The interest in the field of beneficial microbes has emerged multiple folds since its inception by the Russian Noble laureate, Elie Metchnikoff. The term Probiotics, taken as an un-challenged synonym to beneficial microbes, has gained popularity over the years and has found application in several general health and clinical scenarios. Probiotics are live microorganisms, which when administered in adequate amounts confer health benefits to the host (FAO/WHO, 2002). Probiotic formulations are being developed and standardized for both human and animal consumption. Different dairy/functional foods/dietary supplements and pharma formulations harbor probiotic strains, intended for various health benefits in humans. Probiotics have also found application in animal feed for prevention of gastrointestinal infections, with extensive use in the poultry and aquaculture industries (Hong et al., 2005). The consumer awareness, search for alternate, safe and cost-effective treatments, and concern of developing antibiotic resistance has compelled researchers to find an alternate to ongoing therapeutic regimes, mainly dependent over antibiotics. Among the large number of suggested options, probiotic therapy seems to be the most viable one, with long history of consumption and assured safety. LAB and Bifidobacterium spp. are the two globally recognized groups of bacteria that are being consumed for their potential health benefits. Other preferred bacteria include strains of Enterococcus, Streptococcus and Bacillus spp. (Majeed et al., 2016); along with few strains of Saccharomyces spp. Several reference probiotic strains have been shown to play a potential role in management of several clinical scenarios viz. diarrhea, inflammatory bowel disease, obesity, type 2 diabetes, cardiovascular disease, cancer etc. (Mallappa et al., 2012; Panwar et al., 2014, 2016; Ranji et al., 2015). It has been clearly understood that the gut inhabitants and their proper balance is the foremost criteria that determines healthy status, particularly in terms of metabolic disorders (Wang et al., 2015). Research updates from several in vivo (Ellekilde et al., 2014) and human clinical trials (Shimizu et al., 2013; Scott et al., 2015) supports the hypothesis that any strategies targeting the re-customization of the gut inhabitants can help in reverting back to normal healthy phenotype.

Besides the commonly explored strains, bacterial spore formers, mostly of the genus Bacillus do carry probiotic attributes. The value of non-spore former LAB for the maintenance of human and animal health has been acknowledged both scientifically in terms of published research data and commercially in form of the availability of probiotic products. However, in comparison to LAB, bacterial spore formers have not gained high popularity, particularly in terms of research interest (Figure 1). Several Bacillus strains have been screened for their potential probiotic functionalities, in several in vitro and in vivo models. Besides qualifying the mandatory bench marks for a candidate probiotic; Bacillus spp. offers higher acid tolerance and better stability during heat processing and low temperature storage (Bader et al., 2012). Additionally, they have also been shown to possess pathogen exclusion, anti-oxidant, antimicrobial, immuno-modulatory (Lefevre et al., 2015; Shobharani et al., 2015; Ripert et al., 2016) and food fermentation (Terlabie et al., 2006) abilities.

Furthermore, scientific reports supported with evidence of safe use and long history of consumption supports the candidature of spore formers as potential probiotics and as functional food supplements due to their significant capacity of production of extracellular enzymes. Bacillus spp. has been used for production of food grade amylase, glucoamylase, protease, pectinase and cellulase in varying food stuffs (Ghani et al., 2013; Ouattara et al., 2017). Different species of Bacillus has also been used for the production of additional nutraceuticals including vitamins (e.g., riboflavin, cobalamin, inositol) and carotenoids for the synthesis of several health supplements for human consumption (Mohammed et al., 2014; Tanaka et al., 2014; Takano, 2016). Nevertheless, despite above benefits, these strains have not gained much importance and attention in current functional food industry due to their relatedness with few human pathogens. Few of the members of Bacillus spp. particularly, B. cereus, B. weihenstephanensis, B. anthracis, and B. thuringiensis species are known to produce various toxins, including ematic or enterotoxin (Cereulide), Bipartite exotoxins: protective antigen- lethal factor (PA-LF) and PA-edema factor (PA-EF), Cry and Cyt. Among them, Cereulide produced by B. cereus and B. weihenstephanensis is a major cause of food borne intoxications; while PA-LF and PA-EF are B. anthracis generated toxins associated with deadly illness in humans and animals.

Thereby, to understand the nature of beneficial spore former probiotic strains, their probiotic potential and safety concerns are important; not only because of their complexity and behavior in human GIT, but also due to their allochthonous (free living) nature, questioning their ability to colonize in the human gut (Hong et al., 2005). Though, the members of Bacillus genus have been consumed in the form of fermented foods since long time (Tamang et al., 2016), concerns regarding their safety are also raised. This review highlights the probiotic candidature of spore forming Bacillus spp. and presents an overview of the proposed health benefits, including application in food and pharmaceutical industry. The associated safety and licensing issues that influence the use of Bacillus spp. for commercial development has been summarized, together with evidence showing the growing need to evaluate the safety of individual Bacillus strains as well as species on a case by case basis.

Bacillus signifies a Gram-positive, rod shaped, spore-forming, aerobic or facultative anaerobic bacterium. In general, the genus Bacillus is designated as a group of soil inhabitants. However, Bacillus spp. can be isolated from varied sources including air, water, human and animal gut, and also from vegetables and food (Alou et al., 2015; Kotb, 2015). Nevertheless, Bacillus spp. represents the most heterogeneous group in terms of phenotypic and genotypic characters. Some distinct species have also been recognized as opportunistic pathogen or toxin producer in human or animal hosts. The genus Bacillus is closely related to Lactobacillus spp., the distinguished candidate probiotic. Both share the same class, Bacilli under the phylum Firmicutes (Figure 2).

Looking toward the probiotic prospective, it is proclaimed that the candidate probiotic should be isolated from the gut of the target population, which helps them to thrive well within the gut. However, elementary attributes of native flora for survivability are not essential for spore-former(s). Bacillus spores can survive in extreme acidity of stomach, and tolerate bile salts and other hostile conditions of GIT. Besides, bacilli are more stable during processing and storage of food and pharmaceutical preparations, which make them more suitable ingredient for health promoting formulations. Thereby, in addition to human sources, Bacillus strains with probiotic attributes are also isolated from fermented or unfermented food sources (Adewumi et al., 2014; Rao et al., 2015) and are commercialized in the form of diverse range of health supplements (Table 1).

It is believed that Bacillus spp. is not a natural inhabitant of gut. They get colonized in to the intestinal tract after consumption of vegetables or raw food materials contaminated with soil microflora. Moreover, ingestion of fermented cereals or beans, such as Iru and Natto also make their way in to the intestine. Findings from in vitro studies claim that vegetative cells and spores of B. cereus can well defend the GIT stress and adhere to the intestinal epithelium. However commensal gut microbiota possesses inhibitory activity against them (Berthold-Pluta et al., 2015). A study by Tam et al. (2006) demonstrated that spores of Bacillus spp. could readily be recovered in the range of 10³-10⁸cfu/g of human feces. The 16S rRNA gene phylogenetic analysis of isolates demonstrated the presence of 10 different Bacillus species in examined fecal samples of 30 volunteers (Tam et al., 2006). Hoyles et al. (2012) further studied the diversity of Bacillus spp. and related spore-former bacteria in human feces and documented that the majority of recovered isolates belonged to Bacillaceae family. Two species, B. clausii and B. licheniformis were recovered most frequently. To find out the stage of Bacillus in human gut, Casula and Cutting (2002) targeted a genetically engineered chimeric gene, ftsH-lacZ, which is selectively and strongly expressed in the vegetative cells of Bacillus subtilis and reported their presence throughout the GIT. They stated that the spores germinated in significant numbers in the jejunum and ileum, suggesting their colonization into the small intestine. Recently, Ghelardi et al. (2015) documented that the orally administered Bacillus spp. follows transient colonization in to the intestine. Nevertheless, the impact of allochthonous Bacillus strains on the profile of fecal flora of the host during transition period has been proven significant. Nyangale et al. (2014) observed that after 28 day treatment of Bacillus coagulans in elderly subjects, baseline populations of Faecalibacterium prausnitzii, Clostridium lituseburense and Bacillus spp. were significantly higher, relative to the placebo group. Likewise, a study by Adami and Cavazzoni (1999) in piglet model has also shown that the feeding of Bacillus coagulans CNCM I-1061 increased aerobic and anaerobic sporeformers, decreased lactococci, enterococci, anaerobic cocci, and fecal coliforms in the treatment group.

The consumption of vegetative cells and spores of Bacillus spp. by human beings is frequent through fermented foods and raw vegetables. A diverse range of Bacillus species are found to be associated to the natural fermentation of soy, locust been, maize, rice and many more substrates. For example, Natto (Japan), Gari (Africa) TapaiUbi (Malaysia), Douchi (China), Rabadi (India, Pakistan), Soibum (India), Ugba (Nigeria) etc. are among the popular functional foods naturally harboring the blend of Bacillus spp. and LAB. These fermented products exhibit unique sensory attributes, probably due to the activity of extracellular carbohydrate and protein degrading enzymes of Bacillus spp. origin (Table 2). The palatability and health promoting characteristic of these locally produced supplements has also attracted the attention of global market. A diverse range of LAB and Bacillus spp. isolated from such indigenous foods has been studied and are being used for the commercial preparations of functional products (Angmo et al., 2016; Von Mollendorff et al., 2016). Respectively, the strains of B. subtilis, B. subtilis var. natto, B. clausii, B. licheniformis, and B. coagulans etc. are being utilized to improve the quality and demand of functional foods globally (Beaumont, 2002; Chantawannakul et al., 2002; Inatsu et al., 2006).

Bacillus strains are also getting recognition as potential probiotics which could promote human health by direct consumption of high concentrations of viable number of cells (Abdhul et al., 2015; Manhar et al., 2016). Several Bacillus probiotic strains have been approved by regulatory agencies of different countries for human use and are popular as general health promoting pharmaceutical formulations in global market (Table 1). So far commercial products of Bacillus composing functional foods are not popular in nutraceuticals market because the debate over probiotic vs. pathogen tag of Bacillus spp. is persisting in the research and production terrains. Hence, it’s important to clearly understand the phenotypic and genotypic characteristics of selective Bacillus spp. and their substantiation with those having GRAS status, to reach a consensus over the same.

Bacillus spp. has received considerable taxonomic attention because of its economic as well as medical importance. The genus Bacillus has undergone considerable taxonomic changes over time. The number of species allocated to this genus increased to 318 in the “List of prokaryotic names with standing in nomenclature”¹. With the advent of molecular taxonomy, Ash et al. (1991) separated 51 distinct Bacillus species into five phylogenetic clusters. In this review, we are looking over the significance and approach of Bacillus probiotics in current scenario. Thus, it will also be interesting to take note of the evolutionary connections of probiotic Bacillus species/strains with other members of the genera. According to Ash et al. (1991), group 1 of Bacillus forms the largest cluster of 28 species. Evolutionary distance tree showed specific relation between species, for example, there were three distinct clades of closely related species. First clade included B. subtilis, B. atrophaeus, B. amyloliquifaciens, B. lautus, B. lentimorhus, B. licheniformis, B. popilhe, and B. pumilus. Second and third clades comprised of B. anthracis, B. cereus, B. meduso, B. mycoides, B. thuringiensis, B. maroccanus, B. simplex, and B. psychrosaccharolyticus. However, all remaining members of the group did not show any significant relationship with them. Group 2, 3, 4, and 5 consisted of 7, 10, 2, and 3 species respectively. Two species, B. alcalophilus and B. aneurinolyticus remained ungrouped and formed a separate line of descent. Interestingly, the available data points out that both the probiotic Bacillus species (e.g., B. subtilis, B. coagulance, B. licheniformis, and B. megaterium) and potential human pathogens (B. anthracis and B. cereus) fall into group 1; however, both the forms are separated into distinct clans. Therefore, more deep analysis of the taxonomic positions of these species is needed to reach a definite conclusion.

In this context, Xu and Cote (2003) made an effort to determine the phylogenic relationship among 40 Bacillus species using nucleotide sequences of the 16S rDNA and the 16S–23S internal transcribed spacer (ITS). In this study, comparative sequence analysis of the 16S-23S ITS sequences, revealed 10 distinct phylogenetic clusters. Twenty-six evaluated Bacillus species were separated in seven groups; with groups II, V, VI, and X comprising of seven, two, nine and five Bacillus species, respectively (Figure 3). Bacillus subtilis, the type species fall in Group VI along with B. amyloliquefaciens, B. atrophaeus, and B. mojavensis. B. coagulans was placed in group I; B. maroccanus and Bacillus simplex in Group II; and B. anthracis, B. cereus, B. mycoides, and B. thuringiensis in Group X. This study revealed that two major pathogenic spp. of Bacillus (B. anthracis and B. cereus) fall into the Xth group, which is apparently unrelated to the Bacillus spp. used as human and animal probiotics. Interestingly, B. cereus exhibits virulence in a strain specific manner. The pathogenic characteristic depends over strain and variety specific production of several extracellular factors viz. (phospholipase, cereulide (emetic toxin), enterotoxin Hbl, non-haemolytic toxin (Nhe), haemolysin IV) having role in cellular membrane disruption and induction of necrotic enterocolitis cytotoxin (Berthold-Pluta et al., 2015). Toxicity of virulent forms of B. cereus had been linked to the expression of plcR gene, that codes for most of the extracellular virulence factors (Hbl, Nhe, cytK) and proteins (Ramarao and Lereclus, 2006). Recently, data obtained from draft genome assemblies of 25 B. cereus strains clearly indicated sub-division of B. cereus into seven phylogenetic groups. Frequent horizontal transfer of pathogenicity factors among B. cereus has been proposed as an important factor determining the distribution of Bacillus spp. among pathogenic, non-pathogenic and probiotic species. The enterotoxin operons viz. nheABC and hblCDAB are chromosomally located and are abundant within B. cereus, which along with possibility of horizontal transfer raises safety concerns (Bohm et al., 2015).

These studies have revealed the phylogenetic relations among important species of Bacillus genus and are also indicating toward the necessity of more profound process for the selection and identification of Bacillus probiotic candidates. In this way, the complete genome sequencing and comparative analysis of various close relative Bacillus species of different groups has been provided by different research groups (Rey et al., 2004; Kolsto et al., 2009; Earl et al., 2012; Jeong et al., 2016; Krawczyk et al., 2016; Fan et al., 2017). The data of deeply sequenced Bacillus species from different sources can be utilized for the accurate identification and characterization of candidate probiotic strains. This may include characterization using advanced molecular techniques (such as PFGE, 16S rDNA sequencing, AFLP and MLST etc.).

Bacillus spp. are preferentially aerobic to facultative aerobic (Hoffman et al., 1995), germination and outgrowth of spores in the intestine seem difficult to envisage because the mammalian intestine is an anaerobic environment. In order to qualify as a potential probiotic candidate, the Bacillus strains must possess the primary requirement of GIT stress tolerance, besides having good adhesion and bio-therapeutic properties (Thakur et al., 2016). Survival under the GIT stress represents another challenge for safe transit and localization in the gut. Bacilli are normally considered soil organisms however, number of them including B. subtilis have been reported in feces and ileal biopsies of volunteers (Fakhry et al., 2008). In this regard, Hong et al. (2009) reinforced a growing view that B. subtilis and probably other species had adapted to life within the human GIT, including ability to form biofilm, sporulate anaerobically and produce antimicrobials, and should be considered gut commensals, rather than solely soil microorganisms.

Earlier, Hyronimus et al. (2000) evaluated thirteen spore forming lactic acid bacilli for their resistance to acid and bile salt. B. laevolacticus DSM 6475 and B. racemicus IAM 12395 were found to tolerate pH 2.5 for up to six hours. Also, B. racemilacticus and B. coagulans strains were reported to be tolerant to bile concentrations over 0.3% (w/v). This study indicated high acid tolerance of Bacillus spp., however, the same was questionable for bile tolerance for few strains. In a recent study, twenty healthy European subjects were administered orally with Enterogermina^® containing spores of four strains of B. clausii, which could survive transit through the human GIT, during which germination, out-growth and multiplication could happen (Ghelardi et al., 2015). Similar to non-spore forming Lactobacillus spp., the survival rate of spore forming bacilli is also strain specific. Additionally, food matrix also plays an important role in survival of probiotics during simulated gastric juice conditions (Karu and Sumeri, 2016).

Different Bacillus strains have been reported to display antimicrobial, anti-oxidative and immune-modulatory activity in the host. The elements behind beneficial attributes of Bacillus spp. probiotics are explored in various studies, wherein these activities were found connected to their ability to produce antimicrobial peptides, small extracellular effector molecules and their ability to interact with host with the help of adhesion and attachment features (Khochamit et al., 2015). The antagonistic activity of Bacillus spp. has been explored against large number of pathogens. A study by Pinchuk et al. (2001) also reported the anti H. pylori activity of tested probiotic B. subtilis strains, which was attributed to the secretion of aninocoumacin A antibiotic. The antagonistic activity of aninocoumacin A was also documented against enteric E. faecium and Shigella flexneri. An interesting communication by Ripert et al. (2016) revealed that the probiotic B. clausii O/C strain protected vero and Caco-2 cells from the cytotoxic effect of Clostridium difficili and B. cereus toxins. This activity was mediated by serine protease(s) of B. clausii. On the other hand, exclusion of pathogen by the inhibition of bacterial biofilm is another potential attribute proposed for Bacillus strains. In this context, Gobi et al. (2016) demonstrated that the cell free extracts of B. licheniformis Dahb1 decreased the microbial adhesion to hydrocarbon, exopolysaccharide and biofilm metabolic activity, and decreased biofilm formation by the virulent V. parahaemolyticus Dahv2, in Asian catfish.

Recently, a bacteriocin producing strain of probiotic Bacillus coagulans had been isolated from traditional fermented fish of Manipur, India. The purified bacteriocin of low molecular weight displayed broad spectrum of antimicrobial activity against food borne and related clinically relevant pathogens, besides having lower cytotoxicity (Abdhul et al., 2015). Earlier, Joseph et al. (2013) also isolated and characterized bacteriocin producing strain of B. subtilis and displayed high level of antimicrobial activity of partially purified bacteriocin against foot ulcer bacterial pathogens, with highest recorded against Klebsiella spp. Such bacteriocin producing strains of Bacillus spp. have potential to be introduced as food biopreservative and as an antimicrobial in human and animal infections. In spite of pathogenic status of B. cereus, this species has also been explored for probiotic attributes. For example, B. cereus var. vietnami which used in Biosubtly^DL was found to produce bacteriocins like activity against different Bacillus species and it was shown to persist the mouse GIT up to 18 days. However, it was also found to produce enterotoxins (Duc et al., 2004). In addition, B. cereus var. toyoi, B. cereus YB-2, B. cereus G19 and B. cereus BC-01 were studied for their beneficial effect on livestock including rabbit, piglets and sea cucumber (Trocino et al., 2005; Altmeyer et al., 2014; Li et al., 2015).

In the food sector, the global trend is to incorporate probiotics into food matrix in order to provide some health-promoting component(s) beyond its traditional nutrients (Butel, 2014). Lactobacillus and Bifidobacterium spp. have earned many health claims, including their immune-modulation (Shida and Nomoto, 2013; Maneerat et al., 2014), anti-mutagenic (Sah et al., 2014), lowering of plasma triglycerides (Guo et al., 2013; London et al., 2014) and the potential to modulate host physiology via direct and indirect means (Di Caro et al., 2005; Fujiya et al., 2007). On contrary, there are few published reports dealing with the health benefits of probiotic spore formers (Figure 1). Efficacy of Bacillus spp. as probiotic has been screened in several in vitro and in vivo animal models and a few have also been validated in human clinical trials. The available data from these studies has presented the beneficial effects of different strains of Bacillus spp. for human health. For example, several researchers have recognized the preventive role of Bacillus probiotic in gut physiology impairment conditions (Lopetuso et al., 2016; Zhang et al., 2016). The amelioration of dysbiosis and gut inflammation by probiotic Bacillus strains was established by the ability of balancing gut flora toward beneficial microbial population and associated anti-inflammatory agents which helped to recover intestinal mucosa from illness generated injuries. Recently, an in vivo study by Haldar and Gandhi (2016) revealed that the oral administration of skim milk containing Bacillus coagulans B37 and Bacillus pumilus B9 decrease coliform counts in feces of treatment groups. Besides, the beneficial effect of B. coagulans on the gut metabolism is also evaluated by Lee et al. (2016), who reported that feeding of B. coagulans along with soya pulp to cholic acid fed rats, suppressed the production of secondary bile acid, improved intestinal permeability and reduced the bactericidal effect of bile acid which supported the growth of beneficial microbiota into the intestine. An exopolysaccharide (EPS) producing strain of B. cereus SZ-1 delayed DNA damage, increased cell survival and glutathione and catalase expression in H₂O₂ induced PC12 cells. The purified EPS from B. cereus could be useful for preventing oxidative DNA damage and cellular oxidation in pharmaceutical and food products (Zheng et al., 2016). The protective effect of Bacillus probiotics against toxins has also been reported by Ripert et al. (2016). In this interesting communication, authors perceived involvement of secreted serine proteases from B. clausii in normalization of toxin produced by Clostridium difficili and B. cereus. The purified component also exhibited antitoxic potential on Vero cell line treated with cell culture supernatants of both pathogens. Similarly, an antimicrobial peptide, antilisterial Subtilosin A derived from Bacillus tequilensis FR9 was also reported to exhibit pathogen invasion protection ability in HCT-116 human colon carcinoma cell line (Rani et al., 2016). In contrast, the bioavailability of nutraceuticals has seen to be increased in the presence of Bacillus strains. For example, Dudonné et al. (2015) has shown increased microbial degradation products of native cranberry phenolic compounds in B. subtilis CU1 supplemented rats.

The positive effect of Bacillus spp. to distant cells, beyond GIT has also been established by several researchers. In this context, Foligné et al. (2012) studied the effect of probiotic Bacillus subtilis PB6 on cytokine release profile of human immunocompetent peripheral blood mononuclear cells (PBMC). Strain PB6 induced substantial levels of IL-10 but very low levels of IL-12, TNFα, and IFNγ on human PBMC. In an interesting study, Abhari et al. (2016) demonstrated that oral administration of B. coagulans and inulin combination could improve the biochemical and clinical parameters of rheumatoid arthritis in rat model. Briefly, pre-treatment with the symbiotic diet significantly inhibited the fibrinogen, serum amyloid A and TNFα production, and significantly inhibited the development of paw swelling induced by complete Freund’s adjuvant. The immune-modulatory potential of probiotic B. cereus for livestock has also been investigated by few researchers. In an animal study, dietary supplementation of B. cereus var. toyoi to sows and piglets resulted in its recovery from feces, however, interestingly probiotic was detected in piglet feces before its dietary intake, indicating a secondary route of its intake besides diet. Dietary intake of B. cereus var. toyoi reduced the incidence of liquid feces and diarrhea (Taras et al., 2005). Additionally, the positive effect of B. cereus var. toyoi on secretion of interferon gamma and IL-4 and natural killer receptor 2D (NKG2D) expression in intraepithelial CD5+ γδ T cells of piglets has been suggested by few workers (Schierack et al., 2007; Altmeyer et al., 2014). Additionally, components secreted by potential probiotic Bacillus strains also possess anti-cancer activity. In an important analysis by Lee et al. (2012), surfactin like compound of Bacillus subtilis CSY191 could inhibit the growth of MCF-7 human breast cancer cells in a dose-dependent manner. Furthermore, the health benefits of Bacillus probiotic strains have also been proven in human subjects of different health and age groups. Some of the important clinical trials demonstrating the impact of spore-former probiotic Bacillus strains have been highlighted in Table 3.

Besides having direct effect over host health, strains of Bacillus are currently also being employed for protective and therapeutic effect against several systemic clinical syndromes particularly, metabolic disorders. Several studies have established that natural products involving Bacillus spp. can be an alternate, safe and cost effective therapy for the management of metabolic syndromes. In one such study, solid state fermentation of soybean with B. amyloliquefaciens resulted in production of 1-Deoxynojirimycin, a potent alpha-glucosidase inhibitor (Cai et al., 2017). On similar lines, 13 weeks of dietary intervention with B. licheniformis 67 fermented soybean paste significantly prevented obesity related parameters in diet induced obese C57BL/6J mice (Choi et al., 2016). Fermented soybean fed group displayed lower values for blood glucose, insulin, serum and hepatic lipid profile, and body weight compared with high fat diet control group. The anti-obesity activity was attributed to the production of poly gamma glutamic acid by selective strains. The anti-diabetic functionality of B. licheniformis fermented soybean had also been attributed to the reduced accumulation of beta amyloid in brain hippocampus, preventing beta amyloid mediated insulin resistance and beta cell death. The study displayed glucose homeostaisis effects of fermented soybean in diabetic rats with experimental Alzheimer’s type dementia (Yang H.J. et al., 2014). Similarly, Purified exopolysaccharide from B. subtilis suppressed cardiovascular disease related parameters in streptozoticin induced diabetic rats (Ghoneim et al., 2016). In this study, the therapeutic effect of EPS was recorded due to reduced blood glucose, troponin, total serum cholesterol, LDL, and VLDL as well as suppression of ICAM and VCAM expression. Earlier, Zouari et al. (2015) also explored the anti-diabetic and anti-lipidemic properties of biosurfactant produced by B. subtilis SPB1 strain in alloxan induced diabetic rats. Upon oral administration, the biosurfactant reduced the plasma alpha-amylase activity and rendered protection to pancreatic beta cells. Besides displaying hyperglycemic effects, biosurfactant administration regulated serum lipid profile by promoting HDL-cholesterol and delaying the absorption of LDL-cholesterol and triglycerides. Aforesaid studies clearly support the rich bio-therapeutic potential of spore forming Bacillus strains, which further needs validation in human clinical trials. In light of the above reports, it can be stated that the candidate probiotic Bacillus strains themselves or their metabolites could also be considered as a potential candidate for management of metabolic disorder.

Several mechanistic studies have attempted to underline the probable mechanism of action of candidate probiotic Bacillus strains. The mechanisms by which spore forming probiotics (SFP) could enhance health of the host include stimulation of immune system, synthesis of different antimicrobials, like bacteriocins, enzymes and modulation of the composition of gut microbiota (Figure 4). The mechanism behind establishment of gut homeostasis involves promotion of growth of other beneficial microbes and suppression of pathogen and pathogen induced inflammatory response of intestinal mucosa. Microbial interference therapy depends on production of antimicrobial(s) by different probiotic strains. Bacillus spp. are known to produce several antimicrobial substances, e.g., bacteriocins, bacteriocins like inhibitory substances (e.g., Subtilin and Coagulin) and antibiotics (e.g., Surfactin and Bacilysin). B. subtilis var. natto has also been shown to inhibit the growth of Candida albicans in the intestinal tract, which is attributed to production of antibiotic, Surfactin, having activity against yeast (Ozawa et al., 1979; Nagal et al., 1996). In a recent study, B. subtilis R0179 was shown to have significant inhibitory effect on the growth of Candida spp. proposing it as an alternate therapy against oral candidiasis (Zhao et al., 2016). Also, Biosporin^® containing B. subtilis 2335 and B. licheniformis 2336 (Biofarm, Ukraine) had been applied as probiotic supplement for humans and it possess antibacterial activity against Heliobacter pylori (Pinchuk et al., 2001). On the other hand, the positive influence of probiotic Bacillus strains on the growth and composition of commensal and beneficial species on gut could be mediated by the production of extracellular enzymes, vitamins and peptides. The impact of probiotic strains on host physiology is also a major factor behind maintenance of gut homeostasis. A comprehensive study in human subjects using DNA microarray technique observed that the genes involved in inflammation, immune response, defense response, intestinal permeability, cell adhesion, cell growth, cell differentiation, cell signaling, apoptosis, signal transcription, and transduction in intestinal mucosa were modulated upon B. clausii consumption (Di Caro et al., 2005). Surface-associated proteins from vegetative cells and spores of B. cereus might play an important role in interaction between these strains within human GIT (Sanchez et al., 2009). In addition, Fujiya et al. (2007) has also explained the role of quorum sensing molecules (QSMs) secreted by B. subtilis strain JH 642 in preservation of intestinal health. In this study, authors found that quorum sensing pentapeptide, competence and sporulation factor of B. subtilis JH 642 is involved in organic cation transporter mediated activation of p38 and MAPK pathways in Caco2_bbe cells. This interaction serves an example of probiotic mediated change in behavior of host and composition of colonic flora.

The impact of probiotic Bacillus strain has also been reported on distal organs. For instance, the spores of B. clausii (Enterogermina^®) were shown to enhance the production of IFN-γ in murine spleen cells, rabbits and mice animal models (Muscettola et al., 1991, 1992; Kosak et al., 1998). Vegetative cells of B. firmus have been shown to stimulate the proliferation of human peripheral blood lymphocytes in vitro (Prokesova et al., 1994). Also, spores of B. subtilis PB6 from Anaban^TM had displayed anti-inflammatory effect in mice models that has been observed to be mediated through the modulation of IL-10, TNF-α and IFN-γ expression (Foligné et al., 2012).

Safety of a food product signifies the absence of any notable adverse health effects upon consumption under defined conditions (Kalliomäki et al., 2001). Probiotics are recognized for their long history of safe use. However, consumption in large amounts under immune compromised state may raise several safety concerns. Among Bacillus spore-formers, B. anthracis and B. cereus are well known pathogens. In case of B. cereus, pathogenicity varies from case to case; with some strains being the carriers for enterotoxin genes (Rowan et al., 2001). The occurrence of Bacillus spp. in food does not always cause foodborne illnesses or food spoilage; some species likewise, B. subtilis are used for preparation of East Asian fermented foods such as natto (Hosoi and Kiuchi, 2003). B. subtilis causes food-borne illnesses, with different symptoms, mainly vomiting (Kramer and Gilbert, 1989). At least one B. subtilis strain carries all three genes required to produce the Hbl enterotoxin normally produced by B. cereus (Rowan et al., 2001). On the other hand, Bacillus subtilis ATCC 6633 is known to produce a wide variety of antibacterial and antifungal compounds (Stein, 2005).

Furthermore, Bacillus spp. are used widely in transformation, whereas the plasmid encodes conjugative or mobile elements (Mullany et al., 2004). The commercial B. cereus IP5832 (Bactisubtil^®) was isolated from the stools of patients with diarrhea (Kniehl et al., 2003). The strain was later shown to carry genes coding for endotoxin (Duc et al., 2004). Toyocerin^® (Asahi Vet S.A., Tokyo, Japan), containing B. cereus var. toyoi, is licensed in EU for animal feed (reviewed in Cutting, 2011). In market, several probiotic Bacillus subtilis based products like BioGrow^®, mixture of B. subtilis and B. licheniformis (Provita Eurotech Ltd, Omagh, UK); BioPlus^®2B, mixture of Bacillus spp. (CHR. Hansen, Hoersholm, Denmark, EU approved); and AlCare^TM, containing B. licheniformis (Alpha-pharmaInc, Melbourne, VIC, Australia, not licensed in EU) are being used for animal feed and aquaculture.

In South East Asia, different probiotic products containing Bacillus stains, either as single or mixed with other Lactobacillus strains, are used as an alternative to conventional antibiotics. These strains are marketed as antibiotic resistant probiotics. Therefore, there is a risk of transferring antibiotic resistance genes to commensal and pathogens in gut of humans and animals and release of drug resistance genes to the environment through feces (SCAN, 1999, 2003). Enterogermina^® contains spores of four strains of B. clausii, which are resistant toward chloramphenicol and tetracyclin. Suspension of these spores (2 × 10⁹cfu/ml) is used as medical supplement along with antibiotics against infantile diarrhoea (Green et al., 1999; Senesi et al., 2001).

Esporafeed^® Plus, a feed additive containing B. cereus strain carrying a plasmid borne tetB gene was withdrawn from use in different European countries (SCAN, 1999). Also, due to concern of transfer of erythromycin resistance, AlCare^TM was considered unsafe for feeding pigs (SCAN, 2002). In Vietnamese market, several Bacillus spp. products have been applied and licensed for human use such as, Biobaby^® (ILdongPharma Co., Ltd., Korea), which contains three different spore forming probiotics, including B. coagulans (incorrectly, Lactobacillus sporogenes, widely used in India and one strain that has been granted as GRAS by FDA in the United States), B. subtilis and C. butyricum. Also, several in vitro and in vivo studies were performed in order to examine the toxicity of different species including B. subtilis var. natto and Bacillus indicus (Hong et al., 2008), B. licheniformis 2336 (Sorokulova et al., 2008), and B. coagulans (Endres et al., 2009). All appear to show no indications of adverse effects indicating the most occurrence of illness associated with Bacillus probiotic strains supplement of humans are result of either opportunistic infections or miss-diagnosis (reviewed in Cutting, 2011). Recently, Zhu et al. (2016) evaluated the safety of 15 commercial probiotic B. cereus products in China, they found that these products represent a potential risk for public health in China because and they recommended stricter safety regulation for these products is needed.

The “health claims” of commercially available bio-therapeutics are allied to the viability, activity and composition of component microorganisms. Likewise, the entitlements of probiotic products being marketed as functional food, dietary supplement or drug are also elucidated by the state of probiotic strains. Thereby, the quality of commercial probiotic products is an important issue to be considered for regulation. Several researchers have identified discrepancies between labeled and actual contents of commercial probiotic products (Weese and Martin, 2011; Drago et al., 2013). Viability of probiotics, misidentifications at the genus/species level (marking Lactobacillus sporogenes in place of B. coagulans is a common example) and cross contamination by microorganisms are the main non-conformities during the evaluation of the quality of commercial probiotics. Consequently, despite the fact that significant amount of scientific literature is being produced about specific clinical benefits of probiotic microorganisms, there is an increasing demand for the legislative regulation on manufacturing practice, labeling and advertising of probiotic products.

Thereby some countries are developing their regulatory system to warrant the safety and wellbeing of consumers. In Japan, Food for Specified Health Use (FOSHU) system has defined functional food as ‘processed foods containing ingredients that aid specific bodily functions in addition to being nutritious’. The country has also regulation on the prevention of mislabeling of such foods. European countries have Food Products Directive for the regulation of food labeling. Probiotic foods also come under the regulation of this law. According to Directive, the contents in labeling must not be misleading for the purchasers. In UK, Joint Health Claims Initiative (JHCI) defines a health claim as ‘a direct, indirect or implied claim in food labeling, advertising and promotion that consumption of a food carries a specific health benefit or avoids a specific health detriment’. In United States, FDA has approved 12 health claims for foods. In addition, a joint FAO/WHO expert consultation on health and nutritional properties of probiotics in food have given scientific recommendations about the characterization, safety, efficacy, and labeling of the probiotic products. The report of this consultation also stated that the regulatory status of probiotics is not well established on an international basis (FAO/WHO, 2001). Thereby experts of consultation also made a number of recommendations pertaining to regulatory matters which will help to improve the regulatory status of functional food in global market.

The probiotic market share is valued at the size of USD 36.6 billion in 2015 which will be widened with over 7% CAGR growth from 2016 to 2023². The Asia pacific will make the largest industry participant as they accounted for more than 40% of the global industry. India, China, and Japan are the major contributing factors in this field while both India and China will also see maximum growth in upcoming years³. Growing awareness about health, lifestyle, and increasing issues related to metabolic and digestive disorders are important contributing factors in the hike in probiotic market share. Moreover, the presence of international companies is also increasing the attention of consumers toward this health promoting supplements. If we look by the types of organisms, the probiotic market is categorized into five groups, i.e., Lactobacillus, Bifidobacterium, spore formers, yeast and others. Hence, the spore former probiotics are making a major contribution in global nutraceutical as well as pharmaceutical market.

Probiotics enjoy the GRAS status and are freely consumed globally without any safety concern. Their efficacy and safety has been demonstrated in several in vitro, in vivo and human clinical trials. However, few recent studies have raised concern about their safety and dose in immune-compromised people (Redman et al., 2014). Although Bacillus probiotics have an overall excellent health promoting record, especially in preventing and curing of diarrhoea, giggivitis, H. pylori infection and maintaining homeostasis of intestine (Khodadad et al., 2013; Lefevre et al., 2015; Alkaya et al., 2016; Lopetuso et al., 2016). Their application with certain immune deficient population especially for critically ill, neonates and elderly groups should be evaluated and regulated carefully since reports related to bacteremia in immune-compromised patient treated with spore former and other probiotics has been recorded repetitively (Doron and Snydman, 2015). However, the importance of identification to strain level is also important to detect and eliminate any causal link between probiotics and strains isolated from immune-compromised hosts. Thereby, it is important to keep in mind that clinical trials of these formulations should cover the sufficient ratio of target population including people with low immunity.

FE, NR, and HP has drafted the manuscript. FE, NR, RG, CS, and HP equally contributed in writing of manuscript. HP did the editing of manuscript.

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