TECHNICAL FIELD

The present disclosure relates to the technical field of microbiology, and particularly to a novel use of Lactobacillus paracasei ET-22 (deposit number CGMCC 15077) in enhancing resistance of the intestinal tract to bacterial infection and improving intestinal immunity.

BACKGROUND

Intestinal epithelial cells are the first barrier of our body to pathogenic bacteria. The adhesion to or invasion of epithelial cells by pathogenic bacteria stimulates intestinal epithelial cells to produce inflammatory factors or chemokines. Some soluble mediators can modulate the intestinal immune system or induce cellular innate immune responses. Adequate immune responses and a good barrier function of epithelial cells would help protect the host from infection by pathogenic bacteria.

Probiotics refer to a class of living microorganisms that confer health benefits to the human body when ingested in a sufficient amount. As an important component of the intestinal microbiome, probiotics play an unneglectable role in human health, such as nutrient supply, synthesis of vitamins, aid in digestion, promoting angiogenesis and enteric nerve function.

SUMMARY OF THE INVENTION

An objective of the present disclosure is to provide a novel use of Lactobacillus paracasei ET-22.

The present disclosure provides a novel use of a Lactobacillus paracasei strain, which is designated as ET-22 herein. This bacterial strain was deposited with the taxonomic name Lactobacillus paracasei in the China General Microbiological Culture Collection Center (CGMCC) (address: Institute of Microbiology, Chinese Academy of Sciences, NO. 3, Quarter 1, West Beichen Road, Cha oyang District, Beijing, China) on Dec. 18, 2017 with deposit number CGMCC 15077.

In the present disclosure, Lactobacillus paracasei ET-22 was studied for its function in improving intestinal immunity by using an enterotoxigenic Escherichia coli strain ETEC H10407 and an enteropathogenic Escherichia coli strain EPEC 0119 as pathogenic bacterial strains that induce intestinal infection in vitro. Both E. coli strains are common pathogenic bacteria, causing infantile diarrhea and traveler's diarrhea in developing countries or areas of poor sanitation. ETEC H10407 is a well-established model strain commonly used in experiments, and is often used to evaluate the ability of probiotics to adhere to pathogenic bacteria and inflammatory signaling pathways.

It has been discovered in the present disclosure that the Lactobacillus paracasei ET-22 strain (i.e., Lactobacillus paracasei with deposit number CGMCC 15077) has an effect of inhibiting adhesion by intestinal pathogenic bacteria, in that it can significantly inhibit adhesion by ETEC H10407 and EPEC 0119 to Caco-2 cells and improve the integrity of the intestinal barrier, and also has an effect of inhibiting production of intestinal inflammatory factors, in that it can mitigate inflammatory responses caused by ETEC H10407.

As such, in one aspect, the present disclosure provides the use of a Lactobacillus paracasei strain in the preparation of a composition for improving intestinal immunity, wherein the Lactobacillus paracasei strain has a deposit number of CGMCC 15077.

According to an embodiment of the present disclosure, for the use of the present disclosure, the Lactobacillus paracasei strain is used in a form of a solid or liquid formulation of live bacteria and/or dead bacteria for the preparation of the composition.

According to an embodiment of the present disclosure, for the use of the present disclosure, the improving intestinal immunity includes: improving resistance of the intestinal tract to bacterial infection, combating invasion by pathogenic bacteria in the intestinal system, maintaining the intestinal barrier function, and/or preventing diarrhea caused by pathogenic bacteria.

According to an embodiment of the present disclosure, for the use of the present disclosure, the improving intestinal immunity includes: lowering the ability of pathogenic bacteria to adhere to intestinal epithelial cells, and/or reducing the release of the inflammatory factors IL-8 and IP-10 from intestinal cells caused by pathogenic bacteria.

According to an embodiment of the present disclosure, for the use of the present disclosure, the Lactobacillus paracasei strain is administered in an amount of 1.0×10³to 1.0×10¹²CFU/day, or 0.001 μg to 1000 mg per day of the weight of the bacteria strain. Preferably, the Lactobacillus paracasei strain is administered in an amount of 10⁷to 10¹¹CFU/day, or 10 μg to 10 mg per day of the weight of the bacteria strain.

According to an embodiment of the present disclosure, the composition may comprise a food composition, a feed composition, or a pharmaceutical composition.

According to an embodiment of the present disclosure, the composition may be administered to an animal or human. The composition may also include ingredients conventionally used in the art. For example, for a pharmaceutical composition, an appropriate amount of adjuvants may be included, and the adjuvants may be excipients, diluents, fillers, absorption enhancers, and the like. For a food composition, the Lactobacillus paracasei strain of the present disclosure can be produced in accordance with a food product in the art containing Lactobacillus paracasei, and the composition may be in various forms according to the needs of the recipient, for example, powder, lozenges, granules, microcapsules, a liquid formulation, and the like.

In an embodiment of the present disclosure, the composition is a food composition, and the food may be a liquid beverage, a solid beverage, an oral liquid, a diary product, a tablet, or a capsule; for example, it may be a fermented milk product (such as fermented milk, flavored fermented milk, fermented milk beverage, etc.), cheese, a milk-containing beverage, a probiotic solid beverage, milk powder or the like.

In another embodiment of the present disclosure, the composition is a feed composition. The other components in the feed composition may be selected with reference to conventional techniques in the field of probiotic feeds.

In another embodiment of the present disclosure, the composition is a pharmaceutical composition. The other components in the pharmaceutical composition may be selected with reference to conventional techniques in the field of probiotic medicaments.

In another aspect, the present disclosure further provides a method for improving intestinal immunity, the method comprising:

administering to a subject an effective amount of a Lactobacillus paracasei strain to improve intestinal immunity; wherein the Lactobacillus paracasei strain has a deposit number of CGMCC 15077.

Furthermore, the present disclosure provides Lactobacillus paracasei ET-22 for use in improving intestinal immunity.

According to an embodiment of the present disclosure, in the method of the present disclosure, the improving intestinal immunity includes: improving the resistance of the intestinal tract to bacterial infection, combating invasion by pathogenic bacteria in the intestinal system, maintaining the intestinal barrier function, preventing diarrhea caused by pathogenic bacteria, lowering the ability of pathogenic bacteria to adhere to intestinal epithelial cells, and/or reducing the release of the inflammatory factor IL-8 and/or IP-10 from intestinal cells induced by pathogenic bacteria.

According to an embodiment of the present disclosure, in the method of the present disclosure, the Lactobacillus paracasei strain is administered in an amount of 1.0×10³to 1.0×10¹²CFU/day, or 0.001 μg to 1000 mg per day of the weight of the bacteria strain;

- preferably, the Lactobacillus paracasei strain is administered in an amount of 10⁷to 10¹¹CFU/day, or 10 μg to 100 mg per day of the weight of the bacteria strain.

In summary, the present disclosure provides a novel use of Lactobacillus paracasei ET-22, which has effects of significantly reducing the ability of pathogenic bacteria to adhere to intestinal epithelial cells, improving the intestinal barrier function, and activating intestinal immunity. This bacteria strain may be used in the preparation of a food, medicament, or feed product capable of anti-infection and modulating intestinal health and immunity, and may find broad applications.

DESCRIPTION OF DRAWINGS

FIG. 1 shows a curve of viable bacteria counts of Lactobacillus paracasei ET-22.

FIG. 2 shows the effect of Lactobacillus paracasei ET-22 in inhibiting adhesion by pathogenic Escherichia coli ETEC H10407 to Caco-2 (p<0.01).

FIG. 3 shows the effect of Lactobacillus paracasei ET-22 in inhibiting adhesion by pathogenic Escherichia coli EPEC 0119 to Caco-2 (p<0.01).

FIGS. 4A and 4B show the effect of Lactobacillus paracasei ET-22 in combination with a human milk oligosaccharide mix on the intestinal barrier.

FIG. 5 shows the changes in TEER (Ω·cm²) after co-culturing of Lactobacillus paracasei ET-22 and ETEC H10407 for 1 h, 2 h, 3 h, and 4 h.

FIG. 6 shows the effect of Lactobacillus paracasei ET-22 on the expression of the pro-inflammatory factor IL-8 in Caco-2 cells.

FIG. 7 shows the effect of Lactobacillus paracasei ET-22 on the inflammatory factor IP10 in Caco-2 cells.

DEPOSIT OF MICROORGANISM FOR PATENT PROCEDURE

Lactobacillus paracasei ET-22 of the Present Disclosure:

- Date of deposit: Dec. 18, 2017;
- Depositary authority: China General Microbiological Culture Collection Center (CGMCC);
- Address of the depositary authority: Institute of Microbiology, Chinese Academy of Sciences, NO. 3, Quarter 1, West Beichen Road, Chaoyang District, Beijing, China;
- Deposit number: CGMCC 15077;
- Taxonomic designation: Lactobacillus paracasei.

DETAILED DESCRIPTION OF THE INVENTION

In order to provide a better understanding of the technical features, purposes and advantageous effects of the present disclosure, the technical solutions of the present disclosure are described in details hereinafter in connection with specific examples, and it should be understood that these examples are merely illustrative of the present disclosure and not to limit the scope of the present disclosure. In the Examples, the experimental methods, where no specific conditions are indicated, are conventional methods and conditions well known in the art, or are performed as recommended by the instrument manufacturer.

Lactobacillus paracasei ET-22 Used in the Examples:

The Lactobacillus paracasei ET-22 of the present disclosure was deposited at the China General Microbiological Culture Collection Center (CGMCC) (address: Institute of Microbiology, Chinese Academy of Sciences, NO. 3, Quarter 1, West Beichen Road, Chaoyang District, Beijing, China) on Dec. 18, 2017 with a taxonomic designation of Lactobacillus paracasei and a deposit number of CGMCC 15077.

The taxonomic characteristics of the ET-22 strain were confirmed based on the results of 16S rDNA sequence analysis and the API bacterial identification system analysis. Details are provided as follows.

Morphologic characteristics: 1) when cultured in an MRS medium, the bacterium is in a shape of short to medium rods with rounded ends, usually in chains, and occasionally in pairs; 2) the bacterium is Gram positive, does not produce spores, does not have catalase and oxidase, lacks motility, can grow in both aerobic and anaerobic environments at an optimal growing temperature of 37±1° C., belonging to facultative heterogeneous fermentative beacteria, and does not produce gas during glucose metabolism.

Fermentation conditions for the ET-22 strain: MRS liquid medium: peptone, 10.0 g; beef paste, 10.0 g; yeast extract powder, 5.0 g; glucose, 20.0 g; dipotassium hydrogen phosphate, 5.0 g; diammonium hydrogen citrate, 2.0 g; sodium acetate, 5.0 g; magnesium sulfate heptahydrate, 0.5 g; manganese sulfate tetrahydrate, 0.2 g; Tween 80, 1.0 g; agar 15.0 g; distilled water 1000 mL; pH adjusted to 6.2-6.4, and sterilizing at 121° C. for 15 minutes.

Lactobacillus paracasei ET-22 is a micro-aerobic bacterial strain, which grows optimally in a facultative anaerobic environment, produces lactic acid, has acid resistance and can withstand an acidic environment at a pH of 2.5 and a 0.4% bile salt environment for 4 hours. It is a mesophilic bacterial strain, and grows within a temperature range from 15 to 45° C., with an optimal growing temperature at about 37° C.

Viable Bacteria Counts of Lactobacillus paracasei ET-22 Used in the Examples:

A single colony of Lactobacillus paracasei ET-22 (deposit number CGMCC 15077) was picked from a spread plate, and after 16S identification, stored in a glycerin tube at −80° C. Before the experiment, the strain was cultured in an MRS medium at 37° C., grown till the logarithmic phase, and enriched by centrifugation. The number of viable bacteria and bacterial activity were measured by fluorescence activated cell sorting (FACS), and the results are shown in FIG. 1. The strain reached a growth plateau at 8 h, and the number of viable bacteria became stable, and stabilized around 10⁸cfu/mL at 8 h. The viable bacteria count of the strain used in the Examples of the present disclosure was 1×10⁸CFU/mL.

Data Analysis in the Examples:

All data in the experiment were obtained at least in triplicate, and the experimental results were expressed as mean±standard error. Data analysis was performed by using SPSS17.0 software (SPSS, Chicago, IL, USA), and the significance analysis was performed by one-way analysis of variance by the LSD method. P-value<0.05 is considered as a statistically significant difference, and the significant difference is categorized as follows: *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001. Figures were drawn with GraphPad Prism 5.0.

Example 1. Determination of Anti-Adhesion Ability

A co-culturing method was performed to investigate whether Lactobacillus paracasei ET-22 inhibits EPEC 0119 from adhering to Caco-2. Caco-2 cells were cultured in a 24-well plate, washed with a PBS buffer, and co-cultured with the strain for 1 h. EPEC 0119 was added to the Caco-2 cells at a multiplicity of infection (MOI) of 50:1, and co-cultured for 1 h (37° C.), to a final viable bacteria count of 1×10⁷CFU/mL. A group of Caco-2 without addition of Lactobacillus paracasei ET-22 was used as a negative control. As a positive control group, 1 mM zinc oxide (ZnO) was used instead of Lactobacillus paracasei ET-22. After incubation, the Caco-2 cells were washed and lysed, and the pathogenic bacteria were inoculated on agar. After culturing on the agar plate at 37° C. overnight, the number of colonies of the bacteria in CFU was counted to measure the adhesion by the pathogenic bacteria. The number of colonies of growing E. coli was counted and recorded as CFU/mL. In parallel to the anti-adhesion test, E. coli of 10⁷CFU/mL (final concentration) was added to 1 mL of the test substance (ET-22 strain solution) and co-cultured at 37° C. for 1 hour to measure the activity. After the culturing, E. coli was collected from each sample by centrifugation, resuspended in PBS, and inoculated on an agar plate. After culturing on the agar plate at 37° C. overnight, the number of colonies of the bacteria in CFU was counted to measure the adhesion by the pathogenic bacteria. The number of colonies of growing E. coli was counted and recorded as CFU/mL.

With the human intestinal cells Caco-2 described above as a model, it is confirmed in the present disclosure that Lactobacillus paracasei ET-22 has an inhibitory effect on the enteropathogenic Escherichia coli strain EPEC 0119.

In some experiments of the present disclosure, the ability of Lactobacillus paracasei ET-22 at a concentration of 10⁸CFU/mL to inhibit ETEC H10407 is shown in FIG. 2. Without intervention with Lactobacillus paracasei ET-22, the number of the enterotoxigenic E. coli strain ETEC H10407 adhered to Caco-2 cells was as high as 3.75×10⁶CFU/mL (6.57 log CFU/mL). When the enterotoxigenic E. coli strain ETEC H10407 was present together with Lactobacillus paracasei ET-22, the number of the adhered enterotoxigenic E. coli strain ETEC H10407 was 7.67×10⁵CFU/mL (5.88 log CFU/mL), indicating 79.54% inhibition. The experimental results indicate that Lactobacillus paracasei ET-22 has a significant inhibitory effect on the enteropathogenic Escherichia coli strain ETEC H10407 (p<0.01).

In some experiments of the present disclosure, the experimental results of the ability of Lactobacillus paracasei ET-22 at a concentration of 10⁸CFU/mL to inhibit EPEC 0119 are shown in FIG. 3. Without intervention with Lactobacillus paracasei ET-22, the number of the enteropathogenic E. coli strain EPEC 0119 adhered to Caco-2 cells was as high as 1.73×10⁶CFU/mL (6.23 log CFU/mL). When the enteropathogenic E. coli EPEC 0119 was present together with Lactobacillus paracasei ET-22, the number of the adhered enteropathogenic E. coli EPEC 0119 was 6.00×10⁵CFU/mL (5.78 log CFU/mL), indicating 65.32% inhibition. The experimental results indicate that Lactobacillus paracasei ET-22 has a significant inhibitory effect on the enteropathogenic Escherichia coli strain EPEC 0119 (p<0.01).

The above experimental results indicate that Lactobacillus paracasei ET-22 has an inhibitory effect on both the enterotoxigenic E. coli strain ETEC H10407 and the enteropathogenic Escherichia coli strain EPEC 0119.

Example 2. Intestinal Barrier Integrity

An ideal intestinal epithelial barrier function is a prerequisite for protecting the host from pathogenic bacteria invasion and/or pathogen-derived toxins. In this study, in vitro barrier integrity was evaluated by measurement of the transepithelial/transendothelial electrical resistance (TEER) of intestinal cell layers. In order to study the effect of probiotics on infection, the change in TEER over time before and after E. coli infection was measured.

Caco-2 cells were seeded at a concentration of 2×10⁴cells/cm 2 into Transwell polycarbonate cell culture inserts with an average pore size of 0.4 μm and an area of 0.33 cm², until complete differentiation (±1000Ω). Transepithelial/transendothelial electrical resistance (TEER) was measured with an EVOM2 epidermal voltmeter purchased from World Precision Instruments to measure the barrier integrity.

On the day of test, cells were washed and incubated for 1 h at 37° C. in a medium free of antibiotics and serum but containing a test substance. Escherichia coli was then added to the test substance (at an MOI of 200:1) and incubated for 6 h. TEER was measured before the start of the experiment (t=−1), 1 h after exposure to the test substance before addition of the pathogenic bacteria (t=0), and 1 h, 2 h, 3 h, 4 h, 6 h after exposure to the pathogenic bacteria, respectively. The TEER values measured under individual conditions after exposure to the pathogenic bacteria were correlated to their respective TEER values at t=0, and were expressed as ΔTEER (Ω·cm²). Negative controls (with addition of E. coli only) and positive controls (not exposed to the pathogenic bacteria or test substances) were also included in the experiments. All conditions were tested in triplicate, and some control groups were tested in six replicates.

After challenge with ETEC H10407 (MOI=50) for 6 hours, the blank control group showed a poor TEER value, indicating that the survival rate of the cells decreased drastically after 6 h challenge. Thus, it was preliminarily determined that the challenge duration with ETEC H10407 should be kept within 4 h.

As shown in FIGS. 4A and 4B, the effect of the test substance on TEER at various time points was tested, and ET-22 at 1×10⁸CFU/mL had a tendency of increasing the TEER value or preventing its decrease at multiple time points. In these figures, MixA, MixB, MixC, and MixD were human milk oligosaccharides mixtures, and when a combination of ET-22 with these human milk oligosaccharides was added, the tendency of increasing the TEER value or preventing its decrease was more prominent, and showed an improvement over the blank group.

FIG. 5 shows the changes in TEER (Ω·cm²) after co-culturing of Lactobacillus paracasei ET-22 at a concentration of 10⁸CFU/mL and ETEC H10407 for 1 h, 2 h, 3 h, and 4 h in other experiments of the present disclosure. As seen from FIG. 5, after ET-22 was added, TEER increased. After treatment for 4 h, TEER of the ET-22 group decreased in a time-dependent manner, and at t=2 h and t=3 h, there was a significant difference from the ETEC H10407 group (p<0.01). This suggests that the intervention with Lactobacillus paracasei ET-22 significantly mitigated the damage caused by ETEC H10407 to the integrity of the intestinal cell barrier.

Example 3. Determination of Immunomodulatory Ability

The immunomodulatory ability of Lactobacillus paracasei ET-22 was evaluated based on whether it can reduce the production of IL-8 and IP-10 in Caco-2 cells induced by ETCT H10407. Caco-2 cells were cultured in a 96-well plate to an appropriate abundance. At the beginning of the experiment, the cells were washed once with an antibiotic-free medium. A monolayer of cells was co-cultured with a test substance in an antibiotic-free medium for 1 h at 37° C., which was repeated three times. E. coli was added to stimulate the cells (MOI 200:1). After 1 hour of incubation, the cell monolayer was co-cultured with the pathogenic bacteria, washed and incubated overnight with a medium containing a test substance and 50 μg/mL gentamicin. For a blank control (Blank), only the medium was used, without E. coli stimulation. A medium stimulated with E. coli but without a test substance was used as a control for the E. coli response. In addition, as a control for the response of Caco-2 cells, the cells were stimulated with a medium containing a mixture of Rec TNFα (10 ng/mL) and Rec IFNγ (5 ng/mL) (both purchased from R&D Systems, Abingdon, UK). 24 hours after stimulation, supernatant was collected and stored at −20° C. IL-8 and IP-10 were tested with a Bio-Plex kit (BioRad, California, USA) according to the manufacturer's instructions.

FIG. 6 shows the effect of Lactobacillus paracasei ET-22 at a concentration of 10⁸CFU/mL on the inflammatory factor IL-8 in Caco-2 cells. FIG. 7 shows the effect of Lactobacillus paracasei ET-22 at a concentration of 10⁸CFU/mL on the inflammatory factor IP10 in Caco-2 cells. As seen from FIG. 6, after the ETEC H10407 stress, the IL-8 content in the cell culture increased from 2.62±0.44 pg/mL to 473.84±21.9 pg/mL, and after the ET-22 treatment, the expression of IL-8 returned to 17.09±1.89 pg/mL, indicating that Lactobacillus paracasei ET-22 has a significant inhibitory effect on the increase in IL-8 induced by ETEC H10407 (p<0.001). As seen from FIG. 7, after the ETEC H10407 stress, the IP10 content in the cell culture increased from 5±0.00 pg/mL to 1454.08±193.31 pg/mL, and after the ET-22 treatment, the expression of IP10 returned to 10.94±8.41 pg/mL, indicating that Lactobacillus paracasei ET-22 has a significant inhibitory effect on the increase in IP10 induced by ETEC H10407 (p<0.001). The test results indicate that Lactobacillus paracasei ET-22 inhibits the production of inflammatory factors IL-8 and IP10 and significantly inhibits the inflammatory responses caused by ETEC 10407 (p<0.001), which further indicates that ET-22 has a potential for reducing the inflammatory responses caused by ETEC 10407 to a certain extent.

As confirmed from the above research results, Lactobacillus paracasei ET-22 can significantly inhibit the adhesion by ETEC H1407 and EPEC 0119 to Caco-2 cells, and alleviate the inflammatory responses caused by ETEC H10407, indicating that Lactobacillus paracasei ET-22 has a good potential for preventing infant diarrhea, traveler's diarrhea, intestinal inflammation and the like.