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Review

Fermented Mare Milk and Its Microorganisms for Human Consumption and Health

by
Francesca Martuzzi
1,
Piero Franceschi
2,* and
Paolo Formaggioni
2
1
Department of Food and Drug Science, University of Parma, Via delle Scienze, 43124 Parma, Italy
2
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
*
Author to whom correspondence should be addressed.
Foods 2024, 13(3), 493; https://doi.org/10.3390/foods13030493
Submission received: 22 December 2023 / Revised: 26 January 2024 / Accepted: 31 January 2024 / Published: 3 February 2024
(This article belongs to the Special Issue New Insights into Milk and Dairy Products: Quality and Sustainability)
Browse Figure
Versions Notes

Abstract

:
Mare milk is consumed by approximatively 30 million people in the world. In countries in Asia and East Europe, mare milk is mainly consumed as source of fermented products, called koumiss, airag or chigee, alcoholic beverages obtained by means of a culture of bacteria and lactose-fermenting yeasts. Recent research concerning mare milk and its derivatives deals mainly with their potential employment for human health. Studies about the isolation and characterization of Lactobacillus spp. and yeasts from koumiss have been aimed at assessing the potential functional properties of these micro-organisms and to find their employment for the industrial processing of mare milk. The aim of this literature review is to summarize recent research about microorganisms in fermented mare milk products and their potential functional properties.

1. Introduction

Mare milk is a fundamental aliment for the people of the Central Asia steppes. It is consumed also in Europe, in particular in Hungary and in the Netherlands. It was estimated that nearly 30 million people consume it regularly [1]. Besides the use of this milk as a source of valuable nutrients, since ancient times it has been considered as a sort of medication for its health-promoting characteristics in the regions of the former USSR and Western Asia. It has been extolled for its many healing properties in some papers, but clinical studies effectively proving its positive effects are scarce [2,3,4].
In the recent years of the 20th century, in Europe, studies about equine milk have mostly dealt with protein compounds—the identification and characterization of caseins and whey proteins (see reviews by Martuzzi and Doreau [5] and by Uniacke-Lowe et al. [6])—and to a lesser extent other milk components [7], with some interest for its possible use as a substitute for bovine milk for children with intolerance or allergy [8,9,10]. In particular, whereas most studies in the world have dealt with horse’s milk, in Italy interest is more focused on donkey’s milk, traditionally used in the past for orphaned or abandoned children, when formulas were not yet available [11,12,13]. An extensive review about equid milk (horse and donkey) composition and tolerability in human nutrition was published by Salimei and Fantuz [14].
Whereas milk from most domestic ruminants is widely consumed as cheese after processing, cheesemaking from equine milk is not possible, mainly due to its scarce casein content. No curd is formed on the addition of rennet; under acidic conditions only a weak coagulum appears, manufactured especially in the Netherlands for the production of yoghurt-type products with the addition of fruit extract [6,15].
Equine milk is rich in its lactose content, and since most populations in Asia present lactose malabsorption [16,17], in this part of the world mare milk undergoes fermentation before consumption, and the resulting products are called koumiss [18] or qymyz (Eastern Europe, former Soviet Union Republics) [19,20], airag (Mongolia) [21,22] or chigee (Inner Mongolia and Xinjiang, China) [23,24], which are alcoholic beverages obtained by means of a mixed culture of bacteria and yeasts. During fermentation, the lactose is converted into lactic acid, ethanol and carbon dioxide, and the milk becomes an accessible nutriment for lactose-intolerant people. In addition, acidifying fermentation is the oldest method of milk conservation [25]. Organic residue analysis, using δ13C and deuterium isotope (δD) values of fatty acids, has revealed processing of mare milk products in ancient potsherds dating back to about 3500 B.C.E., found in Northern Kazakhstan [26]. Kazakhstan is still at present the nation with the largest koumiss production in the world [27,28].
Nevertheless, until recently, little was known about the numerous studies carried out into koumiss in the former USSR, where this product has been consumed for centuries, due to the difficult accessibility of these papers, written in the Russian language. This lack of knowledge was overcome by a review by Kondybayev et al. [19] which surveyed many studies of soviet authors.
The reader can find a lot of data about the composition of and variability in mare milk in the aforementioned reviews. Recent research about mare milk deals mainly with its derivatives, in particular fermented milk products and the potential probiotic properties of the microorganisms living within [29].
The aim of this review is to present recent advancements in fermented mare milk research, with a particular focus on its potential functional properties and effects on human health.
The following search strategy for the review was adopted: to conduct the literature search and include relevant references, we scanned the databases Medline, PubMed, ScienceDirect, and CNKI for Chinese papers. For the search in the online databases, we used the following keywords: (koumiss), (kumiss), (airag), and (mare milk). In addition, since mare milk is one of the topics of our research group, we had collected most of the considered papers during the preceding years and therefore they were present in our collection of studies already. Regarding the recent literature, at the first screening process, we scanned titles and abstracts of the yielded articles or book chapters. Afterwards, if the publication did not show any signs of incoherence, we screened the full text and searched the sections “similar articles” or “related documents” according to the diverse databases. Three papers were excluded as they studied several traditional fermented foods obtained by the milk of diverse species (such as yak, cow, and camel) together, and it was not possible to select data regarding the specific product obtained by mare milk.

2. Microorganisms in Fermented Mare Milk Products

The most abundant microorganisms naturally present in milk can be classified in order of their possible roles (i) microorganisms involved in dairy fermentation (e.g., Lactococcus, Lactobacillus, Streptococcus, Propionibacterium and fungal populations); (ii) involved in spoilage (e.g., Pseudomonas, Clostridium, Bacillus, and other spore-forming bacteria); (iii) involved in food disease (e.g., Listeria, Salmonella, Escherichia coli, Campylobacter and mycotoxin-producing fungi); and (iv) involved in promoting health (e.g., lactobacilli and bifidobacteria) [30]. Human milk from healthy women contains up to 109 microbes L−1 [31]. These organisms come mainly from the nipple and surrounding skin [31]. Ward et al. studied the complexity of the bacterial community in human milk, finding over 360 prokaryotic genera, mainly belonging to the phyla of Proteobacteria (65%) and Firmicutes (34%), and the genera of Pseudomonas (61.1%), Staphylococcus (33.4%) and Streptococcus (0.5%) [32]. Microbial colonization during the first few weeks of life in the gastrointestinal tracts of humans and farm animals is remarkably similar. Bifidobacteria are the predominant lactic acid bacteria (LAB) in infants, whereas lactobacilli are the primary LAB in the tract of new-born foals [33].
The microbial composition of raw mare milk, like that in other similarly less common milk types, has not been studied in depth: nevertheless, it is known to be widely variable, depending on many factors, such as the breed, season, and region [34]. However, many studies regarding the microbiological composition of fermented mare milk are available.
Koumiss, airag and chigee are the main products obtained through mare milk fermentation. Mare milk fermentation is due to lactic acid bacteria (LAB) and yeast interaction. LAB are mainly involved in milk acidification, whereas the yeasts partly modify its titratable acidity due to the production of acidic compounds, such as acetic acid. On the other hand, yeasts produce ethanol that is very important for determining the properties and increasing the stability of fermented milk [21,35].
The interaction between LAB and yeast can be complex and has to be studied in more depth; however, different theories have been suggested. Positive relationships between the two types of microorganisms can occur because lactic acid bacteria are responsible for the lowering of the pH due to the secretion of organic acids, allowing the yeast population to become competitive in the immediate environment, followed by yeast fermentation [36]. Sudun et al. observed a positive correlation regarding glucose and galactose produced by the lactase of LAB, and consumed by yeast for their growth [21].
In addition, the interaction between the two types of microorganisms is reflected in the product. Regarding its safety, the combination of the acidic condition, saturated with carbon dioxide and alcohol, is inhibitory to many spoilage bacteria [36]. Regarding quality, yeast proteolytic and lypolitic metabolism can stimulate LAB growth and play an important role in aroma development [37].
Koumiss is a lactic acid–alcoholic beverage produced traditionally by the fermentation of mare’s milk by indigenous organisms or by a starter culture. First, lactic acid is formed, and then alcoholic fermentation of the residual sugar content occurs. Koumiss generally contains about 2% alcohol, 0.5–1.5% lactic acid, 2–4% sugar and 2% fat (Kerr and McHale [38]; quoted by Danova et al. [39]). The alcohol has been known to reach a level of 3.5% and, depending on its content, in Russia there is a differentiation between weak koumiss with 0.7–1% ethanol, normal koumiss with 1–1.75% and strong koumiss with 1.75–2.5% [40].
According to Danova et al., another distinction exists: depending on the lactic acid content, three types of koumiss can be distinguished: ‘strong’, ‘moderate’ and ‘light’ koumiss. Lactic acid bacteria (Lactobacillus delbrueckii subsp. bulgaricus and Lactobacillus rhamnosus) acidifying the milk to pH 3.6–3.3 and converting about 80–90% of lactose into lactic acid produce ‘strong’ koumiss. In ‘moderate’ koumiss, other Lactobacillus (Lb.) bacteria (Lb. acidophilus, Lb. plantarum, Lb. casei, and Lb. fermentum) with lesser acidification properties and a conversion ratio of about 50% lower the pH to 4.5–3.9 at the end of the process. ‘Light’ koumiss, produced by Streptococcus thermophilus and Str. cremoris, is slightly acidic (pH 4.5–5.0) [39]. According to several authors, “moderate” koumiss presents a sweet–sour taste and a yeasty odour and is the most appreciated [39,41]. It was demonstrated that acetaldehyde is the most important substance determining aroma in koumiss and the suitable range of its content is 78.25−257.07 μL L−1 [42,43].
Airag, which is called also tsege in Inner Mongolia, contains Lb. helveticus, Lactobacillus fermentum, and Saccharomyces cerevisiae [44]. The traditional technique of production in a cowhide vessel of this product in Mongolia was included in 2019 in the Representative List of the Intangible Cultural Heritage of Humanity.
In an attempt to identify which properties are related to the most appreciated sensory characteristics of airag, it was found that only its electrical conductivity has a statistically significant relationship with its taste score: higher electrical conductivity values are associated with lower taste scores; even though the mean pH values were not different, calcium and phosphorus concentrations were lower in the airag samples rated with high scores, taking in account 51 different airag samples exhibited in a competition in Mongolia [22].
Many mesophilic LAB and yeasts have been detected in koumiss. According to tradition, fresh milk is inoculated with a small quantity of already-fermented milk as natural starter, but many other different substances could be used as well [19]. The use of raw milk and natural undefined starter cultures causes a strong variability in the microbial composition. Many authors have observed a wide variability in species and strains [27,45]. It has been evidenced that milk derivatives from each family have their particular microbiota [46].
A few studies have investigated the relationship between koumiss microbiota and the production of volatile flavour compounds or organic acids, and their effects on taste. Despite the wide variability of microbes and yeasts involved, a “core” microbiota was identified, represented by four bacterial genera (Lactobacillus, Acetobacter, Lactococcus, and Pseudomonas), and two yeast genera (Kazachstania and Candida), and it was observed that notwithstanding the differences depending on the region and production techniques, the basic volatile flavours in traditional koumiss are similar [45,47].
Since this product is administered in hospitals, in the former USSR guidelines were started in 1969 to regulate its production according to a standard: in this case, a pure culture should be used as starter (with L. bulgaricus and S. lactis, which have antibacterial properties). Regardless, according to soviet authors, afterwards old koumiss was commonly used as starter [19].
Like in other fermented dairy products, the genus Lactobacillus (Lb.) plays an important role in affecting the aroma, texture, and acidity of koumiss. Recently, much interest has been focused on the usage and safety of these strains, as the properties of probiotics are more known and appreciated. For this reason, special attention has been paid to the accurate identification and characterization of a potential probiotic microorganism to use as the selected starter. Regarding probiotics selection, it is necessary to assess properties affecting specific health benefits, such as the modulation of the immune system, survival and persistence in the host, and proven safety and stability. Regarding LAB identification, the comparison of molecular sequences, mainly 16S rRNA-encoding genes, is commonly used even if it is not always effective to identify genetically close species. It was stated that if the 16S rRNA gene sequence identity shared by two microorganism is lower than 97%, at the genomic level they are considered to belong to different species. If the shared identity values are higher than 97% or the sequences are identical, the organisms appear closely related and total DNA–DNA hybridization data or more discriminative analyses are needed for species identification [48].
Regarding LAB characterization, several techniques can be used, from the more traditional phenotypic approach like whole-cell protein and cell wall composition analysis, and other morphological, physiological, and biochemical analyses [49] to more recent molecular and genomic characterization [50]. Methods for characterizing probiotics were recommended in the advisory report of the Working Group “8651 Probiotics” of the Belgian Superior Health Council (SHC) by Huys et al. [51].

2.1. Lactic Acid Bacteria

Studies regarding the isolation, identification, and characterization of lactic acid bacteria (LAB) in fermented mare milk have been carried out mainly by Asian research groups in the regions where this production has been a tradition for centuries, namely, Mongolia and Inner Mongolia and the autonomic Region of China.
These kinds of studies began with a notable frequency in the early years of the 2000s, and are still actively going on, probably with the intent to find the most suitable combination of LAB for the industrial production of horse milk derivatives.
The main LAB genera and species characterized in recent years are summarized in Table 1. Different methodological approaches were used, also in consideration of the advent of new increasingly powerful methods.
Most of the knowledge of LAB in fermented mare milk has been gained through culture-dependent methods, and the subsequent isolation and identification of these microorganisms. The number of isolated and identified strains is strongly variable in the manuscripts, depending on the aim of each piece of research, varying from 2 for koumiss [63] to 258 for chigee [52]. In Table 1, the results of 18 studies carried out with several methods are shown. Briefly summarizing the species identified with these approaches, it is possible to conclude that 45 different species have been identified, but the most common were Lb. plantarum, identified in 12 of the 18 studies; Lb. casei, identified in 10 studies; Lb. helveticus, found in 9 studies; Lb. kefiranofaciens, found in 7 studies; and Lb. paracasei, found in 6 studies (Table 1). Less frequent were the species Lb. fermentum, Lb. kefiri, and Leuconostoc mesenteroides, found in 5 studies; Lb. diolivorans, found in 4 studies; Lc. lactis subsp. lactis, Enterococcus faecium and S. thermophilus, found in 3 studies; and Lactococcus lactis subsp. cremoris, Lb. acidophilus, Lb. coryniformis, Lb. curvatus, Lb. farciminis, Lb. pentosus, Weissella kandleri and Lb. delbrueckii, identified in two studies (Table 1). The other species were found only one time (Table 1).
Recently, considerable efforts have been made to develop more rapid, culture-independent methods. One study was carried out with this approach and in particular by means of denaturing gradient gel electrophoresis (DGGE) [64]. The authors concluded that the biodiversity of ten samples of collected koumiss, made by nomadic families in one region of China, was high. In particular, the dominant species identified by DGGE were Lb. acidophilus, Lb. helveticus, Lb. fermentum, and Lb. kefiranofaciens. Less frequent were Enterococcus faecalis, Lactococcus lactis, Lb. paracasei, Lb. kitasatonis, and Lb. kefiri. Leuconostoc mesenteroides, Streptococcus thermophilus, Lb. buchneri, and Lb. jensenii were occasionally found [64].
Comparing all the data, it is possible to highlight that the only species found with high frequency using the two approaches was Lb. helveticus, a thermophilic, homofermentative, proteolytic species traditionally used both for the manufacture of Swiss-type cheeses and long-ripened Italian cheeses or in the production of fermented beverages in north Europe [65]. However, due to its high proteolytic activity, Lb. helveticus is very effective in the production of bioactive peptides such as angiotensin-converting enzyme (ACE) inhibitory peptides [66]. The strain heterogeneity of this species isolated from koumiss was evidenced by an intra-species genotypic and phenotypic characterization [67].
The other three dominant species for DGGE have also been isolated and identified by culture-dependent research, but surprisingly, the species isolated in 12 of the 15 culture-dependent studies, Lb. plantarum, has not been recognized in the samples of koumiss analysed with DGGE. Even if this aspect suggests some considerations about the advantages and disadvantages of both approaches, other culture-independent research should be conducted to discuss this comparison.
More recently, new next-generation sequencing technologies have been applied to explore genes implicated in microbial metabolism: shotgun metagenomic analyses provide taxonomic and functional data about complex microbial communities, with culture-independent methods [68]. In particular, a study investigated bacterial function during several phases of koumiss fermentation by metagenomics. It was observed that the microbial composition of koumiss changes mostly in the first 36 h of fermentation, and the predominant species is Lb. helveticus [68].
The predominance of this species was observed in another study, which analysed the metagenomes of 23 koumiss samples collected in several regions of China: sequences representing 216 different species were found and Lb. helveticus comprised 78.9% of the total sequences in koumiss, followed by Lactobacillus kefiranofaciens (6.0%) and Lactococcus lactis (4.2%) [69].
Analysing the bacterial metagenomes of koumiss from Mongolia and Inner Mongolia by the single-cell genomics technique allowed the identification of rare bacterial species never detected in koumiss before, such as Lb. otakiensis and Streptococcus macedonicus, both present in other fermented foods or dairy products [70].
Since new genetic methods provide more precise metrics to classify bacteria, the genus Lactobacillus was recently re-evaluated and new genus and species names were recently adopted [71]. Therefore, in the more recent studies, LAB names are in accordance with the new taxonomy rules (see note for Table 1) [61,62].
Technological properties and probiotic aptitudes have been considered for strains isolated from koumiss and airag. In particular, probiotic aptitude, such as bile tolerance and other preliminary tests, has been evaluated for strains of Lb. casei, Lb. helveticus and Lb. plantarum [56] and for different strains of Lb. acidophilus [72]. Different technological properties have been investigated in several species. The fermentation properties of four Lb. casei strains were studied by Xu et al. [73], and in Lb. rhamnosus and Lb. paracasei by Zuo et al. [74]. The latter authors were also able to verify the performances of those strains in cheese and yogurt manufacturing [74]. The effects of distinctive proteolytic activity on casein degradation have been studied for six Lb. helveticus strains isolated from home-made airag samples [75].
In airag collected in Mongolia, Watanabe et al. isolated two novel microorganisms belonging to the genus Bifidobacterium. Their phenotypic and genotypic characteristics demonstrated that the strains can be considered a single Bifidobacterium species never observed before, and its proposed name was Bifidobacterium mongoliense sp. nov. [76].

2.2. Yeasts

The yeasts in koumiss are the main aspect responsible for the presence of ethanol and carbon dioxide. The amount of ethanol in koumiss is slightly higher than in kefir because the amount of lactose in mare milk is higher than in cow milk [9]. However, not only are lactose-fermenting yeast species, belonging to the genus Kluyveromices (K.), mainly K. marxianus and K. fragilis, and Candida (C.) kefir, common in koumiss, but also non-lactose-fermenting species, such as Saccharomyces unisporus (S.), are found [77]. A study which explored the correlation between microflora and volatile flavour substances demonstrated a correlation with the genus Candida and ethanol, considered the most important alcohol flavour compound [47].
In the manufacture of koumiss, a considerable amount of free amino acids are produced by yeasts, ranging around 470–490 mg kg−1 [40,43].
Few studies are available about the yeast composition of fermented mare milk. To the authors’ knowledge, six studies have been conducted on koumiss [24,37,47,60,77,78], one on chigee [79], one on airag [46] and one on hurunge, which is a the starter culture for fermented traditional dairy products such as chigee [54]. To briefly summarise, 11 genera and 24 species were isolated but only non-lactose-fermenting species S. cerevisiae was isolated in all the studies, and lactose-fermenting K. marxianus was found in seven of the nine studies. Lactose-fermenting species C. krusei and non-lactose-fermenting yeasts such as Pichia (P.) membranaefaciens, C. kefyr, C. valida, Dekkera anomala, Kazachstania unispora, and Issatchenkia orientalis were found in two studies, and the other species, C. buinensis, C. pararugosa, Geotrichum sp., K. wickerham, P. cactophila, P. deserticola, P. fermentans, P. manshurica, P. membranaefaciens, S. dairensis, S. servazzii, S. unisporus, Trichosporum asaii, Penicillium carneum, Clavispora lusitaniae and Torulaspora delbrueckii, were found in only one study (Table 2).
Interestingly, a polyphasic approach was used in a complete and complex study, using a culture-independent and also culture-dependent method, to study yeasts present in koumiss sampled from three representative regions of China, Mongolia, Xin Jiang and Qing Hai [37]. Using 96 samples, 655 isolates and also DGGE, the authors were able to show how the yeast community in koumiss is complex and rich in different species [37].
Another research article showed that the prevalent yeast found at high altitudes in Kazakhstan was S. unisporus, which was different from lower zones, where lactose-fermenting yeasts are more common, mostly belonging to the Kluyveromyces genus [77]. The authors hypothesized that a high altitude could affect the LAB population composition during the preparation of koumiss, with a selection of LAB not metabolizing galactose, causing therefore an enrichment of this sugar and the prevalence of C. buinensis, which ferments galactose but not lactose, and of the Saccharomyces genus compared with Kluyveromyces [77].
In traditional koumiss from Inner Mongolia, Guo et al. identified 57 fungal species, also, among them the genera Penicillium, Cladosporium and Aspergillus were detected in all samples. These are filamentous fungi considered the cause of spoilage in dairy products. Therefore, the production process of traditional koumiss requires sanitation measures and a better control of environmental hygiene [60].
In conclusion, it could be observed that in comparison with fermented dairy products from other species, in mare milk the higher lactose content (6–7% compared to 4–5% of cow, yak, goat and camel’s milk) usually determines the prevalence of lactose-fermenting yeast strains, but this trait could be modified by the altitude effect, which, when operating in a selection of LAB, can increase the galactose content, causing therefore the major presence of galactose-fermenting yeast strains.

3. Potential Functional Properties of Microorganisms in Fermented Mare Milk for Human Consumption and Health

Probiotics are defined as ‘‘living microorganisms, which upon ingestion in certain numbers, exert health effects beyond inherent basic nutrition’’ [80]. Probiotic cultures in nutritional supplements, pharmaceuticals and functional foods are mainly constituted by LAB belonging to the genera Lactobacillus and Bifidobacterium. The proteolytic systems of LAB are exploited for the production of bioactive peptides in fermented dairy products, because milk proteins need to be hydrolysed into peptides to exert some effect [81].
It is believed, but not yet definitively proven, that probiotics compete with undesirable microorganisms and can inhibit their growth in the intestine. Therefore, probiotics must survive through the stomach and upper intestine, tolerating the acidic and protease-rich environment and the action of bile salts, and need to be numerous enough to exert their effect in the colon [82]. According to several authors, a concentration of at least 106 c.f.u.g−1 of viable and active microorganisms is necessary in the product throughout its specified shelf life [83].
Many recent studies regard koumiss as a source of microorganisms with potential probiotic activities, and trials have been carried out to provide data about these properties [84].
In Figure 1, a synthesis of the main potential functional properties of microorganisms in fermented mare milk is shown.
A Chinese research group has been particularly active in this research field: during the years 2004–2009, 240 Lactobacillus strains were isolated from koumiss and investigated. Among these strains, a novel strain, called Lb. casei Zhang, was screened out and its potential probiotic properties were investigated in many trials, reported initially in national and successively in international journals. According to the combined analyses of a phylogenetic dendrogram and partial sequences of 16S rDNA, this strain was classified as Lb. casei subsp. casei [1,63,73]. The complete genome sequence of Lb. casei Zhang was successively investigated by a whole-genome shotgun strategy, and comparative analyses with other Lb strains evidenced a richer enzyme abundance, which could explain some of its favourable properties in terms of its use of different sugar sources and behaviour in the host environment [85]. Moreover, proteins expressed by Lb. casei Zhang in the exponential and stationary phases were identified and characterized, mainly as stress response proteins, in a proteomics study, evidencing their role in its adaptation to the environment [56]. Therefore, the survival capacity of this strain was initially tested: yoghurt samples fermented with Lb. casei Zhang showed a similar viable count (1.0 × 109 c.f.u. mL−1) as other samples inoculated with selected commercial probiotics after 28 d of refrigerated storage [83]. Similar results were obtained by Zhou et al. [1].
In the following years, the properties of this strain were investigated with in vivo experiments on rats and on humans; some of the results of these studies, showing positive effects on several health problems, are listed by He et al. in the introduction of their paper, concerning the effects of the long-term administration of Lb. casei Zhang on human gut microbiota (see next section) [86].
Particular emphasis about the potential properties of the microorganisms from koumiss in the prevention of chronic diseases is shown in a recent review by Xue et al. [84].
The following sections consider the results of studies aimed at assessing several properties of LAB strains from koumiss as potential probiotics.

3.1. Survival of LAB through the Human Digestive Tract and Cholesterol Reduction Effect

The survival capacity of Lactobacillus strains isolated from mare milk products through the human digestive tract is considered in several studies. In particular, survival under acidic conditions, similar to gastric juice, and resistance to bile salts have been investigated. Bile salts have antibacterial action but do not damage resident microflora. The physiological concentration of human bile ranges from 0.3 to 0.5% (wt vol−1) [87]. It was recently observed that some Lactobacillus strains excrete bile salt hydrolase, an enzyme that catalyses the hydrolysis of conjugated bile salts. This action could reduce serum cholesterol levels, together with various other mechanisms [88]. According to Guo et al. [83], in vitro tests demonstrated Lb. casei Zhang’s tolerance to simulated gastric and intestinal juices and in the presence of 0.3% bile salts. The molecular mechanisms involved in the adaptation of the bacterial cells under bile salt stress were investigated considering the growth and protein expression patterns of Lb. casei Zhang with and without bile salts. It was observed that twenty-six proteins were differentially expressed using two-dimensional gel electrophoresis. These proteins were identified by peptide mass fingerprinting [87].
In the empty human stomach, pH is lower than 3.0 [89]. The tolerance to a low pH of Lb. casei strains from home-made koumiss was investigated considering the expression of H+-ATPase, which is supposed to play an important role in the maintenance of physiological cytoplasmic pH, by means of a mechanism controlling the H+ concentration through the cell membrane. The survival of the Lb. casei Zhang strain in artificial digestion was observed and the expression of H+-ATPase, detected by the reverse transcription–polymerase chain reaction method, increased accordingly to the pH lowering, in accordance with what has been observed regarding other microorganisms. Therefore, it seems that the acid tolerance of Lb. casei could have some relationship with the H+-ATPase gene [89].
It is assumed that an LAB strain could tolerate gastric acid if, after exposure to pH 3.0 with 0.04% pepsin for 3 h, it is detected at over 7 log c.f.u. mL−1. Lb. plantarum 05AM23 isolated from Mongolian airag showed good bile acid tolerance (97% viable colonies), viability in low pH (8.1 log c.f.u. mL−1) and a high capacity of adhesion on Caco-2 cells (72.0 × 103 c.f.u. mL−1) [58].
There is an increasing interest in the research of natural compounds in food with effective abilities to decrease serum cholesterol concentrations, especially in countries where coronary heart disease is the principal cause of death, such as China. It has been known for many years that several Lactobacillus strains exert this property by means of different mechanisms, mostly studied by in vitro experiments [90,91]. According to some studies, which were published in Chinese national journals, several Lb strains have been observed in diverse acidic conditions (pH 3.0 and pH 4.0) and bile salt concentrations (e.g., in media containing 0.6%, 0.4% and 0.3% bile salts) in vitro: some of them showed sufficient tolerance and the cholesterol removed from the growth media was around 50% [72,92]. These properties were confirmed for the strain Lb. helveticus MG2-1, which, moreover, showed a good adhesiveness to Caco-2 cells, an important property to be assessed as a potential probiotic [93].
Evaluation of the cholesterol-reducing effects of LAB has been performed in vivo as well by several studies; e.g., the acid and bile tolerance and cholesterol reduction activity of Lb. fermentum SM-7, isolated from home-made koumiss in Xinjiang, China, were observed in vitro and in vivo in artificially induced hyperlipidaemial ICR mice. The cholesterol reduction rate in vitro observed in this study was 66.8%, and a significant decrease in serum total cholesterol was also observed in vivo, in the groups treated with high and low doses of Lb. fermentum SM-7 [90].
Nevertheless, observing the behaviour of three different strains, screened out from 68 Lb strains from koumiss produced in the same area mentioned above, it was concluded that the results in vitro were not consistent with what was observed in vivo in mice, and a precise explanation of the mechanisms of the hypocholesterolemic action of LAB is seemingly quite difficult, also because different strains show different cholesterol-lowering actions [91].
Regarding this issue, Zhong et al. [94], carrying out one of the aforementioned numerous studies conducted in China into Lb. casei Zhang, investigated in rats how the expression of several genes involved in fatty acid metabolic processes was differently affected by the administration of Lb. casei Zhang, therefore providing some information about the molecular mechanism of the cholesterol-lowering effect exerted by this bacterium [94].
Another quite recent study demonstrated, by metagenomic and metatranscriptomic profiling, that in the human gut, the gene expression of Lb. casei Zhang was very different from what was observed in vitro. Individual variabilities in the intestinal microbiomes among the healthy volunteers were higher than those induced by the probiotic ingestion. Therefore, interactions between probiotics and resident microbiota are a further step in the study of the effects of these promising strains [95]. Moreover, gut microbiota vary along the different life phases, and the differences in the represented phyla in the elderly gut, in comparison with those of younger adults, are well known.
In relation to this issue, He et al. studied the effects of the long-term administration of this strain on the gut microbiota of healthy adults, divided into two groups according to age. Modulating and stabilizing effects of Lb. casei Zhang on gut microbiota were observed in both groups, but with age-dependent differences. According to some indices, the long-time consumption of Lb. casei Zhang changed the microbiota composition in the older adult group, making the microbial community more similar to that of younger people [86].
Another study [96] considered thirteen patients, diagnosed with severe hyperlipidaemia, who consumed 750 g of koumiss every day for 60 days. The composition of the koumiss microbiota and the effects of koumiss consumption on patients’ faecal sample microbiota were investigated by the Pacific Biosciences single-molecule, real-time sequencing technology (SMRT), a state-of-the-art tool which permits the profiling of microbiota. This technique produces long-read sequences, allowing high-resolution taxonomic identification by sequencing the full-length 16S rRNA gene. After 60 days of koumiss consumption, HDL cholesterol values increased significantly, and hyperlipidaemia-associated symptom scores decreased significantly. These results were attributed to the bacterial population of koumiss and its metabolites. According to several indices, participants’ faecal samples reflected a significant increase in the abundance and diversity of gut microbiota. This was the first study which observed the relationship between koumiss consumption and gut microbiota at the species level in hyperlipidaemic patients [96].

3.2. Antioxidative Effect

The action of binding toxins is among the favourable properties attributed to fermented mare milk and its microorganisms, operating like natural chelators to remove the pollutants from the body. This property and the antioxidative effect of koumiss and its LAB strains have been investigated in a rat model: the strain Lb. acidophilus MG2-1, heat-killed or living, extracted from koumiss, was orally administrated for 28 days and an antioxidative effect was observed in serum and in rat liver tissue homogenate. In rats fed living Lb. acidophilus MG2-1, the activity of superoxide dismutase (SOD) and of glutathione peroxidase (GSH-PX) significantly increased in liver tissue and in serum, while the content of malondialdehyde in serum and liver tissue homogenate decreased [97].
The oxidative stress effects and damage induced in the rats, which received 25 ppm mercury (HgCL2) in drinking water for 6 weeks, was alleviated in the rat group fed fermented mare’s milk prepared with starter cultures of Streptococcus thermophilus, Lb. acidophilus and Bifidobacterium bifidum and supplemented with fibre (6% extract of Dandelium root, Taraxacum officinalis). Nevertheless, the mechanism of action was not explained, and the authors declared that it was still under investigation [98].

3.3. Immuno-Modulation Function

Some studies have been performed to assess a potential immuno-modulating function of probiotic species isolated from koumiss [99]. Among them, five studies considered the effects of live or heat-killed probiotic Lb. casei Zhang administration on healthy or liver-injured rats or mice.
For example, varying doses of Lb. casei Zhang, isolated from koumiss, were orally administered to healthy BALB/c mice and positive effects on several parameters of immune response were observed, such as the increased production of interferon-γ (IFN-γ) and decreasing levels of tumour necrosis factor-α (TNF-α). Moreover, interleukin-2 (IL-2) and IL-2 receptor gene transcription increased, and the production of secretory Immunoglobulin A (sIgA) was enhanced. It was concluded that the dose-dependent administration of living Lb. casei Zhang influences immune responses in mice and could be taken into account for the probiotic’s use for humans as well [100,101].
The research group of Wang et al. also observed several protective actions of Lb. casei Zhang in rats with induced liver injury, and demonstrated a positive effect of Lb. casei Zhang upon pro-inflammatory cytokine and hepatic inflammation in rats with acute liver failure [102,103,104].

3.4. ACE Inhibitory Activity

Angiotensin I-converting enzyme (ACE; dipeptidyl carboxypeptidase, EC3.4.15.1) is a multifunctional enzyme which plays a role in the conversion of angiotensin-I to angiotensin-II and in the degradation of bradykinin, causing increased peripheral blood pressure [105]. It has been demonstrated that the proteolytic systems of several LAB produce bioactive peptides exerting an inhibitory activity on the ACE, with a hypotensive effect in the rat model and in clinical studies. In particular, Lb. helveticus cell-wall proteases can activate antihypertensive tripeptides from the hydrolysis of casein. This capacity is strain-dependent and the effect can be exerted by milk fermented by these strains [106,107].
In koumiss collected in the Xilingole region in Inner Mongolia, four ACE-inhibitory peptides, called PI, PK, PM and PP, were identified and analysed: PI was derived from mare milk β-casein (f213–241), and the peptide PK was derived from Actinobacillus succinogenes, which had not been previously found in koumiss, whereas the other two peptides did not correspond to any known milk peptides or proteins. The in vitro studies demonstrated the thermal stability of the four peptides and a high ACE-inhibitory activity, maintained under various pH and ACE treatments [18].
Another antihypertensive property of some LAB strains is the production of gamma-aminobutyric acid (GABA), a neurotransmitter which is effective in lowering blood pressure. Sixteen Lactobacillus strains isolated from koumiss collected in Xinjiang, China, demonstrated high ACE inhibitory activity, and among them two strains produced GABA: the Lb.–ND01 strain, which showed 99% homology to Lb. helveticus according to the sequence of 16S rDNA, possesses both properties, and after further studies regarding its resistance to acidic conditions and its production of free amino nitrogen, it was considered interesting for its possible employment in probiotic dairy products [106].

3.5. Antibacterial Activity of LAB and Yeasts

The growth of pathogenic bacteria could be inhibited by particular toxins, produced by LAB or yeasts present in several fermented foods.
Many LAB produce a high diversity of bacteriocins, proteinaceous or peptidic toxins categorized in several ways, which kill or inhibit the growth of similar bacterial strains. Antimicrobial activity was observed in as many as 53 LAB strains isolated from airag. Class II bacteriocins of LAB are considered to have a large potential for food preservation, due to their anti-Listeria activity and physicochemical properties [108,109]. Bacteriocins produced by LAB isolated from fermented mare’s milk were characterized and tested for their antibacterial effect against yeasts and spoilage bacteria. It was concluded that bacteriocins A5-11A and B, isolated from Enterococcus durans issued from airag, could be used in food preservation due to their anti-pathogenic-bacteria activity, whereas yeasts were not inhibited [110]. Another interesting bacteriocin was identified in airag from the strain Leuc. mesenteroides 406, which showed a narrow antimicrobial spectrum but is effective against Listeria monocytogenes and Clostridium botulinum [108].
Recently, it was demonstrated that a bacteriocin produced by Lb. plantarum NMD-17, isolated from koumiss from Inner Mongolia, has a broad spectrum against Gram-positive and Gram-negative bacteria [111], and a bacteriocin produced by Lb. rhamnosus 1.0320, also extracted from koumiss, besides its wide-spectrum action, is particularly active against E. coli UB1005 [112].
Whereas the antimicrobial properties of LAB are widely documented, less is known about similar properties in yeasts extracted from koumiss. Particular yeast strains produce toxins called mycocins: compounds extracted by Saccharomyces cerevisiae from koumiss exerted antibacterial activity on pathogenic Escherichia coli in in vitro tests [113], and crude extracts of mycocins from K. marxianus showed efficacy against Escherichia coli in mice in vivo as well [114].

4. Conclusions

Research about mare’s milk and derivatives for human consumption is very active especially in Asian countries. The identification and characterization of LAB and yeasts have been performed in many studies: a wide variability of species and strains have been observed. Even if fermented mare’s milk is a very ancient product, a lot of research is still needed: whereas the yeast flora are quite well known, a wide range of scientific activity remains to be carried out to clarify the interdependency and cooperation of its various microbial components, because in fermented mare milk products really complex population structures of yeasts, white moulds, lactic acid bacteria and acetic acid bacteria are present and interacting.
Studies are actively going on to assess the properties of different strains for their optimal employment in the production, at an industrial scale, of koumiss, in particular.
Trials in vitro and in vivo are confirming some of the beneficial effects and healing properties traditionally attributed to mare milk derivatives: some probiotic properties of LAB in fermented milk have been demonstrated, but more necessary experimental steps must be performed to clearly assess their efficacy.

Author Contributions

Conceptualisation, F.M. and P.F. (Piero Franceschi); methodology, F.M., P.F. (Piero Franceschi) and P.F. (Paolo Formaggioni); software, P.F. (Piero Franceschi), F.M. and P.F. (Paolo Formaggioni); formal analysis, F.M. and P.F. (Piero Franceschi); investigation, F.M., P.F. (Piero Franceschi) and P.F. (Paolo Formaggioni); resources, F.M., P.F. (Paolo Formaggioni) and P.F. (Piero Franceschi); data curation, F.M. and P.F. (Piero Franceschi); writing—original draft preparation, F.M., P.F. (Piero Franceschi) and P.F. (Paolo Formaggioni); writing—review and editing, F.M., P.F. (Piero Franceschi) and P.F. (Paolo Formaggioni); visualisation, F.M. and P.F. (Paolo Formaggioni); supervision, F.M. and P.F. (Piero Franceschi); project administration, F.M., P.F. (Piero Franceschi) and P.F. (Paolo Formaggioni). All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Acknowledgments

The authors wish to thank Monica Gatti for her advice and valuable references.

Conflicts of Interest

The authors declare that there are no conflicts of interest in this research article.

References

  1. Zhou, Q.; Wang, J.; Guo, Z.; Yan, L.; Zhang, Q.; Chen, W.; Liu, X.M.; Zhang, H. Fermentation characteristics and transit tolerance of Lactobacillus casei Zhang in reconstituted mare milk during storage. Int. J. Dairy Technol. 2009, 62, 249–254. [Google Scholar] [CrossRef]
  2. Foekel, C.; Schubert, R.; Kaatz, M.; Schmidt, I.; Bauer, A.; Hipler, U.C.; Vogelsang, H.; Rabe, K.; Jahreis, G. Dietetic effects of oral intervention with mare’s milk on the Severity Scoring of Atopic Dermatitis on faecal microbiota and on immunological parameters in patients with atopic dermatitis. Int. J. Food Sci. Nutr. 2009, 60, 41–52. [Google Scholar] [CrossRef]
  3. Schubert, R.; Kahle, C.; Kauf, E.; Hofmann, J.; Hobert, I.; Gruhn, B.; Häfer, R.; Vogelsang, H.; Jahreis, G. Dietetic efficacy of mare’s milk for patients with chronic inflammatory bowel diseases—Clinical study. Ernährung 2009, 33, 314–321. [Google Scholar]
  4. Kushugulova, A.; Kozhakhemtov, S.; Sattybayeva, R.; Nurgozhina, A.; Ziyat, A.; Yadav, H.; Marotta, F. Mare’s milk as a prospective functional product. Funct. Foods Health Dis. 2018, 8, 537–543. [Google Scholar] [CrossRef]
  5. Martuzzi, F.; Doreau, M. Mare milk composition: Recent findings about protein fractions and mineral content. In Nutrition and Feeding of the Broodmare; Miraglia, N., Martin-Rosset, W., Eds.; EAAP Scientific Series; Wageningen Pers: Wageningen, The Netherlands, 2006; Volume 120, pp. 65–76. [Google Scholar]
  6. Uniacke-Lowe, T.; Huppertz, T.; Fox, P.F. Equine milk proteins: Chemistry, structure and nutritional significance. Int. Dairy J. 2010, 20, 609–629. [Google Scholar] [CrossRef]
  7. Doreau, M.; Martuzzi, F. Fat content and composition of mare’s milk. In Nutrition and Feeding of the Broodmare; Miraglia, N., Martin-Rosset, W., Eds.; EAAP Scientific Series; Wageningen Pers: Wageningen, The Netherlands, 2006; Volume 120, pp. 77–87. [Google Scholar]
  8. Curadi, M.C.; Giampietro, P.G.; Lucenti, P.; Orlandi, M. Use of mare milk in pediatric allergology. In Proceedings of the XIV Congress of Associazione Scientifica di Produzione Animale (ASPA), Firenze, Italy, 12–15 June 2001; pp. 647–649. [Google Scholar]
  9. Malacarne, M.; Martuzzi, F.; Summer, A.; Mariani, P. Nitrogen fractions and fat composition of mare milk: Some nutritional remarks with reference to woman and cow milk. Int. Dairy J. 2002, 12, 869–877. [Google Scholar] [CrossRef]
  10. Tidona, F.; Sekse, C.; Criscione, A.; Jacobsen, M.; Bordonaro, S.; Marletta, D.; Vegarud, G.E. Antimicrobial effect of donkeys’ milk digested in vitro with human gastrointestinal enzymes. Int. Dairy J. 2011, 21, 158–165. [Google Scholar] [CrossRef]
  11. Muraro, M.A.; Giampietro, P.G.; Galli, E. Soy formulas and nonbovine milk. Ann. Allergy Asthma Immunol. 2002, 89 (Suppl. S1), 97–101. [Google Scholar] [CrossRef]
  12. Monti, G.; Bertino, E.; Muratore, M.C.; Coscia, A.; Cresi, F.; Silvestro, L.; Fabris, C.; Fortunato, D.; Giuffrida, M.G.; Conti, A. Efficacy of donkey’s milk in treating highly problematic cow’s milk allergic children: An in vivo and in vitro study. Pediatr. Allergy Immunol. 2007, 18, 258–264. [Google Scholar] [CrossRef] [PubMed]
  13. La Torre, G.L.; Saitta, M.; Potortì, A.G.; Di Bella, G.; Dugo, G. High performance liquid chromatography coupled with atmospheric pressure ionization mass spectrometry for sensitive determination of bioactive amines in donkey milk. J. Chromatogr. A 2010, 1217, 5215–5224. [Google Scholar] [CrossRef] [PubMed]
  14. Salimei, E.; Fantuz, F. Equid milk for human consumption. Int. Dairy J. 2012, 24, 130–142. [Google Scholar] [CrossRef]
  15. Bornaz, S.; Guizani, N.; Sammari, J.; Allouch, W.; Sahli, A.; Attia, H. Physicochemical properties of fermented Arabian mares’ milk. Int. Dairy J. 2010, 20, 500–505. [Google Scholar] [CrossRef]
  16. Wang, Y.G.; Yan, Y.S.; Xu, J.J.; Du, R.F.; Flatz, S.D.; Kühnau, W.; Flatz, G. Prevalence of primary adult lactose malabsorption in three populations of northern China. Hum. Genet. 1984, 67, 103–106. [Google Scholar]
  17. Itan, Y.; Powell, A.; Beaumont, M.A.; Burger, J.; Thomas, M.G. The origins of lactase persistence in Europe. PLoS Comput. Biol. 2009, 5, e1000491. [Google Scholar] [CrossRef]
  18. Chen, Y.; Wang, Z.; Chen, X.; Liu, Y.; Zhang, H.; Sun, T. Identification of angiotensin I-converting enzyme inhibitory peptides from koumiss, a traditional fermented mare’s milk. J. Dairy Sci. 2010, 93, 884–892. [Google Scholar] [CrossRef]
  19. Kondybayev, A.; Loiseau, G.; Achir, N.; Mestres, C.; Konuspayeva, G. Fermented mare milk product (Qymyz, Koumiss). Int. Dairy J. 2021, 119, 105065. [Google Scholar] [CrossRef]
  20. Konuspayeva, G.; Baubekova, A.; Akhmetsadykova, S.; Faye, B. Traditional dairy fermented products in Central Asia. Int. Dairy J. 2023, 137, 105514. [Google Scholar] [CrossRef]
  21. Sudun, W.; Arakawa, K.; Miyamoto, M.; Miyamoto, T. Interaction between lactic acid bacteria and yeasts in airag, an alcoholic fermented milk. Anim. Sci. J. 2013, 84, 66–74. [Google Scholar] [CrossRef] [PubMed]
  22. Tsuchiya, R.; Kawai, T.; Bat-Oyun, T.; Shinoda, M.; Morinaga, Y. Electrical conductivity, pH, minerals, and sensory evaluation of airag (Fermented Mare’s Milk). Foods 2020, 9, 333. [Google Scholar] [CrossRef] [PubMed]
  23. An, Y.; Adachi, Y.; Ogawa, Y. Classification of lactic acid bacteria isolated from chigee and mare milk collected in Inner Mongolia. Anim. Sci. J. 2004, 75, 245–252. [Google Scholar] [CrossRef]
  24. Ni, H.J.; Bao, H.H.; Sun, T.S.; Chen, X.; Zhang, H.P. Identification and biodiversity of yeasts isolated from koumiss in Xinjiang of China. Wei Sheng Wu Xue Bao (Acta Microbiol. Sin.) 2007, 47, 578–582. [Google Scholar]
  25. Alais, C. Scienza del Latte, 4th ed.; Tecniche Nuove: Milano, Italy, 2000; p. 717. [Google Scholar]
  26. Outram, A.K.; Stear, N.A.; Bendrey, R.; Olsen, S.; Kasparov, A.; Zaibert, V.; Thorpe, N.; Evershed, R.P. The earliest horse harnessing and milking. Science 2009, 323, 1332–1335. [Google Scholar] [CrossRef] [PubMed]
  27. Dugan, F.M. Dregs of our forgotten ancestors. Fermentative microorganism in the prehistory of Europe, the steppes and Indo-Iranian Asia and their contemporary use in traditional and probiotic beverages. Fungi 2009, 24, 16–39. [Google Scholar]
  28. Siddiqui, S.A.; Salman, S.H.M.; Redha, A.A.; Zannou, O.; Chabi, I.B.; Oussou, K.F.; Bhowmik, S.; Nirmal, N.P.; Maqsood, S. Physicochemical and nutritional properties of different non-bovine milk and dairy products: A review. Int. Dairy J. 2023, 148, 105790. [Google Scholar] [CrossRef]
  29. Martuzzi, F.; Vaccari Simonini, F. Advances on equine milk and derivatives for human consumption. In Proceedings of the 61st Annual Meeting of the European Association of Animal Production, Heraclion, Greece, 23–27 August 2010; Wageningen Academic Publisher: Wageningen, The Netherlands, 2010; p. 40. [Google Scholar]
  30. Quigley, L.; O’Sullivan, O.; Stanton, C.; Beresford, T.P.; Ross, R.P.; Fitzgerald, G.F.; Cotter, P.D. The complex microbiota of raw milk. FEMS Microbiol. Rev. 2013, 37, 664–698. [Google Scholar] [CrossRef] [PubMed]
  31. Mackie, R.I.; Abdelghani, S.; Gaskins, H.R. Developmental microbial ecology of the neonatal gastrointestinal tract. Am. J. Clin. Nutr. 1999, 69, 1035S–1045S. [Google Scholar] [CrossRef] [PubMed]
  32. Ward, T.L.; Hosid, S.; Ioshikhes, I.; Altosaar, I. Human milk metagenome: A functional capacity analysis. BMC Microbiol. 2013, 13, 116. [Google Scholar] [CrossRef] [PubMed]
  33. Lawrence, L.A.; Lawrence, T.J. Development of the equine gastrointestinal tract. In Advances in Equine Nutrition IV; Pagan, J.D., Ed.; Nottingham University Press—Kentucky Equine Research: Versailles, Kentucky, USA, 2008; pp. 173–184. [Google Scholar]
  34. Kondybayev, A.; Konuspayeva, G.; Strub, C.; Loiseau, G.; Mestres, C.; Grabulos, J.; Manzano, M.; Akhmetsadykova, S.; Achir, N. Growth and metabolism of Lacticaseibacillus casei and Lactobacillus kefiri isolated from qymyz, a traditional fermented central Asian beverage. Fermentation 2022, 8, 367. [Google Scholar] [CrossRef]
  35. Guo, L.; Xu, W.; Li, C.; Ya, M.; Guo, Y.; Qian, J.; Zhu, J. Production technology, nutritional, and microbiological investigation of traditionally fermented mare milk (Chigee) from Xilin Gol in China. Food Sci. Nutr. 2020, 1, 257–264. [Google Scholar] [CrossRef]
  36. Viljoen, B. Yeast ecological interactions. Yeast-yeast, yeast-bacteria, yeast-fungi interactions and yeasts as biocontrol agents. In Yeasts in Food and Beverages; Querol, A., Fleet, G., Eds.; Springer: Berlin, Germany, 2006; pp. 83–110. [Google Scholar]
  37. Mu, Z.; Yang, X.; Yuan, H. Detection and identification of wild yeast in Koumiss. Food Microbiol. 2012, 31, 301–308. [Google Scholar] [CrossRef]
  38. Kerr, T.J.; McHale, B.B. Applications in General Microbiology: A Laboratory Manual, 6th ed.; Hunter Textbooks: Winston-Salem, NC, USA, 2001; p. 398. [Google Scholar]
  39. Danova, S.; Petrov, K.; Pavlov, P.; Petrova, P. Isolation and characterization of Lactobacillus strains involved in koumiss fermentation. Int. J. Dairy Technol. 2005, 58, 100–105. [Google Scholar] [CrossRef]
  40. Seiler, H. A review: Yeasts in kefir and koumiss. Milchwissenschaft 2003, 58, 392–396. [Google Scholar]
  41. Lozovich, S. Medical Uses of Whole and Fermented mare Milk in Russia. Cult. Dairy Prod. J. 1995, 30, 18–21. [Google Scholar]
  42. Zhang, L. Studies on orthogonal test of blend fermenting of three phases of intermediate culture of mare’s milk and flavour evaluation of koumiss. China Dairy Ind. 1990, 18, 246–251. [Google Scholar]
  43. Di Cagno, R.; Tamborrino, A.; Gallo, G.; Leone, C.; de Angelis, M.; Faccia, M.; Amirante, P.; Gobbetti, M. Uses of mare’s milk in manufacture of fermented milks. Int. Dairy J. 2004, 14, 767–775. [Google Scholar] [CrossRef]
  44. Akuzawa, R.; Miura, T.; Surono, I.S. Fermented Milks | Asian Fermented Milks. In Encyclopedia of Dairy Sciences, 2nd ed.; Fuquay, J.W., Fox, P.F., McSweeney, P.L.H., Eds.; Academic Press: San Diego, CA, USA, 2011; Volume 2, pp. 507–511. [Google Scholar]
  45. Tang, H.; Ma, H.; Hou, Q.; Li, W.; Xu, H.; Liu, W.; Sun, Z.; Haobisi, H.; Menghe, B. Profiling of koumiss microbiota and organic acids and their effects on koumiss taste. BMC Microbiol. 2020, 20, 85. [Google Scholar] [CrossRef] [PubMed]
  46. Uchida, K.; Hirata, M.; Motoshima, H.; Urashima, T.; Arai, I. Microbiota of ‘airag’, ‘tarag’ and other kinds of fermented dairy products from nomad in Mongolia. Anim. Sci. J. 2007, 78, 650–658. [Google Scholar] [CrossRef]
  47. Meng, Y.; Chen, X.; Sun, Z.; Li, Y.; Chen, D.; Fang, S.; Chen, J. Exploring core microbiota responsible for the production of volatile flavor compounds during the traditional fermentation of Koumiss. LWT Food Sci. Technol. 2021, 135, 110049. [Google Scholar] [CrossRef]
  48. Felis, G.E.; Dellaglio, F. Taxonomy of Lactobacilli and Bifidobacteria. Curr. Issues Intest. Microbiol. 2007, 8, 44–61. [Google Scholar]
  49. Wang, J.; Chen, X.; Liu, W.; Yang, M.; Airidengcaicike; Zhang, H. Identification of Lactobacillus from koumiss by conventional and molecular methods. Eur. Food Res. Technol. 2008, 227, 1555–1561. [Google Scholar] [CrossRef]
  50. de Vos, W. Systems solutions by lactic acid bacteria: From paradigms to practice. Microb. Cell Factories 2011, 10 (Suppl. S1), S2. [Google Scholar] [CrossRef]
  51. Huys, G.; Botteldoorn, N.; Delvigne, F.; De Vuyst, L.; Heyndrickx, M.; Pot, B.; Dubois, J.J.; Daube, G. Microbial characterization of probiotics—Advisory report of the Working Group “8651 Probiotics” of the Belgian Superior Health Council (SHC). Mol. Nutr. Food Res. 2013, 57, 1479–1504. [Google Scholar] [CrossRef]
  52. Burentegusi; Miyamoto, T.; Nakamura, S.; Nozaka, Y.; Aoishi, A. Identification of Lactic Acid bacteria isolated from fermented mare’s milk “chigee” in Inner Mongolia China. Nihon Chikusan Gakkaiho 2002, 73, 441–448. [Google Scholar] [CrossRef]
  53. Menghe, B.; Wu, R.; Wang, L.; Yang, X.; Xu, J.; Dong, Y.; Sun, Z.; Zang, H. Isolation and identification of Lactobacillus from koumiss collected in Inner Mongolia and People’s Republic of Mongolia. China Dairy Ind. 2004, 32, 6–11. [Google Scholar]
  54. Shuangquan; Burentegusi; Yu, B.; Miyamoto, T. Microflora in traditional starter cultures for fermented milk hurunge from Inner Mongolia China. Anim. Sci. J. 2006, 77, 235–241. [Google Scholar] [CrossRef]
  55. Watanabe, K.; Fujimoto, J.; Sasamoto, M.; Dugersuren, J.; Tumursuh, T.; Demberel, S. Diversity of lactic acid bacteria and yeasts in Airag and Tarag traditionally fermented milk products of Mongolia. World J. Microbiol. Biotechnol. 2008, 24, 1313–1325. [Google Scholar] [CrossRef]
  56. Wu, R.; Wang, L.; Wang, J.; Li, H.; Menghe, B.; Wu, J.; Guo, M.; Zhang, H. Isolation and preliminary selection of lactobacilli from koumiss in Inner Mongolia. J. Basic Microbiol. 2009, 49, 318–326. [Google Scholar] [CrossRef] [PubMed]
  57. Sun, Z.H.; Liu, W.J.; Zhang, J.C.; Yu, J.; Gao, W.; Jiri, M.; Menghe, B.; Sun, T.S.; Zhang, H.P. Identification and characterization of the dominant lactic acid bacteria isolated from traditional fermented milk in Mongolia. Folia Microbiol. 2010, 55, 270–276. [Google Scholar] [CrossRef] [PubMed]
  58. Takeda, S.; Yamasaki, K.; Takeshita, M.; Kikuchi, Y.; Tsend-Ayush, C.; Dashnyam, B.; Ahhmed, A.M.; Kawahara, S.; Muguruma, M. The investigation of probiotic potential of lactic acid bacteria isolated from traditional Mongolian dairy products. Anim. Sci. J. 2011, 82, 571–579. [Google Scholar] [CrossRef]
  59. Choi, S. Characterization of airag collected in Ulaanbaatar, Mongolia with emphasis on isolated lactic acid bacteria. J. Anim. Sci. Technol. 2016, 58, 10. [Google Scholar] [CrossRef] [PubMed]
  60. Guo, L.; Ya, M.; Guo, Y.S.; Li, C.D.; Sun, J.P.; Zhu, J.J.; Qian, J.P. Study of bacterial and fungal community structures in traditional koumiss from Inner Mongolia. Int. Dairy Sci. 2019, 102, 1972–1984. [Google Scholar] [CrossRef]
  61. Sun, Y.; Yang, J.; Yuan, J.; Cong, L.; Dang, N.; Sun, T.; Liu, W. Evaluation of lactic acid bacterial communities in spontaneously-fermented dairy products from Tajikistan, Kyrgyzstan and Uzbekistan using culture-dependent and culture-independent methods. Int. Dairy J. 2022, 130, 105281. [Google Scholar] [CrossRef]
  62. Oleinikova, Y.; Alybayeva, A.; Daugaliyeva, S.; Alimzhanova, M.; Ashimuly, K.; Yermekbay, Z.; Khadzhibayeva, I.; Saubenova, M. Development of an antagonistic active beverage based on a starter including Acetobacter and assessment of its volatile profile. Int. Dairy J. 2024, 148, 105789. [Google Scholar] [CrossRef]
  63. Wu, R.; Zhang, H.; Menghe, B. 16S rDNA sequence and cluster analysis of Lb. casei Zhang and ZL12-1 isolated from koumiss. China Dairy Ind. 2005, 33, 4–9. [Google Scholar]
  64. Hao, Y.; Zhao, L.; Zhang, H.; Zhai, Z.; Huang, Y.; Liu, X.; Zhang, L. Identification of the bacterial biodiversity in koumiss by denaturing gradient gel electrophoresis and species-specific polymerase chain reaction. J. Dairy Sci. 2010, 93, 1926–1933. [Google Scholar] [CrossRef]
  65. Slattery, L.; O’Callaghan, J.; Fitzgerald, G.F.; Beresford, T.; Ross, R.P. Invited review: Lactobacillus helveticus—A thermophilic dairy starter related to gut bacteria. J. Dairy Sci. 2010, 93, 4435–4454. [Google Scholar] [CrossRef]
  66. Foster, L.M.; Tompkins, T.; Dahl, W. A comprehensive post-market review of studies on a probiotic product containing Lactobacillus helveticus R0052 and Lactobacillus rhamnosus R0011. Benef. Microbes 2011, 2, 319–334. [Google Scholar] [CrossRef] [PubMed]
  67. Sedláček, I.; Yansanjav, A.; Nováková, D.; Švec, P. Ribotyping of Lactobacillus helveticus from the Koumiss. In Proceedings of the Indonesian Society for Microbiology and Indonesian Society for Lactic Acid Bacteria, Sanur, Bali, Indonesia, 22 October 2015; p. 151. [Google Scholar]
  68. Wu, Y.; Li, Y.; Gesudu, Q.; Zhang, J.; Sun, Z.; Halatu, H.; Menghe, B.; Liu, W. Bacterial composition and function during fermentation of Mongolia koumiss. Food Sci. Nutr. 2021, 9, 4146–4155. [Google Scholar] [CrossRef] [PubMed]
  69. You, L.; Yang, C.; Jin, H.; Kwok, L.Y.; Sun, Z.; Zhang, H. Metagenomic features of traditional fermented milk products. Lwt 2022, 155, 112945. [Google Scholar] [CrossRef]
  70. Yao, G.; Yu, J.; Hou, Q.; Hiu, W.; Liu, W.; Kwok, L.; Menghe, B.; Sun, T.; Zhang, H.; Zhang, W. A perspective study of koumiss microbiome by metagenomics analysis based on single-cell amplification technique. Front. Microbiol. 2017, 8, 165. [Google Scholar] [CrossRef] [PubMed]
  71. Oberg, T.S.; McMahon, D.J.; Culumber, M.D.; McAuliffe, O.; Oberg, C.J. Invited review: Review of taxonomic changes in dairy-related lactobacilli. J. Dairy Sci. 2022, 105, 2750–2770. [Google Scholar] [CrossRef]
  72. Wang, L.; Xu, J.; Yun, Y.; Wu, R.; Menghe, B.; Zhang, H. Assessment of potential probiotic properties of Lactobacillus isolated from traditionally home-made koumiss in Mongolia. China Dairy Ind. 2005, 33, 4–10. [Google Scholar]
  73. Xu, J.; Yun, Y.; Zhang, W.; Shao, Y.; Menghe, B.; Zhang, H. Fermentation properties of 4 strains of Lactobacillus casei isolated from traditionally home-made koumiss in Inner Mongolia of China. China Dairy Ind. 2006, 34, 23–27. [Google Scholar]
  74. Zuo, F.L.; Feng, X.J.; Chen, L.L.; Chen, S.W. Identification and partial characterization of lactic acid bacteria isolated from traditional dairy products produced by herders in the western Tianshan Mountains of China. Lett. Appl. Microbiol. 2014, 59, 549–556. [Google Scholar] [CrossRef] [PubMed]
  75. Myamoto, M.; Ueno, H.M.; Watanabe, M.; Tatsuna, Y.; Seto, Y.; Miyamoto, T.; Nakajima, H. Distinctive proteolytic activity of cell envelope proteinase of Lactobacillus helveticus isolated from airag, a traditional Mongolian fermented mare’s milk. Int. J. Food Microbiol. 2015, 197, 65–71. [Google Scholar] [CrossRef]
  76. Watanabe, K.; Makino, H.; Sasamoto, M.; Kudo, Y.; Fujimoto, J.; Demberel, S. Bifidobacterium mongoliense sp. nov. from airag a traditional fermented mare’s milk product from Mongolia. Int. J. Syst. Evol. Microbiol. 2009, 59, 1535–1540. [Google Scholar] [CrossRef]
  77. Montanari, G.; Zambonelli, C.; Grazia, L.; Kamesheva, G.K.; Shigaeva, M.K. Saccharomyces unisporus as the principal alcoholic fermentation microorganism of traditional koumiss. J. Dairy Res. 1996, 63, 327–331. [Google Scholar] [CrossRef]
  78. Rakhmanova, A.; Wang, T.; Xing, G.; Ma, L.; Hong, Y.; Lu, Y.; Xin, L.; Xin, W.; Zhu, Q.; Lü, X. Isolation and identification of microorganisms in Kazakhstan koumiss and their application in preparing cow-milk koumiss. J. Dairy Sci. 2020, 104, 151–166. [Google Scholar] [CrossRef] [PubMed]
  79. Yu, B.; Miyamoto, T. Isolation and identification of yeasts in chigee, fermented mare’s milk, a traditional drink of Inner Mongolia, China. Milk Sci. 2010, 59, 231–236. [Google Scholar]
  80. Guarner, F.; Schaafsma, G.J. Probiotics. Int. J. Food Microbiol. 1998, 39, 237–238. [Google Scholar] [CrossRef]
  81. Choi, J.; Sabikhi, L.; Hassan, A.; Anand, S. Bioactive peptides in dairy products. Int. J. Dairy Technol. 2012, 65, 11–12. [Google Scholar] [CrossRef]
  82. Del Piano, M.; Morelli, L.; Strozzi, G.P.; Allesina, S.; Barba, M.; Deidda, F.; Lorenzini, P.; Ballare, M.; Montino, F.; Orsello, M.; et al. Probiotics, from research to consumer. Dig. Liver Dis. 2006, 38 (Suppl. S2), S248–S255. [Google Scholar] [CrossRef]
  83. Guo, Z.; Wang, J.; Yan, L.; Chen, W.; Zhang, H. In vitro comparison of probiotic properties of Lactobacillus casei Zhang a potential new probiotic with selected probiotic strains. LWT Food Sci. Technol. 2009, 42, 1640–1646. [Google Scholar] [CrossRef]
  84. Xue, W.; Yuan, X.; Ji, Z.; Li, H.; Yao, Y. Nutritional ingredients and prevention of chronic diseases by fermented koumiss: A comprehensive review. Front. Nutr. 2023, 10, 1270920. [Google Scholar] [CrossRef]
  85. Zhang, W.; Yu, D.; Sun, Z.; Wu, R.; Chen, X.; Chen, W.; Meng, H.; Hu, S.; Zhang, H. Complete genome sequence of Lactobacillus casei Zhang, a new probiotic strain isolated from traditional homemade koumiss in Inner Mongolia, China. J. Bacteriol. 2010, 192, 5268–5269. [Google Scholar] [CrossRef]
  86. He, Q.; Hou, Q.; Wang, Y.; Shen, L.; Sun, Z.; Zhang, H.; Liong, M.T.; Kwok, L.Y. Long-term administration of Lactobacillus casei Zhang stabilized gut microbiota of adults and reduced gut microbiota age index of older adults. J. Funct. Foods 2020, 64, 103682. [Google Scholar] [CrossRef]
  87. Wu, R.; Sun, Z.; Wu, J.; Meng, H.; Zhang, H. Effect of bile salts stress on protein synthesis of Lactobacillus casei Zhang revealed by 2-dimensional gel electrophoresis. J. Dairy Sci. 2010, 93, 3858–3868. [Google Scholar] [CrossRef]
  88. Liong, M.T.; Shah, N.P. Bile salt deconjugation ability, bile salt hydrolase activity and cholesterol co-precipitation ability of lactobacilli strains. Int. Dairy J. 2005, 15, 391–398. [Google Scholar] [CrossRef]
  89. Chen, X.; Sun, Z.; Meng, H.; Zhang, H. The acid tolerance association with expression of H+-ATPase in Lactobacillus casei. Int. J. Dairy Technol. 2009, 62, 272–276. [Google Scholar] [CrossRef]
  90. Pan, D.D.; Zeng, X.Q.; Yan, Y.T. Characterisation of Lactobacillus fermentum SM-7 isolated from koumiss, a potential probiotic bacterium with cholesterol-lowering effects. J. Sci. Food Agric. 2011, 91, 512–518. [Google Scholar] [CrossRef]
  91. Wang, J.; Zhang, H.; Chen, X.; Chen, Y.; Menghebilige; Bao, Q. Selection of potential probiotic lactobacilli for cholesterol-lowering properties and their effect on cholesterol metabolism in rats fed a high-lipid diet. J. Dairy Sci. 2012, 95, 1645–1654. [Google Scholar] [CrossRef]
  92. Zhang, H.; Menghe, B.; Wang, J.; Sung, T.; Xu, J.; Wang, L.; Yun, Y.; Wu, R. Assessment of potential probiotic properties of casei Zhang isolated from traditionally home-made koumiss in Mongolia. China Dairy Ind. 2006, 34, 4–10. [Google Scholar]
  93. Bilighe, M.; Liu, W.; Rina, W.; Wang, L.; Sun, T.; Wang, J.; Li, H.; Zhang, H. Evaluation of potential probiotics properties of the screened Lactobacilli isolated from home-made koumiss in Mongolia. Ann. Microbiol. 2009, 59, 493–498. [Google Scholar] [CrossRef]
  94. Zhong, Z.; Zhang, W.; Du, R.; Meng, H.; Zhang, H. Lactobacillus casei Zhang stimulates lipid metabolism in hypercholesterolemic rats by affecting gene expression in the liver. Eur. J. Lipid Sci. Technol. 2012, 114, 244–252. [Google Scholar] [CrossRef]
  95. Wang, J.; Zhang, J.; Liu, W.; Zhang, H.; Sun, Z. Metagenomic and metatranscriptomic profiling of Lactobacillus casei Zhang in the human gut. NPJ Biofilms Microbiomes 2021, 7, 55. [Google Scholar] [CrossRef] [PubMed]
  96. Hou, Q.; Li, C.; Liu, Y.; Li, W.; Chen, Y.; Siqinbateer; Bao, Y.; Saqila, W.; Zhang, H.; Menghe, B.; et al. Koumiss consumption modulates gut microbiota, increases plasma high density cholesterol, decreases immunoglobulin G and albumin. J. Funct. Foods 2019, 52, 469–478. [Google Scholar] [CrossRef]
  97. Menghe, B.; Zhou, Y.; Zhang, H.; Chen, Y.; Wang, L.; Xu, J.; Zhou, D. Antioxidative effect of Lactobacillus MG2-1 in koumiss. China Dairy Ind. 2005, 33, 21–24. [Google Scholar]
  98. Abdel-Salam, A.M.; Al-Dekheil, A.; Babkr, A.; Farahna, M.; Mousa, H.M. High fiber probiotic fermented mare’s milk reduces the toxic effects of mercury in rats. N. Am. J. Med. Sci. 2010, 2, 569–575. [Google Scholar] [CrossRef] [PubMed]
  99. Rong, J.; Zheng, H.; Liu, M.; Hu, X.; Wang, T.; Zhang, X.; Jin, F.; Wang, L. Probiotic and anti-inflammatory attributes of an isolate Lactobacillus helveticus NS8 from Mongolian fermented koumiss. BMC Microbiol. 2015, 15, 196. [Google Scholar] [CrossRef] [PubMed]
  100. Ya, T.; Su, Y.; Zhang, H. Effect of Lb. casei Zhang on koumiss on the production of cytokines in sera of mouse. Food Sci. 2006, 27, 488–491. [Google Scholar]
  101. Ya, T.; Zhang, Q.; Chu, F.; Merritt, J.; Menhe, B.; Sun, T.; Du, R.; Zhang, H. Immunological evaluation of Lactobacillus casei Zhang, a newly isolated strain from koumiss in Inner Mongolia, China. BMC Immunol. 2008, 9, 68. [Google Scholar] [CrossRef]
  102. Wang, Y.; Li, Y.; Xie, J.; Zhang, Y.; Wang, J.; Sun, X.; Zhang, H. Protective effects of probiotic Lactobacillus casei Zhang against endotoxin- and D-galactosamine-induced liver injury in rats via anti-oxidative and anti-inflammatory capacities. Int. Immunopharmacol. 2013, 15, 30–37. [Google Scholar] [CrossRef]
  103. Wang, Y.; Xie, J.; Wang, N.; Li, Y.; Sun, X.; Zhang, Y.; Zhang, H. Lactobacillus casei Zhang modulate cytokine and Toll-like receptor expression and beneficially regulate poly I:C-induced immune responses in RAW264.7 macrophages. Microbiol. Immunol. 2013, 57, 54–62. [Google Scholar] [CrossRef] [PubMed]
  104. Wang, Y.; Xie, J.; Li, Y.; Dong, S.; Liu, H.; Chen, J.; Wang, Y.; Zhao, S.; Zhang, Y.; Zhang, H. Probiotic Lactobacillus casei Zhang reduces pro-inflammatory cytokine production and hepatic inflammation in a rat model of acute liver failure. Eur. J. Nutr. 2016, 55, 821–831. [Google Scholar] [CrossRef] [PubMed]
  105. Özer, B.H.; Kirmaci, H.A. Functional milks and dairy beverages. Int. J. Dairy Technol. 2009, 63, 1–15. [Google Scholar]
  106. Sun, T.S.; Zhao, S.P.; Wang, H.K.; Cai, C.K.; Chen, Y.F.; Zhang, H.P. ACE-inibitory activity and gamma-aminobutyric acid content of fermented skim milk by Lactobacillus helveticus isolated from Xinjiang koumiss in China. Eur. Food Res. Technol. 2009, 228, 607–612. [Google Scholar] [CrossRef]
  107. Aquilanti, L.; Carbini, A.; Strappati, R.; Santarelli, S.; Silvestri, G.; Garofalo, C.; Clementi, F. Characterisation of Lactobacillus helveticus strains producing antihypertensive peptides by RAPD and inverse-PCR of IS elements. Benef. Microbes 2010, 1, 229–242. [Google Scholar] [CrossRef] [PubMed]
  108. Wulijideligen; Asahina, T.; Hara, K.; Arakawa, K.; Nakano, H.; Miyamoto, T. Production of bacteriocin by Leuconostoc mesenteroides 406 isolated from Mongolian fermented mare’s milk, airag. Anim. Sci. J. 2012, 83, 704–711. [Google Scholar] [CrossRef] [PubMed]
  109. Cui, Y.; Zhang, C.; Wang, C.; Lv, X.; Chen, Z.; Ding, Z.; Wang, Y.; Cui, H. A screening of class IIA bacteriocins produced by lactic acid bacteria isolated from fermented mare milk. J. Food Saf. 2013, 33, 433–439. [Google Scholar] [CrossRef]
  110. Batdorj, B.; Dalgalarrondo, M.; Choiset, Y.; Pedroche, J.; Métro, F.; Prévost, H.; Chobert, J.M.; Haertlé, T. Purification and characterization of two bacteriocins produced by lactic acid bacteria isolated from Mongolian airag. J. Appl. Microbiol. 2006, 101, 837–848. [Google Scholar] [CrossRef]
  111. Li-Li, M.; Xiang, D.J. Effect of LuxS/AI-2-mediated quorum sensing system on bacteriocin production of Lactobacillus plantarum NMD-17. Folia Microbiol. 2023, 68, 855–866. [Google Scholar]
  112. Xu, C.; Fu, Y.; Liu, F.; Liu, Z.; Ma, J.; Jiang, R.; Song, C.; Jiang, Z.; Hou, J. Purification and antimicrobial mechanism of a novel bacteriocin produced by Lactobacillus rhamnosus 1.0320. LWT Food Sci. Technol. 2021, 137, 110338. [Google Scholar] [CrossRef]
  113. Chen, Y.; Wang, C.; Hou, W.; Wang, X.; Gali, B.; Huasai, S.; Yang, S.; Wu, A.; Zhao, Y.; Wu, Y.; et al. Effects of antibacterial compounds produced by Saccharomyces cerevisiae in Koumiss on pathogenic Escherichia coli O8 and its cell surface characteristics. J. Integr. Agric. 2017, 16, 742–748. [Google Scholar] [CrossRef]
  114. Chen, Y.; Aorigele, C.; Wang, C.; Simujide, H.; Yang, S. Screening and extracting mycocin secreted by yeast isolated from koumiss and their antibacterial effect. J. Food Nutr. Res. 2015, 3, 52–56. [Google Scholar] [CrossRef]
Foods 13 00493 g001
Figure 1. Main potential functional properties of microorganisms in fermented mare milk for human consumption and health.
Figure 1. Main potential functional properties of microorganisms in fermented mare milk for human consumption and health.
Foods 13 00493 g001
Table 1. Main LAB species isolated in different studies.
Table 1. Main LAB species isolated in different studies.
12Main LAB SpeciesIdentification MethodProductSampling LocationReferences
10258Enterococcus faecium, Lactobacillus casei, Lactobacillus paracasei, Lactobacillus plantarum, Leuconostoc mesenteroides subsp. dextranicum, Streptococcus thermophilusGrowth condition, gas production, ammonia production, sugar fermentation, hippurate hydrolysischigeeInner MongoliaBurentegusi et al., 2002 [52]
14117Lactobacillus pentosus, Lactobacillus plantarum, Lactococcus lactis subsp. cremorisChemotyping, sugar fermentation, 16S rDNA sequencingchigeeInner Mongolia (Silinguole, Wulanchabu)An et al., 2004 [23]
530Lactobacillus acidophilus, Lactobacillus casei, Lactobacillus plantarumNot mentionedkoumissMongolia Menghe et al., 2004 [53]
2180Lactobacillus acidophilus, Lactobacillus casei, Lactobacillus coryniformis, Lactobacillus curvatus, Lactobacillus fermentum, Lactobacillus kefiranofaciens, Lactobacillus paracasei, Lactobacillus plantarum, Weissella kandleri, Weissella paramesenteroidesNot mentionedkoumissInner Mongolia Menghe et al., 2004 [53]
27Lactobacillus buchneri, Lactobacillus plantarum, Lactobacillus salivariusGrowth condition, gas production, ammonia production, sugar fermentation, hippurate hydrolysislyophilized koumissMongoliaDanova et al., 2005 [39]
366Lactobacillus acetotolerans, Lactobacillus casei, Lactobacillus homohiochii, Lactobacillus kefiranofaciens, Lactobacillus plantarum, Lactococcus lactis subsp. cremoris, Lactococcus lactis spp. lactis, Lactococcus raffinolactis, Leuconostoc mesenteroides subsp. cremorisGrowth condition, gas production, sugar fermentation hurungeInner MongoliaShungquan et al., 2006 [54]
3 Lactobacillus farciminis, Lactobacillus helveticus, Lactobacillus kefiri, Lactobacillus paracasei, Lactobacillus plantarumsugar fermentation, 16S rDNA sequencingairagMongoliaUchida et al., 2007 [46]
12Lactobacillus casei, Lactobacillus fermentum, Lactobacillus helveticus, Lactobacillus plantarumPhysiological tests and 16S rDNA sequencingkoumissChinaWang et al., 2008 [49]
22183Enterococcus faecium, Lactobacillus casei, Lactobacillus diolivorans, Lactobacillus farciminis, Lactobacillus helveticus, Lactobacillus hilgardii, Lactobacillus kefiranofaciens, Lactobacillus kefiri, Lactobacillus parafarranginis, Lactobacillus plantarum, Lactococcus lactis subsp. lactis, Lactococcus spp, Leuconostoc mesenteroides, Leuconostoc pseudomesenteroides, Streptococcus thermophilusRAPD-PCR multiplex and 16S rDNA sequencingairagMongoliaWatanabe et al., 2008 [55]
1648Lactobacillus casei, Lactobacillus coryniformis, Lactobacillus curvatus, Lactobacillus fermentum, Lactobacillus helveticus, Lactobacillus kefiranofaciens, Lactobacillus paracasei, Lactobacillus plantarum, Weissella kandleriGrowth condition, sugar fermentation, acid resistance, bile tolerance, 16S rDNA sequencingkoumissInner MongoliaWu et al., 2009 [56]
526Lactobacillus casei, Lactobacillus helveticus, Lactobacillus plantarumGrowth condition, gas production, ammonia production, sugar fermentation, lactic acid isomers, 16S rRNA sequencingairagMongolia Sun et al., 2010 [57]
77Lactobacillus delbrueckii subsp. Lactis, Lactobacillus fermentum, Lactobacillus helveticus, Lactobacillus kefiri, Lactobacillus pentosus, Lactobacillus plantarum, Lactobacillus sakei, Lactococcus lactis subsp. lactis, Leuconostoc citreum, Leuconostoc garlicum, Weissella confusa, Weissella viridescens16S rDNA sequencing, acid resistance, bile tolerance, adhesion to Caco2 cells, RAPD-PCRairagMongoliaTakeda et al., 2011 [58]
18Lactobacillus helveticus, Lactobacillus kefiranofaciens, Lactobacillus kefiri, Lactobacillus diolivorans, Enterococcus faecium, Enterococcus duransGrowth condition, sugar fermentation, acid resistance, bile tolerance
16S rDNA sequencing
BLAST search program		airagMongoliaChoi, 2016 [59]
11 Lactococcus lactis, Lactobacillus buchneri, Enterococcus italicus, Lactobacillus homohiochii; Lactobacillus hilgardii, Lactobacillus helveticus, Leuconostoc mesenteroides, Streptococcus parauberis16S rDNA sequencing
RAPD-PCR		koumissInner MongoliaGuo et al., 2019 [60]
15109Lacticaseibacillus paracasei, Limosilactobacillus fermentum, Lacticaseibacillus casei, Lentilactobacillus diolivorans, Lactobacillus helveticus, Schleiferilactobacillus harbinensis, Leuconostoc mesenteroides, Lactobacillus kefiranofaciens, Lentilactobacillus parabuchneri, Staphylococcus epidermidis 316S rRNA gene
sequencing,
PacBio SMRT sequencing technology		koumissKyrgyzstanSun et al., 2022 [61]
1526Lactobacillus helveticus, Lactobacillus delbrueckii, Lactobacillus kefiranofaciens, Lentilactobacillus diolivorans, Lentilactobacillus kefiri 316S rRNA gene
sequencing,
PacBio SMRT sequencing technology		koumissUzbekistanSun et al., 2022 [61]
14 Lacticaseibacillus paracasei, Lacticasebacillus casei, Lacticaseibacillus rhamnosus, Lactobacillus delbrueckii, Lactobacillus delbrueckii subsp. bulgaricus, Enterococcus faecalis, Streptococcus thermophilus 316S rRNA gene
sequencing		koumissKazakhstan (Almaty and Zhambyl regions)Oleinikova et al., 2024 [62]
1 Number of samples; 2 Number of isolates; 3 In the studies after 2022, a new nomenclature was adopted for LAB. See http://lactobacillus.ualberta.ca/, (accessed on 19 December 2023).
Table 2. Main yeast species isolated from fermented mare milk in different studies.
Table 2. Main yeast species isolated from fermented mare milk in different studies.
12Main Yeast Species Identification MethodProductSampling LocationReferences
94417Candida buinensis, Kluyveromyces marxianus, Saccharomyces cerevisiae, Saccharomyces unisporusmorphological and physiological testskoumissKazakhstanMontanari et al., 1996 [77]
3ndKulyveromyces wickerham, Issatchenkia orientalis, Saccharomyces cerevisiae, Saccharomyces dairensissugar fermentation, 26S rDNA sequencingairagMongoliaUchida et al., 2007 [46]
96655Candida pararugosa, Dekkera anomala, Geotrichum sp., Issatchenkia orientalis, Kazachstania unispora, Kluyveromyces marxianus, Pichia deserticola, Pichia fermentans, Pichia manshurica, Pichia membranaefaciens, Saccharomyces cerevisiae, Torulaspora delbrueckii5.8S-ITS rDNA and 26S rDNAkoumissMongolia, Xin Jiang, Qing HaiMu et al., 2012 [37]
5108Candida kefyr, Candida krusei, Candida valida, Kluyveromyces marxianus, Pichia cactophila, Saccharomyces cerevisiae, Saccharomyces servazziiAPI ID and physiological testschigeeMongoliaSudun et al., 2010 [79]
2887Kluyveromyces marxianus, Pichia membranaefaciens, Saccharomyces cerevisiae, Saccharomyces unisporusbiochemical tests, 26S rDNA sequencingkoumissXin JiangNi et al., 2007 [24]
330Candida kefyr, Candida krusei, Candida valida, Kluyveromyces marxianus, Saccharomyces cerevisiaeAPI ID and physiological testshurungeInner MongoliaShungquan et al., 2006 [54]
11 Kluyveromyces marxianus, Kazachstania unispora, Dekkera anomala, Saccharomyces cerevisiae, Trichosporum asaii, Penicillium carneum, Pichia membranaefaciens, Clavispora lusitaniaeITS rDNA, 16S rDNA sequencing koumissInner MongoliaGuo et al., 2019 [60]
1 Number of samples; 2 number of isolates.
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Martuzzi, F.; Franceschi, P.; Formaggioni, P. Fermented Mare Milk and Its Microorganisms for Human Consumption and Health. Foods 2024, 13, 493. https://doi.org/10.3390/foods13030493

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Martuzzi F, Franceschi P, Formaggioni P. Fermented Mare Milk and Its Microorganisms for Human Consumption and Health. Foods. 2024; 13(3):493. https://doi.org/10.3390/foods13030493

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Martuzzi, Francesca, Piero Franceschi, and Paolo Formaggioni. 2024. "Fermented Mare Milk and Its Microorganisms for Human Consumption and Health" Foods 13, no. 3: 493. https://doi.org/10.3390/foods13030493

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Martuzzi, F., Franceschi, P., & Formaggioni, P. (2024). Fermented Mare Milk and Its Microorganisms for Human Consumption and Health. Foods, 13(3), 493. https://doi.org/10.3390/foods13030493

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