1. Introduction
According to the current definition of probiotics, “live microorganisms that, when administered in adequate amounts, confer a health benefit on the host” [1], the health-related probiotic traits (e.g., neurological, immunological, endocrinological effects) must be associated to a specific strain and depend on its viability (Live microorganisms) and dose administered (Adequate amounts). Nevertheless, there are also general, so-called Core benefits shared across a genus (e.g., regulation of intestinal transit, competitive exclusion of pathogens, normalization of perturbed microbiota) and species (e.g., direct antagonism, vitamin synthesis, enzymatic activity) level [1].
Most of the scientific literature dealing with the probiotic role of Streptococcus thermophilus strains starts from the assumption of the health benefit of yogurt consumption [2,3,4,5]. Yogurt is defined as a fermented milk based on the association of S. thermophilus and Lactobacillus delbrueckii subsp. bulgaricus. For this reason, strains belonging to these species have often been involved in scientific studies aimed to demonstrate their probiotic traits [6,7,8,9,10]. Due to its safe use in food production over the years, S. thermophilus was granted ‘Generally Recognized as Safe’ (GRAS) status in the USA and the ‘Qualified Presumption of Safety’ (QPS) status in the European Union [11]. Apart from being a constituent of yogurt, which has officially recognized probiotic properties (prerequisite is to contain at least 108 colony-forming units (CFU)/g live microorganisms) [12], health benefits associated with S. thermophilus include production of antioxidant compounds, risk alleviation for some types of cancer, anti-inflammatory effects, antimutagenic effects and stimulation of the gut immune system [11,12,13,14]. The mitigating effect of yogurt consumption on lactose maldigestion has been officially recognized by European Food Safety Authority (EFSA) as a health claim [12]. In compliance with the Food and Agriculture Organization/World Health Organization (FAO/WHO) [15] modified definition of probiotics proposed by Hill and colleagues [1], such a beneficial effect has been attributed to the consumption of live bacterial cultures (S. thermophilus and L. delbrueckii subsp. bulgaricus) by several investigators [16,17,18]. For these reasons, probiotic products that include S. thermophilus strains are produced by multitudinous manufactures all over the world, such as those shown in Table 1. Most of the reported products (Table 1) are blends of several strains belonging to different species of lactic acid bacteria (e.g., Lactobacillus rhamnosus, L. acidophilus, L. bulgaricus, L. reuteri, Bifidobacterium bifidum, B. breve), Bacillus spp. (e.g., Bacillus coagulans, Bacillus subtilis, Bacillus clauslii) or the probiotic yeast Saccharomyces boulardii, with a CFU/dose ranging from 2 to 450 billion. Even though the market offers plenty of probiotic products containing S. thermophilus biomasses, the applicability of the term probiotic for this species itself is still questioned [19] due to its sensitivity to gastrointestinal tract (GIT) transit conditions.
The capability of surviving the GIT is generally considered a key feature of probiotic strains [1,20,21] and must be rigorously assessed. As highlighted by the FAO/WHO [15], typical in vitro tests such as resistance to gastric acidity and bile acid resistance require in vivo validation. One widespread way of doing so is the recovery of viable cells in fecal samples after oral administration, but are S. thermophilus strains easily recovered and correctly identified from stool samples? It is likely that other Streptococcus species, which inhabit the GIT, could be misidentified as S. thermophilus. Therefore, those taxonomic and ecological aspects should be considered in the intervention studies where S. thermophilus biomasses are administered, and in all the studies focused on the characterization of the human microbiota by metagenomics approaches. We review the scientific literature aimed to assess the ability of S. thermophilus strains to survive the human gastrointestinal tract by discussing the scientific validity of the methods applied for the bacterial recovery and identification from stool samples.
2. Existing Knowledge on S. thermophilus Survival in the Gastrointestinal Tract (GIT) Transit Conditions
Several studies attempted to assess the survival to the GIT of S. thermophilus by following different approaches, including culture-dependent and -independent methods or a combination of both [9,20,22,23,24,25,26,27,28] Mater et al. [20] quantified an orally administered streptomycin- and rifampicin-resistant S. thermophilus strain in fecal samples by standard plating, showing its substantial GIT survival in adults consuming yogurt. Similarly, Venturi et al. [22] described the recovery of S. thermophilus after oral administration of a multi-strain probiotic preparation by standard plating and also demonstrated the ability of S. thermophilus to survive the GIT. Subsequently, Brigidi et al. [23,24] and Mimura et al. [26] performed an identification and enumeration of S. thermophilus (combining both culture-dependent and -independent methods) from fecal samples after the administration of the same multi-strain probiotic product or yogurt, where they were able to recover significant numbers of S. thermophilus [23,24,26] as well as to demonstrate its colonization pattern [24]. By contrast, a study by del Campo and colleagues [25] dealing with the recovery of S. thermophilus from fecal samples using plating and polymerase chain reaction (PCR) assay provided negative results for the GIT survival of S. thermophilus in humans during a crossover study after daily yogurt consumption for two weeks. Afterwards, Elli et al. [27] again confirmed that S. thermophilus can be retrieved from human feces after yogurt consumption. Later on, García Hernández and colleagues [9] revealed the GIT survival and colonization pattern of S. thermophilus in some subjects by applying a direct viable count-fluorescence in situ hybridization (DVC-FISH) method to fecal samples.
Since those studies gave contradictory results on the ability of S. thermophilus strains to survive GIT conditions, some authors are still arguing if it should be considered as a probiotic, thus naming S. thermophilus a Transient probiotic [11]. It must be noted that those differences in GIT survival rates observed in different studies could have also been generated by the genetic and phenotypic diversity of S. thermophilus strains and/or by differences in fermentation process parameters adopted for the production of the biomasses or by differences in the absolute number of live cells administered [29].
3. Other Streptococci That Inhabit the Human GIT Could Interfere with the Correct Identification of S. thermophilus in Stool Samples
When attempting to recover Streptococcus thermophilus from fecal samples, one often neglected but critical aspect is its phylogenetic similarity with two other closely related species, namely S. salivarius and S. vestibularis [30]. These three species, which are genetically very similar [30], belong to the S. salivarius subgroup of viridians streptococci. S. salivarius and S. vestibularis are commensal bacteria of the oral and gastrointestinal cavities and of the genital tract [31]. The genetic similarity between S. salivarius and S. thermophilus was so high that the latter was previously classified as a subspecies of S. salivarius (S. salivarius subsp. thermophilus), and it obtained the status of species on its own only in 1991 [32]. S. thermophilus was described as an example of regressive evolution for the adaptation to a food environment [33]. S. thermophilus has lost all pathogenic traits throughout its evolution and adaptation to a well-defined, narrow ecological niche, the milk [33,34]. The regressive evolution of S. thermophilus was supported by the finding of a vestige of pathogenesis-related genes (10% of the total sequence), counterbalanced by the acquisition of relevant traits, like lactose and urea utilization, that have allowed the assembly of a new genome organization suitable for the colonization of the dairy niche [33,34]. The milk-driven speciation of S. thermophilus is also supported by the fact that this species is rarely, if ever, isolated outside the dairy environment [34]. However, the ability of S. thermophilus strains to utilize sucrose [34] with an efficiency comparable to that of lactose utilization led it to be hypothesized that this species could still be able to survive and grow in plant-based environments [35].
Sharing the same and being adapted to more natural and competitive niches, S. salivarius and S. vestibularis show a higher degree of physiological resemblance compared to S. thermophilus. For instance, S. salivarius and S. vestibularis have a higher capability to synthesize extracellular compounds (e.g., adhesins, exopolysaccharides) that are associated with bacterial fitness, resistance, biofilm formation and play a crucial role in cell adhesion, host colonization, or escape from the host immune system [30]. Moreover, the production of active urease, generally related to both health-associated and virulence factors is a common trait for all members of the S. salivarius group of streptococci [36]. The urease gene clusters of S. thermophilus and S. salivarius have similar organization (ureIABCDEFGMQO), with more complex transcriptional regulation in S. salivarius [37,38]. The well-known probiotic strain S. salivarius K12 is urease positive and can colonize the oral mucosae of humans regulating the innate immune responses of human epithelial cells [39]. In the case of the urease activity of S. thermophilus, Arioli and co-authors [40] observed that ammonia provided by urea hydrolysis boosted lactic acid production in both S. thermophilus and in L. delbrueckii, thus proposing urease activity as an altruistic cooperative trait. Regarding carbon sources utilization, S. salivarius can make use of a wider spectrum of compounds including glucose, fructose, galactose, lactose, as well as hydrolyze complex polymers such as starch or glucans [34]. On the other hand, S. thermophilus is well adapted to lactose as the main carbon source, hydrolyzing it to the glucose and galactose moieties. S. thermophilus is not able to metabolize galactose, expelling it outside the cell [34]. However, some galactose positive strains are reported [41]. Recently, multilocus sequence typing (MLST) and comparative genomic analysis gave novel insights into phylogeny, clearly separating these three species as well as indicating that S. thermophilus probably deviated from S. vestibularis [30,42].
Concerning the safety aspect, there is an overall consensus on the safety status of S. thermophilus species, whereas few reports highlighted that S. salivarius and S. vestibularis strains may cause mild to severe human infections [43,44].
Streptococcus spp. represent a notable part of the intestinal microbiota, with S. salivarius as one of the main species, indicating that these bacteria are actually able to colonize this ecological niche, rather than just being washed down with the flow of saliva [30,45,46,47]. S. salivarius has been recovered from fecal samples of infants, thus revealing that this species is one of the first inhabitants of the human gut [48,49]. Moreover, Delorme et al. [30] pointed out that previous metagenomic analysis of human feces revealed the presence of S. salivarius (formerly described as S. thermophilus due to a lack of appropriate genomic references) in more than 90% of the individuals tested [30,50].
In the light of these considerations, the answer to the question “Could S. thermophilus be misidentified with other streptococci that inhabit the human GIT?” is: yes, if the genomic similarities between these species are not considered (Figure 1).
4. The Methods Applied in the Reviewed Literature to Identify S. thermophilus Strains Were Not Selective at Species Level
We previously showed that some studies, dealing with the survival of S. thermophilus to the human GIT, based their assumptions on the recovery of S. thermophilus from the stool of human subjects after the consumption of yogurt or probiotic preparations [9,20,23,24,25,26,27,28]. Most of the studies indicated substantial [9,20,23,24,26,27,28] or no survival [25] of S. thermophilus strains after consumption of yogurt or probiotic products containing this species. What are the reasons for these contradictory conclusions? In most of the studies, the authors have paid little attention to the culture-dependent methods applied to recover live S. thermophilus strains from stool samples. The culture-dependent plating technique on specific selective media (e.g., ST agar, ST agar supplemented with the pH indicators bromocresole purple and bromocresole green, and the antibiotic nalidixic acid) used in some studies [22,23,24,28] was shown [23] to be ineffective for the selective identification and enumeration of S. thermophilus after the administration of a dairy or probiotic product, due to the inability to discriminate S. thermophilus from intestinal streptococci and enterococci as well as the phylogenetically closely related S. salivarius [23]. Therefore, the possibility to misidentify S. thermophilus with S. salivarius, the closest neighbor inhabiting the oral cavity, was likely underestimated. In addition, competitive inhibition by autochthonous bacteria from the gut, which may hinder the growth of S. thermophilus in the plate, cannot be excluded. Mater and colleagues [20] tried to selectively isolate S. thermophilus S85, which was streptomycin and rifampicin resistant, by adding the two antibiotics to the medium used for the recovery from fecal samples; however, the sensitivity of S. salivarius strains to streptomycin and rifampicin was not verified, nor was a molecular identification performed on the isolated colonies to confirm their taxonomy. Therefore, to date, the data about the accurate identification and retrieval of S. thermophilus in human subjects upon administration of yogurt or probiotic preparations are debatable.
4.1. Are the Data Supporting the GIT Survival of S. thermophilus Strains Solid and Unbiased Enough to Generate Scientific Consensus?
A list of molecular tools developed for the identification of S. thermophilus, together with the limitations detected for each of them, is shown in Table 2. Some of the tools listed in Table 2 have been developed aiming to identify S. thermophilus from fermented dairy products. These tools are based on species-specific polymerase chain reaction (PCR) primers targeting the 16S rDNA gene sequence [51,52]. However, the 16S rDNA gene sequence is not specific enough because of a high identity among those sequences in S. thermophilus, S. salivarius and S. vestibuilaris species (99.8% between S. thermophilus and S. salivarius; 99.6% between S. thermophilus and S. vestibularis) [53]. Lick and Teuber [54] designed species-specific oligonucleotide probes based on the 5′ region of the lacZ gene, but they showed both specific and non-specific hybridization signals among different strains of S. thermophilus and S. salivarius. Later on, species-specific PCR primers targeting the lacZ gene were developed [55]. This primer set was validated using several S. thermophilus strains and two S. salivarius strains as a reference [55]. However, subsequent studies demonstrated the inability of lacZ gene primers to correctly identify S. thermophilus strains [27].
In 1997, Tilsala-Timisjärvi and Alatossava [56] designed the ThI/ThII PCR species-specific primer set, based on the internal transcribed spacer between the 16S and the 23S rDNA genes for the detection of S. thermophilus in dairy products. In this study, the authors underlined that this primer set was most probably not able to distinguish between S. thermophilus and S. salivarius, which, being a closely related species, has an almost identical spacer sequence between the 16S rDNA and the 23S rDNA genes. Subsequently, Mora and colleagues [41], analyzing the sequence of the 16S-23S rDNA spacer region, demonstrated that a simple end-point PCR assay carried out using ThI/ThII primers was ineffective to discriminate between S. salivarius, S. thermophilus, S. bovis, S. macedonicus, S. waius and S. infantarius species. Nevertheless, the two primers were used in various intervention studies to carry out the identification of S. thermophilus strains recovered from stool samples [23,24,26]. More specifically, Brigidi et al. [23] performed an identification and enumeration of S. thermophilus from fecal samples of individuals who had been taking a multi-strain probiotic product using ThI/ThII primers, reporting a significant increase of S. thermophilus after administration of this probiotic product. Later, the same group of authors conducted a similar study using a culture-independent quantitative polymerase chain reaction (qPCR) method with the same primer set (ThI/ThII) for the identification and enumeration of several S. thermophilus strains showing its survival as well as colonization pattern after administration of both a probiotic preparation and commercial yogurt [24]. However, quantitative PCR of S. thermophilus was applied directly on feces, thus it was not possible to discriminate between live and dead cells as well as free DNA originated from lysed cells. In this case, a propidium monoazide (PMA-qPCR)-based methodology [57] would have been appropriate to directly quantify live S. thermophilus cells excluding dead cells and free DNA from the fecal samples. Moreover, in this study the primers where accurately tested for specificity against some intestinal and dairy species, among them S. faecium (several strains), Lactobacillus acidophilus (several strains), L. brevis, L. casei, L. crispatus, L. delbrueckii subsp. delbrueckii (several strains), L. delbrueckii subsp. lactis, Lactococcus lactis, (several strains), L. lactis subsp. cremoris (several strains), L. lactis subsp. lactis biovar diacetylactis, Escherichia coli (several strains), Enterococcus fecalis (several strains), Clostridium beijerinkii, C. perfringens, Bacteroides fragilis (several strains), Bifidobacterium bifidum (several strains), B. infantis (several strains), B. longum (several strains), B. adolescentis (several strains) but not against the phylogenetically close S. salivarius. Similarly, Mimura et al. [26] demonstrated higher levels of S. thermophilus after administration of a multi-strain probiotic product using the same primer set. These studies, based on the use of ThI/ThII primers, also showed that some of the subjects harbored S. thermophilus even after the run in and prior to treatment period, where the subjects were asked not to consume any food products containing this species. Therefore, we can speculate that primers may have actually detected S. salivarius strains, providing misleading results.
Contrary to previous data, del Campo and colleagues [25] provided scarce evidence of S. thermophilus recovery in human feces after daily yogurt consumption. In this study, not a single positive amplification for S. thermophilus was obtained from the total fecal DNA of 114 volunteers. The authors attempted to detect S. thermophilus using the THER-F/THER-R primer set, which is targeted to the lacZ gene. Nevertheless, due to some weaknesses in the protocols adopted for DNA extraction from fecal samples, the results obtained may have not been correctly analyzed. In addition, the specificity of the THER-F/THER-R primers for S. thermophilus was questioned in a later study by Elli and colleagues [27] who demonstrated that this primer set was not specific enough to set apart S. salivarius and detect exclusively S. thermophilus. Due to the lack of efficient identification methods, the same authors carried out a pulsed-field gel electrophoresis (PFGE) based on different SmaI digested chromosomes, in order to distinguish these two genetically close species and recover S. thermophilus from the feces of 20 healthy volunteers who had been consuming commercial yogurt. Likewise, it was suggested that there is a need for reliable molecular tools for the identification of orally administered S. thermophilus strains. In a 2012 study, García Hernández and colleagues [9] for the first time applied the DVC-FISH method to fecal samples for the elucidation of the survival rate of S. thermophilus strain CECT 801 to GIT transit. It must be observed, however, that the FISH probe used in the study, namely STH23 targeting the 23S rRNA gene, may not be specific enough for S. thermophilus because only one single base mismatch was present between the FISH probe target region of S. thermophilus and S. salivarius. In 2009, Ongol et al. [58] developed a real-time PCR method targeting a gene encoding a 16S rRNA processing protein (rimM) for the detection of S. thermophilus in dairy products. The authors tested the primer set against several lactic acid bacteria, including S. salivarius, demonstrating its high specificity but failed to amplify some S. thermophilus strains.
In light of the scientific literature cited we can, therefore, conclude that to date there are no taxonomically correct assays that allow to unambiguously identify S. thermophilus strains and distinguish them from those belonging to S. salivarius in a stool sample. 4.2. Culture-Independent Detection and Identification of S. thermophilus
The problems related to the incorrect identification of S. thermophilus are not limited to the studies aimed to verify the recovery of live cells in stool samples during intervention studies. We are living in the microbiota era, and the role of microorganisms is becoming increasingly relevant in all ecosystems, including the human ecosystem. Several studies have been focused on the role of diet- and food-associated microorganisms on gut microbiota and human health. The complexity of the taxonomy of S. thermophilus/S. salivarius/S. vestibularis group was often completely ignored also in this research field. Francavilla and colleagues [59], in a study aimed to characterize the salivary microbiota and metabolome associated with celiac disease, reported that S. thermophilus levels in human saliva were markedly decreased in a group of subjects that undergo a gluten-free diet. In this study saliva microbiota was characterized by 16S rRNA gene amplicon library sequencing, and the authors did not take into consideration both the taxonomy and the ecology of the environment they studied, making the readers erroneously believe that S. thermophilus is a common inhabitant of our oral cavity. More recently, Pasolli and colleagues [60] published an interesting study aimed to elucidate to what extent the lactic acid bacteria we ingest through the consumption of fermented food become members of the gut microbiome. The authors analyzed 9445 metagenomes from human samples and demonstrated that the prevalence and abundance of lactic acid bacteria species in stool samples is generally low and linked to age, lifestyle, and geography, with S. thermophilus being one of the most prevalent species [60]. To reach this conclusion, the authors focused on a defined list of genomes to be used as reference for the quantification of the prevalence of lactic acid bacteria species in the human gut, but unfortunately only the genome of S. thermophilus was present in the list, whereas the genome of S. salivarius was not considered at all [60] although the latter is recognized as a major human commensal [30]. Therefore, how can we provide adequate scientific evidence towards the statement that the increased consumption of yogurts and other dairy products are the sources of S. thermophilus in our gut ecosystem? Moreover, which metabolic features of S. thermophilus would guarantee adaptation of this species to the human gut environment? Why did the authors not consider that S. thermophilus was described as an example of genomic regressive evolution for adaptation to the milk environment [33,34]? In other studies [61,62] aimed to find correlation between the diet and the gut microbiota composition, where the proper reference genomes have been used, S. thermophilus was not considered as a human gut inhabitant.
5. Conclusions
Growing interest in the probiotic market, together with the increasing number of single and multi-strain products, is not always accompanied by scientific studies aimed to address the health benefit on the host of such products. In the last few years, some efforts have been made to evaluate the quality levels of products that are commercialized [63,64,65,66,67]. However, limited efforts have been made to develop molecular or phenotypic tools able to accurately identify the species and/or the strains administered as probiotics in intervention studies. The accurate taxonomic identification is, therefore, a paramount issue to be validated for the compliance of probiotic food and supplement products. Without a correct taxonomy assignment of the species/strains that should contain probiotic traits, the interpretation of the results obtained from the intervention studies is thwarted. This is especially the case of S. thermophilus, whose probiotic status has been in debate for decades. Being S. thermophilus a species with high economic relevance for the probiotic market, and S. salivarius one of the major human commensals able to colonize several human body-related sites, including the digestive tract [30], the correct identification of these taxa should be of high interest for the food and pharma industry. Another important issue arising from the reviewed literature is the absence of guidelines and protocols for the recovery from stool samples of orally ingested probiotics. The guidelines should recommend a proper study design based on a double-blind, placebo-controlled crossover design, an appropriate washout period together with the application of a species-specific plate culture method (if available), and/or the use of strain-specific molecular tools to correctly identify the orally administered probiotic/s. Moreover, among the commonly adopted exclusion criteria used in the intervention studies (e.g., antibiotic consumption prior to the start of the study, consumption of antacids or prokinetic gastrointestinal drugs, history or presence of significant intestinal diseases) the exclusion of the subjects showing a positive detection of probiotic strain in fecal samples during the run in or the placebo intake period should be considered because it might represent a possible compliance violation due to unauthorized probiotic intake.
Enlarge this image.Figure 1. Schematic representation of the criticisms associated to the identification of S. thermophilus strains in human stool samples during intervention studies. Gb, gastric barrier; GIT, gastrointestinal tract.
| Product Brand Name | S. thermophiles Strain | Manufacturer | Colony-Forming Units (CFU)/Dose | Country of Origin |
|---|---|---|---|---|
| Fermental | n.d. | ESI S.r.l. | 2 bilions/capsule | Italy |
| Floratrex | n.d. | Global Healing Center | 75 bilion/0.8 g | USA |
| Lactoflor AB | n.d. | Global Medic | 500 billion/capsule | Ecuador |
| Lactoflor Probiotic | n.d. | Lactoflor | 2 billion/0.4 g | Bulgaria |
| Multibiotics | n.d. | NutriZing | 50 billions/g (capsules) | UK |
| Neuflor | Z57 (BCCM: LMG P-21908) | Yamamoto nutrition | 56 billion/0.8 g | Italy |
| Nexabiotic Advanced | n.d. | DrFormulas | 17.25 billion/capsule | USA |
| NOW Probiotic-10 | St-21 | NOW Foods | 50 billion/capsule | USA |
| Oti Probioti | SP4 | O.T.I. Officine Terapie Innovative S.r.l. | 25.2 billion/4 capsules | Italy |
| Perfect Biotics | n.d. | Probiotic America | 30 billion/capsule | USA |
| Pro-100 Ultra | n.d. | Natures Aid | 100 billion/capsule | UK |
| PRO-30 Max | n.d. | Natures Aid | 30 billion/capsule | UK |
| PRO-B ACTIVE | n.d. | Lilly Drogerie | 14 bilions/capsule | Serbia |
| PROBIO7 | n.d. | PROBIO | 4 billion/capsule | UK |
| Probioguard | n.d. | Lamberts | 4 billion/capsule | UK |
| Probiona Plus | n.d. | Tauron Ventures GmbH | 30 billion/capsule | Germany |
| Probiotic supplement with vitamins | SD5207 | L’Angelica Istituto Erboristico | 18 billions/1.8 g (soluble sticks) | Italy |
| Prodefen | PXN 66 | Italfarmaco S. A | 10 billion L. rhamnosus +1 bilion (other strains)/1 g (sachets) | Spain |
| Protexin Bio-Kult | PXN 66 | Probiotics International L.t.d. | 10 bilion/g (capsule) | UK |
| Synbiotic365 | UASt-09 | United Naturals | 20 billion/capsule | Canada |
| Ultra-potency | ST-21 | Custom Probiotics | 320 billion/0.8 g (powder) | USA |
| Visbiome | DSM24731 | ExeGi Pharma | 1125 billion/g (capsule) | USA |
| Vivomixx | DSM 24731 | Mendes S.A. | 450 billion/4.4 g (sachet) | Switzerland |
| VSL#3 | BT01 | Actial Farmaceutica S.r.l. | 450 billion/4.4 g (sachets) 112 billion/658 mg (capsules) 45 billion/1.5 g (sticks) | Italy |
| Yovis | Z57 (BCCM: LMG P-219089) | AlfaSigma | 50 billion/1.5 g (sachets) 50 billion/0.7 g (capsules) 25 billion/10 mL (falcons) | Italy |
Abbreviations: n.d.: strain code not declared; DSM: German Collection of Microorganisms and Cell Cultures GmbH; BCCM: Belgian Co-ordinated Collections of Micro-organisms.
| Product | Used Tool | Target Species/Gene | Species-Specificity | Other Potentially Detected Species | Reference |
|---|---|---|---|---|---|
| Probiotic food supplement | Standard plating | S. thermophilus | no | S. salivarius, S. vestibularis | [22] |
| Probiotic food supplement | End-point PCR | 16S-23S rDNA spacer region | no | S. salivarius, S. vestibularis | [23] |
| Probiotic food supplement and Yogurt | End-point PCR, qPCR | 16S-23S rDNA spacer region | no | S. salivarius, S. vestibularis | [24] |
| Probiotic food supplement | End-point PCR | 16S-23S rDNA spacer region | no | S. salivarius, S. vestibularis | [26] |
| Yogurt | End-point PCR, DNA-hybridization | lacZ gene | no | S. salivarius, S. vestibularis | [25] |
| Yogurt | End-point PCR, PFGE | lacZ gene, Profiles of SmaI-digested chromosomes | no | S. salivarius, S. vestibularis | [27] |
| Yogurt | DVC-FISH | 23S rRNA | no | S. salivarius, S. vestibularis | [9] |
Abbreviations: PCR: polymerase chain reaction; qPCR: quantitative polymerase chain reaction; PFGE: pulsed-field gel electrophoresis.
Author Contributions
Conceptualization, D.M.; methodology, D.M. and S.A.; investigation, A.M. and R.C.; writing-original draft preparation, A.M. and R.C.; writing-review and editing, D.M., A.M., R.C. and S.A.; supervision, D.M. All authors have read and agreed to the published version of the manuscript.
Funding
University of Milan partially covered the open access APC.
Conflicts of Interest
The authors declare no conflict of interest.
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Anđela Martinović, Riccardo Cocuzzi, Stefania Arioli and Diego Mora*
Department of Food Environmental and Nutritional Sciences (DeFENS), University of Milan, via Celoria 2, 20133 Milan, Italy
*Author to whom correspondence should be addressed.
© 2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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