 37° C. for 3˜4 hours. Upon completion of the culture, centrifugation was performed at 8,000 rpm for 20 minutes and supernatant was recovered. The recovered supernatant was inoculated with Pasteurella multocida at the ratio of 1/1000, followed by shaking culture at 37° C. for 3˜4 hours. When the sample contained the bacteriophage, the above procedure was repeated total 5 times in order to sufficiently increase the titer of the bacteriophage. After repeating the procedure 5 times, the culture solution proceeded to centrifugation at 8,000 rpm for 20 minutes and the resulting supernatant was recovered. The recovered supernatant was filtrated by using a 0.45 μm filter. The resulting filtrate was used in spot assay for examining whether or not the bacteriophage capable of killing Pasteurella multocida was included therein.
Spot assay was performed as follows; TSB medium was inoculated with Pasteurella multocida at the ratio of 1/1000, followed by shaking culture at 37° C. for overnight. 3 ml (1.5 of OD600) of the culture broth of Pasteurella multocida prepared above was spread on the TSA (Tryptic Soy Agar; pancreatic digest of casein, 17 g/L; papaic digest of soybean, 3 g/L; sodium chloride, g/L; agar, 15 g/L) plate. The plate stood in a chamber for about 30 minutes to dry. After drying, 10 μl of the resulting filtrate was spotted directly onto the surface of the Pasteurella multocida lawns and dried for about 30 minutes. Following drying, the plate was incubated at 37° C. for a day and then, examined for the formation of clear zones on the surface of the bacterial lawns. If a clear zone was generated where the filtrate was dropped, it could be judged that the bacteriophage capable of killing Pasteurella multocida was included in the filtrate. Through the above procedure, the filtrate containing the bacteriophage having the killing ability of Pasteurella multocida could be obtained.
After that, the bacteriophage was isolated from the filtrate confirmed above to have the bacteriophage capable of killing Pasteurella multocida. The conventional plaque assay was used for the isolation of pure bacteriophage. In detail, a plaque formed in the course of the plaque assay was picked up by using a sterilized tip, which was then added to the culture solution of Pasteurella multocida, followed by culturing at 37° C. for 4˜5 hours. Upon completion of the culture, centrifugation was performed at 8,000 rpm for 20 minutes to obtain supernatant. The recovered supernatant was inoculated with Pasteurella multocida culture at the ratio of 1/50, followed by culturing at 37° C. for 4˜5 hours. To increase the titer of the bacteriophage, the above procedure was repeated at least 5 times. Then, centrifugation was performed at 8,000 rpm for 20 minutes to obtain supernatant. Plaque assay was performed with the obtained supernatant. In general, the pure bacteriophage isolation is not completed by one-time procedure, so the above procedure was repeated by using the plaque formed above. After at least 5 times of repeated procedure, the solution containing the pure bacteriophage was obtained. The procedure for the isolation of the pure bacteriophage was generally repeated until the generated plaques became similar in sizes and morphologies. And the final pure bacteriophage isolation was confirmed by electron microscopy. Until the pure bacteriophage isolation was confirmed by electron microscopy, the above procedure was repeated. The electron microscopy was performed by the conventional method. Briefly, the solution containing the pure bacteriophage was loaded on copper grid, followed by negative staining with 2% uranyl acetate. After drying thereof, the morphology was observed using a transmission electron microscope. The electron micrograph of the bacteriophage isolated in the present invention is presented in
The solution containing the pure bacteriophage confirmed above proceeded to purification. The culture broth of Pasteurella multocida was added to the solution containing the pure bacteriophage at the volume of 1/50 of the total volume of the bacteriophage solution, followed by culturing again for 4˜5 hours. Upon completion of the culture, centrifugation was performed at 8,000 rpm for 20 minutes to obtain supernatant. This procedure was repeated 5 times to obtain a solution containing enough numbers of the bacteriophage. The supernatant obtained from the final centrifugation was filtered by a 0.45 μm filter, followed by the conventional polyethylene glycol (PEG) precipitation. Particularly, PEG and NaCl were added to 100 ml of the filtrate until reaching 10% PEG 8000/0.5 M NaCl, which stood at 4° C. for 2˜3 hours. Then, centrifugation was performed at 8,000 rpm for 30 minutes to obtain the bacteriophage precipitate. The resulting bacteriophage precipitate was resuspended in 5 ml of buffer (10 mM Tris-HCl, 10 mM MgSO4, 0.1% Gelatin, pH 8.0). This solution was called as the bacteriophage suspension or bacteriophage solution.
As a result, the pure bacteriophage purified above was collected, which was named as the bacteriophage Pas-MUP-1 and then deposited at Korean Collection for Type Cultures, Korea Research Institute of Bioscience and Biotechnology in Nov. 7, 2014 (Accession NO: KCTC 12706BP).
The genome of the bacteriophage Pas-MUP-1 was separated as follows. The genome was separated from the bacteriophage suspension obtained in Example 1. First, in order to eliminate DNA and RNA of Pasteurella multocida cells included in the suspension, DNase I and RNase A were added 200 U each to 10 ml of the bacteriophage suspension, which was incubated at 37° C. for 30 minutes. 30 minutes later, to remove the DNase I and RNase A activity, 500 μl of 0.5 M ethylenediaminetetraacetic acid (EDTA) was added thereto, which was incubated for 10 minutes. The suspension was further incubated at 65° C. for 10 minutes and then added with 100 μl of proteinase K (20 mg/ml) to break the outer wall of the bacteriophage, followed by incubation at 37° C. for 20 minutes. After that, 500 μl of 10% sodium dodecyl sulfate (SDS) solution was added thereto, followed by incubation at 65° C. for 1 hour. 10 ml of the mixture of phenol:chloroform:isoamylalcohol in a ratio of 25:24:1 was added thereto, followed by mixing well. The mixture was centrifuged at 13,000 rpm for 15 minutes to separate each layer. The upper layer was obtained, to which isopropyl alcohol was added at the volume of 1.5 times the volume of the upper layer, followed by centrifugation at 13,000 rpm for 10 minutes to precipitate the genome of the bacteriophage. After collecting the precipitate, 70% ethanol was added to the precipitate, followed by centrifugation at 13,000 rpm for 10 minutes to wash the precipitate. The washed precipitate was recovered, vacuum-dried and then dissolved in 100 μl of water. This procedure was repeated to obtain a sufficient amount of the bacteriophage Pas-MUP-1 genome.
The nucleotide sequence of the genome of the bacteriophage Pas-MUP-1 obtained above was analyzed by Next Generation Sequencing (NGS) using illumina Mi-Seq device at National Instrumentation Center for Environmental Management, Seoul National University. As a result, it is suggested that the final genome of bacteriophage Pas-MUP-1 have 39,497 bp of size and the nucleotide sequence of the whole genome has SEQ. ID. NO: 1.
Based upon the genomic sequence of the bacteriophage Pas-MUP-1 obtained above, its similarity to other genomic sequences previously reported was investigated by using BLAST. From the BLAST result, it is shown that there is no genomic sequence having more than 50% homology with that of the bacteriophage Pas-MUP-1.
Based upon this result, it is concluded that the bacteriophage Pas-MUP-1 is a novel bacteriophage never reported before. Along with this result, it is referred herein that when bacteriophages are different in their kinds, their antibacterial strength and spectrum become different typically. Therefore, it is concluded that the bacteriophage Pas-MUP-1 provides different type of valuable antibacterial activity compared to other bacteriophages aforementioned.
The killing ability of the isolated bacteriophage Pas-MUP-1 against Pasteurella multocida was investigated. To do so, the formation of clear zone was observed by the spot assay by the same manner as described in Example 1. The Pasteurella multocida used for this investigation were total 10 strains which had been isolated and identified as Pasteurella multocida previously by the present inventors. The bacteriophage Pas-MUP-1 demonstrated the killing ability against 9 strains of the Pasteurella multocida used in this experiment. The representative result of the killing ability test is shown in
Therefore, it was confirmed that the bacteriophage Pas-MUP-1 has the specific ability to kill Pasteurella multocida and a broad antibacterial spectrum against Pasteurella multocida, suggesting that the bacteriophage Pas-MUP-1 of the present invention could be used as an active ingredient of the composition for preventing and treating the infections of Pasteurella multocida.
100 μl of the bacteriophage Pas-MUP-1 solution at 1×108 pfu/ml was added to a tube containing 9 ml of TSB. To another tube containing 9 ml of TSB, only the same volume of TSB was added. Then, the Pasteurella multocida culture was added to each tube until OD600 reached about 0.5. After that, the tubes were transferred to an incubator at 37° C., followed by shaking culture, during which the growth of Pasteurella multocida was observed. As presented in Table 1, the growth of Pasteurella multocida was inhibited in the tube adding the bacteriophage Pas-MUP-1 solution, while the growth of Pasteurella multocida was not inhibited in the tube without adding the bacteriophage Pas-MUP-1 solution.
The above results indicate that the bacteriophage Pas-MUP-1 could not only inhibit the growth of Pasteurella multocida but also kill them. Therefore, it is concluded that the bacteriophage Pas-MUP-1 can be used as an active ingredient of the composition for preventing the infections of Pasteurella multocida.
Preventive effect of the bacteriophage Pas-MUP-1 on weaning pigs affected by Pasteurella multocida was investigated. 4 weaning pigs at 25 days of age were grouped together; total 2 groups of pigs were raised in each pig pen (1.1 m×1.0 m). Heating system was furnished and the surrounding environment was controlled. The temperature and the humidity of the pig pen were controlled consistently and the floor was cleaned every day. From the 1st day of the experiment, pigs of the experimental group (adding the bacteriophage) were fed with feeds adding the bacteriophage Pas-MUP-1 at 1×108 pfu/g according to the conventional feed supply procedure, while pigs of the control group (without adding the bacteriophage) were fed with the same feed without adding the bacteriophage Pas-MUP-1 according to the conventional procedure. From the 7th day of the experiment, the feeds of both groups were contaminated with 1×108 cfu/g of Pasteurella multocida for 2 days and thereafter provided twice a day respectively for the experimental and the control groups so as to bring about the infections of Pasteurella multocida. From the next day after providing contaminated feeds for 2 days (the 9th day of the experiment), pigs of the experimental group (adding the bacteriophage) were fed again with the feeds adding the bacteriophage Pas-MUP-1 at 1×108 pfu/g without contaminating Pasteurella multocida according to the conventional feed supply procedure as before, while pigs of the control group (without adding the bacteriophage) were fed with the same feed without adding the bacteriophage according to the conventional procedure. From the 9th day of the experiment, all the test animals were examined whether Pasteurella multocida cells are detected in their nasal discharge or not. In detail, samples of the nasal discharge (nasal swab in the inside of nasal cavity) were smeared onto blood agar plates, incubated at 37° C. for 18˜24 hours to make bacterial colonies. Then, the resulting colonies were screen to select the Pasteurella multocida cells. By using the colony samples selected above, polymerase chain reaction (PCR) specific for Pasteurella multocida was performed so as to identify Pasteurella multocida cells. The result is presented in Table 2.
Pasteurella multocida
From the above results, it is confirmed that the bacteriophage Pas-MUP-1 of the present invention could be very effective to suppress the infections of Pasteurella multocida.
Therapeutic effect of the bacteriophage Pas-MUP-1 on animals affected by Pasteurella multocida was investigated. 4 weaning pigs at 25 days of age were grouped together; total 2 groups of pigs were raised in each pig pen (1.1 m×1.0 m). Heating system was furnished and the surrounding environment was controlled. The temperature and the humidity of the pig pen were controlled consistently and the floor was cleaned every day. On the 4th day of the experiment, all the pigs were sprayed to the nasal cavity with 5 ml of Pasteurella multocida suspension (109 cfu/ml). The Pasteurella multocida suspension inoculated above was prepared as follows: Pasteurella multocida was cultured in TSB medium at 37° C. for 18 hours and then the resulting bacterial cells were recovered. Saline (pH 7.2) was added to the bacterial cell pellet to adjust cell suspension at the concentration of 109 CFU/ml. From the next day of the Pasteurella multocida challenge, the experimental group (adding bacteriophage solution) was sprayed nasally with the bacteriophage Pas-MUP-1 at 109 PFU/head twice a day by the same way as used for the above administration. The control group (without adding bacteriophage solution) was treated with nothing. Feeds and drinking water were equally provided to both the groups. From the 3rd day after the challenge of Pasteurella multocida (the 7th day of the experiment), all the animals were examined every day whether they were suffered from atrophic rhinitis caused by Pasteurella multocida or not. The atrophic rhinitis caused by Pasteurella multocida was evaluated by detecting the presence of Pasteurella multocida cells within the nasal discharge as described in Example 5. The result is presented in Table 3.
Pasteurella multocida colonies per
From the above results, it is confirmed that the bacteriophage Pas-MUP-1 of the present invention could be very effective to treat the infections of Pasteurella multocida.
Feed additives were prepared by adding the bacteriophage Pas-MUP-1 solution at the concentration of 1×108 pfu/g feed additives. The preparation method thereof was as follows: Maltodextrin (50%, w/v) was added to the bacteriophage solution, mixed and then freeze-dried. Lastly, the dried mixture was grinded into fine powders. The drying procedure above can be replaced with drying under a reduced pressure, drying at warm temperature, or drying at room temperature. To prepare the control, feed additives that did not contain the bacteriophage but contained only buffer (10 mM Tris-HCl, 10 mM MgSO4, 0.1% Gelatin, pH 8.0) were prepared.
The above two kinds of feed additives were mixed with the volume of the 1,000 times volume of feed for pig farming respectively, resulting in two kinds of final feeds.
Disinfectants containing bacteriophage Pas-MUP-1 at the concentration of 1×108 pfu/ml were prepared by using the bacteriophage Pas-MUP-1 solution. In detail, to prepare the disinfectant, the bacteriophage Pas-MUP-1 solution at the concentration of 1×108 pfu was added to 1 ml buffer that is used to prepare the bacteriophage solution, and then well mixed. To prepare the control, the buffer itself that is the same with that used for the bacteriophage solution was utilized.
The two kinds of disinfectants prepared above were diluted in water at the ratio of 1:1000, and then used for final disinfectants.
The effect of the feeds and the disinfectants prepared in Example 7 and Example 8 on pig farming was investigated. Particularly, this investigation was conducted by examining degrees of animal growth and clinical signs associated with atropic rhinitis. Total 40 piglets were grouped into two, and each group was composed of 20 piglets (group A: feed test group, group B: disinfectant test group). The experiment was continued for 2 weeks. Each group was divided by two sub-groups comprising 10 piglets. Then, the sub-groups were divided according to the treatment of the bacteriophage Pas-MUP-1 (sub-group-{circle around (1)}: treated with the bacteriophage Pas-MUP-1; and sub-group-{circle around (2)}: not-treated with the bacteriophage). The piglets used in this experiment were weaning pigs at 20 days of age. Each sub-group was raised in a separate room placed at a sufficient distance. Each sub-group was distinguished and designated as presented in Table 4.
Feeds were provided according to the conventional feed supply procedure as shown in Table 4 with the feeds prepared in Example 7. Disinfectants were treated 3 times a week with taking turns with the conventional disinfectants. That is, on the day when the disinfectant of the present invention was sprayed, the conventional disinfectant was not treated. As a consequence, it is demonstrated that the sub-group treated with the bacteriophage Pas-MUP-1 should be significantly outstanding in the degree of growth, compared to the sub-group not-treated with the bacteriophage Pas-MUP-1. Also the clinical sign of atrophic rhinitis was not found in the sub-group treated with the bacteriophage Pas-MUP-1, but it was manifested in about 5% of subjects from the sub-group not-treated with the bacteriophage. Furthermore, as described in Example 5, the sub-groups were examined whether separating Pasteurella multocida cells from the nasal discharge or not. As a result, it is shown that the Pasteurella multocida cells should be detected in the nasal discharge of some animals from the sub-group not-treated with the bacteriophage, while not detected in that of all the animals from the sub-group treated with the bacteriophage Pas-MUP-1.
From the above results, it is confirmed that the feeds and the disinfectants prepared according to the present invention were effective to improve outcomes in animal farming. Therefore, it is concluded that the composition of the present invention could be efficiently applied to increase the productivity in animal farming.
Those skilled in the art will appreciate that the conceptions and specific embodiments disclosed in the foregoing description may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. Those skilled in the art will also appreciate that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended Claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2015-0182593 | Dec 2015 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2016/012906 | 11/10/2016 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2017/111306 | 6/29/2017 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 9358258 | Kim et al. | Jun 2016 | B2 |
| 20040241825 | Mandeville et al. | Dec 2004 | A1 |
| Number | Date | Country |
|---|---|---|
| 1812025 | Sep 2012 | EP |
| 10-0818360 | Apr 2008 | KR |
| 10-2012-0076710 | Jul 2012 | KR |
| 10-1260645 | May 2013 | KR |
| 10-2014-0140698 | Dec 2014 | KR |
| Entry |
|---|
| Ahmad et al., “Development of immunization trials against Pasteurella multocida,” Vaccine 32: 909-917 (Year: 2014). |
| Palocz et al., “Alternative treatment of serious and mild Pasteurella multocida infection in New Zealand White rabbits,” BMC Veterinary Research 10: 276 (Year: 2014). |
| International Search Report dated Feb. 20, 2017 by the International Searching Authority for Patent Application No. PCT/KR2016/012906, which was filed on Nov. 10, 2016 and published as WO 2017/111306 on Jun. 29, 2017 (Inventor—Yoon et al.; Intron Biotechnology, Inc.) (Original—4 pages; Translation—2 pages). |
| Number | Date | Country | |
|---|---|---|---|
| 20180369300 A1 | Dec 2018 | US |
