Patent Application
20250009000
The present application relates to a bacterial strain and a biologically active culture thereof, as well as the uses of said bacterial strain and said biologically active culture in food- or feed-grade substance, food or feed composition and food or feed product.
It is well accepted in the art that probiotics are live micro-organisms contributing to the health and/or the well-being of a subject, such as a human or an animal, when being consumed. For example, it has been observed the influence of probiotics on intestine, wellbeing and balance of immune system of a subject. Also their effect on metabolism, including overcoming and prevention of diseases, protection of body against harmful microbiota and even providing positive effects on mental health has been suggested.
However, probiotics are neither always effective with improvement in the gut microbiota, nor capable of contributing the quality of food or feed substance whereto they are added. In addition, in many cases a mixture of several probiotic strains is necessary for achieving an effect.
Thus, there is a continuous need for new probiotics.
An aim of the invention is to provide a bacterial strain or a culture for probiotic use and other versatile uses, as well as to provide methods for using such strain or culture.
Thus, one aspect of the invention is a bacterial strain of Lactiplantibacillus plantarum Provege, deposited on 24 Aug. 2021 with DSMZ under number DSM 33989, or a mutant or derivative thereof. DSMZ stands for Deutsche Sammlian von Mikroorganismen und Zellkulturen GmbH, German Collection of Microorganisms and Cell Cultures GmbH.
Another aspect of the invention is a biologically active culture comprising the strain of Lactiplantibacillus plantarum Provege, deposited on 24 Aug. 2021 with DSMZ under number DSM 33989, or a mutant or derivative thereof. The biologically active culture comprises the strain and a cultural medium or residues of it.
Another aspect of the invention is an encapsulated product, such as freeze-dried powder, a tablet, or a capsule, comprising the strain of Lactiplantibacillus plantarum Provege, deposited on 24 Aug. 2021 with DSMZ under number DSM 33989, or a mutant or derivative thereof. The biologically active culture may be obtainable by incubating the strain in a cultural medium at 30° C. overnight, and preferably centrifuging the cultural medium to obtain a pellet and redissolving the pellet in another cultural medium or residues of it, for example peptone water containing 0.1% peptone.
Another aspect of the invention is a food or feed composition, a food or feed product, a formulation for food or feed enrichment, a food or feed supplement, or a nutraceutical formulation, comprising the strain, the biologically active culture, or the encapsulated product according to the presently disclosed invention.
Another aspect of the invention is a method of manufacturing a probiotic food or feed composition. Said method comprises preparing, and preferably also fermenting, a mixture of food or feed composition and the strain, the biologically active culture, or the encapsulated product according to the presently disclosed invention.
Another aspect of the invention is a method of increasing nutritional value of food- or feed-grade substance. Said method comprises fermenting a mixture of food- or feed-grade substance and the strain, the biologically active culture, or the encapsulated product according to the presently disclosed invention.
Another aspect of the invention is a method of prolonging shelf-life of a food or feed product. Said method comprises fermenting a mixture of a food or feed product or a starting material of a food or feed product and the strain, the biologically active culture, or the encapsulated product according to the presently disclosed invention.
Another aspect of the invention is use of the strain, the biologically active culture, or the encapsulated product as described herein, for example in manufacturing a food or feed composition, a food or feed product, a formulation for food or feed enrichment, a food or feed supplement, or a nutraceutical formulation.
The main embodiments are characterized in the independent claims. Various embodiments are disclosed in the dependent claims and the description. The features recited in dependent claims and in the embodiments are mutually freely combinable unless otherwise explicitly stated.
The following strain deposition according to the Budapest Treaty on the International Recognition of Deposit of Microorganisms for the Purposes of Patent Procedure were made at the German Collection of Microorganisms and Cell Cultures GmbH, Mascherroder Weg I-Lb 38123 Braunschweig, Germany (DE) on 24 Aug. 2021: Lactiplantibacillus plantarum Provege assigned accession number DSM 33989. Said bacterial strain Lactiplantibacillus plantarum Provege is herein referred to as a bacterial strain according to the present invention, or L. plantarum Provege, or simply Provege. The strain was deposited by Probitat Oy, Kuopio, Finland. In the present specification, German Collection of Microorganisms and Cell Cultures GmbH is referred as DSMZ, which stands for its German name Deutsche Sammlian von Mikroorganisrmen und Zellkulturen GmbH.
Unless being specified differently, the unit “vol. %”, as used herein throughout the specification, refers to volume/volume percentage, or volume fraction expressed in percent, defined as the volume of a constituent divided by the volume of all constituents of the mixture prior to mixing, expressed in percent.
The present invention relates to a new bacterial strain of Lactiplantibacillus plantarum Provege, isolated from the feces of humans. It has been surprisingly demonstrated that the strain has versatile benefits in various uses, such as for probiotic use, especially for improving digestibility and gut health of humans, for increasing nutritional value of food or feed-grade substance, and for prolonging self-life of food or feed products.
Thus, the present invention includes the presently disclosed bacterial strain L. plantarum Provege, as well as its mutant forms or derivatives which possess the same properties as the L. plantarum Provege. The L. plantarum Provege and its mutants or derivatives defined above are collectively referred herein as the bacterial strains according to the present invention.
One aspect of the present invention provides a biologically active culture comprising the strain L. plantarum Provege or a mutant or derivative thereof.
The biological activity as used herein refers especially to viability and adhesion properties of the strain or the culture. Expression “viable” means that the cells are alive and viable in the body, such as in the intestine, of a subject, for at least the standard intestinal transit time (usually 12 to 48 hours). Viability is defined as the number of bacteria (cfu g−1) that remain viable in their site of action to produce a beneficial health effect to the host. The number of bacteria may be calculated using conventional methods, e.g. based on microbe counts 10 in a Petri dish. Expression “adhesion ability” means that the strain or culture is able to adhere to intestinal mucosa or to other desired target in the body of a subject. Good adherence prolongs the time that said strain can be active in the body of the subject.
The biologically active culture according to the present invention may be prepared from a frozen stock of the strain or from freeze-dried powder.
For preparing such a biologically active culture, Lactiplantibacillus plantarum Provege may be incubated at a cultural medium, for example a selective cultural medium, at 30° C. overnight, centrifuging the cultural medium to obtain a pellet and redissolving the pellet in another culture medium, such as a non-selective cultural medium. Types of culture media for microorganisms are well known to the skilled person in the art. For example, the strain may be inoculated using a 1 μl loop to scratch a frozen bacterial stock and adding it into 10 ml MRS broth (Lab M, Bury, Lancashire, UK) and incubated at 30 C overnight. The overnight broth is then centrifuged, the supernatant discarded, and the pellet redissolved in peptone water (0.1% peptone) or 0.9% sodium chloride. The biologically active culture containing the strains according to the present invention is thus ready for further use.
Freeze-dried powder of the strains according to the present invention may be prepared using conventional methods. Freeze drying bacteria is a multistep process which involves culturing the microbes, suspending them in a lyophilization medium/buffer, subjecting them to the freeze drying process, and then subsequently storing them properly.
Besides freeze drying bacteria, other stored forms of products of the bacterial strains according to the present invention may be prepared, such as capsules, tablets or similar products, which are collectively referred as encapsulated products.
Thus, the present invention provides an encapsulated product comprising the strain L. plantarum Provege or a mutant or derivative thereof. The encapsulated product may be, for example, freeze-dried powder, a tablet, a capsule, an effervescent tablet, or so on.
The term encapsulation refers to a process of entrapping a substance, i.e. the bacterial in the present application, into another substance, producing particles in the nanometer, micrometer or millimeter scale. A substance used to encapsulate is called coating membrane, shell, carrier or wall material, external phase or matrix. For specific encapsulation processes such as freeze-drying, the substances used to encapsulate are also called cryoprotectants. The wall material used in food products or processes should be food grade and must be able to form a barrier between the active agent and its surroundings. Encapsulation technologies used to keep to keep probiotic cell viable throughout storage, commercialization and use in food products, are known by the skilled person in the art.
As mentioned, one object of the invention is to provide the bacteria strains as disclosed herein for probiotic use.
It is demonstrated that a food or feed composition comprising bacterial strains according to the present invention increases the level of many types of gut bacteria, whose existence has positive influence on some heath conditions, while decreases the level of many types of gut bacteria, whose existence has negative influence on certain conditions in a subject, such as a human or an animal, especially humans and pets. Thus, the bacterial strains according to the present invention contribute to the health condition of gut microbiota of a subject, such as a human or an animal, especially humans and pets.
Accordingly, the present invention provides a method of manufacturing a probiotic food or feed composition.
Examples of above-mentioned gut bacteria having positive influence on some heath conditions include, but not limited to, Fusicatenibacter, Tyzzerella, Oscillospira and Eubacterium. By increasing the level of the gut bacterial is meant to increase the amount said gut bacterial from a naturally existing level in a subject. The Statistical significance is determined using the Students t-test.
Examples of above-mentioned gut bacteria having negative influence on some heath conditions include, but not limited to, Prevotella 2, Prevotella 7, Alloprevotella and Tyzzerella 4. By decreasing the level of the gut bacterial is meant to decrease the amount said gut bacterial from a naturally existing level in a subject. The Statistical significance is determined using the Students t-test.
A food or feed composition as disclosed herein refers a consumable composition comprising at least one food- or feed-grade substance. A food or feed-grade substance is a non-toxic and safe for consumption substance consumable to provide nutritional support for a subject, for example humans and animals. All ingredients comprised in a food or feed composition as disclosed herein are non-toxic and safe for consumption for the subject meant to consume such composition. Thus, a food- or feed-grades substance may be human food or animal feed, or in the synonymous expression such as food for humans, fodder for livestock or food/feed for pets. A food- or feed-grade substance may be plant, animal or fungal origin, containing nutrients, such as carbohydrates, fats, proteins, vitamins, and/or minerals. A food- or feed-grade substance according to the present invention includes but is not limited to a substance originally from dairy-, grain-, legumes-/pulses-, vegetable-, fruit-, berry-, fungus-, fish-, or meat-based material. The term “based material” is herein defined that the food or feed-grade substance is produced from a specific raw material such as dairy, grain, legumes/pulses, vegetable, fruit, berry, fungus, fish, or meat, and preferably the food or feed-grade substance contains at least 70% of the raw material(s). The food or feed-grade substance may be based on a mixture of different raw materials e.g. a mixture of dairy and grain or a mixture of meat and fruit. The food or feed-grade substance may be in its natural form or processed, such as fermented, baked, cooked, etc. A probiotic food or feed composition refers to a food or feed composition having probiotic properties. A probiotic food or feed composition according to the present invention comprises at least one food or feed-grade substance, and the bacterial strain according to the present invention, the biologically active culture, or the encapsulated product according to the present invention.
The present invention further provides a food or feed product, a formulation for food or feed enrichment, a food or feed supplement, or a nutraceutical formulation, comprising the strain according to the present invention, the biologically active culture, or the encapsulated product according to the present invention.
A food or feed product as disclosed herein refers to a product intended for being commercially available for consumers, and such product comprises the food or feed composition as defined. A food or feed product or a food or feed composition may be in the form of solid, semi-solid, gel or liquid. Examples of food or feed product include, but not limited to cheese, butter, bread, porridge, juice, smoothie, yogurt, milk, pudding, coffee, or the like.
Such food or feeds may be prepared in a manner known per se, e.g. by adding the encapsulated product, biologically active culture or the bacterial strain according to the present invention to a suitable food or feed or food or feed-grade substance, in a suitable amount. For example, the bacterial strain according to the present invention, or the biologically active culture or the encapsulated product according to the present invention may be used in a manner known per se for the preparation of a fermented food or feed or food or feed-grade substance, e.g. in a manner known per se for the preparation of fermented food or feed products using the bacterial strain according to the present invention, the biologically active culture or the encapsulated product according to the present invention. In such methods, the bacterial strain according to the present invention, the biologically active culture or the encapsulated product according to the present invention may be used in addition to the micro-organism usually used, and/or may replace one or more or part of the micro-organism usually used. For example, in the preparation of fermented products such as smoothie, the bacterial strain according to the present invention, the biologically active culture or the encapsulated product according to the present invention may be added to or used as part of a starter culture or may be suitably added during such a fermentation.
Accordingly, there is provided according to the present invention a method of manufacturing a probiotic food or feed composition, comprising the steps:
In one preferred embodiment, the method comprises the step b) fermenting the food or feed composition obtained from the step a)
Such food or feed composition having the probiotic properties may be made by e.g. adding the bacterial strains according to the present invention into a food or feed composition and proceed to fermentation. For example, the food or feed composition having the probiotic properties may be made by adding the biologically active culture as disclosed herein into food or feed or drink in a concentration of 0.01-10.00 vol. %. Unless being specified differently, the unit “vol. %”, as used herein throughout the specification, refers to volume/volume percentage, or volume fraction expressed in percent, defined as the volume of a constituent divided by the volume of all constituents of the mixture prior to mixing, expressed in percent. Thus, in this case, the expression “adding the biologically active culture into food or feed or drink in a concentration of 0.01-10.00 vol. %” refers to the volume of the additive/constituent, i.e. the biologically active culture, in the volume of the whole composition, in this case food or feed composition, e.g. food or feed or drink, and the biologically active culture.
It is also possible to use freeze-dried sachets of bacterial strains according to the present invention for preparing such probiotic food or feed composition. The food or feed composition comprising the strain may then be fermented, thereby obtaining the probiotic food or feed composition, food or feed composition having the probiotic properties. It is noted that the concentration of bacterial strain added in to the food or feed composition may be tailored according to the applications. Likewise, the incubating/fermenting time may also be tailored according to the actual applications. For example, the inoculated food or feed may be incubated at 30° C. for 4-48 hours. It is found that a final dose of 106 cfu of Lactiplantibacillus plantarum Provege is sufficient to provide probiotic effect.
In some examples, the probiotic food or feed composition contains 107-109 cfu/ml of Lactiplantibacillus plantarum Provege. In some preferred examples, a final dose of 109 cfu of Lactiplantibacillus plantarum Provege may be recommended for consumers who would like to improved the gut conditions.
In some embodiments, the food or feed composition having the probiotic properties may be made by the steps of:
To have the probiotic effect, the bacteria must remain viable in the product at least until it is consumed. Thus, incubating temperature shall not exceed 40° C.
In some examples, the biologically active culture according to the present invention is added into the food or feed composition in a concentration of 0.10-1.00 vol. %, based on total volume of the whole composition having the active culture added in, and the incubating time is 6-24 hours at 30° C., thereby obtaining the probiotic food or feed composition.
It is found that the bacteria strains according to the present invention contributes to the nutrient level of a food or feed-grade substance. Accordingly, the invention provides the bacteria strains as disclosed herein for increasing nutritional value of a food or feed-grade substance. Thus, there is provided a method of increasing nutritional value of a food or feed-grade substance, by fermenting a mixture of the food or feed-grade substance and the bacterial strains according to the present invention.
The meaning of food or feed-grade substance has been defined. Further examples of good-grade substance include, but not limited to, crops as food for humans, fodder for livestock or food/feed for pets, including grains or legumes/pulses, such as oat, quinoa or fava bean.
The phrase “increasing the nutritional value” refers to the amount of nutrients, including at least an amino acid and/or at least a mineral and/or at least a vitamin in the food or feed-grade substance, is increased from the naturally existing level in the unprocessed food or feed-grade substance. Furthermore, it is noted that the amount of γ-aminobutyric acid (GABA), vitamin B12 and folic acid, may also be increased by the present method. It is to be noted that, although GABA is sometimes not classified as an amino acid in the art, here GABA is covered by the meaning of amino acid of the claimed invention.
According to some embodiments of the present method, at least the following nutrients may be simultaneously and significantly increased: Alanine, Arginine, Aspartic acid, Glutamic acid, Glycine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Proline, Serine, Taurine, Threonine, Tyrosine, Valine, and GABA.
According to some embodiments of the present method, at least the following nutrients may be simultaneously and significantly increased: Alanine, Aspartic acid, Cysteine, Glutamic acid, Glycine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Ornithine, Phenylalanine, Proline, Serine, Taurine, Threonine, Valine, and GABA.
According to some embodiments of the present method, at least the following nutrients may be simultaneously and significantly increased: calcium, iron, and zinc.
Such food or feed-grade substance having increased nutritional value may be made by e.g. adding the bacterial strains according to the present invention into a food or feed-grade substance and proceed to fermentation. For example, the food or feed-grade substance having increased nutritional value may be made by adding the biologically active culture as disclosed herein into a food or feed-grade substance, e.g. grans or legumes/pulses, in a concentration of 0.01-10.00 vol. %, based on total volume of the whole substance having the active culture added in.
It is noted that the amount of bacterial strain added in to the food or feed-grade substance may be tailored according to the applications. Likewise, the incubating/fermenting time may also be tailored according to the actual applications. For example, the inoculated food or feed may be incubated at 30° C. for 4-48 hours.
In some embodiments, the method of increasing nutritional value of a food or feed-grade substance may comprise
The food or feed-grade substance may be pre-treated. For example, the food or feed-grade substance may be sterilized, e.g. by boiling, from endogenous bacteria.
In some embodiments, the biologically active culture according to the present invention is added into the food or feed-grade substance in a concentration of 0.10-1.00 vol. %, based on total volume of the whole substance having the active culture added in, and the incubating time is 12-24 hours at 30° C., and the drying time is 24-48 hours at 65° C.
It is found that the bacteria strains according to the present invention contributes to the shelf-life of a food or feed product or a starting material of a food or feed product. It is found that the bacteria strains according to the present invention have antifungal activity. Accordingly, the invention provides the bacteria strains as disclosed herein for prolonging shelf-life of a food or feed product or a starting material of a food or feed product. Thus, there is provided a method prolonging shelf-life of a food or feed product, by fermenting a mixture of the food or feed product or a starting material of the food or feed product and the bacterial strains according to the present invention. The term “starting material of a food or feed product” refers to an ingredient or material that is used to manufacturing a food or feed product. A starting material may be an unprocessed raw material or processed material meant for further use in making the food or feed product. A starting material may be a food or feed-grade substance as defined herein. For example, grains or legumes/pulses, or flour or dough of grains or legumes/pulses, fall within the meaning of a starting material of a food or feed product which may be bread, baking and so on. It is to be noted that in this example flour as such falls within the meaning of a good product as well.
Is it found that when a food or feed product or a starting material of a food or feed product fermented with the bacterial strain according to the present invention or with the biologically active culture or the encapsulated product according to the present invention, the molding process of the food or feed product is a lot suppressed. For example, after contacting with a fungal source, the food or feed product fermented with the bacterial strain according to the present invention may start to grow mold at least one day later than those without the bacterial strain according to the present invention. Further, the growing speed of the mold of the food or feed product fermented with the bacterial strain according to the present invention may be as twice slower as those without the bacterial strain according to the present invention. Thus, by using the bacterial strain according to the present invention there is no need to add preservatives into the food or feed product.
Such food or feed product having prolonged shelf-life may be made by e.g. adding the bacterial strains according to the present invention into a product and proceed to fermentation. For example, the food or feed product substance having prolonged shelf-life may be made by adding the biologically active culture as disclosed herein into a food or feed product, e.g. flour, in a concentration of 0.01-10.00 vol. %, based on total volume of the whole product having the active culture added in.
It is noted that the amount of bacterial strain added in to the food or feed product may be tailored according to the applications. Likewise, the incubating/fermenting time may also be tailored according to the actual applications. For example, the inoculated food or feed may be incubated at 30° C. for 4-48 hours.
In some embodiments, the method of prolonging shelf-life of a food or feed product may comprise
The food or feed product may be pre-treated. For example, the food or feed product may be sterilized, e.g. by boiling, from endogenous bacteria.
In some embodiments, the biologically active culture according to the present invention is added into the food or feed-grade substance in a concentration of 0.10-1.00 vol. %, based on total volume of the whole substance having the active culture added in, and the incubating time is 12-24 hours at 30° C., and the drying time is 24-48 hours at 65° C. Afterwards, the food or feed-grade substance is made into a food or feed product.
The present invention is further described by the following examples which should not be construed as limiting the scope of the invention.
PLANTARUM PROVEGE
10 g of human faeces were mixed with 90 ml of peptone water (0.1% peptone or 0.85% NaCl) and homogenized in a waring blender (Stomacher 400). This was the 10-1 dilution.
Tenfold dilutions of each sample were prepared using peptone water.
De Mann, Rogosa and Sharpe (MRS) agar (Lab M, Bury, Lancashire, UK) was used to make agar plates. This media allows the growth of lactic acid bacteria.
Bacterial numbers were determined by plating 0.1 ml of three appropriated dilutions, in duplicate, in MRS agar plates and incubated at 30° C. for 48 hours.
100 differently looking bacterial colonies were picked and re-inoculated in MRS agar plates and incubated for their purification.
API 50 CH strips and API 50 CHL medium (Bio Me'rieux, Marcy-l'Etoile, France) were used to identify lactic acid bacteria at the species level.
Genomic DNA was extracted with Nucleo® Tissue Kit (Macherey-Nagel, Düren, Germany) using Support protocol for bacteria.
The genetic diversity of the 100 isolates was analysed by Random Amplification of Polymorphic DNA (RAPD-PCR) with primers P2 (50-GAT CGG ACGG-30), P16 (50-TCG CCA GCC A-30) and P17 (50-CAG ACA AGC C-30). The RAPD fingerprints were, analysed using the software GELCOMPAR II (Applied Maths, Version 6.5, Sint-Martens-Latem, Belgium). RAPD dendrograms were obtained with hierarchical cluster analysis (UPGMA, Unweighted Pair Group Method with Arithmetic Mean). The similarity of band profiles was calculated based on the Pearson's correlation coefficient.
At least one representative of each RAPD cluster was chosen for identification by 16S rRNA gene sequencing. Primers 27f (50-AGA GTT TGA TCC TGG CTC AG-30) and 685r (50-TCT ACG CAT TTC ACC GCT AC-30) were used to obtain a fragment of approx. 650 bp. PCR products were purified with NucleoSpin® Extract II kit (Macherey-Nagel) prior to sequencing (LGC Genomics GmbH, Berlin, Germany). The identification of isolates was obtained through the GenBank DNA database using the BLAST algorithm (http://www.ncbi.nlm.mnih.gov). Sequences showing at least 99% similarity levels are accepted.
A Lactiplantibacillus plantarum strain was identified this way and named Lactiplantibacillus plantarum Provege (L. plantarum Provege)
Stool samples from all participants (control and probiotic groups) were obtained before (run-in), during and after (washout) the consumption of the quinoa smoothie, with and without 109 cfu/ml of Lactiplantibacillus plantarum Provege.
Stool samples were kept frozen after collection at −20° C. until they were delivered to the laboratory and then stored at −80° C. until analysis.
DNA extraction was performed by using KingFisher and InviMag® Stool DNA kit (Invitek GmbH, Berlin, Germany). The DNA was harvested using an automatic magnetic-particle purifying system, KingFisher (type: 700, Thermo Fischer Scientific Oy, Vantaa, Finland).
The V3-V4 region of 16S rDNA gene was amplified by PCR using Illumina adapter overhang nucleotide sequences following Illumina protocols. After 16S rDNA gene amplification, the mutiplexing step was performed using Nextera XT Index Kit. 1 μl of the PCR product was checked with a Bioanalyzer DNA 1000 chip and libraries were sequenced using a 2×300 pb paired-end run (MiSeq Reagent kit v3) on a MiSeq-Illumina platform (FISABIO sequencing service, Valencia, Spain).
The quality-filtered sequences were checked for chimera, and the non-chimeric sequences were processed using a QIIME pipeline (version 1.9.0). The sequences were clustered at 97% of identity into operational taxonomic units (OTUs), and representative sequences were taxonomically classified based on the Greengenes 16S rRNA gene database (version 13.8).
The microbial differences between the two developmental stages and the two treatment groups were analyzed using Calypso version 8.56 with data normalized by cumulative sum scaling, which corrects the bias in the assessment of differential abundance introduced by total sum normalization.
For the multivariate analysis of bacterial genera, a discriminant analysis of principal components (DAPC) was run considering groups based on developmental stage and GBH treatment. An analysis of variance (ANOVA) test was used to analyze the differences between the relative abundances of microbial groups in the Colorado potato beetle and between the Shannon diversity index, species richness and Chao1 index.
Hereunder shows the results of samples taken during the consumption of the quinoa smoothie.
In patients with ulcerative colitis there was a significant decrease in the genus Fusicatenibacter. We found an increase of Fusicatenibacter in the probiotic group when consuming the probiotic strain as shown in
It has also been associated a decrease in Tyzzerella and Fusicatenibacter in patients with esophageal cancer and therefore, an increase of these bacteria in the probiotic consuming group might result in a protective effect. We found an increase of Tyzzerella in the probiotic group when consuming the probiotic strain as shown in
Recently, several human gut microbiota investigations have detected Oscillospira and demonstrated its underlying significance for host health. Oscillospira was reported to be less abundant in patients with inflammatory bowel disease and pediatric nonalcoholic steatohepatitis.
We found that Oscillospira is closely related to human health because its abundance was positively correlated with microbial diversity, high density lipoprotein, and sleep time, and was inversely correlated with diastolic blood pressure, systolic blood pressure, fasting blood glucose, triglyceride, uric acid and Bristol stool type. Moreover, random forest analysis with five-fold cross validation showed Oscillospira could be a predictor of low BMI and constipation in the subset. We found an increase of Oscillospira in the probiotic group when consuming the probiotic strain as shown in
The genus consists of phylogenetically, and quite frequently phenotypically, diverse species, making Eubacterium a taxonomically unique and challenging genus. Several members of the genus produce butyrate, which plays a critical role in energy homeostasis, colonic motility, immunomodulation and suppression of inflammation in the gut. Eubacterium spp. also carry out bile acid and cholesterol transformations in the gut, thereby contributing to their homeostasis. Gut dysbiosis and a consequently modified representation of Eubacterium spp. in the gut, have been linked with various human disease states. We found an increase of Eubacterium in the probiotic group when consuming the probiotic strain as shown in
It has been suggested that Prevotella is a beneficial bacteria as it is associated with a plant-rich diet, however, high levels of Prevotella have also been linked to obesity and significantly associated with BMI, insulin resistance in non-diabetic people, hypertension and non-alcoholic fatty liver disease. Furthermore, Prevotella has also been linked to high blood pressure and impaired glucose metabolism. Prevotella 2, Prevotella 7 Alloprevotella and Tyzzerella 4 have also been associated with cardiovascular disease (CVD) risk.
Thus, a reduction in the abundance of Prevotella 2, Prevotella 7 Alloprevotella and Tyzzerella 4 in the group consuming L. plantarum Provege might suggest an improvement in their gut microbiota, as shown in
During the quinoa smoothie intervention, the balance gut microbiota was studied. The intervention consisted in two groups. The first group consumed a probiotic quinoa smoothie and the second, a control quinoa smoothie. The only difference between the two groups was the added probiotic bacteria. The levels of bacteria in the probiotic smoothie were 109 cfu/ml.
This study was done using culture dependent method based on growing and selecting microbes and focused on Enterobacteria, known to have negative influence on gut microbiota, and Lactic acid bacteria, known to have positive influence on gut microbiota.
Enterobacteria are in higher amounts than Lactic acid bacteria, which indicates a normal state of gut microbiota.
The amount of Enterobacteria are reduced while the amount of Lactic acid bacteria are increased.
Lactic acid bacteria stays in high amounts.
The results suggest that the beneficial effect of consuming the probiotic bacteria was still present at least two weeks after stopping their consumption. Thus, consuming the probiotic stimulates beneficial bacteria and this stimulation is present even after the probiotic is not present anymore.
Enterobacteria are in higher amounts than Lactic acid bacteria, which indicates a normal state of gut microbiota.
The amount of Enterobacteria is reduced while the amount of Lactic acid bacteria increases.
These results are not statistically significant. This means that there is a tendency to reduce Enterobacteria and increase Lactic acid bacteria but the difference is very small.
Lactic acid bacteria are still in high amounts.
This result is also not statistically significant, so Lactic acid bacteria stayed higher than in the original levels but the difference is very small.
CONCLUSION: The consumption of the probiotic quinoa smoothie containing Lactiplantibacillus plantarum Provege can stimulate intestinal good bacteria and protect a subject from any intestinal dysregulation. This stimulation is still present even after the probiotic is not present anymore. From the control group, we can conclude that even without the probiotic, the gut microbiota has a tendency to reduce the Enterobacteria and increase the Lactic acid bacteria. This effect is most likely due to the quinoa, which contains fiber (prebiotic). The prebiotic is the “food” that Lactic acid bacteria needs to be also stimulated.
When the Lactic acid bacteria of gut microbiota is stimulated (higher amounts than normal), the gut is more protected to different disturbances (stress, infections, etc.).
Grains or legumes/pulses were boiled to sterilize them from any endogenous bacteria. Wet grains or legumes/pulses were inoculated with 1% of Lactiplantibacillus plantarum Provege and incubated at 30° C. for 12-24 hours. After the fermentation step, they were dried at 65° C. for 24-48 hours. Once dried, they were milled into flour.
Flours were analyzed at Eurofins Scientific Finland.
LAB were inoculated on MRS agar plates as two-centimeter-long lines. After 24 hours of incubation at 30° C. the plates were overlaid with 10 ml LB soft agar (2.5% LB, 0.7% agar) which was inoculated with 0.1% molds (Aspergillus oryzae 1011 or Aspergillus oryzae 66222). The plates were then incubated at 30° C. for 48 hours. Clear zones of inhibition around the bacteria lines on the plates were examined and the areas of the clear zones were measured.
As the results show, plates with L. plantarum Provege had the largest clear zones as compared with other strains tested, suggesting the antifungal activity of L. plantarum Provege.
2. Antifungal Activity in L. plantarum Provege Fermented Quinoa Bread
Dark bread and white bread were prepared according to a recipe commonly known in the industry, using flours with and without Provege fermentation obtained according to Example 4.
The sliced breads were studied according to their ability to resist fungal growth. Duplicates of each sample were made. The slices were inoculated with 50 μl Aspergillus oryzae suspension (a loop of mold diluted in 1 ml of peptone water). The plates were covered and stored in plastic bags. Samples were incubated at room temperature. Samples without inoculation were as controls and stored in the same way. The growth of the mold was examined every day during eight days by observing the appearance and measuring the growth diameter, as shown in
| Number | Date | Country | Kind |
|---|---|---|---|
| 21208495.8 | Nov 2021 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2022/075385 | 9/13/2022 | WO |
