Probiotic mixed preparation with anti-influenza ability and application thereof

Abstract

The disclosure discloses a probiotic mixed preparation with anti-influenza ability and application thereof, and belongs to the technical fields of microorganisms and medicines. The probiotic mixed preparation has anti-influenza effects, which are embodied in: (1) significantly reducing the degree of weight loss of influenza mice; (2) significantly improving the blood indexes of the influenza mice; (3) significantly improving the inflammation status of respiratory tract infections in the influenza mice; (4) significantly reducing the viral load in the lungs of the influenza mice (i.e., significantly inhibiting the replication and multiplication of influenza viruses in the influenza mice); and (5) significantly increasing the expression quantity of antiviral protein MxA in the lungs of the influenza mice. Therefore, the probiotic mixed preparation has great application prospects in preparation of a product for preventing and/or treating atopic dermatitis and even preventing and/or treating influenza.

Claims

1. A probiotic preparation, comprising a fermentation agent, wherein the fermentation agent comprises Bifidobacterium breve (B. breve) and Lactobacillus mucosae, and wherein the fermentation agent is produced by: inoculating B. breve and L. mucosae each separately into an individual medium at an inoculation amount of 5% to 8% of total mass of the medium; culturing the B. breve inoculant in an anaerobic environment at 37° C. for 30 hours, and culturing the L. mucosae inoculant at 37° C. for 18 hours, to obtain individual culture solutions of each; centrifuging the culture solutions to obtain B. breve and L. mucosae bacterial cell pellets; washing the bacterial cell pellets 2 to 4 times with a phosphate buffer solution with a pH value of 7.2; resuspending the bacterial cell pellets in 100 g/L trehalose to obtain individual resuspension solutions; and freeze-drying the resuspension solutions individually by vacuum freezing to obtain B. breve and L. mucosae bacterial powders; and mixing the obtained L. mucosae bacterial powder and the B. breve bacterial powder to obtain a fermentation agent, wherein the probiotic preparation comprises the fermentation agent, wherein the L. mucosae, is deposited at Guangdong Microbial Culture Collection Center, 5th Floor, Building 59, Grand Courtyard 100, Xianlie Middle Road, Guangzhou, with deposit number GDMCC No. 60460; and wherein the B. breve is deposited at Guangdong Microbial Culture Collection Center 5th Floor, Building 59, Grand Courtyard 100, Xianlie Middle Road, Guangzhou, with deposit number GDMCC No. 60459.

2. The probiotic preparation of claim 1, wherein a viable count of L. mucosae in the probiotic preparation is not less than 1×10.sup.6 CFU/mL; and a viable count of B. breve in the probiotic preparation is not less than 1×10.sup.6 CFU/mL.

3. A product for treating influenza, comprising the probiotic preparation of claim 1.

4. The product for treating influenza of claim 3, wherein the product comprises food, medicine, or health food.

5. The product for treating influenza of claim 4, further comprising a pharmaceutical carrier or a pharmaceutical excipient.

6. The product for treating influenza of claim 4, wherein the food comprises a dairy product, a bean product, a fruit and vegetable product or a beverage.

7. The product for treating influenza of claim 6, wherein a mass ratio of the trehalose to the bacterial cells is 2:1.

8. The product for treating influenza of claim 3, wherein a pH value of the medium is 6.8.

Description

BRIEF DESCRIPTION OF FIGURES

(1) FIG. 1 shows comparison of body weight changes of different groups of influenza mice (L. mucosae).

(2) FIG. 2 shows comparison of the blood test index (neutrophils) of different groups of influenza mice (L. mucosae).

(3) FIG. 3 shows comparison of the blood test index (lymphocytes) of different groups of influenza mice (L. mucosae).

(4) FIG. 4 shows comparison of histopathological sections of lungs of different groups of influenza mice (L. mucosae).

(5) FIG. 5 shows comparison of viral load of lungs of different groups of influenza mice (L. mucosae).

(6) FIG. 6 shows comparison of body weight changes of different groups of influenza mice (B. breve).

(7) FIG. 7 shows comparison of the blood test index (neutrophils) of different groups of influenza mice (B. breve).

(8) FIG. 8 shows comparison of the blood test index (lymphocytes) of different groups of influenza mice (B. breve).

(9) FIG. 9 shows comparison of histopathological sections of lungs of different groups of influenza mice (B. breve).

(10) FIG. 10 shows comparison of expression quantity of antiviral protein MxA in lungs of different groups of influenza mice (B. breve).

(11) FIG. 11 shows comparison of body weight changes of different groups of influenza mice (mixed bacteria).

(12) FIG. 12 shows comparison of the blood test index (neutrophils) of different groups of influenza mice (mixed bacteria).

(13) FIG. 13 shows comparison of the blood test index (lymphocytes) of different groups of influenza mice (mixed bacteria).

(14) FIG. 14 shows comparison of histopathological sections of lungs of different groups of influenza mice (mixed bacteria).

(15) FIG. 15 shows comparison of viral load of lungs of different groups of influenza mice (mixed bacteria).

(16) FIG. 16 shows comparison of expression quantity of antiviral protein MxA in lungs of different groups of influenza mice (mixed bacteria).

DETAILED DESCRIPTION

(17) Media Involved in the Following Examples are as Follows:

(18) MRS plate (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.

EXAMPLE 1-1

Screening and Identification of L. mucosae

(19) 1. Screening

(20) Human feces was used as a sample. After being pretreated, the sample was stored in about 20% glycerol in a refrigerator at −80° C. After being taken out and thawed, the sample was mixed, and 0.5 mL of the sample was pipetted and added to 4.5 mL. The sample was subjected to gradient dilution with 0.9% normal saline containing 0.05% cysteine. An appropriate gradient diluent was selected and coated on an MRS plate supplemented with 0.05% cysteine, and was cultured at 37° C. for 48 h. Typical colonies were selected and streaked on the MRS plate for purification. Single colonies were selected and transferred to a liquid MRS medium (containing 0.05% cysteine) for enrichment culture. The bacteria were preserved in 30% glycerol to obtain a strain GDMCC60460 and a strain F1.

(21) 2. Identification

(22) The genomes of the GDMCC60460 and the F1 were extracted. The 16S rDNAs of the GDMCC60460 and the F1 were subjected to amplification and sequencing (Shanghai Sangon Biotech Co., Ltd.). The sequences were compared in GenBank, and the results showed that the strains were L. mucosae and were named as L. mucosae GDMCC60460 and L. mucosae F1.

EXAMPLE 1-2

Culture of L. mucosae

(23) The L. mucosae GDMCC60460 was inoculated into an MRS solid medium (containing 0.05% cysteine) and cultured at 37° C. for 48 h. The colonies were observed and the bacterial cells were observed under a microscope. It was found that the colonies were round, rough and transparent, and the bacterial cells were short rod-shaped.

(24) The L. mucosae GDMCC60460 was inoculated into an MRS medium (containing 0.05% cysteine) and cultured at 37° C. for 48 h. A growth curve was made, and it was found that the strain reached a stationary phase after being cultured at 37° C. for 12 h. At the same time, it was observed that the strain performs heterofermentation, and produces acid and gas from glucose.

(25) The L. mucosae GDMCC60460 was inoculated into MRS media (containing 0.05% cysteine) and cultured at 10, 15, 20, 25, 30, 35, 40, 45 and 50° C. for 48 h respectively, and the growth conditions were observed. It was found that the strain grows well at 20-35° C. and can still grow at 45° C., but hardly grows at or below 15° C. or at 50° C.

(26) After being inoculated into the MRS medium (containing 0.05% cysteine) and cultured at 37° C. for 48 h, the L. mucosae GDMCC60460 was transferred into a fresh MRS medium (containing 0.05% cysteine) and cultured under the same conditions for 30 h. The bacterial cells were centrifuged at 6000 g for 15 min. After being washed with 0.9% normal saline, the bacterial cells were centrifuged again at 6000 g for 10 min. The bacterial cells were resuspended in a 30% sucrose solution, and frozen and stored at −80° C. for later use.

EXAMPLE 1-3

Effect of L. mucosae on Body Weight of Influenza Mice

(27) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae GDMCC60460 (GDMCC60460), and a L. mucosae intervention group with intragastric administration of L. mucosae F1 (F1), with 8 mice in each group.

(28) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria every day, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria every day, and the other groups (Control, Model, Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(29) On the first day of the experiment, except for the blank control group (Control), the mice in the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(30) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(31) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(32) During the 5 days of the experiment, the mice were weighed each day before intragastric administration, and the changes in body weight were continuously recorded for five days. The results are shown in FIG. 1.

(33) It can be seen from FIG. 1 that the body weight of mice began to decrease on the third day after challenge, and the weight loss was the most obvious on the fourth day (P<0.05). Compared with the control group (Control), the body weight of the model group (Model) decreased by more than 10%, the body weight of the drug treatment group (Treatment) decreased by about 5%, the body weight of the L. mucosae F1 intervention group decreased by about 5.5%, and the body weight of the L. mucosae GDMCC60460 intervention group decreased by only 3%.

(34) It shows that the L. mucosae GDMCC60460 in the disclosure can significantly improve the weight loss symptoms of influenza mice.

EXAMPLE 1-4

Effect of L. mucosae on Blood Indexes of Influenza Mice

(35) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae (GDMCC60460), and a L. mucosae intervention group with intragastric administration of L. mucosae F1 (F1), with 8 mice in each group.

(36) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae suspension diluent containing 10.sup.9 CFU of bacteria every day, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria every day, and the other groups (Control, Model, Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(37) On the first day of the experiment, except the blank control group (Control), the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(38) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(39) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(40) The mice were sacrificed after blood collection on the fifth day after challenge. The collected mouse blood was placed in an anticoagulant tube and shaken gently to make the blood fully contact an anticoagulant. Then the blood was sent to an animal hospital for routine analysis and detection of blood (in the early stage of influenza virus infection, a large number of natural immune cells such as neutrophils and lymphocytes will participate in the defense process, therefore, the routine analysis and detection of blood focuses on detecting changes in the neutrophils and lymphocytes). The results are shown in FIGS. 2-3.

(41) As can be seen from FIGS. 2-3, compared with the blank control group (Control), the neutrophils in the model group (Model) significantly increased and the lymphocytes in the model group (Model) significantly decreased, while the other four groups had no significant change.

(42) It is shown that the L. mucosae GDMCC60460 in the disclosure can play the same immune regulating function on the body as the ribavirin drug.

EXAMPLE 1-5

Effect of L. mucosae on Inflammation of Respiratory Tract Infection in Influenza Mice

(43) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae (GDMCC60460), and a L. mucosae intervention group with intragastric administration of L. mucosae F1 (F1), with 8 mice in each group.

(44) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria every day, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria every day, and the other groups (Control, Model, Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(45) On the first day of the experiment, except the blank control group (Control), the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(46) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(47) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the blank control group and influenza model group (Control and Model) were intragastrically administered with 0.2 mL of normal saline every day.

(48) The mice were sacrificed after blood collection on the fifth day after challenge. The left lungs of the mice were immediately removed and fixed in 4% paraformaldehyde. The lungs were histopathologically sectioned after fixation. The histopathological sections of the mouse lungs were subjected to hematoxylin-eosin staining after sectioning. The histopathological sections of the mouse lungs were histopathologically scored by professional technicians. The results are shown in FIG. 4.

(49) It can be seen from FIG. 4 that the lung tissue structures of the mice of the blank control group (Control) are relatively complete, and have no infiltration of inflammatory cells; the mice of the model group (Model) show large-scale characterization of inflammation and even hyperemia; the lungs of the mice of the treatment group (Treatment) and the L. mucosae intervention group (GDMCC60460) have mild infiltration of inflammatory cells, which occurs near the bronchus.

(50) The above animal experiments show that influenza infection can cause influenzal pneumonia in mice. After the lungs are infected by the virus, the tissue structure is destroyed and massive inflammatory infiltration occurs. The L. mucosae GDMCC60460 of the disclosure can alleviate lung inflammation and pneumonia symptoms in mice, and is equivalent in effect to the ribavirin drug treatment commonly used for influenza.

EXAMPLE 1-6

Effect of L. mucosae on Viral Load in Lungs of Influenza Mice

(51) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae (GDMCC60460), and a L. mucosae intervention group with intragastric administration of L. mucosae F1 (F1), with 8 mice in each group.

(52) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae suspension diluent containing 10.sup.9 CFU of bacteria every day, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria every day, and the other groups (Control, Model, Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(53) On the first day of the experiment, except the blank control group (Control), the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(54) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the L. mucosae F1 intervention group (F1) was intragastrically administered with a L. mucosae F1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model, Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(55) The mice were sacrificed after blood collection on the fifth day after challenge. After the mice were sacrificed, the right lung tissues of the mice were taken out and placed in 1 mL of TRIZOL, and cryopreserved in a refrigerator at −80° C. for later use. During extraction, the right lung tissue samples were thawed on ice, and then ground using a DEPC-treated sterile grinder. 200 μL of chloroform was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and 500 μL of supernatant was removed. An equal volume of isopropanol was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. 75% ethanol was added for washing RNA once, the mixture was centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. After the ethanol evaporated to dryness, 40 μL of DEPC treating water was added to dissolve the RNA. The extracted RNA was cryopreserved in the refrigerator at −80° C. for later use.

(56) A qPCR method was used to determine the viral load, GAPDH was used as the internal reference, a classic 2.sup.−ΔΔt calculation method was used, and the model group was used as contrast processing data. The results are shown in FIG. 5.

(57) It can be seen from FIG. 5 that the viral load in the lungs of mice of the drug treatment group (Treatment) is 38.03% of that of the model group, while the viral load in the lungs of mice of the L. mucosae intervention group (GDMCC60460) was only 16.30% of that of the model group.

(58) The above experiments show that the L. mucosae GDMCC60460 of the disclosure can significantly reduce the viral load in the lungs of mice infected with influenza, with significant difference (P=0.0022). The reduction in viral load in the lungs of mice of both the L. mucosae F1 group and the drug treatment group (Treatment) has significance (P values are 0.0309 and 0.0170, respectively). It is sufficient to show that the therapeutical effect of the L. mucosae GDMCC60460 of the disclosure is better than that of influenza drugs in terms of resistance to virus infection.

EXAMPLE 2-1

Screening and Identification of B. breve

(59) 1. Screening

(60) Human feces was used as a sample. After the sample was pretreated, the sample was stored in about 20% glycerol in a refrigerator at −80° C. After being taken out and thawed, the sample was mixed, and 0.5 mL of the sample was pipetted and added to 4.5 mL. The sample was subjected to gradient dilution with 0.9% normal saline containing 0.05% cysteine. An appropriate gradient diluent was selected and coated on an MRS plate supplemented with 0.05% cysteine, and was cultured at 37° C. for 48 h. Typical colonies were selected and streaked on the MRS plate for purification. Single colonies were selected and transferred to a liquid MRS medium (containing 0.05% cysteine) for enrichment culture. The bacteria were preserved in 30% glycerol to obtain a strain CCFM1026 and a strain B1.

(61) 2. Identification

(62) The genomes of the CCFM1026 and the B1 were extracted. The 16S rDNAs of the CCFM1026 and the B1 were subjected to amplification and sequencing (Shanghai Sangon Biotech Co., Ltd.). The sequences were compared in GenBank. The results showed that the Query cover of the strain and B. breve is 100% and the identity (Ident) is 99%, so the strains were determined to be B. breve and were named as B. breve CCFM1026 and B. breve B1.

EXAMPLE 2-2

Culture of B. breve

(63) The B. breve CCFM1026 was inoculated into an MRS solid medium (containing 0.05% cysteine) and cultured at 37° C. for 48 h. The colonies were observed and were found to be round and white.

(64) The bacterial cells were observed and stained under a microscope, and it was found that the bacterial cells are short rod-shaped, are Gram-positive, are irregularly stained with methylene blue staining, have no spores, flagella and capsules, and do not move.

(65) The B. breve CCFM1026 was inoculated into an MRS liquid medium (containing 0.05% cysteine) and cultured at 37° C. for 48 h. A growth curve was made, and it was found that the strain reached a stationary phase after being cultured at 37° C. for 30 h. The strain performs atypical heterolactic fermentation using glucose.

(66) After being cultured in the MRS medium (containing 0.05% cysteine) at 37° C. for 48 h, the B. breve CCFM1026 was transferred into a fresh MRS medium (containing 0.05% cysteine) and cultured under the same conditions for 30 h. The bacterial cells were centrifuged at 6000 g for 15 min. After being washed with 0.9% normal saline, the bacterial cells were centrifuged again at 6000 g for 10 min. The bacterial cells were resuspended in a 30% sucrose solution, and frozen and stored at −80° C. for later use.

EXAMPLE 2-3

Effect of B. breve on Body Weight of Influenza Mice

(67) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a B. breve intervention group with intragastric administration of B. breve B1 (B1), with 8 mice in each group.

(68) Two weeks before the experiment, the B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(69) On the first day of the experiment, except the blank control group (Control), the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(70) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(71) Intragastric administration was continued for 4 days after challenge. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(72) During the 5 days of the experiment, the mice were weighed each day before intragastric administration, and the changes in body weight were continuously recorded for five days. The results are shown in FIG. 6.

(73) It can be seen from FIG. 6 that the body weight of mice began to decrease on the third day after challenge, and the weight loss was the most obvious on the fourth day (P<0.05). Compared with the control group (Control), the body weight of the model group (Model) decreased by more than 10%, the body weight of the drug treatment group (Treatment) decreased by about 5%, while the body weight of the B. breve intervention group (CCFM1026) and the B. breve B1 group decreased by only 5%.

(74) It shows that the B. breve CCFM1026 and B1 in the disclosure can significantly improve the weight loss symptoms of influenza mice.

EXAMPLE 2-4

Effect of B. breve on Blood Indexes of Influenza Mice

(75) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a B. breve intervention group with intragastric administration of B. breve B1 (B1), with 8 mice in each group.

(76) Two weeks before the experiment, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(77) On the first day of the experiment, except the blank control group (Control), the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(78) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(79) Intragastric administration was continued for 4 days after challenge. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(80) The mice were sacrificed after blood collection on the fifth day after challenge. The collected mouse blood was placed in an anticoagulant tube and shaken gently to make the blood fully contact an anticoagulant. Then the blood was sent to an animal hospital for routine analysis and detection of blood (in the early stage of influenza virus infection, a large number of natural immune cells such as neutrophils and lymphocytes will participate in the defense process, therefore, the routine analysis and detection of blood focuses on detecting changes in the neutrophils and lymphocytes). The results are shown in FIGS. 7-8.

(81) As can be seen from FIGS. 7-8, compared with the blank control group (Control), the percentages of neutrophils and lymphocytes in mice of the model group (Model) were significantly abnormal, and were significantly different from those of the control group (control) (p values are 0.0015 and 0.0011, respectively). Yet, the percentages of neutrophils and lymphocytes in mice of the B. breve intervention group (CCFM1026) and the drug treatment group (Treatment) tended to those of the blank control group (Control) without significant differences.

(82) It is shown that the B. breve of the disclosure has the same effect as the ribavirin drug, and can actively participate in the influenza-related immune regulation of mice and alleviate the symptoms of influenza in mice.

EXAMPLE 2-5

Effect of B. breve on Inflammation of Respiratory Tract Infection in Influenza Mice

(83) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a B. breve intervention group with intragastric administration of B. breve B1 (B1), with 8 mice in each group.

(84) Two weeks before the experiment, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(85) On the first day of the experiment, except the blank control group (Control), the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(86) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(87) Intragastric administration was continued for 4 days after challenge. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(88) The mice were sacrificed after blood collection on the fifth day after challenge. The left lungs of the mice were immediately removed and fixed in 4% paraformaldehyde. The lungs were histopathologically sectioned after fixation. The histopathological sections of the mouse lungs were subjected to hematoxylin-eosin staining after sectioning. The histopathological sections of the mouse lungs were histopathologically scored by professional technicians. The results are shown in FIG. 9.

(89) It can be seen from FIG. 9 that the lung tissue structures of the mice of the blank control group (Control) are relatively complete, and have no infiltration of inflammatory cells; the mice of the model group (Model) have severe inflammatory infiltration, and even local hemorrhage; the B. breve B1 intervention group (B1) showed moderate inflammatory infiltration near the bronchus; while the treatment group (Treatment) and the B. breve intervention group (CCFM1026) had relatively mild inflammation in the lungs of mice.

(90) The above animal experiments show that influenza infection can cause influenzal pneumonia in mice. After the lungs are infected by the virus, the tissue structure is destroyed and massive inflammatory infiltration occurs. The B. breve of the disclosure can alleviate lung inflammation and pneumonia symptoms in mice, and is equivalent in effect to the ribavirin drug treatment commonly used for influenza.

EXAMPLE 2-6

Effect of B. breve on Viral Load in Lungs of Influenza Mice

(91) 40 healthy ICR female mice weighing 20-24 g were randomly divided into five groups. The five groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a B. breve intervention group with intragastric administration of B. breve B1 (B1), with 8 mice in each group.

(92) Two weeks before the experiment, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(93) On the first day of the experiment, except the blank control group (Control), the other four groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(94) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(95) Intragastric administration was continued for 4 days after challenge. The B. breve intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve B1 intervention group (B1) was intragastrically administered with a B. breve B1 suspension diluent containing the same amount of bacteria, and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(96) The mice were sacrificed after blood collection on the fifth day after challenge. After the mice were sacrificed, the right lung tissues of the mice were taken out and placed in 1 mL of TRIZOL, and cryopreserved in a refrigerator at −80° C. for later use. During extraction, the right lung tissue samples were thawed on ice, and then ground using a DEPC-treated sterile grinder. 200 μL of chloroform was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and 500 μL of supernatant was removed. An equal volume of isopropanol was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. 75% ethanol was added for washing RNA once, the mixture was centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. After the ethanol evaporated to dryness, 40 μL of DEPC treating water was added to dissolve the RNA. The extracted RNA was cryopreserved in the refrigerator at −80° C. for later use.

(97) A qPCR method was used to determine the relative expression quantity of MxA (the body will react defensively to the influenza virus to clear the invading virus and restore health, MxA is an antiviral protein secreted by the body, which can effectively prevent the virus from replicating), GAPDH was used as the internal reference, a classic 2.sup.−ΔΔt calculation method was used, and the model group was used as the contrast processing data. The results are shown in FIG. 10.

(98) It can be seen from FIG. 10 that the expression quantity of MxA in the lungs of mice of the drug treatment group (Treatment) is 2.62 times that of the model group (Model), and the expression quantity of MxA in the lungs of mice of the B. breve B1 intervention group is 2.67 times that of the model group (Model), with no significant difference. Yet, the expression quantity of MxA in the lungs of mice of the B. breve intervention group (CCFM1026) is 3.46 times that of the model group (Model), which is significantly improved (p value is 0.0292).

(99) The above experiments show that the B. breve CCFM1026 of the disclosure can significantly enhance the immunity ability of influenza mice, and promote increase of the expression quantity of MxA antiviral protein, thereby counteracting virus replication, and helping the body to recover. The B. breve CCFM1026 significantly alleviates the respiratory tract inflammation, and has even better effect than drug treatment.

EXAMPLE 3-1

Effect of Mixed Bacteria on Body Weight of Influenza Mice

(100) 48 healthy ICR female mice weighing 20-24 g were randomly divided into six groups. The six groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae GDMCC60460 (GDMCC60460), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a bacterial preparation intervention group with intragastric administration of a probiotic mixed preparation (GDMCC60460+1026), with 8 mice in each group.

(101) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(102) On the first day of the experiment, except the blank control group (Control), the other five groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(103) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(104) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(105) During the 5 days of the experiment, the mice were weighed each day before intragastric administration, and the changes in body weight were continuously recorded for five days. The results are shown in FIG. 11.

(106) It can be seen from FIG. 11 that the body weight of mice began to decrease on the third day after challenge, and the weight loss was the most obvious on the fourth day (P<0.05). Compared with the control group (Control), the body weight of the model group (Model) decreased by more than 10%, the body weight of the drug treatment group (Treatment) decreased by about 5%, the body weight of the L. mucosae intervention group (GDMCC60460) decreased by about 3%, the body weight of the B. breve intervention group (CCFM1026) decreased by about 5%, and the bacterial preparation intervention group (GDMCC60460+1026) mice had the smallest weight loss of less than 3%, and had better intervention effect than those of the drug treatment group (Treatment), the L. mucosae intervention group (GDMCC60460), and the B. breve intervention group (CCFM1026). It is sufficient to explain that ingestion of the probiotic mixed preparation of the disclosure can obviously alleviate weight loss of influenza mice caused by influenza cold.

EXAMPLE 3-2

Effect of Mixed Bacteria on Blood Indexes of Influenza Mice

(107) 48 healthy ICR female mice weighing 20-24 g were randomly divided into six groups. The six groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae GDMCC60460 (GDMCC60460), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a bacterial preparation intervention group with intragastric administration of a probiotic mixed preparation (GDMCC60460+1026), with 8 mice in each group.

(108) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(109) On the first day of the experiment, except the blank control group (Control), the other five groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(110) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(111) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(112) The mice were sacrificed after blood collection on the fifth day after challenge. The collected mouse blood was placed in an anticoagulant tube and shaken gently to make the blood fully contact an anticoagulant. Then the blood was sent to an animal hospital for routine analysis and detection of blood (in the early stage of influenza virus infection, a large number of natural immune cells such as neutrophils and lymphocytes will participate in the defense process, therefore, the routine analysis and detection of blood focuses on detecting changes in the neutrophils and lymphocytes). The results are shown in FIGS. 12-13.

(113) As can be seen from FIGS. 12-13, after the mice have caught influenza cold, the proportion of natural immune cells in the mice will change differently. That is, the levels of the immune cells such as neutrophils and lymphocytes in the mice of the model group (Model) show changes in different trends, and are significantly different from those in the blank control group (Control). Yet, the indexes of the mice in the intervention group ingesting probiotics tend to normal values and have no significant difference from those of the blank control group (Control). Compared with the model group, in the groups ingesting probiotics, the percentage of neutrophils decreased (Control: 22.60%, GDMCC60460+1026: 33.10%, GDMCC60460: 35.75%, CCFM1026: 37.10%), and correspondingly, the percentage of lymphocytes increased (Control: 73.70%, GDMCC60460+1026: 63.95%, GDMCC60460: 60.56%, CCFM1026: 62.10%). It can be seen that the probiotic mixed preparation group (GDMCC60460+1026) tends to the blank control group (Control) to a slightly stronger extent than the two single-bacterium (GDMCC60460 and CCFM1026) groups. It shows that the probiotics ingested by the mice can participate in the immune regulation of the body, help the body to resist the invasion of influenza virus, and maintain the health of the body, and the effect of the mixed bacterial preparation is better than that of the single bacterium.

EXAMPLE 3-3

Effect of Mixed Bacteria on Inflammation of Respiratory Tract Infection in Influenza Mice

(114) 48 healthy ICR female mice weighing 20-24 g were randomly divided into six groups. The six groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae GDMCC60460 (GDMCC60460), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a bacterial preparation intervention group with intragastric administration of a probiotic mixed preparation (GDMCC60460+1026), with 8 mice in each group.

(115) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(116) On the first day of the experiment, except the blank control group (Control), the other five groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(117) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(118) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(119) The mice were sacrificed after blood collection on the fifth day after challenge. The left lungs of the mice were immediately removed and fixed in 4% paraformaldehyde. The lungs were histopathologically sectioned after fixation. The histopathological sections of the mouse lungs were subjected to hematoxylin-eosin staining after sectioning. The histopathological sections of the mouse lungs were histopathologically scored by professional technicians. The results are shown in FIG. 14.

(120) It can be seen from FIG. 14 that the lung tissue structures of the mice of the blank control group (Control) are relatively complete, and have no infiltration of inflammatory cells; the mice of the model group (Model) show large-scale characterization of inflammation and even hyperemia; and some moderate and mild inflammation can be observed in the lungs of the mice of the treatment group (Treatment) and the probiotic mixed preparation intervention group (GDMCC60460+1026), but the bronchus and other structures are still complete, and the degree of pathology has been relieved to certain extent. Compared with the two single bacterial intervention groups, the mixed bacterial preparation intervention group (GDMCC60460+1026) has better villous integrity of the bronchus and less peripheral inflammation. Although the histopathological scores of the groups are similar, it can still be explained that the mixed bacterial preparation intervention group (GDMCC60460+1026) can reduce the degree of respiratory tract infection in influenza-infected mice to a certain extent, and the effect of the mixed bacterial preparation is better than that of a single bacterium.

EXAMPLE 3-4

Effect of Mixed Bacteria on Viral Load in Lungs of Influenza Mice

(121) 48 healthy ICR female mice weighing 20-24 g were randomly divided into six groups. The six groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae GDMCC60460 (GDMCC60460), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a bacterial preparation intervention group with intragastric administration of a probiotic mixed preparation (GDMCC60460+1026), with 8 mice in each group.

(122) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(123) On the first day of the experiment, except the blank control group (Control), the other five groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(124) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(125) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(126) The mice were sacrificed after blood collection on the fifth day after challenge. After the mice were sacrificed, the right lung tissues of the mice were taken out and placed in 1 mL of TRIZOL, and cryopreserved in a refrigerator at −80° C. for later use. During extraction, the right lung tissue samples were thawed on ice, and then ground using a DEPC-treated sterile grinder. 200 μL of chloroform was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and 500 μL of supernatant was removed. An equal volume of isopropanol was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. 75% ethanol was added for washing RNA once, the mixture was centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. After the ethanol evaporated to dryness, 40 μL of DEPC treating water was added to dissolve the RNA. The extracted RNA was cryopreserved in the refrigerator at −80° C. for later use.

(127) A qPCR method was used to determine the viral load, GAPDH was used as the internal reference, a classic 2.sup.−ΔΔt calculation method was used, and the model group was used as the contrast processing data. The results are shown in FIG. 15.

(128) It can be seen from FIG. 15 that the viral load in the lungs of mice of the intervention groups ingesting probiotics decreased, all being less than 50%. The mixed bacterial preparation intervention group (GDMCC60460+1026) and the L. mucosae intervention group significantly decreased, with the p values being 0.0097 and 0.0032 respectively, and average values being 27.68% and 16.3% respectively. The average value of the relative viral load of the drug treatment group was 38.03%. The data shows that the probiotic mixed preparation can significantly reduce the viral load in the lungs of mice infected with influenza, and has better effect than drug treatment.

EXAMPLE 3-5

Effect of Mixed Bacteria on Viral Load in Lungs of Influenza Mice

(129) 48 healthy ICR female mice weighing 20-24 g were randomly divided into six groups. The six groups were respectively named: a blank control group (Control), an influenza model group (Model), a drug treatment group with administration of ribavirin (Treatment), a L. mucosae intervention group with intragastric administration of L. mucosae GDMCC60460 (GDMCC60460), a B. breve intervention group with intragastric administration of B. breve CCFM1026 (CCFM1026), and a bacterial preparation intervention group with intragastric administration of a probiotic mixed preparation (GDMCC60460+1026), with 8 mice in each group.

(130) Two weeks before the experiment, the L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1206 intervention group (CCFM1206) was intragastrically administered with a B. breve CCFM1206 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(131) On the first day of the experiment, except the blank control group (Control), the other five groups were challenged with influenza virus by nasal drip after mild anesthesia with ether. Intragastric administration was still performed on the day. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(132) On the second day of the experiment, the drug treatment group with administration of ribavirin (Treatment) was injected intraperitoneally with the drug ribavirin for treatment.

(133) Intragastric administration was continued for 4 days after challenge. The L. mucosae intervention group (GDMCC60460) was intragastrically administered with a L. mucosae GDMCC60460 suspension diluent containing 10.sup.9 CFU of bacteria, the B. breve CCFM1026 intervention group (CCFM1026) was intragastrically administered with a B. breve CCFM1026 suspension diluent containing 10.sup.9 CFU of bacteria, the bacterial preparation intervention group of the probiotic mixed preparation (GDMCC60460+1026) was intragastrically administered with the probiotic mixed preparation containing 10.sup.9 CFU of bacteria (the probiotic mixed preparation contains 5×10.sup.8 CFU bacterial amount of L. mucosae GDMCC60460 and 5×10.sup.8 CFU bacterial amount of B. breve CCFM1026), and the other groups (Control, Model and Treatment) were intragastrically administered with 0.2 mL of normal saline every day.

(134) The mice were sacrificed after blood collection on the fifth day after challenge. After the mice were sacrificed, the right lung tissues of the mice were taken out and placed in 1 mL of TRIZOL, and cryopreserved in a refrigerator at −80° C. for later use. During extraction, the right lung tissue samples were thawed on ice, and then ground using a DEPC-treated sterile grinder. 200 μL of chloroform was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and 500 μL of supernatant was removed. An equal volume of isopropanol was added, the mixture was mixed thoroughly and centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. 75% ethanol was added for washing RNA once, the mixture was centrifuged at 4° C. and 12000 rpm for 10 min, and the supernatant was removed. After the ethanol evaporated to dryness, 40 μL of DEPC treating water was added to dissolve the RNA. The extracted RNA was cryopreserved in the refrigerator at −80° C. for later use.

(135) A qPCR method was used to determine the relative expression quantity of MxA (the body will react defensively to the influenza virus to clear the invading virus and restore health, MxA is an antiviral protein secreted by the body, which can effectively prevent the virus from replicating), GAPDH was used as the internal reference, a classic 2.sup.−ΔΔt calculation method was used, and the model group was used as the contrast processing data. The results are shown in FIG. 16.

(136) It can be seen from FIG. 16 that the expression quantity of the antiviral protein MxA in the lungs of mice of the bacterial preparation intervention group (GDMCC60460+1026) is the highest and can reach 5.311 times that of the model group, which indicates that the probiotic mixed preparation of the disclosure can effectively participate in the anti-influenza virus process of the body, enhance the expression quantity of the antiviral protein MxA, and help the body to inhibit virus replication. The B. breve intervention group (CCFM1026) and L. mucosae (GDMCC60460) can also increase the expression quantity of the antiviral protein MxA to a certain extent (the expression quantity is 3.464 and 3.074 times that of the model group, respectively), and the expression quantity is higher than that in the drug treatment group (Treatment), but not as good as that of the mixed bacterial preparation intervention group (GDMCC60460+1026).

EXAMPLE 3-6

Preparation of Solid Beverage Containing Mixed Bacteria

(137) Specific steps are as follows:

(138) B. breve CCFM1026 was inoculated into a medium at an inoculation amount of 5-8% of the total mass of the medium, and cultured in an anaerobic environment of 37° C. for 30 h to obtain a culture solution. The culture solution was centrifuged to obtain bacterial cells. The bacterial cells were washed 2-4 times with a phosphate buffer solution with a pH of 7.2, and then resuspended with a 100 g/L trehalose freeze-drying protectant (the mass ratio of the freeze-drying protectant to the bacterial cells is 2:1) to obtain a resuspension solution. The resuspension solution was freeze-dried by vacuum freezing to obtain B. breve CCFM1026 bacterial powder.

(139) L. mucosae GDMCC60460 was inoculated into a medium at an inoculation amount of 5-8% of the total mass of the medium, and cultured 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 2-4 times with a phosphate buffer solution with a pH of 7.2, and then resuspended with a 100 g/L trehalose freeze-drying protectant (the mass ratio of the freeze-drying protectant to the bacterial cells is 2:1) to obtain a resuspension solution. The resuspension solution was freeze-dried by vacuum freezing to obtain L. mucosae GDMCC60460 bacterial powder.

(140) The L. mucosae GDMCC60460 bacterial powder and B. breve CCFM1026 bacterial powder containing 10.sup.10 CFU of bacteria were respectively mixed with 1 g of maltodextrin to obtain a solid beverage containing the L. mucosae GDMCC60460 and the B. breve CCFM1026.

(141) 10 g of the solid beverage containing the L. mucosae GDMCC60460 and the B. breve CCFM1026 was taken and redissolved with 20 mL of normal saline. Each mouse was intragastrically administered with 200 microliters of the beverage for two consecutive weeks, which could effectively relieve the symptoms of influenza mice, and had excellent effects on the treatment and/or prevention of influenza.