Patent Grant
8470579
The present invention relates to novel strains of lactic acid bacteria that are effective in preventing necrotizing enterocolitis.
Necrotizing enterocolitis (NEC), occurring most often in preterm infants, is a common gastrointestinal disorder with high mortality rate. About 12% of babies weighing less than 3 lbs.-5 oz. (1,500 grams) experience NEC. The symptoms of NEC include poor tolerance to feedings, weight loss, abdominal distention, bloody stools, peritonitis, sepsis, and shock, and severe cases of NEC cause death. Risk factors including prematurity (Wilson R et al., Am J Dis Child 136: 814-816, 1982), hypoxia (Kliegman R M, J Pediatr 117: S2-S5, 1990), intestinal ischemia (Abanese C T et al., Semin Pediatr Surg 4: 200-206, 1995), bacterial infection (Scheifele D W, J Pediatr 117: S44 S46, 1990), and formula feeding (Go L L et al., J Pediatr Surg 29: 1059-1063, 1994) have been implicated in the pathogenesis of NEC. However, it is not clear exactly what causes NEC.
Treatments for NEC include stopping feedings, supportive therapies, antibiotics for infection, surgery, and etc. However, the risks of surgery for preterm newborns are high and treatment with antibiotics although inhibits the growth of pathogenic bacteria in the gut, but on the other hand hurts other beneficial bacteria, destroying the equilibrium between bacterial species. Therefore, a safe and effective pharmaceutical or dietary composition for prevention or treatment of necrotizing enterocolitis is desired.
The present invention relates to novel strains of lactic acid bacteria, Lactobacillus plantarum subsp. plantarum PM-A0087 deposited as NRRL accession number B-50523, Bifidobacterium longum PM-A0101 deposited as NRRL accession number B-50525, and Bifidobacterium bifidum PM-A0218 deposited as NRRL accession number B-50524.
In one aspect, the present invention provides biologically pure culture of a strain of lactic acid bacteria selected from the group consisting of Lactobacillus plantarum subsp. plantarum PM-A0087 deposited as NRRL accession number B-50523, Bifidobacterium longum PM-A0101 deposited as NRRL accession number B-50525, and Bifidobacterium bifidum PM-A0218 deposited as NRRL accession number B-50524.
In another aspect, the present invention is based on the unexpected finding that either or combination of the strains of lactic acid bacteria according to the invention, including Lactobacillus plantarum subsp. plantarum PM-A0087, Bifidobacterium longum FM-A0101, and Bifidobacterium bifidum PM-A0218, is beneficial for maintaining the intestinal health of preterm infants via oral administration, and effective in prevention of the occurrence of necrotizing enterocolitis (NEC).
Accordingly, the present invention provides a composition for preventing necrotizing enterocolitis (NEC), comprising a biologically pure culture of Lactobacillus plantarum subsp. plantarum PM-A0087, Bifidobacterium longum PM-A0101, Bifidobacterium bifidum PM-A0218, or a combination thereof, in an amount effective in preventing NEC. In one example of the present invention, the composition is a pharmaceutical composition or a dietary composition.
In one embodiment of the invention, the composition comprises a biologically pure culture of Lactobacillus plantarum subsp. plantarum PM-A0087, a biologically pure culture of Bifidobacterium longum PM-A0101, and a biologically pure culture of Bifidobacterium bifidum PM A0218, wherein the bacterial numbers of these strains are in a ratio of 1:1:1.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawings will be provided by the Office upon request and payment of the necessary fee.
For the purpose of illustrating the invention, there are shown in the drawings embodiments which are presently preferred. It should be understood, however, that the invention is not limited to the preferred embodiments shown.
In the drawings:
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by a person skilled in the art to which this invention belongs. All publications mentioned herein are incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited.
As used herein, the singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a sample” includes a plurality of such samples and equivalents thereof known to those skilled in the art.
In one aspect, the present invention provides a biological pure culture of one strain of lactic acid bacteria selected from the group consisting of Lactobacillus plantarum subsp. plantarum PM-A0087 (the “PM-A0087 strain”), Bifidobacterium longum PM-A0101 (the “PM-A0101 strain”), and Bifidobacterium bifidum PM-A0218 (the “PM-A0218 strain”).
The three lactic bacteria strains, including the PM-A0087 strain, the PM-A0101 strain and the PM-A0218 strain, were deposited under the Budapest Treaty on Jul. 15, 2011 with an International Depositary Authority, the Agricultural Research Culture Collection (NRRL) at 1815 N. University Street, Peoria, Ill., 61601, U.S.A., and have been assigned NRRL accession numbers B-50523, B-50525, and B-50524, respectively.
According to the present invention, it was unexpectedly found that the PM-A0087 strain, the PM-A0101 strain and the PM-A0218 strain are effective in preventing necrotizing enterocolitis (NEC).
Another aspect of the present invention thus provides a composition for preventing necrotizing enterocolitis (NEC), comprising a biologically pure culture of Lactobacillus plantarum subsp. plantarum PM-A0087. Bifidobacterium longum PM-A0101, Bifidobacterium bifidum PM-A0218, or a combination thereof, in an amount effective in preventing NEC.
The term “necrotizing enterocolitis (NEC)” as used herein refers to a disorder with acute partial or chronic intestinal ulcer that causes intestinal tissue necrosis, occurring most often in preterm infants.
According to the present invention, the Lactobacillus plantarum subsp. plantarum PM-A0087 was isolated by screening from a fermentation plant, e.g., a pickled vegetable, or kimchi. The microbiological characteristics of the PM-A0087 strain are shown below:
(1) Morphological Characteristics:
(2) Cultural Characteristics:
(3) Physiological Characteristics:
The Lactobacillus plantarum subsp. plantarum PM-A0087 was deposited under the Budapest Treaty on Jul. 15, 2011 with the Agricultural Research Culture Collection (NRRL) and has been assigned NRRL accession number B-50523.
According to the present invention, the Bifidobacterium longum strain Bifidobacterium longum PM-A0101 was isolated by screening from newborn infant feces. The microbiological characteristics of the PM-A0101 strain are shown below:
(1) Morphological Characteristics:
(2) Cultural Characteristics:
(3) Physiological Characteristics:
The Bifidobacterium longum PM-A0101 was deposited under the Budapest Treaty on Jul. 15, 2011 with the Agricultural Research Culture Collection (NRRL) and has been assigned NRRL accession number B-50525.
According to the present invention, the Bifidobacterium bifidum strain Bifidobacterium bifidum PM-A0218 was isolated by screening from newborn infant feces. The microbiological characteristics of the PM-A0218 strain are shown below:
(1) Morphological Characteristics:
(2) Cultural Characteristics:
(3) Physiological Characteristics:
The Bifidobacterium bifidum PM-A0218 was deposited under the Budapest Treaty on Jul. 15, 2011 with the Agricultural Research Culture Collection (NRRL) and has been assigned NRRL accession number B-50524.
The present invention provides a composition for preventing NEC. The composition of the present invention may comprise a biologically pure culture of the PM-A0087 strain, a biologically pure culture of the PM-A0101 strain and a biologically pure culture of the PM-A0218 strain, wherein the bacterial numbers or colony-forming units (CFUs) of these strains are in an appropriate ratio providing a good efficacy in preventing NEC. In one example of the invention, the bacterial numbers of these three strains are preferably in a ratio of 1:1:1, or the composition contains 0.1-10×109 CFU/ml of each strain.
In one preferred embodiment of the present invention, the composition comprises a biologically pure culture of the PM-A0087 strain, a biologically pure culture of the PM-A0101 strain and a biologically pure culture of the PM-A0218 strain, wherein the bacterial numbers of these strains are in a ratio of 1:1:1, or the composition contains about 1×109 CFU/ml of each strain.
In another embodiment, the composition according to the present invention comprises a biologically pure culture of the PM-A0087 strain, a biologically pure culture of the PM-A0101 strain and a biologically pure culture of the PM-A0218 strain, in a ratio of 1:1:1, wherein each strain is of about 1.5×109 CFU/ml bacteria.
According to one embodiment of the present invention, the composition may be administered orally and formulated as any appropriate forms. The composition can be manufactured as food, a drink or a medicament. In addition, a variety of additives can be included. Examples of additives include but are not limited to colorings (e.g., beta-carotene, anatto, tumeric, paprika and FD & C dyes); flavors, aromas, sweeteners; emulsifiers and/or thickening agents; preservatives, vitamins and antioxidants (e.g., vitamins A, C, D, E, B-1, B-5, B-6, zinc, selenium, calcium, alpha-tocopherol, glutathione, butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), and cysteine).
In one embodiment of the present invention, the composition is a pharmaceutical composition comprising a biologically pure culture of the PM-A0087 strain, a biologically pure culture of the PM-A0101 strain, a biologically pure culture of the PM-A0218 strain, or a combination thereof, and a pharmaceutically acceptable carrier. The term “pharmaceutically acceptable carrier” as used herein includes, but is not limited to: saline, buffered saline, dextrose, water, glycerol, ethanol or combination thereof.
In another embodiment of the invention, the composition is a dietary composition comprising a biologically pure culture of the PM-A0087 strain, a biologically pure culture of the PM-A0101 strain, a biologically pure culture of the PM-A0218 strain, or a combination thereof. The dietary composition may be in the form of milk, fermented dairy product, drink, sports drink, a nutritional additive, health food, candy, or jelly.
The present invention is further illustrated by the following examples, which are provided for the purpose of demonstration rather than limitation.
Lactobacillus plantarum subsp. plantarum PM-A0087
Kimchi sample was added to the following medium:
(1) MRS− anaerobic: to isolate anaerobic or facultative Lactobacillus.
(2) MRS− aerobic: to isolate aerobic Enterococus.
(3) MRS+ Cysteine-anaerobic: to isolate anaerobic or facultative Bifidobacterium.
(4) LBS− anaerobic: to isolate anaerobic or facultative Lactobacillus.
(5) LBS+ acetic acid-anaerobic: to isolate anaerobic or facultative Lactobacillus.
(6) TS− aerobic: to isolate aerobic bacillus.
(7) LB− aerobic: to isolate E. coli.
(8) BCP− anaerobic: to isolate blue colony non-lactic acid bacteria.
(9) BCP− aerobic: to isolate yellow colony lactic acid bacteria.
The isolation was carried out by performing a four quadrant streak plate method.
The MRS medium contains (final pH 6.5±0.2):
10.0 g of proteose peptone,
10.0 g of beef extract,
5.0 g of yeast extract,
20.0 of glucose,
1.0 g of sorbitan monooleate (Tween 80),
2.0 g of ammonium citrate,
5.0 g of sodium acetate,
0.1 g of magnesium sulfate,
0.05 g of manganese (II) sulfate,
2.0 g of dipotassium hydrogen phosphate,
15 g of agar, and
1000 mL of distilled/de-ionized water.
A picture of the isolated bacteria under microscope is shown in
Bifidobacterium longum PM-A0101
The sample of newborn infant feces was used and followed the same isolation procedure as described above.
A picture of the isolated bacteria under microscope is shown in
Bifidobacterium bifidum PM-A0218
The sample of newborn infant feces was used and the strain was isolated following the procedures as described above.
The picture of the isolated bacteria under microscope is shown in
Preparation of the Cultures of the Strains
Lactobacillus plantarum subsp. plantarum PM-A0087 was cultured in MRS medium at 37° C. Bifidobacterium longum PM-A0101 and Bifidobacterium bifidum PM-A0218 were cultured in MRS medium supplemented with 5% Cysteine at 37° C. in anaerobic condition. After a culture for 3 days, the cells of each strain in the bacterial culture tube were dispersed thoroughly and subjected to optical density (OD) measurement to evaluate the number of bacteria. Then, each of the cultures was adjusted to 1.5×109 CFU/ml, and 1 ml of the culture was taken and centrifuged at 3,000 rpm for 10 minutes. The supernatant was removed, and refrigerated at 4° C. for 30 minutes, and then moved for storage at −20° C. Before feeding the animals, the cultures of Lactobacillus plantarum subsp. plantarum PM-A0087, Bifidobacterium longum PM-A0101, and Bifidobacterium bifidum PM-A0218 were removed from the −20° C. refrigerator and mixed with 1 mL milk.
Preparation of the NEC Pathogenic Composition
Single colonies of Klebsiella pneumonia, Serratia marcescens, and Escherichia coli were added to 5 mL normal saline, respectively, mixed in 2:2:3, aliquoted into 1.5 mL centrifuge tubes, and stored at 4° C. before use.
Animal Model
Time-dated pregnant Sprague-Dawley rats were anesthetized with CO2 anesthesia (50 seconds) on the 21st day of gestation and delivered via abdominal incision. Newborn rats were collected and placed in a neonatal incubator for humidification and temperature control. Animals were randomly divided into experimental group and control group. At 3 hours of life, animals were fed with 50 μl of the NEC pathogenic composition. At 6 hours of life, animals were fed with 50 μl of milk, or 50 μl of milk comprising any one of the three lactic bacterial strains. Then animals were stressed with asphyxia twice daily by breathing 100% nitrogen gas for 60 seconds and then cold exposure to 4° C. for 10 minutes. At 9 hours of life, animals were fed with 50 μl of the NEC pathogenic composition, and at 12 hours Of life, animals were fed with 50 μl of milk, or 50 μl of milk comprising any one of the three lactic bacterial strains. By the 24 hours of life, animals developed clinical and pathological signs similar to neonatal NEC, e.g. bloody stools, shortness of breath, poor tolerance to feedings, and weight loss.
Upon death of the newborn rats, the small intestine and colon were collected and fixed; histological sections were prepared and subjected to evaluation of the degree of intestinal necrosis.
Results
As shown in
Lactobacillus plantarum
Bifidobacterium longum
Bifidobacterium bifidum
Bifidobacterium longum
Bifidobacterium bifidum
Lactobacillus plantarum
longum PM-A0101 and
Bifidobacterium bifidum
The results were subject to nonparametric Mann-Whitney test using SPSS 12.0 (p-value<0.05 indicates statistical significance, see Table 2 below).
Lactobacillus plantarum
Bifidobacterium longum PM-
Bifidobacterium bifidum PM-
Bifidobacterium longum PM-
bifidum PM-A0218)
Lactobacillus plantarum
Bifidobacterium longum PM-
bifidum PM-A0218)
As shown in Table 1, Table 2 and
It was concluded that the composition comprising each of the strains of the invention or their combination is effective in preventing NEC.
It is believed that a person of ordinary knowledge in the art where the present invention belongs can utilize the present invention to its broadest scope based on the descriptions herein with no need of further illustration. Therefore, the descriptions and claims as provided should be understood as of demonstrative purpose instead of limitative in any way to the scope of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 100117110 A | May 2011 | TW | national |
| Number | Date | Country | |
|---|---|---|---|
| 20120294833 A1 | Nov 2012 | US |
