Lactic acid bacterial composition for treating or preventing jaundice

Abstract

The present invention provides a lactic acid bacterial composition for inhibiting the activity of Escherichia coli and/or treating or preventing jaundice, the composition including: a Bifidobacterium animalis subsp. lactis CP-9 strain and a Lactobacillus salivarius subsp. salicinius AP-32 strain. The present invention further provides a method for inhibiting growth of Escherichia coli, the method including the step(s) of: administering the foregoing lactic acid bacterial composition to a subject in need thereof. The present invention additionally provides a method for treating or preventing jaundice, the method including the step(s) of: administering the foregoing lactic acid bacterial composition to a subject in need thereof.

Claims

1. A method for treating jaundice, comprising: administering a lactic acid bacterial composition to a subject in need thereof; and performing phototherapy on the subject; wherein the lactic acid bacterial composition comprises: a Bifidobacterium animalis subsp. lactis CP-9 strain and a Lactobacillus salivarius subsp. salicinius AP-32 strain; wherein the CP-9 strain is deposited at the China Center for Type Culture Collection with accession number: CCTCC M2014588 and the AP-32 strain is deposited at the China Center for Type Culture Collection with accession number: CCTCC M2011127; wherein a CFU ratio of the CP-9 strain and the AP-32 strain is 1:1 to 9:1; wherein the jaundice is jaundice derived from urinary tract infection caused by Escherichia coli.

2. The method as claimed in claim 1, wherein, a CFU ratio of the CP-9 strain and the AP-32 strain is 1:1.

3. The method as claimed in claim 1, wherein the phototherapy is performed on the subject before, during, and/or after the composition administering step.

4. The method as claimed in claim 1, wherein a CFU ratio of the CP-9 strain and the AP-32 strain is 9:1.

5. The method as claimed in claim 2, wherein the phototherapy is performed on the subject before, during, and/or after the composition administering step.

6. The method as claimed in claim 4, wherein the phototherapy is performed on the subject before, during, and/or after the composition administering step.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1A is a bar graph illustrating the effect of different Bifidobacterium animalis subsp. lactis stains on the growth of Escherichia coli;

(2) FIG. 1B is a bar graph illustrating the effect of different Lactobacillus salivarius subsp. salicinius stains on the growth of Escherichia coli;

(3) FIG. 1C is a bar graph illustrating the effect of different mixing ratios of Bifidobacterium animalis subsp. lactis CP-9 strains and Lactobacillus salivarius subsp. salicinius AP-32 strains on the growth of Escherichia coli;

(4) FIG. 1D is a bar graph illustrating the effect of various bacterial compositions on the growth of Escherichia coli;

(5) FIG. 2 is a bar graph illustrating the effect of administration of different lactic acid bacterial strains in conjugation with phototherapy on the icteric indices; and

(6) FIG. 3 is a bar graph illustrating the effect of administration of different lactic acid bacterial strains in conjugation with phototherapy on the total irradiation hours.

DETAILED DESCRIPTION OF THE INVENTION

(7) The detailed description and preferred embodiments of the invention will be set forth in the following content, and provided for people skilled in the art to understand the characteristics of the invention.

(8) Each lactic acid bacterial strain according to the present invention is deposited at the Food Industry Research and Development Institute in No. 331 Shih-Pin Road, Hsinchu, Taiwan and at the China Center for Type Culture Collection in Wuhan University, Wuhan City, China in the form of freeze-dried culture. The deposition information is listed in Table 1 below.

(9) TABLE-US-00001 TABLE 1 Deposition Information Accession Deposition Strain Classification Related Patent Number Date CP-9 Bifidobacterium Taiwan Invention BCRC Aug. 21, 2014 animalis Patent No. 910645 subsp. lactis 1572713 China Invention CCTCC Nov. 24, 2014 Patent No. M2014588 CN105985918B AP- Lactobacillus Taiwan Invention BCRC Jul. 30, 2009 32 salivarius Patent No. 910437 subsp. salicinius 1384990 China Invention CCTCC Apr. 10, 2011 Patent No. M2011127 CN102835666B

(10) It is found in the present invention that a Bifidobacterium animalis subsp. lactis CP-9 strain and a Lactobacillus salivarius subsp. salicinius AP-32 strain can inhibit the growth of enteropathogenic Escherichia coli, which can produce β-glucuronidase, so that the icteric index and the irradiation hours both can decrease. Especially, the combination of these bacterial strains can bring a synergistic effect on the inhibition of the Escherichia coli growth. Therefore, these bacterial strains can be used for inhibiting the activity of Escherichia coli and/or treating or preventing jaundice, alone or together.

(11) An embodiment of the present invention discloses a lactic acid bacterial composition. The composition can inhibit the activity of Escherichia coli and/or treat or prevent jaundice, and comprises: a Bifidobacterium animalis subsp. lactis CP-9 strain or a Lactobacillus salivarius subsp. salicinius AP-32 strain. Preferably, the composition comprises: the Bifidobacterium animalis subsp. lactis CP-9 strain and the Lactobacillus salivarius subsp. salicinius AP-32 strain. Preferably, the composition is a food composition or a pharmaceutical composition. Preferably, the composition additionally comprises: a physiologically acceptable excipient, diluent, or carrier.

(12) On the condition that the composition is a food composition, the physiologically acceptable excipient, diluent, or carrier is an edible acceptable excipient, diluent, or carrier, and an example thereof is a food, but not limited thereto. The food may be a fluid milk product (e.g., a milk or an evaporated milk), a fermented milk product (e.g., a fermented milk), a milk powder, an ice cream, a cheese, a soy milk, a fermented soy milk, a vegetable juice, a fruit juice, a sports drink, a jelly, a cookie, an energy bar, a healthy food, an animal feed, or a dietary supplement, but not limited thereto.

(13) On the condition that the composition is a pharmaceutical composition, the physiologically acceptable excipient, diluent, or carrier is a pharmaceutically acceptable excipient, diluent, or carrier and an example thereof is a solution, a buffer, an emulsifier, a suspension agent, a decomposing agent, a disintegrant, a dispersant, a binder, a stabilizer, a chelation agent, a gelling agent, a humectant, a lubricant, an absorption delaying agent, and a liposome, but not limited thereto. The composition may be in the oral dosage form or the parenteral dosage form. An example of the oral dosage form is a powder, a lozenge, a tablet, a troche, a pill, a capsule, a solution, a suspension, an emulsion, a syrup, an elixir, a thick paste, or a drop, but not limited thereto; an example of the parenteral dosage form is a liquid, but not limited thereto. The term “parenteral dosage form” used in the present content comprises: a subcutaneous dosage form, an intramuscular dosage form, an intravertebral dosage form, an intravenous dosage form, or a sublingual dosage form, but not limited thereto.

(14) The Bifidobacterium animalis subsp. lactis CP-9 strain and the Lactobacillus salivarius subsp. salicinius AP-32 strain may be separately be a viable bacterial strain or a deactivated bacterial strain. On the condition that the composition comprises: the Bifidobacterium animalis subsp. lactis CP-9 strain and the Lactobacillus salivarius subsp. salicinius AP-32 strain, the number ratio of the CP-9 strain and the AP-32 strain may be 1:9 to 9:1, preferably 1:1 to 9:1.

(15) Another embodiment of the present invention discloses a method for inhibiting growth of Escherichia coli and a method for treating or preventing jaundice. Each method comprises: administering the foregoing lactic acid bacterial composition to a subject in need thereof.

(16) The foregoing composition can be administered to the subject in need of inhibiting growth of Escherichia coli to achieve the purpose of inhibition of the Escherichia coli growth. The term “subject” used in the present content comprises: a mammal, but not limited thereto; an example thereof is a human, a monkey, a cow, a sheep, a horse, a swine, a goat, a dog, a cat, a mouse, or a rat, but not limited thereto. The phrase “inhibiting growth of Escherichia coli” used in the present content comprises: reducing, alleviating, or terminating the growth or spread of Escherichia coli, or preventing the growth or spread of Escherichia coli. Based on the composition's property to inhibit growth of Escherichia coli, the composition can be administered to a subject in need of treating or preventing a disease caused by Escherichia coli, e.g., urinary tract infection or gastrointestinal infection.

(17) The foregoing composition can be administered to the subject in need of treating or preventing jaundice to achieve the purpose of jaundice treatment or prevention. Additionally, phototherapy can be performed on the subject before, during, and/or after the composition administration. What's more, the foregoing composition can be administered to the subject in need of treating or preventing jaundice to decrease the icteric index so as to achieve the purpose of jaundice treatment or prevention. Furthermore, the foregoing composition can be administered to the subject in need of treating or preventing jaundice to decrease the irradiation hours. The term “subject” used in the present content comprises: a mammal, but not limited thereto; an example thereof is a human, a monkey, a cow, a sheep, a horse, a swine, a goat, a dog, a cat, a mouse, or a rat, but not limited thereto. The term “jaundice” used in the present content comprises: jaundice resulted from high content of conjugated bilirubin caused by adult liver disease or biliary disease, e.g., jaundice caused by virus hepatitis (hepatitis B or hepatitis C) or jaundice caused by biliary disease (e.g., biliary obstruction, stone, tumor, cholangitis, or primary biliary cirrhosis), but not limited thereto. The term “jaundice” used in the present content comprises: jaundice caused by infant's immature liver or jaundice derived from urinary tract infection caused by Escherichia coli, but not limited thereto.

(18) The following examples are offered to further illustrate the present invention:

Example 1

(19) Manufacture of Bacterial Powders

(20) All bacterial strains were cultivated in an MRS medium containing 0.05% cysteine at 37° C. for 24 hours to activate these strains. 1×10.sup.8 CFU activated bacterial strains were seeded into a 5 mL MRS medium containing 60 mg/mL glucose and 0.05% cysteine at a volume concentration of 2%, and cultivated at 37° C. for 20 hours. Afterwards, the thus-obtained culture was centrifugated at a rate of 3,000 rpm for 10 minutes, and the supernatant was removed and the precipitate was washed with 0.1M PBS. After which, the strain concentration of the bacterial solution was adjusted to 1×10.sup.10 CFU/mL with PBS, and the bacterial solution was lyophilized to obtain bacterial powders for the following experiment.

Example 2

(21) Analysis for Escherichia coli Growth

(22) Lactic acid bacterial strains (total bacterial concentration of 1×10.sup.9 CFU/mL) were coated on a solid medium to form a width of 2 cm; a blank solid medium was used as the control group. After cultivation for 2 days, a 14 mL medium for pathogenic bacteria was injected and solidified. Afterwards, the pathogenic bacterial solution containing Escherichia coli was uniformly coated on the solidified medium. After cultivation for a proper period, the zone diameter of inhibition on the bacterial plate was measured with a ruler to analyze the inhibitory activity by lactic acid bacterial strains.

(23) As shown in FIG. 1A, with the same total bacterial number, the zone diameter of Escherichia coli inhibition by CP-9 strains was 5.3±0.2 cm; the zone diameter of Escherichia coli inhibition by L-53 strains was 3.2±0.1 cm. The foregoing result implies that although CP-9 strains and L-53 strains all belong to Bifidobacterium animalis subsp. lactis, the inhibitory activity for Escherichia coli by CP-9 strains is greater than that by L-53 strains.

(24) As shown in FIG. 1B, with the same total bacterial number, the zone diameter of Escherichia coli inhibition by AP-32 strains was 3.9±0.2 cm; the zone diameter of Escherichia coli inhibition by L-28 strains was 2.6±0.2 cm. The foregoing result implies that although AP-32 strains and L-28 strains all belong to Lactobacillus salivarius subsp. salicinius, the inhibitory activity for Escherichia coli by AP-32 strains is greater than that by L-28 strains.

(25) According to the conclusion made from FIGS. 1A to 1B, different bacterial strains belonging to the same species have various inhibitory activities for Escherichia coli.

(26) As shown in FIG. 1C, with the same total bacterial number, the zone diameter of Escherichia coli inhibition by CP-9 strains and AP-32 strains at a number ratio of 1:9 was 3.9±0.2 cm; the zone diameter of Escherichia coli inhibition by CP-9 strains and AP-32 strains at a number ratio of 1:1 was 6.7±0.2 cm; the zone diameter of Escherichia coli inhibition by CP-9 strains and AP-32 strains at a number ratio of 9:1 was 5.9±0.2 cm. Since the zone diameter of Escherichia coli inhibition by CP-9 strains and AP-32 strains at a number ratio of 1:1 and the zone diameter of Escherichia coli inhibition by CP-9 strains and AP-32 strains at a number ratio of 9:1 were greater than the zone diameter of Escherichia coli inhibition only by CP-9 strains and the zone diameter of Escherichia coli inhibition only by AP-32 strains, this result implies that on the condition that CP-9 strains and AP-32 strains are at a number ratio of 1:1 to 9:1, the combination of these kinds of strains has a synergistic activity on the inhibition of the Escherichia coli growth.

(27) As shown in FIG. 1D, with the same total bacterial number, the zone diameter of Escherichia coli inhibition by CP-9 strains and AP-32 strains at a number ratio of 1:1 was 6.3±0.2 cm; the zone diameter of Escherichia coli inhibition by CP-9 strains and L-28 strains at a number ratio of 1:1 was 3.4±0.1 cm. Since the zone diameter of Escherichia coli inhibition by CP-9 strains and AP-32 strains at a number ratio of 1:1 was greater than the zone diameter of Escherichia coli inhibition only by CP-9 strains and the zone diameter of Escherichia coli inhibition only by AP-32 strains, and the zone diameter of Escherichia coli inhibition by CP-9 strains and L-28 strains at a number ratio of 1:1 was greater than the zone diameter of Escherichia coli inhibition only by L-28 strains but smaller than the zone diameter of Escherichia coli inhibition only by CP-9 strains, this result implies that although AP-32 strains and L-28 strains all belong to Lactobacillus salivarius subsp. salicinius, only the combination of CP-9 strains and AP-32 strains brings a synergistic effect on the inhibition of the Escherichia coli growth.

Example 3

(28) Analysis for Irradiation Hours and Icteric Index

(29) 137 infants were preliminarily chosen from the Pediatric Newborn Observation Room in the China Medical University Children's Hospital. All infants were full-term infants (≥37 weeks) and had the icteric index on the 4th day after birth of greater than 15 mg/dL. However, 16 infants were excluded based on that each had one of the following diseases: (1) hypothyroidism; (2) Down syndrome; (3) ABO hemolytic disease; (4) gastrointestinal disease; (5) G6PD deficiency (favism); (6) hemangioma; (7) cephalematoma; (8) severe perinatal asphyxia; (9) neonatal chromosome disorder; (10) cyanotic congenital heart disease; (11) omphalocele; (12) early onset sepsis; and (13) liver failure, and finally the other 121 infants were used as testers.

(30) Subsequently, the 121 testers were randomly divided in three groups: (1) a group with CP-9 strain administration and phototherapy; (2) a group with AP-32 strain administration and phototherapy; and (3) a group with placebo administration and phototherapy. All testers received phototherapy, in which the light for irradiation was blue light with a wavelength of 425 nm to 457 nm, and the irradiation hours were determined according to the gestational age, the infant's age and the symptoms of the complication. The phototherapy standard is listed in Table 2 below.

(31) TABLE-US-00002 TABLE 2 Phototherapy Standard Against Jaundice Condition Gestational age of 35 weeks to 37 weeks and 6 days; Gestational age ≥38 weeks but having the risk Gestational to suffer from other complications age ≥38 weeks Normal Intensive Normal Intensive Infant's age irradiance irradiance irradiance irradiance 12 hours 6 7.5 7.5 9 24 hours 8 10 10 11.5 36 hours 9.5 11.5 11.5 13.5 48 hours 12 13 13 15 60 hours 12.5 14.5 14.5 16.5 72 hours 13.5 15.5 15.5 17.5 3.5 days 14 16.5 16.5 19 4 days 14.5 17 17 20 4.5 days 15 18 18 20.5 ≥5 days 15 18 18 21

(32) The group with CP-9 strain administration and phototherapy and the group with AP-32 strain administration and phototherapy were fed with 5×10.sup.9 CFU bacterial strains every morning and every afternoon during the phototherapy course; the group with placebo administration and phototherapy were fed with maltodextrin at the same content as the foregoing bacterial strains every morning and every afternoon during the phototherapy course. Before feeding, the corresponding powders were mixed with breast milk or infant formula for feeding. Additionally, the blood samples were taken from the admission day to the discharge day, and the bilirubin concentrations were analyzed.

(33) Firstly, serum bilirubin concentrations of all testers on the admission day were not significantly different, and serum bilirubin concentrations of all testers on the discharge day were also not significantly different. Next, the descent rate of each tester's icteric index was measured with the following formula:

(34) $\mathrm{Descent}\mathrm{rate}\left(\mathrm{mg}/\mathrm{dL}/\mathrm{hr}\right)=\frac{\mathrm{Decrement}\mathrm{of}\mathrm{icteric}\mathrm{index}}{\mathrm{Irradiation}\mathrm{hours}}.$

(35) As shown in FIG. 2, the descent rate of the icteric index of the group with CP-9 strain administration and phototherapy was 0.16±0.02 mg/dL/hr, and the descent rate of the icteric index of the group with AP-32 strain administration and phototherapy was 0.155±0.017 mg/dL/hr. Both were greater than the descent rate of the icteric index of the group with placebo administration and phototherapy, 0.1±0.01 mg/dL/hr. This result implies that CP-9 strains and AP-32 strains can reduce the icteric index.

(36) As shown in FIG. 3, the total irradiation hours of the group with CP-9 strain administration and phototherapy were 44.82±3.23 hr, and the total irradiation hours of the group with AP-32 strain administration and phototherapy were 45.49±3.91 hr. Both were lower than total irradiation hours of the group with placebo administration and phototherapy, 57.80±4.02 hr. This result implies that CP-9 strains and AP-32 strains can reduce the total irradiation hours.

(37) While the invention has been described in connection with what is considered the most practical and preferred embodiments, it is understood that this invention is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretation so as to encompass all such modifications and equivalent arrangements.