REVIEW article

Front. Nutr., 27 April 2022

Sec. Food Chemistry

Volume 9 - 2022 | https://doi.org/10.3389/fnut.2022.871896

Biotechnological Processes Simulating the Natural Fermentation Process of Bee Bread and Therapeutic Properties—An Overview

  • 1. Institute of Life Sciences, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Cluj-Napoca, Romania

  • 2. Faculty of Food Science and Technology, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Cluj-Napoca, Romania

  • 3. Advanced Horticultural Research Institute of Transylvania, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Cluj-Napoca, Romania

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Abstract

Recent signs of progress in functional foods and nutraceuticals highlighted the favorable impact of bioactive molecules on human health and longevity. As an outcome of the fermentation process, an increasing interest is developed in bee products. Bee bread (BB) is a different product intended for humans and bees, resulting from bee pollen's lactic fermentation in the honeycombs, abundant in polyphenols, nutrients (vitamins and proteins), fatty acids, and minerals. BB conservation is correlated to bacteria metabolites, mainly created by Pseudomonas spp., Lactobacillus spp., and Saccharomyces spp., which give lactic acid bacteria the ability to outperform other microbial groups. Because of enzymatic transformations, the fermentation process increases the content of new compounds. After the fermentation process is finalized, the meaningful content of lactic acid and several metabolites prevent the damage caused by various pathogens that could influence the quality of BB. Over the last few years, there has been an increase in bee pollen fermentation processes to unconventional dietary and functional supplements. The use of the chosen starters improves the bioavailability and digestibility of bioactive substances naturally found in bee pollen. As a consequence of enzymatic changes, the fermentation process enhances BB components and preserves them against loss of characteristics. In this aspect, the present review describes the current biotechnological advancements in the development of BB rich in beneficial components derived from bee pollen fermentation and its use as a food supplement and probiotic product with increased shelf life and multiple health benefits.

Introduction

Nowadays, the concept of “food as medicine and medicine as food” assimilated to Hippocrates is increasingly common in the food sector, where the production of functional foods is a significant part of human lifestyle (1). All over the world, consumers have extensive knowledge regarding the effect of food on wellbeing and having positive food expectations (2).

Bee products have been used to treat and prevent disorders such as burns, wounds, diabetic foot ulcers, allergic rhinitis, hyperlipidemia, and rheumatoid arthritis through the history of the traditional medicine (36). Recently, bee products developed due to the fermentation process have gained colossal interest and became a severe topic for future research due to the positive impact on the food market.

Bee bread (BB) is a fermented assortment of bee pollen (BP), nectar, and bee saliva, having a caramel-like color and a sharp taste given by flowers, citrus, or other fruit flavors (7). The outcome of lactic acid fermentation of BP collected from flowers by bees and combined with their digestive enzymes is the primary food for larvae and young bees in the hive (8). In the cells of the honeycombs, bees pack the components and then secure the mixture with honey and wax, protecting the pollen mass from oxygen, starting an anaerobic lactic fermentation process, which after approximately seven days generates BB (9).

According to Habryka et al. BB incorporates a well-balanced nutritional content and more prosperous chemical composition than BP, having a significant assimilation rate and a better absorption at the level of the human body (10). Since the BB components are fermented in part, the high BP content is more straightforward incorporated and utilized as the walls have partly deteriorated through the lactic fermentation (9). The studies on its chemical composition demonstrated that BB is a trustworthy source of proteins, vitamins (B, C, E, K, and P), and polyphenols, like quercetin, kaempferol, apigenin, naringenin, chrysin, caffeic, gallic and ferulic acids (11). Besides, free amino acids, carbohydrates, and fatty acids are essential elements of BB composition, which depend on environmental conditions, seasonal discrepancy and differ from region to region, based on the melliferous plant's (12).

The recent studies on BB chemical composition established that it has a higher nutritional value than BP; nevertheless, research on BB is scarce and focused only on its chemical composition (13, 14). Because collecting BB from the hive is too costly and time-consuming, BB purchases for human consumption are limited; moreover, beekeepers feel more comfortable extracting BP using traps. Unfortunately, due to this method, there is a danger of harmful mold growth due to the high humidity. Furthermore, storage treatments are required to avoid spoiling (1517). The traditional methods used have several disadvantages; the nutritional value is affected, and the operating cost is high; therefore, alternative opportunities should be considered to overcome these impediments. A unique opportunity is the biotechnological fermentation of BP, simulating the natural process in the hive leading to a high nutritional product, as in BB (18).

Fermentation is one of the most widely used methods in the production and economic preservation of food, being perceived as an essential constituent of the nutritional culture of every world's society supporting the cultural history of ethnic communities (19). Globally, a multifariousness of fermented products is widely consumed as daily human food, from yogurt, kefir, sausages to pickles and fermented cereals, thanks to their biological functions and enrichment of nutritional value. In the beehive, the natural fermentation improves the bioavailability of fresh BP and the possibility of long-time storage, avoiding losing its nutritional value as it is converted to BB (20). Because of its beneficial components, BP represents a valuable raw material that allows the microorganisms' development during the fermentation process (21). In the past years, researchers attempted to induce the natural fermentation of BP at a lab scale by inoculating diverse microorganisms under specific process conditions.

The purpose of the review was to present an overview of the biotechnological processes used to obtain BB from harvested BP in laboratory conditions by an assortment of chosen starters reproducing the microbial consortium implicated in the fermentation of BB. Changes in the bioactive compounds and antioxidant activity are also pointed out along with the final's probiotic product shelf life and health benefits. Furthermore, the effectiveness of BB and strains isolated or found in BB are investigated in the prevention and treatment of several anti-cancer agent-induced toxicities in animal models and patients with cancer.

Similarities and Differences Between Bee Pollen and Bee Bread

Because of their nutritional and medicinal properties, natural products such as unique bee brands have piqued the curiosity of academics in recent years. Even though these have been well-known products for millennia, they have only lately become the subject of recorded scientific investigation (2).

BP is recognized as the oldest nutritive supplement in history and includes roughly all of the dietary nutrition compounds, the main ingredient of BB (14). BP is the male gametophyte of flowering plants. After gathering pollen grains from flowers, bees combine their saliva and secretions. This procedure enables BP to be hydrated and pelleted, which subsequently sticks to the pollen basket on the bees' rear leg and carries to hive. BP is a source of nutrients that honeybees need to grow and develop appropriately throughout their larval stage until maturity (22, 23). BP is deposited into honeycomb cells by bees, which seal them with honey and wax. Collected and stored, BP is exposed to lactic fermentation under the beehive conditions, resulting in BB, which is fermented BP (2).

BP and BB are used for apitherapeutic benefits as they are rich in vitamins, valuable bio-elements, and nutrients. Still nevertheless, the two components differ from a biochemical point of view (Table 1) (25).

Table 1

CompositionBPBB
Proteins4.50–40.70%14–37%
Carbohydrates24.0–60.0%%24–74.82%
Lactic acid0.56%3.2%
Lipids1–18%6–13%
Cellulose3.7%2.7%
Nucleic acid0.6–4.8%n.a.
pH3.8–6.34.3
Fiber0.15–31.26%n.a.
Glucose13.41/100 g5.7 ± 0.4
Fructose15.36 g/100 g11.8 ± 0.6 g/100 g
Sucrose4.25 g/100 gn.a.
Potassium (K)3.06–13366.6 mg/kg338 ± 8 mg/100 g
Phosphorus (P)234.40–9587 mg/kg251 ± 4 mg/100 g
Calcium (Ca)1.09–5752.19 mg/kg198 ± 4 mg/100 g
Magnesium (Mg)44.0–4680.53 mg/kg61 ± 2 mg/100 g
Zinc (Zn)0.1–105.8 mg/kg3.31 ± 0.04 mg/100 g
Iron (Fe)2.6–1180.0 mg/kg27.3 ± 0.3 mg/100 g
Total phenolic content0.69–213.2 mg GAE/g9.2 ± 0.1 mg GAE/g

Chemical and nutritious compounds of BP and BB adapted after Kieliszek et al. and Bakour et al. (2, 14, 24).

n.a., no data available; GAE, gallic acid equivalents.

The nutritional composition of BB varies based on the pollen's local and seasonal value and availability to different plant species. Compared to BP, BB is high in reducing sugars and has significant amounts of tocopherols (26, 27). BB has low protein and fat content but increased carbohydrate and lactic acid content. Due to its structure, it possesses increased bioavailability, which can be partly assimilated by fermentation and demonstrates high resistance against the degradation action of digestive media. Furthermore, the functional and actively rich components of BP are easily absorbed and utilized (Figure 1) (2, 28).

Figure 1

Figure 1

Chemical composition and bioactive compounds of BB (image created using BioRender and King Draw applications).

BB is more digestible than BP due to the breakdown of the multilayer wall during fermentation. Moreover, this process enhances BB bioavailability, resulting in higher absorption by human intestinal epithelial cells (3, 18). Also, during fermentation, bacteria break down cellulose, which constitutes the internal coating (also known as intine) of BP, lowering BB's cellulose ratio in contrast to BP (22). Furthermore, throughout the fermentation process, certain innovative products are deliberated. For instance, several proteins in BP are converted to amino acids by digestive enzymes, increasing the protein level, whereas, in BB, an increasing content in amino acids is noticed (2). According to DeGrandi-Hoffman et al., the content of threonine and leucine in BB is approximately 60% higher than BP (29). As a primary food source for bees, BP includes amino acids such as leucine, isoleucine, histidine, lysine, valine, arginine, phenylalanine, methionine threonine, and tryptophan (30). According to Bayram et al., in comparison to BP, BB samples had considerably less L-asparagine (5891.1–2475.4 μg/g), but L-proline (22212.8–4939.2 μg/g), L-aspartic acid (5207.37–2833.3 μg/g), and GABA (4588.4–2703.2 μg/g) were detected as significant amino acids. Furthermore, considerable amounts of L-phenylalanine were found in BP and BB samples, with values ranging from 3353.8–1298.9 μg/g to 3345.6–1308.4 μg/g, respectively (30). The lower content in L-asparagine in BB may be due to the fermentation development and acidic environment that cause this amino acid field's deamination (29).

In 2008, Venskutonis et al. investigated the fatty acid content of BB in summer and spring and discovered 22 fatty acids, as well as five ω-3, four ω-6, and three ω-9 polyunsaturated fatty acids (PUFAs). The primary fatty acids found in BB were arachidonic and oleic acids, with α-linolenic concentrations varying the most between the botanical origins of samples. There was also a substantial difference in the α-linolenic and eicosapentaenoic acids (31).

BP has a high concentration of polyphenolic chemicals, primarily flavonoids and phenolic acids (32). Flavonoids in BP vary from 3.7 to 10.1 mg/g, according to Pascoal et al. (33). At the same time, the total flavonoid content of five BB samples showed values ranging between 13.56 and 18.24 g QE/g DW (quercetin equivalents/g dry weight) (34). Also, in 2015 Zuluaga et al. established that BB originated from Colombia has a total flavonoid content between 1.9 and 4.5 mg QE/g (18).

Vitamins are a diverse group of active ingredients required for the optimal health and growth of all organisms. BB is characterized by higher levels of phenolics with 4.87 mg GAE/g, flavonoids with 59.06 mg QE/g, vitamin C (0.36 ng/g), and E (32.55 ng/g) (35). In addition, K, P, Ca, Mg, Zn, Fe, and Mn (Manganese) levels in spring BB collected from honey bee colonies were also tested at the Institute for Forage Crops, the results demonstrating a strong relationship between the mineral content and the sources of floral pollen (25). Adequate amounts of macro-and microelements in the human organism are critical for the effective operation of many distinct metabolic processes. Minerals are required for appropriate physiological functions and metabolic pathways regulation (36).

BB includes a variety of enzymes, as well as acid leucine aminopeptidase, phosphatase, and glucosidase, which hydrolyze carbohydrates such as amygdalin, salicin, cellobiose, and centipoise (3). The BB fermentation technique results in higher amounts of lactic acid due to microbial metabolism, which provides long-term defense against pathogens while also increasing the nutritious qualities of BB (3).

In summary, BB includes a wide range of nutritional phytochemicals with valuable characteristics, including vitamins, carotenoids, phenolic acids, and, most notably, flavonoids. BB was found to possess antioxidant, antibacterial, antiviral, anti-inflammatory, and anti-cancer benefits because of their complex chemical composition. In recent years, there has been a surge in interest in the chemicals responsible for these effects; hence, taking into account food productions and the beneficial impacts on human wellbeing, these bee products, with enormous production perspectives and usage as natural and valuable components, provide a broad topic of study (3741).

The growing global interest in functional products and rising health consciousness adds burden to the upcoming production of bee products. BB has the advantage, apart from a distinct chemical profile, the further production of microbial fermentation, which contributes to its nutritional and health properties. BB is quickly absorbed and digested and contains a variety of macro-and micronutrients that are beneficial to the human body, including flavonoids and polyphenols (3). In addition to the well-known bee products, such as BP, honey, and royal jelly, BB might be the potentially exploited gold mine in the culinary sector and medicine development.

BB Natural Fermentation Process

After fermentation of BP, the resulting product (BB) has an amber-like color and a rich aroma of flowers and citrus flavor (7). The digestive enzymes of bees naturally contain lactic acid bacteria (LAB), due to which a lactic fermentation begins, leading to BB (15, 22, 29).

According to the indoor beehive conditions, the process of obtaining BB is based on the progression of the appearance/disappearance of colonizing microorganisms, particularly LAB, under anaerobic conditions (18). Also, through the saliva of bees, enzymes are segregated, causing fermentation and enzymatic processes, biochemical transformations necessary to break the outer layer known as exine, that covers the pollen, consisting of sporopollenin that provides resistance to chemicals and preservation of bioactive substances inside the pollen grain (42). As a result of microbial metabolism and biochemical changes, BP is transformed to BB via lactic acid fermentation generated mainly by bacteria, like Pseudomonas spp., Lactobacilli spp., and yeasts as Saccharomyces spp. (Figure 2).

Figure 2

Figure 2

The natural process of producing BB by bees (image created using BioRender and King Draw applications).

In addition, Bacillus species in Melipona panamica nests were shown to secrete enzymes that catalyze the breakdown of lipids, carbohydrates, and proteins. This bacterial genus was found predominant in BP, and some species are known to ferment glucose. Therefore, this suggests that Bacillus species is a significant genus that could be involved in the BB formation (43, 44).

Inside the hive, BP turns into BB in about 7 days, fulfilling several biochemical stages, starting after the development of LAB, indole-producing bacteria (Escherichia spp.), aerobic bacteria, and yeast. In the next step, the anaerobic LAB (Streptococcus spp.) use the nutrients created by bacteria and yeast, causing the pH of BP to decrease. Then, when the concentration of Streptococcus bacteria decreases, Lactobacilli bacteria begin to increase at the end of the 7 days when the LAB and yeasts die. Moreover, due to lactic acid fermentation, the BB reaches a pH of 4.0, becoming microbiologically sterile, all in the last stage (3). Certainly, BB is pollen stored in the hive, which undergoes a fermentation process, most likely due to the glandular secretions of bees and its microbial group, involving mold, yeast, and bacteria, and LAB with a critical role in this process (45). The resulted product is more stable and more nutritious than fresh BP and has higher vitamin content, especially vitamin K because of the pollen degradation (3, 46). Due to the metabolism of microorganisms involved in the fermentation process, the content of LAB increases, resulting in long-term protection against microorganisms and strengthening the nutritional properties of BB (47).

The chemical composition of BB, such as flavor, color, and texture, changes considerably after being stored, and these characteristics vary among bee species. For example, the BB of stingless bee Frieseomelitta and Tetragonisca are dry and sweet, while the ones produced by Melipona and Scaptotrigona are moist and sour (48).

The process of collecting BB from the hive is more laborious than BP, where the traps placed at the hive entrance are sufficient to manage it. Complex techniques like machinery separation or freezing followed by a manual crushing of the combs are required to obtain BB as it is fixed with beeswax and tightly stuffed in the combs by bees (22). Therefore, BB is more costly than other bee products (49).

The current tendency relating to the consumer's behavior and food inclination determined the production of novel products. Therefore, new technologies for their development, challenging companies from several food enterprises to commence the action of organic products. As a result of fermentation, the obtained bee products have become an increasingly studied niche. Solid-state fermentation is a bioprocess naturally produced in the hive when BP is used as the primary nutrient source for microorganisms (21). The advantage of using BP in future processes, like solid-state fermentation, will be discussed in the following section to demonstrate the necessity of obtaining BB via the biotechnological route.

Biotechnological Processes Simulating the Natural Fermentation Process of BB

Nowadays, more and more scientific research proposes using LAB as a noteworthy part of future production chains. The food industries focused on producing value-added products with significant bio-elements, macro and micro-nutrients, vitamins, and health benefits (50). LAB are gram-positive bacteria, non-spore-forming, fermentative, facultative anaerobic, with a significant impact on the food industry (51). Furthermore, LAB has important significance since they fulfill the safety conditions for people and animals (GRAS—-Generally Recognized as Safe). Each has a distinct fermentation metabolism and energy gained due to the saccharides conversion (52).

In consequence, throughout fermentation, in addition to lactic acid, the specific LAB strains produce multiple metabolites like exopolysaccharides, enzymes, diacetyl, hydrogen peroxide, and bactericidal proteins or bacteriocins. These compounds confer the functional properties of LAB, for instance, probiotic and fibrinolytic effects antioxidant activity, in addition to providing fermented products with their remarkable consistency, color, flavor, and aroma (53). LAB has a long history of application in various industrial sectors used as starter cultures. Thus, microbial preparations of many microorganisms are introduced in raw material to develop a fermented product by an accelerated and guided process (54, 55). In recent years, numerous researchers attempted to simulate the natural fermentation of BP via microorganisms' inoculation under various process conditions at the lab scale to obtain nutritional and functional BB (Figure 3).

Figure 3

Figure 3

The biotechnological process of simulating the natural fermentation process of BB (image created using BioRender and King Draw applications).

Moreover, other studies have carried out enzymatic hydrolysis and sonication as alternative methods to improve BP nutrient bioavailability (56). Concerning LAB, 45 bacteria species were identified and isolated from honeybees, flowers, and bee products, as shown in Table 2 (87). Studies have shown that bees possess specific microbiota, different from other beings, but closely related to the thread Firmicutes, Actinobacteria, and Proteobacteria, the essential intestinal bacteria (88). A unique LAB group, different from the classic consortium that prefers glucose, has been identified in the stomach of bees, fructophilic lactic acid bacteria (FLAB), which can use fructose from richer sources, for instance, flowers (57). Recently, FLAB was regarded as unconventional LAB, as they have a unique growth characteristic due to a partially bi-functional alcohol/acetaldehyde dehydrogenase encoded gene, generating a disequilibrium in NAD/NADH (nicotinamide adenine dinucleotide/reduced nicotinamide adenine dinucleotide) and the necessity of supplementary acceptors for metabolizing glucose (58). According to recent studies, fructose-feeding insects, like bees, possess in their guts high amounts of FLAB cells belonging to the Fructobacillus and Lactobacilli spp. (59).

Table 2

Host speciePrimary locationIsolated microbial strainsReferences
Honeybee
Apis and Bombus spp.Adult hindgut (rectum)B. asteriodes(5760)
Adult hindgut (rectum)B. coryneforme(57)
MidgutB. indicum(61, 62)
Adult cropBifidobacterium spp.(63)
Adult crop, larval gut, not present in adult hindgutApilactobacillus kunkeei(56, 57, 59, 61, 6366)
Adult hindgut (rectum)Lactobacillus johnsonii(59, 67)
Adult hindgut (rectum)Lactiplantibacillus plantarum(59, 68)
Larval gut, adult cropApilactobacillus apinorum(69, 70)
Adult hindgut (rectum)Lactobacillus mellis(69)
Adult crop, midgut and rectumA. kunkeei(56, 57, 59, 61, 6366)
Apis cerana and A. cerana indicaMidgutLactobacillus kullabergensis, Bifidobacterium longum(59, 69, 71)
A. dorsataAdult cropBombilactobacillus mellifer, Lactobacillus insectis, Enterococcus durans, Oenococcus spp.(56, 69, 72, 73)
A. floreaAdult hindgut (rectum)Enterococcus faecium(67)
A. mellifera and A. mellifera BuckfastAdult cropL. kullabergensis(59, 69)
Adult crop and hindgutB. mellifer(69)
Adult crop, midgut and rectumLactobacillus melliventris(69)
A. melliferaAdult cropLactobacillus apis, Lactobacillus acidophilus, Lactobacillus alvei, Lentilactobacillus buchneri(56, 74, 75)
Adult crop, midgut and rectumLactobacillus helsingborgensis, Lactobacillus kimbaldii(59, 69)
MidgutLactobacillus brevis(61)
Adult gut, variably presentAlpha 1(58)
Adult gutFructobacillus pseudoficulneus, Fructobacillus tropaeoli(72, 76)
A. mellifera intermissaAdult hindgut (rectum)Enterococcus faecalis(63)
A. mellifera, Bombus terrestris, Osmia bicornis (red mason bee)Adult gutLactobacillus intestinalis(74)
A. mellifera, Heterotrigona itama, Bombus spp.Adult gutFructobacillus fructosus(76)
Honey
Apis and Bombus spp.A. kunkeei, L. acidophilus, Lactobacillus crispatus ST1, Furfurilactobacillus rossiae, Companilactobacillus versmoldensis, Ligilactobacillus araffinosus(56, 57, 71, 77, 78)
Bifidobacterium steroids, Bifidobacterium catenulatum, Bifidobacterium longum(59, 60, 71)
H. itamaF. fructosus(76)
BP
Apis and Bombus spp.Lactobacillus kefiranofaciens(56)
Holzapfelia floricola, Apilactobacillus ozensis, Lactobacillus frumenti(56)
A. dorsataL. insectis(56)
A. floreaLactobacillus helsingborgensis(69)
A. melliferaA. kunkeei, L. plantarum, Apilactobacillus apinorum, Lactobacillus alvei, Latilactobacillus curvatus(45, 56)
A. mellifera intermissaE. faecalis(79)
A. mellifera, B. terrestrisL. intestinalis, Limosilactobacillus reuteri, Lactococcus lactis(56, 80)
Meliponula bocandeiLactobacillus kimbaldii, Lactobacillus kullabergensis(69)
Royal jelly
A. dorsata and A. melliferaA. kunkeei, L. insectis, Bifidobacterium spp.(56)
BB
A. dorsataE. durans, Oenococcus spp.(72, 73)
A. melliferaA. kunkeei, L. plantarum, A apinorum, L. helsingborgensis, Weissella paramesenteroides; Zygosaccharomyces favi spp. nov(56, 63, 69, 72, 81, 82)
A. mellifera lingusticaA. kunkeei, L. plantarum, F. fructosus, F.fructosus JCM 1119 and NBRC 3516, Levilactobacillus brevis (Lvb. brevis) and Lactobacillus delbrueckii subsp. lactis(83, 84)
A. mellifera, B. terrestrisLimosilactobacillus mucosae, Bifidobacterium spp.(56)
H. itamaLactobacillus spp., Carnimonas spp., Escherichia-Shigella and Acinetobacter spp.(85)
M. bocandeiLactobacillus kimbladii, L. kullabergensis(69)
Stingless bee Tetragonula pagdeniBacillus spp., Streptomyces spp.(86)
Flowers
Paeonia suffruticosa and Chrysanthemoides moniliferaFructilactobacillus florum(70)
Hedera helixLactobacillus lactis(45)
Mountain flowersApilactobacillus ozensis(56)
Acacia spp. And Mesquite spp.Weissella spp.(63)

LAB from the colony environment of honeybees.

Foods fermented with selected Bifidobacterium strains are known to present a variety of probiotics, prophylactic and therapeutic properties (89). Members of the Bifidobacterium genus are found as gut microbiota components. They are thought to play a significant function in sustaining and improving human health by evoking various positive qualities. Bifidobacteria may use a wide variety of dietary carbohydrates, most of them being oligo- and polysaccharides derived from plants, that avoid decomposing in the intestine's upper section (90). Bifidobacteria spp. are Gram-positive, hetero-fermentative microorganisms that do not generate spores (90). The Bifidobacteria pathway consists of a carbohydrate metabolism mechanism found in all Bifidobacterium spp., due to their ability to metabolize different polysaccharides leading to the degradation of those undigested sugars (91). Vamanu et al. (92) used a substrate of prebiotics such as lactulose, inulin, and raffinose with Bifidobacterium bifidum 1 and 2 to evaluate their impact on lactic acid production, cell viability, and antioxidant activity. The BP and honey-based medium supplemented with prebiotics, ground pollen, and inulin provided the best results in viability and total antioxidant activity (92). These findings demonstrate the feasibility of BB functional foods that can be used in both medicine and food sectors (93).

Lactobacilli spp. on the Biotechnological Process and the Use of Probiotics

Lactobacilli are gram-positive, non-spore-forming bacteria that at the end of fermentation release lactic acid as the primary end product of fermentation, which also contributes to the texture and sensory profile of a food (94). Lactobacillus was the most numerous genera within the LAB group belonging to the phylum Firmicutes, class Bacilli, order II Lactobacillales and family Lactobacillaceae. According to the recent reclassification, the Lactobacillus genus has been split into 23 new genera (95). Some of them (for example, Lacticaseibacillus casei and Ligilactobacillus salivarius) provide particularly L (+) lactic acid, while other microorganisms like Lactobacillus bulgaricus and Lactobacillus jensenii generate only D – lactic acid, and microorganisms like Lactobacillus acidophilus and Lactobacillus helveticus can create a combination of D (+) and L– lactic acid. (63). The live microorganism belonging to these genera has recently gained further attention. They are immune to gastrointestinal acidity, improve the intestinal microbiota, and reduce the growth of undesirable bacteria (65). Further, the available studies in the literature describe a biotechnological way to obtain BB by using collected BP as substrate and specific Lactobacilli spp. as starter culture according to their particular growing conditions (Table 3).

Table 3

Floral sampleFermented productFermentation methodsSubstrate formulationFermentation conditionsOptimum fermentation conditions and observationsReferences
Hedera helix BPFermented BP and BBAssorted inoculum of A. kunkeei strains and H. uvarum in fresh BPWater:pollen (1:4)30°C for 216 hOptimal fermentation: unstarted BP;
↑ mesophilic microorganisms and LAB after 40 days;
↑ yeasts afer 20 days in started and unstarted BP;
↓ yeasts in raw BP after 20 days;
↑ protein digestibility in started BP after 216 h at 30°C;
↑ free aminoacids in started and unstarted BP; RawBP and unstarted BP populated by A. parasiticus following 10 days of storage; 15 days of hive-storage: L. plantarum, A. kunkeei, Latilactobacillus curvatus, Leuconostoc citreum, Lactococcus lactis, F. fructosus; 30 days of hive-storage: A. kunkeei and F. fructosus
(45)
Hedera helix BPStarted-BP; Unstarted-BP; Raw-BPComparison between BP fermented with selected strains (Started-BP), spontaneously fermented BP (Unstarted-BP) and unprocessed raw BP (Raw-BP).Water:pollen (1:4)30°C for 216 h↑ bioaccessible phenolics in started BP compared to raw BP;
↑ volatile free fatty acids and acetic acid content in Unstarted-BP
(66)
Brassica campestris L. BP from ChinaFermented BPLactobacillus delbrueckii subsp. bulgaricus, St. thermophilusand active dry yeastWater:pollen ratio (1:1)50 g of BP/WBP mixtures combined with 3% LAB, fermented for 48 h at 42°C; 50 g of BP/WBP mixtures combined with yeast 3%, fermented for 48 h at 37°C; 50 g of BP/WBP mixtures combined with 3% LAB and 3% yeast, fermented for 48 h at 37°C↑ PUFA, FA and aminoacids in yeast fermented BP; Alpha 2.2 bacteria, A. kunkeei, Actinobacteria in unstarted-BP(96)
Brassica napus BP from SlovakiaFermented pollen cansWithout selected strainsWater (75 ml), honey (45 g) and BP (300 g)1st Fermentation:
V1: 30°C for 2 days, no O2
V2: 23°C for 5 days, O2
V3: 30 °C for 2 days, no O2
2nd Fermentation:
V1: 23 °C for 16 days, no O2
V2: 23 °C for 13 days, no O2
V3: 23 °C for 6 days, no O2
↓ filamentous microscopic fungi by fermentation(56)
Pinus spp. BPFermented BP, yeast-fermented BPLacticaseibacillus paracasei Lc-3200 mL medium after inoculation with 5–15% (v/v) of starter culture35–45°C on a shaker for 1–5 dayInoculum size: 11.92%, at 39.6°C, and pH = 7.22; Viable count = 4.24 × 109 CFU/mL and crude protein = 15.35%(77)
Pinus spp. BP from ChinaFermented BPL. paracasei Lc-3;
Isolated and characterized strain of Bacillus coagulans
200 mL medium after inoculation with 5–15% (v/v) of the starter culture35–55°C on a shaker for 6–72 hOptimum viable count production: inoculum size = 9.22%, 49.21°C, and pH = 6.82; treatment of fermented products was carried out by spray-drying(72)
BP (Apis mellifera) from ColombiaFermented BPS1: L. delbrueckii ssp. bulgaricus, ssp. lactis, and St. thermophilus; S2: L. delbrueckii ssp. lactis, ssp. cremoris, and ssp. biovar. diacetylactis); S3: L. acidophilus NCFMWater:BP ratio (1:1 and 2:1), temperature of 115°C between 10 and 20 min; pH = 5.872 h at 37°CFermented BP with L. acidophilus considered as optimum and probiotic; Optimal conditions in 2:1 water:BP mixture with pH = 5.8, heat/pressure pre-treatment for 10 min; at 115°C(67)
Hypochaeris spp. and Brassica spp. BP from ColombiaFermented BP (probiotic characterized product)S1: fresh BP, S2: BB and BP fermented with Choozit®, S3: L. plantarum, S4: S. cerevisiae, S5: Commercial S.cerevisiae, S6: ATCC Mixture, S7: commercial mixWater:pollen (1:1)37°C, 72 hOptimal: Choozit® (mixture of St. thermophilus, L. delbrueckii subsp. lactis and subsp. bulgaricus) and Commercial mix;
↑ total phenolics and flavonoids content and antioxidant activity
↑ LAB content which gave it a probiotic characteristic
(68)
Polyfloral BPFermented BP and BBBP fermented with and without L. rhamnosusWater:pollen (1:5)32°C, 288 h for 12 days↑ total phenolics and flavonoids content and antioxidant activity in BP fermented with L. rhamnosus(97)
BP from ColombiaFermented BPL. acidophilus, L. plantarum, S. cerevisiae, and mixture of L. plantarum and S. cerevisiaeFresh BP, dry BP: Water: pollen ratio 2:1 and 1:135 and 40°C for 72 hBP: water (1:1) at 35°C
↑ bioactive compounds compared to raw material
(21)
pollen, borage honeyBBWithout selected strainsT0: BP without inoculum, T1: natural BB, T2: BP + 5% inoculum, T3: BP + 10% inoculum, T4: BP + 15% inoculum, T5: BP + 20% inoculum35°C, 480 h↑ acidity (4.83%) in T5 similar to natural BB(69)
BP from CubaFermented BPL. acidophilus, L. casei, Loigolactobacillus coryniformis, L. delbrueckii, L. plantarumpollen silage, honey35°C, 360 hL. plantarum and L delbrueckii at 36–40% humidity were the most promising, with > 1% lactic acid and total inhibition of E. coli.(70)
BP from ColombiaFermented BPL. acidophilus, L. paracasei subsp. paracasei, and two mixed cultures: Yomixtm 205 Lyo And Choozit Tm My800 from Danisco® (108CFU/g)pollen:water (2:1)35°C, 72 hL. acidophilus was the most promising inoculum; 121°C/15 min treatment improved the microbiological characteristics;
↑ acidification capacity (0.16 g lactic acid/kg*h) and survival rate (108 CFU/g 24 h in incubation) in L. acidophilus
(98)
BP and honeyProbiotic productLimosilactobacillus fermentum BS2, L. plantarum BS1, BS3, L. paracasei BS6, Bifidob. bifidum BS4, BS5B1: unground BP, honey, water (4:1:1); B2: ground BP, honey, water (4:1:1); B3 –unground pollen, honey, water (4:1:1) and 1% lactulose; B2: ground37°C for 48 h and incubation for 7 and 14 daysOptimal method using ground pollen and inulin;
↑ probiotic viability in B2;
↑ antioxidant activity in B2 after 7 and 14 days;
↑ lactic acid content (%) after 4 days
(80)
BP, honey, water (4:1:1) and 1% lactulose
Canola BPBreaking the pollen wallGanoderma lucidum and Saccharomyces cerevisiaeBB1: G. lucidum fermentation: pH = 5.5; BB2: S. cerevisiae fermentation: pH = 5.0BB1: 30°C; 8 days;
BB2: 36°C; 8 days
↓ reducing sugar level
↑ CMCase activity of G. lucidum at day 3
↑protease activity in the 5th day for G. lucidum and in the 6th day for S. cerevisiae
↑ pectinase activity in BB1 (83.99 ± 2.81 U/mL) at day 4 and in BB2 (90.51 ± 5.53) U/mL at day 5 Optimal laccase activity in BB1 at day 3 (546.30 ± 8.18 U/L)
(99)
Honey, BP (pellets or ground)Symbiotic productFermented product with L. plantarum and L. acidophilus administration daily in Wistar rats (n = 10): G1: 2 mg/kg; G2: 20 mg/kg; G3: 200 mg/kg; G4: controlBP1: 20 g unground BP, 3 g honey, 5 mL distilled water; BP2: 20 g ground BP, 3 honey, 5 mL distilled water; BP3: 20% unground BP, 3%honey; BP4: 20% ground pollen, 3% honey37°C, 72 h↑ lactic acid content in BP2 after 24, 48 and 72 h;
↑ viability of L. plantarum and L. acidophilus strains in BP2 and BP4;
↓ cholesterol levels at an intake of 20 mg kg−1 of BP;
↑ body weight after 4 weeks in the BP1 and BP2 groups
(75)

Recent advances in the biotechnological processes to obtain fermented products using BP.

CFU, colony forming units; FA, fatty acids; PUFA, polyunsaturated fatty acids; ↑, increase; ↓, decrease.

The most important mechanism for the fermenting of microorganisms is carbon metabolism, in which carbohydrates are converted into essential compounds such as alcohols, acids, and carbon dioxide as the main end–products (100). To produce lactic acid, L. bulgaricus, and Streptococcus thermophilus consume sugar up to 3.2%, but in an acidic environment, those species become inactive (101). In this aspect, following fermentation, the levels of maltose and turanose decreased. The contents of free and total phenolic compounds increased by 18.3 and 17.8% after fermentation, whereas the content of bound phenolic compounds decreased. Fermentation with various microbial strains was demonstrated to enhance the quality of phenolic compounds in BB attributed to BP's structure (23, 102). Most bioactive compounds can be changed during fermentation due to the microbes' metabolic actions; thus phenolic acids are released under acidic conditions—field (103). Furthermore, peptides play critical roles in enhancing food taste and flavor. Most people cannot eat BP due to its distinctive aroma; however, active–taste peptides may solve this limitation (104).

BP is well-known to be rich in nicotinic, pantothenic acids, and riboflavin, while the riboflavin content of BP is the highest among all plant-based materials. The contents of riboflavin, nicotinamide, nicotinic acid, and amino acids were increased after fermentation in both pollen mediums, emphasizing the fermentation with L. bulgaricus and S. thermophilus can enhance vitamin content (105). In addition, the proteins degrade into smaller molecules through the fermentation process, making digestion and consumption much more accessible. Aside from that, wall-breaking pollen demonstrated more significant advantages in nutrient transformation during the fermentation process (96). In 2019, Di Cagno et al. (45) attempted to reproduce the natural process of BB fermentation by performing an actual solid-state fermentation process with BP as the primary substrate. Furthermore, they established a biotechnological protocol in which the role of LAB is precisely emphasized, and specific parameters, like temperature, pH, use of selected starters, time, influence the quality of the product developed at the fermentation end (Table 3).

Since fermentation is the most cost-effective method to improve the availability of high-quality nutrients for the human body, Knazovická et al. (73) simulated the function of bees with BP using a natural fermentation model analyzed the final product, which they dubbed pollen can. Physico-chemical analyzes of pollen can (BB) showed a 60% increase in water content, a 40% increase in free acidity, and a 17% decrease in pH, along with a reduction of 2% of fat compared to the results of analyzes performed on raw BP. The drop in pH is caused by lactic and acetic acid fermentation and alcoholic fermentation, thus ensuring a defensive role and spoilage avoidance of BB.

In 2019, another study found a potential improvement in the nutrient content of the resulting product through the solid fermentation of BP with LAB (96). The study aimed to obtain a nutritionally improved novel natural food product from BP that can be used as a nutritional supplement or a valuable ingredient in other foods. The LAB produced lactic acid by using the carbohydrates found in BP. During fermentation, the lactic acid content increased slightly after 168 h, with the final level of 6.10%, while in control, it remained unchanged, and the total sugar content decreased by 31.60%. The protein level in BP before fermentation was 26.80 mg/g, which increased by 12.53 mg/g after fermentation. Further details can be seen in Table 3.

Yeast on the Biotechnological Process and Probiotic Usage

Foods have been fermented to enhance their organoleptic and nutritional characteristics from ancient times. In the 20th century, industrial microbiology grew even further when new opportunities for producing a wide range of goods by fermentative processes emerged (90). Recent developments in yeast taxonomy, ecology, biochemistry, genetics, and molecular biology have piqued the interest in their role and importance in beverages and foods. This has led to a better understanding of the fermentation functions of well-known products and their role in the fermentation processes of other substrates (93). During their development in beverages and foods, they absorb nitrogen and carbon substrates and produce a wide range of volatile and non-volatile metabolites that influence the product's chemosensory properties. At the same time, other yeasts create extracellular amylases, proteases, lipases, and pectinases which also affect the aroma and texture of products (106). Yeast enzymatic activity is now critical in the processing of wide varieties of fermented food products; thus through a fermentation process under anaerobic or oxygen rich-conditions, it is likely to obtain ethanol and carbon dioxide (107). Compared to LAB, yeasts are not especially nutritionally demanding, but even so, the presence of simple compounds such as fermentable sugars, vitamins, minerals, amino acids, and oxygen stimulate their growth (108).

During a study, Yan et al. (96) fermented BP with various yeast or yeast mixtures the following fermentation. The overall phenolic compound contents of BP or wall-breaking pollen increased in the next order: fermentation with a microbial combination> fermentation with yeasts > LAB fermentation. The findings indicate that peptides with lower molecular weight significantly increased throughout fermentation. Peptides are either released during protein hydrolysis or formed by microorganisms involved in fermentation (97). A surprising aspect is that the following fermentation with yeasts, peptides with lower molecular weight (<1,000 Da), also known as oligopeptides, carry out a variety of active functions such as blood pressure regulators, anticoagulants, and antioxidants (109).

Yeast fermented BP may contain more carbohydrates, generate oligopeptides, free essential amino acids, PUFAs, and polyphenols than BP fermented by LAB; thus, yeast fermentation is a viable option for improving BP's nutritional properties (29). In this aspect, Zhang et al. (99) investigated the fermentation mechanisms of Canola BP by S. cerevisiae and Ganoderma lucidum to facilitate the breaking of the pollen wall. The pollen wall cannot fully decompose in the human digestive system, and its contents are only released through the germinal aperture, resulting in a nutrient consumption reduction. As a result, deterioration of the pollen wall is needed to maximize the use of nutrients present inside BP (58). On day 1, the Canola BP coating disappeared, the germinal apertures continued to expand with fermentation until the 8th day when the contents were released, and the wall's structure was damaged. G. lucidum broth comprises higher amounts of nutrients compared to S. cerevisiae. The results showed a suitable fermentation method for breaking the pollen wall and releasing nutritional compounds (e.g., polysaccharides, ganoderic acid) (110).

Hanseniaspora uvarum, a unique yeast species that can grow at 1.5 pH (most yeasts grow better at pH 4.5–7.0), along with A. kunkeei, was used by Di Cagno et al. to reproduce the natural process of BB by performing an initial solid-state fermentation process with BP as the main substrate (45). Yeasts were detected at the uppermost cell densities in raw BP throughout their first 20 days of storage and unstarted BP throughout their last 20 days. H. uvarum pectin-degrading enzymes were required to break down the pollen walls, resulting in nutrient release; this hypothesis emphasizes the close interaction between LAB and other microbial groups during BB fermentation (111). This study linked the growth process of BB to the active role of native LAB in collaboration with yeasts. Furthermore, it highlighted the critical role of A. kunkeei and the development of a fermentation protocol for BP that nearly reproduces the natural process of BB fermentation, resulting in a well-constructed and consistent fermented product with a high nutritional value, ideal for human consumption (45). Further details can be seen in Table 3.

The present studies indicate the favorable influence of BP solid-state fermentation on the nutritional content of the resulting product, BB, by boosting the bioavailability and digestibility of nutrients and bioactive substances. Furthermore, since all of the studies listed above have achieved positive features in their field of research, biotechnological BB can be considered a different food with a great source of natural nutrients and a product that is beneficial to human nutrition and health (14, 112).

Potential Therapeutic Properties of LABs Found in BB and/or Used in the Fermentation Process of BP

Probiotics from bee products possess several health benefits, including controlling gastrointestinal infections, improvement in lactose metabolism, anticarcinogenic and antimutagenic properties, cholesterol reduction, immune system stimulation, and improvement in inflammatory bowel disease (Table 4). Probiotics from BB produce bacteriocins and short-chain fatty acids, which help lower gut pH, enhance the available nutrients, colonize the colon with available microorganisms, stimulate mucosal barrier function, and increase immunity (Table 5). Moreover, several studies demonstrated the stimulatory effect of probiotics of the natural and gained immune response by inducing secretory and systemic IgA secretion (135137).

Table 4

Functional propertiesProductIsolated or used strainsHealth effectsReference
Antibiotic susceptibilityApis mellifera BBA. kunkeei K18, K34 and K45,
Lact. rhamnnosus GG (ATCC 53103)
K18, K34 resistant to Ampicillin and Kanamycin(81)
Apis mellifera BBCompanilactobacillus musae SGMT17, Companilactobacillus crustorum SGMT19, SGMT20, Companilactobacillus mindensis SGMT22↑ resistance to Vancomycin, Teicoplanin, Kanamycin, Streptomycin, Gentamicin(113)
n.a.LGG↑ decrease in optical density of preformed biofilms of Corynebacterium and antibiotic-resistant gram-negative bacteria(114)
Apis mellifera BBA. kunkeei AP-2, AP-8, AP-13, AP-15, AP-16, AP-18↑ resistance to Kanamycin and Streptomycin(115)
AntibacterialFresh BBMetschnikowia pulcherrima↑ activity against Candida parapsilosis, Debaryomyces occidentalis, Proteus vulgaris, and S. cerevisiae(116, 117)
Apis mellifera BBLGG and isolated EPS↑ inhibition against C. albicans
↑ inhibition against hyphal formation of C. albicans Isolated EPS reduced adhesion of C. albicans to VK2/E6E7 (30%) and Calu-3 (27%) at 200 μg/mL
(118)
BB of stingless bee H. itamaBacillus safensis BB2, Bacillus amyloliquefaciens BB5, Bacillus pumilus U1, Bacillus cereus U22, MPS3↑ Haemolytic activity(113)
BB of stingless bee H. itamaC. musae SGMT17↑ antibacterial activity against Escherichia coli, Staphylococcus aureus, Salmonella typhimurium, Pseudomonas aeruginosa(113)
BB of stingless bee H. itamaLeuconostoc mesenteroides U39↑ antibacterial activity against E. coli, S. aureus, Salm. typhimurium, Pseud. aeruginosa(113)
BB of stingless bee H. itamaC. crustorum SGMT20↑ antibacterial activity against Pseud. aeruginosa(113)
Apis mellifera BBBacillus amyloliquefaciens SGMT3↑ antibacterial activity against Staphylococcus aureus(113)
Apis mellifera BBLeuconostoc mesenteroides subsp. suionicum strain M6S3B6↑ inhibitory activity against Pseudomonas aeruginosa (ATCC 27853) Escherichia coli (ATCC 11775) Bacillus subtilis (ATCC 21332) Staphylococcus aureus (ATCC 25923) Klebsiella pneumoniae (KU593478)(113)
BB Hedera helixL. plantarum PLB1↑ inhibition in Bacillus megaterium F6(45)
BB Hedera helixA. kunkeei PFB13, PFA7, PFA35↑inhibition in Bacillus megaterium F6 and Pantoea agglomerans DTB8
Moderate to ↓ inhibition in Listeria monocytogenes ATCC 19115, Escherichia coli DSM 30083, Serratia marcescens DR8 and DR10
(45)
BB Hedera helixA. kunkeei PLA14↑ inhibition in Bacillus megaterium F6, Pantoea agglomerans DTB8, Escherichia hermannii PS2(45)
BB Hedera helixA. kunkeei PLA21↑ inhibition against Bacillus megaterium F6, Pantoea agglomerans DTB8 and Serratia marcescens DR10(45)
BB Hedera helixA. kunkeei PFA15↑ inhibition in Bacillus megaterium F6(45)
Apis mellifera BBA. kunkeei AP-2, AP-8, AP-13, AP-15, AP-16, AP-18↑ levels of antibacterial activity against S. aureus ATCC 29213, B. cereus ATCC 11778, E. coli ATCC 25922, and S. typhimurium RSSK 95091(115)
Bile toleranceBB of stingless bee H. itamaFructobacillus fructosus U47, C. mindensis SGMT22↓ bile tolerance (75.66% survival rate) after exposure to 0.3% bile for 4 h(113)
Apis mellifera BBA. kunkeei AP-2, AP-8, AP-13, AP-15, AP-16, AP-18↑ inhibition levels (60–80%)(115)
pH survival rateApis mellifera BBA. kunkeei AP-2, AP-8, AP-13, AP-15, AP-16, AP-18↑ tolerance to low pH conditions(115)
Bile toleranceApis mellifera BBLeuconostoc mesenteroides U39, F. fructosus U45, C. musae SGMT17, C. crustorum SGMT19, SGMT20, E. faecalis MPS15↑ bile tolerance after exposure to 0.3% bile for 4 h(113)
Pepsin toleranceApis mellifera BBC. musae, C. mindensis, C. crustorum↑ survivability rate (98.20–100%) after 3-h exposure to pepsin(113)
Pancreatin toleranceApis mellifera BBC. musae, C. crustorum↑ survival rate of L. musae SGMT 17 (99.38%) followed by L. crustorum SGMT20 (99.23%) to exposure to pancreatin(113)
Cell autoaggregationApis mellifera BBC. mindensis SGMT22↑ autoaggregation ability (41.16%)(113)
Apis mellifera BBA. kunkeei AP-2, AP-8, AP-13, AP-15, AP-16, AP-18↑ autoaggregation ability (65%)(115)
Cell surface hydrophobicityApis mellifera BBLc. mesenteroides U39, C. mindensis SGMT22 and C. musae↑ cell surface hydrophobicity (80.52, 74.51, and 59.41%, respectively)(113)
AntifungalBB Hedera helixA. kunkeei PFB13↓ inhibition in Aspergillus versicolor CBS 117286(45)
BB Hedera helixA. kunkeei PLA13↑ inhibition in Aspergillus versicolor CBS 117286 and Penicillium roqueforti DPPMA1(45)
BB Hedera helixL. plantarum PLB16Moderate to ↓ inhibition in Penicillium albocoremium CBS 109582 and Penicillium roqueforti DPPMA1(45)
Apis mellifera BBA. kunkeei AP-2, AP-8, AP-13, AP-15, AP-16, AP-18↑ activity of all tested strains against A. paraciticus and B. cinerea
↑ activity of A. kunkeei AP-2 against A. alternata, A. paraciticus and B. cinerea
↑ activity of A. kunkeei AP-20 against F. oxysporum, A. paraciticus and B. cinerea
(115)
n.a.LGG↑ activity against Candida hyphae formation(118)
Safety and probiotic potentialCamellia sinensis BBLactobacillus jensenii, F. fructosus and Lactococcus plantarumProduction of organic acids in BB(119)
n.a.LGG↑ auto-aggregation of LGG after 24 h incubation
↑ biofilm formation in TSB with 0–1% glucose
↑ Co-aggregation percentages with E. coli DSM 5698, E. coli K12-DH5, P. mirabilis ATCC 29906, Ec. faecalis ATCC 2912, S. aureus ATCC 29213, and Lb. acidophilus ATCC 4356 evaluated after 5 and 24 h of incubation
(120)
Caries preventionn.a.LGG↑ viable cell numbers with glucose and sucrose in 64.5-h multispecies experimental oral biofilms
↓ pH values of spent media at each time point with lactose No harmful effects detected on dental hard tissues
(121)

Therapeutic properties of probiotic bacterial isolates found in BB and/or used in the fermentation process of BP.

NCM460, normal mucosa intestinal cells; IL, Interleukin; APEC, Avian pathogenic E. coli; HGC-27, Gastric carcinoma cells; ODC, Ornithine decarboxylase; SSAT, spermidine/spermine N1-acetyltransferase; AGS, gastric adenocarcinoma cells; LGG, Lacticaseibacillus rhamnosus GG (ATCC 53103); HCT-116, human colon carcinoma cell line; ↑, increase; ↓, decrease.

Table 5

DisorderLAB strainStudy modelEffectsReferences
Bladder cancerLive and Lyo LGG (lyophilized)MB49-PSA cells↑ TNF-a in live LGG (414.27 ± 251.96 pg /mL) and Lyo LGG (318.46 ± 208.28 pg /mL)
↑ IL-12p40 in live LGG (76.45 ± 2.97 pg /mL) and Lyo LGG (102.30 ± 31.64 pg /mL)
↑ IL-10 in live LGG (193.14 ± 93.35 pg /mL) and Lyo LGG (393.42 ± 225.19 pg /mL)
↑ number of dendritic cells to the bladder
↓ number of dendritic cells in local lymph nodes
↑ immune cell recruitment into the bladder
(122)
Gastric adenocarcinomaLGGHGC-27 cells↓ODC mRNA and activity, polyamine content, neoplastic proliferation after 24 and 48 h
↑ SSAT mRNA and activity
(123)
Live and heat-killed LGGAGS cells↓reduced adhesion of H. pylori by 50% on AGS cells at a concentration of 1010 CFU/mL
↓ IL-8 (5,500 ± 1,600 pg /mL) with live LGG
(124)
Viable and heat-killed LGG (108 CFU/mL)HGC-27 Gastric cell line↑ adhesion of LGG (75.4%−90.9%)
↑ proliferation activity after 48 h
↑ proapoptotic effect of viable and heat-killed LGG after 24 and 48 h
(125)
LGG homogenate (1 × 108, 5 × 107 and 2 × 107 CFU/mL)HGC-27 Gastric cell line↑ antiproliferative action with increasing concentrations of LGG after 24 h and 48 h of treatment
↓ conversion of the MTT tetrazolium salt at 1 × 108 CFU/mL compared with the untreated control cells after 24 h
↓ in [3H]-thymidine incorporation in DNA of cells with 5 × 107 CFU/mL compared with the untreated control cells
↓ spermine, spermidine and total polyamine content 1 × 108 CFU/mL compared to untreated control cells after 24 and 48 h
↑ Bax/Bcl-2 ratio compared to untreated cells with 1 × 108 CFU/mL after 24 h and 48 h
(126)
Colorectal cancerLive and UV-Inactivated LGGCaco-2 Cells↓ IL-8 expression by both LGG
↓ Ub-IκB expression by UV-inactivated LGG
(127)
LGGHCT-116↓ cell invasion to 49%
↓ MMP-9 activity to 72%
↑ ZO-1 protein levels to 170%
↓ cell invasion to 30%
(128)
L. plantarumNCM460 cells↓ IL-17F (0.17–1.00 pg/mL) and
↓ IL-23 (16.9–18.6 pg/mL) in inflamed NCM460 cells
(83, 129)
Viable and heat-killed LGG (108 CFU/mL)DLD-1 Colon Cell Line↑ adhesion of LGG (90%−98%)
↑ proapoptotic effect of viable and heat-killed LGG after 24 and 48 h
(125)
Live (1 × 106 CFU/mL) and heat-killed (1 × 108, 1 × 109 and 1 × 1010 CFU/mL) LGGCaco-2 cells↓ chemoxine (CCL20, CXCL8 and CXCL10) expression in Caco-2 cells
↑ suppression of E. coli-induced expression of all 3 chemokines
↑ suppression on the expression of CXCL8 in Caco-2 cells after stimulation with PGN
↑ suppression on the expression of CCL20 and CXCL10 in Caco-2 cells after stimulation with PGN and flagellin
↑ HSPA1 and HSPA6 expression in Caco-2 cells with (10 10 CFU/mL) of heat-killed LGG
(130)
Freeze-dried LGGHuman T84 colon epithelial cells↑ expression of COX2 protein in a concentration-dependent manner in T84 after 72 h(131)
Live and heat-killed LGGCaco-2 cells↓TER levels in Caco-2 cells
↑ TER levels (24 h post TNF-a stimulation) in the presence of LGG (105)
↓ TER levels (24 h post TNF-a stimulation) in the presence of heat-killed LGG and LGG+ chloramphenicol (20 μg mL−1)
(132)
↓ CXCL-8 and CCL-11 secretion from cytokine-stimulated epithelial monolayers
Chronic colitisLGGRAW 264.7 macrophages and spontaneous mutant, RAW 264.7 gamma NO(–)↑ inhibition of TNF-α production by LPS-activated macrophages
↑ inhibition of TNF-a production by LTA-activated macrophages
(133)
Irritable bowel syndromeLGGHT-29, Caco-2 cells, and intestinal epithelial cells↑ SERT mRNA levels in HT-29 cells treated with increased concentration of LGG for 12 and 24 h
↑ SERT protein expression in HT-29 cells treated with increased concentration of LGG for 12 and 24 h
↑ SERT mRNA expression and protein levels of SERT in Caco-2 cells treated with increased concentration of LGG for 12 and 24 h
↑ SERT mRNA levels in mice intestinal epithelial cells at the 1st week
↓ SERT mRNA levels in mice intestinal epithelial cells at the 2nd week
(134)

In vitro studies regarding the potential therapeutic properties of LABs found in BB and/or used in the fermentation process of BP.

HCT-116, human colon carcinoma cell line; HGC-27, Human gastric cancer cell line; DLD-1, colon cancer cell line; Caco-2, human colon adenocarcinoma cell line; PGN, peptidoglycan; RAW 264.7, mouse monocyte/macrophage cell lines; LPS, lypopolysacharides; LTA, lipoteichoic acid; CXCL-8, interleukin-8; CCL-11, eotaxin; SERT, serotonin transporter.

Multiple human and animal studies have been conducted and suggest that probiotics are GRAS and practical for clinical application on human diseases, such as acute pediatric diarrhea (138), rotavirus-related diarrhea (139), infantile colic (140), necrotizing enterocolitis in shallow birth weight infants (141), type 1 diabetes (142), allergic asthma (143) inflammatory bowel disease (144), bone loss (145), and bacterial vaginosis (146), and virus infection (147). Further details can be seen in Table 6.

Table 6

Functional propertiesLAB strainTreatment schemeTreatment durationHealth effectsReferences
Anti-inflammatoryA. kunkeei YB3811 subjects took 1 g heat-killed YB38 once a day4 weeksSignificant ↑ in SIgA concentration
↑ IgA production in mouse Peyer's Patch cells
↓ mitogenic activity and ↓ effect on IL-2 production in mouse spleen cells
(135)
A. kunkeei YB38IFV sublethal infection in mice:
6-week-old BALB/c mice divided into 2 groups (n = 100) administered daily oral doses of YB38 saline dilution (0 or 100 mg/kg) for 22 days
IFV lethal infection in mice:
6-week-old BALB/c mice were divided in 3 groups (n = 60) and daily administered oral doses of 0, 10, or 100 mg/ kg of YB38 saline dilution
n.a.↓ numbers of T cells, NK cells, neutrophils, and macrophages in the mice inoculated with the heat-killed YB38 treatment compared to control at 4, 4–8, 4–6, and 8 days after infection;
IL-6 production was significantly suppressed in the heat-killed YB38-treated group
↑ IgA concentration in YB38-treated group
↓ tissue damage in YB38-treated group
(137)
A. kunkeei YB3829 female subjects consumed 0 (placebo), 2, 10, and 50 mg of heat-killed YB38n.a.↓ in intestinal levels of Bacteroides fragilis(136)
Capsule with LGG (109)home residents (n = 196; >65 years old)
G1 (treatment, n = 100) = 2 capsules/day G2 (control, n = 96): placebo (calcium carbonate capsule)
6 months↓ respiratory viral infections observed in 14 (15.0%) residents in G1
Moderate respiratory viral infections observed in 21 (22.9%) residents in G2
(148)
LGG-derived protein (p40)4–6 week-old C57BL/6 mice
G1: gavaged with pectin/zein beads with p40 from LGG (10 mg per day)
G2: pectin/zein beads
3 weeks↑IgA level in LGG treatment group
April gene expression in MSIE cells
(128)
LGGHuman intestinal mucus isolated from 114 fecal samples collected from healthy infants and adultsn.a.↑adhesion properties to adult human mucus
↓ adhesion properties to neonatal and infant mucus
(149)
LGG20 ulceritive-colitis (UC) patients and 22 normal subjects)
G1 (n = 10): negative control
G2 (n = 12): dose of 1.2 × 1010 CFU/d LGG (2 packets/day) G3 (UC, n = 10): 1.2 × 1010 CFU/d) dose of LGG
G4 (UC, n = 10): 2.4 × 1010 CFU/d dose of LGG
7 days↑ adhesion in the normal colon after 7 days of LGG administration in G4 (6.83 ± 2.97) compared to control
↓ mucosal TNFα (1.68 ± 0.22) and IL-17 (1.05 ± 0.11) expression in G4
(150)
Safety and tolerabilityLGG15 volunteers (aged 66–80 years) received 2 capsules (1010) daily for 28 days and were followed through day 5656 days↓ adverse effects, most common were gastrointestinal (bloating, gas, and nausea)
↓ IL-8 during LGG consumption
↓ hemoglobin in 2 patients at day 28
↑ Blood Urea Nitrogen in 2 patients at day 28 and 1 patient at day 56
↑ White Blood Count in 1 patient at day 56
↓ glucose level in 1 patient at day 28
↑ glucose level in 1 patient at day 28
(151)
ImmunomodulationLGGFemale (4–6 weeks old) C57BL/6 mice (n = 12/group) immunized by oral gavage with 108 CFU LGG on days 0, 14 and 28
G1: live LGG-GFP
G2: LGG IL-2-GFP
G3: wild type LGG
G4: sterile PBS
28 days↑ survival of LGG-IL-2-GFP
↑ cytokine gene expression at 12 h and ↓ by 24 h
↑ IgA producing B cells and CD86 positive DC in G2
↑ GFP specific IgG titres in G2
↑ GFP specific sIgA in fecal extracts from 24th to 35th day
↑ GFP specific CD8+ T cells in G2
↓ GFP specific CD8+ T cells in G1
↑ CTL activity in G1 and G2
(152)
Immnunotherapy against bladder cancerLGGC57BL/ 6 female mice aged 4–6 weeks divided in 5 groups (n = 50)
G1: live LGG
G2: Lyo LGG
G3: oral 1 × 108 live LGG 1 day before intravesical Lyo (O + I) LGG
G4(control): intravesical instillations of PBS
G5 (control): oral PBS 1 day before intravesical PBS
6 weeks↑ PF4, XCL1, and P-selectin in LGG-treatment groups
↓ OPN, Pro-MMP9, Thymus CK-1, and VEGFR2 in LGG-treatment groups
↑ bladder VEGF-D
↑ splenic Mac3+ cells in LGG-treatment groups
↑ number of cured mice
(122)
Intestinal crypt lossLGG8-week-old C57BL/6 by gavage of Gavage of 5 × 107 LGGn.a.↓ epithelial apoptosis
↓ radiation-induced epithelial injury
↑ crypt survival
(153)
ImmunomodulationLGG (ATCC 53103)Forty-five 6-week-old female BALB/c mice divided in 3 groups
G1 (control): intragastrically administered PBS (200 μL) every other day for 7 total treatments
G2 (LLGG): intragastrically administered LGG every other day for 7 total treatments (doses from 103 to 109CFU)
G3: intragastrically administered 109CFU every other day for 7 total treatments
n.a.↑ OTU, Chao1, ACE, and Shannon indices
↓ Simpson index
↑ abundances of intestinal Firmicutes, Bacteroides and Actinomycetes
↓ intestinal Proteobacteria
↑ immunity
↑ expression of Th1-type cytokines (IFN-γ) and Th2 cytokines (IL-4) in CD4+ T cells
↑ expression of IL-17 in CD4+ T cells
↑ percentage of CD4+CD25+Foxp3+ Treg cells
(154)
HepatotoxicityLGG (ATCC 53103)Twenty-four male Holstein calves divided in 3 groups received oral administration in 50 mL of phosphate-buffered saline
G1: untreated control
G2: 4.80 mg of AFB1
G3: 1 × 1010 cfu of LGG suspension and 4.80 mg of AFB1
Treatment duration: 14 days
14 days↑ ADG in G3 nad G1 compared to G2
↓ AST and LDH compared to G2
↓ concentration of AFB1 and AFM1 in rumen fluid, urine and plasma in G3
↑ concentration of AFB1 and AFM1 in feces
(155)
Diarrhea treatmentLGGFour weeks old Female Sprague Dawley rats (n = 64) divided in 4 groups
G1: control
G2: oral daily dose of LGG 1 × 109 CFU lactobacilli/1 ml
25 weeks↓β-catenin expression in G2 and G4
↓ NFκB-p65, COX-2 and TNFα inflammatory proteins
↑ pro-apoptotic proteins Bax casp3 and p53
↓ VEGFα expression in G4
↓ tumor incidence in G2
(156)
G3: weekly single dose of 40 mg/kg body weight of DMH intraperitoneally for 10 consecutive weeks
G4: weekly single dose of 40 mg/kg body weight of DMH intraperitoneally for 10 weeks and daily oral dose of LGG 1 × 109 CFU lactobacilli/1 ml for 25 weeks
Atopic dermatitis (AD)LGG39 infants with AD divided in 2 groups
G1 (n = 19): 5.01 × 107 CFU/g LGG to achieve a daily intake of 3.4 × 109CFU
G2 (control): Casein hydrolysate
3 months↓ number of Ig-secreting cells in G1
↓ IgA- and IgM-secreting cells in G1 from 1–3 months
↑ IgA- and IgM-secreting cells in G2
↑ Number of Bifidobacterium species in G1 compared to control
↑ % colonization with Bifidobacterium longum in G1 compared to control
↓ % colonization with B. fragilis compared to control
(157)
LGG105 pregnant women with AD divided in 2 groups:
G1 (n = 50): 5 × 109 CFU/g LGG twice daily
G2 (n = 44):placebo
4–6 weeks before delivery and a postnatal period of 6 monthsrisk of AD in children on probiotics relative to placebo was 0.96
no difference between groups regarding the cumulative incidence of atopic symptoms
no difference in total IgE concentrations or numbers of specific sensitization to inhalant allergens between groups
(158)
Freeze-dried LGGFemale NC/Nga mice divided in 2 groups
G1 (n = 17): control
G2 (n = 16): LGG 4 x 109 CFU/g (~30–50 mg/adult mouse)
12 day of pregnancy to 12 weeks after birth↓ grades of dermatitis G2 compared to control
↑ suppression of onset and development of atopic leasions in G2 compared to control
↓ mast cells number and eosinophils in G2 compared to control
↑ IL-10 levels compared to control
↑ expressions of IFN-g and IL-4 compared to control
(159)
LGGG1 (n = 27): Cow's milk elimination diet + formula milk with or without LGG
G2 (n = 11): LGG (5 × 108 CFU/g or 2 × 1010 CFU twice/day) during breastfeeding
4 weeks↓SCORAD in probiotic group
No significant difference between groups after 2 months
(160)
LGGG1 (n = 52): probiotic (1x1010 CFU/g LGG + 0.01 mg of vitamin D3 + 0.6 mg zinc)
G2 (n= 44): placebo
n.a.↓ reduction in SCORAD in probiotic group(161)
Alcoholic liver diseaseLGG supernatant10-weeks old male C57BL/6 mice
G1: alcohol (5% w/v, AF, n = 6)
G2: isocaloric maltodextrin (PF, n = 6)
G3: alcohol + 109 CFU/ml LGG (AF + LGG-s, n = 6)
5 days↓ Serum ALT and AST levels in G3 compared to G1 and G2
↓ claudin-1 and ZO-1 mRNA expression in G3 compared to control and G2
↑ villus-crypt junction in ileum
E. coli protein level compared compared to alcohol exposure in G2
↓ frequency of TH17 in G3 compared to G2
↓ serum IL-17 level in G3 compared to G2
(162)
LGG supernatant9-week old Male C57BL/6N mice
G1: Control
G2: alcohol at 6 g/kg body wt via gavage
G3: 1 × 109 CFU/mL + alcohol
5 days↓ Hepatic tissue TG levels after 6 h alcohol exposure in G3 compared to G2
↓ plasma ALT and plasma LDH in G3 compared to G2 after 1.5 and 6 h
↓ liver and ileum reactive oxygen species (ROS) formation compared to G2
↓ plasma endotoxemia, ileum permeability in G3 compared to G2
↑ mRNA levels of ileum tight junction proteins and adaptors and of ileum mucus protecting factors in G3 compared to G2
↑ hypoxiainducible factor (HIF)-1α/2α expression in G3
(163)
LGG supernatantMale C57BL/6 N mice divided in 3 groups
G1 (PF): isocaloric maltose–dextrin
G2: alcohol-fed
G3: alcohol + LGG (109 CFU/mouse/day)
8 weeks↓ MPO activity, TNFα protein levels and TNFα mRNA expression in G3 and G1 compared to G2
↓ Cyp2E1 mRNA and protein levels in G3 and G1 compared to G2
↓ hepatic TLR (toll-like receptors) mRNA expression
(164)
Alcohol-induced liver injuryLGG supernatantMale C57BL/6N mice divided in 3 groups
G1 (PF): isocaloric maltose–dextrin
G2: alcohol-fed
G3: alcohol + LGG (109 CFU/mouse/day)
8 weeks↑bw, ITF and VEGF
↑ mRNA levels of ZO-1, claudin-1, and occluding
↓ Epithelial Cell Permeability in Caco-2 Cells
↓ Alcohol-Induced ROS Formation in the Ileum and in Caco-2 cells
(165)
Non-alcoholic fatty liver disease (NAFLD)LGG6 weeks old female C57BL/6 mice (n = 24) divided in 4 groups
G1: water and mouse breeding (MZ)-diet
G2: 30% fructose solution+ enriched MZ-diet
G3: LGG (5.2*107 CFU/g bw daily in water and MZ-diet
G4: 30% fructose solution with LGG in water and enriched MZ-diet
n.a.↓ ALT in G3 compared to G2
↓ liver fat accumulation in G3 and G4
↓ Hepatic ChREBP, ACC1 and FAS mRNA expressions in G3 and G4 compared to high-fructose diet (G2)
↓ TNF-α, IL-1β (B) and IL-8R (C) mRNA expressions
↑ occludin, and claudin-1 molecules
↓ pIkB kinase protein expression and LPS
(166)
Alcohol-induced intestinal oxidative stress and liver injuryLive LGGMale Sprague–Dawley rats
G1 (n = 11): alcohol gavage (~2–3 mL) twice daily (initial dose: 2 g/kg/day; final dose: 8 g/kg/day)+ powdered rat chow
G2 (n = 9): alcohol gavage+ live LGG (2.5 × 107/once daily)
G3 (control, n = 5): isocaloric amount of dextrose, by gavage
G4 (n = 3): dextrose + intragastric feedings of live LGG
10 weeks↓ liver necroinflammation score (%) in G2 and G4 compared to G1
↓ liver MPO levels and liver fat content in G2 and G4 compared to G1
↓ liver carbonyl and nitrotyrosine levels in G2 and G4 compared to G1
↓ intestinal permeability to sucralose in G2 and G4 compared to G1
(167)
GastroenteritisLGGChildren aged 6 months to 5 years positive for either rotavirus (G1 and G2, n = 82)or Cryptosporidium species (G3 and G4, n = 42)
G1: probiotic:1 × 1010CFU/capsule LGG+ 170 mg of microcrystalline cellulose
G2: 170 mg cellulose
G3: LGG+ cellulose
G4: 170 mg cellulose
4 weeks↓ repeated diarrheal episodes in G1 (25%) compared to G2 (46%)
↓ impaired intestinal function in G1 (48%) compared to G2 (72%)
↑ IgG levels postintervention in G1
↑ improvement in intestinal permeability in G3
(140)
Necrotizing enterocolitisLGG640 infants aged between 26.3 and 30.6 weeksn.a.↓ severe necrotizing enterocolitis and mortality in LGG-supplemented infants compared with non-supplemented infants(168)
Bone lossLGGC57BL6/J mice divided in: G1 (control): normal saline (NS) vehicle by oral gavage
G2: LGG+TDF (0.86 mg) daily
G3: 5 × 108 CFU LGG (109 CFU/ml, dissolved in NS) twice a week
G4: E. coli+TDF daily
G5: TDF daily
G6: ZOL+TDF daily
n.a.↑ trabecular bone microarchitecture, cortical bone volume, and biomechanical properties in G2 compared to G5
↑ intestinal barrier integrity, expanded regulatory T cells in G3
↓ Th17 cells and osteoclastogenesis-related cytokines in the bone marrow, spleen, and gut
↑ expression of lysophosphatidylcholines
(169)
Gingival healthLGG108 schoolboys (13–15 years)
G1 (n = 54): placebo
G2 (n = 54): 1 g probiotic mixture (LGG 4.4 × 108 and BB-12 4.8 × 108)
4 weeks↓ gingival and plague index in G2
Aggregatibacter actinomycetemcomitans levels in saliva and plague
↓ total bacterial count in the saliva and plaque sample in both groups
(170)
PeriodontitisLGG6–8 week old BALB/c female mice (n = 36)
G1: Control
G2: PD (periodontitis)
G3: LGG (200 μl of 2-9 × 109 CFU/ml of LGG) gavage + PD
G4: LGG gavage
G5: LGG oral + PD
G6: LGG oral
44 days↓mean bone loss (p > 0.05) in the LGG groups compared to G2
↓ inflammatory scores in LGG groups compared to G2
↓ TRAP positive cells (3.99 ± 2.05) and circulating levels of LIX in blood serum (61% lower) compared to G2
(145)
Human rotavirus (HRV) infectionLGGHuman gut microbiota (HGM) transplanted gnotobiotic (Gn) pig model
G1: control with
G2: 14 doses of LGG
G3: AttHRV alone,
G4: AttHRV + 9 doses of LGG
G5: AttHRV + 14 doses of LGG
n.a.↑ fecal and intestinal LGG counts in HGM transplanted Gn pigs after 23 days in G5
↑ Rotavirus-specific IFN-γ producing T cell responses in ileum, IEL, spleen and blood
↑ Rotavirus-specific serum IgA and IgG antibody responses in LGG treated groups
↑ rotavirus-specific IgA antibody responses in small intestine contents of Gn pigs fed with higher LGG doses
(170)

In vivo studies regarding the potential therapeutic properties of LABs found in BB and/or used in the fermentation process of BP.

GFP, green fluorescence protein; Il-2, Interleukin-2; IgG, Immunoglobulin G; sIgA, secretory immunoglobulin A; CTL, cytotoxic T lymphocyte; CD8+ T cells, killer T cells; VK2/E6E7 ATCC-CRL-2616; normal human vagina epithelial cells; DMH, Dimethyl hydrazine; VEGFα, vascular endothelial growth factor A; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells; COX 2, cyclooxygenase 2; TNFα, Tumor Necrosis Factor α; casp3, caspase3; p53, Tumor protein; PBS, Phosphate-buffered saline; PF, pair-fed; IgA, Immunoglobulin A; IgM, Immunoglobulin M; MSIE, mouse small intestine epithelial cells; APRIL, proliferation-inducing ligand; AFB1, aflatoxin B1; AFM1, aflatoxin M1; ADG,average daily gain; AST, aspartate aminotransferase; LDH, lactate dehydrogenase; ALT, Alanine aminotransferase; ITF, Intestinal trefoil factor; VEGF, vascular endothelial growth factor; BW, body weight; NAFLD, non-alcoholic fatty liver disease; ChREBP, carbohydrate response element-binding protein; ACC1, acetyl-CoA carboxylase 1; FAS, fatty acid synthase; IL-1b, interleukin 1 beta; IL-8R, interleukin 8 receptor; MZ-diet, mouse breeding diet; MPO, myeloperoxidase; HGM, human gut microbiota; Gn, transplanted gnotobiotic pig model; T1D, Type 1 diabetes; IgE, immunoglobulin E; SCORAD, Severity Scoring for Atopic Dermatitis; ZOL, zoledronic acid.

So far, Lacticaseibacillus rhamnosus ATCC 53103 (formerly Lactobacillus rhamnosus LGG) is the most characterized, and studied probiotics, extensively used in the fermentation process of BP with promising results (171). It has multiple health benefits; for instance, it produces a biofilm that acts as a mucosa-protecting agent, enhances the intestinal pit survival through diverse soluble factors beneficial to the gut, diminishes apoptosis of the intestinal epithelium, preserves cytoskeletal strength along with pathogen inhibition, promotes immune awareness by reducing expression of inflammation markers and increasing production of IL-10 (interleukin-10), IL-12 and TNF- α (α-tumor necrosis factor) (172). Thus, the combination of BP fermented with different lactobacilli strains is significant for developing a novel product used both as food and medicine.

Antibiotic Susceptibility

Several reports demonstrated that Lactobacilli strains have antibiotic resistance genes which can be transferred to the host gut of other bacteria. Therefore, it is significant to evaluate the antibiotic resistance properties of probiotics. Furthermore, characteristics linked to safety, survival in the host gut, and colonizing abilities are substantial to assess the proposed probiotic bacteria.

The prevalence of antibiotic-associated diarrhea varies based on diagnosis, with values between 5 and 30% in children and up to 70% in adults. In this aspect, treatment with LGG reduced the risk of antibiotic-associated diarrhea from 22 to 12% in adults and from 23 to 9.6% in children. In the LGG-groups, there was no need for antibiotic treatment discontinuation or intravenous rehydration (173). Korpela et al. evaluated whether long-term consumption of probiotics influences the antibiotic-associated changes in children's microbiota. Their results showed that long-term LGG-supplementation increased the levels of Lactococcus, Prevotella, and Ruminococcus and decreased the levels of Escherichia, as well as reduced the frequency of gastrointestinal complaints after the use of macrolides (174).

Salmonellosis is usually treated with antibiotics, which can cause side effects, including antibiotic resistance and enteric dysbacteriosis. Also, antibiotic therapy can worsen Salmonella-induced diarrhea. In this aspect, Lactobacilli strains are a promising alternative for Salmonella infection as they help prevent it, have fewer side effects, and have higher safety. Several Lactobacilli strains were found to attenuate the intestinal epithelial barrier dysfunction induced by Salmonella lipopolysaccharide (175). De Keersmaecker et al. demonstrated the potential antibacterial activity of LGG-spent culture supernatant (SCS) against S. typhimurium (176). Their results showed that several compounds, such as acetic, pyroglutamic, formic, and lactic acids, might be responsible for the antibacterial efficiency against Salmonella spp. Furthermore, infection with Salmonella spp. causes gut inflammation, which changes in the cytokine profile can detect. LGG reduced the levels of TNF-α in the colon while maintaining IL-10 and significantly reducing MPO (myeloperoxidase) levels (177).

Antibacterial Activity

Several reports showed the antibacterial activity of BB due to its high content of polyphenols and LAB. Also, the antimicrobial potential of BB for the prevention and treatment of bacterial and fungal infections in animals and humans has been demonstrated in (1, 178). In a recent study, several polish BB samples exerted higher inhibitory potential against Staphylococcus aureus ATCC 25923 and ATCC 29213. Furthermore, several pieces effectively inhibited the growth of S. aureus and MRSA (methicillin-resistant S. aureus), strains at concentrations between 2.5 and 5.0% (179). In the following study, the bacterial isolates of mature BB exhibited moderate antagonistic effects against S. aureus ATCC 25923, ATCC 29213, S. epidermidis ATCC 12228, P. aeruginosa ATCC 27853, and lower results against Escherichia coli ATCC 25922 (180).

Despite the progress in antimicrobial therapy, sepsis and meningitis caused by E. coli K1 remain the primary cause of mortality and severe neurological morbidity, particularly in preterm and very-low-birth-weight infants (181). In this aspect, He et al. in 2017 evaluated whether LGG supernatant has a preventive effect against gut-derived systemic neonatal E. coli K1 infection in human colonic carcinoma cell line Caco-2 and neonatal rat models. The in vitro results showed that LGG up-regulated mucin and maintained intestinal integrity by blocking the adhesion of E. coli K1 to Caco-2 monolayer. In contrast, the in vivo results showed a decrease of E. coli K1 infection susceptibility in neonatal rats who received oral administration of LGG and reduced bacterial intestinal colonization (182). Furthermore, the LGG-treated rats had increased intestinal expression of MUC2 (intestinal mucin), Ki67 (intestinal epithelial cell proliferation marker), IgA (immunoglobulin A), ZO-1 (zonula occludens-1), and mucin layer, and decreased barrier permeability compared to untreated rats.

Antiviral Activity

Influenza is an infectious disease that affects both animals and humans. The most common symptoms in humans are fever, coughing, muscle pain, chills, headaches, and weakness. In severe cases, it can cause pneumonia which can be fatal in children and the elderly. To investigate whether probiotics protect the host against influenza virus (IFV), BALB/c mice were infected with IFV A/PR/8/34 (H1N1) and administered intranasal LGG. It was shown that mice treated with LGG had lower symptoms frequency and higher survival rates than control. Also, increased mRNA expression of IL-8, TNF, and MCP-1 (monocyte chemotactic protein) were noticed in Ispirli and Dertli (183).

It was reported to reduce IL-2, IL-6, and IL-8, either by oral feeding or intraperitoneal injection with Apilactobacillus spp. The administration of heat-killed A. kunkeei YB38 reduced the symptoms of murine influenza pneumonia by enhancing SIgA production in mice infected with the influenza virus. The intake of A. kunkeei YB38 by healthy adults significantly improved secretory immunoglobulin A (SIgA) levels in saliva compared with baseline concentrations. Also, it decreased levels of the Bacteroides fragilis group.

Gastrointestinal Disorders

Based on their viability, probiotics can survive in simulated gastrointestinal conditions. LAB and their bioactive specific cellular components exert many pivotal effects on the ecosystem of the human GI tract, including maintenance of the gut microbiota and control of the enteric mucosal pathogens, and modulation of the cell-mediated immune response. Auto-aggregation and cell surface hydrophobicity properties of the bacterial cells are essential characteristics to reveal their potential as probiotics which can be associated with the cells adhesion to the gastrointestinal, demonstrating their health-promoting functions. The EPS (exopolysaccharide) production levels in A. kunkeei strains from BB had values between 0.17 (A. kunkeei AP-13) and 2.79 (A. kunkeei AP-15) g/L (115). Also, supplementation with LGG in colicky breastfed infants resulted in reduced daily crying and fecal calprotectin and increased total bacteria and Lactobacilli compared to the placebo group (140).

LGG has beneficial effects on the organism as to be considered probiotic. In particular, LGG can withstand gastric acidity and bile salts, effectively adhering to the gastrointestinal mucosa. The ability to resist gastric acidity and bile salts is a consequence of the power of the bacterium to produce anti-stress proteins that give it greater survival capacity in intestinal transit after oral intake (Table 4).

As neonatal necrotizing enterocolitis (NEC) is one of the significant causes of mortality in premature infants, oral administration of Bifidobacterium bifidum has been suggested as a promising preventive treatment. Thus, B. bifidum (5 × 106 CFU/day) administered to premature rat models of NEC decreased the ailment incidence from 57 to 17% and increased the levels of IL-6, mucin-3, and Tff3 (trefoil factor 3). The protective effect of B. bififdum is related to a decreased inflammatory reaction in the ileum, regulation of main components of the mucus layer, and intestinal integrity improvement (184).

Bone Loss Prevention

Osteoporosis is a chronic syndrome of excessive skeletal fragility characterized by bone mass loss and bone micro-architecture deterioration. Patients with human immunodeficiency virus (HIV) (185) or subjected to antiretroviral therapy with tenofovir disoproxil fumarate (TDF) (186) are strongly correlated to bone loss. Recently, it has been suggested that the gut microbiota is linked to bone homeostasis (187). Thus, Liu et al. evaluated the effectiveness of LGG in attenuation of TDF-induced bone loss in 6-week old C57BL6/J mice. LGG treatment reconstructed the gut microbiota structure and increased the intestinal barrier integrity, proving an effective treatment against TDF-induced osteoporosis (169).

Periodontitis, a chronic inflammatory condition, affects the soft and hard tissues that support teeth. It is influenced by specific pathogenic bacteria (i.e., Porphyromonas gingivalis and Fusobacterium nucleatum), which have been shown to aggravate inflammation and alveolar bone loss in mice (188). In a recent study, LGG administration to P. gingivalis and F. nucleatum-inoculated mice reduced tissue inflammation in the duodenum and IL-6 levels in ileum compared to control. Oral gavage with LGG induced a protective effect against intestinal inflammation and reduced the changes in the gut microbiome (189). LGG also attenuated bone loss in ovariectomy-induced postmenopausal mice models. Inhibition of bone loss was due to increased anti-osteoclastogenic CD4+Foxp3+Tregs and CD8+Foxp3+Tregs and reduced bone marrow, peyer's patch, spleen, and lymph nodes levels (190).

Liver Disease

Alcoholic liver disease is one of the major liver diseases and has increased morbidity and mortality rates. Continued alcohol consumption might cause intestinal microbiota homeostasis, intestinal tight junction barrier dysfunction, endotoxemia, and ultimately steatohepatitis. LGG and bacteria-free LGG culture supernatant have shown promising results in terms of liver protection, such as promoting intestinal epithelial integrity and protecting the intestinal barrier in both animal and human subjects. In this aspect, Zhao et al. demonstrated that supplementation with LGG (109 CFU/day/mouse) decreased ethanol-elevated miR122a expression levels and attenuated ethanol-induced liver injury in mice (191).

Cholestatic liver disease is characterized by gut dysbiosis and increased toxic hepatic bile acids.

The mechanism of action by LGG on hepatic bile acids, liver injury, fibrosis, were evaluated in bile duct ligation (BDL) and multidrug resistance protein two knockout (Mdr2−/−) mice. LGG-treated mice had reduced hepatic concentration of taurine-β-muricholic acid and normalized levels of chenodeoxycholic acid compared to BDL mice. Also, the LGG-group mice had increased serum and ileum fibroblast growth factor 15 expression levels and reduced hepatic cholesterol 7α-hydroxylase (192). Further details can be seen in Table 6.

Immunomodulatory Effects

In recent years, immunotherapy has become an increasing anti-cancer treatment due to its fewer side effects compared to conventional ones. LABs in the gut microbiome of patients under immunotherapy had favorable, responsive rates compared to patients lacking them. Viable and heat-killed LGG were administered to colonic cancer mice models to assess the gut immune background changes. LGG-supplemented rats had increased colonic CD8 T-cell (cytotoxic T lymphocytes) responses and decreased tumor burden in the murine gut cancer models by a CD8 Tcell–dependent manner (193).

Mast cells are multifunctional regulator cells responsible for defense against pathogenic microbes. Thus, the effect of LGG on human mast cell gene expression using microarray analysis was investigated. LGG suppressed genes encoded allergy-related high-affinity IgE receptor subunits α and γ (FCER1A and FCER1G) and histamine H4 receptor. Also, LGG up-regulated the expression levels of genes involved in mast cell immune system regulation and genes that encode proteins with a pro-inflammatory impact (IL-8) and with anti-inflammatory functions (IL-10) (194).

Giardiasis causes intestinal malabsorption and diarrhea in malnourished and immunodeficient individuals, but frequently in children <3 years old. Thus, the immunomodulatory effect of orally administered LGG in Giardia-infected mice was investigated. Pre-and post-probiotic oral administration for 25 days modulated the mucosal immune system response, as the levels of IgA antibody, IgA+ cells, and CD4+ T lymphocytes increased, as well as increased levels of anti-inflammatory cytokines (i.e., IL-6 and Il-10) and decreased levels of pro-inflammatory cytokine INF-γ (195).

Using several BP fermentation variants, Knazovická et al. noticed a decrease in Enterobacteriaceae, making the fermented products appropriate for consumption by people with lower immunity. Apart from the types of fermentation involved in the process, natural products with antibiotic attributes developed by the existing microbiota in stored BP, interactions among living microorganisms can control and enhance the microbiota (73). Furthermore, the resulting BB is more suitable for the organism due to its increased digestibility (196).

Allergic Asthma

Asthma is an airway inflammatory disorder, and its prevalence is increasing by each year. Recent epidemiological studies demonstrated the relationship between asthma, allergic disorder development, and altered intestinal microbiota in both animal models (197200) and human clinical trials (201203). Intestinal colonization with freeze-dried LGG in pregnant and during lactation of BALB/c female mice for 48 days resulted in reduced allergic airway, peribronchial inflammation, goblet cell hyperplasia, and increased TNF-α levels (198). Also, pre-and post-treatment with LGG suppressed the airway hyper-responsiveness to methacholine and metalloproteinase nine expressions in lung tissue. Also, it significantly decreased the number of infiltrating inflammatory cells and Th2 cytokines in bronchoalveolar lavage fluid and serum compared with the OVA-sensitized mice (204). Recently, it was demonstrated that pre-and post-supplementation with LGG suppressed Th2 cytokine (T helper type II cells), TNF-α, IL-17, and HMGB (high mobility group box 1) in the BALF (Bronchoalveolar Lavage Fluid) levels and increased the levels of proteins involved in immune system responses, namely T-bet and Foxp3 in ARN (205).

The efficacy of LGG administration was studied on at-risk infants, as children of allergic mothers have an increased risk of developing allergies. Thus, LGG administration for 6 months diminished by almost 50% the incidence of allergy to expecting mothers and their infant's (197). No significant differences in asthma and allergic rhinitis were shown between early probiotic and placebo supplementation in infants (206).

Atopic Dermatitis

Atopic dermatitis (AD) is an increasing chronic skin disease in children with a prevalence reaching 10% in many industrialized countries (207). The rising incidence of atopic dermatitis might be associated with shifts in gastrointestinal microbiota, namely from a rich flora in non-pathogenic bacteria (i.e., Lactobacilli or Bifidobacterium) to one with increased pathogenic bacteria (i.e., Clostridium) (208). The preventive effect of Lactobacillus on the incidence of atopic dermatitis was demonstrated in pre-and postnatal infants who were less likely to develop this disease compared to placebo group infants. In a randomized, double-blind trial, pregnant women with atopic eczema, allergic rhinitis, or asthma received LGG (1 × 1010 CFU/day) between 2 and 4 weeks before the estimated delivery date. After delivery, infants received LGG for 6 months. In the 4th year, at the end of the trial, 46% of the children in the placebo group developed AD, compared to 26% in the probiotic group (201, 209). In a subsequent randomized, placebo-controlled trial, the children completing the previous studies were invited to complete a 7-year treatment. The LGG group had a lower risk of developing eczema (42%) compared to the placebo group (66%) (210). Rautava, Kalliomäki, and Isolauri in 2002 found that the levels of transforming growth factor (TGF)-β was significantly higher in the breast milk of LGG-administered mothers (2 × 1010 CFU/day) before labor and 3 months after birth (211). Furthermore, AD development was significantly lower in infants receiving LGG in the first 2 years compared to the placebo group. In multiple studies, no significant differences were observed between the probiotic and placebo-treated patients (212214) or in IL-4, IL-5, and interferon γ (IFN γ) (215). Also, no significant differences between the probiotic and placebo groups regarding the eczema frequencies and atopic eczema were noticed (206, 216). Recently, Filipovic et al., in 2020, demonstrated that LGG formulation with Zn and vitamin D3 supplementation in infancy and early childhood proves to be an effective treatment against AD (161).

Lowering Cholesterol Levels

Excess cholesterol is associated with coronary artery disease, the most common cardiovascular disease with increased worldwide mortality by each year. Thus, there is a need for natural therapeutic products that lower cholesterol levels besides the existing treatment schemes. In this aspect, Kim et al. orally administered LGG to high-fat diet (HFD) mice for 13 weeks. A significant reduction of weight and adipose tissues were noticed in LGG-treated HFD-fed mice compared to control. The triglyceride serum levels and cholesterol were also significantly reduced (217).

In 2008, Vamanu et al. performed a study analyzing the evolution of L. acidophilus 1a, and L. plantarum 2s strains on a media with BP and honey. The study aimed to demonstrate the outcome of fermented products on cholesterol levels in Wistar rats (n = 40) and possible bio-productive effects. An increase in sugar consumption after 72 h of fermentation was noticed in the milled pollen grains groups and an aroma specific to BP and lactic acid. The results showed that increased weight was seen in all treated groups with the symbiotic product compared to control. Other monitored parameters were taste and aroma, highlighting that once lactic acid is produced, the sweet flavor converts to a mix between sweet and sour (218).

Safety and Digestibility

Understanding intestinal health and disease is strongly linked to identifying the functional elements behind the gut epithelia's effective growth and homeostasis. Recently, it was demonstrated that the intake of LGG elevated the leptin levels in the gut epithelia important in normal metabolism function and intestinal development and triggered cell proliferation (219).

According to the results presented in previous studies, in 2011, Fuenmayor et al. assessed the conditions required for a better BP fermentation from Columbia. Their results showed the possibility to use L. acidophilus inoculum in a matrix of BP to induce lactic fermentation and generate a probiotic product with additional functional characteristics, which might be used as a protein food supplement suitable for human consumption or as an ingredient in the development of other functional foods (98).

The massive role of A. kunkeei in preserving BB has been demonstrated in previous studies that have recognized BB's stability to the influences caused by nectar, honey, bee secretions, and BP natural properties (7). The fermentation protocol developed during this study emulates the natural BB fermentation process, generating a stable and safe fermented product with increased digestibility and bioavailability of nutrients due to the use of specific strains of lactobacilli as A. kunkeei (45).

Confectionary foods contain large numbers of titanium dioxide nanoparticles (TiO2 NPs), proving to be at a high risk of developing diet-induced metabolism syndrome (MetS). In this aspect, LGG-oral supplementation to MetS mice ameliorates TiO2 NPs-induced inflammation and metabolic abnormality caused by fructose. In LGG-supplemented mice, the gut dysbiosis was improved, and the inflammation-related bacteria (Clostridia, Desulfovibrionaceae, and Proteobacteria) were decreased; thus LGG acted as a defensive system against TiO2 NPs-induced severe inflammation damage (220).

Urinary symptoms are common in people suffering from neurogenic lower urinary tract dysfunction (NLUTD). As there are no non-prescription treatment methods (221), assessed the safety and tolerability of LGG in adults and children with NLUTD due to spinal cord injury or disease. At the end of the 18-month study, two doses of self-installed intravesical LGG were safe and well-tolerated among the tested individuals. This aspect was further confirmed by LGG installation in asymptomatic patients with neuropathic bladder. No adverse effects were reported after installation (222).

Impact Assessment of Current BB Production

Because collecting BB from the hive is time-consuming and harmful, it's marketing for human use is hampered. On the other hand, pollen removal through traps is handy for beekeepers and harmless to the hive (17). Harvesting BB can be a profitable option, but it is rarely applied in apiaries due to high costs and time-consuming. However, it is an auspicious opportunity, thanks to the rising consumer awareness of functional foods (i.e., food with positive and pro-health effects on human individuals, primarily due to the naturally present bioactive substances) (223).

The process of acquiring the final product can technically be entirely automated. However, in conventional apiaries, which are the most common in EU nations and have an average of 21 hives per beekeeper, it is not economically justified (224). A 3-year study began in the spring of 2015 to establish the volume of BB production in honeybee colonies and analyze the economic effects of such output. Each year, 28 honeybee colonies participated in the experiment, separated into four groups. Each group tried alternative brood nest configurations or frame positioning against the hive entrance for collected BB. All costs, including labor, were associated with the BB production process. Depending on the group, it gathered between 0.51 and 1.23 kg of BB from a single colony. The average yield was 0.7 kg, while the apiary as a whole produced 20 kg of BB each year.

Moreover, the annual expenditures associated with BB manufacturing were 679.5 EUR, whereas the projected sales gain was 1110 EUR. As a result, the income was 430.5 EUR or 21.5 EUR per kilogram of collected BB. The most significant expenses were associated with labor, which might be a factor restricting the growth of BB manufacturing in apiaries (49).

Challenges and Opportunities for Developing Improved Fermented Functional Foods

Fermented foods and beverages are global edible products of significant scientific, social, and economic importance. A fermented nutritive matrix represents one-third of all foods produced for human consumption (225). Furthermore, the attention of prestigious international institutions, such as the World Health Organization (WHO) and the Food and Agriculture Organization (FAO) of the United Nations (UN), to the importance of microbiological risks assessment and of traditional fermented food and beverages contribute to testify to the relevance of the discussed topic (226). The intake of fermented foods and drinks is typically connected with beneficial properties (227). This increased nutritional and functional quality would serve as an additional reason to establish a risk management plan to minimize contamination (225). The establishment of a multi-strain starter culture based on genotypic and technical characterization of microbial diversity connected with natural food fermentation to increase the “unique characteristics” defined as fermented attributes (228). It is critical to differentiate between the risk associated with microbial genera/species that are not generally present in fermented matrices and the risks associated with spontaneous fermentation. Pathogens are classified as the first class, whereas mycotoxins, ethyl carbamate, and biogenic amines are second. Because the same species includes both technologically beneficial and harmful strains, the second category is more subtle (229). Controlling the microbiology of fermented foods may be an essential step toward harnessing the biotechnological potential of strains developed via spontaneous fermentation (230). Recent economic, productive, and social trends have rediscovered the possibility of spontaneous fermentation in increasing the uniqueness of fermented goods.

Future Perspectives and Conclusions

Over the last decade, aspects of artificial food additives and consumer demands for balanced and healthy diets may have accelerated research on natural products, such as BB. As a result, researchers are working to uncover its nutritional importance and health-promoting effects. A comparison of expenses and earnings generated by the production of BB, obtained in nature in the hive, showed that the financial impact could sometimes be less satisfactory. Labor costs can be a problem that restricts the development of this beekeeping product, so a biotechnological approach may be a better way to improve the market's presence. In the case of fermented BP consumed by humans, the chosen starters improved the bioavailability and digestibility of nutrients and bioactive compounds naturally found in BP.

Moreover, from an economic standpoint, the biotechnological development of BB may be an alternative and efficient way to diversify the beekeeping activity, which is gradually susceptible to frequent problems and increasing beekeepers' incomes. Further research into the classification of aromatic compounds, the flavor impact of organic acid-aroma interactions, chosen LAB starters and fermentation protocols, as well as consumer demands, will lead to noteworthy advancements in the flavor of fermented bee products for a promising market. Additionally, the need for value-added products with numerous health properties, macro-, and micronutrients, important bio-elements, probiotics, and vitamins is gaining popularity.

Funding

This work was supported by the National Research, Development, and Innovations Programme for 2015-2020-PNII, developed with the support of UEFISCDI PN-III-P1-1.1-TE-2019-1748 (TE 184/2020), and the publication was supported by funds from the National Research Development Projects to finance excellence (PFE)-14/2022-2024 granted by the Romanian Ministry of Research and Innovation.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Statements

Author contributions

DGB and MC-C: conceptualization, methodology, and writing—original draft preparation. RM: validation, supervision, and writing—review & editing. DCV: funding acquisition, supervision, and writing—review and editing. All authors read and approved the manuscript.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Summary

Keywords

bee bread, lactic acid bacteria, fermented product, food supplement, a probiotic product

Citation

Barta DG, Cornea-Cipcigan M, Margaoan R and Vodnar DC (2022) Biotechnological Processes Simulating the Natural Fermentation Process of Bee Bread and Therapeutic Properties—An Overview. Front. Nutr. 9:871896. doi: 10.3389/fnut.2022.871896

Received

08 February 2022

Accepted

21 March 2022

Published

27 April 2022

Volume

9 - 2022

Edited by

Sandrina A. Heleno, Polytechnic Institute of Bragança (IPB), Portugal

Reviewed by

Elena Sorrentino, University of Molise, Italy; Filomena Nazzaro, National Research Council (CNR), Italy

Updates

Copyright

*Correspondence: Dan Cristian Vodnar Rodica Margaoan

†These authors have contributed equally to this work and share first authorship

This article was submitted to Food Chemistry, a section of the journal Frontiers in Nutrition

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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