Bifidobacterium Longum with the Ability to Relieve Atopic Dermatitis and its Application

Abstract

The disclosure discloses Bifidobacterium longum with the ability to relieve atopic dermatitis and its application, and belongs to the technical fields of microorganisms and medicine. The Bifidobacterium longum of the disclosure has the effects of relieving atopic dermatitis, and the effects are specifically embodied in: (1) significantly improving the degree of ear swelling in mice with atopic dermatitis; (2) significantly improving skin pathological symptoms and inflammatory cell infiltration in mice with atopic dermatitis; (3) significantly reducing the serum IgE level in mice with atopic dermatitis; (4) significantly reducing the levels of IL-4 and IL-13 in the skin tissues of mice with atopic dermatitis; and (5) significantly reducing the level of histamine in the skin tissues of mice with atopic dermatitis. Therefore, the Bifidobacterium longum has great application prospects in the preparation of products for the prevention and/or treatment of atopic dermatitis.

Claims

1. A composition comprising Bifidobacterium longum, wherein the Bifidobacterium longum was deposited at the Guangdong Microbial Culture Collection Center on Oct. 11, 2018, with the accession number of GDMCC No. 60461, and the deposit address of 5.sup.th Floor, Building No. 59, Courtyard No. 100, Xianlie Middle Road, Guangzhou.

2. The composition of claim 1, wherein viable count of the Bifidobacterium longum is not less than 1×10.sup.6 CFU/mL or 1×10.sup.6 CFU/g.

3. A product comprising the composition of claim 2, wherein the product comprises food, medicine or health care products, and the product treats or prevents atopic dermatitis.

4. The product of claim 3, further comprises a drug carrier and/or pharmaceutical excipients.

5. A product for prevention and/or treatment of atopic dermatitis, wherein the product comprises Bifidobacterium longum, the Bifidobacterium longum was deposited at the Guangdong Microbial Culture Collection Center on Oct. 11, 2018, with the accession number of GDMCC No. 60461, and the deposit address of 5.sup.th Floor, Building No. 59, Courtyard No. 100, Xianlie Middle Road, Guangzhou, and the product treats or prevents atopic dermatitis.

6. The product of claim 5, wherein in the product, the viable count of the Bifidobacterium longum is not less than 1×10.sup.6 CFU/mL or 1×10.sup.6 CFU/g.

7. The product of claim 6, wherein the product comprises food, medicine or health care products.

8. The product of claim 7, wherein the medicine further comprises a drug carrier and/or pharmaceutical excipients.

9. The product of claim 7, wherein the food comprises dairy products, soybean products, or fruit and vegetable products produced using a starter containing the Bifidobacterium longum; or the food comprises solid beverages containing the Bifidobacterium longum.

10. The product of claim 9, wherein a preparation method of the starter is as follows: inoculating a culture medium with the Bifidobacterium longum at an inoculum concentration of 2-4% of the total mass of the culture medium, and performing culturing at 37° C. for 18 h to obtain a culture solution; centrifuging the culture solution to obtain bacterial cells; washing the bacterial cells with a phosphate buffer with the pH of 7.2-7.4 for 3 times and then resuspending with a freeze-drying protective agent to obtain a resuspension; and freeze-drying the resuspension by a vacuum freezing process to obtain the starter.

11. The product of claim 10, wherein the mass ratio of the freeze-drying protective agent to the bacterial cells is 2:1.

12. The product of claim 10, wherein the culture medium comprises 87.7% water, 10% skim milk, 0.5% glucose, 1.5% tryptone, and 0.3% yeast extract solution, of the total mass of the culture medium.

13. The product of claim 10, wherein the pH of the culture medium is 6.8.

14. The product of claim 10, wherein the freeze-drying protective agent comprises 100 g/L skimmed milk powder, 150 g/L trehalose, and 10 g/L sodium L-glutamate.

Description

BRIEF DESCRIPTION OF FIGURES

[0032] FIG. 1: Comparison of the effects of different groups in reducing ear thickness of mice with atopic dermatitis.

[0033] FIG. 2: Comparison of the effects of different groups in relieving skin pathological symptoms in mice with atopic dermatitis.

[0034] FIG. 3: Comparison of the effects of different groups in reducing skin eosinophil infiltration in mice with atopic dermatitis.

[0035] FIG. 4: Comparison of the effects of different groups in reducing the total serum IgE level in mice with atopic dermatitis.

[0036] FIG. 5: Comparison of the effects of different groups in reducing the IL-4 level in the skin tissues of mice with atopic dermatitis.

[0037] FIG. 6: Comparison of the effects of different groups in reducing the IL-13 level in the skin tissues of mice with atopic dermatitis.

[0038] FIG. 7: Comparison of the effects of different groups in reducing the level of histamine in the skin tissues of mice with atopic dermatitis.

[0039] Among them, “*” indicates a significant difference from a Model group (P<0.05), and “**” indicates an extremely significant difference from the Model group (P<0.01).

DETAILED DESCRIPTION

[0040] In the following examples, the skim milk was purchased from Brightdairy Co., Ltd., the glucose and yeast extract were purchased from Sinopharm Chemical Reagent Co., Ltd., the tryptone was purchased from OXOID, UK, and enzyme-linked immunosorbent assay kits were purchased from Nanjing SenBeiJia Biological Technology Co., Ltd.

[0041] The culture media involved in the following examples are as follows:

[0042] MRS solid culture medium (g/L): peptone 10 g/L, beef extract 10 g/L, glucose 20 g/L, sodium acetate 2 g/L, yeast powder 5 g/L, diammonium hydrogen citrate 2 g/L, K.sub.2PO.sub.4.3H.sub.2O 2.6 g/L, MgSO.sub.4.7H.sub.2O 0.1 g/L, MnSO.sub.4 0.05 g/L, Tween 80 1 mL/L, agar 20 g/L, and cysteine hydrochloride 0.5 g/L.

[0043] MRS liquid culture medium (g/L): peptone 10 g/L, beef extract 10 g/L, glucose 20 g/L, sodium acetate 2 g/L, yeast powder 5 g/L, diammonium hydrogen citrate 2 g/L, K.sub.2PO.sub.4.3H.sub.2O 2.6 g/L, MgSO.sub.4.7H.sub.2O 0.1 g/L, MnSO.sub.4 0.05 g/L, Tween 80 1 mL/L, and cysteine hydrochloride 0.5 g/L.

Example 1: Screening and Strain Identification of Bifidobacterium longum

[0044] 1. Screening

[0045] Healthy human feces from Hangzhou, Zhejiang was taken as a sample. The sample was pretreated and stored in a refrigerator at −80° C. in about 20% glycerol. After the sample was taken out and thawed, the sample was mixed uniformly. 0.5 mL of the sample was pipetted and added to 4.5 mL, and the sample was subjected to gradient dilution with 0.9% normal saline containing 0.05% cysteine. An appropriate gradient dilution was selected and spread on an MRS solid culture medium added with 0.05% cysteine. The dilution was cultured at 37° C. for 48 h. Typical colonies were picked and streaked on an MRS solid culture medium for purification. A single colony was picked and transferred to an MRS liquid culture medium (containing 0.05% cysteine) for enrichment, and the bacteria were preserved with 30% glycerol to obtain a strain CCFM1029, a strain A1 and a strain A2.

[0046] 2. Identification

[0047] The genomes of CCFM1029, A1 and A2 were extracted. The 16S rDNAs of CCFM1029, A1 and A2 were amplified and sequenced (by Invitrogen (Shanghai) Trading Co., Ltd., wherein the amplified nucleotide sequences of the 16S rDNAs of CCFM1029, A1 and A2 are shown in SEQ ID NO. 1, SEQ ID NO. 2 and SEQ ID NO. 3, respectively; the sequence of a forward primer 27F for strain identification is shown in SEQ ID NO. 4: 5′-AGAGTTTGATCCTGGCTCAG-3′; and the sequence of a reverse primer 1492R is shown in SEQ ID NO. 5: 5′-GGTTACCTTGTTACGACTT-3′). The sequences were subjected to nucleic acid sequence alignment in NCBI, and the results showed that the strains were Bifidobacterium longum, named Bifidobacterium longum CCFM1029, Bifidobacterium longum A1 and Bifidobacterium longum A2.

Example 2: Culture of Bifidobacterium longum

[0048] An MRS solid culture medium (containing 0.05% cysteine) was inoculated with the Bifidobacterium longum CCFM1029 and culturing was performed at 37° C. for 48 h. It was found that the convex surface of the colony was cushion-shaped, with complete edges, and is soft, moist, white and shiny, through observation of the colony.

[0049] An MRS liquid culture medium (containing 0.05% cysteine) was inoculated with the Bifidobacterium longum CCFM1029 and anaerobic culturing was performed at 37° C. for 24 h. The culture solution was transferred into a fresh MRS liquid culture medium (containing 0.05% cysteine) and cultured at same conditions for 24 h. Bacterial cells were centrifuged at 6000 g for 15 min, and then the bacterial cells were washed with 0.9% normal saline and recentrifuged at 6000 g for 10 min to obtain bacterial cells. The bacterial cells were resuspended with a 30% sucrose solution and cryopreserved at −80° C. for later use.

Example 3: Effects of Different Bifidobacterium longum on Ear Thickness of Mice with Atopic Dermatitis

[0050] 50 healthy female C57BL/6 mice weighing 18-20 g were randomly divided into 5 groups, each with 10 mice. The 5 groups were respectively: a blank group (Control), a model group (Model) administered with 2,4-dinitrofluorobenzene (DNFB), a CCFM1029 group administered with Bifidobacterium longum CCFM1029, an A1 group administered with Bifidobacterium longum A1, and an A2 group administered with Bifidobacterium longum A2. The CCFM1029 group, the A1 group and the A2 group were all treatment groups.

[0051] The experiment lasts for four weeks in total. The first week was the adaptation period of mice. Gavage was started from the second week to the end of the experiment. The treatment groups were given bacterial solutions of the Bifidobacterium longum CCFM1029, A1 and A2 by gavage. 0.2 mL of bacterial solution (the total amount of viable bacteria in a single gavage was 1×10.sup.9 CFU) was given per mouse per time by gavage. The blank group and the model group were not treated with the intervention of bacterial solutions, and only the same amount of normal saline was given by gavage as a control. The third to fourth weeks were the modeling period. On the 1st day of modeling, 50 μL of 0.5% DNFB solution was applied to the right ears of the mice in the model group and the treatment groups to sensitize and stimulate skin lesions. On the 5.sup.th, 8.sup.th, 11.sup.th, and 14.sup.th days, 20 μL of 0.2% DNFB solution was applied to the right ears of the mice in the model group and the treatment groups. Only the same amount of acetone/olive oil matrix solution was applied to the right ears of the mice in the blank group as a control. All groups were free access to water and food.

[0052] Before modeling (that is, day 0), the ear thickness of the 5 groups of mice was measured with a digital spiral micrometer. After the modeling (that is, on the 15.sup.th day), blood was taken and the mice were sacrificed. Then the ear thickness of the mice was measured immediately. The test results are shown in FIG. 1.

[0053] It can be seen from FIG. 1 that both the Bifidobacterium longum CCFM1029 and the Bifidobacterium longum A1 can significantly reduce the ear thickness of mice with atopic dermatitis and relieve the degree of ear swelling of the mice; while the Bifidobacterium longum A2 has no obvious relieving effect.

[0054] The experimental results show that the Bifidobacterium longum CCFM1029 has the effect of relieving the thickness and degree of swelling of the ears of mice with atopic dermatitis.

Example 4: Effects of Different Bifidobacterium longum on Skin Pathological Symptoms in Mice with Atopic Dermatitis

[0055] 50 healthy female C57BL/6 mice weighing 18-20 g were randomly divided into 5 groups, each with 10 mice. The 5 groups were respectively: a blank group (Control), a model group (Model) administered with 2,4-dinitrofluorobenzene (DNFB), a CCFM1029 group administered with Bifidobacterium longum CCFM1029, an A1 group administered with Bifidobacterium longum A1, and an A2 group administered with Bifidobacterium longum A2. The CCFM1029 group, the A1 group and the A2 group were all treatment groups.

[0056] The experiment lasts for four weeks in total. The first week was the adaptation period of mice. Gavage was started from the second week to the end of the experiment. The treatment groups were given bacterial solutions of the Bifidobacterium longum CCFM1029, A1 and A2 by gavage. 0.2 mL of bacterial solution (the total amount of viable bacteria in a single gavage was 1×10.sup.9 CFU) was given per mouse per time by gavage. The blank group and the model group were not treated with the intervention of bacterial solutions, and only the same amount of normal saline was given by gavage as a control. The third to fourth weeks were the modeling period. On the 1st day of modeling, the back skin of the 5 groups of mice was depilated for an area of approximately 2.5 cm×2.5 cm, and 50 μL of 0.5% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups to sensitize and stimulate skin lesions. On the 5.sup.th, 8.sup.th, 11.sup.th, and 14.sup.th days, 20 μL of 0.2% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups. Only the same amount of acetone/olive oil matrix solution was applied to the depilated areas on the back of the mice in the blank group as a control. All groups were free access to water and food.

[0057] After the modeling (that is, on the 15.sup.th day), blood was taken and the mice were sacrificed. The skin of the depilated areas on the back of the mice was taken for histopathological analysis. Histopathological sections of the back skin of mice were subjected to hematoxylin-eosin staining, and then histopathological scoring was performed by professional technicians (the results are shown in FIG. 2).

[0058] It can be seen from FIG. 2 that the structure of the epidermal cells on the back of mice in the blank group (Control) was normal, and there was no inflammation in all layers of the epidermis. The pathology of the skin lesions on the back of mice in the model group (Model) shows obvious inflammatory and proliferative changes and infiltration of lymphocytes and plasma cells, and the back skin was eroded and had proliferation of fibrous tissue. The structure of the epidermal cells on the back of mice in the Bifidobacterium longum CCFM1029 treatment group was almost normal, and there was no serious inflammation in all layers of the epidermis. There is obvious proliferation of fibrous tissue and relatively small amount of inflammation in the Bifidobacterium longum A1 and Bifidobacterium longum A2 treatment groups, and the pathological symptoms of atopic dermatitis in the skin of mice were relieved. The structure of epidermal cells in the remaining groups was obviously incomplete, and it was speculated that the skin was ulcerated and crusted, and had severe inflammation.

[0059] The experiment shows that the Bifidobacterium longum CCFM1029 can significantly improve skin inflammation in mice with atopic dermatitis.

Example 5: Effects of Different Bifidobacterium longum on Eosinophil Infiltration in Mice with Atopic Dermatitis

[0060] 50 healthy female C57BL/6 mice weighing 18-20 g were randomly divided into 5 groups, each with 10 mice. The 5 groups were respectively: a blank group (Control), a model group (Model) administered with 2,4-dinitrofluorobenzene (DNFB), a CCFM1029 group administered with Bifidobacterium longum CCFM1029, an A1 group administered with Bifidobacterium longum A1, and an A2 group administered with Bifidobacterium longum A2. The CCFM1029 group, the A1 group and the A2 group were all treatment groups.

[0061] The experiment lasts for four weeks in total. The first week was the adaptation period of mice. Gavage was started from the second week to the end of the experiment. The treatment groups were given bacterial solutions of the Bifidobacterium longum CCFM1029, A1 and A2 by gavage. 0.2 mL of bacterial solution (the total amount of viable bacteria in a single gavage was 1×10.sup.9 CFU) was given per mouse per time by gavage. The blank group and the model group were not treated with the intervention of bacterial solutions, and only the same amount of normal saline was given by gavage as a control. The third to fourth weeks were the modeling period. On the 1st day of modeling, the back skin of the 5 groups of mice was depilated for an area of approximately 2.5 cm×2.5 cm, and 50 μL of 0.5% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups to sensitize and stimulate skin lesions. On the 5.sup.th, 8.sup.th, 11.sup.th, and 14.sup.th days, 20 μL of 0.2% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups. Only the same amount of acetone/olive oil matrix solution was applied to the depilated areas on the back of the mice in the blank group as a control. All groups were free access to water and food.

[0062] After the modeling (that is, on the 15.sup.th day), blood was taken and the mice were sacrificed. The skin of the depilated areas on the back of the mice was taken for histopathological analysis. Histopathological sections of the back skin of mice were subjected to hematoxylin-eosin staining, and then eosinophil counting and analysis were performed by professional technicians (the results are shown in FIG. 3).

[0063] It can be seen from FIG. 3 that the Bifidobacterium longum CCFM1029 significantly reduced the number of eosinophils in the skin tissues, reduced the inflammatory infiltration produced by the eosinophils, and thereby inhibited skin tissue inflammation. However, the Bifidobacterium longum A1 group and Bifidobacterium longum A2 group cannot inhibit the number of eosinophils in the tissues, has no significant effect on tissue inflammatory infiltration, and cannot relieve skin inflammation in mice.

[0064] The experiment shows that the Bifidobacterium longum CCFM1029 can significantly inhibit the inflammatory infiltration produced by eosinophils in the skin of mice with atopic dermatitis.

Example 6: Effects of Different Bifidobacterium longum on the Total Serum IgE Level in Mice with Atopic Dermatitis

[0065] 50 healthy female C57BL/6 mice weighing 18-20 g were randomly divided into 5 groups, each with 10 mice. The 5 groups were respectively: a blank group (Control), a model group (Model) administered with 2,4-dinitrofluorobenzene (DNFB), a CCFM1029 group administered with Bifidobacterium longum CCFM1029, an A1 group administered with Bifidobacterium longum A1, and an A2 group administered with Bifidobacterium longum A2. The CCFM1029 group, the A1 group and the A2 group were all treatment groups.

[0066] The experiment lasts for four weeks in total. The first week was the adaptation period of mice. Gavage was started from the second week to the end of the experiment. The treatment groups were given bacterial solutions of the Bifidobacterium longum CCFM1029, A1 and A2 by gavage. 0.2 mL of bacterial solution (the total amount of viable bacteria in a single gavage was 1×10.sup.9 CFU) was given per mouse per time by gavage. The blank group and the model group were not treated with the intervention of bacterial solutions, and only the same amount of normal saline was given by gavage as a control. The third to fourth weeks were the modeling period. On the 1st day of modeling, the back skin of the 5 groups of mice was depilated for an area of approximately 2.5 cm×2.5 cm, and 50 μL of 0.5% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups to sensitize and stimulate skin lesions. On the 5.sup.th, 8.sup.th, 11.sup.th, and 14.sup.th days, 20 μL of 0.2% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups. Only the same amount of acetone/olive oil matrix solution was applied to the depilated areas on the back of the mice in the blank group as a control. All groups were free access to water and food.

[0067] After the modeling (that is, on the 15.sup.th day), blood was taken and the mice were sacrificed. The serum of mice was taken, and the total serum IgE level was measured with an enzyme-linked immunosorbent assay kit (the results are shown in FIG. 4).

[0068] It can be seen from FIG. 4 that compared with the model group (Model), the Bifidobacterium longum CCFM1029 significantly reduced the total serum IgE level in mice, and was beneficial to inhibiting the Th2-type immune response, thereby helping relieve the pathological inflammation of atopic dermatitis. However, the Bifidobacterium longum A1 group and the Bifidobacterium longum A2 group cannot inhibit the synthesis of serum IgE, so the intervention of the Bifidobacterium longum A1 and A2 has no significant effect on the pathological inflammation of atopic dermatitis.

[0069] The experiment shows that the Bifidobacterium longum CCFM1029 can significantly reduce the total serum IgE level in mice, and is beneficial to relieving the pathological inflammation of atopic dermatitis.

Example 7: Effects of Different Bifidobacterium longum on the Levels of IL-4 and IL-13 in the Skin Tissues of Mice with Atopic Dermatitis

[0070] 50 healthy female C57BL/6 mice weighing 18-20 g were randomly divided into 5 groups, each with 10 mice. The 5 groups were respectively: a blank group (Control), a model group (Model) administered with 2,4-dinitrofluorobenzene (DNFB), a CCFM1029 group administered with Bifidobacterium longum CCFM1029, an A1 group administered with Bifidobacterium longum A1, and an A2 group administered with Bifidobacterium longum A2. The CCFM1029 group, the A1 group and the A2 group were all treatment groups.

[0071] The experiment lasts for four weeks in total. The first week was the adaptation period of mice. Gavage was started from the second week to the end of the experiment. The treatment groups were given bacterial solutions of the Bifidobacterium longum CCFM1029, A1 and A2 by gavage. 0.2 mL of bacterial solution (the total amount of viable bacteria in a single gavage was 1×10.sup.9 CFU) was given per mouse per time by gavage. The blank group and the model group were not treated with the intervention of bacterial solutions, and only the same amount of normal saline was given by gavage as a control. The third to fourth weeks were the modeling period. On the 1st day of modeling, the back skin of the 5 groups of mice was depilated for an area of approximately 2.5 cm×2.5 cm, and 50 μL of 0.5% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups to sensitize and stimulate skin lesions. On the 5.sup.th, 8.sup.th, 11.sup.th, and 14.sup.th days, 20 μL of 0.2% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups. Only the same amount of acetone/olive oil matrix solution was applied to the depilated areas on the back of the mice in the blank group as a control. All groups were free access to water and food.

[0072] After the modeling (that is, on the 15.sup.th day), blood was taken and the mice were sacrificed. Then the skin tissues of the depilated areas on the back of mice were taken, and the levels of Th2-type immune response cytokines IL-4 and IL-13 were measured with an enzyme-linked immunosorbent assay kit (the results are shown in FIG. 5 to FIG. 6).

[0073] It can be seen from FIG. 5 to FIG. 6 that compared with the model group (Model), the Bifidobacterium longum CCFM1029 significantly reduced the levels of IL-4 and IL-13 in the skin tissues of mice, and significantly inhibited the Th2-type immune response, thereby helping relieve the pathological inflammation state caused by Th2-type abnormal immune response. However, the Bifidobacterium longum A1 group and the Bifidobacterium longum A2 group cannot reduce the levels of IL-4 and IL-13 in the skin tissues, so the intervention of the Bifidobacterium longum A1 and A2 has no significant effect on the pathological inflammation of atopic dermatitis.

[0074] The experiment shows that the Bifidobacterium longum CCFM1029 can significantly reduce the levels of cytokines IL-4 and IL-13 related to Th2-type immune response, and help relieve the pathological inflammation state caused by the Th2-type abnormal immune response.

Example 8: Effects of Different Bifidobacterium longum on the Level of Histamine in the Skin Tissues of Mice with Atopic Dermatitis

[0075] 50 healthy female C57BL/6 mice weighing 18-20 g were randomly divided into 5 groups, each with 10 mice. The 5 groups were respectively: a blank group (Control), a model group (Model) administered with 2,4-dinitrofluorobenzene (DNFB), a CCFM1029 group administered with Bifidobacterium longum CCFM1029, an A1 group administered with Bifidobacterium longum A1, and an A2 group administered with Bifidobacterium longum A2. The CCFM1029 group, the A1 group and the A2 group were all treatment groups.

[0076] The experiment lasts for four weeks in total. The first week was the adaptation period of mice. Gavage was started from the second week to the end of the experiment. The treatment groups were given bacterial solutions of the Bifidobacterium longum CCFM1029, A1 and A2 by gavage. 0.2 mL of bacterial solution (the total amount of viable bacteria in a single gavage was 1×10.sup.9 CFU) was given per mouse per time by gavage. The blank group and the model group were not treated with the intervention of bacterial solutions, and only the same amount of normal saline was given by gavage as a control. The third to fourth weeks were the modeling period. On the 1st day of modeling, the back skin of the 5 groups of mice was depilated for an area of approximately 2.5 cm×2.5 cm, and 50 μL of 0.5% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups to sensitize and stimulate skin lesions. On the 5.sup.th, 8.sup.th, 11.sup.th, and 14.sup.th days, 20 μL of 0.2% DNFB solution was applied to the depilated areas on the back of the mice in the model group and the treatment groups. Only the same amount of acetone/olive oil matrix solution was applied to the depilated areas on the back of the mice in the blank group as a control. All groups were free access to water and food.

[0077] After the modeling (that is, on the 15.sup.th day), blood was taken and the mice were sacrificed. Then the skin tissues of the depilated areas on the back of mice were taken, and the inflammatory factor histamine related to degranulation of mast cells was measured with an enzyme-linked immunosorbent assay kit (the results are shown in FIG. 7).

[0078] It can be seen from FIG. 7 that compared with the model group (Model), the Bifidobacterium longum CCFM1029 significantly reduced the level of histamine in the skin tissues of mice. It can be inferred that the Bifidobacterium longum CCFM1029 significantly reduced the degranulation of mast cells, prevented the release of histamine in the damaged skin tissues, and relieved skin itching of mice. However, the Bifidobacterium longum A1 group and the Bifidobacterium longum A2 group cannot reduce the level of histamine in the skin tissues, and even promotes the release of histamine. Therefore, the Bifidobacterium longum A1 group and the Bifidobacterium longum A2 group cannot inhibit degranulation of mast cells in the tissues or further prevent the release of histamine, and cannot relieve skin itching of the mice.

[0079] The experiment shows that the Bifidobacterium longum CCFM1029 can significantly reduce the level of histamine in skin tissues, and inhibit the degranulation of mast cells in skin tissues, thereby relieving skin itching of mice and preventing further development of atopic dermatitis.

Example 9: Preparation of Solid Beverage Containing Bifidobacterium longum CCFM1029

[0080] A culture medium was inoculated with the Bifidobacterium longum CCFM1029 at an inoculum concentration of 3% of the total mass of the culture medium and culturing was performed at 37° C. for 18 h to obtain a culture solution. The culture solution was centrifuged to obtain bacterial cells. The bacterial cells were washed with a phosphate buffer with the pH of 7.2-7.4 for 3 times, and then resuspended with a trehalose freeze-drying protective agent with the trehalose concentration of 100 g/L (the mass ratio of the freeze-drying protective agent to the bacterial cells was 2:1) to obtain a resuspension. The resuspension was freeze-dried by a vacuum freezing process to obtain Bifidobacterium longum CCFM1029 bacterial powder. The culture medium includes 87.7% water, 10% enzymatically hydrolyzed skim milk, 0.5% glucose, 1.5% tryptone and 0.3% yeast extract solution, of the total mass of the culture medium. The pH of the culture medium was 6.8.

[0081] The Bifidobacterium longum CCFM1029 bacterial powder containing 1×10.sup.10 CFU was mixed with maltodextrin with the total mass of the bacterial powder and the maltodextrin being 1 gram to obtain a solid beverage containing the Bifidobacterium longum CCFM1029.

[0082] 10 grams of the solid beverage containing the Bifidobacterium longum CCFM1029 was reconstituted with normal saline and the volume was set to 20 mL. 0.2 mL of the dilution was given to each mouse per day by gavage for three consecutive weeks. The solid beverage can effectively relieve the symptoms of atopic dermatitis in mice, and has excellent effects in the prevention and/or treatment of atopic dermatitis.