Prophylactic and therapeutic agent against swine dysentery

This invention relates to an agent for preventing or treating swine dysentery and for promoting the growth of growing animals. More particularly, it relates to a prophylactic or therapeutic composition against swine dysentery which comprises, as effective ingredient(s), one or more compound(s) selected from WS-1627A, WS-1627B, WS-1627C and WS-1627D, or salts thereof, to a use of one or more compound(s) selected from WS-1627A, WS-1627B, WS-1627C and WS-1627D or salt thereof, for the manufacture of a veterinary medicine for preventing or treating swine dysentery, and to a method for preventing or treating swine dysentery by administering an effective amount of said compound(s) to swine suffering from or susceptible to swine dysentery.
Further, it relates to an animal growth promotant composition comprising the same ingredient(s) as mentioned above.
Heretofore, the breeding of swines has been developing in a large scale, swine dysentery has been prevalent and thereby a great deal of damage was done to the swine industry. On the other hand, it has been found from various investigations that the major causative microorganism of swine dysentery is Treponema hyodysenteriae.
Many chemotherapeutic agents and antibiotics have been evaluated for their prophylactic or therapeutic effectiveness against swine dysentery. However, these substances are not satisfactory in respects of their effects, side effects and/or toxicities. For example, the most broadly used synthetic antimicrobial agent for this purpose, carbadox is a strong mutagenic substance.
In the course of screening program for novel prophylactic or therapeutic agents from soil samples, the inventors of the present invention newly found out that four substances obtained from a cultured broth of a newly isolated microorganism, Streptomyces noboritoensis subsp. amamiensis subsp. nov. No. 1627, have strong antimicrobial activities against Treponema hyodysenteriae. Then, these substances were named WS-1627A, WS-1627B, WS-1627C and WS-1627D, respectively.
Further, the inventors of this invention also found out that these substances have an animal growth promoting effect.
The WS-1627A, WS-1627B, WS-1627C and WS-1627D have the following physicochemical properties.
WS-1627A
(a) Appearance: White powder.
(b) Melting point: 104-107.degree. C.
(c) Optical rotation: [.alpha.].sub.D.sup.22 =-125.0.degree. (C=1.0, H.sub.2 O).
(d) Molecular weight: 513 [SIMS:m/z 514 (M.sup.+ +1)].
(e) Elemental analysis (%): C 53.71; H 6.07; N 2.91.
(f) UV absorption spectrum: .lambda..sub.max H.sub.2 O nm (.epsilon.): 300 (sh, 22800), 270 (34800), 214 (46000). .lambda..sub.max 0.1NHCl nm (.epsilon.): 300 (sh, 22500), 270 (34600), 214 (45900). .lambda..sub.max 0.1N NaOH nm (.epsilon.): 323 (sh, 15350), 285 (sh, 25900), 249 (45400), 230 (sh, 41500).
(g) IR absorption spectrum: .nu..sub.max KBr: 3700-3000, 2930, 1720, 1700, 1640, 1610, 1510, 1420, 1360, 1320, 1270, 1250, 1200, 1130, 1100, 1060, 1025, 960, 900, 840, 800 cm.sup.-1.
(h) .sup.1 H NMR absorption spectrum: (D.sub.2 O) (as shown in FIG. 1) .delta. ppm: 212 (6H, s), 3.51 (3H, s), 3.72-3.76 (1H, m), 3.99-4.15 (4H, m), 4.18-4.39 (3H, m), 4.62-4.65 (1H, m), 5.62 (1H, d, J=4.3 Hz), 6.86-6.95 (2H, m), 7.20-7.25 (2H, m).
(i) Solubility: Soluble: Water, methanol. Insoluble: Acetone, ethyl acetate, chloroform.
(j) Color reaction: Positive: Ferric chloride reaction, reaction with cerium sulfate and iodine vapor. Negative: Molish's reaction, Ninhydrin reaction.
(k) Property of substance: Acidic substance.
From the above physicochemical properties and other investigations, it can be judged that the WS-1627A is a known antibiotic, KA-3093 [Cf. Japan Kokai No. 99495/1981].
WS-1627B
(a) Appearance: White powder.
(b) Melting point: 107-110.degree. C.
(c) Optical rotation: [.alpha.].sub.D.sup.20 =-126.5.degree. (C=1.0, H.sub.2 O).
(d) Molecular weight: 511 [SIMS: m/z 512 (M.sup.+ +1)]. (e) Elemental analysis (%): C 53.83; H 5.86; N 2.63.
(f) UV absorption spectrum: .lambda..sub.max H.sub.2 O nm (.epsilon.): 300 (sh, 22700), 270 (34700), 214 (46000). .lambda..sub.max 0.1NHCl nm (.epsilon.): 300 (sh, 22500), 270 (34500), 214 (45800). .lambda..sub.max 0.1NaOH nm (.epsilon.): 323 (15300), 285 (sh, 25800), 249 (45200), 232 (sh, 41400).
(g) IR absorption spectrum: .nu..sub.max KBr: 3700-3000, 2920, 1720, 1700, 1640, 1610, 1510, 1430, 1360, 1320, 1270, 1250, 1210, 1160, 1130, 1100, 1060, 1000, 960, 920, 840, 810 cm.sup.-1.
(h) .sup.1 H NMR absorption spectrum: D.sub.2 O) .delta. ppm: 2.12 (6H, s), 3.80-3.84 (1H, m), 3.95-4.00 (1H, m) 4.17-4.40 (6H, m), 4.49-4.53 (1H, m), 4.80 (1H, s), 5.23 (1H, s), 5.62 (1H, d, J=4.3 Hz), 6.87-6.95 (2H, m), 7.20-7.26 (2H, m).
(i) Solubility: Soluble: Water, methanol. Insoluble: Acetone, ethyl acetate, chloroform.
(j) Color reaction: Positive: Ferric chloride reaction, reaction with cerium sulfate and iodine vapor. Negative: Molish's reaction, Ninhydrin reaction.
(k) Property of substance: Acidic substance.
From the above physicochemical properties and other investigations, it can be judged that the WS-1627B is a known antibiotic, hygromycin [cf. THE MERCK INDEX TENTH EDITION Page 708 (1983)].
WS-1627C
(a) Appearance: White powder.
(b) Melting point: 110-113.degree. C.
(c) Optical rotation: [.alpha.].sub.D.sup.20 =-62.0.degree. (C=1.0, H.sub.2 O).
(d) Molecular weight: 513 [SIMS: m/z 514 (M.sup.+ +1)].
(e) Elemental analysis (%): C 53.65; H 6.33; N 2.95.
(f) UV absorption spectrum: .lambda..sub.max H.sub.2 O nm (.epsilon.): 300 (sh, 22,750), 270 (34,750), 214 (46,000). .lambda..sub.max 0.1NHCl nm (.epsilon.): 300 (sh, 22,500), 270 (34,750), 214 (46,000). .lambda..sub.max 0.1N NaOH nm (.epsilon.): 323 (15,350), 285 (sh, 25,800), 249 (45,200), 232 (sh, 41,400).
(g) IR absorption spectrum: .nu..sub.max KBr: 3700-3000, 2900, 2700, 1720, 1700, 1640, 1600, 1510, 1420, 1350, 1330, 1260, 1250, 1200, 1120, 1100, 1050, 1020, 960, 900, 830, 800 cm.sup.-1.
(h) .sup.1 H NMR absorption spectrum: (CD.sub.3 OD) (as shown in FIG. 2) .delta. ppm: 2.12 (3H, s), 2.21 (3H, s), 3.51 (3H, s), 3.73-3.75 (1H, m), 4.00-4.14 (4H, m), 4.20-4.30 (2H, m), 4.55-4.65 (2H, m), 5.83 (1H, d, J=4 Hz), 6.85-6.94 (2H, m), 7.21-7.25 (2H, m).
(i) Solubility: Soluble: Water, methanol. Insoluble: Acetone, ethyl acetate, chloroform.
(j) Color reaction: Positive: Ferric chloride reaction, reaction with cerium sulfate and iodine vapor. Negative: Molish's reaction, Ninhydrin reaction.
(k) Property of substance: Acidic substance.
From the above physicochemical properties and other investigations, it can be judged that the WS-1627C is a new epimer of KA-3093.
WS-1627D
(a) Appearance: White powder.
(b) Melting point: 114.degree.-117.degree. C.
(c) Optical rotation: [.alpha.].sub.D.sup.20 =-93.1.degree. (C=1.0, H.sub.2 O).
(d) Molecular weight: 511 [m/z 512 (M.sup.+ +1)].
(e) Elemental analysis (%): C 53.91; H 5.82; N 2.80.
(f) UV absorption spectrum: .lambda..sub.max H.sub.2 O nm (.epsilon.): 300 (sh, 22,700), 270 (34,700), 214 (46,000). .lambda..sub.max 0.1NHCl nm (.epsilon.): 300 (sh, 22,500), 270 (34,600), 214 (45,900). .lambda..sub.max 0.1N NaOH nm (.epsilon.): 323 (sh, 15,300), 285 (sh, 25,900), 249 (45,400), 232 (41,400).
(g) IR absorption spectrum: .nu..sub.max.sup.KBr : 3700-3000, 2900, 1720, 1710, 1640, 1620, 1600, 1510, 1430, 1350, 1270, 1250, 1210, 1130, 1100, 1050, 1020, 960, 920, 900, 880, 840, 810 cm.sup.-1.
(h) .sup.1 H NMR absorption spectrum: (CD.sub.3 OD) .delta. ppm: 2.12 (3H, m), 2.21 (3H, s), 3.80-3.82 (1H, m), 3.94-4.00 (1H, m), 4.16-4.29 (4H, m), 4.49-4.59 (2H, m), 4.79 (1H, s), 5.23 (1H, s), 5.82 (1H, d, J=4 Hz), 6.85-6.89 (2H, m), 7.20-7.25 (2H, m).
(i) Solubility: Soluble: Water, methanol. Insoluble: Acetone, ethyl acetate, chloroform.
(j) Color reaction: Positive: Ferric chloride reaction, reaction with cerium sulfate and iodine vapor. Negative: Molish's reaction, Ninhydrin reaction.
(k) Properties of substance: Acidic substance.
From the above physicochemical properties and other investigations, it can be judged that WS-1627D is a known antibiotic, epi-hygromycin [cf. THE JOURNAL OF ANTIBIOTICS VOL. XXXIII Pages 695 (1980)].
From the above data, chemical structures of WS-1627A, WS-1627B, WS-1627C and WS-1627D can be represented as follows. ##STR1##
The WS-1627A, WS-1627B, WS-1627C and WS-1627D can be prepared by culturing a WS-1627A, WS-1627B, WS-1627C and/or WS-1627D-producing strain belonging to the genus Streptomyces in a nutrient medium and recovering the WS-1627A, WS-1627B, WS-1627C and WS-1627D from the cultured broth.
Among a WS-1627A, WS-1627B, WS-1627C and/or WS-1627D-producing strain belonging to the genus Streptomyces, Streptomyces noboritoensis subsp. amamiensis No. 1627 was newly isolated from a soil sample collected at Amami-Oshima, Japan.
Lyophilized samples of the newly isolated Streptomyces noboritoensis subsp. amamiensis No. 1627 have been deposited with an International Depositary Authority on Budapest Treaty, Fermentation Research Institute, Agency of Industrial Science and Technology residing at Yatabe-cho higashi No. 1-1-3, Tsukuba-gun, Ibaraki-ken, Japan, under the number FERM BP-1275(formerly, FERM P-8069) since January 25, 1985.
Further, Streptomyces hygroscopicus IFO 13472 can also produce the WS-1627A, WS-1627B, WS-1627C and WS-1627D in the cultured broth thereof.
It is to be understood that the production of the WS-1627A, WS-1627B, WS-1627C and WS-1627D is not limited to the use of the particular organisms described herein, which are given for illustrative purpose only. This invention also includes the use of any mutants which can be produced from the described organisms by conventional means, such as X-rays, ultra-violet radiation, treatment with N-methyl-N'-nitro-N-nitrosoguanidine, 2-aminopurine and the like.
Streptomyces noboritoensis subsp. amamiensis No. 1627 has the following morphological, cultural and physiological characteristics.
Morphological observations were made with light and electron microscopes from cultures grown at 30.degree. C. for 14 days on yeast-malt extract agar, oatmeal agar and inorganic salts-starch agar. The mature sporophores were formed Rectiflexibiles with more than 30 spores in each chain. Aerial mycelium was poorly developed on some of examined media. The spore surfaces were smooth.
Cultural characteristics were observed on ten kinds of media described by Shirling and Gottlieb [Vide. International Journal of Systematic Bacteriology 16, 313-340 (1966)] and by Waksman [Vide. S. A. Waksman "The Actinomycetes Vol. 2 (1961)]. The incubation was made at 30.degree. C. for 14 days. The color names used in this study were based on Color Standard (Nihon Shikisai Co., Ltd.). Colonies belonged to the gray or red color series when grown on yeast-malt extract agar and inorganic salt-starch agar. Melanoid pigment was produced on tyrosine agar, but not on peptone-yeast extract-iron agar. Soluble pigment was produced in some of examined media. The results are shown in the following Table 1 in comparison with characteristics of Streptomyces noboritoensis IFO 13065.
TABLE 1______________________________________Cultural characteristics of the strain No. 1627and Streptomyces noboritoensis IFO 13065Medium No. 1627 IFO 13065______________________________________Oatmeal agar G Poor to moderate Poor A None None R Dark yellowish Dark yellowish brown brown S Pale yellowish Pale yellow orange brownYeast-malt G Moderate Moderateextract agar A Light gray Gray R Dark brown Reddish brown S Brown BrownInorganic G Moderate Moderatesalts-starch A Pale pinkish white Pale yellow orange,agar cottony powdery R Reddish brown Reddish brown to black S None NoneGlucose- G Moderate Moderateasparagine agar A Grayish white, Grayish white, cottony powdery R Light brown Brown S Pale yellow orange Pale yellow orangeGlycerin- G Moderate Moderateasparagine agar A Light gray Light gray R Reddish brown Dull reddish brown S Pale brown BrownCzapek agar G Poor Poor A None White R Colorless Colorless S None NoneNutrient agar G Poor Poor A None None R Colorless Colorless S None NonePotato-dextrose G Moderate Moderateagar A Gray, poor None R Grayish black Dull red S Brown NoneTyrosine agar G Moderate Moderate A Gray, poor Light gray, poor R Dark gray to Dark brown dark brown S Brown BrownPeptone-yeast G Moderate Moderateextract- A None Noneiron agar R Colorless Colorless S None Brown______________________________________ Abbreviation: G = growth, A = aerial mycelium, R = reverse side color, S = soluble pigment
Cell wall analysis was performed by the methods of Becker et al [Vide. Applied Microbiology 12, 421-423 (1964)] and Yamaguchi [Vide. Journal of Bacteriology 89, 444-453 (1965)]. Analysis of whole cell hydrolysates showed the presence of LL-diaminopimelic acid. Accordingly, the cell wall of this strain is believed to be of type I.
Physiological properties of the strain No. 1627 were determined according to Shirling and Gottlieb [Vide. The same literature as mentioned above]. Temperature range for growth was from 12.degree. C. to 36.degree. C. with optimum temperature from 26.degree. C. to 28.degree. C. Starch hydrolysis, melanin production and gelatin liquefaction were positive. The results are summarized in Table 2 in comparison with characteristics of Streptomyces noboritoensis IFO 13065.
TABLE 2______________________________________Physiological properties of the strain No. 1627and Streptomyces noboritoensis IFO 13065. No. 1627 IFO 13065______________________________________Temperature range for growth 12.degree. C.-36.degree. C. 8.degree. C.-38.degree. C.Optimum temperature 26.degree. C.-28.degree. C. 24.degree. C.-28.degree. C.Nitrate reduction Negative NegativeStarch hydrolysis Positive PositiveMilk coagulation Negative NegativeMi1k peptonization Negative PositiveMelanin production Positive PositiveGelatin liquefaction Positive PositiveH.sub.2 S producticn Negative PositiveNaCl tolerance 7%<-<10% 7%<-<10%______________________________________
Utilization of carbon sources was examined according to the method of Pridham and Gottlieb [Vide. Journal of Bacteriology 56, 107-114 (1948)]. The growth was observed after 14 days incubation at 30.degree. C. Carbon sources utilization of this strain is shown in Table 3 in comparison with those of Streptomyces noboritoensis IFO 13065.
TABLE 3______________________________________Carbon sources utilization of strain No. 1627and Streptomyces noboritoensis IFO 13065.Carbon source No. 1627 IFO 13065______________________________________D-Glucose + +Sucrose + +Glycerin + +D-Xylose + +D-fructose - +Lactose + +Maltose + +Rhamnose - -Raffinose + +D-Galactose + +L-Arabinose + +D-Mannose + +D-Trehalose + +Inositol + -Mannitol - +Inulin - -Cellulose - -Salicin - +Chitin - -Sodium citrate + +Sodium succinate + +Sodium acetate = -______________________________________ Symbols: + = utilization, .+-. = doubtful utilization, - = no utilization
Microscopic studies and cell wall composition analysis indicate that the strain No. 1627 belongs to the genus Streptomyces Waksman and Henrici 1943. Accordingly, a comparison of this strain was made with various Streptomyces species in the light of the published descriptions [Vide. International Journal of Systematic Bacteriology 18, 69-189, 279-392 (1968) and 19, 391-512 (1969), and Bergey's Manual of Determinative Bacteriology 8th Edition (1974)].
As the results of the comparison, the strain No. 1627 was considered to resemble Streptomyces noboritoensis Isono et al. 1957. Therefore, the strain No. 1627 was compared with the corresponding S. noboritoensis IFO 13065.
As the results of comparison, cultural characteristics of the strain No. 1627 are different from those of S. noboritoensis on inorganic salts-starch agar, potato-dextose agar and peptone-yeast extract-iron agar. Milk peptonization and H.sub.2 S production of the strain No. 1627 are negative, but those of S. noboritoensis are positive. In carbon utilization, the strain No. 1627 can utilize inositol, but S. noboritoensis can not utilize it. And, the strain No. 1627 can not utilize D-fructose, mannitol and salicin, but S. noboritoensis can utilize them. As the results of comparison as mentioned above, there are some differences between the strain No. 1627 and S. noboritoensis. However, morphological and cultural characteristics were similar each other on numerous media. Therefore, the strain No. 1627 can be considered to belong to S. noboritoensis. Considering several differences of the strain No. 1627 from S. noboritoensis, it is reasonable that the strain No. 1627 is regarded as new subspecies of S. noboritoensis. Therefore, the strain No. 1627 has been designated as Streptomyces noboritoensis subsp. amamiensis No. 1627.
The WS-1627A, B, C and D can be produced by culturing a WS-1627 A, B, C and/or D producing strain belonging to the genus Streptomyces in a nutrient medium.
In general, the WS-1627A, B, C and D can be produced by culturing the WS-1627A, B, C and/or D producing strain in a nutrient medium containing assimilable sources of carbon and of nitrogen, preferably under aerobic conditions (e.g. shaking culture, submerged culture, etc.).
The preferred sources of carbon in the nutrient medium are carbohydrates such as glucose, fructose, glycerin and starch. Other sources which may be included are lactose, arabinose, xylose, dextrin, molasses and the like.
The preferred sources of nitrogen are yeast extract, peptone, gluten meal, cottonseed meal, soybean meal, corn steep liquor, dried yeast, etc., as well as inorganic and organic nitrogen compounds such as ammonium salts (e.g. ammonium nitrate, ammonium sulphate, ammonium phosphate, etc.), urea, amino acid and the like.
The carbon and nitrogen sources, though advantageously employed in combination, need not be used in their pure form because less pure materials which contain traces of growth factors and considerable quantities of mineral nitrients, are also suitable for use. When desired, there may be added to medium such as mineral salts as calcium carbonate, sodium or potassium phosphate, sodium or potassium iodide, magnesium salt, cobalt chloride and the like. If necessary, especially when the culture medium is foamed remarkably, a defoaming agent such as liquid paraffin, higher alcohol, plant oil, mineral oil and silicones may be added.
As conditions for the production in massive amounts, submerged aerobic cultural condition is preferred for the production of the WS-1627A, B, C and D.
For the production in small amounts, a shaking or surface culture in a flask or bottle is employed. Furthermore, when the growth is carried out in large tanks, it is preferable to use the vegetative form of the organism for inoculation in the production tanks in order to avoid growth lag in the process of production of the object compounds. Accordingly, it is desirable first to produce a vegetative inoculum of the organism by inoculating a relatively small quantity of culture medium with spores or mycelia of the organism and culturing said inoculated medium, and then to transfer the cultured vegetative inoculum aseptically to large tanks. As the medium, in which the vegetative inoculum is produced, there can be used the substantially same as or somewhat different medium from medium utilized for main production of the object compounds.
Agitation and aeration of the culture mixture may be accomplished in a variety of ways. Agitation may be provided by a propeller or the similar mechanical agitation equipment, by revolving or shaking the fermenter, by various pumping equipment or by the passage of sterile air through the medium. Aeration may be effected by passing sterile air through the fermentation mixture.
The fermentation is usually conducted at a temperature about between 20.degree. C. and 40.degree. C., preferably around 30.degree. C., for a period of 50 hours to 100 hours, which may be varied according to the fermentation conditions and scale.
Thus produced WS-1627A, B, C and D can be recovered from the culture medium by conventional means which are commonly used for the recovery of other fermentation products such as antibiotics.
In general, most of the WS-1627A, B, C and D produced are found in the culture filtrate, and accordingly the object compounds can be isolated from the filtrate, which is obtained by filtering or centrifuging the broth, by a conventional method such as concentration under reduced pressure, lyophilization, extraction with a conventional solvent, pH adjustment, treatment with a conventional resin (e.g. anion or cation exchange resin, non-ionic adsorption resin), treatment with a conventional adsorbent (e.g. activated charcoal, silicic acid, silica gel, cellulose, alumina), crystallization, recrystallization and the like.
The WS-1627A, B, C and D can be separated each other and isolated, for example, by subjecting a crude material comprising WS-1627A, B, C and D to a low pressure and high performance liquid chromatography using reverse phase silica gel [e.g. Lichroprep RP-8, RP-18 (trademark, made by E. Merk), .mu.Bondapak C.sub.18 (trademark, made by Waters Associates)].
The WS-1627A, B, C and D as obtained in their free forms may be converted to a salt with inorganic or organic base such as sodium salt, potassium salt, triethylamine salt and the like. The WS-1627A, B, C and D or their salts can orally or parenterally be administered as a prophylactic and therapeutic agent against swine dysentery to swine and as a growth promoting agent to growing animals (e.g. piglet, chick, etc.) in a conventional manner. In cases that the WS-1627A, B, C and D and their salts are orally administered to animals one or more effective ingredient(s) selected from the WS-1627A, B, C, D and their salts may usually be administered as it is or in admixture with a suitable carrier (e.g. water, kaolin, talc, calcium carbonate, lactose, etc.) or in admixture with a feed. More particularly, the effective ingredient(s) may be administered to animals as a drinking water in the form of aqueous solution; or as a tablet, granule or capsule in the form of preparations which comprises the effective ingredient(s) and suitable non-toxic carrier(s) as exemplified above; or as a ration in the form of the composition which comprises the effective ingredient(s) and animal feed.
Further, in cases that the WS-1627A, B, C or D or mixture thereof is parenterally administered to animals, a conventional and suitable injection preparations which comprises the effective ingredient(s) and suitable non-toxic carrier(s) (e.g. water, etc.) can be employed.
In connection of the form of administering the feed composition as mentioned above, the ration comprising one or more effective ingredient(s) selected from the WS-1627A, B, C and D and their salts can be prepared in a conventional manner, namely by admixing the effective ingredient(s) with basal ration.
The dosage of the effective ingredient(s) to animals may be varied over a very wide range depending upon various factors such as kind of animals, growth period, administration route and the like. In general, for the purpose of the treatment of swine dysentery, preferred dosage of the effective ingredients to swine may be selected from the range within 0.1-100 mg/kg/day. Levels of the effective ingredient(s) in the feed and drinking water which are construed as preferably and anticipated to treat the swine dysentery and to promote growth of growing animals may be in an amount between about 1 and about 500 ppm, and 0.5-250 ppm, respectively.
For the purpose of the prophylaxis of swine dysentery, preferred dosage of the effective ingredients to swine may be selected from the range within 0.02-25 mg/kg/day.
Further, in the acute toxicity test, each of five ddy mice (5-week old, male, 20 g in weight), was intraveneously given a single dose of WS-1627A, B, C or D 20 mg (lg/kg) and all survived. During 10 days of observation after injection, no toxic symptom was observed.
The following Tests and Examples are given to illustrate this invention, but it should be understood that they are not intended to limit this invention.
TEST 1.
(In vitro activity of WS-1627A, B, C and D against Treponema hyodysenteriae)
The test organisms were grown anaerobically for 96 hours on Trypticase soy agar plate supplemented with 5% sheep blood. Appropriate amounts of physiological saline solution were poured into each agar plate to make a cell-suspension of test organism, which was finally adjusted at the cell density of 10.sup.6 colony forming units (CFU)/ml. Freshly prepared Trypticase soy agar plates supplemented with 5% sheep blood which were containing serial two-fold dilutions of each of the compounds as mentioned below were inoculated with a loopful (about 5 .mu.l) of the above-mentioned cell-suspension. The MIC (minimum inhibitory concentration) values were determined after 72 hours of anaerobical incubation at 37.degree. C. in Gas Pak jars.
The results are shown in the following table.
TABLE 3______________________________________Stains ofTreponema MIC (.mu.g/ml)hyodysenteriae WS1627A WS1627B WS1627C WS1627D______________________________________ATCC 31212 3.2 <0.8 6.3 <0.8DJ70 1.6 <0.8 3.2 <0.8TH81013 6.4 <0.8 12.8 <0.8S5709 <0.8 <0.8 1.6 <0.8______________________________________
TEST 2.
(Protective effect of the WS-1627A, B, C and D against experimental infection of Treponema hyodysenteriae in mice)
5 week-old mice (ddy, .male.) were used in these experiments. Mice were orally infected with 1.8.times.10.sup.7 cells of Treponema hyodysenteriae S5709 grown for 96 hours on Trypticase soy agar plate supplemented with 5% sheep blood. On the first and second day after challenge, test compounds were given by oral administration once a day. One week after infection, the efficacy of the antibiotics on mice suffering from dysentery was determined as follows. Cecum contents from infected mice were suspended in 2 ml of saline solution, diluted twenty times with Trypticase soy medium supplemented with 5% sheep blood and cultured for T. hyodysenteriae on agar plate of Trypticase soy medium supplemented with 5% sheep blood at 37.degree. C. for 72 hours in Gas Pak jars. The numbers of T. hyodysenteriae colony appeared on the plates were counted. Mice that gave no colony formations of T. hyodysenteriae were regarded as cured mice.
The results are shown in the following table.
TABLE 4______________________________________Test compound andDosage cured/treated______________________________________Vehicle (water) 0/7WS1627A 5 mg/kg 4/7WS1627B 5 mg/kg 7/7WS1627C 5 mg/kg 4/7WS1627D 5 mg/kg 4/7______________________________________

EXAMPLE 1
Preparation of WS-1627 A and C
An aqueous seed medium (80 ml) containing 1% corn starch, 1% glycerin, 0.5% glucose, 1% cotton seed meal, 0.5% dried yeast, 0.5% corn steep liquor, 0.2% calcium carbonate (pH 6.5) into each of ten 250 ml Erlenmeyer flasks and sterilized at 120.degree. C. for 30 minutes. A loopful of Streptomyces noboritoensis subsp. amamiensis No. 1627 on matured slant culture was inoculated to the seed medium. The flasks were shaken on a rotary shaker at 30.degree. C. for 3 days.
An aqueous production medium (18 l) containing 3% starch, 2% sucrose, 0.5% cotton seed meal, 0.5% dried yeast, 0.5% gluten meal, 0.05% magnesium sulfate heptahydrate, 0.05% sodium chloride, 0.0004% cobaltous chloride hexahydrate, 0.00005% sodium iodide, 0.2% calcium carbonate (pH 6.8) was poured into each of two 30 l stainless steel fermenters and sterilized at 120.degree. C. for 30 minutes. The resultant seed culture broth (360 ml) was inoculated to each of the production medium and cultured at 30.degree. C. for 3 days, agitated at 300 rpm and aerated at 20 liters per minute.
The cultured broth (35 l) was filtrated with the aid of diatomaceous earth (500 g). The filtrate (32 l, pH 7.2) was passed through a column of activated charcoal (3.2 l). The column was washed with water (7 l) and eluted with 60% aqueous acetone (15 l). The eluate was concentrated to a volume of 1 liter under reduced pressure. The concentrate was chromatographed on CM-Sephadex C-25 (H.sup.+, made by Pharmacia Fine Chemicals A B) column (2 l). The column was developed with water. The active fraction (4 l) was concentrated under reduced pressure. The residue was chromatographed on a column (200 ml) of silica gel using saturated aqueous n-butanol as developing solvent. The active fraction (320 ml) was combined and concentrated to a volume of 50 ml under reduced pressure. The resultant solution was chromatographed on a column (50 ml) of nonionic adsorption resin, HP-20 (trademark, made by Mitsubishi Chemical Industries Ltd.) to remove the silica gel. The column was washed with water (200 ml) and 20% aqueous methanol (200 ml) and then eluted with 40% aqueous methanol (250 ml). The eluate was concentrated under reduced pressure and the resultant solution was freeze-dried to give a pale yellow powder (900 mg).
The crude powder was dissolved in 30% aqueous methanol (9 ml) and applied to a column of low pressure liquid chromatography using reverse phase silica gel [Lichroprep RP-8 (trademark) made by E. Merck, size B: 310.times.25 mm, 40-63 .mu.m, detected by UV absorbance at 254 nm, flow rate 10 ml/min] with 30% aqueous methanol. The first fractions (from 220 ml to 290 ml) were collected and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (Powder I, 150 mg) containing WS-1627A and WS-1627C. The continuous fractions (from 310 ml to 360 ml) were collected and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (Powder II, 12.7 mg) containing WS-1627B and WS-1627D. The powder I (140 mg) was further purified, in seven separate runs, using a high performance liquid chromatography. Each portion (20 mg) of the starting charge was dissolved in 20% aqueous methanol (0.2 ml) and applied to a column of reverse phase silica gel (.mu.Bondapak C.sub.18 (trademark) made by Waters Associates, 7.8.times.30 mm, 8-10 .mu.m, detected by UV absorbance at 254 nm, flow rate 2.5 ml/min) with 20% aqueous methanol. The first fractions (from 45 ml to 50 ml) of each of the seven chromatographic separation were combined and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (15.8 mg) of WS-1627C. The continuous fractions (from 52 ml to 60 ml) of each of the seven chromatographic separations were combined and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (117 mg) of WS-1627A.
EXAMPLE 2
Preparation of WS-1627B and D
An aqueous seed medium (160 ml) containing 1% corn starch, 1% glycerin, 0.5% glucose, 1% cotton seed meal, 0.5% dried yeast, 0.5% corn steep liquor, 0.2% calcium carbonate (pH 6.5) into each of twenty three 500 ml Erlenmeyer flasks and sterilized at 120.degree. C. for 30 minutes. A loopful of Streptomyces noboritoensis subsp. amamiensis No. 1627 on matured slant culture was inoculated to the seed medium. The flasks were shaken on a rotary shaker at 30.degree. C. for 3 days. An aqueous production medium (180 l) containing 3% starch, 2% glycerin, 0.5% soy bean meal, 2% gluten meal, 0.05% magnesium sulfate heptahydrate, 0.05% sodium chloride, 0.0004% cobaltous chloride hexahydrate, 0.00005% sodium iodide, 0.2% calcium carbonate (pH 6.8) was poured into a 200 l stainless steel fermenter and sterilized at 120.degree. C. for minutes. The resultant seed culture broth (3.6 l) was inoculated to the production medium and cultured at 30.degree. C. for 4 days, agitated at 250 rpm and aerated at 20 liters per minute.
The culture broth (180 l) was filtrated with the aid of diatomaceous earth (2.5 kg). The filtrate (170 l, pH 7.2) was passed through a column (15 l) of activated charcoal. The column was washed with water (60 l) and 20% aqueous acetone (60 l) and then eluted with 60% aqueous acetone (75 l). The eluate was concentrated to a volume of 17 liters under reduced pressure. The concentrate was chromatographed on a column (4 l) of CM-Sephadex C-25 (H.sup.+). The column was developed with water. The activated fractions (3 l) was combined and concentrated under reduced pressure. The residue was chromatographed on a column (200 ml) of silica gel using saturated aqueous n-butanol as developing solvent. The active fractions were combined and concentrated to a volume of 100 ml under reduced pressure. The resultant solution was chromatographed on a column of HP-20 (200 ml) to remove the silica gel. The column was washed with water (800 ml) and 20% aqueous methanol (1200 ml) and then eluted with 40% aqueous methanol (1200 ml). The eluate was freeze-dried to give a pale yellow powder (3.62 g).
The crude powder was dissolved in 30% aqueous methanol (36 ml) and applied to a column of low pressure liquid chromatography using reverse phase silica gel [Lichroprep RP-8 (trademark) made by E. Merck, size B: 310.times.25 mm, 40-63 .mu.m, detected by UV absorbance at 254 nm, flow rate 10 ml/min] with 30% aqueous methanol, in four separate runs. The first fractions (from 250 ml to 275 ml) of each of the four chromatographic separations were combined and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (Powder I, 108 mg) containing WS-1627A and WS-1627C. The continuous fractions (from 285 ml to 370 ml) of each of the four chromatographic separations were combined and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (Powder II, 2.07 g) containing WS-1627B and WS-1627D. The powder II (500 mg) was further purificated, in twenty five separated runs, using a high performance liquid chromatography. Each portion (20 mg) of the starting charge was dissolved in 20% aqueous methanol (0.2 ml) and applied to a column of reverse phase silica gel (.mu.Bondapak C.sub.18 (trademark) made by Waters Associates, 7.8.times.30 mm, 8.times.10 .mu.m, detected by UV absorbance at 254 nm, flow rate 2.5 ml/min) with 20% aqueous methanol. The first fractions (from 83 ml to 88 ml) of each of the twenty five chromatographic separations were combined and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (350 mg) of WS-1627D. The continuous fractions (from 93 ml to 100 ml) of each of twenty five chromatographic separations were combined and concentrated under reduced pressure. The resultant solution was freeze-dried to give a white powder (407 mg) of WS-1627B.
EXAMPLE 3
Preparation of WS-1627A, B, C and D
The WS-1627A, B, C and D were prepared in substantially the same manner as those of Example 1 and 2 except using Streptomyces hygroscopicus IFO 13472 in place of Streptomyces noboritoensis subsp. amamiensis No. 1627.
EXAMPLE 4
Therapeutic effect on experimentally induced swine dysentery
Seven piglets, LW (Landace.times.Large White crossbred) male, were used. The initial body weight at the time of inoculation of infective materials ranged from 6.5 to 8.5 kg. Piglets were divided into 4 groups (2 groups of 2 heads and 1 group of 1 head) and were maintained in stainless cages (90.times.90 cm) with raised plastic net floors at 28.+-.2.degree. C. Feed [Milk replacer for piglet] and water were supplied ad libitum except the duration of fasting. Infective materials used were prepared as follows. A total of 300 g of mucous haemorrhagic feces, large intestinal (from caecum through rectum) contents, and mucosa obtained from a clinically affected pig (3 days after onset of swine dysentery), which was previously inoculated into its caecum with pure culture of Treponema hyodysenteriae ATCC31212 (about 3.times.10.sup.9 colony forming units/head) by surgical operation, were suspended, diluted finally 2.5 times with phosphate-bufferized saline and minced by biotron homogenizer (trademark, made by Biotrona Co., Ltd.).
For the purpose of infection, all piglets were inoculated individually with about 90 g of the infective materials after 22 hours' fasting.
All of those showed the clinical sign (watery and/or mucous haemorrhagic diarrhea) within 4 days after inoculation.
Treatment were done once a day for 2 consecutive days from the 5th day post inoculation.
The results are shown in the following Table.
TABLE 5______________________________________ No. (average) days of (average) days ofVeterinary of recovery to disappearance**medicine pig normal stool of fecal T. h***______________________________________Vehicle* 2 >5 >5(Sterile water, orally1 ml/kg bodyweight .times. 2 day)WS1627 B 2 2 2(Solution in water,orally 2.5 mg/kgbody weight .times. 2 day)WS1627 B 1 1 1(Solution in water,intramuscularly10 mg/kg bodyweight .times. 2 day)______________________________________ *Vehicle treatment means an infected, nonmedicated group. **Disappearance means the fecal treponemal number less than detection limit (10.sup.2 colonyforming units/g of feces). ***T. h is the abbreviation of Treponema hyodysenteriae.
EXAMPLE 5
Growth promoting effect
Five sets of 24 pigs (33 days-old, LWD strain) were used. Each 24 pigs were divided into 4 groups, i.e. 3 treatment groups and a control group. Each group consisted of 3 barrows and 3 female pigs. They were fed continuously with the feed described in Table 6. Their body weight and feed consumption were observed for 6 weeks. The results are shown in Table 7.
TABLE 6-(a)______________________________________Basal ration IIngredient %______________________________________Yellow maize 63Wheat flour 8Defatted Soybean meal 16Skim milk 5Fish meal 3Vegetable oil 1.5Tricalcium phosphate 0.8Calcium carbonate 1.2Sodium chloride 0.4Zeolite 1Nutritious premix* 0.1______________________________________ *Note: The premix is composed of Vitamin A, D.sub.3, E, B.sub.1, B.sub.2, B.sub.6, B.sub.12, nicotinic acid, Pantothenic acid, biotin, choline, lysine, methionine, zinc carbonate, calcium iodate, cobalt sulfate, ferri sulfate, cupric sulfate, manganese sulfate, ferrous fumarate, ethoxiquin and saccharin
TABLE 6-(b)______________________________________Feed composition fed to animals______________________________________Feed Composition fed The above basal ration Ito Control groupFeed Composition fed The above basal ration I +to Treatment group I WS-1627B 10 ppmFeed Composition fed The above basal ration I +to Treatment group II WS-1627B 20 ppmFeed Composition fed The above basal ration I +to Treatment group III WS-1627B 40 ppm______________________________________
TABLE 7______________________________________ Control Treatment group group I II III______________________________________Average initial body 10.0 10.0 10.0 10.0weight (kg)Average final bodyweight (kg) at the6th week after the 28.0 29.6 29.2 28.9starting of thefeedingAverage body weightgain (kg) at the 18.0 19.6 19.2 18.96th week after thefeedingEfficiency of 2.19 2.05 2.11 2.09feed utilization*______________________________________ *Note: ##STR2##
EXAMPLE 6
Growth promoting effect
8-Days-old male broiler chickens (chunky) were divided into 3 groups i.e. 2 treatment groups and a control group, each group of which consisted of 10 chicks. They were fed continuously with the feed described in Table 8. Their body weight and feed consumption were observed for one week. The results are shown in Table 9.
TABLE 8-(a)______________________________________Basal ration IIIngredient %______________________________________Sucrose 55.7Soybean oil meal 29.3Alfalfa meal 2.0white fish meal 8.0Animal fat 3.2Calcium carbonate 0.3Calcium phosphate 0.7Salt 0.2DL-methionine 0.15Choline hydrochloride 0.05Vitamin premix*.sup.1 0.2Mineral premix*.sup.2 0.2______________________________________ Note: *.sup.1 Vitamin premix is composed of Vitamin A, B.sub.1, B.sub.2, B.sub.6, B.sub.12, D.sub.3 and E, biotin, folic acid and calcium pantothenate. *.sup.2 Mineral premix is composed of ferrous sulfate, manganese sulfate, zinc sulfate, cupric sulfate, cobalt sulfate and potassium iodide.
TABLE 8-(b)______________________________________Feed composition fed to animals______________________________________Feed composition fed The above Basal ration IIto Control groupFeed composition fed The above Basal ration II +to Treatment group I WS-1627 B 10 ppmFeed composition fed The above Basal ration II +to Treatment group II WS-1627 B 50 ppm______________________________________
TABLE 9______________________________________ Treatment Control group group I II______________________________________Average initial body 88.5 88 88weight gain (g)Average final bodyweight (g) at one 183.8 204.5 209week after thefeedingAverage body weightgain (g) at one week 95.3 116.5 121after the feedingEfficiency of feed 2.02 2.00 1.67utilization*______________________________________ *Note: ##STR3##
EXAMPLE 7
Injection Preparation
Some sterile samples of WS-1627B are distributed into vials, thereby containing 100 mg of the active ingredient. The vials are sealed hermetically to exclude bacteria. Whenever the vials are required for use, 2 ml of sterile distilled water for injection is added to the vial and the vial is subjected to administration.
TABLE 10______________________________________Example 8 [Feed preparation]Ingredient______________________________________Skim milk 270 kgDried whey 100 kgfish meal 50 kgWheat flour 350 kgGlucose 50 kgTallow 30 kgDried yeast 100 kgStarch 21 kgCasein sodium 10 kgTricalcium phosphate 10 kgSodium chloride 4 kgDL-Methionine 500 gLysine hydrochloride 1 kgVitamin A D E premix 2 kgVitamin B premix*.sup.1 2 kgTrace mineral premix*.sup.2 1 kgWS-1627 B 100 g______________________________________ Note: *.sup.1 Vitamin B premix is composed of vitamin B.sub.1, vitamin B.sub.2, vitamin B.sub.6, vitamin B.sub.12, biotin, folic acid and calcium pantothenate. *.sup.2 Trace mineral premix is composed of ferrous sulphate, manganese sulphate, zinc sulphate, cupric sulphate, cobalt sulphate and potassium iodide.

Prophylactic and therapeutic agent against swine dysentery

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